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Allanon - Shannara Wiki - Exploring The Magical World Of Shannara, Allernon

Allanon

Allanon is a main character in The Shannara Chronicles . based on the lead character of the same name from the original Shannara trilogy. He is the last remaining member of the Druids of Paranor.

Biography Edit

Early Life Edit

Much of Allanon's early life is a mystery, save that after his parents abandoned him, most likely due to his magic, he served as apprentice to the seer and Druid Bremen. eventually succeeding him as the world's last known Druid.

Thirty years prior to the events of the Shannara Chronicles the third War of the Races, also known as the War of the Warlock Lord. took place. Allanon fought in that war alongside the young Elven King Eventine Elessedil and Shea Ohmsford. the last heir of the magical Shannara bloodline. Together they defeated the Warlock Lord and brought peace to The Four Lands.

During this time Allanon had a brief romantic relationship with Eventine's sister Pyria. However, this did not stop Allanon from leaving her to enter the Druid Sleep. a state of suspended animation, once the war was over. Pyria refused to give up her love for Allanon in spite of Eventine forbidding her from marrying the Druid, and she estranged herself from her brother, choosing to live in Wing Hove instead of at the palace in Arborlon.

Quest to Save the Ellcrys Edit

Thirty years later, Allanon awakes when he senses the diminishing of the Ellcrys and the reemergence of the Dagda Mor. He immediately goes in search of Shea's son Wil Ohmsford in the hopes that the magic he inherited from Shea would aid in the coming fight against the Demons. Allanon finds Wil in an abandoned home the morning after he was drugged and robbed of his Elfstones by the Rover girl Eretria.

Though Wil is initially reluctant to travel with Allanon, he relents and the two eventually find the Elven Princess Amberle Elessedil in Wing Hove, visiting her great-aunt Pyria. Amberle, the last of the Chosen. had run away from Arborlon because she had been receiving visions from the Ellcrys of a demonic apocalypse and the murder of her boyfriend.

Allanon is reunited with Pyria only to learn she waited for him for thirty years after the War of the Races, not knowing that he had succumbed to the Druid Sleep. She is also shocked that he hasn't aged a day. Allanon barely has time to explain his absence and apologize before he is knocked out and she is killed by a Fury that is after the last of the Chosen.

Allanon manages to come to and kill the Fury, but he is wounded in the fight. He orders Amberle and Wil to ride for Arborlon while he hides and recuperates in a cave using a process that seems related to that of the Druid Sleep.

Once healed, Allanon saves Wil and Amberle and recovers the stolen Elfstones from Eretria's group of Rovers. On their way back to Arborlon, he meets a young Elf named Bandon chained and muzzled inside an abandoned house by his parents. Because Bandon was regularly kept hidden and locked away, he happened to avoid being killed by the Demons that killed his parents. Allanon warns Amberle that he cannot sense the boy's thoughts, meaning that Bandon is either actively hiding magic powers or possesses magic he is unaware of. Despite the warning Amberle insists that Bandon be taken to Arborlon where he can be cared for.

Allanon realizes that Bandon is a seer when he learns that Bandon's power is the ability to see visions of death for those whom he touches, and that his parents had probably kept him chained up out of a fear of his magic. The Druid tells Bandon that it isn't death he is always fated to see, but future possibilities. He insists that Bandon's ability is a gift, and he begins training Bandon to hone his potentially immense powers. However, the Dagda Mor takes notice and seizes Bandon's mind, locking it away from Allanon's reach and incapacitating the boy.

In the meantime, the Changeling had infiltrated Arborlon. The Demon kills Eventine while in the form of his son Arion. and then it assumes Eventine's form and takes the throne. As Eventine, the Changeling convinces Arion that the Druid is conspiring against the Elves, and he orders Arion to retrieve the Warlock Sword from the tunnels beneath Arborlon and to use it against Allanon. Arion uses the sword against Allanon and the Druid vanishes, apparently dead.

However, Allanon had been transported back to his cave, where he tries to heal himself for a time but is unable to muster the strength. As he lays dying, he is confronted by the shade of Bremen, who tells him that there was still more work to be done before healing him and giving him a powerful magical staff.

Renewed, Allanon journeys to the Northland just in time to protect Prince Ander from a suicidal attempt to kill the Dagda Mor. The false Eventine had ordered Arion and Ander to fight the Dagda Mor alone, using the Warlock Sword. Upon facing the two brothers, the Dagda Mor reveals that Arion had done his bidding by recovering the sword and killing Allanon, and that Eventine has already been killed. The Dagda Mor then spirits the sword away from Arion before killing him with it. Ander is saved by Allanon using a protective wall of magic, and he returns to the palace and kills the Changeling.

With the deaths of Eventine and Arion, Ander becomes the de facto King of the Elves. He drinks heavily after their deaths, intending to abdicate the throne to Kael Pindanon, a member of the Elven High Council, at his brother and father's funeral. It is only after some stern words from Allanon and memories of his family members dying with honor that he changes his mind while speaking at the funeral, vowing to fight for the Elves as their king, and to battle bravely in the name of The Four Lands.

While saving Ander from the Dagda Mor, Allanon managed to free Bandon from his mental imprisonment as well. He tells Bandon that he wants to train him to become the next Druid, the same way he was trained after his own parents abandoned him. Bandon refuses, but Allanon insists that under the current Demon onslaught, he doesn't have that choice anymore.

As Allanon begins teaching Bandon to harness his magic properly, Bandon becomes resentful of the Druid's harsh training and preoccupied with the feeling that he is only being valued for and defined by his magic. It soon becomes apparent that the Dagda Mor's hold on Bandon's mind has not been completely undone. When Bandon and Catania are alone together, Bandon is at first affectionate, but as their intimacy begins to increase Bandon gets a vision from the Dadga Mor and ends up trying to strangle Catania. She manages to get away, and Allanon decides to hide her from Bandon for her own safety.

Allanon confronts Bandon and tells him he will have to let go of Catania for her own good. Bandon refuses to accept the idea and lashes out with his increasingly powerful magic, catching the Druid unawares. Allanon quickly recovers, and manages to knock Bandon unconscious.

Later, Catania visits Bandon and brings him food to his prison cell in Arborlon. He convinces her to help him deceive a guard into unlocking his shackles, but after he is freed he flies into a rage when the guard manhandles Catania. To Catania's horror Bandon doesn't just incapacitate the guard; he brutally beats him to death and flees.

After the last leaf of the Ellcrys has fallen, Allanon, King Ander, and Slanter 's Gnomes prepare to defend Arborlon long enough for Amberle to return. During the battle, Allanon engages the Dagda Mor in single combat to allow Wil and Amberle passage to the Ellcrys. Though the two were evenly matched for much of the fight, the Dagda Mor gained the upper hand and attempted to kill Amberle, who had arrived during the battle. He was held off by Wil and the Elfstones long enough for Allanon to recover and decapitate him, after which Amberle became the new Ellcrys and banished the Demon horde.

Wil is angry at Allanon for withholding his knowledge of what Amberle's ultimate fate would be if she saved the Ellcrys, but the Druid insists to Wil that if would not have helped any of them to know the truth in advance. He also tells Wil that he is proud of him.

Ultimately, Allanon and Wil part on amicable terms: Wil thanks Allanon for granting him better self-knowledge, and Allanon remarks that their time together probably isn't done yet, as a new evil seems to have been awoken.

Catania is left to explain to Allanon what happened with Bandon and how he escaped. She tells Allanon that she has failed Bandon, and the Druid commiserates with her, saying that he's failed Bandon as well.

Bandon is later seen carrying the Warlock Sword with his eyes gone completely black, standing at the magical henge where the Dagda Mor had once imprisoned his mind.

Changes made for the TV Adaptation Edit

Along with his magic, Allanon carries a sword and engages in physical combat quite frequently in the TV series; in the original trilogy he fights almost solely with his magic, the Druid fire.

Allanon regularly uses his Druid cave as a quick way to heal himself from serious injuries. In the books, Allanon has no such recourse, aside from the Druid Sleep which would put him to sleep for decades, if not longer.

Allanon fights the Demons using a staff given to him by the shade of Bremen; in The Elfstones of Shannara he received a staff from the Ellcrys that was a piece of the tree itself. He gave this staff to both King Eventine and King Ander to use.

Allanon is overpowered by the Dagda Mor and it is only later later when Wil Ohmsford uses the Elfstones against the Demon that Allanon is able to decapitate him. In Elfstones . Allanon defeats the Dagda Mor in a one-on-one duel designed to buy time for Wil and Amberle's return to Arborlon.

Allanon is physically unchanged by the war against the Demons; in Elfstones . he is visibly aged by at the end of the war due to overusing his magic, and he has large streaks of white in his hair.

Allanon is of average height in the TV series. In the books he is exceptionally tall and is specifically described as being seven feet in height.

Pyria Elessedil was added to the TV series as a romantic interest for Allanon, most likely in an attempt to humanize him. There is no such romantic relationship for Allanon in the books.

Gallery Edit

Allanon is a main character in the original Shannara trilogy. For nearly all of his life he was the last of the Druids. He dedicated his life to the protection and preservation of the Four Lands and repeatedly recruited members of the House of Shannara in the Ohmsford family to aid him on various quests to defeat evil.

Biography Edit

Background Edit

Allanon was a young boy wandering through the ruins of Varfleet. having lost his parents to the destruction of the city, when he met the aged Druid Bremen. Bremen took the boy in and the two became attached to each other. Eventually Allanon sought to become like Bremen, and the old man taught him the Druid arts. Allanon participated in the Second War of the Races alongside Bremen, and studied in Paranor after the war for several years, until Bremen's passing.

Like Bremen, Allanon was the last of the Druids after the Druid Order had been eradicated by the Warlock Lord. He carried on Bremen's legacy as the only Druid of the Four Lands, preserving two kinds of knowledge: knowledge that had been salvaged from the Old World as well as the knowledge of magic that the first Druid Order had rediscovered. Initial descriptions of Allanon call him "the mysterious wanderer of the Four Lands, historian of the Races, philosopher and teacher, and practitioner of the mystic arts."

Allanon was enigmatic and secretive, appearing in the Four Lands only when needed, and passing decades of time in a form of suspended animation called the Druid Sleep. He was never completely honest with those whose help he requested: his words were few and clouded in half-truths, and his companions were kept on a "need-to-know" basis. Beginning with Shea Ohmsford. he repeatedly called on the aid of the descendants of Jerle Shannara 's bloodline. Many believe Allanon to be the greatest of the Druids and the last Druid of the second Druid Order, to which Bremen belonged.

Quest to Defeat the Warlock Lord Edit

Allanon first reveals himself to the Ohmsford family when he calls on Shea Ohmsford to retrieve the lost Sword of Shannara and use it to destroy the Warlock Lord. He gave Shea the Elfstones to protect himself on his journey.

Quest to Save the Ellcrys Edit

When the Ellcrys begins to fail, causing the Forbidding to crumble, Demons start escaping the Forbidding and attacking the Elves and the Four Lands. To stop them, Allanon sends Shea's grandson Wil Ohmsford and the Elven princess Amberle Elessedil on a quest to restore the Ellcrys, while Allanon remains behind in the Elven city of Arborlon to battle the Demon hordes.

A dying Allanon wipes his blood on Brin Ohmsford 's forehead, imbuing her with the Druid trust that her bloodline will carry. Artwork by Darrell K. Sweet for the original edition of The Wishsong of Shannara .

Quest to Destroy the Ildatch Edit

Allanon goes on one last journey with Wil's daughter, Brin Ohmsford. to enter the Maelmord and destroy the Ildatch. a malevolent book from the Age of Faerie which was also responsible for the corruption of the Druid Brona into the Warlock Lord. During their journey Allanon locks Paranor. the Druid Keep, away in another dimension to prevent its destruction at the hands of Mord Wraiths and their Gnome warriors. He also imbues the Sword of Leah with the magic of the Hadeshorn to aid Rone Leah in his role as Brin's protector.

During the journey with Brin and Rone, Allanon is mortally wounded in battle with an ancient being called a Jachyra and dies soon after. Before passing away, he wipes a bit of his blood on Brin's forehead, imbuing her with a trust meant to preserve and revive his legacy. At the Hadeshorn, the shade of Bremen appears and carries the dying Druid away, down into the lake.

Despite Allanon's death, Brin succeeds in destroying the Ildatch, with the help of her brother Jair. At the time of his death, Allanon had been walking the Four Lands for five hundred years.

Death Edit

Allanon's spirit dwells in the Hadeshorn along with the spirits of his predecessors, Bremen and Galaphile. Centuries after his death, he summons the descendants of Brin and Jair to him and charge them with saving the Four Lands from the threat of the Shadowen. He orders Par Ohmsford to recover the Sword of Shannara, Wren Ohmsford to find the Elves and return them to the Four Lands, and Walker Boh to restore Paranor and the Druid Order.

Legacy Edit

Centuries after Allanon gave Shea Ohmsford the Elfstones, they still belong to the House of Shannara. Although they are in the hands of the Elessedils, the House of Elessedil has been a part of the House of Shannara since the time of the Elf Queen Ellenroh Elessedil.

Usage of the Elfstones by Shea's grandson Wil contaminates his body with the Elven magic, a consequence of attempting to use the Elfstones while not possessing a high enough amount of Elven blood. The magic that becomes a part of Wil's body later manifests in Wil's children Brin and Jair as the wishsong. Centuries after Brin and Jair, their descendants often carry the magic of the wishsong, and innate magic has become an indelible a part of the Shannara bloodline.

Walker Boh, a descendant of Brin Ohmsford, eventually becomes Allanon's successor, ultimately fulfilling the trust given to Brin by restoring Paranor and absorbing Allanon's spirit and life experience with the power of the Black Elfstone. During his time as the last of the Druids, Walker consults the shade of Allanon at the Hadeshorn.

Although he restores Paranor and becomes the last of the Druids, Walker is ultimately unable to create a new Druid Order. As Walker lays dying, he wipes a bit of his blood on Grianne Ohmsford 's forehead, who at the time was still the Ilse Witch, surreptiously imbuing her with his trust in the way Allanon had done with Brin. After Bek Ohmsford and Truls Rohk take the dying Walker to an underground lake, the shade of Allanon appears to bear him away to an afterlife in the Hadeshorn.

Later, after Grianne has renounced her life as the Ilse Witch and accepted Walker's trust, she creates the third Druid Order and becomes the order's Ard Rhys. Like Walker had done before her, Grianne consults with Allanon's shade.

Allanon's shade appears to Khyber Elessedil. Ard Rhys of the fourth Druid Order, before Khyber and others embark on a quest to find the missing sets of Elfstones. which have been lost since the Age of Faerie. His shade also appears for the Ard Rhys Aphenglow Elessedil. when Aphenglow is ready to die and travels to the Hadeshorn. Allanon's shade carries Aphenglow down into the lake.

Physical Appearance Edit

Allanon is described as seven feet tall, with a dark face, a booming voice, and a hooded cowl that covers his disturbingly penetrating eyes.

Computer Game Edit

In the Shannara computer game. twenty years after the defeat of the Warlock Lord, Allanon appears in Shady Vale right on time to save Shea's son, Jak Ohmsford. from a monster. He orders Jak to go to Leah and warn Menion Leah of an oncoming peril, and stays with Shea in the Vale to defend the village. Allanon is later seen in Leah, after Menion was cured of a poison. There he explains that the Warlock Lord has returned from the dead and tasks Jak with traveling to Tyrsis to warn King Balinor Buckhannah and to claim the Sword of Shannara like his father. Allanon then leaves for the Valley of Shale to speak with the shade of Bremen.

Dexamethasone Oral Medlineplus Drug Information, Dexamethazon

Dexamethasone Oral

Dexamethasone, a corticosteroid, is similar to a natural hormone produced by your adrenal glands. It often is used to replace this chemical when your body does not make enough of it. It relieves inflammation (swelling, heat, redness, and pain) and is used to treat certain forms of arthritis; skin, blood, kidney, eye, thyroid, and intestinal disorders (e. g. colitis); severe allergies; and asthma. Dexamethasone is also used to treat certain types of cancer.

This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

How should this medicine be used?

Dexamethasone comes as a tablet and a solution to take by mouth. Your doctor will prescribe a dosing schedule that is best for you. Follow the directions on your prescription label carefully, and ask your doctor or pharmacist to explain any part you do not understand. Take dexamethasone exactly as directed. Do not take more or less of it or take it more often than prescribed by your doctor.

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tell your doctor if you are pregnant, plan to become pregnant, or are breast-feeding. If you become pregnant while taking dexamethasone, call your doctor.

if you are having surgery, including dental surgery, tell the doctor or dentist that you are taking dexamethasone.

if you have a history of ulcers or take large doses of aspirin or other arthritis medication, limit your consumption of alcoholic beverages while taking this drug. Dexamethasone makes your stomach and intestines more susceptible to the irritating effects of alcohol, aspirin, and certain arthritis medications: this effect increases your risk of ulcers.

What special dietary instructions should I follow?

Keep all appointments with your doctor and the laboratory. Your doctor will order certain lab tests to check your response to dexamethasone. Checkups are especially important for children because dexamethasone can slow bone growth.

If your condition worsens, call your doctor. Your dose may need to be adjusted.

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Brand names

Z Prenatal Oral Drug Information On Uses, Side Effects, Interactions, And User Reviews On Rxlist, Or

Z + Prenatal oral

Z + Prenatal oral Uses

This medication is a multivitamin product used to treat or prevent vitamin deficiency due to poor diet, certain illnesses, or during pregnancy. Vitamins are important building blocks of the body and help keep you in good health.

How to use Z + Prenatal oral

Take this medication by mouth, usually once daily or as directed. Follow all directions on the product package, or take as directed by your doctor. Do not take more than the recommended dosage. If you are uncertain about any of the information, consult your doctor or pharmacist.

Take this medication regularly in order to get the most benefit from it. To help you remember, take it at the same time each day.

Z + Prenatal oral Side Effects

Constipation, diarrhea, or upset stomach may occur. These effects are usually temporary and may disappear as your body adjusts to this medication. If any of these effects persist or worsen, contact your doctor or pharmacist promptly.

If your doctor has prescribed this drug, remember that he or she has judged that the benefit to you is greater than the risk of side effects. Many people using this medication do not have serious side effects.

A very serious allergic reaction to this drug is rare. However, seek immediate medical attention if you notice any of the following symptoms of a serious allergic reaction: rash, itching/swelling (especially of the face/tongue/throat), severe dizziness, trouble breathing.

This is not a complete list of possible side effects. If you notice other effects not listed above, contact your doctor or pharmacist.

Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088 or at www. fda. gov/medwatch.

In Canada - Call your doctor for medical advice about side effects. You may report side effects to Health Canada at 1-866-234-2345.

Z + Prenatal oral Precautions

Before taking this product, tell your doctor or pharmacist if you are allergic to any of its ingredients; or to soy/peanut found in some brands; or if you have any other allergies. This product may contain inactive ingredients, which can cause allergic reactions or other problems. Talk to your pharmacist for more details.

Before taking this medication, tell your doctor or pharmacist your medical history, especially of: use/abuse of alcohol, liver problems, stomach/intestinal problems (e. g. ulcer, colitis).

If your brand of multivitamin also contains folic acid, be sure to tell your doctor or pharmacist if you have vitamin B12 deficiency (pernicious anemia) before taking it. Folic acid may affect certain laboratory tests for vitamin B12 deficiency without treating this anemia. Untreated vitamin B12 deficiency may result in serious nerve problems (e. g. peripheral neuropathy). Consult your doctor or pharmacist for details.

Tell your doctor if you are pregnant before using this medication.

This medication passes into breast milk. Consult your doctor before breast-feeding.

Z + Prenatal oral Interactions

Your doctor or pharmacist may already be aware of any possible drug interactions and may be monitoring you for them. Do not start, stop, or change the dosage of any medicine before checking with them first.

Before taking this medication, tell your doctor or pharmacist of all prescription and nonprescription/herbal drugs you may use, especially: other vitamin/nutritional supplements.

If your brand of multivitamin also contains iron, avoid taking this product at the same time as antacids, bisphosphonates (for example, alendronate), levodopa, thyroid medications (for example, levothyroxine), or some antibiotics (for example, tetracyclines, quinolones such as ciprofloxacin). Ask your doctor or pharmacist about how long you should wait between doses and for help finding a dosing schedule that will work with all your medications.

If your brand of multivitamin also contains folic acid, be sure to tell your doctor or pharmacist if you take certain anti-seizure drugs (e. g. hydantoins such as phenytoin).

This document does not contain all possible interactions. Therefore, before using this product, tell your doctor or pharmacist of all the products you use. Keep a list of all your medications with you, and share the list with your doctor and pharmacist.

Z + Prenatal oral Overdose

If overdose is suspected, contact a poison control center or emergency room right away. US residents can call their local poison control center at 1-800-222-1222. Canada residents can call a provincial poison control center. Symptoms of overdose may include: stomach pain, nausea, vomiting, diarrhea.

If your doctor has prescribed this medication, do not share it with others.

Keep all regular medical and laboratory appointments.

Some brands may also contain ingredients such as docusate. Ask your doctor or pharmacist if you have questions about the ingredients in your brand.

This product is not a substitute for a proper diet. Remember that it is best to get your vitamins from healthy foods. Maintain a well-balanced diet and follow any dietary guidelines as directed by your doctor.

If you are taking this product on a prescribed schedule and miss a dose, take it as soon as you remember. If it is near the time of the next dose, skip the missed dose and resume your usual dosing schedule. Do not double the dose to catch up.

Store at room temperature between 59-86 degrees F (15-30 degrees C) away from light and moisture. Do not store in the bathroom. Keep all medicines away from children and pets.

Do not flush medications down the toilet or pour them into a drain unless instructed to do so. Properly discard this product when it is expired or no longer needed. Consult your pharmacist or local waste disposal company for more details about how to safely discard your product.

Information last revised October 2015. Copyright(c) 2015 First Databank, Inc.

Progut® Rumen, Progut

Progut® Rumen

Progut Rumen is new generation yeast product. The patented (EP 0946108) hydrolysis process used to break down the yeast cell. Yeast cells from the brewing industry are deactivated by heat treatment and then hydrolysed to release soluble, bioactive particles.

Research has shown that the unique composition of bioactive particles enhances rumen fermentation by increasing the number of rumen microbes. More microbes can produce more volatile fatty acids, which positively impacts milk production. More over, the amino acid composition of microbial protein is optimal for milk protein synthesis. Cows fed using Progut Rumen have in trials increased milk production up to 6 % (table 2). The effect has been similar throughout the entire lactation period. Progut Rumen enhances also animal’s natural immunity, which has been seen in fitter calves.

Recommended dosage rates

Dairy cows 2 weeks before calving and during the lactation

Sheep and goats

2 weeks before calving and during the lactation

lambs and kids

Contact us

Hankkija

Company address

Hankkija Oy PL 390 (Peltokuumolantie 4) 05801 HYVINKAA

Ranitidine Indications, Side Effects, Warnings, Raxide

Ranitidine

Ranitidine is used for:

Treating certain conditions that cause your body to make too much stomach acid (eg, Zollinger-Ellison syndrome). It is also used to treat ulcers of the small intestine that have not responded to other treatment. It may be used as a short-term alternative to oral ranitidine, in patients who are not able to take medicine by mouth. It may also be used for other conditions as determined by your doctor.

Ranitidine is an H 2 - receptor blocker. It works by blocking the action of histamine in the stomach. This reduces the amount of acid the stomach makes. Reducing stomach acid helps to reduce heartburn, heal irritation of the esophagus, and heal ulcers of the stomach or intestines.

Do NOT use ranitidine if:

you are allergic to any ingredient in ranitidine

you have a history of the blood disease porphyria

you are taking dasatinib

Contact your doctor or health care provider right away if any of these apply to you.

Before using ranitidine:

Some medical conditions may interact with ranitidine. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have a history of kidney or liver problems

if you have abnormal blood electrolyte levels or a history of irregular heartbeat

Some MEDICINES MAY INTERACT with ranitidine. Tell your health care provider if you are taking any other medicines, especially any of the following:

Certain benzodiazepines (eg, midazolam, triazolam), glipizide, procainamide, or warfarin because the risk of their side effects may be increased by ranitidine

Dasatinib, delavirdine, gefitinib, certain HIV protease inhibitors (eg, atazanavir), itraconazole, or ketoconazole because their effectiveness may be decreased by ranitidine

This may not be a complete list of all interactions that may occur. Ask your health care provider if ranitidine may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use ranitidine:

Use ranitidine as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Ranitidine is usually given as an injection at your doctor's office, hospital, or clinic. If you will be using ranitidine at home, a health care provider will teach you how to use it. Be sure you understand how to use ranitidine. Follow the procedures you are taught when you use a dose. Contact your health care provider if you have any questions.

Do not use ranitidine if it contains particles, is cloudy or discolored, or if the vial is cracked or damaged.

Keep this product, as well as syringes and needles, out of the reach of children and pets. Do not reuse needles, syringes, or other materials. Ask your health care provider how to dispose of these materials after use. Follow all local rules for disposal.

You may take antacids while you are using ranitidine if you are directed to do so by your doctor.

Continue to use ranitidine even if you feel well. Do not miss any doses.

If you miss a dose of ranitidine, use it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not use 2 doses at once.

Ask your health care provider any questions you may have about how to use ranitidine.

Important safety information:

Ranitidine may rarely cause drowsiness, dizziness, or blurred vision. These effects may be worse if you take it with alcohol or certain medicines. Use ranitidine with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.

Ranitidine may interfere with certain lab tests, including urine protein tests. Be sure your doctor and lab personnel know you are taking ranitidine.

Lab tests, including liver function, may be performed while you use ranitidine. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Ranitidine should be used with extreme caution in CHILDREN younger than 1 month old; safety and effectiveness in these children have not been confirmed.

PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using ranitidine while you are pregnant. Ranitidine is found in breast milk. Do not breast-feed while taking ranitidine.

Possible side effects of ranitidine:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Constipation; diarrhea; headache; nausea; stomach upset.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue; unusual hoarseness); change in the amount of urine produced; confusion; dark urine; depression; fast, slow, or irregular heartbeat; fever, chills, or sore throat; hallucinations; severe or persistent headache or stomach pain; unusual bruising or bleeding; yellowing of the eyes or skin.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA .

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center. or emergency room immediately. Symptoms may include dizziness; trouble walking.

Proper storage of ranitidine:

Ranitidine is usually handled and stored by a health care provider. If you are using ranitidine at home, store ranitidine as directed by your pharmacist or health care provider. Keep ranitidine out of the reach of children and away from pets.

General information:

If you have any questions about ranitidine, please talk with your doctor, pharmacist, or other health care provider.

Ranitidine is to be used only by the patient for whom it is prescribed. Do not share it with other people.

If your symptoms do not improve or if they become worse, check with your doctor.

Check with your pharmacist about how to dispose of unused medicine.

This information should not be used to decide whether or not to take ranitidine or any other medicine. Only your health care provider has the knowledge and training to decide which medicines are right for you. This information does not endorse any medicine as safe, effective, or approved for treating any patient or health condition. This is only a brief summary of general information about ranitidine. It does NOT include all information about the possible uses, directions, warnings, precautions, interactions, adverse effects, or risks that may apply to ranitidine. This information is not specific medical advice and does not replace information you receive from your health care provider. You must talk with your healthcare provider for complete information about the risks and benefits of using ranitidine.

Review Date: August 8, 2016

Disclaimer: This information should not be used to decide whether or not to take this medicine or any other medicine. Only your health care provider has the knowledge and training to decide which medicines are right for you. This information does not endorse any medicine as safe, effective, or approved for treating any patient or health condition. This is only a brief summary of general information about this medicine. It does NOT include all information about the possible uses, directions, warnings, precautions, interactions, adverse effects, or risks that may apply to this medicine. This information is not specific medical advice and does not replace information you receive from your health care provider. You must talk with your healthcare provider for complete information about the risks and benefits of using this medicine.

More about ranitidine

Acicvir, Acicvir

Acivir

Important Notice: The Drugs. com international database is in BETA release. This means it is still under development and may contain inaccuracies. It is not intended as a substitute for the expertise and judgement of your physician, pharmacist or other healthcare professional. It should not be construed to indicate that the use of any medication in any country is safe, appropriate or effective for you. Consult with your healthcare professional before taking any medication.

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Celecoxib Informaci - N Espa - Ola De La Droga, Caditar

celecoxib

¿Qué es celecoxib?

Celecoxib es un antiinflamatorio no esteroide (AINE, NSAID por sus siglas en ingles). Celecoxib funciona reduciendo hormonas en su cuerpo que causan inflamación, dolor y fiebre.

Celecoxib se usa para reducir el dolor y la inflamación causados por condiciones como la artritis, la espondilitis anquilosante, y el dolor menstrual. Celecoxib se usa para tratar la artritis reumatoide juvenil en los niños que tienen al menos 2 años de edad. También se usa en el tratamiento de pólipos hereditarios en el colon.

Celecoxib puede también usarse para fines no mencionados en esta guía del medicamento.

¿Cuál es la información más importante que debo saber sobre celecoxib?

Celecoxib puede aumentar su riesgo de ataques al corazón o accidentes cerebrovasculares fatales, especialmente si usted la usa por largo tiempo o toma dosis elevadas, o si tiene enfermedad del corazón. No use esta medicina justo antes o después de tener una cirugía de puente (bypass) aortocoronario con injerto (CABG por sus siglas en Inglés).

Celecoxib también puede causar sangrado del estómago o intestino, lo que podría ser fatal. Estas condiciones pueden ocurrir sin ninguna advertencia mientras esté usando celecoxib, especialmente en los adultos mayores. Usted no debe tomar esta medicina si ya tienen un sangrado en su estómago o en los intestinos.

¿Qué debería discutir con el profesional de la salud antes de tomar celecoxib?

Celecoxib puede aumentar su riesgo de ataques al corazón o accidentes cerebrovasculares fatales, especialmente si usted la usa por largo tiempo o toma dosis elevadas, o si usted tiene enfermedad del corazón. Aun las personas sin enfermedad del corazón o factores de riesgo podrían tener un accidente cerebrovascular o ataque al corazón mientras toman esta medicina.

No use esta medicina justo antes o después de tener una cirugía de puente (bypass) aortocoronario con injerto (CABG por sus siglas en Inglés).

Celecoxib también puede causar sangrado del estómago o intestino, lo que podría ser fatal. Estas condiciones pueden ocurrir sin ninguna advertencia mientras esté usando celecoxib, especialmente en los adultos mayores.

Usted no debe usar celecoxib si es alérgico a éste, o si tiene:

sangrado en el estómago o los intestinos;

una alergia a las drogas sulfas; o

un historial de ataque de asma o reacción alérgica severa después de tomar aspirin o un AINE.

Para asegurarse que celecoxib es seguro para usted, dígale a su médico si usted tiene:

enfermedad del corazón, presión arterial alta, colesterol elevado, diabetes, o si fuma;

un historial de ataque al corazón, accidente cerebrovascular, o coagulo sanguíneo;

un historial de úlcera en el estómago o sangrado;

retención de líquido;

enfermedad del hígado;

enfermedad del riñón; o

Tomar celecoxib durante los últimos 3 meses de embarazo puede hacer daño al bebé nonato. Dígale a su médico si usted está embarazada o planea quedar embarazada mientras está usando celecoxib.

Celecoxib puede pasar a la leche materna y causarle daño al bebé lactante. Dígale a su médico si está dando de amamantar a un bebé.

Celecoxib no está aprobada para usarse en cualquier persona menor de 2 años de edad.

¿Cómo debo tomar celecoxib?

Siga todas las instrucciones en la etiqueta de su prescripción. No tome esta medicina en cantidades mayores, o por más tiempo de lo recomendado. Use la dosis más baja que sea efectiva para el tratamiento de su condición.

Usted puede tomar celecoxib con o sin comida.

Tome con comida si celecoxib molesta su estómago.

Para que sea más fácil tragarla, usted puede abrir la cápsula de celecoxib y rociar la medicina en una cuchara de puré de manzana. Trague de inmediato sin masticar. Bote la cápsula vacía. Si no toma la mezcla de inmediato, guárdela en el refrigerador y tómela dentro de 6 horas.

Si usted usa esta medicina a largo plazo, usted puede necesitar pruebas médicas frecuentes.

Guarde a temperatura ambiente, lejos de la humedad y el calor.

Lea toda la información para el paciente, las guías del medicamento y las hojas de instrucción que le proporcionaron. Hable con su médico o farmacéutico si tiene alguna pregunta.

¿Qué sucede si me salto una dosis?

Ya que celecoxib a veces se usa cuando se necesita, usted tal vez no esté en un horario de dosis. Si usted está en un horario de dosis, use la dosis que dejó de usar tan pronto se acuerde. Sáltese la dosis que dejó de usar si ya casi es hora para la siguiente dosis. No use más medicina para alcanzar la dosis que dejó de usar.

¿Qué sucedería en una sobredosis?

Busque atención médica de emergencia o llame a la línea de Poison Help al 1-800-222-1222.

¿Qué debo evitar mientras tomo celecoxib?

Evite beber alcohol. Le puede aumentar su riesgo de sangrado en el estómago.

Evite tomar aspirin u otros AINEs mientras esté tomando celecoxib.

Pregúntele a su médico o farmacéutico antes de usar cualquier medicamento para el resfriado, alergias, o el dolor. Muchas de las medicinas que se consiguen sin receta contienen aspirin u otras medicinas similares a celecoxib. El tomar ciertos productos juntos puede hacer que tome demasiado de este tipo de medicamento. Revise la etiqueta para ver si una medicina contiene aspirin, ibuprofen, ketoprofen, o naproxen.

¿Cuáles son los efectos secundarios posibles de celecoxib?

Busque atención médica de emergencia si tiene síntomas de una reacción alérgica: estornudo, nariz mocosa o congestionada; silbido o dificultad para respirar; ronchas; hinchazón de la cara, labios, lengua, o garganta.

Busque ayuda médica de emergencia si usted tiene síntomas de un ataque al corazón o accidente cerebrovascular: dolor del pecho que se extiende a la mandíbula u hombro, entumecimiento o debilidad repentina en un lado de su cuerpo, habla arrastrada, sensación de que le falta aire al respirar.

Deje de usar celecoxib y llame a su médico de inmediato si usted tiene:

el primer signo de cualquier sarpullido, no importa que sea muy leve;

falta de aire al respirar (aún cuando la actividad es leve);

hinchazón o aumento rápido de peso;

signos de sangrado en el estómago-- heces con sangre o alquitranadas, tos con sangre o vómito que parece café molido;

problemas del hígado--náusea, dolor en la parte superior del estómago, picazón, sensación de cansancio, síntomas parecidos a la gripe, pérdida del apetito, orina oscura, heces fecales de color arcilla, ictericia (color amarillo de la piel u ojos);

problemas del riñón--orinar poco o nada, dolor o dificultad al orinar, hinchazón en sus pies o tobillos, sensación de cansancio o de que le falta aire al respirar;

bajo conteo de glóbulos rojos (anemia)--piel pálida, sentir que se va a desmayar o le falta aire al respirar, latido cardíaco rápido, dificultad para concentrarse; o

reacción severa de la piel--fiebre, dolor de garganta, hinchazón en su cara o lengua, quemazón en sus ojos, dolor de la piel seguido por un sarpullido rojo o púrpura que se extiende (especialmente en la cara o la parte superior del cuerpo) y causa ampollas y descamación.

Efectos secundarios comunes pueden incluir:

dolor de estómago, indigestión, gas, diarrea;

hinchazón de las manos o los pies;

síntomas de resfrío como nariz congestionada, estornudo, dolor de garganta.

Esta lista no menciona todos los efectos secundarios y puede ser que ocurran otros. Llame a su médico para consejos médicos relacionados a efectos secundarios. Usted puede reportar efectos secundarios llamando al FDA al 1-800-FDA-1088.

¿Qué otras drogas afectarán al celecoxib?

Pregúntele a su médico antes de usar celecoxib si usted toma un antidepresivo como citalopram, escitalopram, fluoxetine (Prozac), fluvoxamine, paroxetine (Paxil), sertraline (Zoloft), trazodone, o vilazodone. Tomar cualquiera de estas medicinas con un AINE puede causarle moretones o sangrado fácil.

Dígale a su médico todas las medicinas que usa, y cualquiera que comience o deje de usar, especialmente:

un anticoagulante (warfarin, Coumadin, Jantoven);

medicamento para el corazón o la presión arterial, incluyendo un diurético o "pastilla para eliminar el agua"; o

medicina esteroide (como prednisone).

Esta lista no está completa. Otras drogas pueden interactuar con celecoxib, incluyendo medicinas que se obtienen con o sin receta, vitaminas, y productos herbarios. No todas las interacciones posibles aparecen en esta guía del medicamento.

¿Dónde puedo obtener más información?

Su farmacéutico le puede dar más información acerca de celecoxib.

Recuerde, mantenga ésta y todas las otras medicinas fuera del alcance de los niños, no comparta nunca sus medicinas con otros, y use este medicamento sólo para la condición por la que fue recetada.

Se ha hecho todo lo posible para que la información que proviene de Cerner Multum, Inc. ('Multum') sea precisa, actual, y completa, pero no se hace garantía de tal. La información sobre el medicamento incluida aquí puede tener nuevas recomendaciones. La información preparada por Multum se ha creado para uso del profesional de la salud y para el consumidor en los Estados Unidos de Norteamérica (EE. UU.) y por lo cual Multum no certifica que el uso fuera de los EE. UU. sea apropiado, a menos que se mencione específicamente lo cual. La información de Multum sobre drogas no sanciona drogas, ni diagnóstica al paciente o recomienda terapia. La información de Multum sobre drogas sirve como una fuente de información diseñada para la ayuda del profesional de la salud licenciado en el cuidado de sus pacientes y/o para servir al consumidor que reciba este servicio como un suplemento a, y no como sustituto de la competencia, experiencia, conocimiento y opinión del profesional de la salud. La ausencia en éste de una advertencia para una droga o combinación de drogas no debe, de ninguna forma, interpretarse como que la droga o la combinación de drogas sean seguras, efectivas, o apropiadas para cualquier paciente. Multum no se responsabiliza por ningún aspecto del cuidado médico que reciba con la ayuda de la información que proviene de Multum. La información incluida aquí no se ha creado con la intención de cubrir todos los usos posibles, instrucciones, precauciones, advertencias, interacciones con otras drogas, reacciones alérgicas, o efectos secundarios. Si usted tiene alguna pregunta acerca de las drogas que está tomando, consulte con su médico, enfermera, o farmacéutico.

Copyright 1996-2012 Cerner Multum, Inc. Version: 14.01. Revision Date: 9/8/2015 10:43:42 AM.

Pediazole Indications, Side Effects, Warnings, Pediazole

Pediazole

Treating ear infections caused by certain bacteria. It may also be used for other conditions as determined by your doctor.

Pediazole is a macrolide and sulfonamide antibiotic combination. It works by slowing the growth of and killing sensitive bacteria.

Do NOT use Pediazole if:

you are allergic to any ingredient in Pediazole or to any other sulfonamide medicine (eg, sulfamethoxazole)

you are pregnant and at term (38 to 42 weeks)

you are breast-feeding a child younger than 2 months old

the patient is a child younger than 2 months old

you have severe kidney problems, bladder blockage, or anemia caused by folic acid deficiency

you have a very slow heartbeat or a certain type of irregular heartbeat (QT prolongation, long QT syndrome)

you have low blood potassium or magnesium levels

you are taking certain antiarrhythmics (eg, amiodarone, dofetilide, dronedarone, procainamide, propafenone, quinidine, sotalol), asenapine, astemizole, cisapride, diltiazem, eletriptan, an ergot alkaloid (eg, dihydroergotamine, ergotamine), an HIV protease inhibitor (eg, ritonavir), certain imidazole antifungals (eg, itraconazole, ketoconazole, voriconazole), nilotinib, pimozide, a streptogramin (eg, quinupristin/dalfopristin), terfenadine, tetrabenazine, tolvaptan, or verapamil

Contact your doctor or health care provider right away if any of these apply to you.

Before using Pediazole:

Some medical conditions may interact with Pediazole. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have diarrhea or throat inflammation

if you have a history of asthma, blood problems, a glucose-6-phosphate dehydrogenase (G6PD) deficiency, kidney or liver problems, heart problems (eg, fast, slow, or irregular heartbeat), low blood potassium or magnesium levels, myasthenia gravis, or the blood disease porphyria

if you take any medicine that may increase the risk of a certain type of irregular heartbeat (prolonged QT interval). Check with your doctor or pharmacist if you are unsure if any of your medicines may increase the risk of this type of irregular heartbeat

Some MEDICINES MAY INTERACT with Pediazole. Tell your health care provider if you are taking any other medicines, especially any of the following:

Many prescription and nonprescription medicines (eg, used for aches and pains, allergies, blood thinning, breathing problems, cancer, diabetes, erection problems, gout, hepatitis C infection, high blood calcium levels, high blood pressure, high cholesterol, HIV infection, inflammation, infections, irregular heartbeat or other heart problems, low blood sodium levels, migraine, mood or mental problems, nausea and vomiting, overactive bladder, Parkinson disease, prevention of organ transplant rejection, seizures, stomach problems, trouble sleeping), multivitamin products, and herbal or dietary supplements (eg, herbal teas, coenzyme Q10, garlic, ginseng, ginkgo, St. John's wort) may also interact with Pediazole. Ask your doctor or pharmacist if you are unsure if any of your medicines might interfere with Pediazole

This may not be a complete list of all interactions that may occur. Ask your health care provider if Pediazole may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Pediazole:

Use Pediazole as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Take Pediazole by mouth with or without food. If stomach upset occurs, take with food to reduce stomach irritation.

Drinking extra fluids while you are taking Pediazole is recommended. Check with your doctor for instructions.

Do not eat grapefruit or drink grapefruit juice while you use Pediazole.

Pediazole works best if it is taken at the same time(s) each day.

To clear up your infection completely, take Pediazole for the full course of treatment. Keep taking it even if you feel better in a few days.

If you miss a dose of Pediazole, take it as soon as possible. If it is almost time for the next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Pediazole.

Important safety information:

Pediazole may cause dizziness. This effect may be worse if you take it with alcohol or certain medicines. Use Pediazole with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.

Mild diarrhea is common with antibiotic use. However, a more serious form of diarrhea (pseudomembranous colitis) may rarely occur. This may develop while you use the antibiotic or within several months after you stop using it. Contact your doctor right away if stomach pain or cramps, severe diarrhea, or bloody stools occur. Do not treat diarrhea without first checking with your doctor.

Pediazole only works against bacteria; it does not treat viral infections (eg, the common cold).

Be sure to use Pediazole for the full course of treatment. If you do not, the medicine may not clear up your infection completely. The bacteria could also become less sensitive to this or other medicines. This could make the infection harder to treat in the future.

Long-term or repeated use of Pediazole may cause a second infection. Tell your doctor if signs of a second infection occur. Your medicine may need to be changed to treat this.

Infrequently, a serious stomach problem called infantile hypertrophic pyloric stenosis (IHPS) has been reported in infants taking erythromycin. Contact your child's doctor right away if severe vomiting or irritability with feeding occurs.

Tell your doctor or dentist that you take Pediazole before you receive any medical or dental care, emergency care, or surgery.

Rarely, patients taking Pediazole have developed reversible hearing loss. This risk is greater if you have kidney problems or you take high doses of Pediazole. Contact your doctor if you develop decreased hearing or hearing loss.

Pediazole may cause you to become sunburned more easily. Avoid the sun, sunlamps, or tanning booths until you know how you react to Pediazole. Use a sunscreen or wear protective clothing if you must be outside for more than a short time.

Pediazole may interfere with certain lab tests. Be sure your doctor and lab personnel know you are taking Pediazole.

Lab tests, including liver function, kidney function, complete blood counts, and urinalysis, may be performed while you use Pediazole. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Pediazole should not be used in CHILDREN younger than 2 months old; safety and effectiveness in these children have not been confirmed.

Use Pediazole with caution in the ELDERLY; they may be more sensitive to its effects, especially irregular heartbeat (prolonged QT interval).

PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Pediazole while you are pregnant. Do not take Pediazole if you are pregnant and at term (38 to 42 weeks). Pediazole is found in breast milk. Do not breast-feed while taking Pediazole.

Possible side effects of Pediazole:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Dizziness; headache; loss of appetite; mild diarrhea; nausea; stomach pain; vomiting.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue; unusual hoarseness); bloody or dark urine; bloody stools; change in the amount of urine produced; decreased hearing or hearing loss; fainting; fast or irregular heartbeat; fever, chills, or sore throat; mood or mental changes; numbness or tingling of the hands or feet; pale skin; red, swollen, blistered, or peeling skin; ringing in the ear; seizures; severe or persistent diarrhea, dizziness, or headache; severe stomach pain; shortness of breath; sore mouth or tongue; stomach cramps; symptoms of liver problems (eg, yellowing of skin or eyes; pale stools; severe or persistent nausea, vomiting, or loss of appetite; dark urine); unusual bruising or bleeding; unusual weakness or fatigue; vision changes.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA .

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center. or emergency room immediately. Symptoms may include blood in the urine; high fever; loss of consciousness; severe nausea, dizziness, drowsiness, headache, or vomiting; severe or persistent loss of appetite.

Proper storage of Pediazole:

Store Pediazole in the refrigerator, between 36 and 46 degrees F (2 and 8 degrees C). Do not freeze. Throw away any unused medicine after 14 days. Store away from heat, moisture, and light. Do not store in the bathroom. Keep tightly closed. Keep Pediazole out of the reach of children and away from pets.

General information:

If you have any questions about Pediazole, please talk with your doctor, pharmacist, or other health care provider.

Pediazole is to be used only by the patient for whom it is prescribed. Do not share it with other people.

If your symptoms do not improve or if they become worse, check with your doctor.

Check with your pharmacist about how to dispose of unused medicine.

This information should not be used to decide whether or not to take Pediazole or any other medicine. Only your health care provider has the knowledge and training to decide which medicines are right for you. This information does not endorse any medicine as safe, effective, or approved for treating any patient or health condition. This is only a brief summary of general information about Pediazole. It does NOT include all information about the possible uses, directions, warnings, precautions, interactions, adverse effects, or risks that may apply to Pediazole. This information is not specific medical advice and does not replace information you receive from your health care provider. You must talk with your healthcare provider for complete information about the risks and benefits of using Pediazole.

Review Date: August 8, 2016

Disclaimer: This information should not be used to decide whether or not to take this medicine or any other medicine. Only your health care provider has the knowledge and training to decide which medicines are right for you. This information does not endorse any medicine as safe, effective, or approved for treating any patient or health condition. This is only a brief summary of general information about this medicine. It does NOT include all information about the possible uses, directions, warnings, precautions, interactions, adverse effects, or risks that may apply to this medicine. This information is not specific medical advice and does not replace information you receive from your health care provider. You must talk with your healthcare provider for complete information about the risks and benefits of using this medicine.

More about Pediazole (erythromycin / sulfisoxazole)

Nurofen - Definition Of Nurofen By The Free Dictionary, Neurofen

ibuprofen

References in periodicals archive ?

PHARMACISTS' stranglehold over the sale of some non-prescription, over-the-counter painkillers shows no sign of loosening despite a four-year-old court ruling that ibuprofen-based Nurofen should be freely available in supermarkets and kiosks.

The Australian Competition and Consumer Commission has instituted proceedings in the Federal Court of Australia against Reckitt Benckiser (Australia) Pty Ltd (Reckitt Benckiser), alleging that it made false or misleading claims that its Nurofen Specific Pain Products were each formulated to treat a specific kind of pain, when the products are identical.

WOMEN are becoming more hooked on everyday painkillers, such as Nurofen Plus.

A TODDLER was left fighting for her life after suffering a massive allegic reaction to a child's dose of Nurofen .

The move was announced as Reckitt, which sells Durex condoms, Lysol disinfectant and Nurofen painkilling tablets, reported better-thanexpected half-year profits of PS1.

In fact we have looked at this outfit for so long we are going to have to take a Nurofen and have a lie down.

uk Nurofen for Children Cold, Pain & Fever SUGAR and colour-free orange or strawberry flavour oral suspension which helps manage children's cold and flu symptoms including fever, sore throats, headaches and minor body aches.

A SURGE in winter cold and flu bugs helped Nurofen and Strepsils maker Reckitt Benckiser report better than expected profits.

A SURGE in winter cold and flu bugs has helped Nurofen and Strepsils maker Reckitt Benckiser report betterthan-expected profits The firm, whose brands also include Durex and Dettol, finished last year with quarterly like-for-like sales growth of 6%, with its Europe and North America region up 3% due to strong seasonal demand.

DRUGS and hygiene giant Reckitt Benckiser has revealed under-pressure revenues in Europe and North America as fewer cases of the common cold and flu hit sales of its Nurofen pain-relief range.

Summary: A codeine addict, who contaminated packets of Nurofen Plus in order to fund his habit, has been jailed for eighteen months.

RB would increase its focus on the higher-margin health and hygiene products among its 'power brands' - including Nurofen. Strepsils, Durex and Dettol, said CEO Rakesh Kapoor.

Oxitriptan - Information; Why It Is Recommended, Tript-Oh

Oxitriptan

Source

Oxitriptan is supplied in 50mg or 10mg tablets under the trade names Cincofarm, Levotonine, Levothym, Oxyfan, Serotonyl™, Serovit, Telesol, Trimag, Tript-OG, Tript-OH, Triptene and Triptum™.

Function; Why it is Recommended

Oxitriptan is converted into the brain hormone serotonin in the body. Serotonin is a key factor in mood regulation, eating disorders, and anxiety. Serotonin is also the precursor to the pineal gland 's production of melatonin .

Oxitriptan's anti-aging benefits may include the prevention and treatment of depression. maintenance of serotonin levels as the body ages, prevention and treatment of compulsive disorders like overeating, improved daytime alertness and treatment of insomnia.

Side-Effects

Side-effects include nausea and mild gastric discomfort.

Diagnose your symptoms now!

understand what's happening to your body

see your health summarized and in detail

have a doctor review your case (optional)

Doxazosin Side Effects In Detail, Doxaben

Doxazosin Side Effects

In Summary

Commonly reported side effects of doxazosin include: fatigue, vertigo, dizziness, hypertension, symptomatic orthostatic hypotension, malaise, and orthostatic effect. Other side effects include: syncope, edema, drowsiness, and dizziness. See below for a comprehensive list of adverse effects.

For the Consumer

Applies to doxazosin: oral tablet, oral tablet extended release

In addition to its needed effects, some unwanted effects may be caused by doxazosin. In the event that any of these side effects do occur, they may require medical attention.

Severity: Moderate

If any of the following side effects occur while taking doxazosin, check with your doctor or nurse as soon as possible:

More common:

Dizziness or lightheadedness

Less common:

Blurred vision

confusion

dizziness, faintness, or lightheadedness when getting up from a lying or sitting position

fainting (sudden)

fast and pounding heartbeat

irregular heartbeat

shortness of breath

sweating

swelling of feet or lower legs

Rare

Painful or prolonged erection of the penis (called priapism), although extremely rare, must have immediate medical attention. If painful or prolonged erection occurs, call your doctor or go to an emergency room as soon as possible

Incidence not known:

Abdominal or stomach pain

area rash

black, tarry stools

bleeding gums

blood in urine or stools

chest pain or discomfort

chills

clay-colored stools

cough

dark urine

diarrhea

difficulty breathing

difficult, burning, or painful urination

fever

general tiredness and weakness

headache, sudden and severe

inability to speak

itching

lab results that show problems with liver

light-colored stools

loss of appetite

noisy breathing

pain or discomfort in arms, jaw, back or neck

pinpoint red or purple spots on skin

rash

seizures

slow or irregular heartbeat

slurred speech

sore throat

sores, ulcers, or white spots on lips or in mouth

swollen glands

temporary blindness

tightness in chest

unpleasant breath odor

unusual bleeding or bruising

upper right abdominal pain

vomiting

vomiting of blood

weakness in arm and/or leg on one side of the body, sudden and severe

wheezing

yellow eyes and skin

Minor Side Effects

Some of the side effects that can occur with doxazosin may not need medical attention. As your body adjusts to the medicine during treatment these side effects may go away. Your health care professional may also be able to tell you about ways to reduce or prevent some of these side effects. If any of the following side effects continue, are bothersome or if you have any questions about them, check with your health care professional:

More common:

Headache

lack or loss of strength

unusual tiredness or weakness

Less common:

Acid or sour stomach

back pain

belching

bladder pain

cloudy urine

difficulty in moving

frequent urge to urinate

heartburn

indigestion

joint pain

lower back or side pain

muscle aching, cramping, or weakness

muscle pains or stiffness

nausea

nervousness, restlessness, unusual irritability

runny nose

sleepiness or drowsiness

sneezing

sore throat

stomach discomfort, upset or pain

swollen joints

Incidence not known:

Anxiety

burning, crawling, itching, numbness, prickling, “pins and needles”, or tingling feeling

change in frequency or urination

dry mouth

feeling of warmth

frequent urination

general feeling of discomfort or illness

hair loss

hives or welts

hyperventilation

increased urge to urinate during the night

increased volume of pale dilute urine

loss of appetite

painful urination

redness of skin

redness of the face, neck, arms and occasionally upper chest

shaking

swelling of the breasts or breast soreness in both females and males

thinning of hair

trouble in holding or releasing urine

trouble sleeping

waking to urinate at night

weight loss

For Healthcare Professionals

Applies to doxazosin: oral tablet, oral tablet extended release

General

Doxazosin is generally well-tolerated. Side effects are usually mild to moderate in intensity and may resolve with continued therapy. [Ref ]

Cardiovascular

Like other alpha-blockers, doxazosin has been associated with significant decreases in total and LDL serum cholesterol and serum triglycerides. This beneficial effect on the lipid profile may be important in some patients with ischemic heart disease.

Data from ALLHAT (which led to the discontinuation of the doxazosin-treatment arm of the study) indicated that users of doxazosin had 25% more cardiovascular events and were twice as likely to be hospitalized for congestive heart failure compared to users of chlorthalidone. However, these two drugs were found to be similarly effective in preventing heart attacks and in reducing the risk of death from all causes. [Ref ]

Cardiovascular side effects are the most common. Dizziness has been reported in 3% to 14% of patients and is most likely to occur 2 to 6 hours after dosing. It may be minimized by administration of the drug at bedtime, particularly at the beginning of therapy. Rarely, syncope has been associated with doxazosin, and appears to be more likely in patients greater than 65 years old. Peripheral edema, palpitations, chest pain, and tachycardia have been reported in 7%, 4%, 3%, and 2% of patients, respectively.

Cerebrovascular accidents, postural dizziness, bradycardia, cardiac arrhythmias, and myocardial infarction have been reported in postmarketing studies.

Patients treated with doxazosin during the Antihypertensive and Lipid Lowering Treatment to Prevent Heart Attack Trial (ALLHAT) had a greater likelihood of developing congestive heart failure. [Ref ]

Ocular

Ocular side effects including Intraoperative Floppy Iris Syndrome (IFIS) have been observed in some patients undergoing phacoemulsification cataract surgery while being treated with alpha-1 blockers.

Blurred vision has been reported in postmarketing studies. [Ref ]

Most reports were in patients treated with an alpha-1 blocker at the time IFIS occurred, but in some instances the alpha-1 blocker had been stopped prior to surgery. The manufacturer recommends that patients be questioned to determine whether or not they have taken alpha-1 blockers prior to being considered for cataract surgery. If it is determined that the patient has taken an alpha-1 blocker, the patient's ophthalmologist should be prepared for possible modifications to their surgical technique that may be necessary should IFIS be observed during the procedure. [Ref ]

Nervous system

Anxiety, insomnia, and paresthesias have each been reported in 2% of patients. Dry mouth and flushing have been reported in less than 2% of patients. [Ref ]

Nervous system side effects have included dizziness in up to 17%, headache or fatigue/lethargy in 10% to 15%, and somnolence in 5% of patients. Hypoesthesia and paresthesia have been reported in postmarketing studies. [Ref ]

Respiratory

Respiratory system complaints of dyspnea and rhinitis have been reported in 3% to 4% of patients. Aggravated bronchospasm has been reported in postmarketing studies. [Ref ]

Gastrointestinal

Gastrointestinal side effects are unusual, and are mainly limited to nausea or diarrhea in 1% to 3% of patients. [Ref ]

Dyspepsia, general abdominal pain, flatulence, and constipation have each been reported in about 1% of patients. [Ref ]

Musculoskeletal

Musculoskeletal pain has been reported in 1% to 5% of patients. Muscle cramps and muscle weakness have been reported in postmarketing studies. [Ref ]

Genitourinary

Genitourinary complaints are rare. Approximately 3% of men have reported impotence and about 1% have reported urinary frequency. Hematuria, micturition disorder, micturition frequency, nocturia, polyuria, and gynecomastia have been reported in postmarketing studies. In addition, at lease one case of priapism associated with doxazosin use has been reported. [Ref ]

The Treatment of Mild Hypertension Study (TOMHS), a randomized, placebo-controlled, double-blind study has shown that there is a slightly and significantly higher incidence of sexual dysfunction (obtaining and maintaining erections) among male patients who were taking doxazosin for 48 months compared with placebo [Ref ]

Psychiatric

In a study of 23 hypertensive patients with renal insufficiency, a single case of a personality change has been associated with the use of doxazosin. [Ref ]

Psychiatric abnormalities including depression and anxiety have been reported in less than 2% of patients. Anorexia and nervousness have been reported in postmarketing studies. In addition, at least one case of psychosis associated with doxazosin use has been reported. [Ref ]

Hematologic

The manufacturer has reported 4 possible doxazosin-related cases of neutropenia from a database of 2,400 patients. In cases where follow-up was available the white blood cell count and differential cell count returned to normal after drug discontinuation. No patients became symptomatic as a result of the low white blood cell or neutrophil counts. [Ref ]

Hematologic abnormalities are extremely rare. Decreases in baseline white blood cell and neutrophil counts of 2.4% and 1.0%, respectively, have been reported from controlled clinical trials. Leukopenia, purpura, and thrombocytopenia have been reported in postmarketing studies. [Ref ]

Hypersensitivity

From a study of 1,548 patients, less than 2% reported a rash. [Ref ]

Hypersensitivity to doxazosin has been rarely reported. [Ref ]

Hepatic

Hepatic side effects including abnormal liver function tests, hepatitis, cholestatic hepatitis, and jaundice have been reported in postmarketing studies. [Ref ]

Dermatologic

Dermatologic side effects have included urticaria. Alopecia has been reported in postmarketing studies. [Ref ]

Other

Other side effects including fatigue, hot flashes, and malaise have been reported in postmarketing studies. [Ref ]

References

1. "Multum Information Services, Inc. Expert Review Panel"

2. Kaplan SA, Soldo KA, Olsson CA "Effect of dosing regimen on efficacy and safety of doxazosin in normotensive men with symptomatic prostatism: a pilot study." Urology 44 (1994): 348-52

3. Roehrborn CG, Siegel RL "Safety and efficacy of doxazosin in benign prostatic hyperplasia: a pooled analysis of three double-blind, placebo-controlled studies." Urology 48 (1996): 406-15

4. Messerli FH "Implications of discontinuation of doxazosin arm of ALLHAT." Lancet 355 (2000): 863-4

5. Bartels AC, de Vries PM, Oe LP, van Bronswyk H, Donker AJ, Reveillaud RJ, Fillastre JP, Zech P "Doxazosin in the treatment of patients with mild or moderate hypertension and mild or moderate renal insufficiency." Am Heart J 116 (1988): 1772-7

6. Ball SG "Discontinuation of doxazosin arm of ALLHAT." Lancet 355 (2000): 1558

7. Gillenwater JY, Conn RL, Chrysant SG, Roy J, Gaffney M, Ice K, Dias N "Doxazosin for the treatment of benign prostatic hyperplasia in patients with mild to moderate essential hypertension: a double-blind, placebo-controlled dose-response multicenter study." J Urol 154 (1995): 110-5

8. Fulton B, Wagstaff AJ, Sorkin EM "Doxazosin: an update of its clinical pharmacology and therapeutic applications in hypertension and benign prostatic hyperplasia." Drugs 49 (1995): 295-320

9. Young RA, Brogden RN "Doxazosin. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic efficacy in mild or moderate hypertension." Drugs 35 (1988): 525-41

10. Scott PJ, Hosie J, Scott MG "A double-blind and cross-over comparison of once daily doxazosin and placebo with steady-state pharmacokinetics in elderly hypertensive patients." Eur J Clin Pharmacol 34 (1988): 119-23

11. Kazumi T, Shima F, Hotta K, Hozumi T, Ishida Y, Yoshino G "Effects of doxazosin on blood pressure and serum lipid levels in hypertensive patients." Curr Ther Res Clin Exp 55 (1994): 843-50

12. Langdon CG, Packard RS "Doxazosin in hypertension - results of a general practice study in 4809 patients." Br J Clin Pract 48 (1994): 293-8

13. Troffa C, Manunta P, Dessifulgheri P, Pazzola A, Sabino G, Patteri G, Tonolo G, Pupita G, Glorioso N, Gitti M, Rappelli A "Efficacy and tolerability of doxazosin alone or in combination with chlorthalidone in essential hypertension." Curr Ther Res Clin Exp 55 (1994): 22-31

14. Lehtonen A, et al "Doxazosin effects on insulin and glucose in hypertensive patients." Am Heart J 121 (1991): 1307-11

15. Takata Y, Yoshizumi T, Ito Y, Hirota Y, Fujishima M "Effect of administration and withdrawal of doxazosin on ambulatory blood pressure in patients with essential hypertension." Angiology 46 (1995): 11-8

16. Fawzy A, Braun K, Lewis GP, Gaffney M, Ice K, Dias N "Doxazosin in the treatment of benign prostatic hyperplasia in normotensive patients: a multicenter study." J Urol 154 (1995): 105-9

17. Torvik D, Madsbu HP "An open one-year comparison of doxazosin and prazosin for mild to moderate essential hypertension." Am J Cardiol 59 (1987): g68-72

18. Fulton B, Wagstaff J, Sorkin EM "Doxazosin: an update of its clinical pharmacology and therapeutic applications in hypertension and benign prostatic hyperplasia." Drugs 49 (1995): 295-320

19. Ahaneku JE, Taylor OG, Walker D, Agbedana OE, Salako LA "Blood pressure and biochemical changes during doxazosin monotherapy in nigerian hypertensive patients." Curr Ther Res Clin Exp 55 (1994): 1067-74

20. Messerli FH "Implications of discontinuation of doxazosin arm of ALLHAT (Vol 355, pg 863, 1920)." Lancet 355 (2000): 1280

21. Levy D, Walmsley P, Levenstein M "Principal results of the hypertension and lipid trial (HALT): a multicenter study of doxazosin in patients with hypertension." Am Heart J 131 (1996): 966-73

22. Stoschitzky K, Stoschitzky G, Wonisch M, Brussee H "Differential effects of urapidil and doxazosin on heart rate." Eur J Clin Pharmacol 63 (2007): 259-62

23. "Product Information. Cardura (doxazosin)." Pfizer US Pharmaceuticals, New York, NY.

24. Avisrror MU, Fernandez IA, Sanchez AS, Garcia-Pando AC, Arias LM, Del Pozo JG "Doxazosin and priapism." J Urol 163 (2000): 238

25. Grimm RH, Granditis GA, Prineas RJ, et al. "Long-term effects on sexual function of five antihypertensive drugs and nutritional hygienic treatment in hypertensive men and women: treatment of mild hypertension study (TOMHS)." Hypertension 29 (1997): 8-14

26. Evans M, Perera PW, Donoghue J "Drug induced psychosis with doxazosin." BMJ 314 (1997): 1869

Not all side effects for doxazosin may be reported. You should always consult a doctor or healthcare professional for medical advice. Side effects can be reported to the FDA here .

Reclipsen, Reclipsen

Reclipsen

Reclipsen is an oral contraceptive that is available only by prescription. This birth control pill is a combined oral contraceptive, meaning it contains an estrogen and a progestin, and works primarily by stopping ovulation. It comes in the form of a tablet, and it is important to take it at the same time every day. There is only one standard dose of Reclipsen, regardless of age, weight, or medical conditions.

What Is Reclipsen?

Reclipsen™ (desogestrel/ethinyl estradiol) is a prescription oral contraceptive (commonly known as a birth control pill ) and is a generic version of Desogen ®. There are several other birth control pills that are equivalent to Reclipsen, including:

Desogen ® (made by Organon USA, Inc.)

Emoquette ™ (made by Patheon, Inc. for Qualitest Pharmaceuticals)

Enskyce ™ (made by Lupin Pharmaceuticals)

Ortho-Cept ® (made by Ortho-McNeil Pharmaceutical, Inc.)

Apri ® (made by Barr Pharmaceuticals, Inc.)

Solia ™ (made by Prasco Laboratories).

(Click What Is Reclipsen Used For? for more information on what Reclipsen is used for, including possible off-label uses.)

Side Effects of Reclipsen

As with any medicine, side effects are possible with Reclipsen. However, not everyone who uses the contraceptive will experience side effects. In fact, most people tolerate it quite well. If side effects do occur, in most cases, they are minor and either require no treatment or can easily be treated by you or your healthcare provider. Serious side effects are less common.

Common side effects of Reclipsen include, but are not limited to:

Nausea

Vomiting

Breakthrough bleeding or spotting (between periods)

Breast tenderness

Headaches .

(Click Side Effects of Reclipsen to learn more, including potentially serious side effects that you should report immediately to your healthcare provider.)

Kalmoxilin 500mg, Kalmoxillin

Komposisi Tiap kaplet mengandung : Amoksisilin Trihidrat setara dengan Amoksisilin. 500 mg

Farmakologi Amoksisilin adalah turunan dari penisilin semi sintetik yang aktif terhadap mikroorganisme Gram-positif dan Gram-negatif. Ekskresi amoksisilin dihambat jika diberikan bersamaan dengan probenesid, sehingga dapat memperpanjang efek terapi. Kapsul, Kaplet dan Sirup Kering Amoksisilin stabil dalam suasana asam lambung. Amoksisilin diabsorpsi dengan cepat dan baik pada saluran cerna serta tidak dipengaruhi oleh adanya makanan. Amoksisilin terutama diekskresikan dalam bentuk tidak berubah di dalam urin.

Injeksi Pemberian 250 mg atau 500 mg amoksisilin injeksi intramuskular, diperoleh kadar puncak 5,5 – 10 μg/mL dalam 60 menit. Ekskresi amoksisilin sebagian besar melalui ginjal. Pada fungsi ginjal normal sekitar 70% amoksisilin akan diekskresikan dalam bentuk yang tidak berubah (pada pemberian i. m. dan i. v. yang cepat) setelah 6 jam.

Indikasi Amoksisilin injeksi diberikan bila pemberian oral tidak memungkinkan. Amoksisilin diindikasikan untuk terapi infeksi yang disebabkan oleh galur-galur bakteri yang peka : • Infeksi kulit dan jaringan lunak: Staphylococcus sp. bukan penghasil penisilinase, Streptococcus sp. E. coli. • Infeksi saluran nafas: Haemophilus influenzae, Streptococcus sp. termasuk Streptococcus pneumoniae, Staphylococcus sp. bukan penghasil penisilinase, E. coli. • Infeksi saluran genitourinaria: E. coli, P. mirabilis dan Streptococcus faecalis. • Gonore: N. gonorrhoeae (bukan penghasil penisilinase).

Dosis dan Cara Pemberian Kapsul, Kaplet dan Sirup Kering • Dewasa dan anak-anak > 20 kg. 250 – 500 mg tiap 8 jam. • Anak-anak < 20 kg. 20 – 40 mg/kg BB sehari dalam dosis terbagi tiap 8 jam. • Penderita gangguan ginjal, perlu dilakukan pengurangan dosis. Pada penderita yang menjalani dialisa peritoneal, dosis maksimum yang dianjurkan 500 mg sehari. • Uretritis gonokokus. 3 g dosis tunggal.

Injeksi Penderita dengan fungsi ginjal normal : • Infeksi saluran nafas bagian atas, infeksi saluran genitourinaria, infeksi kulit dan jaringan lunak : Dewasa. 250 mg tiap 6-8 jam, tergantung kondisi penderita. Anak-anak (< 20 kg). 20 mg/kg/hari dalam dosis terbagi tiap 6-8 jam. Pada infeksi berat, dosis dapat ditingkatkan menjadi 500 mg tiap 6-8 jam (dewasa) dan 40 mg/kg/hari dalam dosis terbagi tiap 6-8 jam (anak-anak). • Infeksi saluran nafas bagian bawah : Dewasa. 500 mg tiap 6-8 jam. Anak-anak (< 20 kg). 40 mg/kg/hari dalam dosis terbagi tiap 6-8 jam. • Septikemia bakterialis : Dewasa. Pada infeksi yang lebih serius. 1 gram tiap 6 jam injeksi i. v. perlahanlahan atau infus i. v. dalam waktu 30-60 menit. Anak-anak (< 20 kg). 20 – 40 mg/kg/hari tiap 6 jam.

Penderita dengan gangguan fungsi ginjal : Klirens kreatinin > 30 mL/menit Tidak perlu penyesuaian dosis.

Sedang 1 gr --> 500 mg/ 12 jam (Klirens kreatinin 10 –30 mL/menit)

Berat 1 gr --> 500 mg/ 24 jam (Klirens kreatinin < 10 ml/menit)

Peringatan dan Perhatian • Hati-hati untuk pemberian obat ini pada penderita leukemia limfatik karena dapat menimbulkan reaksi hipersensitivitas berupa ruam kulit. • Dapat menyebabkan terjadinya kolitis berat. • Sebelum pengobatan dengan amoksisilin harus dilakukan uji kepekaan terhadap penisilin. • Amoksisilin harus digunakan dengan hati-hati pada wanita hamil dan menyusui. • Pengobatan dengan amoksisilin dalam jangka waktu lama harus disertai dengan pemeriksaan terhadap fungsi ginjal, hati dan darah. • Dapat menimbulkan superinfeksi (biasanya penyebabnya Enterobacterium, Pseudomonas, Staphylococcus aureus, Candida). Bila terjadi hal tersebut, hentikan pengobatan dan diberikan alternatif antimikroba lain. • Penderita dengan gagal fungsi ginjal, harus dilakukan monitor kadarnya di dalam plasma dan urin serta perlu dilakukan penyesuaian dosis. • Amoksisilin oral tidak untuk pengobatan meningitis atau infeksi pada tulang sendi karena amoksisilin oral tidak menembus ke dalam cairan serebrospinal atau sinovial. • Amoksisilin injeksi tidak boleh dicampur dengan produk darah atau cairan protein seperti hidrolisat protein atau dengan emulsi lipid intravena. • Penggunaan bersama aminoglikosida, tidak boleh dicampur di dalam satu siringe/wadah cairan infus karena aktivitas aminoglikosida akan berkurang. • Pada pengobatan dengan amoksisilin dosis tinggi, terutama pada bolus injeksi pemasukan cairan dan pengeluaran air kemih harus diperhatikan agar cukup banyak. • Amoksisilin injeksi stabil bila dicampur dengan cairan intravena pada 23oC jika infus diberikan dalam jangka waktu tidak lebih dari 6 jam. • Cairan harus diganti setelah 1 jam jika amoksisilin injeksi diberikan dalam cairan yang mengandung dekstrose atau karbohidrat lainnya, atau diganti setelah tiga jam jika cairan mengandung natrium laktat.

Efek Samping • Reaksi kepekaan seperti erythematous maculopapular rashes, urtikaria, serum sickness. • Reaksi kepekaan yang serius dan fatal adalah reaksi anafilaksis terutama terjadi pada penderita yang hipersensitif terhadap penisilin. • Gangguan saluran cerna seperti mual, muntah, diare. • Reaksi-reaksi hematologi (biasanya bersifat reversibel). • Khusus pada pemberian injeksi dapat menyebabkan flebitis dan rasa sakit pada tempat injeksi.

Kontraindikasi Penderita hipersensitif atau mempunyai riwayat hipersensitif terhadap antibiotik beta laktam (penisilin, sefalosporin).

Interaksi Obat • Probenesid dapat meningkatkan dan memperpanjang kadar amoksisilin dalam darah. • Penggunaan bersamaan alopurinol dapat menyebabkan peningkatan terjadinya reaksi kulit.

Kemasan • Kaplet 500 mg. Dos berisi 3 strip x 10 kaplet Reg. No. DKL7811607404A1

Gunakan segera setelah dilarutkan. Setelah dilarutkan. Penyimpanan pada suhu kamar maksimal 1 jam. Penyimpanan pada lemari es maksimal 3 jam.

Kapsul, Kaplet dan Sirup kering Simpan pada suhu di bawah 30oC. Injeksi Simpan pada suhu di bawah 25oC.

HARUS DENGAN RESEP DOKTER

• HARGA BLM DISC: Rp. 2.662,-

Buy Heart Disease - Durabeta (Brand Name Tenormin) Online - Order Atenolol - Purchase Heart Disease

Common use Tenormin is a beta-adrenergic blocking agent. Its role is to block the effects of adrenergic drugs, such as adrenaline or epinephrine, on nerves of the sympathetic nervous system. Tenormin reduces the heart rate and is used for treatment of abnormally rapid heart rhythms, arterial hypertension, angina, acute myocardial infraction, tachycardia (different types), ventricular fibrillation and others.

Dosage and direction Take Tenormin before meals or at bedtime. Your dose depends on your condition and should be administered by your doctor. Take the medication exactly as prescribed. Do not change the dose and do not stop suddenly treatment even if you feel better as hypertension often has no symptoms. Avoid drinking alcohol. Let your surgeon know if you are taking Tenormin if you plan to be operated.

Precautions Do not take Tenormin if it was not Tenormin should be taken with a glass of water once a day at the same time. Do not stop taking the medication suddenly as it may worsen your condition. Continue taking the medication even if you feel fine as hypertension and diseases of a heart maybe a life long illness. Inform your surgeon if you take Tenormin, if you need to be operated.

Hypersensitivity, sick sinus syndrome, sinus bradycardia (rate slower than 50 per minute), atrioventricular block (degree II and III), arterial hypotension, acute or chronic heart failure, peripheral blood flow disorders, breastfeeding. Cautiousness should be exercised in patients with diabetes, hypopotassemia, pulmonary emphysema, asthma, liver and kidney diseases pregnancy and with other conditions.

Possible side effect Side effects are rare and transient if occur. They may include weakness, fatigue, dizziness, headache, depression, dreaming, insomnia, memory loss, abdominal cramps, diarrhea, constipation, nausea, fever, impotence, lightheadedness, slow heart rate, low blood pressure, numbness, tingling, cold extremities, and sore throat and also allergy.

Drug interaction Tenormin can aggravate conditions of patients with asthma, chronic bronchitis, or emphysema. In patients with slow heart rates and heart blocks, Tenormin can slow up heart rates considerably. Tenormin reduces the force of heart muscle contraction and worsens conditions of patients with heart failure. Non-steroidal anti-inflammatory drugs, estrogens, sympathomimetics, xanthines weaken hypotensive effect of Tenormin.

Missed dose Never take a double dose of this medication. If it is almost time of the next dose just skip the missed portion and continue taking the medicine according to the schedule.

Overdose Symptoms of an overdose are uneven heartbeats, shortness of breath, dizziness, weakness, fainting, bluish-colored fingernails, convulsions. If you experience this, call your doctor immediately.

Storage Tablets should be stored at room temperature between 25-25 C (68-70 F) away from light and moisture.

Disclaimer We provide only general information about medications which does not cover all directions, possible drug integrations, or precautions. Information at the site cannot be used for self-treatment and self-diagnosis. Any specific instructions for a particular patient should be agreed with your health care adviser or doctor in charge of the case. We disclaim reliability of this information and mistakes it could contain. We are not responsible for any direct, indirect, special or other indirect damage as a result of any use of the information on this site and also for consequences of self-treatment.

Electronic Version) 2015, Teedex

Ricesteele Manufacturing Ltd

4.8 Undesirable effects

Adverse effects of paracetamol are rare but hypersensitivity including skin rash may occur. There have been a few reports of blood dyscrasias including thrombocytopenia and agranulocytosis but these were not necessarily causally related to paracetamol.

Chronic hepatic necrosis has been reported in a patient who took daily therapeutic doses of paracetamol for about a year and liver damage has been reported after daily ingestion of excessive amounts for shorter periods.

A review of a group of patients with chronic active hepatitis failed to reveal differences in the abnormalities of liver function in those who were long-term users of paracetamol nor was the control of the disease improved after paracetamol withdrawal.

Nephrotoxic effects following therapeutic doses of paracetamol are uncommon. Papillary necrosis has been reported after prolonged administration.

Diphenhydramine Side Effects

CNS effects: Drowsiness (usually diminishes within a few days), paradoxical stimulation, headache, psychomotor impairment.

Antimuscarinic effects: Urinary retention, dry mouth, blurred vision, gastrointestinal disturbances, thickened respiratory tract secretions.

Rare side-effects: Hypotension, extrapyramidal effects, dizziness, confusion, depression, sleep disturbances, tremor, convulsions, palpitation, arrhythmia, hypersensitivity reactions, blood disorders and liver dysfunction.

Liver damage is possible in adults who have taken 10g or more of paracetamol. Ingestion of 5g or more of paracetamol may lead to liver damage if the patient has risk factors, including the following ones:

a) Long term treatment with carbamazepine, phenobarbitone, phenytoin, primidone, rifampicin, St John's Wort or other drugs that induce liver enzymes, or

b) regular consumption of ethanol in excess of recommended amounts, or

c) likely glutathione depletion, e. g. eating disorders, cystic fibrosis, HIV infection, starvation, cachexia.

Symptoms of paracetamol overdosage in the first 24 hours are pallor, nausea, vomiting, anorexia and abdominal pain. Liver damage may become apparent 12 to 48 hours after ingestion. Abnormalities of glucose metabolism and metabolic acidosis may occur. In severe poisoning, hepatic failure may progress to encephalopathy, haemorrhage, hypoglycaemia, cerebral oedema and death. Acute renal failure with acute tubular necrosis, strongly suggested by loin pain, haematuria, and proteinuria, may develop even in the absence of severe liver damage. Cardiac arrhythmias and pancreatitis have been reported.

Immediate treatment is essential in the management of paracetamol overdose. Despite a lack of significant early symptoms, patients should be referred to hospital urgently for immediate medical attention. Symptoms may be limited to nausea or vomiting and may not reflect the severity of overdose or the risk of organ damage. Management should be in accordance with established treatment guidelines.

Treatment with activated charcoal should be considered if the overdose has been taken within 1 hour. Plasma paracetamol concentration should be measured at 4 hours or later after ingestion (earlier concentrations are unreliable). Treatment with N-acetylcysteine may be used up to 24 hours after ingestion of paracetamol, however, the maximum protective effect is obtained up to 8 hours post-ingestion. The effectiveness of the antidote declines sharply after this time. If required the patient should be given intravenous N-acetylcysteine, in line with the established dosage schedule. If vomiting is not a problem, oral methionine may be a suitable alternative for remote areas, outside hospital. Management of patients who present with serious hepatic dysfunction beyond 24h from ingestion should be discussed with a liver unit.

Mild cases of overdose with antihistamines are mainly characterised by prominent anticholinergic effects including dry mouth, headache, nausea, tachycardia and urinary retention. Larger overdoses will have additional antihistamine effects which may depress or stimulate the CNS. In small children, the stimulatory effects predominate and clinical features include hallucinations, ataxia and convulsions. The child may be hot, flushed and have dilated pupils. Cardiorespiratory depression and coma can subsequently develop followed by rapid death. Overdosing diphenhydramine in adults usually results in drowsiness followed by convulsions and coma. Fever and flushing are uncommon. Overdosed patients are best treated by gastric lavage and supportive measures. Administration of activated charcoal may be useful. Convulsions can be controlled with diazepam. Peripheral anticholinergic effects can be controlled with subcutaneous neostigmine.

5. PHARMACOLOGICAL PROPERTIES

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DISCLAIMER: MediGuard is not intended to be a substitute for professional medical advice. MediGuard cannot and does not take into consideration every possible interaction or account for individual responses to medicine. Different individuals may respond to medication in different ways. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective, or appropriate for any given patient. Always seek the advice of a qualified health provider with any questions you may have before making any changes to your treatment. The use of the MediGuard site and its content is at your own risk. The MediGuard site and the information contained in it is intended for users in the United States and information in other countries may be different.

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Repriza progona

Synopsis

Autenticna autobiografska prica bliska povijesnom dnevniku kroz spoj autor-selo govori istovremeno o prozivljenom logoru i pripremi progona sela. Dramaturgija desavanja, strahovi, emocije, stav politike i humanost pojedinca cine put izdrzavanja nicim ogranicene i od nikog izrecene kazne veoma dirljivim. Ponovljena sudbina autora i sela kroz dva rata uokviruju naslov i otvaraju pitanje trazenja rjesenja za odmicanje od osvetnickih ciklusa.

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Repriza progona

Synopsis

Autenticna autobiografska prica bliska povijesnom dnevniku kroz spoj autor-selo govori istovremeno o prozivljenom logoru i pripremi progona sela. Dramaturgija desavanja, strahovi, emocije, stav politike i humanost pojedinca cine put izdrzavanja nicim ogranicene i od nikog izrecene kazne veoma dirljivim. Ponovljena sudbina autora i sela kroz dva rata uokviruju naslov i otvaraju pitanje trazenja rjesenja za odmicanje od osvetnickih ciklusa.

People who read this also enjoyed

Modern Chinese (BOOK 1) - Learn Chinese in a Simple and Successful Way - Series BOOK 1, 2, 3, 4

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Anacin - Pain Relief, Becetamol

Anacin is a pain reliever intended for the temporary relief of minor aches and pains. Anacin is a combination salicylate and stimulant. It works by blocking several different chemical processes within the body that cause pain, inflammation, and fever. It also reduces the tendency for blood to clot.

Availability: In Stock (17 packs)

Anacin is used for treating pain including, headache, muscle aches, sprains, tooth extraction and toothache, menstrual cramps, arthritis and rheumatism, and pain and fever of the common cold. It may also be used for other conditions as determined by your doctor.

Use Anacin as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Take Anacin by mouth with or without food. If stomach upset occurs, take with food to reduce stomach irritation. Taking it with food may not decrease the risk of stomach or bowel problems (eg, bleeding, ulcers) that may occur while taking Anacin.

Take Anacin with a full glass of water (8 oz/240 mL). Do not lie down for 30 minutes after taking Anacin.

Use Anacin exactly as directed on the package, unless instructed differently by your doctor. If you are taking Anacin without a prescription, follow any warnings and precautions on the label.

If you miss a dose of Anacin and you are taking it regularly, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Anacin.

Store Anacin at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Anacin out of the reach of children and away from pets.

Anacin may cause dizziness. These effects may be worse if you take it with alcohol or certain medicines. Use Anacin with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.

Avoid large amounts of food or drink that have caffeine (eg, coffee, tea, cocoa, cola, chocolate). This includes any medicines that contain caffeine.

Anacin has aspirin in it. Before you start any new medicine, check the label to see if it has aspirin in it too. If it does or if you are not sure, check with your doctor or pharmacist.

Talk to your doctor before you take Anacin or other pain relievers/fever reducers if you drink more than 3 drinks with alcohol per day. Serious stomach ulcers or bleeding can occur with the use of Anacin. Taking it in high doses or for a long time, smoking, or drinking alcohol increases the risk of these side effects. Taking Anacin with food will NOT reduce the risk of these effects. Contact your doctor or emergency room at once if you develop severe stomach or back pain; black, tarry stools; vomit that looks like blood or coffee grounds; or unusual weight gain or swelling.

Do NOT take more than the recommended dose or use for longer than prescribed without checking with your doctor. Taking more than the recommended dose or taking Anacin regularly may be habit-forming.

Anacin may reduce the number of clot-forming cells (platelets) in your blood. To prevent bleeding, avoid situations in which bruising or injury may occur. Report any unusual bleeding, bruising, blood in stools, or dark, tarry stools to your doctor.

Aspirin has been linked to a serious illness called Reye syndrome. Do not give Anacin to a child or teenager who has the flu, chickenpox, or a viral infection. Contact your doctor with any questions or concerns.

Diabetes patients - Anacin may affect your blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.

If Anacin has a strong vinegar-like smell upon opening, do not use. It means the medicine is breaking down. Throw the bottle away safely and out of the reach of children; contact your pharmacist and replace.

Tell your doctor or dentist that you take Anacin before you receive any medical or dental care, emergency care, or surgery.

Do not take Anacin for at least 7 days after any surgery unless directed by your health care provider.

Do not take Anacin for more than 10 days for pain or for more than 3 days for fever unless directed to do so by your health care provider.

Different brands of Anacin may have different dosing instructions for CHILDREN. Follow the dosing instructions on the package labeling. If your doctor has given you instructions, follow those. If you are unsure of the dose to give a child, check with your doctor or pharmacist.

Do NOT use Anacin if:

you are allergic to any ingredient in Anacin

you are a child or teenager with influenza (flu) or chickenpox

you have bleeding problems such as hemophilia, von Willebrand disease, or low blood platelets, or you have active severe bleeding

you have had a severe allergic reaction (eg, severe rash, hives, breathing difficulties, dizziness) to aspirin, tartrazine, or a nonsteroidal anti-inflammatory drug (NSAID) (eg, ibuprofen, naproxen, celecoxib)

you are taking anticoagulants (eg, heparin, warfarin) or methotrexate

Before using Anacin:

Some medical conditions may interact with Anacin. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have alcoholism or if you consume 3 or more alcohol-containing drinks every day

if you have asthma, bleeding or clotting problems, growths in the nose (nasal polyps), kidney or liver problems, stomach or intestinal problems (eg, ulcer, inflammation), heart problems, heartburn, upset stomach, stomach pain, hives, influenza (flu) or chickenpox, or vitamin K deficiency

if you have anxiety, trouble sleeping, or heart problems

if you are a child with a stroke, a weakened blood vessel (cerebral aneurysm) or bleeding in the brain, rheumatic disease (eg, rheumatoid arthritis), or Kawasaki syndrome (a rare inflammation causing heart problems in children)

Some MEDICINES MAY INTERACT with Anacin. Tell your health care provider if you are taking any other medicines.

PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Anacin while you are pregnant. Anacin is not recommended during the last 3 months (third trimester) of pregnancy because it may cause harm to the fetus. Anacin is found in breast milk. If you are or will be breast-feeding while you use Anacin, check with your doctor. Discuss any possible risks to your baby.

All medicines may cause side effects, but many people have no, or minor, side effects. Anacin's side effects may include dizziness, heartburn, irritability, nausea, nervousness, rashes, hives, bloody stools, drowsiness, hearing loss, ringing in the ears, and trouble sleeping.

Check with your doctor if any of the listed above most COMMON side effects persist or become bothersome.

Seek medical attention right away if any of these SEVERE side effects occur: severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); black or bloody stools; confusion; diarrhea; drowsiness; hearing loss; ringing in the ears; severe or persistent dizziness; severe or persistent stomach pain or heartburn; shakiness; trouble sleeping; vomiting.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects.

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Important Notice: The Drugs. com international database is in BETA release. This means it is still under development and may contain inaccuracies. It is not intended as a substitute for the expertise and judgement of your physician, pharmacist or other healthcare professional. It should not be construed to indicate that the use of any medication in any country is safe, appropriate or effective for you. Consult with your healthcare professional before taking any medication.

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Cefuroxime - Side Effects, Dosage, Interactions, Cefuzime

Cefuroxime

Cefuroxime is a prescription drug available under the brand names Ceftin and Zinacef.

It's an antibiotic used to treat certain infections caused by bacteria, such as sinus infections, throat infections, Lyme disease. and gonorrhea.

Cefuroxime was originally approved by the Food and Drug Administration (FDA) under the brand name Ceftin, manufactured by GlaxoSmithKline, in 1987.

Cefuroxime Warnings

You should not take cefuroxime if you:

Are allergic to cefuroxime or any of the other ingredients contained in the drug

Are taking Theracrys (BCG live intravesical)

Talk to your doctor before taking cefuroxime if you:

Are allergic to penicillin

Are allergic to other antibiotics such as ceflacor, cefdinir, Keflex (cephalexin), or antibiotics in the cephalosporin class

Have kidney or liver problems

Have seizures

Have poor eating habits or suffer from malnutrition

Have recently had an either infection or inflammation of your intestines while or after taking antibiotics

Cefuroxime may reduce the effects of your birth control (pills, patches, or injections).

You may need to use a back-up form of birth control while taking cefuroxime.

Pregnancy and Cefuroxime

Cefuroxime falls under the FDA's Pregnancy Category B, which means that it's generally safe for your unborn baby.

Regardless, you should tell your doctor if you are pregnant or plan to become pregnant before taking this medication.

Cefuroxime is found in breast milk. Tell your doctor if you are breastfeeding or plan to breastfeed before you take this medication.

Cefuroxime (Ceftin) Side Effects

Common side effects of cefuroxime include:

Nausea, vomiting, and diarrhea

Kidney problems

Diaper rash

Yeast infection

An allergic reaction

Serious side effects of cefuroxime include but are not limited to:

Life-threatening allergic reaction called anaphylaxis in which you may have trouble breathing, your throat closes up, and your skin breaks out into hives

Swelling of the face, including eyes, lips, mouth, tongue, and throat

Severe and possibly life-threatening skin-reactions like Steven-Johnsons syndrome or toxic epidermal necrolysis (TENs)

Blood disorders like low platelet count or low levels of all blood cells

Low levels of white blood cells

Seizures

A severe form of diarrhea noted by loose, watery stool and a foul smell that is much worse than normal

Cefuroxime (Ceftin) Interactions

It's always important to share with your doctor and pharmacist all of the medications you are taking.

This includes prescription and over-the-counter (OTC) medications, supplements like vitamins and other dietary supplements (nutritional shakes, protein powders, etc.), herbals, and any illegal or recreational drugs.

You should not take cefuroxime if you are taking Theracrys (BCG live intravesical).

Some other medications that have serious interactions with Cefuroxime include:

Acid-reflux medications like Tagamet (cimetidine), Dexilant (deslansoprazole), and Aciphex (rabeprazole)

Other acid-reflux medications like Pepcid (famotidine), Zantac (ranitidine), and Axid (nizatidine)

Vivotif (live typhoid vaccine)

Aluminum hydroxide, calcium carbonate, magnesium hydroxide, sodium bicarbonate

Cellcept (mycophenolate mofetil) and Myfortic (mycophenolic acid)

Cefuroxime and Alcohol

You should avoid or limit alcohol consumption while taking cefuroxime.

Cefuroxime and Grapefruit Juice

You should avoid eating grapefruit and drinking grapefruit juice while taking cefuroxime.

Grapefruit juice slows down how quickly the body is able to break down cefuroxime, which could cause levels in the blood to rise dangerously high.

Cefuroxime (Ceftin) Dosage

Cefuroxime comes in 250 mg and 500 mg tablets.

Doses typically range from 250 mg twice a day to 500 mg twice a day to be taken for 5 to 10 days for most infections.

Lyme disease symptoms may be treated for up to 20 days.

For gonorrhea, your doctor may prescribe a one-time dose of 1000 mg.

It is very important to take cefuroxime exactly as your doctor prescribes and to finish taking all of the medication -- even if you start to feel better or your symptoms disappear.

Otherwise, the infection might return and become much more difficult to treat.

Cefuroxime Overdose

If you suspect an overdose of cefuroxime you should contact a poison control center or emergency room immediately.

You can get in touch with a poison control center at (800) 222-1222.

Missed Dose of Cefuroxime

If you miss a dose of Cefuroxime, try to take it as soon as you remember.

If it's almost time for the next dose, skip the missed dose and take your next dose at the regular time.

Do not take two doses of the medication at the same time.

Nexterone (Amiodarone Hcl), Nexterone

It's about time

It's time to consider the first and only premixed amiodarone

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NEXTERONE (amiodarone HCl) Premixed Injection is indicated for initiation of treatment and prophylaxis for frequently recurring ventricular fibrillation (VF) and hemodynamically unstable ventricular tachycardia (VT) in patients refractory to the therapy. Nexterone also can be used to treat patients with VT/VF for whom oral amiodarone is indicated, but who are unable to take oral medication. During or after treatment with NEXTERONE, patients may be transferred to oral amiodarone therapy.

At a moment's notice

Manufacturer-prepared amiodarone for multiple healthcare settings

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NEXTERONE (amiodarone HCl) Premixed Injection is indicated for initiation of treatment and prophylaxis for frequently recurring ventricular fibrillation (VF) and hemodynamically unstable ventricular tachycardia (VT) in patients refractory to the therapy. Nexterone also can be used to treat patients with VT/VF for whom oral amiodarone is indicated, but who are unable to take oral medication. During or after treatment with NEXTERONE, patients may be transferred to oral amiodarone therapy.

When needed in time

It's time to consider the first and only premixed amiodarone

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NEXTERONE (amiodarone HCl) Premixed Injection is indicated for initiation of treatment and prophylaxis for frequently recurring ventricular fibrillation (VF) and hemodynamically unstable ventricular tachycardia (VT) in patients refractory to the therapy. Nexterone also can be used to treat patients with VT/VF for whom oral amiodarone is indicated, but who are unable to take oral medication. During or after treatment with NEXTERONE, patients may be transferred to oral amiodarone therapy.

Manufacturer Prepared Premixed Amiodarone Nexterone - Ready to Administer

In the ER. The CCU. The ICU. The Cath Lab. NEXTERONE premixed amiodarone is ready and at your fingertips. Plus, it's manufacturer prepared so it can help minimize medication errors related to compounding and is ready to deliver to patients without the need for admixing

Scroll down for indications, important risk information and full prescribing information

Two-Year Shelf Life Nexterone - Extended stability

Currently, admixing generic forms of amiodarone limit you to 2-24 hours of room temperature stability. NEXTERONE premixed amiodarone has a shelf life of 24 months. That's right, months-not hours. Our proprietary GALAXY containers and cGMP aseptic-fill technology enable us to create an amiodarone formulation that is premixed with a long shelf life.* In addition, GALAXY containers are non-PVC and non-DEHP.

Store in carton to protect from light until ready to use.

Ready To Use Nexterone - There When You Need It

Extended shelf life means that NEXTERONE Premixed Injection can be stored in crash carts, automated dispensing cabinets. standing by. until the instant it is needed.* And if you're not a 24/7 pharmacy-enough said.

Store in carton to protect from light until ready to use.

Scroll down for Indications, Important Risk Information and Full Prescribing Information

Indications and Usage

NEXTERONE (amiodarone HCl) Premixed Injection is indicated for initiation of treatment and prophylaxis of frequently recurring ventricular fibrillation (VF) and hemodynamically unstable ventricular tachycardia (VT) in patients refractory to other therapy. NEXTERONE also can be used to treat patients with VT/VF for whom oral amiodarone is indicated, but who are unable to take oral medication. During or after treatment with NEXTERONE, patients may be transferred to oral amiodarone therapy.

Use NEXTERONE for acute treatment until the patient's ventricular arrhythmias are stabilized. Most patients will require this therapy for 48 to 96 hours, but NEXTERONE may be safely administered for longer periods if necessary.

Important Risk Information

NEXTERONE (amiodarone HCl) Premixed Injection is contraindicated in patients with:

Known hypersensitivity to any of the components of NEXTERONE, including iodine

Cardiogenic shock

Marked sinus bradycardia

Second - or third-degree atrio-ventricular (AV) block unless a functioning pacemaker is available

NEXTERONE should be administered only by physicians who are experienced in the treatment of life-threatening arrhythmias, who are thoroughly familiar with the risks and benefits of amiodarone therapy, and who have access to facilities adequate for monitoring the effectiveness and side effects of treatment.

Because of the long half-life of amiodarone and its metabolite desethylamiodarone, the potential for adverse reactions or interactions, as well as observed adverse effects, can persist following amiodarone withdrawal.

Hypotension is the most common adverse reaction seen with intravenous amiodarone. Clinically significant hypotension during infusions was seen most often in the first several hours of treatment and appeared to be related to the rate of infusion. Monitor the initial rate of infusion closely and do not exceed the recommended rate. In some cases, hypotension may be refractory and result in a fatal outcome. Treat hypotension initially by slowing the infusion; additional standard therapy may be needed, including: vasopressors, positive inotropic agents and volume expansion.

Drug-related bradycardia that was not dose-related occurred while patients were receiving intravenous amiodarone for life-threatening VT/VF. Treat bradycardia by slowing the infusion rate or discontinuing NEXTERONE. Treat patients with a known predisposition to bradycardia or AV block with NEXTERONE in a setting where a temporary pacemaker is available.

Elevations of blood hepatic enzyme values ALT, AST, GGT are commonly seen in patients with immediately life-threatening VT/VF. Elevated bilirubin levels have been reported in patients administered intravenous amiodarone. In patients with life-threatening arrhythmias, the potential risk of hepatic injury should be weighed against the potential benefit of NEXTERONE therapy. Carefully monitor patients receiving NEXTERONE for evidence of progressive hepatic injury. In such cases, consider reducing the rate of administration or withdrawing NEXTERONE.

NEXTERONE may cause worsening of existing arrhythmias or precipitate a new arrhythmia sometimes leading to fatal outcomes. Monitor patients for QTc prolongation during infusion with NEXTERONE. Reserve the combination of amiodarone with other antiarrhythmic therapies that prolong the QTc to patients with life-threatening ventricular arrhythmias who are incompletely responsive to a single agent. Amiodarone causes thyroid dysfunction in some patients, which may lead to potentially fatal breakthrough or exacerbated arrhythmia.

Two percent (2%) of patients were reported to have acute respiratory distress syndrome (ARDS) during clinical studies involving 48 hours of therapy. There have been reports of early development of pulmonary fibrosis (within 1 to 3 months) following initiation of amiodarone treatment. Pulmonary toxicity including pulmonary fibrosis is a well-recognized complication of long-term amiodarone use.

Cases of optic neuropathy and optic neuritis, usually resulting in visual impairment, have been reported in patients treated with oral or intravenous amiodarone. In some cases, visual impairment has progressed to permanent blindness. Optic neuropathy and neuritis may occur at any time following initiation of therapy. A causal relationship to the drug has not been clearly established. Perform an ophthalmic examination if symptoms of visual impairment appear, such as changes in visual acuity and decreases in peripheral vision. Re-evaluate the necessity of amiodarone therapy if optic neuropathy or neuritis is suspected. Perform regular ophthalmic examination, including fundoscopy and slit-lamp examination, during administration of NEXTERONE.

Amiodarone inhibits peripheral conversion of thyroxine (T4) to triiodothyronine (T3) and may cause increased T4 levels, decreased T3 levels, and increased levels of inactive reverse T3 (rT3) in clinically euthyroid patients. Amiodarone can cause either hypothyroidism or hyperthyroidism. Evaluate thyroid function prior to treatment and periodically thereafter, particularly in elderly patients, and in any patient with a history of thyroid nodules, goiter, or other thyroid dysfunction. Because of the slow elimination of amiodarone and its metabolites, high plasma iodide levels, altered thyroid function, and abnormal thyroid function tests may persist for several weeks or even months following NEXTERONE withdrawal. Amiodarone causes hyperthyroidism in about 2% of patients. Thyrotoxicosis and arrhythmia with fatal outcome has been reported in the presence of pre-existing hyperthyroidism even following a single intravenous amiodarone dose. Consider the possibility of hyperthyroidism if any new signs of arrhythmia appear. Hypothyroidism has been reported in 2-10% of patients receiving amiodarone. Cases of severe hypothyroidism and myxedema coma, sometimes fatal, have been reported in association with amiodarone therapy. Manage hypothyroidism by reducing the dose of or discontinuing NEXTERONE and considering the need for thyroid hormone supplement.

Inform the patient that amiodarone can cause fetal harm if NEXTERONE is administered during pregnancy or if the patient becomes pregnant while taking NEXTERONE

Anaphylactic/anphylactoid reactions have been reported with intravenous amiodarone including shock (sometimes fatal), cardiac arrest, and the following manifestations: hypotension, tachycardia, hypoxia, cyanosis, rash, flushing, hyperhidrosis and cold sweat. Since NEXTERONE contains dextrose, patients with allergy to corn or corn products are at risk for allergic reaction.

The most important adverse reactions were hypotension, asystole/cardiac arrest/pulseless electrical activity (PEA), cardiogenic shock, congestive heart failure, bradycardia, liver function test abnormalities, VT, and AV block. The most common adverse reactions leading to discontinuation of intravenous amiodarone therapy were hypotension (1.6%), asystole/cardiac arrest/PEA (1.2%), VT (1.1%), and cardiogenic shock (1%).

Amiodarone is metabolized to the active metabolite desethylamiodarone (DEA) by the cytochrome P450 (CYP450) enzyme group, specifically CYP3A and CYP2C8. Amiodarone has the potential for interactions with drugs or substances that may be substrates, inhibitors or inducers of CYP450 enzymes. Amiodarone and DEA inhibits p-glycoprotein and certain CYP450 enzymes CYP1A2, CYP2C9, CYP2D6, and CYP3A, increasing exposure to other drugs. The metabolism of quinidine . procainamide . flecainide can be inhibited by amiodarone. In patients receiving digoxin therapy, administration of oral amiodarone results in an increase in serum digoxin concentration. Reduce dose of digoxin by half or discontinue digoxin. If digitalis treatment is continued, monitor serum levels. Limit the dose of simvastatin in patients on amiodarone to 20 mg daily. Limit the daily dose of lovastatin to 40 mg. Lower starting and maintenance doses of other CYP3A4 substrates (e. g. atorvastatin) may be required as amiodarone may increase the plasma concentration of these drugs. Potentiation of warfarin - type (CYP2C9 and CYP3A substrate) anticoagulant response is almost always seen in patients receiving amiodarone and can result in serious or fatal bleeding, therefore reduce the dose of the anticoagulant by one-third to one-half, and monitor INR closely. Monitor cyclosporine drug levels and renal function in patients taking both drugs. Increased steady-state levels of phenytoin during concomitant therapy with amiodarone have been reported. Monitor phenytoin levels in patients taking both drugs.

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Movileps, Movileps

Other - Movileps (Brand name: dilantin)

Dilantin is used to control seizures. It is not made to treat all types of seizures, and your doctor will determine if it is the right medication for you. Dilantin is an anti-epileptic drug, also called an anticonvulsant. It works by slowing down impulses in the brain that cause seizures.

Use Dilantin as directed by your doctor.

Do not take in larger or smaller amounts or for longer than recommended.

Do not crush, chew, break, or open a capsule. Swallow it whole. Breaking or opening the pill may cause too much of the drug to be released at one time.

To be sure Dilantin is helping your condition, your blood may need to be tested often.

If you miss a dose of Dilantin, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Dilantin.

Store Dilantin at room temperature. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Dilantin out of the reach of children and away from pets.

Active Ingredient: Phenytoin.

you are allergic to any ingredient in Dilantin or to another hydantoin (eg, fosphenytoin).

Some medical conditions may interact with Dilantin. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have a blood disease (eg, porphyria), liver disease, diabetes, or a history of lymph gland problems

if you are in very poor heath

if you drink alcohol or have a history of alcohol abuse

if you have been tested and know whether or not you have a gene type called HLA-B*1502.

Some medicines may interact with Dilantin. Tell your health care provider if you are taking any other medicines, especially any of the following:

Many other prescription and nonprescription medicines (eg, used for asthma, blood thinning, diabetes, infections, inflammation, aches and pains, high blood pressure, heart problems, high cholesterol, birth control, hormone replacement, mental or mood problems, sleep seizures), multivitamin products, and herbal or dietary supplements (eg, herbal teas, coenzyme Q10, garlic, ginseng, ginkgo, St. John's wort) may interact with Dilantin, increasing the risk of side effects. Ask your doctor or pharmacist if you are unsure if any of your medicines might interfere with Dilantin.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Dilantin may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

Important safety information:

Dilantin may cause dizziness. This effect may be worse if you take it with alcohol or certain medicines. Use Dilantin with caution. Do not drive or perform other possible unsafe tasks until you know how you react to it.

Check with your doctor before you drink alcohol while you are taking Dilantin. Alcohol may increase or decrease the amount of medicine in your blood.

Do not change brands or dose forms (eg, tablets, suspension, injection) of Dilantin without talking with your doctor.

Do not take more than the recommended dose without checking with your doctor.

Proper dental care is important while you are taking Dilantin. Brush and floss your teeth and visit the dentist regularly.

Dilantin may raise your blood sugar. High blood sugar may make you feel confused, drowsy, or thirsty. It can also make you flush, breathe faster, or have a fruit-like breath odor. If these symptoms occur, tell your doctor right away.

There have been reports of lymph node problems, including cancer, in patients who take Dilantin. It is not known if Dilantin may be the cause. Contact your doctor right away if you develop swollen lymph nodes, fever, rash, dark urine, stomach pain, or yellowing of the eyes or skin.

Tell your doctor or dentist that you take Dilantin before you receive any medical or dental care, emergency care, or surgery.

Hormonal birth control (eg, birth control pills) may not work as well while you are using Dilantin. To prevent pregnancy, use an extra form of birth control (eg, condoms).

Patients who have a certain gene type called HLA-B*1502 may have an increased risk for serious skin reactions from Dilantin. This gene type is found most commonly in Asian patients. Tell your doctor if you have been tested and know whether or not you have the HLA-B*1502 gene type. Discuss any questions or concerns with your doctor.

Dilantin may interfere with certain lab tests. Be sure your doctor and lab personnel know you are taking Dilantin.

Lab tests, including blood phenytoin levels, may be performed while you use Dilantin. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Use Dilantin with caution in the elderly; they may be more sensitive to its effects.

Women who take Dilantin may experience an increase in seizure activity if they become pregnant. Discuss any questions or concerns with your doctor. If you think you may be pregnant, contact your doctor.

Pregnancy and breast-feeding: Dilantin may cause harm to the fetus. If you think you may be pregnant, contact your doctor. You will need to discuss the benefits and risks of using Dilantin while you are pregnant. Dilantin is found in breast milk. Do not breastfeed while taking Dilantin.

All medicines may cause side effects, but many people have no, or minor, side effects.

Check with your doctor if any of these most common side effects persist or become bothersome:

Constipation; dizziness; headache; mild nervousness; nausea; trouble sleeping; vomiting.

Seek medical attention right away if any of these severe side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); bone pain; butterfly-shaped rash on the face; clumsiness or unsteadiness; confusion; dark urine; delirium; high blood sugar (flushing; fruit-like breath odor; increased thirst, hunger, or urination; rapid breathing); mental or mood changes; numbness or tingling of the hands or feet; red, swollen, blistered, or peeling skin; signs of infection (eg, chills, fever, sore throat); slurred speech; stomach pain; swollen lymph nodes; swollen or tender gums; tremor; unusual bruising or bleeding; unusual eye movements; unusual muscle movements; yellowing of the skin or eyes.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider.

Fasarax, Fasarax

Un comprimido de FASARAX cada 12 horas, se sugiere iniciar el tratamiento con la mitad de la dosis, hasta ajustar a la respuesta del paciente.

Entre 2 y 6 años 0,5 mg/kg de peso día.

Entre 6 y 12 años 10 mg/cada 12 horas.

Cada COMPRIMIDO contiene: Hidroxizina clorhidrato 20 mg;

Cada 5 mL de JARABE contienen: Hidroxizina clorhidrato 10 mg.

Antecedentes de hipersensibilidad a la droga, lactancia y primer trimestre de embarazo.

FASARAX es una antagonista H1 selectivo, con un potente efecto antipruriginoso, por lo que es especialmente útil en el tratamiento de alergias de distinta etiología; atopias, urticarias de contacto.

La molecula de hidroxizina, cruza la barrera hematoencefálica desencadenado un efecto sedante, útil en el control de afecciones psicosomáticas y cuadros moderados de ansiedad y tensión.

Puede ser utilizado con éxito en niños hiperactivos.

Estuche con 20 comprimidos.

Frasco con 120 mL de jarabe.

Avda. Pedro Aguirre Cerda 5291 - Cerrillos

Telf. 870 7500 Fax: 557 4336

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Atarax (hydroxyzine hydrochloride)

Atarax (Hydroxyzine) is used as an antihistamine for the treatment of itching, allergies, hyperalgesia, motion sickness-induced nausea, and insomnia, as well as notably for the treatment of mild anxiety. Even though it is an effective sedative, hypnotic, analgesic, and tranquilizer, it shares almost none of the abuse, dependence, addiction, and toxicity potential of other drugs used for the same range of therapeutic reasons. This drug may also be used to prevent/treat motion sickness, nausea, and vomiting related to certain conditions (e. g. traveling, after surgery). Atarax (hydroxyzine hydrochloride) is used for the short-term treatment of nervousness and tension that may occur with certain mental/mood disorders (e. g. anxiety, dementia). Atarax is prescribed for the relief of anxiety and tension brought about by psychoneurosis.

Atarax may also be used for the containment of pruritus due to allergic reactions such as chronic uticaria and contact dermatitis. Atarax may be used as a sedative when used as a premedication following general anesthesia.

Other Names : Alamon, Atazina, Durrax, Orgatrax, Quiess, Sedaril, Vistaril, Hydroxyzine, Ataraxone, Hyderax, Hixizine, Prurizin, Dalun, Fasarax, AH 3 N, Elroquil N, Iremofar, Qualidrozine, Otarex, Serecid, Iterax, Neurax, Phymorax, Abacus, Allerax, Antizine, Atano, Cerax, Drazine, Hadarax, Histan, Hizin, Honsa, Katrax, Validol, Ucerax, Neucalm

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Hyaluronic Acid, Nicozet

Other - Nicozet (Brand name: hyaluronic acid)

Hyaluronic Acid enhances proteoglycans in the joint matrix, thereby providing support for healthy joint function and maintaining joint shock absorption and cushioning.

As a dietary supplement, take 2 capsules daily, or as directed by a health care practitioner. Take with 8-10 ounces of water, with or without food.

Consult your Health Provider about the dosage appropriate for you.

If you miss a dose of Hyaluronic Acid, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Store Hyaluronic Acid at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Keep Hyaluronic Acid out of the reach of children and away from pets.

Do not take Nicozet unless administered by a healthcare professional if:

You are pregnant or breast-feeding.

Hyaluronic Acid is not known to have any side effects if taken as per the prescribed dosage.

Syntrend, Syntrend

Syntrend

Important Notice: The Drugs. com international database is in BETA release. This means it is still under development and may contain inaccuracies. It is not intended as a substitute for the expertise and judgement of your physician, pharmacist or other healthcare professional. It should not be construed to indicate that the use of any medication in any country is safe, appropriate or effective for you. Consult with your healthcare professional before taking any medication.

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Vytorin - Cholesterol Lowering, Simvahex

Vytorin (Ezetimibe/Simvastatin) is used for reducing total cholesterol, LDL cholesterol, and triglycerides and for increasing HDL cholesterol.

Vytorin is available in a 20 mg dosage ( 10 mg of ezetimibe and 10 mg of simvastatin) and in a 30 mg dosage (10 mg of ezetimibe, and 20 mg of simvastatin).

The recommended dose range of Vytorin is 10/10 mg to 10/80 mg, and it is administered once daily in the evening with or without food. Therapy is usually initiated with 10/20 mg daily, but individuals who need more than a 55% reduction in LDL cholesterol can be started on 10/40 mg daily.

Drug Class and Mechanism

Vytorin is a combination of ezetimibe (Zetia) and simvastatin (Zocor) that is used for treating high levels of cholesterol in the blood. Vytorin reduces total cholesterol and low density lipoprotein cholesterol while it increases high density lipoprotein cholesterol. The ezetimibe component of Vytorin lowers blood cholesterol by blocking the absorption of cholesterol, including dietary cholesterol, from the intestine. It does not affect the absorption of triglycerides. The simvastatin component of Vytorin belongs to a class of drugs called HMG-CoA reductase inhibitors, commonly called "statins". Statins reduce cholesterol by blocking an enzyme in the liver (HMG-CoA reductase) that produces cholesterol. Statins lower total and LDL cholesterol in the blood as well as triglycerides. They also increase HDL cholesterol. LDL cholesterol is believed to be an important cause of coronary artery disease. Lowering LDL cholesterol levels slows and may even reverse coronary artery disease. Raising HDL cholesterol levels also may slow down coronary artery disease. Vytorin was approved by the FDA in July, 2004.

Take the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not take extra medicine to make up the missed dose.

Vytorin should be stored at room temperature, 20-25 degrees C (68-77 degrees F).

Before taking ezetimibe/simvastatin, tell your doctor or pharmacist if you think you are allergic to it; or to other drugs called "statins"; or if you have any other allergies. This medication should not be used if you have certain medical conditions. Before using this medicine, consult your doctor or pharmacist if you have: active liver disease. Before using this medication, tell your doctor or pharmacist your medical history, especially of: heart disease, history of liver disease, kidney disease, underactive thyroid (hypothyroidism), poorly controlled diabetes, alcohol use. Developing severe muscle damage, which is rare, can sometimes lead to serious kidney problems (see the Side Effects section in this handout). This medication is usually temporarily stopped if you have any condition which can increase your risk of developing kidney problems. Before you stop taking your medication, notify your doctor immediately if you have any of the following conditions: major surgery, trauma, serious illness (e. g. sepsis or severe metabolic, endocrine, or electrolyte disorders), very low blood pressure, uncontrolled seizures. Limit alcoholic beverages. Daily use of alcohol may increase your chance for serious side effects. Caution is advised when using this drug in the elderly because they may be more sensitive to its side effects, especially muscle damage. This medication must not be used during pregnancy. If you become pregnant or think you may be pregnant, inform your doctor immediately. It is recommended that young girls and women of child-bearing age use effective birth control to prevent pregnancy while taking this drug. One of these drugs (simvastatin) may cause harm to your unborn child. It is not known if either drug passes into breast milk. A drug similar to simvastatin passes into breast milk, and because of this drug's potential risk of undesirable effects on a nursing infant, breast-feeding is not recommended while using ezetimibe/simvastatin. Consult your doctor before breast-feeding.

Possible Side Effects

Headache may occur. If this effect persists or worsens, notify your doctor or pharmacist promptly. This drug can sometimes cause muscle damage. Although uncommon, this may lead to very serious muscle damage called rhabdomyolysis, which in rare cases can be fatal. Seek immediate medical attention if you develop: muscle pain/tenderness/weakness (especially with fever or unusual tiredness). Tell your doctor immediately if any of these highly unlikely but very serious side effects occur: yellowing eyes and skin, dark urine, severe fatigue, stomach/abdominal pain, persistent nausea, change in the amount of urine. A serious allergic reaction to this drug is unlikely, but seek immediate medical attention if it occurs. Symptoms of a serious allergic reaction include: rash, itching, swelling, dizziness, trouble breathing. If you notice other effects not listed above, contact your doctor or pharmacist.

Do not share this medication with others. Laboratory and/or medical tests (e. g. blood cholesterol levels, liver function tests) should be performed periodically to monitor your progress or check for side effects. Consult your doctor for more details. For best results, this product should be used along with exercise, a low-cholesterol or low-fat diet, and a weight-loss program if you are overweight. Also to help reduce your risk of heart attacks and strokes, check your blood pressure regularly, seek medical treatment if your blood pressure is high, and stop smoking. Consult your doctor for more details.

Cholesterol Lowering - Simvahex (Brand name: vytorin)

Vytorin (Ezetimibe/Simvastatin) is used for reducing total cholesterol, LDL cholesterol, and triglycerides and for increasing HDL cholesterol.

Vytorin is available in a 20 mg dosage ( 10 mg of ezetimibe and 10 mg of simvastatin) and in a 30 mg dosage (10 mg of ezetimibe, and 20 mg of simvastatin).

The recommended dose range of Vytorin is 10/10 mg to 10/80 mg, and it is administered once daily in the evening with or without food. Therapy is usually initiated with 10/20 mg daily, but individuals who need more than a 55% reduction in LDL cholesterol can be started on 10/40 mg daily.

Drug Class and Mechanism

Vytorin is a combination of ezetimibe (Zetia) and simvastatin (Zocor) that is used for treating high levels of cholesterol in the blood. Vytorin reduces total cholesterol and low density lipoprotein cholesterol while it increases high density lipoprotein cholesterol. The ezetimibe component of Vytorin lowers blood cholesterol by blocking the absorption of cholesterol, including dietary cholesterol, from the intestine. It does not affect the absorption of triglycerides. The simvastatin component of Vytorin belongs to a class of drugs called HMG-CoA reductase inhibitors, commonly called "statins". Statins reduce cholesterol by blocking an enzyme in the liver (HMG-CoA reductase) that produces cholesterol. Statins lower total and LDL cholesterol in the blood as well as triglycerides. They also increase HDL cholesterol. LDL cholesterol is believed to be an important cause of coronary artery disease. Lowering LDL cholesterol levels slows and may even reverse coronary artery disease. Raising HDL cholesterol levels also may slow down coronary artery disease. Vytorin was approved by the FDA in July, 2004.

Take the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not take extra medicine to make up the missed dose.

Vytorin should be stored at room temperature, 20-25 degrees C (68-77 degrees F).

Before taking ezetimibe/simvastatin, tell your doctor or pharmacist if you think you are allergic to it; or to other drugs called "statins"; or if you have any other allergies. This medication should not be used if you have certain medical conditions. Before using this medicine, consult your doctor or pharmacist if you have: active liver disease. Before using this medication, tell your doctor or pharmacist your medical history, especially of: heart disease, history of liver disease, kidney disease, underactive thyroid (hypothyroidism), poorly controlled diabetes, alcohol use. Developing severe muscle damage, which is rare, can sometimes lead to serious kidney problems (see the Side Effects section in this handout). This medication is usually temporarily stopped if you have any condition which can increase your risk of developing kidney problems. Before you stop taking your medication, notify your doctor immediately if you have any of the following conditions: major surgery, trauma, serious illness (e. g. sepsis or severe metabolic, endocrine, or electrolyte disorders), very low blood pressure, uncontrolled seizures. Limit alcoholic beverages. Daily use of alcohol may increase your chance for serious side effects. Caution is advised when using this drug in the elderly because they may be more sensitive to its side effects, especially muscle damage. This medication must not be used during pregnancy. If you become pregnant or think you may be pregnant, inform your doctor immediately. It is recommended that young girls and women of child-bearing age use effective birth control to prevent pregnancy while taking this drug. One of these drugs (simvastatin) may cause harm to your unborn child. It is not known if either drug passes into breast milk. A drug similar to simvastatin passes into breast milk, and because of this drug's potential risk of undesirable effects on a nursing infant, breast-feeding is not recommended while using ezetimibe/simvastatin. Consult your doctor before breast-feeding.

Possible Side Effects

Headache may occur. If this effect persists or worsens, notify your doctor or pharmacist promptly. This drug can sometimes cause muscle damage. Although uncommon, this may lead to very serious muscle damage called rhabdomyolysis, which in rare cases can be fatal. Seek immediate medical attention if you develop: muscle pain/tenderness/weakness (especially with fever or unusual tiredness). Tell your doctor immediately if any of these highly unlikely but very serious side effects occur: yellowing eyes and skin, dark urine, severe fatigue, stomach/abdominal pain, persistent nausea, change in the amount of urine. A serious allergic reaction to this drug is unlikely, but seek immediate medical attention if it occurs. Symptoms of a serious allergic reaction include: rash, itching, swelling, dizziness, trouble breathing. If you notice other effects not listed above, contact your doctor or pharmacist.

Do not share this medication with others. Laboratory and/or medical tests (e. g. blood cholesterol levels, liver function tests) should be performed periodically to monitor your progress or check for side effects. Consult your doctor for more details. For best results, this product should be used along with exercise, a low-cholesterol or low-fat diet, and a weight-loss program if you are overweight. Also to help reduce your risk of heart attacks and strokes, check your blood pressure regularly, seek medical treatment if your blood pressure is high, and stop smoking. Consult your doctor for more details.

Marina - Ko Olina, Olina

The 43-acre Ko Olina Marina is a boater’s dream, with 330 full-service slips able to accommodate up to 200-foot vessels. The marina features state-of-the-art Bellingham floating docks, a fuel dock for gas, diesel and pump-out and the Ko Olina Marina Shop.

Marina Shop

Visit the Ko Olina Marina Shop to book a tour or activity from a diverse selection of coastline cruises and water activities from family snorkel tours to romantic sunset cruises. Guests can also indulge in an assortment of delicious snacks and refreshing drinks or enjoy a stylish collection of Ko Olina apparel, aloha shirts, towels, sunscreen, disposable cameras and sundry essentials.

Ko Olina Boat Ramp

Information and Rules for Use of the Ko Olina Boat Ramp and Parking (Updated, July 29, 2015)

This is a brief summary of the requirements and rules that boaters must meet in order to obtain authorization to use the boat ramp and designated parking. The full terms and conditions of boat ramp and parking use are set forth in the Ko Olina Boat Ramp and Parking Agreement (“Agreement”), which can be obtained from the Ko Olina Community Association (“KOCA”) by calling (808) 671-2512 .

Ko Olina Resort is equipped with a boat ramp and 30 parking stalls for vehicles and trailers. The facilities are located on private property with allowed non-commercial public use.

Ko Olina Marina leases an access easement over the deep draft channel for Kalaeloa Harbor from the State of Hawaii, therefore the following procedures, requirements, state rules, and Coast Guard regulations must be observed by all boats operating in the same channel:Decals will be issued by the Ko Olina Aloha Team upon verification of the following documents and requirements:

Decals will be issued by the Ko Olina Aloha Team upon verification of the following documents and requirements:

Owner Information Form and a signed copy of the Ko Olina Boat Ramp and Parking Agreement along with proof of insurance required by the Agreement.

Copy of current registration for vehicle, boat, and boat trailer, vehicle safety inspection, valid driver’s license, and a valid no-fault or liability insurance identification card.

Certificate of completion from a National Association of State Boating Law Administrators (NASBLA) approved course on the safe use and operation of a power driven boat as required by Hawaii Administrative Rules 13-244-15.5.

Compliance with all state regulations.

All boats shall be equipped with a marine VHF transceiver with Channel 71 and a motor or engine in good operating condition.

Watercraft liability certificate of insurance that complies with the insurance provision in the Agreement. Watercraft liability coverage will have minimum limits of insurance of $500,000 for Each Occurrence for Bodily Injury and Property Damage. In addition, this insurance must maintain coverage for salvage costs associated with grounding & sinking, damage to docks, pollution contamination, and wreck removal.

The total length of vehicle and trailer shall not exceed 40 feet.

Owner agrees to pay the following fees, as applicable:

Daily Launch Fee of $15

Daily Parking Fee of $10

Hours of Operation (Boat Ramp): The boat ramp and vehicle/trailer parking will generally be open from sunrise to sunset.

Boat Ramp Access: Vehicles with trailered boats must enter/exit the Ko Olina Resort front gate via the right lane. KOCA reserves the right to alter the access route to the boat ramp in the future. See attached access and location map.

Trailer-only and vehicle-only parking prohibited in 40’ stalls. Trailers must be hitched to a vehicle in the parking stall. Registered vehicles/trailers left in the boat ramp parking lot after sunset will be allowed to remain for one night only. Vehicles/trailers in the lot for a second night will be subject to tow. Transient dockage at Ko Olina Marina may be available for late returnees at the posted rate.

Registration and boat ramp use is by appointment only. Please call (808) 676-4853 to schedule an appointment or (808) 671-2512 for information.

Obtain clearance from the Ko Olina Harbor Master on VHF channel 71 prior to and while transiting the channel.

Boats are not permitted to tie up to any pier or to cruise or anchor within Kalaeloa Harbor basin without prior permission from the Honolulu Harbor Master’s Office or the Aloha Tower Marine Traffic Controller.

Boats are not permitted to anchor in Ko Olina Marina except in the event of an emergency.

Boat traffic entering and departing Ko Olina Marina must yield to commercial shipping traffic in the entrance channel.

Sailing and other boats must be under auxiliary power while transiting the entrance channel. Sailboats must have their sails lowered while in the entrance channel.

The Rules of the Road, Hawaii Administrative Rules Title 13, Subtitle 11, Chapter 244 shall be applicable to the use of all boats transiting the entrance channel and while in Ko Olina Marina.

Boat traffic entering and departing Ko Olina must follow visual warning and traffic control signals, as well as directions and commands from the chase boat provided by Ko Olina Marina.

The use of personal floatation devices shall at all times be required within Ko Olina Marina and as required by all applicable state and federal laws.

The use of any dock within Ko Olina Marina, except those appurtenant to the ramp, is prohibited.

No boat shall be operated in any manner that unnecessarily interferes with any other boat’s free and proper navigation within Ko Olina Marina.

The consumption of alcohol and the use of any illegal substance at the Ko Olina boat ramp and parking facility are strictly prohibited. The consumption of alcohol and the use of any illegal substance in the boat while in Ko Olina Marina are likewise prohibited.

Any suspicious behavior must be reported to the Aloha Team at (808) 676-6547 .

The Ko Olina Marina Harbor Master can be reached at (808) 679-1050 .

Please refer to the Ko Olina Boat Ramp and Parking Agreement for additional rules, regulations, and details.

Key Contacts: General Information: Ko Olina Community Association (808) 671-2512 Registration and Boat Ramp Use Appointments: Aloha Team (808) 676-4853

Safe Boating is No Accident

Who can use Ko Olina’s boat ramp?

Valproic Acid - Brand Name List From, Valpakine

Valproic acid

See also.

Disclaimer: The indications, uses and warnings for individual medications outside the USA are determined by local regulatory bodies in each country or region. The Drugs. com website is intended primarily for audiences in the United States and its territories. Indications, uses and warnings on Drugs. com patient information leaflets are derived from FDA product labels and may differ in countries outside the USA. Every effort has been made to ensure that the information provided on this page is accurate, up-to-date and complete, but no guarantee is made to that effect. Drugs. com does not endorse drugs, diagnose patients or recommend specific therapies. The information on this page is not a substitute for the expertise, skill, knowledge and judgment of healthcare practitioners. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that a drug or drug combination is safe, effective or appropriate for any given patient. Drugs. com does not assume any responsibility for any aspect of healthcare administered with the aid of information provided here. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. Always consult your doctor or healthcare specialist for medical advice.

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Level Cap, Tera-Cap

Posts tagged level cap

Originally posted on ThisIsGame, this Q&A about the TERA Open Beta translated by TeraFans has a great deal of information about the game. The answers are from Hyun-Kyu Park, Executive Developer, Kang-Suk Kim, CEO, and Lead Graphic artist Chul-Woon Hwang. Some of the topics discussed are graphics, endgame content, battlefields, the political system, changes made More >

Want to learn the best insider tricks and start dominating in TERA Online? Want to level up at lightning speed and learn more about crafting, weapons, armor, crystals, gold making and more? If your answer is yes, then check out this Tera Strategy Guide and read all the secrets every other player doesn't want you to know! Learn More

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Sotret Oral Uses, Side Effects, Interactions, Pictures, Warnings - Dosing, Sotret

Sotret

GENERIC NAME(S): ISOTRETINOIN

Warnings

Women who are pregnant must not use isotretinoin. Women must avoid becoming pregnant while taking this medication. Serious (sometimes fatal) birth defects. miscarriages, and premature births have occurred when this drug has been used during pregnancy .

For female patients, two effective forms of birth control (or complete avoidance of sexual intercourse) must be used for 1 month before starting isotretinoin, during use, and for 1 month after stopping this drug. You must also have monthly pregnancy-avoidance counseling from your doctor. Do not use "minipills" for birth control (non-estrogen - containing pills) since they may not work as well with isotretinoin. If you are late in having your period, or if you have sexual intercourse at any time without using two effective forms of birth control. stop taking this medication and contact your doctor right away. (See also the Precautions section.)

After December 31, 2005, only patients enrolled in the iPLEDGE program may obtain and use isotretinoin. You will need to register with iPLEDGE and view a video at your doctor's office before receiving your prescription. Only physicians enrolled in iPLEDGE may prescribe isotretinoin, and only pharmacies enrolled in the program may dispense it. Consult your doctor or pharmacist for more details about the iPLEDGE program and for more information about the risks and benefits of using this medication.

For female patients who are able to become pregnant (even if not sexually active), you will need to contact iPLEDGE every month, either through the internet or by telephone, and answer required questions every time you fill your prescription and 1 month after your last dose.

These requirements apply in the United States. If you live in Canada or any other country, consult your doctor and pharmacist for your specific regulations.

Uses

This medication is used to treat severe cystic acne (also known as nodular acne ) that has not responded to other treatment (e. g. benzoyl peroxide or clindamycin applied to the skin or tetracycline or minocycline taken by mouth ). It belongs to a class of drugs known as retinoids. It works by decreasing facial oil (sebum) production. High amounts of sebum can lead to severe acne. If left untreated, severe acne may cause permanent scarring.

OTHER USES: This section contains uses of this drug that are not listed in the approved professional labeling for the drug but that may be prescribed by your health care professional. Use this drug for a condition that is listed in this section only if it has been so prescribed by your health care professional.

This medication may also be used to treat a certain type of cancer (neuroblastoma ).

How to use Sotret

Read the Medication Guide provided by your pharmacist before you start using isotretinoin and each time you get a refill. Read and sign a Patient Information/Informed Consent form before you start taking this medication. If you have any questions about isotretinoin, consult your doctor or pharmacist before taking the medication.

Swallow capsules whole. Do not crush or chew them. Isotretinoin is usually taken twice daily for 15-20 weeks, or as directed by your doctor. Directions for most generic forms of isotretinoin state that it should be taken with meals. However, the FDA has indicated that the Absorica brand may be taken with or without food. Food helps increase absorption of this drug into your bloodstream. Ask your doctor or pharmacist for more information. Take this drug with a full glass of water, and do not lie down for 10 minutes after taking it.

The dosage is based on your medical condition, weight. and response to treatment.

Your acne may worsen during the first few days of taking this drug, and it may take up to 1-2 months before you notice the full benefit of this medication. If severe acne returns, a second course of treatment may be started after you have stopped taking the drug for 2 months. The manufacturer does not recommend long-term use of isotretinoin. Do not take more than the recommended dose.

Since this drug can be absorbed through the skin and lungs and may harm an unborn baby, women who are pregnant or who may become pregnant should not handle this medication or breathe the dust from the capsules.

Side Effects

Dry lips and mouth. minor swelling of the eyelids or lips, crusty skin, nosebleeds. upset stomach. or thinning of hair may occur. If any of these effects persist or worsen, tell your doctor or pharmacist promptly.

To relieve dry mouth. suck on (sugarless) hard candy or ice chips, chew (sugarless) gum, drink water, or use a saliva substitute.

Remember that your doctor has prescribed this medication because he or she has judged that the benefit to you is greater than the risk of side effects. Many people using this medication do not have serious side effects.

Tell your doctor right away if you have any of these unlikely but serious side effects: mental/mood changes (e. g. depression. aggressive or violent behavior, and in rare cases, thoughts of suicide ), tingling feeling in the skin, quick/severe sunburn (sun sensitivity), back/joint/muscle pain. signs of infection (e. g. fever, persistent sore throat ), painful swallowing, peeling skin on palms/soles.

Isotretinoin may rarely cause disease of the pancreas (pancreatitis ) that may rarely be fatal. Stop taking this medication and tell your doctor right away if you develop: severe stomach pain. severe or persistent nausea/vomiting .

Stop taking this medication and tell your doctor right away if you develop these unlikely but very serious side effects: severe headache. vision changes, ringing in the ears. hearing loss. chest pain. yellowing eyes /skin, dark urine, severe diarrhea. rectal bleeding .

A very serious allergic reaction to this drug is rare. However, seek immediate medical attention if you notice any symptoms of a serious allergic reaction, including: rash, itching/swelling (especially of the face/tongue/throat), severe dizziness, trouble breathing.

This is not a complete list of possible side effects. If you notice other effects not listed above, contact your doctor or pharmacist.

Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088 or at www. fda. gov/medwatch.

In Canada - Call your doctor for medical advice about side effects. You may report side effects to Health Canada at 1-866-234-2345.

Precautions

Before taking isotretinoin, tell your doctor or pharmacist if you are allergic to it; or to vitamin A-related drugs (other retinoids such as tretinoin); or if you have any other allergies. This product may contain inactive ingredients (such as soybean, parabens), which can cause allergic reactions or other problems. Some people who are allergic to peanuts may also be allergic to soy. Talk to your pharmacist for more details.

Before using this medication, tell your doctor or pharmacist your medical history, especially of: diabetes, family or personal history of high blood fats (triglycerides), family or personal history of psychiatric disorders (including depression), liver disease, obesity, eating disorders (e. g. anorexia nervosa), alcohol abuse, pancreatitis, bone loss conditions (e. g. osteoporosis/osteomalacia, decreased bone density).

Do not donate blood while you are taking isotretinoin and for at least 1 month after you stop taking it.

This medication may make you more sensitive to the sun. Avoid prolonged sun exposure, tanning booths, and sunlamps. Use a sunscreen and wear protective clothing when outdoors.

Isotretinoin can affect your night vision. Do not drive, use machinery, or do any activity that requires clear vision after dark until you are sure you can perform such activities safely.

If you wear contact lenses, you may not tolerate them as well as usual while using this medication. Contact your doctor for more information.

Do not have cosmetic procedures to smooth your skin (e. g. waxing, laser, dermabrasion) during and for 6 months after isotretinoin therapy. Skin scarring may occur.

Avoid the use of alcohol while taking this medication because it may increase the risk of certain side effects (e. g. pancreatitis).

Limited information suggests isotretinoin may cause some bone loss effects. Therefore, playing contact or repetitive impact sports (e. g. football, basketball, soccer, tennis) may result in bone problems, including an increased risk of broken bones. Limited information also suggests isotretinoin may stop normal growth in some children (epiphyseal plate closure). Consult your doctor for more details.

Caution is advised when using this drug in the elderly because they may be more sensitive to its effects, especially the effects on bones.

Caution is advised when using this drug in children because they may be more sensitive to its effects, especially back/joint/muscle pain.

This drug must not be used during pregnancy or by those who may become pregnant during treatment. If you become pregnant or think you may be pregnant, inform your doctor right away. See also Warning section.

Since this drug can be absorbed through the skin and lungs and may harm an unborn baby, women who are pregnant or who may become pregnant should not handle this medication or breathe the dust from the capsules.

You must have two negative pregnancy tests before starting this medication. You must have a monthly pregnancy test during treatment with isotretinoin. If the test is positive, you must stop taking this medication and consult your doctor right away.

It is unknown if this medication passes into breast milk. However, similar drugs pass into breast milk. Breast-feeding while using this drug is not recommended. Consult your doctor before breast-feeding.

Interactions

Your doctor or pharmacist may already be aware of any possible drug interactions and may be monitoring you for them. Do not start, stop, or change the dosage of any medicine before checking with your doctor or pharmacist first.

Before using this medication, tell your doctor or pharmacist of all prescription and nonprescription/herbal products you may use, especially of: tetracyclines (e. g. minocycline, tetracycline), vitamin A-type drugs (e. g. acitretin, bexarotene), vitamin A, drugs that cause bone loss (e. g. anti-seizure drugs such as phenytoin, corticosteroids such as prednisone).

Tell your doctor when you start any new drug, and discuss if you should use additional reliable birth control. Also tell your doctor if you have any new spotting or breakthrough bleeding, because these may be signs that your birth control is not working well. (See also Warning section.)

This document does not contain all possible interactions. Therefore, before using this product, tell your doctor or pharmacist of all the products you use. Keep a list of all your medications with you, and share the list with your doctor and pharmacist.

Overdose

If overdose is suspected, contact a poison control center or emergency room right away. US residents can call their local poison control center at 1-800-222-1222. Canada residents can call a provincial poison control center. Symptoms of overdose may include: vomiting, stomach pain, facial flushing, headache, loss of balance.

Notes

Do not allow anyone else to take this medication. It can cause birth defects and other serious health problems.

Laboratory and/or medical tests should be performed (e. g. pregnancy, blood cholesterol/triglyceride levels, liver function, white blood count, eye exams) to monitor for side effects.

Missed Dose

If you miss a dose, take it as soon as you remember. If it is near the time of the next dose, skip the missed dose and resume your usual dosing schedule. Do not double the dose to catch up.

Storage

Store at room temperature between 59-86 degrees F (between 15-30 degrees C) away from light and moisture. Do not store in the bathroom. Keep all medicines out of reach of children and pets.

Do not flush medications down the toilet or pour them into a drain unless instructed to do so. Properly discard this product when it is expired or no longer needed. Consult your pharmacist or local waste disposal company for more details about how to safely discard your product.

Information last revised October 2015. Copyright(c) 2015 First Databank, Inc.

Images

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Selected from data included with permission and copyrighted by First Databank, Inc. This copyrighted material has been downloaded from a licensed data provider and is not for distribution, expect as may be authorized by the applicable terms of use.

CONDITIONS OF USE: The information in this database is intended to supplement, not substitute for, the expertise and judgment of healthcare professionals. The information is not intended to cover all possible uses, directions, precautions, drug interactions or adverse effects, nor should it be construed to indicate that use of a particular drug is safe, appropriate or effective for you or anyone else. A healthcare professional should be consulted before taking any drug, changing any diet or commencing or discontinuing any course of treatment.

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ADHD Drug Side Effects

Drug Overdose

Motrin - Pain Relief, Neuralprona

Motrin is used for treating rheumatoid arthritis, osteoarthritis, menstrual cramps, or mild to moderate pain. Motrin is an NSAID. NSAIDs treat the symptoms of pain and inflammation. They do not treat the disease that causes those symptoms.

Use Motrin as directed by your doctor.

Take Motrin by mouth with or without food. It may be taken with food if it upsets your stomach. Taking it with food may not lower the risk of stomach or bowel problems (eg, bleeding, ulcers). Talk with your doctor or pharmacist if you have persistent stomach upset.

Take Motrin with a full glass of water (8 oz/240 mL) as directed by your doctor.

If you miss a dose of Motrin and you are taking it regularly, take it as soon as possible. If it is almost time for your next dose, skip the missed dose. Go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about the proper use of Motrin .

Store Motrin at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Motrin out of the reach of children and away from pets.

Active Ingredient: Ibuprofen.

Do NOT use Motrin if:

you are allergic to any ingredient in Motrin

you have had a severe allergic reaction (eg, severe rash, hives, trouble breathing, growths in the nose, dizziness) to aspirin or an NSAID (eg, ibuprofen, celecoxib)

you have recently had or will be having bypass heart surgery

you are in the last 3 months of pregnancy.

Contact your doctor or health care provider right away if any of these apply to you.

Some medical conditions may interact with Motrin. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal product, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have a history of kidney or liver disease, diabetes, or stomach or bowel problems (eg, bleeding, perforation, ulcers)

if you have a history of swelling or fluid buildup, lupus, asthma, or growths in the nose (nasal polyps), or mouth inflammation

if you have high blood pressure, blood disorders, bleeding or clotting problems, heart problems (eg, heart failure), or blood vessel disease, or if you are at risk for any of these diseases

if you have poor health, dehydration or low fluid volume, or low blood sodium levels, you drink alcohol, or you have a history of alcohol abuse.

Some medicines may interact with Motrin. Tell your health care provider if you are taking any other medicines, especially any of the following:

Anticoagulants (eg, warfarin), aspirin, corticosteroids (eg, prednisone), heparin, or selective serotonin reuptake inhibitors (SSRIs) (eg, fluoxetine) because the risk of stomach bleeding may be increased

Probenecid because it may increase the risk of Motrin 's side effects

Cyclosporine, lithium, methotrexate, or quinolones (eg, ciprofloxacin) because the risk of their side effects may be increased by Motrin

Angiotensin-converting enzyme (ACE) inhibitors (eg, enalapril) or diuretics (eg, furosemide, hydrochlorothiazide) because their effectiveness may be decreased by Motrin.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Motrin may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

Important safety information:

Motrin may cause dizziness or drowsiness. These effects may be worse if you take it with alcohol or certain medicines. Use Motrin with caution. Do not drive or perform other possible unsafe tasks until you know how you react to it.

Serious stomach ulcers or bleeding can occur with the use of Motrin. Taking it in high doses or for a long time, smoking, or drinking alcohol increases the risk of these side effects. Taking Motrin with food will NOT reduce the risk of these effects. Contact your doctor or emergency room at once if you develop severe stomach or back pain; black, tarry stools; vomit that looks like blood or coffee grounds; or unusual weight gain or swelling.

Do not take more than the recommended dose or use for longer than prescribed without checking with your doctor.

Motrin has ibuprofen in it. Before you start any new medicine, check the label to see if it has ibuprofen in it too. If it does or if you are not sure, check with your doctor or pharmacist.

Do not take aspirin while you are using Motrin unless your doctor tells you to.

Lab tests, including kidney function, complete blood cell counts, and blood pressure, may be done to monitor your progress or to check for side effects. Be sure to keep all doctor and lab appointments.

Use Motrin with caution in the elderly; they may be more sensitive to its effects, including stomach bleeding and kidney problems.

Motrin should be used with extreme caution in children; safety and effectiveness in children have not been confirmed.

Pregnancy and breast-feeding: Motrin may cause harm to the fetus. Do not take it during the last 3 months of pregnancy. If you think you may be pregnant, contact your doctor. You will need to discuss the benefits and risks of taking Motrin while you are pregnant. It is not known if Motrin is found in breast milk. Do not breastfeed while taking Motrin .

All medicines can cause side effects, but many people have no, or minor, side effects.

Check with your doctor if any of these most common side effects persist or become bothersome:

Constipation; diarrhea; dizziness; gas; headache; heartburn; nausea; stomach pain or upset.

Seek medical attention right away if any of these severe side effects occur:

Severe allergic reactions (rash; hives; itching; trouble breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); bloody or black, tarry stools; change in the amount of urine produced; chest pain; confusion; dark urine; depression; fainting; fast or irregular heartbeat; fever, chills, or persistent sore throat; mental or mood changes; numbness of an arm or leg; one-sided weakness; red, swollen, blistered, or peeling skin; ringing in the ears; seizures; severe headache or dizziness; severe or persistent stomach pain or nausea; severe vomiting; shortness of breath; stiff neck; sudden or unexplained weight gain; swelling of hands, legs, or feet; unusual bruising or bleeding; unusual joint or muscle pain; unusual tiredness or weakness; vision or speech changes; vomit that looks like coffee grounds; yellowing of the skin or eyes.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider.

Tadalafil Uses, Dosage, Side Effects, Tadalafilo

Tadalafil

Tadalafil relaxes muscles found in the walls of blood vessels and increases blood flow to particular areas of the body.

Tadalafil under the name of Cialis is used to treat erectile dysfunction (impotence) and symptoms of benign prostatic hypertrophy (enlarged prostate). Another brand of tadalafil is Adcirca, which is used to treat pulmonary arterial hypertension and improve exercise capacity in men and women.

Do not take Cialis while also taking Adcirca, unless your doctor tells you to.

Tadalafil may also be used for purposes not listed in this medication guide.

Important information

Some medicines can cause unwanted or dangerous effects when used with tadalafil. Tell your doctor about all your current medicines, especially riociguat (Adempas).

Do not take tadalafil if you are also using a nitrate drug for chest pain or heart problems, including nitroglycerin, isosorbide dinitrate, isosorbide mononitrate, and some recreational drugs such as "poppers". Taking tadalafil with a nitrate medicine can cause a sudden and serious decrease in blood pressure.

Contact your doctor or seek emergency medical attention if your erection is painful or lasts longer than 4 hours. A prolonged erection (priapism) can damage the penis.

Stop using tadalafil and get emergency medical help if you have sudden vision loss.

Before taking this medicine

You should not take tadalafil if you are allergic to it, or:

if you take other medicines to treat pulmonary arterial hypertension, such as riociguat (Adempas).

Do not take tadalafil if you are also using a nitrate drug for chest pain or heart problems. This includes nitroglycerin, isosorbide dinitrate, and isosorbide mononitrate. Nitrates are also found in some recreational drugs such as amyl nitrate or nitrite ("poppers"). Taking tadalafil with a nitrate medicine can cause a sudden and serious decrease in blood pressure.

To make sure tadalafil is safe for you, tell your doctor if you have any of these other conditions:

heart disease or heart rhythm problems, coronary artery disease;

a recent heart attack (within the past 90 days);

a recent history (in the past 6 months) of a stroke, or congestive heart failure;

angina (chest pain), high or low blood pressure;

liver or kidney disease (or if you are on dialysis);

a blood cell disorder such as sickle cell anemia, multiple myeloma, or leukemia;

a bleeding disorder such as hemophilia;

a stomach ulcer;

retinitis pigmentosa (an inherited condition of the eye);

a physical deformity of the penis (such as Peyronie's disease); or

if you have been told you should not have sexual intercourse for health reasons.

Tadalafil can decrease blood flow to the optic nerve of the eye, causing sudden vision loss. This has occurred in a small number of people taking Viagra or other drugs similar to tadalafil. Most of these people also had certain pre-existing eye problems or risk factors for blood vessel disorders (such as heart disease, diabetes, high blood pressure, high cholesterol, coronary artery disease, smoking, or being over 50 years old). It is not clear whether tadalafil is the actual cause of vision loss.

This medicine is not expected to harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant.

It is not known whether tadalafil passes into breast milk or if it could harm a nursing baby. Tell your doctor if you are breast-feeding a baby.

How should I take tadalafil?

Tadalafil is usually taken only once per day. Follow all directions on your prescription label. Do not take this medicine in larger or smaller amounts or for longer than recommended.

Tadalafil can be taken with or without food.

Do not break or split a Cialis tablet. Swallow it whole.

For erectile dysfunction, take Cialis just before sexual activity but not more than once per day.

Cialis can help achieve an erection when sexual stimulation occurs. An erection will not occur just by taking a pill. Follow your doctor's instructions.

During sexual activity, if you become dizzy or nauseated, or have pain, numbness, or tingling in your chest, arms, neck, or jaw, stop and call your doctor right away. You could be having a serious side effect of tadalafil.

Do not take Cialis for erectile dysfunction if you are taking Adcirca for pulmonary arterial hypertension.

Store at room temperature away from moisture and heat.

What happens if I miss a dose?

If tadalafil is used as needed, you are not likely to be on a dosing schedule.

If you take tadalafil every day and you miss a dose, take the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not take extra medicine to make up the missed dose.

What happens if I overdose?

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

What should I avoid while taking tadalafil?

Drinking alcohol with this medicine can cause side effects.

Grapefruit and grapefruit juice may interact with tadalafil and lead to unwanted side effects. Avoid the use of grapefruit products while taking this medicine.

Avoid using any other medicines to treat impotence, such as alprostadil or yohimbine, without first talking to your doctor.

Tadalafil side effects

Get emergency medical help if you have any signs of an allergic reaction to tadalafil: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.

Stop using tadalafil and get emergency medical help if you have:

erection is painful or lasts longer than 4 hours (prolonged erection can damage the penis);

vision changes or sudden vision loss; or

heart attack symptoms - chest pain or pressure, pain spreading to your jaw or shoulder, nausea, sweating.

Also call your doctor right away if you have:

ringing in your ears, or sudden hearing loss;

swelling in your hands, ankles, or feet;

shortness of breath;

seizure (convulsions); or

a light-headed feeling, like you might pass out.

Common tadalafil side effects may include:

sinus pain, sore throat; or

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

Tadalafil dosing information

Usual Adult Dose for Erectile Dysfunction:

Use as needed for ED: - Initial dose: 10 mg orally once a day, as needed, prior to sexual activity - Maintenance dose: 5 to 20 mg orally once a day, as needed, prior to sexual activity based on individual efficacy and tolerability

Comment: Consider that this drug has shown to improve erectile dysfunction up to 36 hours following dosing, when used as needed.

Once a day use for ED: - Initial dose: 2.5 mg orally once a day at approximately the same time, without regard to timing of sexual activity - Maintenance dose: 2.5 to 5 mg orally once a day based on individual efficacy and tolerability.

Once daily use for ED and Benign Prostatic Hyperplasia (BPH): -5 mg orally once a day at approximately the same time, without regard to timing of sexual activity

Use: Treatment of erectile dysfunction (ED)

Usual Adult Dose for Pulmonary Hypertension:

Adcirca (R): -40 mg orally once a day

Comment: Dividing the 40 mg dose over the course of the day is not recommended.

Usual Adult Dose for Benign Prostatic Hyperplasia:

Once daily use for BPH: -5 mg orally once a day at approximately the same time

Concomitant administration with finasteride: -5 mg orally once a day at approximately the same time, for up to 26 weeks

Comments: The incremental benefit of this drug decreases from 4 weeks until 26 weeks. The incremental benefit of this drug beyond 26 weeks is unknown.

Once daily use for ED and BPH: -5 mg orally once a day at approximately the same time, without regard to timing of sexual activity

Use: Treatment of the signs and symptoms of benign prostatic hyperplasia (BPH)

What other drugs will affect tadalafil?

Tell your doctor about all your current medicines and any you start or stop using, especially:

an antibiotic or antifungal medicine;

antiviral medicine to treat hepatitis C or HIV/AIDS;

drugs to treat high blood pressure or a prostate disorder; or

This list is not complete. Other drugs may interact with tadalafil, including prescription and over-the-counter medicines, vitamins, and herbal products. Not all possible interactions are listed in this medication guide.

More about tadalafil

Consumer resources

Professional resources

Related treatment guides

Where can I get more information?

Your pharmacist can provide more information about tadalafil.

Remember, keep this and all other medicines out of the reach of children, never share your medicines with others, and use tadalafil only for the indication prescribed.

Disclaimer: Every effort has been made to ensure that the information provided by Cerner Multum, Inc. ('Multum') is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. Multum information has been compiled for use by healthcare practitioners and consumers in the United States and therefore Multum does not warrant that uses outside of the United States are appropriate, unless specifically indicated otherwise. Multum's drug information does not endorse drugs, diagnose patients or recommend therapy. Multum's drug information is an informational resource designed to assist licensed healthcare practitioners in caring for their patients and/or to serve consumers viewing this service as a supplement to, and not a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. Multum does not assume any responsibility for any aspect of healthcare administered with the aid of information Multum provides. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

Copyright 1996-2016 Cerner Multum, Inc. Version: 10.04. Revision Date: 2016-05-16, 11:32:51 AM.

Drug Status

Colchicina

FORMA FARMACпїЅUTICA Y FORMULACIпїЅN:

Cada TABLETA contiene:

Colchicina. 1 mg

Excipiente, c. b.p. 1 tableta.

COLCHICINA estпїЅ indicada como coadyuvante en el tratamiento de la gota y de la cirrosis hepпїЅtica; alivia el dolor y la inflamaciпїЅn propios del ataque agudo de gota. Puede administrarse combinado con alopurinol y salicilatos.

COLCHICINA estпїЅ indicada para reducir la frecuencia y severidad de ataques agudos de gota artrпїЅtica en pacientes con gota crпїЅnica. En algunos pacientes пїЅpuede ocurrir completa remisiпїЅn de tales ataques. La administraciпїЅn profilпїЅctica de COLCHICINA puede ser especialmente importante durante los primeros meses de tratamiento con un agente antihiperuricпїЅmico (alopurinol, probenecid o sulfinpirazona) porque la frecuencia de los ataques agudos pueden ser incrementados cuando la terapia es iniciada. COLCHICINA es usada en el tratamiento primario de cirrosis biliar. COLCHICINA tal vez provee beneficio adicional cuando es usada concurrentemente con ursodiol para esta indicaciпїЅn.

Hipersensibilidad a COLCHICINA insuficiencia hepпїЅtica y/o renal, afecciones gastrointestinales, embarazo y lactancia.

Los pacientes geriпїЅtricos pueden ser mпїЅs sensibles a la toxicidad acumuпїЅlativa por COLCHICINA.

Posiblemente grandes cantidades de alcohol pueden incrementar el riesgo de toxicidad gastrointestinal.

Los efectos leucopпїЅnico y trombocitopпїЅnico de COLCHICINA pueden producir aumento en la incidencia de infecciпїЅn microbiana, retraso en la cicatrizaciпїЅn y hemorragia gingival. Si aparece leucopenia o trombocitoпїЅpenia, el trabajo odontolпїЅgico debe retrasarse hasta que los recuentos sanguпїЅneos hayan vuelto a la normalidad y se debe instruir al paciente en la higiene oral adecuada, incluyendo la precauciпїЅn en la utilizaciпїЅn de cepillos, seda y palillos dentales.

RESTRICCIONES DE USO DURANTE EL EMBARAZO Y LA LACTANCIA:

No se administre durante estos periodos, en caso necesario debe valorarse la existencia de otros antiinflamatorios пїЅtiles, ya que COLCHICINA interfiere con la divisiпїЅn celular. No se sabe si es excretada en la leche materna, por lo que se debe considerar el riesgo-beneficio.

REACCIONES SECUNDARIAS Y ADVERSAS:

Algunos pacientes han llegado a mostrar trastornos gastrointestinales relaпїЅcionados con la dosis como nпїЅuseas, vпїЅmito y diarrea. Con la utilizaciпїЅn a largo plazo o prolongado se puede presentar entumecimiento, hormigueo, dolor o debilidad en manos y pies; rash cutпїЅneo, dolor de garganta, fiebre y escalofrпїЅos, cansancio o debilidad no habitual.

INTERACCIONES MEDICAMENTOSAS Y DE OTRO GпїЅNERO:

Alcohol: El uso concurrente con COLCHICINA aumenta el riesgo de toxicidad gastrointestinal especialmente en alcohпїЅlicos; tambiпїЅn el alcohol aumenta las concentraciones de пїЅcido пїЅrico en la sangre y puede disminuir la terapia proпїЅfilпїЅctica de la gota. Bumetamicida, diasпїЅxido, diurпїЅticos, tiazidas, furesamida y pirazinamida pueden aumentar las concentraciones sпїЅricas del пїЅcido пїЅrico y disminuir la eficacia de la terapia profilпїЅctica de la gota.

Vitamina B 12 : La absorciпїЅn de esta vitamina puede ser impedida por la administraciпїЅn crпїЅnica o de altas dosis de COLCHICINA; el requerimiento puede ser aumentado.

PRECAUCIONES EN RELACIпїЅN CON EFECTOS DE CARCINOGпїЅNESIS, MUTAGпїЅNESIS, TERATOGпїЅNESIS Y SOBRE LA FERTILIDAD:

Fertilidad: COLCHICINA detiene la divisiпїЅn celular en animales y plantas; se ha reportado disminuciпїЅn de la espermatogпїЅnesis en humanos.

COLCHICINA ha mostrado ser teratogпїЅnica en ratones (en dosis de 1.25 пїЅ 1.5 mg por kg).

Aunque existen estudios controlados en humanos se tienen reportes de posible teratogenicidad inducida por COLCHICINA. Debe considerarse el riesgo-beneficio.

DOSIS Y VпїЅA DE ADMINISTRACIпїЅN:

La vпїЅa de administraciпїЅn de COLCHICINA es oral.

Dosis inicial: Se sugiere 1 tableta cada dos horas hasta un mпїЅximo de 6 en 24 horas.

Dosis de mantenimiento: 1 tableta 2 a 3 veces al dпїЅa.

Cirrosis biliar: 1 tableta al dпїЅa en dosis divididas.

MANIFESTACIONES Y MANEJO DE LA SOBREDOSIFICACIпїЅN O INGESTA ACCIDENTAL: Tratamientos de efectos adversos o sobredosis:

Para signos tempranos de sobredosis: DiscontinпїЅe la administraciпїЅn de COLCHICINA.

Administre un opioide antidiarreico.

Administre morfina o atropina para dolor abdominal.

Para sobredosis severas: Remueva el medicamento no absorbido (si se toma oralmente) efectuando un lavado gпїЅstrico.

MantпїЅngase en constante revisiпїЅn el status hemodinпїЅmica, cardiaco y respiratorio, asпїЅ como los electrпїЅlitos en la sangre.

Evite la deshidrataciпїЅn y medidas generales para prevenir el estado de shock.

RECOMENDACIONES SOBRE ALMACENAMIENTO:

ConsпїЅrvese a temperatura ambiente a no mпїЅs de 30пїЅC y en lugar seco.

ProtпїЅjase de la luz.

NOMBRE Y DOMICILIO DEL LABORATORIO

VпїЅase PresentaciпїЅn o Presentaciones.

PRESENTACIпїЅN O PRESENTACIONES:

Fuente: S. S.A. CatпїЅlogo de Medicamentos GenпїЅricos Intercambiables para farmacias y pпїЅblico en general al 3 de agosto de 2007. Con el objeto de demostrar la intercambiabilidad a que se refiere el artпїЅculo 75 del reglamento de Insumos para la Salud, los medicamentos que integran el CatпїЅlogo de Medicamentos GenпїЅricos Intercambiables han sido comparados, siguiendo los lineamientos indicados por la NOM-177SSA1-1998, contra los productos innovadores o de referencia enlistados en las pпїЅgs. 11 a 22 donde usted lo podrпїЅ consultar.

Diclofenac Uses, Dosage - Side Effects, Difenac

Diclofenac

Diclofenac is a nonsteroidal anti-inflammatory drug (NSAID). This medicine works by reducing substances in the body that cause pain and inflammation.

Diclofenac is used to treat mild to moderate pain, or signs and symptoms of osteoarthritis or rheumatoid arthritis. The Cataflam brand of this medicine is also used to treat menstrual cramps.

Diclofenac powder (Cambia) is used to treat a migraine headache attack. Cambia will only treat a headache that has already begun. It will not prevent headaches or reduce the number of attacks.

Important information

You should not use diclofenac if you have a history of allergic reaction to aspirin or NSAIDs (non-steroidal anti-inflammatory drugs).

Diclofenac can increase your risk of fatal heart attack or stroke, especially if you use it long term or take high doses, or if you have heart disease. Do not use this medicine just before or after heart bypass surgery (coronary artery bypass graft, or CABG).

Diclofenac may also cause stomach or intestinal bleeding, which can be fatal. These conditions can occur without warning while you are using this medicine, especially in older adults.

Before taking this medicine

Diclofenac can increase your risk of fatal heart attack or stroke, especially if you use it long term or take high doses, or if you have heart disease. Even people without heart disease or risk factors could have a stroke or heart attack while taking this medicine.

Do not use this medicine just before or after heart bypass surgery (coronary artery bypass graft, or CABG).

Diclofenac may also cause stomach or intestinal bleeding, which can be fatal. These conditions can occur without warning while you are using this medicine, especially in older adults.

You should not use diclofenac if you are allergic to it, or if you have ever had an asthma attack or severe allergic reaction after taking aspirin or an NSAID.

Do not use Cambia to treat a cluster headache. Do not use Zipsor if you are allergic to beef or beef protein.

To make sure diclofenac is safe for you, tell your doctor if you have:

heart disease, high blood pressure, high cholesterol, diabetes, or if you smoke;

a history of heart attack, stroke, or blood clot;

a history of stomach ulcers or bleeding;

liver or kidney disease;

Taking diclofenac during the last 3 months of pregnancy may harm the unborn baby. Tell your doctor if you are pregnant or plan to become pregnant.

It is not known whether diclofenac passes into breast milk or if it could harm a nursing baby. You should not breast-feed while using this medicine.

Diclofenac is not approved for use by anyone younger than 18 years old.

How should I take diclofenac?

Different brands of diclofenac contain different amounts of this medicine, and may have different uses . If you switch brands, your dose needs may change. Follow your doctor's instructions about how much medicine to take. Ask your pharmacist if you have any questions about the brand you receive at the pharmacy.

Follow all directions on your prescription label. Your doctor may occasionally change your dose to make sure you get the best results. Do not take this medicine in larger amounts or for longer than recommended. Use the lowest dose that is effective in treating your condition.

Take Zorvolex on an empty stomach, at least 1 hour before or 2 hours after a meal.

Do not crush, chew, or break an extended-release tablet or delayed-release tablet . Swallow it whole.

Dissolve Cambia powder in to 2 ounces of water. Do not use any other type of liquid. Stir this mixture and drink all of it right away. Cambia works best if you take it on an empty stomach.

Call your doctor if your headache does not completely go away after taking Cambia. Do not take a second dose of diclofenac powder without your doctor's advice.

If you use diclofenac long-term, you may need frequent medical tests.

Store at room temperature away from moisture and heat. Keep the bottle tightly closed when not in use.

Read all patient information, medication guides, and instruction sheets provided to you. Ask your doctor or pharmacist if you have any questions.

What happens if I miss a dose?

Take the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not take extra medicine to make up the missed dose.

What happens if I overdose?

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

What should I avoid while taking diclofenac?

Avoid drinking alcohol. It may increase your risk of stomach bleeding.

Avoid taking aspirin or other NSAIDs while you are taking this medicine.

Ask a doctor or pharmacist before using any cold, allergy, or pain medication. Many medicines available over the counter contain aspirin or other medicines similar to diclofenac. Taking certain products together can cause you to get too much of this type of medication. Check the label to see if a medicine contains aspirin, ibuprofen, ketoprofen, or naproxen.

Diclofenac side effects

Get emergency medical help if you have signs of an allergic reaction to diclofenac: sneezing, runny or stuffy nose; wheezing or trouble breathing; hives; swelling of your face, lips, tongue, or throat.

Get emergency medical help if you have signs of a heart attack or stroke: chest pain spreading to your jaw or shoulder, sudden numbness or weakness on one side of the body, slurred speech, feeling short of breath.

Stop using diclofenac and call your doctor at once if you have:

the first sign of any skin rash, no matter how mild;

shortness of breath (even with mild exertion);

swelling or rapid weight gain;

signs of stomach bleeding - bloody or tarry stools, coughing up blood or vomit that looks like coffee grounds;

liver problems - nausea, upper stomach pain, itching, tired feeling, flu-like symptoms, loss of appetite, dark urine, clay-colored stools, jaundice (yellowing of the skin or eyes);

kidney problems - little or no urinating, painful or difficult urination, swelling in your feet or ankles, feeling tired or short of breath;

high blood pressure - severe headache, pounding in your neck or ears, nosebleed, anxiety, confusion;

low red blood cells (anemia) - pale skin, feeling light-headed or short of breath, rapid heart rate, trouble concentrating; or

severe skin reaction - fever, sore throat, swelling in your face or tongue, burning in your eyes, skin pain followed by a red or purple skin rash that spreads (especially in the face or upper body) and causes blistering and peeling.

Common diclofenac side effects may include:

indigestion, gas, stomach pain, nausea, vomiting;

headache, dizziness, drowsiness;

itching, increased sweating;

increased blood pressure; or

swelling or pain in your arms or legs.

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

Diclofenac dosing information

Usual Adult Dose for Osteoarthritis:

Diclofenac free acid capsules: 35 mg orally 3 times a day Diclofenac potassium immediate-release tablets: 50 mg orally 2 or 3 times a day Diclofenac sodium enteric-coated tablets: 50 mg orally 2 or 3 times a day or 75 mg orally 2 times a day Maximum dose: 150 mg daily

Diclofenac sodium extended-release tablets: 100 mg orally once a day

Use: For the relief of signs and symptoms of osteoarthritis.

Usual Adult Dose for Ankylosing Spondylitis:

Diclofenac sodium enteric-coated and delayed-release tablets: 25 mg orally 4 times a day. An additional 25 mg dose may be administered at bedtime, if necessary Maximum dose: 125 mg per day

Use: For acute or long-term use in the relief of signs and symptoms of ankylosing spondylitis.

Usual Adult Dose for Dysmenorrhea:

Diclofenac potassium immediate-release tablets: 50 mg orally 3 times a day

Comments: An initial dose of 100 mg orally followed by 50 mg oral doses may provide better relief for some patients; initiate treatment upon appearance of the first symptoms and continue for a few days.

Use: For the relief of signs and symptoms of primary dysmenorrhea.

Usual Adult Dose for Rheumatoid Arthritis:

Diclofenac potassium immediate-release tablets: 50 mg orally 3 or 4 times a day Diclofenac sodium enteric-coated and delayed-release tablets: 50 mg orally 3 to 4 times a day or 75 mg orally twice a day Maximum dose: 225 mg daily

Diclofenac sodium extended-release tablets: 100 mg orally once a day Maximum dose: 100 mg orally 2 times a day; this would be for the rare patient in whom the benefits outweigh the clinical risks.

For the relief of signs and symptoms of rheumatoid arthritis

Usual Adult Dose for Migraine:

Diclofenac potassium for oral solution packets: 50 mg (1 packet) orally once

Comments: This drug is not indicated for the prophylactic therapy of migraine or for use in cluster headaches; the safety and efficacy of a second dose has not been established.

Use: For acute treatment of migraine with or without aura.

Usual Adult Dose for Pain:

Oral: Diclofenac potassium liquid-filled capsules: 25 mg orally 4 times a day Diclofenac free acid capsules: 18 mg or 35 mg orally 3 times a day Diclofenac potassium immediate-release tablets: 50 mg orally 3 times a day; an initial dose of 100 mg orally followed by 50 mg oral doses may provide better relief in some patients.

Comment: Neither the potassium base liquid filled capsules nor the free acid capsules are interchangeable with each other or with other diclofenac products containing the sodium or potassium salt.

Parenteral: 37.5 mg IV bolus over 15 seconds every 6 hours as needed for pain Maximum Dose: 150 mg per day

Comment: Patients should be well hydrated prior to IV administration of this drug in order to reduce the risk of adverse renal reactions.

Uses: For the management of mild to moderate acute pain (oral, IV) and moderate to severe pain alone or in combination with opioid analgesics (IV).

What other drugs will affect diclofenac?

Ask your doctor before using diclofenac if you take an antidepressant such as citalopram, escitalopram, fluoxetine (Prozac), fluvoxamine, paroxetine, sertraline (Zoloft), trazodone, or vilazodone. Taking any of these medicines with an NSAID may cause you to bruise or bleed easily.

Tell your doctor about all your current medicines and any you start or stop using, especially:

Colospas Soria Natural, Colospas

Segun el apartado 2 del articulo 22 de la LSSI. los prestadores de servicios deberan INFORMAR y CONSEGUIR CONSENTIMIENTO de los usuarios, puesto que si no es de ese modo la privacidad de ellos se veria afectada con contenido que sobrepasaria los limites legales de nueva normativa. Esta tienda online utiliza cookies para ofrecer una mejor experiencia de navegacion al usuario. Para seguir navegando es necesario aceptar el uso de cookies en la misma.

Politica de Cookies

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Colospás Soria Natural

Colospas es un producto de Soria Natural compuesto principalmente por aceite esencial de menta. El aceite esencial de menta es utilizado comunmente por su accion antiseptica (antibacteriana y antifungica), digestiva, carminativa y antiespastica.

Colospas esta recomendado como suplemento alimenticio para ayudar en digestiones pesadas despues de comidas copiosas, malas digestiones por acidez o gases.

Ingredientes principales: Aceite esencial de menta, Estabilizador: Celulosa microcristalina y Sal magnesica de acidos grasos: Estearato de magnesio.

Modo de empleo: se recomienda tomar de 1 a 2 comprimidos al dia.

Presentacion: Envase con 30 comprimidos de 1100Mg. de Colospas .

Conservacion: Mantener en lugar fresco y seco.

- No utilizar como sustituto de una dieta equilibrada.

- Mantengase fuera del alcance de los ninos mas pequenos.

- No superar la dosis recomendada.

30 Otros productos de la misma categoria

Horario de Atencion al Cliente

De Lunes a Viernes

De 10 -14 y de 16 -19

Tlf: 91 262 05 20 / 91 239 38 35

ENVIOS 24/72 HORAS

Su pedido sera preparado en un plazo de 24/48h siempre que dispongamos de stock

Realice su pago de la forma mas segura, gracias a los modulos de PAYPAL y CECA

Nuestros clientes pueden ofrecer sus propias valoraciones de nuestros servicios.

ATENCION AL CLIENTE

Nuestro servicio de atencion al cliente esta disponible de Lunes a Viernes de 10 a 14h y de 16 a 19h

Motrin - Pain Relief, Ponstil Mujer

Motrin is used for treating rheumatoid arthritis, osteoarthritis, menstrual cramps, or mild to moderate pain. Motrin is an NSAID. NSAIDs treat the symptoms of pain and inflammation. They do not treat the disease that causes those symptoms.

Use Motrin as directed by your doctor.

Take Motrin by mouth with or without food. It may be taken with food if it upsets your stomach. Taking it with food may not lower the risk of stomach or bowel problems (eg, bleeding, ulcers). Talk with your doctor or pharmacist if you have persistent stomach upset.

Take Motrin with a full glass of water (8 oz/240 mL) as directed by your doctor.

If you miss a dose of Motrin and you are taking it regularly, take it as soon as possible. If it is almost time for your next dose, skip the missed dose. Go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about the proper use of Motrin .

Store Motrin at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Motrin out of the reach of children and away from pets.

Active Ingredient: Ibuprofen.

Do NOT use Motrin if:

you are allergic to any ingredient in Motrin

you have had a severe allergic reaction (eg, severe rash, hives, trouble breathing, growths in the nose, dizziness) to aspirin or an NSAID (eg, ibuprofen, celecoxib)

you have recently had or will be having bypass heart surgery

you are in the last 3 months of pregnancy.

Contact your doctor or health care provider right away if any of these apply to you.

Some medical conditions may interact with Motrin. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal product, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have a history of kidney or liver disease, diabetes, or stomach or bowel problems (eg, bleeding, perforation, ulcers)

if you have a history of swelling or fluid buildup, lupus, asthma, or growths in the nose (nasal polyps), or mouth inflammation

if you have high blood pressure, blood disorders, bleeding or clotting problems, heart problems (eg, heart failure), or blood vessel disease, or if you are at risk for any of these diseases

if you have poor health, dehydration or low fluid volume, or low blood sodium levels, you drink alcohol, or you have a history of alcohol abuse.

Some medicines may interact with Motrin. Tell your health care provider if you are taking any other medicines, especially any of the following:

Anticoagulants (eg, warfarin), aspirin, corticosteroids (eg, prednisone), heparin, or selective serotonin reuptake inhibitors (SSRIs) (eg, fluoxetine) because the risk of stomach bleeding may be increased

Probenecid because it may increase the risk of Motrin 's side effects

Cyclosporine, lithium, methotrexate, or quinolones (eg, ciprofloxacin) because the risk of their side effects may be increased by Motrin

Angiotensin-converting enzyme (ACE) inhibitors (eg, enalapril) or diuretics (eg, furosemide, hydrochlorothiazide) because their effectiveness may be decreased by Motrin.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Motrin may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

Important safety information:

Motrin may cause dizziness or drowsiness. These effects may be worse if you take it with alcohol or certain medicines. Use Motrin with caution. Do not drive or perform other possible unsafe tasks until you know how you react to it.

Serious stomach ulcers or bleeding can occur with the use of Motrin. Taking it in high doses or for a long time, smoking, or drinking alcohol increases the risk of these side effects. Taking Motrin with food will NOT reduce the risk of these effects. Contact your doctor or emergency room at once if you develop severe stomach or back pain; black, tarry stools; vomit that looks like blood or coffee grounds; or unusual weight gain or swelling.

Do not take more than the recommended dose or use for longer than prescribed without checking with your doctor.

Motrin has ibuprofen in it. Before you start any new medicine, check the label to see if it has ibuprofen in it too. If it does or if you are not sure, check with your doctor or pharmacist.

Do not take aspirin while you are using Motrin unless your doctor tells you to.

Lab tests, including kidney function, complete blood cell counts, and blood pressure, may be done to monitor your progress or to check for side effects. Be sure to keep all doctor and lab appointments.

Use Motrin with caution in the elderly; they may be more sensitive to its effects, including stomach bleeding and kidney problems.

Motrin should be used with extreme caution in children; safety and effectiveness in children have not been confirmed.

Pregnancy and breast-feeding: Motrin may cause harm to the fetus. Do not take it during the last 3 months of pregnancy. If you think you may be pregnant, contact your doctor. You will need to discuss the benefits and risks of taking Motrin while you are pregnant. It is not known if Motrin is found in breast milk. Do not breastfeed while taking Motrin .

All medicines can cause side effects, but many people have no, or minor, side effects.

Check with your doctor if any of these most common side effects persist or become bothersome:

Constipation; diarrhea; dizziness; gas; headache; heartburn; nausea; stomach pain or upset.

Seek medical attention right away if any of these severe side effects occur:

Severe allergic reactions (rash; hives; itching; trouble breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); bloody or black, tarry stools; change in the amount of urine produced; chest pain; confusion; dark urine; depression; fainting; fast or irregular heartbeat; fever, chills, or persistent sore throat; mental or mood changes; numbness of an arm or leg; one-sided weakness; red, swollen, blistered, or peeling skin; ringing in the ears; seizures; severe headache or dizziness; severe or persistent stomach pain or nausea; severe vomiting; shortness of breath; stiff neck; sudden or unexplained weight gain; swelling of hands, legs, or feet; unusual bruising or bleeding; unusual joint or muscle pain; unusual tiredness or weakness; vision or speech changes; vomit that looks like coffee grounds; yellowing of the skin or eyes.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider.

Motrin is used for treating rheumatoid arthritis, osteoarthritis, menstrual cramps, or mild to moderate pain. Motrin is an NSAID. NSAIDs treat the symptoms of pain and inflammation. They do not treat the disease that causes those symptoms.

Use Motrin as directed by your doctor.

Take Motrin by mouth with or without food. It may be taken with food if it upsets your stomach. Taking it with food may not lower the risk of stomach or bowel problems (eg, bleeding, ulcers). Talk with your doctor or pharmacist if you have persistent stomach upset.

Take Motrin with a full glass of water (8 oz/240 mL) as directed by your doctor.

If you miss a dose of Motrin and you are taking it regularly, take it as soon as possible. If it is almost time for your next dose, skip the missed dose. Go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about the proper use of Motrin .

Store Motrin at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Motrin out of the reach of children and away from pets.

Active Ingredient: Ibuprofen.

Do NOT use Motrin if:

you are allergic to any ingredient in Motrin

you have had a severe allergic reaction (eg, severe rash, hives, trouble breathing, growths in the nose, dizziness) to aspirin or an NSAID (eg, ibuprofen, celecoxib)

you have recently had or will be having bypass heart surgery

you are in the last 3 months of pregnancy.

Contact your doctor or health care provider right away if any of these apply to you.

Some medical conditions may interact with Motrin. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal product, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have a history of kidney or liver disease, diabetes, or stomach or bowel problems (eg, bleeding, perforation, ulcers)

if you have a history of swelling or fluid buildup, lupus, asthma, or growths in the nose (nasal polyps), or mouth inflammation

if you have high blood pressure, blood disorders, bleeding or clotting problems, heart problems (eg, heart failure), or blood vessel disease, or if you are at risk for any of these diseases

if you have poor health, dehydration or low fluid volume, or low blood sodium levels, you drink alcohol, or you have a history of alcohol abuse.

Some medicines may interact with Motrin. Tell your health care provider if you are taking any other medicines, especially any of the following:

Anticoagulants (eg, warfarin), aspirin, corticosteroids (eg, prednisone), heparin, or selective serotonin reuptake inhibitors (SSRIs) (eg, fluoxetine) because the risk of stomach bleeding may be increased

Probenecid because it may increase the risk of Motrin 's side effects

Cyclosporine, lithium, methotrexate, or quinolones (eg, ciprofloxacin) because the risk of their side effects may be increased by Motrin

Angiotensin-converting enzyme (ACE) inhibitors (eg, enalapril) or diuretics (eg, furosemide, hydrochlorothiazide) because their effectiveness may be decreased by Motrin.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Motrin may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

Important safety information:

Motrin may cause dizziness or drowsiness. These effects may be worse if you take it with alcohol or certain medicines. Use Motrin with caution. Do not drive or perform other possible unsafe tasks until you know how you react to it.

Serious stomach ulcers or bleeding can occur with the use of Motrin. Taking it in high doses or for a long time, smoking, or drinking alcohol increases the risk of these side effects. Taking Motrin with food will NOT reduce the risk of these effects. Contact your doctor or emergency room at once if you develop severe stomach or back pain; black, tarry stools; vomit that looks like blood or coffee grounds; or unusual weight gain or swelling.

Do not take more than the recommended dose or use for longer than prescribed without checking with your doctor.

Motrin has ibuprofen in it. Before you start any new medicine, check the label to see if it has ibuprofen in it too. If it does or if you are not sure, check with your doctor or pharmacist.

Do not take aspirin while you are using Motrin unless your doctor tells you to.

Lab tests, including kidney function, complete blood cell counts, and blood pressure, may be done to monitor your progress or to check for side effects. Be sure to keep all doctor and lab appointments.

Use Motrin with caution in the elderly; they may be more sensitive to its effects, including stomach bleeding and kidney problems.

Motrin should be used with extreme caution in children; safety and effectiveness in children have not been confirmed.

Pregnancy and breast-feeding: Motrin may cause harm to the fetus. Do not take it during the last 3 months of pregnancy. If you think you may be pregnant, contact your doctor. You will need to discuss the benefits and risks of taking Motrin while you are pregnant. It is not known if Motrin is found in breast milk. Do not breastfeed while taking Motrin .

All medicines can cause side effects, but many people have no, or minor, side effects.

Check with your doctor if any of these most common side effects persist or become bothersome:

Constipation; diarrhea; dizziness; gas; headache; heartburn; nausea; stomach pain or upset.

Seek medical attention right away if any of these severe side effects occur:

Severe allergic reactions (rash; hives; itching; trouble breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); bloody or black, tarry stools; change in the amount of urine produced; chest pain; confusion; dark urine; depression; fainting; fast or irregular heartbeat; fever, chills, or persistent sore throat; mental or mood changes; numbness of an arm or leg; one-sided weakness; red, swollen, blistered, or peeling skin; ringing in the ears; seizures; severe headache or dizziness; severe or persistent stomach pain or nausea; severe vomiting; shortness of breath; stiff neck; sudden or unexplained weight gain; swelling of hands, legs, or feet; unusual bruising or bleeding; unusual joint or muscle pain; unusual tiredness or weakness; vision or speech changes; vomit that looks like coffee grounds; yellowing of the skin or eyes.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider.

Klont, Klont

Klont

Important Notice: The Drugs. com international database is in BETA release. This means it is still under development and may contain inaccuracies. It is not intended as a substitute for the expertise and judgement of your physician, pharmacist or other healthcare professional. It should not be construed to indicate that the use of any medication in any country is safe, appropriate or effective for you. Consult with your healthcare professional before taking any medication.

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Track Name: TorsoKiller Mad butcher of Kingsbury Run Butchered both women and men He castrated and decapitated Terrorrised Cleveland in the '30's Severed arms Severed legs Mutilate Cleveland Torso Killer Severed arms Severed legs Corpse Cleveland Torso killer ( 2x ) The killings stopped as suddenly they had began No one knows who's responsible For the Cleveland Torso Killings Severed arms Severed legs mutilated corpse Cleveland Torso Killer Track Name: I Will Kill I’m hans van Zon I’ll kill for gain and fun I butchered five people With na lead pipe and a knife i went out and take another life A woman or a man, it means nothing to me Strangulation, beaten to death Cut her throat, i will kill I’ll kill male or female It doesn’t matter to me I’ll take my lead pipe And when the beating is done I’ll rape you once more And with my knife, slash a throat will end your life, so sick i am! But what is this? I cannot kill anymore Let my last victim live And i was caught But thanks to the dutch legalsystem I’ve only spend seventeen years behind bars That’s why i’m the bloody bi Track Name: LeTeuerDeLose Le teuer de L'Oise, Marcel barbeault, what did you do. with a .22 Le teuer de L'Oise, Marcel Barbeault, late at night, rainy weather suits you best Le Teuer de Loise, Marcel Barbeault, murdered eight people in Nogent-sur-L'oise Le Teuer de Loise, Marcel Barbeault, was a frequent visitor of the local graveyard Ooh no, Why me? How can she recognise me? 2x Le Teuer de l'Oise, Marcel Barbeault, kidnapped two women, but one of them got away Le Teuer de L'Oise, marcel barbeault was apprehended and made a foolish mistake. Ooh no Why me? How can she (still) recognise me?2x Track Name: BlueBeardKiller Drenth was a bluebeard killer Luring women to his hideaway Introduce them to his execution lab A concrete, soundproof gas chamber

Herman drenth was a bluebeard killer (3x) ohohohohblubberblehheheheh ( zoiets )

Death agonies filled him with intense sexual gratification In his scientific laboratory As he watched his victims die

Herman Drenth was a dutchman immigrated to the Usa And took the name harry Powers for the power he had over his victims

Drenth was a bluebeard killer luring women to their death As they brought their children He hammered them to death Drenth was a bluebeard killer Answering adds in ther paper When they come tot visit him He would gas them to death Drenth was a bluebeard killer Luring women to his lab And they’ll meet their death Killing, Killing, Killing, killing, Dead! Track Name: DeathOfAHundredChildren This is the story of a pakistani killer Who claimed to have murdered a 100 children Iqbal was an entrepeneur who got beaten up By his young servants who were fed up Lure them – Feed them – Kill them He went to the police to press charges But was arrested for sodomy instead Iqbal as mad as he was wanted revenge Revenge for his mother who cried that night oooohohohohohoo The death of a 100 children ( 2x ) Lure them – feed them – Kill them He would lure outcasts and homeless children To his house, feed them and then he'd kill them By using cyanide and an acid bath Threw the remains in a drain in an alley Iqbal kept a diary and a detailed report Turning himself in by reaching a hundred The court sentenced him to death but he hanged himself with bedsheets instead ooohohohohohoho The Death of a 100 children ( 2x ) ohohhhohoohhho.

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Avlida Hotel - Pafos, Kipr, Avidal

Avlida Hotel

Посмотреть все отзывы

Отель Avlida расположен в центре города Пафос, всего в 250 метрах от пляжа. К услугам гостей крытый и открытый бассейны, тренажерный зал, сауна и гидромассажная ванна. Поблизости можно посетить популярную достопримечательность «Царские гробницы». Все …

Отель Avlida расположен в центре города Пафос, всего в 250 метрах от пляжа. К услугам гостей крытый и открытый бассейны, тренажерный зал, сауна и гидромассажная ванна. Поблизости можно посетить популярную достопримечательность «Царские гробницы».

Все номера отеля Avlida оснащены кондиционером и телевизором с плоским экраном и спутниковыми каналами, а также располагают собственной ванной комнатой.

В отеле Avlida гости найдут удобства для различных видов спорта, включая бильярд, теннис, дартс и настольный теннис. Окрестности славятся хорошими местами для дайвинга. В распоряжении гостей сауна и паровая баня. За дополнительную плату можно заказать массажные процедуры. Для юных гостей обустроена детская игровая площадка.

В отеле работает пункт проката автомобилей и велосипедов. На территории обустроена бесплатная общественная парковка. В числе прочих услуг — занятия аквааэробикой и водным поло.

Кроме того, в отеле можно посетить 3 бара и 2 ресторана, где подают блюда интернациональной кухни. В чайном лаундже организуют вечерние развлекательные мероприятия, в том числе живые концерты и караоке.

Это отзыв от Гуру по городу ().

Гуру по городу — тот, кто посетил определенный город по крайней мере 3 раз и написал полезные отзывы о городе и о своем проживании.

Это отзыв от Гуру деловых поездок

Гуру деловых поездок часто бывают в командировках, а потом описывают свои наблюдения в отзывах.

Это отзыв от Гуру семейных путешествий

Гуру семейных путешествий знают все о путешествиях с детьми и всегда делятся впечатлениями о своих приключениях.

Это отзыв от Гуру групповых поездок

Гуру групповых поездок часто путешествуют компанией и любят делиться своими историями.

Это отзыв от Гуру путешествий с животными

Гуру путешествий с животными часто берут с собой в путешествие своих домашних питомцев — а потом делятся своими историями!

Отзывы гостей отражают личное мнение клиентов Booking. com, ответивших на вопросы анкеты после проживания в отеле. Данные суждения могут не совпадать с мнением Booking. com.

Avlida Hotel

Посмотреть все отзывы

Отель Avlida расположен в центре города Пафос, всего в 250 метрах от пляжа. К услугам гостей крытый и открытый бассейны, тренажерный зал, сауна и гидромассажная ванна. Поблизости можно посетить популярную достопримечательность «Царские гробницы». Все …

Отель Avlida расположен в центре города Пафос, всего в 250 метрах от пляжа. К услугам гостей крытый и открытый бассейны, тренажерный зал, сауна и гидромассажная ванна. Поблизости можно посетить популярную достопримечательность «Царские гробницы».

Все номера отеля Avlida оснащены кондиционером и телевизором с плоским экраном и спутниковыми каналами, а также располагают собственной ванной комнатой.

В отеле Avlida гости найдут удобства для различных видов спорта, включая бильярд, теннис, дартс и настольный теннис. Окрестности славятся хорошими местами для дайвинга. В распоряжении гостей сауна и паровая баня. За дополнительную плату можно заказать массажные процедуры. Для юных гостей обустроена детская игровая площадка.

В отеле работает пункт проката автомобилей и велосипедов. На территории обустроена бесплатная общественная парковка. В числе прочих услуг — занятия аквааэробикой и водным поло.

Кроме того, в отеле можно посетить 3 бара и 2 ресторана, где подают блюда интернациональной кухни. В чайном лаундже организуют вечерние развлекательные мероприятия, в том числе живые концерты и караоке.

Это отзыв от Гуру по городу ().

Гуру по городу — тот, кто посетил определенный город по крайней мере 3 раз и написал полезные отзывы о городе и о своем проживании.

Это отзыв от Гуру деловых поездок

Гуру деловых поездок часто бывают в командировках, а потом описывают свои наблюдения в отзывах.

Это отзыв от Гуру семейных путешествий

Гуру семейных путешествий знают все о путешествиях с детьми и всегда делятся впечатлениями о своих приключениях.

Это отзыв от Гуру групповых поездок

Гуру групповых поездок часто путешествуют компанией и любят делиться своими историями.

Это отзыв от Гуру путешествий с животными

Гуру путешествий с животными часто берут с собой в путешествие своих домашних питомцев — а потом делятся своими историями!

Отзывы гостей отражают личное мнение клиентов Booking. com, ответивших на вопросы анкеты после проживания в отеле. Данные суждения могут не совпадать с мнением Booking. com.

Buy Hyalart Hyaluronic Acid, Hyaludermin

Hyaluronic Acid enhances proteoglycans in the joint matrix, thereby providing support for healthy joint function and maintaining joint shock absorption and cushioning.

As a dietary supplement, take 2 capsules daily, or as directed by a health care practitioner. Take with 8-10 ounces of water, with or without food.

Consult your Health Provider about the dosage appropriate for you.

If you miss a dose of Hyaluronic Acid, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Store Hyaluronic Acid at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Keep Hyaluronic Acid out of the reach of children and away from pets.

Do not take hyaluronic acid unless administered by a healthcare professional if:

You are pregnant or breast-feeding.

Hyaluronic Acid is not known to have any side effects if taken as per the prescribed dosage.

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