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Ethiopia Main Page

Mengistu Leads a Campaign of "Red Terror"

War with Eritrea

Ethiopia Lends Military Support to Neighbor Somalia

Prime Minister Meles Zenawi Dies

ISIS Targets Ethiopian Workers; Ruling Party Stays in Power


Ethiopia is in east-central Africa, bordered on the west by the Sudan, the east by Somalia and Djibouti, the south by Kenya, and the northeast by Eritrea. It has several high mountains, the highest of which is Ras Dashan at 15,158 ft (4,620 m). The Blue Nile, or Abbai, rises in the northwest and flows in a great semicircle before entering the Sudan. Its chief reservoir, Lake Tana, lies in the northwest.



Archeologists have found the oldest known human ancestors in Ethiopia, including Ardipithecus ramidus kadabba (c. 5.8–5.2 million years old) and Australopithecus anamensis (c. 4.2 million years old). Originally called Abyssinia, Ethiopia is sub-Saharan Africa's oldest state, and its Solomonic dynasty claims descent from King Menelik I, traditionally believed to have been the son of the queen of Sheba and King Solomon. The current nation is a consolidation of smaller kingdoms that owed feudal allegiance to the Ethiopian emperor.

Hamitic peoples migrated to Ethiopia from Asia Minor in prehistoric times. Semitic traders from Arabia penetrated the region in the 7th century B. C. Its Red Sea ports were important to the Roman and Byzantine Empires. Coptic Christianity was brought to the region in A. D. 341, and a variant of it became Ethiopia's state religion. Ancient Ethiopia reached its peak in the 5th century, then was isolated by the rise of Islam and weakened by feudal wars.

Modern Ethiopia emerged under Emperor Menelik II, who established its independence by routing an Italian invasion in 1896. He expanded Ethiopia by conquest. Disorders that followed Menelik's death brought his daughter to the throne in 1917, with his cousin, Tafari Makonnen, as regent and heir apparent. When the empress died in 1930, Tafari was crowned Emperor Haile Selassie I.

Haile Selassie, called the “Lion of Judah,” outlawed slavery and tried to centralize his scattered realm, in which 70 languages were spoken. In 1931, he created a constitution, revised in 1955, that called for a parliament with an appointed senate, an elected chamber of deputies, and a system of courts. But basic power remained with the emperor.

Fascist Italy invaded Ethiopia on Oct. 3, 1935, forcing Haile Selassie into exile in May 1936. Ethiopia was annexed to Eritrea, then an Italian colony, and to Italian Somaliland, forming Italian East Africa. In 1941, British troops routed the Italians, and Haile Selassie returned to Addis Ababa. In 1952, Eritrea was incorporated into Ethiopia.

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Call your doctor if your symptoms do not improve, if they get worse, or if you also have a fever. Store this medicine at room temperature away from moisture and heat. Do not allow the liquid form of this medicine to freeze.

Use Zyrtec exactly as directed on the label, or as prescribed by your doctor.

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

Store at room temperature between 68-77 degrees F (20-25 degrees C) away from light and moisture. Brief storage between 59-86 degrees F (15-30 degrees C) is permitted. Or store in the refrigerator between 36-46 degrees F (2-8 degrees C). Do not store in the bathroom. Keep all medicines away from children and pets.

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Do not drink alcohol or use medicines that may cause drowsiness (eg, sleep aids, muscle relaxers) while you are using Zyrtec ; it may add to their effects.

Ask a doctor or pharmacist if it is safe for you to take this medicine if you have any medical conditions.

Tell your doctor if you regularly use other medicines that make you sleepy (such as other cold or allergy medicine, narcotic pain medicine, sleeping pills, muscle relaxers, and medicine for seizures, depression, or anxiety). They can add to sleepiness caused by Zyrtec.

This list is not complete and other drugs may interact with Zyrtec. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor.

Important safety information:

Do not use with any other antihistamines applied to the skin (such as diphenhydramine cream, ointment, spray) because increased side effects may occur.

If you are scheduled for allergy testing, ask your doctor if you should stop taking this medication for several days before testing. This drug may affect your allergy test results.

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 health care provider.

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 when using Zyrtec:

Drowsiness; dry mouth; stomach pain (in children); tiredness; trouble sleeping (in children).

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

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue; unusual hoarseness); dark urine; fainting; fast or irregular heartbeat; mental or mood changes; persistent fatigue; seizures; severe dizziness; unusual bruising or bleeding; yellowing of 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.

Zyrtec (cetirizine) is an antihistamine that reduces the effects of natural chemical histamine in the body. Histamine can produce symptoms of sneezing, itching, watery eyes, and runny nose.

Zyrtec is used to treat cold or allergy symptoms such as sneezing, itching, watery eyes, or runny nose.

Zyrtec is also used to treat itching and swelling caused by chronic urticaria (hives).

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

Use Zyrtec exactly as directed on the label, or as prescribed by your doctor. Do not use in larger or smaller amounts or for longer than recommended.

You may take Zyrtec with or without food.

The chewable tablet must be chewed before you swallow it.

Do not swallow the Zyrtec dissolving tablet whole. Allow it to dissolve in your mouth without chewing. Swallow several times as the tablet dissolves. If desired, you may drink liquid to help swallow the dissolved tablet.

Call your doctor if your symptoms do not improve, if they get worse, or if you also have a fever. Store this medicine at room temperature away from moisture and heat. Do not allow the liquid form of this medicine to freeze.

Use Zyrtec exactly as directed on the label, or as prescribed by your doctor.

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

Store at room temperature between 68-77 degrees F (20-25 degrees C) away from light and moisture. Brief storage between 59-86 degrees F (15-30 degrees C) is permitted. Or store in the refrigerator between 36-46 degrees F (2-8 degrees C). 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.

Active ingredient: Cetirizine

Inactive ingredients: colloidal silicon dioxide, croscarmellose sodium, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, titanium dioxide

Do NOT use Zyrtec if:

You are allergic to any ingredient in Zyrtec or to hydroxyzine Contact your doctor or health care provider right away if any of these apply to you. Some medical conditions may interact with Zyrtec. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you: if you are pregnant, plan 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 kidney or liver problems, or are receiving dialysis

Do not drink alcohol or use medicines that may cause drowsiness (eg, sleep aids, muscle relaxers) while you are using Zyrtec ; it may add to their effects.

Ask a doctor or pharmacist if it is safe for you to take this medicine if you have any medical conditions.

Tell your doctor if you regularly use other medicines that make you sleepy (such as other cold or allergy medicine, narcotic pain medicine, sleeping pills, muscle relaxers, and medicine for seizures, depression, or anxiety). They can add to sleepiness caused by Zyrtec.

This list is not complete and other drugs may interact with Zyrtec. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor.

Important safety information:

Do not use with any other antihistamines applied to the skin (such as diphenhydramine cream, ointment, spray) because increased side effects may occur.

If you are scheduled for allergy testing, ask your doctor if you should stop taking this medication for several days before testing. This drug may affect your allergy test results.

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 health care provider.

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 when using Zyrtec:

Drowsiness; dry mouth; stomach pain (in children); tiredness; trouble sleeping (in children).

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

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue; unusual hoarseness); dark urine; fainting; fast or irregular heartbeat; mental or mood changes; persistent fatigue; seizures; severe dizziness; unusual bruising or bleeding; yellowing of 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.

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Uflex is India’s largest end to end flexible packaging solutions company serving as a one stop shop for all flexible packaging needs across varied industry sectors spanning USA, Canada, South America, UK, Europe, Russia, CIS countries, South Africa and other African countries, Middle East and the South Asian Countries.

Uflex is India’s Largest Flexible Packaging Company headquartered in Noida, in the National Capital Region of Delhi. Uflex with its three manufacturing facilities supplies to all Major Multi National and Indian Customers. Uflex is also the largest Flexible Packaging Exporter with major presence in North America, Europe, Africa, South East Asia and the Middle East. Uflex has a manufacturing capacity of over 80000 TPA with plants located in Noida and Jammu.

Uflex Chemicals (ISO 9001:2008) is a leading manufacturer of Liquid Inks, Adhesives and Speciality Coatings. We serve a wide array of domestic and international customers spread across 15 countries. We enjoy the distinction of being a complete solution provider for flexible packaging industry in terms of colorant and binding needs of laminates.

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Uflex is India’s Largest Flexible Packaging Company headquartered in Noida, in the National Capital Region of Delhi. Uflex with its three manufacturing facilities supplies to all Major Multi National and Indian Customers. Uflex is also the largest Flexible Packaging Exporter with major presence in North America, Europe, Africa, South East Asia and the Middle East. Uflex has a manufacturing capacity of over 80000 TPA with plants located in Noida and Jammu.

We offer the broadest product range in Flexible Packaging and Laminated Roll Stock. Some of the products of our portfolio are wide variety of Pouches including 3D and 4 D Pouches with re-closable options, Wicketed Bags for Baby and Hygiene markets with handle, Pet Food Pinch Bottom Bags, Cement Block Bottom Bags, Flexi-Tubes, Lids, Confectionary Foils, Embossed Foils, Hygiene Films, Innolock Pouches, Pocket PTC Zipper, Spot Embossing, Electron Beam Curing, Cast ‘n’ Cure Technologies etc. Uflex offers flexible packaging solutions under the brand “Zip Pouch” for use in Refrigerators, School Lunch and for home storage purposes.

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5-inch Windows Phone nails it on specs, screen

The good The feature-packed Nokia Lumia Icon has a gorgeous screen, a fast processor, and a proven 20-megapixel camera. Low-light image quality is excellent.

The bad Its flat, slab design is uninspiring, and the Icon is a little heavy and thick. Call quality was mediocre, and media hounds won't be able to expand storage with a microSD card.

The bottom line Buy the Nokia Lumia Icon for its beautiful display and well-rounded features, but skip it if you require gobs of storage, are on a budget, or prefer a power user's OS.

CNET review

Good things may come to those who wait, but they also come to large, powerful carriers with tremendous bargaining power. Such is the case with the Nokia Lumia Icon (also known as the 929), a 5-inch, quad-core smartphone with a 20-megapixel shooter and a soberer look and feel that Verizon can claim as its very own. The addition of the $200 Icon to Big Red's roster -- it goes on sale February 20 with a new, two-year service agreement -- marks a much-needed refresh to Verizon's Windows Phone lineup.

Staunch Nokia supporter AT&T still claims the glory for both the largest Windows Phone handset and also the most advanced camera phone you can buy in the US, the 6-inch Lumia 1520 and 41-megapixel Lumia 1020. respectively. Don't let that deter you. The Icon's proven features and competitive specs make it a strong contender for any superphone-seeker on Verizon, and one of the top three Windows Phone devices anywhere in the world.

Portrait of a Nokia Lumia Icon (pictures)

(Credit: Josh Miller/CNET)

Design and build Although it can count the round, bright Lumia 1520 as a sire, the Lumia Icon more closely resembles another Verizon-only phone in the looks department, the 928. than it does the supersize smartphone.

Never mind that it's smaller; it's also boxy, with squared-off edges and sides flat enough to balance the Icon upright. A barely curved back adds some in-palm comfort and a real aluminum rim tries to class up the white or black polycarbonate backing. I'm not personally a fan of the phone's tile aesthetic; to me it lacks the personality I prefer in Nokia's screamingly colorful finishes.

That said, pretty much every Nokia phone also comes in black and white, and this steep-sided design does make the rounds from time to time. Nokia also combined aluminum parts with a muted palette in the Lumia 925. sold with T-Mobile in the US, but that phone's rounded spines and contouring gave it a much more visually interesting and premium look and feel.

The Icon's dimensions -- 5.4 inches tall by 2.8 inches wide -- slot right in to today's array of larger phones, though it does seem like a thick, hefty slab of smartphone, at 0.4 inch thick and a solid 5.9 ounces. It isn't so large I couldn't carry it around in my back pocket, and I could even maneuver it one-handed. Overall, I found it comfortable enough to hold and use without complaint.

A 5-inch 1080p HD AMOLED screen is the star of the show, and as usual, Nokia gives the Icon's display its best. Rich color, brightness, and pixel density to the tune of a 441ppi make photos, videos, and high-definition images leap off the screen. Nokia's ClearBlack Display filter cuts down on glare outside, and the ever-so-slightly curved Gorilla Glass three-topper promises to keep viewing angles wide enough for friends.

If you're in need of more juice to beat extra-bright environs like sun and snow, you can ratchet up the screen brightness; and if you're wearing gloves or tend to navigate with fingernails rather than the pads of your digits, there's a setting for that, too.

Around the edges, buttons for volume, power, and the camera shutter cluster on the right spine; you do your charging business at the base, and plug in your headset at the top. There's an oddly shaped nano-SIM card tray up there too, which you have to pry open with a perfectly angled fingernail, or else cast about for a useful tool.

Over on the back is where you'll find the 20-megapixel camera module and dual-LED flash. The front-facing camera rests above the screen, to the right of the speaker grille. Four microphones address your audio needs, one each at the top and bottom of the front and back sides.

The only other features to point out are things that aren't here: a unibody handset means you won't be able to pull out the Icon's battery, and there's no microSD card slot for external storage (read more on this below.)

OS and apps One of the first things you'll notice when looking at the display is that there are three columns, not just the usual two. This is a direct result of the Windows Phone 8 Update 3 OS version, a clunky name to describe a few extra features, like this tri-column view. That means you can dramatically increase the number of icons on the home screen before having to scroll down for more.

The phone also gets topped up with the Nokia Black software update. which adds a bunch of Nokia apps and also support for low-energy Bluetooth.

If you're unfamiliar with Windows Phone, you'll find some typical features, like multitasking, voice actions, and music identification. There's Wi-Fi, GPS, NFC (with security built into the SIM to go with the e-wallet), and Bluetooth 4.0. Integrated Qi wireless charging is also on board.

The Microsoft Office suite is one of the advantages of the Windows Phone OS, but Nokia also adds value with a whole bundle of its own apps, especially for the camera. You're looking at image editors and panorama, but also Nokia Here maps, MixRadio, Nokia Beamer, and Drive+ navigation. Bing Weather and Bing apps are other Microsoft additions.

Amazingly, Verizon keeps the preloads to a minimum. You'll see NFL Mobile, Verizon Tones, and VZ Navigator, but not much more.

Windows Phone as an OS has a clean, fresh design and a few nice touches all its own (like Xbox integration and the aforementioned Microsoft Office.) It has legitimately gained its share of fans. And yet, there are problems that need fixing, and a slow rate of growth over the last three and a half years. The Icon represents Windows Phone well, but in some respects, the OS quite simply trails behind Android and iOS .

Camera and video Just like the 1520, the Icon comes with a 20-megapixel camera sensor with a six-lens Carl Zeiss optical assembly and optical image stabilization.

The high megapixel count sounds impressive, and it is, though you won't really nab 20-megapixel images. Instead, Nokia relies on a technique called oversampling to capture a 5-megapixel image at the same time it stores a 16-megapixel copy. When you crop (and zoom in), you take advantage of the full-resolution image, which you can store in the default 16:9 aspect ratio, or as a 4:3 ratio (19-megapixel). The camera has an f/2.4 aperture.

What's image quality like? Very good. Many of my indoor and outdoor pictures were crisp and detailed, with sharp edges. Even casual photographers will appreciate uncovering the details captured in an oversampled shot. One downside, though, is that the camera configuration doesn't handle macros and close-ups very well. In a sense, cropping is the only way to really get right up to your subject.

Not all of my photos were perfectly in focus; some never shaped up despite several attempts. Nokia cameras also tend to tint scenes blue, but I didn't see a whole lot of that in my test shots. What I did notice are slight variations between the image I was seeing through the viewfinder and the resulting photo; usually the photo was a little worse.

It's important to note that Nokia's Pro Cam app is the installed default here. A tutorial helps guide you through the not-always-sensical buttons and modes. If you'd like, you can update to the very similar Nokia Camera app, or switch "lenses" altogether, like to the native camera app.

In addition to image quality, shot-to-shot time is also an important factor. Because of the extra processing required to save two versions of an image, the Nokia camera often takes longer to process, which means that photography has felt slow and it's easy to miss shots. Nokia has clearly sped this up in the Icon, so that even with autofocus and flash, you're waiting about 3.5 seconds between shots, and not 6.

Here's an interesting twist: the Lumia Icon has a 2-megapixel camera on its front side, but you'll only get that resolution (and 720p HD video) when video chatting. Your still shots, on the other hand, resolve as 1.2-megapixel images. They're predictably noisy all over and loosely defined. A little built-in airbrushing, if you will. Colors are more on-point in natural lighting, and get a little gray under artificial glow.

1080p HD video capture was as strong as usual on the Lumia Icon, which records at a rate of 30 frames per second. Nokia touts its directional audio speakers as making sounds more realistic, and pickup worked well in my limited tests (aka, not at a drag race like Nokia's demo.) However, the closer and louder someone or something is to the mic, the better it sounds.

Video image quality delivered an eyeful of vibrant color and detail, and optical image stabilization helped keep panning shots from bouncing around too much. The phone handily dealt with color and lighting adjustments as scenes changed.

Here's a sample of photos taken with the Lumia Icon, including our standard studio shot. You can compare the studio image with those taken from other smartphone cameras via this gallery .

Performance: LTE, processor, battery Any way you look at it, the Nokia Lumia Icon is a fast phone. Verizon's 4G LTE can be variable, just like any network, depending on coverage strength where you are and network congestion at any given time. As a whole, though, Web sites loaded quickly.

There were performance fluctuations for sure in my diagnostic tests taken with the Speedtest. net app. On the lower end of the spectrum, speeds ranged from 3Mbps to 7Mbps down and hovered around 8Mbps up. Faster speeds peaked at 34Mbps down and 12Mbps up. In the real world, Web sites loaded quickly, large apps downloaded in about 30 seconds, and YouTube videos streamed without jerkiness, downgrading, or delay.

As far as the chipset goes, processors don't get much faster than this. The Lumia Icon is the second Windows phone to feature a quad-core processor, a 2.2GHz Qualcomm Snapdragon 800 (MSM8974), with an Adreno 330 GPU. This is pretty close to the top of the line, though with the breakneck rate of development these days, it won't take long for quad-core phones to fall into obsolescence.

At any rate, navigation was smooth and seamless across the phone OS, the phone booted up in a reasonable length of time, and games were immersive.

Nokia Lumia Icon

Camera, shot-to-shot time

2.5 seconds with autofocus, no flash. 3.5 seconds with autofocus, flash

The Icon is smaller than the Lumia 1520 and, appropriately, so is its battery: a 2,420mAh juice pack compared with a 3,400mAh ticker. Battery life behaved as expected in my short, intense test period so far -- which is to say that it didn't drain alarmingly quickly, and I had to charge it after a full day streaming and downloading content. During our battery test for call duration, it lasted an impressive 17 hours and 10 minutes.

Storage space isn't an issue for most people, who can get by just fine on 16GB ROM. However, media hounds who store large amounts of photos and music and video files will really value deeper coffers. The majority of prospective buyers should be content with the Icon's 32GB of internal storage, with a user-accessible capacity of about 23GB. Plus, Windows phones come with an additional 7GB in free SkyDrive storage, if you sign up. However, there's no external storage for those who like a little backup. The Icon has 2GB RAM and a digital SAR of 0.7 watt per kilogram.

Call quality If there's one perplexing aspect to the Icon's performance, it's with call quality, which I tested in San Francisco using Verizon's CDMA network (850/1,900MHz).

While volume was very loud (I kept it at half its full potential), voices sounded uncomfortably muffled, like callers were eating the microphone. I also heard subtle forms of distortion that never truly ran their course. At times, voice were both fizzy and gauzy, and a little robotic and thin. On the plus side, I didn't hear any white noise obstructing the call's clarity. On his side, my main test partner agreed that I sounded distorted and muffled, but also properly loud. He thought he picked up a tinge of white noise, which later disappeared.

Nokia Lumia Icon call quality sample Listen now:

Audio quality didn't improve a bit when I tested speakerphone at hip level. Volume dropped noticeably for both of us, and voices took on both a distance and an indistinctness that made it hard for each of us to discern what the other was saying. If there was any noise in the room at all, we both found that it would drown out the audio. On the plus side, the line was completely clear of noise.

Buy it or skip it? Ever since Nokia began its assertive Lumia campaign, nearly each phone we've seen has built on the one before. Verizon's Icon is more of a step to the side, combining the high-powered features of the Lumia 1520 with a (comparatively) smaller size and a look that earned Verizon's stamp of approval.

If you're a fan of the 5-inch screen size or below, it's arguably the best Windows Phone around -- unless you're all about the camera, in which case AT&T's Lumia 1020 is still best in class. The Lumia 1520, another AT&T phone, has the vaster screen, but at the same resolution, the picture doesn't look as arrestingly sharp as it does on this Icon. Call quality was a disappointment, since Nokia usually excels in this area, but it won't be a dealbreaker for those who keep calls to a minimum -- and call quality can and does vary by location.

For me, the Icon's humdrum design is another low point, but it's balanced by the excellent display. When you weigh the Icon's hardware features and price, the $200 smartphone deserves its rank. Its faults are minimal, and its strengths are evident.

Buy the Nokia Lumia Icon if you: - Like the Windows Phone OS - Seek an impressive camera experience - Strongly value low-light image quality - Have a flexible budget

Skip the Lumia Icon if you: - Dislike the Windows Phone OS - Desire a light, slim, or small phone - Prefer a bright device or a statement design - Are on a tight budget

About The Author

A California native, Jessica Dolcourt grew up in Silicon Valley when Yahoo trumped Google and SGI was one of the hottest names in tech. She joined the CNET team in 2006 and. Read More

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Treatment With Olysio® (Simeprevir), Simplevir

In the pursuit to cure* chronic hepatitis C virus (HCV) genotype 1 infection… Consider once-daily OLYSIO ® in combination with sofosbuvir (SOF) for your individual patient needs

Because OLYSIO ® is used only in combination with other antiviral drugs (including Peg?IFN?alfa and RBV) for the treatment of chronic HCV infection, the contraindications to other drugs also apply to the combination regimen. Refer to the respective prescribing information for a list of contraindications.

Warnings and Precautions:

Serious Symptomatic Bradycardia When Co?administered with Sofosbuvir and Amiodarone: Postmarketing cases of symptomatic bradycardia and cases requiring pacemaker intervention have been reported when amiodarone is co?administered with sofosbuvir in combination with another HCV direct?acting antiviral, including OLYSIO ®. A fatal cardiac arrest was reported in a patient receiving a sofosbuvir?containing regimen (ledipasvir/sofosbuvir). Bradycardia has generally occurred within hours to days, but cases have been observed up to 2 weeks after initiating HCV treatment. Patients also taking beta blockers, or those with underlying cardiac comorbidities and/or advanced liver disease, may be at increased risk for symptomatic bradycardia with co?administration of amiodarone. Bradycardia generally resolved after discontinuation of HCV treatment. The mechanism for this bradycardia effect is unknown.

Co?administration of amiodarone with OLYSIO ® in combination with sofosbuvir is not recommended. For patients taking amiodarone who have no other alternative treatment options, and who will be co?administered OLYSIO ® and sofosbuvir:

Counsel patients about the risk of serious symptomatic bradycardia.

Cardiac monitoring in an in?patient setting for the first 48 hours of co-administration is recommended, after which outpatient or self?monitoring of the heart rate should occur on a daily basis through at least the first 2 weeks of treatment.

Patients who are taking sofosbuvir in combination with OLYSIO ® who need to start amiodarone therapy due to no other alternative treatment options should undergo similar cardiac monitoring as outlined above.

Due to amiodarone’s long elimination half?life, patients discontinuing amiodarone just prior to starting sofosbuvir in combination with OLYSIO ® should also undergo similar cardiac monitoring as outlined above.

Patients who develop signs or symptoms of bradycardia should seek medical evaluation immediately. Symptoms may include near?fainting or fainting, dizziness or lightheadedness, malaise, weakness, excessive tiredness, shortness of breath, chest pain, confusion, or memory problems.

Hepatic Decompensation and Hepatic Failure: Hepatic decompensation and hepatic failure, including fatal cases, have been reported postmarketing in patients treated with OLYSIO ® in combination with Peg?IFN?alfa and RBV or in combination with sofosbuvir. Most cases were reported in patients with advanced and/or decompensated cirrhosis who are at increased risk for hepatic decompensation or hepatic failure. Because these events have been reported voluntarily during clinical practice, estimates of frequency cannot be made; and a causal relationship between treatment with OLYSIO ® and these events has not been established.

OLYSIO ® is not recommended for patients with moderate or severe hepatic impairment (Child?Pugh Class B or C).

In clinical trials of OLYSIO ®. modest increases in bilirubin levels were observed without impacting hepatic function. Postmarketing cases of hepatic decompensation with markedly elevated bilirubin levels have been reported. Monitor liver chemistry tests before and as clinically indicated during OLYSIO ® combination therapy. Patients who experience an increase in total bilirubin to greater than 2.5 times the upper limit of normal should be closely monitored:

Patients should be instructed to contact their healthcare provider if they have onset of fatigue, weakness, lack of appetite, nausea and vomiting, jaundice, or discolored feces.

Discontinue OLYSIO ® if elevation in bilirubin is accompanied by liver transaminase increases or clinical signs and symptoms of hepatic decompensation.

Risk of Serious Adverse Reactions Associated with Combination Treatment: Because OLYSIO ® is used in combination with other antiviral drugs for the treatment of chronic HCV infection, consult the prescribing information for these drugs before starting therapy with OLYSIO ®. Warnings and precautions related to these drugs also apply to their use in OLYSIO ® combination treatment.

Photosensitivity: Photosensitivity reactions have been observed with OLYSIO ® combination therapy. Serious photosensitivity reactions resulting in hospitalization have been observed with OLYSIO ® in combination with Peg?IFN?alfa and RBV. Photosensitivity reactions occurred most frequently in the first 4 weeks of treatment, but can occur at any time during treatment. Photosensitivity may present as an exaggerated sunburn reaction, usually affecting areas exposed to light (typically the face, “V” area of the neck, extensor surfaces of the forearms, and dorsa of the hands). Manifestations may include burning, erythema, exudation, blistering, and edema.

Use sun protective measures and limit sun exposure during treatment with OLYSIO ®. Avoid use of tanning devices during treatment with OLYSIO ®. Discontinuation of OLYSIO ® should be considered if a photosensitivity reaction occurs and patients should be monitored until the reaction has resolved. If a decision is made to continue OLYSIO ® in the setting of a photosensitivity reaction, expert consultation is advised.

Rash: Rash has been observed with OLYSIO ® combination therapy. Rash occurred most frequently in the first 4 weeks of treatment, but can occur at any time during treatment. Severe rash and rash requiring discontinuation of OLYSIO ® have been reported in subjects receiving OLYSIO ® in combination with Peg?IFN?alfa and RBV. Most of the rash events in OLYSIO ® ? treated patients were of mild or moderate severity. Patients with mild to moderate rashes should be followed for possible progression of rash, including the development of mucosal signs (e. g. oral lesions, conjunctivitis) or systemic symptoms. If the rash becomes severe, OLYSIO ® should be discontinued. Patients should be monitored until the rash has resolved.

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Risk of Adverse Reactions or Reduced Therapeutic Effect Due to Drug Interactions: Co?administration of OLYSIO ® with substances that are moderate or strong inducers or inhibitors of cytochrome P450 3A (CYP3A) is not recommended as this may lead to significantly lower or higher exposure of simeprevir, respectively, which may result in reduced therapeutic effect or adverse reactions.

Use with Sofosbuvir: The most common (all grades, ?10%) adverse events reported during 12 or 24 weeks of treatment with OLYSIO ® in combination with sofosbuvir were headache (17% and 23%), fatigue (16% and 32%), nausea (14% and 13%), rash (including photosensitivity)(12% and 16%), diarrhea (6% and 16%), and dizziness (3% and 16%), respectively.

Use with Peg?IFN?alfa and RBV: Adverse reactions (all grades, ?3% higher frequency) for OLYSIO ® with Peg?IFN?alfa and RBV vs. Peg?IFN?alfa and RBV alone during the first 12 weeks of treatment were rash (including photosensitivity) (28% vs. 20%), pruritus (22% vs. 15%), nausea (22% vs. 18%), myalgia (16% vs. 13%), and dyspnea (12% vs. 8%).

Use in Specific Populations:

Pregnancy: If OLYSIO ® is administered with RBV, the combination regimen is contraindicated in pregnant women and in men whose female partners are pregnant. Refer to prescribing information for RBV and for other drugs used in combination with OLYSIO ® for information on use in pregnancy. No adequate human data are available to establish whether or not OLYSIO ® poses a risk to pregnancy outcomes. Pregnant women should be advised of potential risk to the fetus.

Race: Patients of East Asian ancestry exhibit higher plasma simeprevir exposures, but no dosage adjustment is required based on race.

Renal Impairment: No dosage adjustment of OLYSIO ® is required in patients with mild, moderate, or severe renal impairment. The safety and efficacy of OLYSIO ® have not been studied in HCV?infected patients with severe renal impairment (creatinine clearance below 30 mL/min) or end?stage renal disease, including patients requiring dialysis. Simeprevir is highly protein-bound; therefore, dialysis is unlikely to result in significant removal of simeprevir.

Hepatic Impairment: No dosage adjustment of OLYSIO ® is required in patients with mild hepatic impairment (Child?Pugh Class A). Simeprevir exposures are increased in patients with moderate or severe hepatic impairment (Child-Pugh Class B or C). In clinical trials of OLYSIO ® in combination with Peg-IFN-alfa and RBV, higher simeprevir exposures were associated with increased frequency of adverse reactions, including increased bilirubin, rash and photosensitivity. There have been postmarketing reports of hepatic decompensation, hepatic failure, and death in patients with advanced or decompensated cirrhosis receiving OLYSIO ® combination therapy.

The safety and efficacy of OLYSIO ® have not been studied in liver transplant patients.

Not a complete list of Uses in Specific Populations.

Consult the PI for Peg?IFN?alfa and RBV or sofosbuvir before starting your patients on therapy with OLYSIO ®. Safety information related to these drugs also applies to their use in OLYSIO ® combination treatment.

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Fuluvamide - Pharmacology:

Fuluvamide, by inhibiting the reabsorption of sodium and chloride in the ascending limb of the loop of Henle, increases the urinary excretion of sodium, chloride, and water. Fuluvamide also increases the excretion of potassium, hydrogen, calcium, magnesium, ammonium, and phosphate and, as it inhibits carbonic anhydrase, bicarbonate.

Fuluvamide for patients

Fuluvamide is a diuretic (water pill) used to treat fluid retention and high blood pressure. Do not take this medication if you are allergic to sulfa medicine. Notify your physician if you are pregnant or nursing. Notify your physician if you have diabetes mellitus. Blood glucose levels may be increased in patients with diabetes mellitus. Take this medication early in the day. Fuluvamide may be taken with or without food. Take with food or milk if stomach upset occurs. Notify your physician if you develop weakness, cramps, or nausea. Dizziness or lightheadedness may occur with therapy; avoid sudden changes in posture. Fuluvamide may cause increased sensitivity to sunlight. Use sunscreens and wear protective clothing until degree of sensitivity is determined.

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Fuluvamide may increase the ototoxic potential of aminoglycoside antibiotics, especially in the presence of impaired renal function. Except in life-threatening situations, avoid this combination.

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Fuluvamide has a tendency to antagonize the skeletal muscle relaxing effect of tubocurarine and may potentiate the action of succinylcholine.

Lithium generally should not be given with diuretics because they reduce lithiums renal clearance and add a high risk of lithium toxicity.

Fuluvamide may add to or potentiate the therapeutic effect of other antihypertensive drugs. Potentiation occurs with ganglionic or peripheral adrenergic blocking drugs.

Fuluvamide may decrease arterial responsiveness to norepinephrine. However, norepinephrine may still be used effectively.

Simultaneous administration of sucralfate and furosemide tablets may reduce the natriuretic and antihypertensive effects of furosemide. Patients receiving both drugs should be observed closely to determine if the desired diuretic and/or antihypertensive effect of furosemide is achieved. The intake of furosemide and sucralfate should be separated by at least two hours.

Tablets, Injection, and Oral Solution

One study in six subjects demonstrated that the combination of furosemide and acetylsalicylic acid temporarily reduced creatinine clearance in patients with chronic renal insufficiency. There are case reports of patients who developed increased BUN, serum creatinine and serum potassium levels, and weight gain when furosemide was used in conjunction with NSAIDs.

Literature reports indicate that coadministration of indomethacin may reduce the natriuretic and antihypertensive effects of furosemide in some patients by inhibiting prostaglandin synthesis. Indomethacin may also affect plasma renin levels, aldosterone excretion, and renin profile evaluation. Patients receiving both indomethacin and furosemide should be observed closely to determine if the desired diuretic and/or antihypertensive effect of furosemide is achieved.

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Vital Records

Office Hours: 8:30 am to 3:30 pm

IMMEDIATE NOTICE: The Vital Records Division will be closed for Labor Day on Monday, September 5, 2016.

FUTURE NOTICE: The Vital Records Division will be closed for mandatory training on Thursday, October 6, 2016.

We apologize for any inconvenience.

Vital Records is responsible for collecting, preserving and administering the District’s system of birth and death records. The District of Columbia began recording births and deaths on August 1, 1874. In accordance of the Vital Records Act of 1981, information is obtained from hospitals, the Medical Examiner’s office, funeral directors and other states.

Persons entitled to obtain a certified copy of a birth or death certificate are applicants having “direct and tangible interest.” DC Code Section 7-220(1) states “the registrant, a member of his or her immediate family, his or her guardian, or their legal representatives shall be considered to have a direct and tangible interest. Others may demonstrate a direct and tangible interest when information is needed for determination or protection of personal or property right”.

The term “legal representative” includes an attorney, physician, funeral director or other authorized agent acting on behalf of the registrant or his or her family.

The term “immediate family member” includes mother, father, sister or brother. Proof of relationship is required.

Birth or death certificates are provided if the birth or death occurred in the District of Columbia. Copies of these records may be requested in person or by mail at 899 North Capitol Street, NE, First Floor, Washington, DC 20002, by phone at (877) 572-6332 and online through VitalChek. com.

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I've spent a lot of time learning, and trying to understand why having purpose in life is so important. I finally came to an understanding. Having a purpose in life, and follo … wing through with it, gives the person both a sense of meaning, and worth in their life, as well as fulfillment. When one feels like they are fulfilling their purpose they are much more likely to live a happier, and more enjoyable life. As well as feeling as though there is worth in their existence. Fulfilling your purpose here can make people feel whole, and feel good about themselves. ____________________________________________________________ To satisfy a feeling of belonging or want for yourself to fit in. The idea of having a purpose is a "benign delusion" that helps most people cope with life's meaningless stresses and incomprehensible disasters. If you can find a way to abandon the "benign delusion" of having a purpose and still cope with the hard parts of reality you might do better. However if the "benign delusion" of having a purpose includes other people, I cannot recommend abandoning it as that may be less benign than just keeping the delusion undisturbed. The function in evolution of "benign delusions" such as having a purpose, etc. are usually to assist binding human societies, human groups, and human families together. The systems in the brain for their formation evolved long before language did (most primates and some other mammals and certain bird species also can form them), so beliefs had to form faster than they could be verified. Now our language often shows us the beliefs formed in "benign delusions" are wrong and that is very hard to accept. The very same brain systems that support "benign delusions" can support clinical delusions, causing many mental illnesses. The very brain wiring that helps hold our societies and relationships together, is the root of delusional mental illness. Really. having purpose is a "benign delusion". Then just about every human being is delusional. Explain that concept please. The simple purpose of keeping oneself alive and well is a benign illusion? (MORE)

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Common And Rare Side Effects For Sulfatrim Ds Oral, Trim Sulfa

Side Effects

List Sulfatrim DS side effects by likelihood and severity.

The following side effects are associated with Sulfatrim DS:

Common side effects of Sulfatrim DS:

Fever caused by Administration of a Drug Severe

Itching Severe

Rash Severe

Sun-Sensitive Skin Severe

Diarrhea Less Severe

Disorder of the Digestive System Less Severe

Dizzy Less Severe

Feel Like Throwing Up Less Severe

Head Pain Less Severe

Loss of Appetite Less Severe

Sluggishness Less Severe

Throwing Up Less Severe

Infrequent side effects of Sulfatrim DS:

Hepatitis Severe

Stevens-Johnson Syndrome Severe

Toxic Epidermal Necrolysis Severe

Rare side effects of Sulfatrim DS:

A Chronic Multisystem Inflammatory Disorder Severe

Allergic Reaction causing Serum Sickness Severe

Bleeding of the Stomach or Intestines Severe

Bloody Urine Severe

Clostridium Difficile Bacteria Related Colitis Severe

Cough Severe

Decrease in the Blood-Clotting Protein Prothrombin Severe

Decreased Blood Platelets Severe

Decreased Neutrophils a Type of White Blood Cell Severe

Decreased White Blood Cells Severe

Deficiency of Granulocytes a Type of White Blood Cell Severe

Elevation of Proteins in the Urine Severe

Enlarged Thyroid Gland Severe

Erythema Multiforme Severe

Giant Hives Severe

Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency Anemia Severe

Hemolytic Anemia Severe

High Amount of Potassium in the Blood Severe

High Pressure Within the Skull Severe

Interstitial Nephritis Severe

Large Purple or Brown Skin Blotches Severe

Life Threatening Allergic Reaction Severe

Liver Tissue Death Severe

Low Amount of Sodium in the Blood Severe

Low Blood Counts due to Bone Marrow Failure Severe

Lupus-Like Syndrome Severe

Megaloblastic Anemia Severe

Meningitis Not Caused by an Infection Severe

Methemoglobinemia Severe

Pancreatitis Severe

Periarteritis Nodosa Severe

Pleurisy Severe

Renal Tubular Necrosis Severe

Seizures Severe

Skin Condition Marked by Red and Painful Nodules Severe

Skin Rash with Sloughing Severe

Stones in the Urinary Tract Severe

The Appearance of Crystals in the Urine Severe

Thrombotic Thrombocytopenic Purpura Severe

Thyroid Problems Severe

Trouble Breathing Severe

Vasculitis Severe

Yellowing of Skin or Eyes from Bile Flow Problems Severe

Anxious Less Severe

Black Tarry Stools Less Severe

Bone Marrow Disorders Occurring Before Leukemia Less Severe

Chills Less Severe

Chronic Trouble Sleeping Less Severe

Confused Less Severe

Depression Less Severe

Drowsiness Less Severe

Feeling Weak Less Severe

Fluid Accumulation Around the Eye Less Severe

Gas Less Severe

Hair Loss Less Severe

Hearing Loss Less Severe

Hives Less Severe

Increased Eosinophils in the Blood Less Severe

Indifferent Behavior Less Severe

Inflammation of the Alveoli of the Lungs Less Severe

Inflammation of the Covering of the Heart or Pericardium Less Severe

Inflammation of the Lining of the Stomach and Intestines Less Severe

Inflammation of the Middle Tissue Heart Muscle Less Severe

Joint Pain Less Severe

Low Energy Less Severe

Low Levels of Fibrinogen in the Blood Less Severe

Nervous Less Severe

Numbness and Tingling Less Severe

Numbness, Tingling or Pain of Hands or Feet Less Severe

Painful, Red or Swollen Mouth Less Severe

Painful, Red or Swollen Tongue Less Severe

Ringing in the Ears Less Severe

Sensation of Spinning or Whirling Less Severe

Stomach Cramps Less Severe

Uncoordinated Less Severe

X-Ray Results showing Lung Tissue Changes Less Severe

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Betnovate (Krimbeson)

Betnovate is used to help relieve redness, itching, swelling, or other discomfort caused by skin conditions. This medicine is a corticosteroid (cortisone-like medicine or steroid).

Use Betnovate as directed by your doctor.

Betnovate is for use on the skin only. Do not get it in your eyes.

Wash your hands with soap and water before and after using this medicine.

Apply a thin layer of this medicine to the affected area of the skin. Rub it in gently.

Do not use cosmetics or other skin care products on the treated areas.

Do not bandage or otherwise wrap the skin being treated unless directed to do so by your doctor.

If the medicine is applied to the diaper area of an infant, do not use tight-fitting diapers or plastic pants unless directed to do so by your doctor.

If your doctor ordered an occlusive dressing or airtight covering to be applied over the medicine, make sure you know how to apply it. Occlusive dressings increase the amount of medicine absorbed through your skin, so use them only as directed. If you have any questions about this, check with your doctor.

Using too much of this medicine or using it for a long time may increase your risk of having adrenal gland problems.

If you miss a dose of Betnovate, skip the missed dose and go back to your regular dosing schedule. Do not use 2 doses at once.

The dose of this medicine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so.

The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.

For redness, itching, and swelling of the skin:

Adults: Apply to the affected area of the skin one to three times per day.

Children: Use and dose must be determined by your doctor.

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

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

Active Ingredient: Betamethasone.

Do NOT use Betnovate if:

you are allergic to any ingredient in Betnovate

you are taking mifepristone

you have a systemic fungal infection

you are scheduled to have a smallpox vaccine

you have a certain bleeding disorder (idiopathic thrombocytopenic purpura).

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

Some medical conditions may interact with Betnovate. 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 bleeding problems, heart problems (eg, congestive heart failure [CHF]), heart attack, high blood pressure, kidney problems, liver problems, diabetes, seizures, an underactive thyroid, adrenal gland problems, any mental or mood problems, or low blood potassium levels

if you have or have recently had a bacterial, fungal, malarial, viral, or other type of infection; herpes infection of the eye; chickenpox; measles; shingles; or a head or brain injury

if you have HIV infection or tuberculosis (TB), or if you have ever had a positive TB skin test

if you have any stomach problems (eg, ulcers), intestinal problems (eg, blockage, perforation, infection, unexplained diarrhea, diverticulitis, ulcerative colitis), recent intestinal surgery, or inflammation of the esophagus

if you have weak bones (eg, osteoporosis) or muscle problems (eg, myasthenia gravis)

if you have had any recent vaccinations (eg, smallpox)

if you have a history of joint surgery or any joint problems (eg, fracture, infection).

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

Aprepitant, clarithromycin, cyclosporine, diltiazem, erythromycin, itraconazole, ketoconazole, or troleandomycin because side effects, such as adrenal gland or nervous system problems (eg, seizures), may occur

Barbiturates (eg, phenobarbital), carbamazepine, hydantoins (eg, phenytoin), lithium, or rifampin because they may decrease Betnovate's effectiveness

Aspirin, live vaccines, mifepristone, or ritodrine because the risk of their side effects may be increased by Betnovate.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Betnovate 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:

Betnovate may lower the ability of your body to fight infection. Avoid contact with people who have colds or infections. Tell your doctor if you notice signs of infection like fever, sore throat, rash, or chills.

If you have not had chickenpox, shingles, or measles, avoid contact with anyone who does.

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

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

If you use Betnovate for an extended period of time, your body may not produce enough natural steroids for up to several months after you stop using it. Severe symptoms may occur if you experience injury, surgery, infection, or loss of blood electrolytes. Contact your doctor immediately if you experience any of these events. You may need to begin taking additional corticosteroids.

If you have had Betnovate injected into a joint and you experience increased pain along with swelling, decreased joint movement, fever, and general feeling of being unwell, contact your doctor.

Talk with your doctor before you receive any vaccine while you are using Betnovate.

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

Betnovate may have benzyl alcohol in it. Do not use it in newborns or infants. It may cause serious and sometimes fatal nervous system problems and other side effects.

Corticosteroids may affect growth rate in children and teenagers in some cases. They may need regular growth checks while they use Betnovate.

Betnovate should be used with extreme caution in children; safety and effectiveness in 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 Betnovate while you are pregnant. Betnovate is found in breast milk. If you are or will be breast-feeding while you use Betnovate, check with your doctor. Discuss any possible risks to your baby.

If you suddenly stop taking Betnovate, you may have withdrawal symptoms, These may include unbalanced hormones (in both men and women).

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:

Acne; clumsiness; dizziness; facial flushing; general body discomfort; headache; increased appetite; increased sweating; lightheadedness; nausea; nervousness; sleeplessness; upset stomach.

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, tarry stools; changes in body fat; changes in menstrual periods; changes in skin color; chest pain; easy bruising or bleeding; irregular heartbeat; mental or mood changes (eg, depression); muscle pain, wasting, or weakness; seizures; severe nausea or vomiting; sudden severe dizziness or headache; swelling of feet or legs; symptoms of infection (eg, chills, fever, sore throat); tendon or bone pain; thinning of the skin; unusual skin sensation; unusual weight gain; vision changes or other eye problems; vomit that looks like coffee grounds.

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.

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Why register with MediGuard?

We are a free monitoring service designed for patients like you who want to be in the driver seat of your medical treatment. We have a community of more than 2.6 million members and offer the services below.

Medication Information Personalized Risk Rating Easy to understand overview Serious Side Effects Printable Medication List

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The risk of serious side effects for taking this medicine can be different if you take other medicines or if you suffer from a condition. Get your Risk Rating by creating a profile in a few steps.


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Share your story! Tell us how MediGuard has helped you or someone you love. Download the MediGuard Mobile App to manage your prescription and over-the-counter medications, for free. Taking multiple medications puts you at risk for possible drug-drug interactions Monitor the medical treatment of you and your loved ones.

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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Why register with MediGuard?

We are a free monitoring service designed for patients like you who want to be in the driver seat of your medical treatment. We have a community of more than 2.6 million members and offer the services below.

Medication Information Personalized Risk Rating Easy to understand overview Serious Side Effects Printable Medication List

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What is your Risk Rating for this medicine?

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Share your story! Tell us how MediGuard has helped you or someone you love. Download the MediGuard Mobile App to manage your prescription and over-the-counter medications, for free. Taking multiple medications puts you at risk for possible drug-drug interactions Monitor the medical treatment of you and your loved ones.

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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Kapidex decreases the amount of acid produced in the stomach.

Kapidex is used to treat heartburn caused by gastroesophageal reflux disease (GERD), and to heal erosive esophagitis (damage to the esophagus from stomach acid).

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

Important information

Before taking Kapidex, tell your doctor if you are allergic to any drugs, or if you have liver disease. You may need a dose adjustment or special tests to safely take Kapidex. Take this medicine for the entire length of time prescribed by your doctor. Your symptoms may get better before your treatment is completed.

When treating heartburn, Kapidex is usually given for 4 weeks. To best heal erosive esophagitis, you may need to take this medicine for several months. Follow your doctor's instructions.

Heartburn can be confused with early symptoms of heart attack. Seek emergency medical attention if you have chest pain or heavy feeling, dizziness, pain spreading to the arm or shoulder, sweating, nausea or vomiting, and a general ill feeling.

Before taking this medicine

You should not use Kapidex if you are allergic to dexlansoprazole. Before taking Kapidex, tell your doctor if you are allergic to any drugs, or if you have liver disease. You may need a dose adjustment or special tests to safely take Kapidex.

FDA pregnancy category B. Kapidex is not expected to be harmful to an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant during treatment. It is not known whether dexlansoprazole passes into breast milk or if it could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.

How should I take Kapidex?

Take Kapidex exactly as it was prescribed for you. Do not take the medication in larger amounts, or take it for longer than recommended by your doctor. Follow the directions on your prescription label.

Take each dose with a full glass (8 ounces) of water.

Kapidex may be taken with or without food.

Do not crush, break, or open a delayed-release capsule. Swallow the pill whole. It is specially made to release medicine slowly in the body. Breaking or opening the pill would cause too much of the drug to be released at one time.

If you are unable to swallow a delayed-release capsule whole: Open the capsule and sprinkle the medicine into a spoonful of applesauce. Swallow this mixture right away without chewing. Do not save the mixture for later use. Discard the empty capsule.

It is important to use Kapidex regularly to get the most benefit. Get your prescription refilled before you run out of medicine completely.

When treating heartburn, Kapidex is usually given for 4 weeks. To best heal erosive esophagitis, you may need to take Kapidex for several months. Follow your doctor's instructions.

Store this medication at room temperature away from moisture and heat.

What happens if I miss a dose?

Take the missed dose as soon as you remember. If it is almost time for your next dose, skip the missed dose and take the medicine at the next regularly scheduled time. Do not take extra medicine to make up the missed dose.

What happens if I overdose?

Seek emergency medical attention if you think you have used too much of this medicine.

An overdose of Kapidex is not expected to produce life-threatening symptoms.

What should I avoid?

Follow your doctor's instructions about any restrictions on food, beverages, or activity while you are using Kapidex.

Kapidex side effects

Get emergency medical help if you have any of these signs of an allergic reaction to Kapidex: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Call your doctor at once if you have a serious side effect such as:

chest pain, fast or pounding heartbeats;

severe stomach pain; or

Less serious Kapidex side effects may include:

nausea, vomiting, stomach pain, gas;

stuffy nose, sneezing, or other cold symptoms.

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.

What other drugs will affect Kapidex?

Before taking Kapidex, tell your doctor if you are using any of the following drugs:

ampicillin (Omnipen, Principen);

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Abefen Para Que Sirve, Abefen


Tenga especial cuidado durante el embarazo .

No usar Abefen con lactantes.

Revise siempre que no sea alergico a ninguno de los componentes de Abefen . podria poner en peligro su salud

Recuerda antes de tomar este medicamento consultar siempre con su medico, la informacion que ofrecemos es orientativa y no sustituye en ningun caso la de su medico u otro profesional de la salud.

Prospecto e indicaciones

FORMULA: El frasco ámpula con polvo contiene:

Succinato sódico de cloramfenicol equivalente a 1 g

La ampolleta contiene:

Agua inyectable 5 ml

Fiebre tifoidea y paratifoidea, tosferina, brucelosis, rickettsiosis, infecciones broncopulmonares, infecciones quirúrgicas, tracoma y en algunas infecciones del ojo y de sus anexos.


El cloramfenicol es un antibiótico de amplio espectro con acción bacteriostática. Puede llegar a ser bactericida a concentraciones elevadas o contra microorganismos altamente susceptibles.

Difunde a través de la membrana celular por ser liposoluble y se une en forma reversible a la subunidad 50s de los ribosomas bacterianos donde evita la transferencia de aminoácidos a las cadenas peptídicas en formación, probablemente por supresión de la actividad de la peptidiltransferasa, inhibiendo de este modo la formación del enlace peptídico y la síntesis de proteína subsiguiente. Aun no se ha establecido el mecanismo de la anemia aplásica irreversible después del uso de cloramfenicol.

El cloramfenicol se difunde fácilmente y se distribuye ampliamente, pero no en forma uniforme a todo el organismo. La distribución del cloramfenicol es muy diversa y se realiza de la siguiente manera:

Hígado y riñones: Donde se encuentran las concentraciones mayores.


También a concentraciones elevadas.


Alcanza una concentración en el feto entre el 30 y el 80% de las de la madre.


Logra alcanzar niveles terapéuticos en humor vítreo y humor acuoso.


Cuando las meninges no están inflamadas se alcanza un 21 a 50% de la concentración sérica y en estado de inflamación aumenta a un 45 a 89% con respecto al nivel sérico.

Otros Líquidos: Líquido pleural, ascítico, sinovial y saliva. El volumen de distribución es de 0.92 litros/kg.

Su unión a proteínas es moderada. Se metaboliza a nivel de hígado, plasma, pulmones y riñones. El feto y el neonato no pueden conjugar el cloramfenicol y se acumulan concentraciones tóxicas del fármaco activo, produciendo el "síndrome gris".

En adultos la vida media es la siguiente:

* Función renal y hepática normal: De 1.5 a 3.5 horas.

* Alteración renal: De 3 a 4 horas.

* Alteración hepática severa: Prolongada.

En lactantes la vida media es la siguiente:

* Lactantes de 1 a 2 días de edad: 24 horas o más.

* Niños de 10 a 16 días de edad: 10 horas.

La eliminación se realiza por filtración glomerular en el riñón en un 5 a 10% sin alteración: El resto se excreta en forma hidrolizada.

Se contraindica el uso de Abefen® en personas con antecedentes de hipersensibilidad o antecedentes de reacciones tóxicas a este.

El embarazo y la lactancia. No deberá utilizarse en padecimientos triviales que puedan ser tratados con otros medicamentos ni como agente profiláctico ni su insuficiencia hepática.

El uso de Abefen® deberá emplearse solo cuando sea el antibiótico de primera elección.

Durante el tratamiento se deberá practicar recuentos sanguíneos periódicos.

La duración del tratamiento se limitará al tiempo necesario para lograr la curación. Se evitará utilizarlo como profiláctico.

Se evitará el empleo simultáneo de medicamentos que puedan ocasionar depresión de la médula ósea.

La dosificación deberá ser lo más precisa posible para evitar intoxicaciones ("Síndrome del niño gris")

6. Existen reportes de superinfecciones por gérmenes no susceptibles, especialmente Cándida albicans.


El Abefen® atraviesa la placenta y se excreta por la leche materna.

Aún no se han precisado las posibles reacciones sobre el feto, por lo cual su uso se contraindica en el embarazo y la lactancia.


Con el uso de Abefen® se pueden presentar las siguientes alteraciones:

a) Discrasias sanguíneas: Se han llegado a reportar casos de reacciones sanguíneas graves que han llegado a ser fatales (anemia aplásica o hipoplásica, trombocitopenia, granulocitopenia y pancitopenia). Generalmente al interrumpir el tratamiento se revierte la reacción, sin embargo puede presentarse en forma irreversible.

Esta reacción parece no guardar relación con la dosis empleada sino con la sensibilidad del paciente.

Asimismo, se han reportado pacientes con hemoglobinuria paroxística nocturna.

b) Reacciones gastrointestinales: En una baja proporción de casos pueden presentarse náuseas, vómito, glositis, estomatitis y diarrea.

c) Reacciones neurotóxicas: Se han reportado casos de cefalea, depresión emocional leve, confusión mental, delirio, neuritis óptica y periférica. En estos casos se deberá suspender de inmediato el tratamiento.

d) Hipersensibilidad: En estos casos el paciente podrá presentar fiebre, erupciones maculares y vesiculares, angioedema, urticaria y anafilaxis. Cuando se ha tratado la fiebre tifoidea se han llegado a presentar reacciones de Herxheimer.

"Síndrome del niño gris": En el prematuro y en el recién nacido se han presentado intoxicaciones que se manifiestan en forma de signos y síntomas denominadas en conjunto como "Síndrome del niño gris".


Pueden presentarse interacciones con los siguientes medicamentos:

Alfentanilo, fenitoína, medicamentos depresores de la médula ósea, hipoglucemiantes orales, eritromicina, lincomicina, penicilinas, piridoxina y cianocobalamina.


No se han reportado a la fecha estudios que indiquen que Abefen® sea carcinogénico, mutagénico o teratógenico, ni que altere la fertilidad.


Abefen® puede alterar la prueba de bentiromida y deberá suspenderse al menos 3 días antes de realizar esta prueba.

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Dianabol History and Overview

Dianabol, known by its scientific and chemical name as Methandrostenolone (and/or Methandienone), is the most popular and widely utilized anabolic steroid by bodybuilders and athletes today. It gained its popularity in the late 1950s and throughout the “Golden Era of Bodybuilding” of the 1960s and 1970s. Methandrostenolone was introduced to the pharmaceutical and medical community by Dr. John Ziegler in the mid-1950s as an American response to the Soviet use of Testosterone in their Olympic athletes[1]. Dr. Ziegler and his team created Methandrostenolone as a result, which was then introduced to the prescription market under the trade name of Dianabol by the Ciba pharmaceutical company. It was the first orally active anabolic steroid to be synthesized and sold on the prescription market.

Dianabol possesses a half-life of 4.5 – 6 hours, contains a moderate level of Estrogenic effects in the body[2]. and has less of a rate of conversion into a stronger androgenic metabolite via the 5-alpha reductase enzyme[3]. It is for these reasons that Dianabol tends to be favored by bodybuilders and athletes in the quest for mass and strength above all else.

Chemical Properties of Dianabol

Dianabol is methylated at carbon 17-alpha on its structure (this is simply the addition of a methyl group at the 17 th carbon). This process, known as C17-Alpha Alkylation, allows the anabolic steroid to be administered orally and still have a measurably strong effect on the body. Without this modification, it is impossible for any anabolic steroid to survive liver metabolism in significant enough quantities to promote any measurable effects in the body – the result is that extremely miniscule amounts of the anabolic steroid reaches the bloodstream to perform its job. Dianabol also possesses a double-bond between carbons 1 and 2. This modification in particular is what grants it a ‘milder’ androgenic strength in comparison to its parent hormone Testosterone. This double-bond is what limits Dianabol’s affinity to bind to the androgen receptor in different tissues in comparison to Testosterone. It is these modifications that also allow Dianabol’s half-life to exceed that of Testosterone (Dianabol’s half-life is 4.5 – 6 hours). An additional benefit of these chemical modifications is Dianabol’s lower affinity for binding proteins to bind to it, such as Sex Hormone Binding Globulin (SHBG). These binding globulins (in this case SHBG), which are proteins, bind to sex hormones such as Testosterone, Estrogen, Dianabol, etc. and render them inactive temporarily. What results is essentially a bound hormone that floats around in the bloodstream and does nothing – it cannot bind to receptors or do anything – and is essentially useless. These are the chemical features of Dianabol that grant it its status of being a significantly potent anabolic steroid. One interesting point to note, however, is that Dianabol possesses a weaker interaction with the androgen receptor in comparison to Testosterone and many other anabolic steroids, yet it is a very strong and potent hormone in comparison. It is therefore speculated that much of Dianabol’s activity is that of non-receptor mediated activity. With this being said, Dianabol’s anabolic rating is known to be a rating of 210 in contrast with Testosterone’s anabolic rating of 100. What can be seen here is that Dianabol possesses slightly over double the anabolic strength of Testosterone, and this is because of the described structural modifications it possesses.

The Effects of Dianabol (D-Bol)

Dianabol does succumb to some limitations of its own, with the first being its C17-Alpha Alkylated property. As previously mentioned, C17-Alpha Alkylation allows an anabolic steroid to become orally active and bioavailable – without it, the anabolic steroid would not survive liver metabolism. However, the negative downside in this case is that of increased hepatotoxicity (increased liver toxicity). C17-Alpha Alkylation allows an anabolic steroid to become more resistant to hepatic breakdown, and any compound that is further resistant to hepatic breakdown with always have greater hepatotoxicity associated with it. As a result, it is a smart choice to run Dianabol for periods no greater than 4-6 weeks at any given time in a cycle. This is to ensure healthy liver function, and for proper liver recovery following the cycle. It is because of the risk of hepatotoxicity that Dianabol’s main function in a cycle is to serve as a supportive kickstarting compound. Dianabol, nor any oral anabolic steroid, should ever be run solitarily on its own. Testosterone in some form no lower than a TRT (Testosterone Replacement Therapy) dose should always be run with an oral anabolic steroid such as Dianabol.

Dianabol contains moderate Estrogenic activity and is a compound that is exposed to aromatization by the aromatase enzyme, which is the enzyme responsible for converting androgens into Estrogen. This is why Dianabol is commonly known for its Estrogenic side effects of water retention, risk of gynecomastia, elevated blood pressure (often as a result of water retention), and possible fat retention/gain due to Estrogen. It has been mentioned already that Dianabol expresses far less androgenic strength and activity than does Testosterone, but it is important to understand that androgen-related side effects and issues are still a concern with Dianabol, although they are not as pronounced as Testosterone. Dianabol possesses an androgenic rating of 40-60, and when compared to Testosterone’s androgenic rating of 100, we can see there is quite a significant reduction – however, the risk of androgenic side effects can still be prominent especially in those individuals sensitive to androgenic side effects. Androgenic side effects can include: increased risk for male pattern baldness (MPB) if the individual possesses the genetic trait responsible for it, increased sebum secretion (oily skin) and associated acne, and increased facial hair and bodily hair growth. In addition, the 5-Alpha Reductase enzyme which is the enzyme responsible for converting Testosterone into the much stronger androgen Dihydrotestosterone (DHT) does also interact with Dianabol. In this case, Dihydrotestosterone is not created but instead Dianabol’s own more androgenic metabolite is the result. A positive note on this issue, however, is that Dianabol possesses a lower binding affinity for the 5-Alpha Reductase enzyme

Dianabol Side Effects

Dianabol’s side effect profile is variable. The most significant Dianabol side effect is that of Estrogen-related effects, although studies have stated that Dianabol’s action on the aromatase enzyme (CYP19) is moderate[6].

This includes water retention and bloating which will mean this oral steroid will increase blood pressure [7] as well as acne and gynecomstia (development of breast tissue). The most prominent Dianabol side effect tends to be the bloating and water retention, followed by gynecomastia. These side effects can be mitigated through the use of anti-estrogens such as aromatase inhibitors Exmestane (Aromasin ) and Arimidex. Estrogen blockers (SERMs) Nolvadex (Tamoxifen Citrate) and Clomid .

Secondary to the Estrogenic side effects, Dianabol can produce androgenic side effects as well (though less pronounced than Testosterone). There are risks of experiencing acne, oily skin, male pattern baldness, and benign prostatic hyperplasia.

The next most concerning Dianabol side effect is its increased stress imposed on the hepatic system (i. e. the liver). It is advised to limit cycle lengths to no greater than 4 – 6 weeks, supplement with liver support compounds, and avoid high dosages.

Lastly, D bol is very well known for its strong inhibitive nature on the HPTA (Hypothalamic Pituitary Testicular Axis). Clinical studies have been conducted on Dianabol’s testosterone inhibitive action in humans, and they have demonstrated that doses as low as 15mg per day for 8 weeks caused total plasma Testosterone levels to decline by 69%[4].

Aside from these side effects, Dianabol does impose those side effects that are also typical with any anabolic steroid. These include negative cholesterol alterations, negative cardiovascular effects, and disruption of the HPTA (Hypothalamic Pituitary Testicular Axis).

Dianabol Cycles and Uses

Dianabol cycles are very straightforward in most cases of its application. The use of Dianabol is normally during periods of bulking and strength gaining where the bodybuilder or athlete is not overly concerned with water retention and bloating. These types of Dianabol cycles are therefore normally during the “off-season” period where bodybuilders are in the midst of achieving this goal, and it is normally cycled with some kind of injectable anabolic steroid that achieves similar results – normally some variant of Testosterone, such as Testosterone Enanthate.

Most of these Dianabol cycles involve its use as a kickstarting compound, where it is used only during the first 4 – 6 weeks of the cycle in order to experience strength and size gains while the user waits for the longer acting injectable compound (i. e. Testosterone Enanthate) to achieve its full effects and “kick in”. It is advised to run Dianabol cycles for no longer than 4 – 6 weeks due to its nature as a C-17 alpha alkylated compound, which exerts negative effects on the liver (and especially cholesterol levels). This is an additional reason as to why Dianabol cycles are typically kickstarter cycles for no greater than 4 – 6 weeks in length.

Shorter Dianabol cycles can be run, but in this case it should be run with a short-estered (fast acting) base injectable. Referencing back to Testosterone in this case, the preferred choice would be Testosterone Propionate. However, Dianabol cycles in these instances should still be limited to 4 – 6 weeks (while the Testosterone Propionate, for example, can be extended well beyond this length if desired).

Dianabol is very rarely employed as a cutting or fat loss agent, although it can be done. It is generally undesirable to do so because of Dianabol’s negative Estrogenic effects (such as water retention and bloating). Because of this, the physique’s definition during dieting can be difficult to gauge as the water retention blurs this. Dianabol cycles intended for cutting or fat loss should be run no differently than previously outlined cycles, as fat loss is first and foremost achieved through the athlete’s diet and nutritional intake and not determined by which anabolic steroid is utilized.

Dianabol Dosages and Administration

Being that Dianabol is considered a very potent anabolic steroid where anabolism (the buildup of muscle tissue) is concerned, its dosages need not be as high as many other commonly used oral anabolic steroids. Dianabol dosages need to be considered carefully especially where negative effects on the liver are concerned, as the higher dosage is used, there is a corresponding increase in the negative effects here.

Dr. Ziegler originally issued prescription guidelines of 5mg per day for no longer than 6 weeks. Being that 5mg is on the lowest end of the dosage spectrum, more modern beginner Dianabol dosages range between 15 – 30mg per day. This Dianabol dosage. especially the higher end, is quite considerably strong in terms of anabolic effects and does not necessitate an increase beyond it even after years of cycles. Intermediate as well as advanced dosages for Dianabol are in the area of 30 – 50mg per day, and it is generally advised to go no higher than this despite the fact that some very advanced users are known to venture well into the 80mg or greater range. It is very unadvisable to even attempt to approach this range due to excess stressors on the body’s organ systems and side effects.

It should also be mentioned that the difference between beginner, intermediate, and advanced users is not that of increasing Dianabol dosages, and that many advanced users tend to utilize a low beginner dosage of 15mg per day with a high degree of effect.

That said, some studies have looked at the adverse side effects of 100mg per day and were found to have shown no serious complications in health[5].

Looking at this study in more detail, 100mg per day for 6 weeks meant total testosterone declined 40%, LH dropped to 80% of its original baseline value, FSH decreased 33%, human growth hormone (hGH) rose 30% and Fat Free Mass also increased from 2-7kgs.

Female Dianabol dosages are relatively unheard of due to the fact that Dianabol is not a commonly used anabolic steroid by female athletes due to its unsuitability as a result of harsher virilization effects on the female physiology. Those females that do venture into Dianabol use have been known to utilize 2.5 – 5mg per day, and 10mg daily being the uppermost limit. These dosages can produce very dramatic results for the few female users that exist.

How to Buy Dianabol

Dianabol is bought and sold through many different avenues and sub-avenues. The two most prominent avenues are: in-person dealers and the internet. The internet is by far the most popular and widely used avenue today, making older methods (such as mail-order) generally obsolete. Incidentally, the old method of mail-order has now in many ways transformed into e-mail order, which is one of the internet methods of buying Dianabol. This method involves the buyer contacting a seller who makes sales and processes payments via an email address. Other and more popular internet sources include websites and lesser-known e-commerce websites.

There are two types of Dianabol that shoppers will encounter no matter where they look: pharmaceutical grade Dianabol and underground lab (UGL) grade Dianabol. As the names imply, pharmaceutical grade drugs are those which are manufactured by fully licensed and FDA-approved pharmaceutical companies that manufacture these drugs for sale on the prescription market. However, in the case of off-label use for bodybuilding and athletic purposes, these drugs are often diverted clandestinely into the black market. UGL products are simply manufactured by unlicensed, unapproved, and often amateur underground laboratories that sell their products for far cheaper than their pharmaceutical grade counterparts.

In this area, D-Bol prices can vary a great deal. It is generally difficult to quantify prices due to the massive variation (e. g. Dianabol is frequently available in 5mg, 10mg, 50mg, and even 100mg tablets – and packaged in different counts per bottle/package as well). Underground grade Dianabol is generally sold in the range of $1 – $1.50 per 50mg tablet ($0.02 – $0.03 per 1mg). Pharmaceutical grade Dianabol is often sold for $2.8 per 50mg tablet ($0.056 per 1mg). There is not much variation in the price difference between pharmaceutical and underground grade Dianabol products in this case, which is due to the sheer fact that Dianabol is extremely easy to produce, and it is manufactured by almost every single underground lab and various European and Middle Eastern pharmaceutical manufacturers making it an extremely common product to come by on the market. Those wishing to buy Dianabol should have no issues locating it very easily or for very cheap prices.

Dianabol Information:

Methandrostenolone (AKA Dianabol) Chemical Name: 17a-methyl-17b-hydroxy-1,4-androstadien-3-one Molecular Weight: 300.441 g/mol Formula: C20H28O2 Original Manufacturer: Ciba (originally) Half Life: 4.5 – 6 hours Detection Time: 5 – 6 weeks Anabolic Rating: 90 – 210 Androgenic Rating: 40 – 60

Dianabol References:

Vischer E, Meystre C, Wettstein A. Helv Chim Acta 38 (1955):1502

Kruskemper, H L, Anabolic Steroids, Academic Press, New York, 1968

Relative importance of 5alpha reduction for the androgenic and HL-inhibiting activities of delta-4-3-ketosteroids, Steroids 29 (1997):331-48.

Effect of anabolic steroid (metandionon) on plasma LH-FSH, and testosterone and on the response to intravenous administration of LRH. Holma P. Adlecreutz. Acta Endocrinol (Copenh) 1976 Deca;83(4):856-64

Clin Sci (Lond). 1981 Apr;60(4):457-61

Brain Res. 1998 May 11;792(2):271-6.

Br Med J. 1975 May 31;2(5969):471-3.

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Product Description Common use This medicine is a proton pump inhibitor (PPI) used to treat ulcers, heartburn, gastroesophageal reflux, erosive esophagitis, or Zollinger-Ellison syndrome and also ulcers generated by long-term use of non-steroidal anti-inflammatory drugs (NSAIDs). To treat ulcers caused by bacterial infections this medicine may be used in combination with antibiotics such as amoxicillin or clarithromycin. Prilosek significantly alleviates such their symptoms as heartburn, difficulty swallowing, coughing, and sleep problems. Prilosek works by blocking acid production in the stomach. The medicine may be used to treat other conditions diagnosed by your doctor.

Dosage and directions Follow all the directions provided by your doctor. Take this medication (15-30 mg) orally once a day in morning before a meal with a full glass of water or according to your doctor's recommendations. Swallow the tab whole, do not chew, crush, or open the capsule as may destroy the drug and/or increase side effects. Antacids drugs can be taken together with this medicine, if necessary. Dosage and duration of treatment depends on your medical condition and response to the therapy. Take it the same time each day to avoid missing a dose. In the case of aggravation or worsening of your illness notify your doctor immediately. It may take 1 - 4 days before Prilosek acts in full measure. Treatment with Prilosec should not be stopped even if certain amelioration is achieved. Improvement of symptoms is observed within 4 to 8 weeks in treatment of gastric ulcers or reflux disease. Treatment of heartburn usually lasts for 14 days. If heartburn persists after this period of time or even worsens, or if you need more than one course of treatment every 4 months, contact your doctor or pharmacist.

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Possible side effects Adverse reactions that may disappear during treatment include headache, constipation, cough, dizziness, or rash. If they continue or are bothersome, let your doctor know about it. An allergic reaction to this medicine is not expected, but seek immediate medical help if it happens. Symptoms of an allergic reaction appear as rash, itching, dizziness, swelling, or difficult breathing. If you notice other reactions of your body which are not listed above, contact your doctor or pharmacist.

Prilosec can decreases elimination of diazepam, warfarin and phenytoin. These are medications metabolized in the liver by oxidation. Drugs which are metabolized with help of cytochrome P-450 system (e. g. cyclosporine, disulfiram, benzodiazepines) may also interact with Prilosec because it is metabolized the same way. Clarithromycin is also metabolized by cytochrome P450, concomitant administration of clarithromycin with Prilosec may result in increases in plasma levels of Prilosec. Concomitant use of Prilosec and clarithromycin may result in increases in plasma levels of erithromycin, and 14-hydroxy-clarithromycin. You may need additional monitoring of your condition if you are taking ampicillin, cilostazol, cyclosporine, diazepam, digoxin, disulfiram, iron, itraconazole, ketoconazole, moclobemide, phenytoin, sucralfate, vorconizole, or warfarin. This medicine may be combined with antacids if they were prescribed by your doctor. Potent acid-reducing drugs such as Prilosec diminish the effectiveness of sucralfate, and other medicaitons such as the antifungals ketoconazole and itraconazole. If instructed to take any of these medicines while taking Prilosec, consult your doctor or pharmacist regarding the proper timing of each dose, usually Prilosec is taken 30 minutes before sucralfate.

Missed dose If you missed a dose take the medication as soon as you remember. If it is almost time of your next dose, just skip its intake and return to your regular schedule.

Overdose If suppose that took too much of Prilosec contact your local poison control center or emergency room immediately. Symptoms of overdose are confusion, blurred vision, unusual sweating, or unusually fast heartbeat.

Storage Store at room temperature between 59-77 F (15-25 C). Do not expose to high humidity or keep in a bathroom. Hide Prilosec away from children and pets. If your treatment requires an extended period of time, take care about refills before your supply is over.

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.

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Hydroxyprogesterone Caproate Im And Prednisolone Oral Drug Interactions, Prednisolon Caproate

Drug interactions with hydroxyprogesterone caproate im and prednisolone oral

hydroxyprogesterone caproate im brand names and other generic formulations include:

Delalutin IM, Delalutin Unimatic IM, Delta-Lutin IM, Deprolutin-250 IM, Duralutin IM, Gesterol La 250 IM, Hydrosterone IM, Hydroxon IM, Hylutin IM, Hyprogest 250 IM, Hyproval IM, Hyproval Pa IM, La Progesterone IM, Long Acting Corporalute IM, Makena IM. Pro Rone La IM, Pro-Depo IM, Prodrox IM, Prolutin IM, Pro-Span IM

All generic drug interactions for hydroxyprogesterone caproate im (lists will include brand and generic names):

prednisolone oral brand names and other generic formulations include:

Delta-Cortef Oral, Fernisolone-P Oral, Millipred DP Oral, Predoxine-5 Oral, Prelone Oral. Sterane Oral

All generic drug interactions for prednisolone oral (lists will include brand and generic names):

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Rino-Clenil Generic Name Beclomethasone Online, Rino-Clenil

Rino-Clenil General Information

Rino-Clenil - Pharmacology:

Unbound corticosteroids cross cell membranes and bind with high affinity to specific cytoplasmic receptors. The result includes inhibition of leukocyte infiltration at the site of inflammation, interference in the function of mediators of inflammatory response, suppression of humoral immune responses, and reduction in edema or scar tissue. The antiinflammatory actions of corticosteroids are thought to involve phospholipase A2 inhibitory proteins, lipocortins, which control the biosynthesis of potent mediators of inflammation such as prostaglandins and leukotrienes.

Rino-Clenil for patients

(beclomethasone dipropionate HFA)

It is important that you read these instructions before using QVAR. Correct and regular use of the inhaler will prevent or lessen the severity of asthma attacks.

1. Remove the plastic cap and be sure there are no foreign objects in the mouthpiece.

2. As with all aerosol medications, it is recommended to prime the QVAR inhaler before using for the very first time after purchase, and in cases where the inhaler has not been used for more than ten days. Prime by releasing two actuations into the air, away from your eyes and face. Be sure the canister is firmly seated in the plastic mouthpiece adapter before each use.

3. BREATHE OUT AS FULLY AS YOU COMFORTABLY CAN. Close your lips around the mouthpiece, keeping your tongue below it.

4. WHILE BREATHING IN DEEPLY AND SLOWLY, PRESS DOWN ON THE CAN WITH YOUR FINGER. When you have finished breathing in, hold your breath as long as you comfortably can (i. e. 5 - 10 seconds).

5. TAKE YOUR FINGER OFF THE CAN and remove the inhaler from your mouth. Breathe out gently.

6. If your physician has told you to take more than one inhalation per treatment repeat steps 3 through 5.

7. You should rinse your mouth with water after treatment.

8. For normal hygiene, the mouthpiece of your inhaler should be cleaned weekly with a clean, dry tissue or cloth. DO NOT WASH OR PUT ANY PART OF YOUR INHALER IN WATER.

9. DISCARD THE CANISTER AFTER the date calculated by your physician or pharma-cist. The correct amount of medication in each inhalation cannot be assured after 100 actuations from the 7. 3 g canister even though the canister is not completely empty. The canister should be discarded when the labeled number of actuations have been used. Before the discard date you should consult your physician to determine whether a refill is needed. It is advisable to keep track of the number of doses taken from the canister to better predict when a refill is necessary.

Just as you should not take extra doses without consulting your physician, you also should not stop taking QVAR without consulting your physician.

IMPORTANT QVAR is preventive therapy for asthma and must be used regularly and at the times your physician has prescribed.


Your physician will decide whether other medication is needed should you require immediate relief. If you also use another medicine by inhalation, you should consult your physician for instructions on when to use it in relation to using QVAR. If this is the first time you will be using QVAR, it may take from 1 to 4 weeks before you feel the full benefits.

QVAR Inhalation Aerosol canister should only be used with the QVAR Inhalation Aerosol mouthpiece and the mouthpiece should not be used with any other inhalation drug product.

DOSAGE . Use only as directed by your physician.

CONTENTS UNDER PRESSURE Do not puncture. Do not use or store near heat or open flame. Exposure to temperatures above 49?C (120?F) may cause bursting. Never throw container into fire or incinerator.

Keep out of reach of children.

Avoid spraying in eyes.

Store at 25?C (77?F). For optimal results, the canister should be at room temperature when used.

Store QVAR Inhalation Aerosol when not being used, so that the product rests on the concave end of the canister with the plastic actuator on top.

This description is suitable for active ingredient Beclomethasone

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Dangerous Waters by Kowit Wattanarach click to view this painting in full

oops! by Kowit Wattanarach click to view this painting in full

Summer Fun by Douglas Stewart click to view this painting in full

Malikijarra Jukurrpa (411/15; left) and (437/15; right) by Murdie Nampijinpa Morris click to view this painting in full

About asart

Over 35 years of experience . tertiary qualifications in Fine Art, extensive networks of both artists and dealers allow asart's director, Anthony Smith, to offer a rare level of judgement and connoisseurship

Asian art

Anthony Smith's knowledge and understanding of the art movements in Asia, particularly Southeast Asia . and his relationship with artists ensure that asart is able to secure the finest pieces for collectors

Australian art

asart specialises in elder Australian Aboriginal art . Considered one of the greatest movements of contemporary art, Indigenous art from Australia is based on traditions that go back more than 40,000 years.

Western art

After many years dealing with Asian art and Aboriginal art only, the talent of international contemporary artists Douglas Stewart and Phil Couture made asart decide to focus on a new area: Western art.

"We sought asart's assistance with the decor of a newly refurbished apartment in Bangkok. asart guided us in our choice of antiques and artifacts and identified a shortlist of original artworks, subsequently sourcing and hanging our choices. The result is stunning. asart's ability to interpret our brief and deliver it was sensational."   –Slater

"Anthony and I have been working together for about the last decade and it is always a pleasure. His obvious enthusiasm and passion for sourcing new works is uplifting and his committment to service is second to none. He listens and delivers. Anthony's knowledge is extensive."   –Rebecca

"I found asart on the web when I was looking to buy a piece of modern Aboriginal art. I bought my first work from Anthony Smith in February 2014 and two more since. All pieces arrived in Sydney in excellent condition within a week of purchase. Anthony provides the highest level of customer service from initial contact to receipt of goods. "   –Angela

" I have dealt with Anthony Smith for over 10 years and have bought a number of artworks from him. He deals with very high quality art from Asia and South East Asia. I have found him extremely professional and a pleasure to deal with. He provides not only accurate details of the works but gives very enlightening background information."   –Dr Alan Segal

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Frequently Asked Questions - Travel To Kosovo, Losamet


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Frequently Asked Questions

You do not need a Kosovo visa if you are a part of this list .

I am a citizen of a country that needs Kosovo visa, but I have a valid biometric residence permit in one of the Schengen countries. Do I still need Kosovo visa?

You do not need a Kosovo visa if you hold a valid biometric residence permit in one of the Schengen countries.

Do I still need a Kosovo visa if I have a valid multi-entry Schengen visa?

You do not need a Kosovo visa if you have a valid multi-entry Schengen visa.

Do I still need a Kosovo visa if I have a valid one-entry Schengen visa?

If you have a valid one-entry Schengen visa, you need a Kosovo visa to enter.

Does a diplomatic or official passport automatically guarantee me a free entry in Kosovo?

You do not need a Kosovo visa if you are a holder of diplomatic or official passport of a country which does not need a visa or Russian Federation States, People’s Republic of China, Egypt, Indonesia and Ukraine.

I am a citizen of an EU/Schengen country. Do I need a passport to enter Kosovo?

You do not need a Kosovo visa if you hold a valid EU passport or EU biometric ID card.

I have an EU ID card, but it’s not biometric. Can I enter Kosovo only with this old ID card?

To enter Kosovo, you need a valid EU biometric ID card.

Do I need a Kosovo visa if I have a United Nations Laissez-Passer travel document?

You do not need a Kosovo visa if you have a Laissez-Passer travel document issued either by United Nations Organizations or NATO, OSCE, Council of Europe and European Union.

Where can I get the Kosovo visa?

You can apply and get a Kosovo visa in the following Diplomatic or Consular Missions :

How do I apply for a Kosovo visa?

To submit your visa application, you need to personally show up at the respective Diplomatic or Consular Mission of the Republic of Kosovo unless you are:

Invited by the state institutions of the Republic of Kosovo and other international institutions for official purposes

A person with special needs who cannot submit applications in person (documents proving the disability should be attached)

A person known to the diplomatic or consular mission for their integrity and credibility.

Where do I download the visa application form?

You can download the visa application form at http://www. mfa-ks. net/?page=2,165

What documents do I need to submit in order to get a Kosovo visa?

Your visa application should include the following:

A completed and signed application form. Persons included in the applicant’s travel document shall submit a separate application form. Minors shall submit an application form signed by a person exercising permanent or temporary parental authority or legal guardianship;

A copy of your travel document. Its validity shall extend at least three months after the intended date of departure from the territory of the Republic of Kosovo. It shall contain at least two blank pages;

A recent (not older than 1 month) photograph in accordance with the international standards as set out in the International Civil Aviation Organization (ICAO) document 9303 Part 1, 6th edition;

documents indicating the purpose of the journey;

documents in relation to accommodation, or proof of sufficient means to cover his/her accommodation;

documents indicating that the applicant possesses sufficient means of subsistence both for the duration of the intended stay and for the return to his country of origin or residence, or for the transit to a third country into which he is certain to be admitted, or that he is in a position to acquire such means lawfully;

Information enabling an assessment of the applicant’s intention to leave the territory of the Republic of Kosovo before the expiry of the visa applied for;

Travel medical insurance valid throughout the territory of the Republic of Kosovo which covers the entire period of the person’s intended stay or transit;

Applicants shall pay a visa fee of EUR 40 unless they are holders of diplomatic and official passports; children nder six (6) years old; or school children, students and teachers accompanying and visiting for studying or training purposes Note: For bank details please check with the Diplomatic or Consular Mission .

The Consular Officer may request from the applicant additional supporting documents;

All supporting documents should be translated in one of the Kosovo’s official languages (Albanian or Serbian) or in English;

All the documents must be submitted in two copies;

Only possessing a valid visa does not automatically guarantee entry in Kosovo.

Do I need to pay a Kosovo visa fee and how much does it cost?

Kosovo visa fee costs 40 EUR. In order to get a Kosovo visa, all applicants need to pay the visa fee unless they are:

Holders of diplomatic and official passports

Children under six (6) years old

School children, students and teachers accompanying them and visiting for studying or training purposes.

How can I pay for the Kosovo visa?

You can pay the Visa fee through bank. For bank details contact the respective Diplomatic or Consular Mission.

Do I need to show up at your consulate to get the visa sticker on my passport or can I do it by mail?

Depending on the decision, sending and receiving of the passport with a visa sticker can be arranged by mail.

Can I apply on behalf of a family member?

To submit your visa application, you need to personally show up at the respective Diplomatic or Consular Mission of the Republic of Kosovo. For specific cases, please contact:

Ministry of Foreign Affairs, Department for Consular Affairs

Tel. +381 38 200 11 101

Can I travel in the region with a Kosovo visa?

With a Kosovo visa you can enter, transit, or stay in Kosovo only.

How long can I stay in Kosovo with a Kosovo visa?

With a Kosovo visa you can stay for a maximum of 90 days within a period of 6 months.

My passport will expire in two months. Am I still eligible to apply for a Kosovo visa?

To apply for a Kosovo visa, your passport should be valid for at least three months from the intended day of leaving Kosovo.

How do I travel to Kosovo?

Prishtina International Airport is well connected with main destinations around the world.

There are also convenient connections with other means of transport that take you to Kosovo.

Who do I contact if I have more questions?

If you have more questions, you can contact:

Ministry of Foreign Affairs, Department for Consular Affairs

Tel. +381 38 200 11 101

If I am denied, whom do I complain to?

The applicant can file a complaint within 8 calendar days from the notification day to the respective Diplomatic or Consular Mission where initially applied. The complaint should be filed through an official letter, not through e-mail.

How long does it take to receive an answer on Kosovo visa application?

It may take up to 1 month to receive an answer on the visa application.

Can I work in Kosovo with a long-term Kosovo visa?

If you wish to work in Kosovo, you need to apply for a Residence Permit at the Ministry of Internal Affairs in Kosovo .

Can I live in Kosovo with a long-term Kosovo visa?

If you wish to stay longer than your visa expiration date, you need to apply for a Residence Permit at the the Ministry of Internal Affairs in Kosovo .

Explore Kosovo

Travel Information


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