Acacia Gum And Vitinoin Drug Interactions, Vitinoin

Drug interactions between acacia gum and Vitinoin

Drug Interaction Classification

The classifications below are a guideline only. The relevance of a particular drug interaction to a specific patient is difficult to determine using this tool alone given the large number of variables that may apply.

Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit.

Moderately clinically significant. Usually avoid combinations; use it only under special circumstances.

Minimally clinically significant. Minimize risk; assess risk and consider an alternative drug, take steps to circumvent the interaction risk and/or institute a monitoring plan.

Do not stop taking any medications without consulting your healthcare provider.

Disclaimer: Every effort has been made to ensure that the information provided by Multum is accurate, up-to-date and complete, but no guarantee is made to that effect. In addition, the drug information contained herein may be time sensitive and should not be utilized as a reference resource beyond the date hereof. This material does not endorse drugs, diagnose patients, or recommend therapy. Multum's information is a reference resource designed as supplement to, and not a substitute for, the expertise, skill, knowledge, and judgement of healthcare practitioners in patient care. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective, or appropriate for any given patient. Multum Information Services, Inc. does not assume any responsibility for any aspect of healthcare administered with the aid of information Multum provides. Copyright 2000-2016 Multum Information Services, Inc. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. If you have questions about the drugs you are taking, check with your doctor, nurse, or pharmacist.

How to Prevent Deadly Drug Interactions

Some mixtures of medications can lead to serious and even fatal consequences.

Exondys 51 Exondys 51 (eteplirsen) is a morpholino antisense oligomer for the treatment of Duchenne muscular.

Yosprala Yosprala (aspirin and omeprazole) is a platelet aggregation inhibitor and proton pump inhibitor.

Cuvitru Cuvitru (immune globulin subcutaneous (human)) is indicated as replacement therapy in the treatment.

Erelzi Erelzi (etanercept-szzs) is a tumor necrosis factor (TNF) blocker biosimilar to Enbrel indicated.

FDA Consumer Updates

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Terminate Solution, Termicon

A Miraculous product for Termite!

One of the most stubborn pests is the Termites. These white or lotion colored creatures, resembling an ant can create a havoc if still left uncontrolled. Termites are a group of eu-social insects, with more than 2500 of species. These insects can cause severe destruction to wooden structures. They have the capacity to nest on nearly anything and almost everything. They commonly feed on wood, leaves or branches of bushes, papers and many others. These insects can cause severe destruction to wooden structures. They generally build nests in trees or underground, as well as building large mounds above ground. Like bees, wasps and ants, termites divide labor among castes, produce overlapping generations and take care of young collectively. Termites mostly feed on dead plant material, generally in the form of wood, leaf litter, soil, or animal dung, and can cause serious structural damage to buildings, crops or plantation forests.

That’s a whole lot of money wasted because of termite and pest infestation in homes, which is one of the primary causes of such damages. Have you heard of the phrase, “small but terrible”? This can very well describe the small but terrible termites that invade your home and cause so much damage to your precious property. Unfortunately, termites and similar pests are quite common in most parts of the world. These destructive creatures invade your nice homes through any kind of wood THAT COMES IN CONTACT WITH THESOIL.

WHAT IS TERMITE?

One of the most stubborn pests are the Termites. These white or lotion colored creatures, resembling an ant can create a havoc if still left uncontrolled. Termites are a group of eu-social insects, with more than 2500 of species. These insects can cause severe destruction to wooden structures. They have the capacity to nest on nearly anything and almost everything. They commonly feed on wood, leaves or branches of bushes, papers and many others. These insects can cause severe destruction to wooden structures. They generally build nests in trees or underground, as well as building large mounds above ground. Like bees, wasps and ants, termites divide labor among castes, produce overlapping generations and take care of young collectively. Termites mostly feed on dead plant material, generally in the form of wood, leaf litter, soil, or animal dung, and can cause serious structural damage to buildings, crops or plantation forests.

The extent of infestation is world wide, however if we look at India, there does not seem to be a single state where the termite infestation cannot be seen. Total damage caused by termites alone runs in the order of several billion of rupees.

That’s a whole lot of money wasted because of termite and pest infestation in homes, which is one of the primary causes of such damages. Have you heard of the phrase, “small but terrible”? This can very well describe the small but terrible termites that invade your home and cause so much damage to your precious property. Unfortunately, termites and similar pests are quite common in most parts of the world. These destructive creatures invade your nice homes through any kind of wood THAT COMES IN CONTACT WITH THESOIL. In some cases, termites have the capacity to build mud tubes, if there is not much wood around, and in turn, these tubes grow into colonies that contain thousands of termites in one area alone.

They are really so powerful that they even destroy the entire construction if left unattended. On the other hand the eradication of termites is however, a serious issue and fairly troublesome. There is no sole tactic in eradicating the menace and its reoccurrence cannot be avoided. It depends on the seriousness of infestation, the style of termites and its habitat. That speaks for the special attention of this issue. The main reason is that these small creatures (termites) have the ability to withstand the worst climate situation.

Termites mostly have a bad reputation in the human world, but in the overall ecosystem, that isn't so. Since they feed on wood, termites serve an important function by recycling dead trees into organic matter, or humus, which is then available to nourish living trees.

Unfortunately, the wood in our homes is just as palatable to termites as dead/dying trees in the forest. The latest industry estimates place the annual cost of damage to property and treatment cost at $5 billion worldwide. It is said that `no pest is more threatening to a structure than termites'. How to avoid the termite infestation in homes? Here are some points that could be of help

Termites become a serious problem when they start consuming structural lumber. Each year thousands of housing units require treatment for the control of termites. Termites may also damage utility poles and other wooden structures. There are four types of termites such as Drywood termite, Dampwood termite, Formosan termites and Subterranean termites. These pests cause serious damage to wooden structures and posts and may also attack stored food, books, and household furniture. The total weight of all of the termites in the world is more than the weight of all the humans in the world.

The social organization of termites includes reproductives, workers and soldiers. Termites are social and can form large nests or colonies, consisting of very different looking individuals or castes. PHYSICALLY THE LARGEST INDIVIDUAL IS THE QUEEN. Her function is to lay eggs, sometimes thousands in a single day. A king is always by her side. Other individuals have large heads with powerful jaws, or a bulblike head that squirts liquid. These individuals are called soldiers. But the largest group of termites in a colony is the workers. They toil long hours tending the queen, building the nest, or GATHERING FOOD. While other species of social insects have workers, termites are unique among insects in that workers can be male or female. Surprisingly, termites can be long-lived: queens and kings can live for decades while individual workers can survive for several years.

WHAT ARE SUBTERRANEAN TERMITES?

There are three major groups of termites which occur in the World drywood termites, Subterranean termites and Formosan termites. Termites are identified by the appearance of the swarmers, their damage, and the droppings they leave behind. Subterranean termites or soil termites are social insects that live in societies whose members are mostly immature individuals. Their colonies, which can contain thousands to millions of termites, are formidable, even though each individual termite is soft-bodied and delicate. In nature, subterranean termites are closely ASSOCIATED WITH THE SOIL habitat where they tunnel to locate water and food like wood, fallen logs, and other cellulose-containing materials. Termites become a serious problem to humans when structures containing cellulose are built over or near their colonies in the ground. Termites are the major wood-destroying structural pests. On the average, there could be as many as 13 to 14 subterranean termite colonies per acre, which means that a typical home may easily have three to four colonies situated under or around it. And because there can be as many as 1,000,000 subterranean termites per colony, the threat of infestation becomes a very real big one. They are able to find weakened areas in the structure, or areas of direct wood to ground contact, and feed on the cellulose. Soil termites cause about 95% of the termite-related damage found in the world wide scenario. Like other types, this particular variety of termite eats cellulose for nutrition. Cellulose is found in wood and wood products.

Soil termites build earthen shelter tubes from the ground into the structure for protection from predators and to help maintain a moist environment. Many times these tubes are built on inside walls, porches, or chimneys where they cannot be seen.

Termites excavate galleries throughout their food as they consume it. They conceal their workings and can completely honeycomb wood by feeding along the grain and following the softer spring wood, leaving little more than a thin wooden exterior. Subterranean termites construct aboveground earthen runways that protect them from the drying effects of air as well as from natural enemies, such as ants. Termites are very susceptible to desiccation, and thus they are dependent on moisture sources. Termites work 24 hours a day. "Worker" termites bring food to the colony through tunnels, without ever resting.

Termites need moisture to survive and will die if exposed to sunlight or open air. Their tunnels protect them from the elements. High moisture areas like basements and crawl spaces are very attractive to termites and can serve as starting points for infestation.

In some rare situations, if water and wood are available from a source other than the soil, subterranean termites can establish a colony with no ground contact. Isolated, above-ground infestations may occur in buildings where termites have access to water from condensation, leaking pipes, roofs, or other sources. These type of termites are the most destructive insect pests of wood since they cause billions of dollars in damage each year and have a negative impact on a family’s most valuable possession — the home.

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Parol, Parol

parol

Did You Know?

Since the 18th century, parol has been pretty much confined to oral contracts and the realm of law. No longer is anyone likely to refer to the "sweet parols" of a paramour, as in one 16th-century work. Parol brings to mind that other legal word, parole. Both words lack any connection with law in their original form. They come from Latin parabola, which means "parable" or "speech." The Latin, in turn, is from Greek parabole, meaning "comparison." The French created two words (which we then borrowed) from parabola . parol, meaning "spoken words," and parole, for "word of honor." Originally, a parole was a prisoner of war's promise to fulfill certain conditions on consideration of his release.

Origin and Etymology of parol

Middle French parole

Az Ofteno Solucion Oftalmica Para Que Sirve, Az Ofteno

AZ OFTENO SOLUCION OFTALMICA

Acceso rapido al contenido

Tenga especial cuidado durante el embarazo .

No usar AZ OFTENO SOLUCION OFTALMICA con lactantes.

Revise siempre que no sea alergico a ninguno de los componentes de AZ OFTENO SOLUCION OFTALMICA . 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

SOLUCION OFTALMICA Antialergico

SOPHIA, S. A. de C. V. LABORATORIOS

DENOMINACION GENERICA:

FORMA FARMACEUTICA Y FORMULACION:

Cada ml contiene:

Clorhidrato de azelastina. 0.5 mg

Vehiculo, cbp. 1.0 ml

INDICACIONES TERAPEUTICAS:

AZ OFTENO esta indicado para el tratamiento de los signos y sintomas de la conjuntivitis alergica.

FARMACOCINETICA Y FARMACODINAMIA EN HUMANOS:

La azelastina tiene una selectiva y potente afinidad por los receptores H1 de histamina in vitro y ejerce un efecto antihistaminico en estudios in vitro e in vivo.

La azelastina tiene actividad anticolinergica e inhibe la serotonina inducida por anafilaxis cutanea en ratas a dosis (25 mg/kg) in vitro, la agregacion de plaquetas, el edema y la broncoconstriccion son inducidas por el factor de activacion plaquetaria y son inhibidas por azelastina.

En voluntarios sanos, una sola dosis oral de azelastina es casi completamente absorbida (95%). Las concentraciones plasmaticas pico de 3 mg/lt. ocurren 4 o 5 horas despues de una sola dosis oral de 4 mg.

Multiples dosis de azelastina (4 mg, 2 veces al dia) alcanzaron una concentracion plasmatica pico de 10 mg/lt. en 2.3 horas. En animales, la azelastina es distribuida primariamente a tejidos perifericos: las concentraciones son bajas en el cerebro. La azelastina se liga a proteinas en 78 a 88%. La vida media de eliminacion es de 25 horas despues de una dosis oral y 35.5 horas despues de una dosis multiple.

Las propiedades antialergicas han sido demostradas en la mayoria de estudios animales. Los estudios realizados para investigar la farmacocinetica, su distribucion sistemica y ocular, asi como la excrecion, despues de una sola instilacion ocular de azelastina en ratas albinas con y sin conjuntivitis alergica inducida, han concluido que las concentraciones de azelastina en la mayoria de las muestras oculares tratadas de ojos normales y con conjuntivitis alergica excedieron la constante inhibitoria contra los receptores de histamina H1 calculados de los sitios de union al receptor por al menos 48 horas despues de la instilacion.

Los resultados indican que la azelastina despues de su aplicacion ocular esta disponible en suficientes concentraciones y por largo tiempo en los sitios de liberacion de los eventos alergicos oculares, y sus propiedades farmacocineticas pueden ser beneficas para el tratamiento ocular de la alergia en humanos con un intervalo de dosificacion de 12 horas.

CONTRAINDICACIONES:

AZ OFTENO esta contraindicado en pacientes con hipersensibilidad a los componentes de la formula.

PRECAUCIONES GENERALES:

Para prevenir la contaminacion de la punta del frasco gotero y de la solucion, se debe tener cuidado de no tocar el parpado o las areas subyacentes.

RESTRICCIONES DE USO DURANTE EL EMBARAZO Y LA LACTANCIA:

La azelastina no tuvo influencia sobre las condiciones generales durante la gestacion y la lactancia en estudios realizados en ratas.

No hay estudios controlados en la mujer embarazada. La azelastina debera ser utilizada durante el embarazo solamente si los beneficios potenciales justifican los riesgos potenciales al feto.

No se sabe si la azelastina topica puede excretarse en la leche humana. Se recomienda administrarla con precaucion durante la lactancia.

REACCIONES SECUNDARIAS Y ADVERSAS:

Los efectos adversos mas frecuentemente reportados son percepcion alterada del sabor y ardor transitorio a la aplicacion.

INTERACCIONES MEDICAMENTOSAS Y DE OTRO GENERO:

No se conocen a la fecha.

ALTERACIONES EN LOS RESULTADOS DE PRUEBAS DE LABORATORIO:

No existe evidencia de alteraciones de pruebas de laboratorio en relacion a la azelastina.

PRECAUCIONES EN RELACION CON EFECTOS DE CARCINOGENESIS, MUTAGENESIS, TERATOGENESIS Y SOBRE LA FERTILIDAD:

No fueron encontrados efectos teratogenicos en ratas y conejos.

Esto puede ser debido al hecho de que la estructura quimica de la azelastina difiere marcadamente de los antihistaminicos convencionales. No fueron encontrados efectos sobre la fertilidad, mutagenesis, teratogenesis o carcinogenesis.

DOSIS Y VIA DE ADMINISTRACION:

Dosis: Instilar una gota en el(los) ojo(s) afectado(s) cada 12 horas.

Via de administracion: Oftalmica.

MANIFESTACIONES Y MANEJO DE LA SOBREDOSIFICACION O INGESTA ACCIDENTAL:

Si se ingiere accidentalmente, administre liquidos orales para diluirlo.

PRESENTACIONES:

Caja con frasco gotero con 5 ml de solucion.

RECOMENDACIONES SOBRE ALMACENAMIENTO:

Conservese a temperatura ambiente a no mas de 30°C.

LEYENDAS DE PROTECCION:

Su venta requiere receta medica. No se deje al alcance de los ninos.

LABORATORIO Y DIRECCION:

LABORATORIOS SOPHIA, S. A. de C. V. Hidalgo Num. 738 Sector Hidalgo 44290 Guadalajara, Jal.

Reg. Num. 225M98, SSA IV JEAR-314728/RM2002/IPPA

EDEMA . Es la tumefaccion de los tejidos debido a un aumento del liquido existente en ellos y suele aparecer tras una lesion.

City National Rochdale Fxd Inc Opps Fund (Rimox), Rimox

City National Rochdale Fxd Inc Opps Fund

About RIMOX

The investment seeks a high level of current income. The fund normally invests at least 80% of its net assets in fixed income securities. It will invest in both fixed rate and floating rate fixed income securities and may invest in fixed income securities of any credit rating. The fund seeks to invest its net assets across a spectrum of income yielding securities and primarily focuses on investments in high yield bonds issued by corporate and municipal issuers, in securities issued by corporate issuers, sovereign issuers or quasi-sovereign issuers, in fixed and floating rate loans made to U. S. and foreign borrowers, and in domestic and foreign corporate bonds.

Rankings

U. S. News evaluated 802 High Yield Bond Funds. Our list highlights the top-rated funds for long-term investors based on the ratings of leading fund industry researchers.

RIMOX is listed as:

Scorecard

Trailing Total Returns Monthly

Barclays US Agg Bond TR USD

Performance

The fund has returned 1.24 percent over the past year, 3.57 percent over the past three years, and 4.33 percent over the past five years.

Fees

Fees are Average compared to funds in the same category. City National Rochdale Fxd Inc Opps Fund has an expense ratio of 1.10 percent.

Net Expense Ratio

Aerosol Nasal De Budesonida Medlineplus Medicinas, Budemar

Aerosol nasal de budesonida

?Para cuales condiciones o enfermedades se prescribe este medicamento?

El aerosol nasal de budesonida se usa para aliviar los estornudos, la secrecion nasal, la congestion nasal o la comezon en la nariz causada por la fiebre del heno u otras alergias (provocadas por una alergia al polen, al moho, al polvo o a las mascotas). El aerosol nasal de budesonida no se debe usar para tratar sintomas (por ejemplo, estornudos, nariz congestionada, secrecion nasal, comezon en la nariz) provocados por el resfriado comun. El aerosol nasal de budesonida se encuentra en una clase de medicamentos llamados corticoesteroides. Funciona al bloquear la liberacion de ciertas sustancias naturales que causan sintomas de alergia.

?Como se debe usar este medicamento?

La presentacion de la budesonida es en forma de suspension (liquido) (con y sin receta medica) para rociar en la nariz. El aerosol nasal de budesonida usualmente se rocia en cada fosa nasal una vez al dia. Si usted es un adulto, comenzara el tratamiento con una dosis mas alta de aerosol nasal de budesonida y luego reducira la dosis cuando mejoren los sintomas. Si le esta administrando el aerosol nasal de budesonida a un nino, comenzara el tratamiento con una dosis mas baja del medicamento y aumentara la dosis si los sintomas del nino no mejoran. Disminuya la dosis cuando mejoren los sintomas del nino. Siga atentamente las instrucciones que se encuentran en la etiqueta de su receta medica y pida a su medico o farmaceutico que le explique cualquier parte que no comprenda. Use la budesonida exactamente como se indica. No use una cantidad mayor ni menor del medicamento, ni lo use con mas frecuencia de lo que su medico le indique.

Un adulto debe ayudar a los ninos menores de 12 anos a usar el aerosol nasal de budesonida. Los ninos menores de 6 anos de edad no deben usar este medicamento.

El aerosol nasal de budesonida es para usarlo unicamente en la nariz. No se trague el aerosol nasal y tenga cuidado de no rociarlo en los ojos o la boca.

Solo una persona debe usar cada frasco de aerosol nasal de budesonida. No comparta el aerosol nasal de budesonida, ya que esto puede propagar los germenes.

El aerosol nasal de budesonida controla los sintomas de la fiebre del heno o las alergias, pero no cura estas condiciones. Sus sintomas podrian empezar a mejorar 1 a 2 dias despues del primer uso de budesonida, pero podria tomar hasta 2 semanas antes que sienta el beneficio completo de la budesonida. La budesonida funciona mejor cuando se usa de manera regular. Use budesonida en un horario regular a menos que su medico le haya indicado que lo use segun sea necesario. Llame a su medico si los sintomas empeoran o no mejoran despues de usar el aerosol nasal de budesonida todos los dias durante 2 semanas.

El aerosol nasal de budesonida esta disenado para proporcionar cierta cantidad de aplicaciones. Despues de haber usado el numero de aplicaciones marcado, las aplicaciones que quedan en el frasco podrian no contener la cantidad correcta de medicamento. Debe llevar un registro del numero de aplicaciones que ha usado y tirar el frasco a la basura despues de haber usado el numero de aplicaciones marcado, incluso si aun contiene algo de liquido.

Antes de aplicarse el aerosol nasal de budesonida por primera vez, lea las instrucciones escritas que vienen en el empaque. Siga estos pasos:

Agite el frasco suavemente antes de cada uso.

Retire la tapa.

Si va a usar la bomba por primera vez o no la ha usado durante 2 o mas dias seguidos, debe prepararla siguiendo los pasos 4 a 5 a continuacion. Si ha usado la bomba antes y no ha dejado de usarla durante 2 dias seguidos de medicamento, vaya al paso 6.

Sostenga la bomba con el aplicador entre su dedo indice y el dedo medio con la parte de abajo del frasco apoyada sobre su pulgar. Apunte el aplicador lejos de su cara.

Si esta utilizando la bomba por primera vez, presione y libere la bomba ocho veces. Si ha usado la bomba antes, pero no dentro de los ultimos 2 dias, presione y libere la bomba una vez hasta que vea un aerosol fino. Si no ha usado la bomba durante mas de 14 dias, enjuague la punta del aplicador y preparela con dos o mas aplicaciones hasta que vea un aerosol fino.

Limpiese la nariz hasta que las fosas esten despejadas.

Mantenga una fosa nasal cerrada con el dedo.

Incline la cabeza ligeramente hacia adelante y coloque cuidadosamente la punta del aplicador nasal en la otra fosa nasal. Asegurese de mantener el frasco en posicion vertical.

Sostenga la bomba con el aplicador entre su dedo indice y el dedo medio con la parte de abajo apoyada sobre su pulgar.

Comience a inhalar por la nariz.

Mientras respira, use su dedo indice y el medio para presionar el aplicador firmemente hacia abajo y liberar el aerosol.

Incline su cabeza hacia atras y aspire lentamente por la fosa nasal y exhale por la boca.

Si su medico le indico que use aplicaciones adicionales en esa fosa nasal, repita los pasos 6 al 12.

Repita los pasos 6 al 13 en la otra fosa nasal.

No se suene la nariz durante 15 minutos despues de usar el aerosol nasal.

Limpie el aplicador con un pano limpio y tapelo con la cubierta de plastico.

Pida a su farmaceutico o medico una copia de la informacion del fabricante para el paciente.

?Que otro uso se le da a este medicamento?

Este medicamento se puede recetar para otros usos; para obtener mas informacion pregunte a su medico o farmaceutico.

?Cuales son las precauciones especiales que debo seguir?

Antes de usar el aerosol nasal de budesonida,

informe a su medico y farmaceutico si es alergico a la budesonida, a cualquier otro medicamento o a alguno de los ingredientes que contiene el aerosol nasal de budesonida. Revise la etiqueta del empaque para ver la lista de los ingredientes.

Informe a su medico y farmaceutico que medicamentos con y sin receta medica, vitaminas, suplementos nutricionales y productos a base de hierbas esta tomando o tiene planificado tomar. Asegurese de mencionar cualquiera de los siguientes: claritromicina (Biaxin, en Prevpac); inhibidores de la proteasa del VIH como atazanavir (Reyataz, en Evotaz), indinavir (Crixivan), nelfinavir (Viracept), ritonavir (Norvir, en Kaletra, en Technivie), o saquinavir (Invirase); itraconazol (Onmel, Sporanox); ketoconazol (Extina, Nizoral, Xolegel); nefazodona; telitromicina (Ketek). Tambien informe a su medico o farmaceutico si esta utilizando medicamentos esteroides como la dexametasona, metilprednisolona (Medrol) y prednisona (Rayos) para el asma, alergias o una erupcion cutanea. Es posible que su medico deba cambiar las dosis de sus medicamentos o monitorearle atentamente para saber si sufre efectos secundarios.

Informe a su medico si le realizaron una cirugia de nariz recientemente, si se ha golpeado la nariz de alguna manera o si tiene alguna lesion en la nariz. Tambien informe a su medico si tiene o alguna vez ha tenido cataratas (empanamiento del lente del ojo), glaucoma (una enfermedad de los ojos), asma (episodios repentinos de jadeo, falta de aliento y dificultad para respirar), cualquier tipo de infeccion, una infeccion por herpes en el ojo (una infeccion que causa un dolor en el parpado o la superficie del ojo) o enfermedad hepatica. Informe a su medico si tuvo varicela, paperas o tuberculosis (TB; un tipo de infeccion pulmonar) o si ha estado cerca de alguien que tenga una de estas condiciones.

Informe a su medico si esta embarazada, tiene planificado embarazarse o esta amamantando. Llame a su medico si queda embarazada mientras usa budesonida.

?Que tengo que hacer si me olvido de tomar una dosis?

Use la dosis que omitio tan pronto como lo recuerde. Sin embargo, si ya casi es hora de la proxima dosis, omita la dosis que le falto y continue con su programa regular de dosificacion. No duplique la dosis para compensar la dosis omitida.

?Cuales son los efectos secundarios que podria provocar este medicamento?

El aerosol nasal de budesonida puede ocasionar efectos secundarios. Informe a su medico si cualquiera de estos sintomas es intenso o no desaparece:

resequedad, escozor, ardor o irritacion en la nariz

cansancio

debilidad

vomitos

nauseas

dolor de articulaciones o musculos

sangrado de nariz

Algunos efectos secundarios pueden ser graves. Si experimenta algunos de los siguientes sintomas, deje de usar el aerosol nasal de budesonida y llame a su medico de inmediato o busque tratamiento medico de emergencia:

problemas de la vista

fiebre, dolor de garganta, escalofrios, tos y otras senales de infeccion

sonido de silbido de la nariz

urticaria

sarpullido

picazon

inflamacion del rostro, garganta, lengua, labios, ojos, manos, pies, tobillos o parte inferior de las piernas

ronquera

sibilancia

opresion del pecho

dificultad para respirar o tragar

parches blancos en su garganta, en su boca o nariz

Debe saber que este medicamento puede ocasionar que los ninos crezcan despacio. Hable con el medico de su hijo si necesita usar este medicamento durante mas de 2 meses al ano.

El aerosol nasal de budesonida puede causar otros efectos secundarios. Llame a su medico si tiene algun problema inusual mientras usa este medicamento.

Si desarrolla un efecto secundario grave, usted o su doctor puede enviar un informe al programa de divulgacion de efectos adversos 'MedWatch' de la Administracion de Alimentos y Medicamentos (FDA, por su sigla en ingles) en la pagina de Internet (http://www. fda. gov/Safety/MedWatch ) o por telefono al 1-800-332-1088.

?Como debo almacenar o desechar este medicamento?

Mantenga este medicamento en su envase original, cerrado hermeticamente y fuera del alcance de los ninos. Almacenelo a temperatura ambiente y lejos de la luz, del exceso de calor y de la humedad (no en el bano). No lo congele.

Los medicamentos que ya no son necesarios se deben desechar de una manera apropiada para asegurarse de que las mascotas, los ninos y otras personas no puedan consumirlos. Sin embargo, no debe desechar estos medicamentos por el inodoro. En su lugar, la mejor manera de deshacerse de sus medicamentos es a traves de un programa de devolucion de medicamentos. Hable con su farmaceutico o pongase en contacto con su departamento de basura/reciclaje local para conocer acerca de los programas de devolucion de medicamentos de su comunidad. Consulte el sitio web de la Administracion de Medicamentos y Alimentos (FDA), (http://goo. gl/c4Rm4p ) para obtener mas informacion de como desechar de forma segura los medicamentos, si no tiene acceso al programa de devolucion de medicamentos.

?Que otra informacion de importancia deberia saber?

Debe limpiar el aplicador de aerosol nasal periodicamente. Tendra que quitar la tapa de plastico y luego tirar suavemente del aplicador para extraerlo del frasco. Lave la tapa de plastico y el aplicador con agua tibia y enjuaguelo con agua fria, deje secar a temperatura ambiente y luego vuelva a ponerlos en el frasco.

Si la punta del aerosol esta tapada, lavela con agua tibia y luego enjuaguela con agua fria y sequela. No utilice alfileres u otros objetos afilados para eliminar la obstruccion.

Haga a su farmaceutico cualquier pregunta que tenga sobre el aerosol nasal de budesonida.

Es importante que Ud. mantenga una lista escrita de todas las medicinas que Ud. esta tomando, incluyendo las que recibio con receta medica y las que Ud. compro sin receta, incluyendo vitaminas y suplementos de dieta. Ud. debe tener la lista cada vez que visita su medico o cuando es admitido a un hospital. Tambien es una informacion importante en casos de emergencia.

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Online Language Dictionaries

Diccionario de la lengua espanola © 2005 Espasa-Calpe:

todo, da

adj. y pron. Que se toma o se considera por entero o en conjunto: todo el mundo esta de acuerdo.

Se usa para ponderar el exceso de algo o intensificar una cualidad: es toda una mujer.

Seguido de un sustantivo en singular y sin articulo, equivale a cualquiera: toda persona.

pl. Puede equivaler a cada: cobra todos los meses.

m. Cosa integra, o que consta de la suma y conjunto de sus partes integrantes, sin que falte ninguna: la sinecdoque designa una parte por el todo o viceversa.

adv. m. Por completo, enteramente: Carmen es todo espontaneidad y simpatia.

a todo loc. adv. col. Con el maximo esfuerzo o rendimiento: a toda maquina.

a todo esto loc. adv. Entre tanto, mientras: a todo esto, ella nos ignoraba abiertamente.

ante todo loc. adv. Primera o principalmente, antes que otra cosa: ante todo quiero daros la enhorabuena.

asi y todo loc. conjunt. A pesar de eso, no obstante: discuten mucho, pero asi y todo se adoran.

con todo loc. conjunt. Sin embargo, no obstante: no me cae mal, pero, con todo, no me fio de el.

de todas todas loc. adv. Con seguridad, irremediablemente: esto es asi de todas todas, te lo digo yo.

del todo loc. adv. Sin excepcion, completamente: es del todo imposible.

jugar(se) el todo por el todo loc. Arriesgarse mucho para conseguir algo que se desea mucho: al sacar a aquel jugador demostro que se estaba jugando el todo por el todo.

ser todo uno loc. col. Ser consecuencia logica e inevitable: darle yo la noticia y que se echara a llorar fue todo uno.

Acabar siendo iguales cosas que parecen muy diferentes.

sobre todo loc. adv. Con especialidad, mayormente: es una persona sobre todo generosa.

y todo loc. adv. Hasta, tambien, incluso: volco el carro con mulas y todo.

' todo ' aparece tambien en las siguientes entradas:

Preguntas en los foros con la(s) palabra(s) 'todo' en el titulo:

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Carlitex Marketing Information

Carlitex Description

Carlitex is an angiotensin II receptor antagonist. It works by inhibiting the action of a chemical transmitter (angiotensin II) and allowing the blood vessels to dilate (widen) and the kidneys to eliminate extra sodium and fluids. These actions combine to help lower blood pressure.

Generic name of Carlitex is Olmesartan.

Brand name of Carlitex is Carlitex.

Carlitex Dosage

Carlitex is available in:

20mg Low Dosage40mg Standard Dosage

Take Carlitex orally with or without food.

If you want to achieve most effective results do not stop taking Carlitex suddenly.

Carlitex Missing of dose

Do not take double dose. If you miss a dose you should take it as soon as you remember about your missing. If it is the time for the next dose you should continue your regular dosing schedule.

Carlitex Overdose

If you overdose Carlitex and you don't feel good you should visit your doctor or health care provider immediately.

Carlitex Side effects

Carlitex has its side effects. The most common are:

abdominal or stomach paincoughdiarrheadizzinessheadacheunusual tiredness

Less common but more serious side effects during taking Carlitex:

allergy reactions (urticaria, breathing difficulties, rash, and eruption)faintingincreased heartbeatlightheadedness

Side effects manifestations are not only depend on medicine you are taking but also depend on your health state and on the other factors.

Carlitex Contra-indications

Do not take Carlitex if you are allergic to Carlitex components.

Do not take Carlitex if you're pregnant or you plan to have a baby, or you are a nursing mother.

Avoid machine driving.

Patients who take medicine for high blood pressure often feel tired or run down for a few weeks after starting treatment.

Be careful if you use salt substitute or a product that has potassium in it.

Do not stop taking Carlitex suddenly.

Carlitex Frequently asked questions

Q: What is Carlitex?

A: Carlitex is used for treating high blood pressure, alone or with other medicines. It may also be used for other conditions. Carlitex is an angiotensin II receptor antagonist. It works by inhibiting the action of a chemical transmitter (angiotensin II) and allowing the blood vessels to dilate (widen) and the kidneys to eliminate extra sodium and fluids. These actions combine to help lower blood pressure.

Q: How should I take Carlitex?

A: Carlitex is available in tablets (20 mg, 40 mg). Take Carlitex orally with or without food. If you want to achieve most effective results do not stop taking Carlitex suddenly.

Q: What should I do in case of overdose?

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Betnovate helps to reduce the redness, itching, and swelling of skin conditions such as eczema, psoriasis, contact dermatitis, and seborrhea.

Use Betnovate as directed by your doctor.

This medication is usually applied 2 or 3 times daily or according to the instruction. Enough medication should be applied to completely cover the affected area with a thin film. The medication should be gently and thoroughly massaged into the affected area. In certain conditions, the doctor will order the application to be covered with a dressing. Ask your health care provider any questions you may have about how to use Betnovate.

Drug Class and Mechanism

Betnovate is a corticosteroid that is used for the topical treatment of skin irritations.

If you miss a dose, take it as soon as possible and continue with your regular schedule. If it is almost time for your next dose, skip the missed dose and continue with your regular dosing schedule. Do not take a double dose to make up for a missed one.

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.

Betnovate should not be taken by anyone who:

is allergic to betamethasone valerate or any of the ingredients of the medication; has chickenpox; has fungal, yeast, or viral skin lesions; has herpes simplex; has tuberculosis of the skin; has vaccinia.

Possible Side Effects

Side effects that you should report to your prescriber or health care professional as soon as possible:

burning or itching of the skin; dark red spots on the skin; infection; lack of healing of the skin condition; painful, red, pus-filled blisters in hair follicles; severe burning and continued itching of the skin; thinning of the skin, with easy bruising, sunburn more likely especially on the face. Other serious side effects can develop if you use Betnovate for a long time, or if you use too much. Contact your prescriber or health care professional if you notice any unusual effects.

Side effects that usually do not require medical attention (report to your prescriber or health care professional if they continue or are bothersome): burning, itching, or irritation of the skin; dry skin; increased redness or scaling of the skin.

Betnovate is to be used only by the patient for whom it is prescribed. Do not share it with other people. If your symptoms do not improve or if they become worse, check with your doctor.

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Aciclovir is indicated for the treatment of HSV and VZV infections, including:

Genital herpex simplex

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Herpes zoster (shingles)

Acute chickenpox in immunocompromised patients

Herpes simplex encephalitis

Acute mucocutaneous HSV infections in immunocompromised patients

Herpes simplex keratitis (ocular herpes)

Herpes simplex blepharitis

Bell's Palsy

Aciclovir is an antiviral. It works by stopping viral replication. However, Aciclovir does not eliminate the virus, is not a cure, and does not prevent transmission to others.

Use Aciclovir as directed by your doctor!

Take Aciclovir by mouth with or without food.

Start therapy with Aciclovir at the earliest sign or symptom of shingles or genital herpes (pain, burning, blisters).

If treating an acute outbreak, continue using Aciclovir for the full course of treatment even if you feel better in a few days.

For suppressive therapy, Aciclovir works best if it is taken at the same times each day.

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

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

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

Do NOT use Aciclovir if:

you are allergic to any ingredient in Aciclovir or to valacyclovir

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

Some medical conditions may interact with Aciclovir. 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 kidney problems or a weakened immune system.

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

Medicines that may harm the kidney (eg, aminoglycoside antibiotics [eg, gentamicin], amphotericin B, cyclosporine, nonsteroidal anti-inflammatory drugs [NSAIDs] [eg, ibuprofen], tacrolimus, vancomycin) because the risk of kidney side effects may be increased. Ask your doctor if you are unsure if any of your medicines might harm the kidney.

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

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

Aciclovir may cause dizziness, lightheadedness, or fainting; alcohol, hot weather, exercise, or fever may increase these effects. To prevent them, sit down or stand up slowly, especially in the morning. Sit or lie down at the first sign of any of these effects.

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

Aciclovir is not a cure for genital herpes and will not prevent the virus from spreading. Avoid sexual intercourse when sores are present to prevent infecting your partner. You can also be contagious and spread the herpes virus but not have any signs or symptoms at all. This is called asymptomatic viral shedding.

Lab tests, including kidney function and serum urea nitrogen (BUN), may be performed while you use Aciclovir. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Use Aciclovir with caution in the elderly; they may be more sensitive to its effects, especially confusion, drowsiness, or hallucinations.

Aciclovir is not recommended for use in children younger than 2 years old as safety and effectiveness for 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 Aciclovir while you are pregnant. Aciclovir is found in breast milk. If you are or will be breast-feeding while you use Aciclovir, check with your doctor. Discuss any possible risks to your baby.

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

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

Diarrhea; general body discomfort; headache; nausea/vomiting.

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

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); aggressive behavior; blood in the urine; confusion; decreased consciousness; decreased urination; hallucinations; lower back pain; mental or mood changes; red, swollen, blistered, or peeling skin; seizures; unusual bruising or bleeding.

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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An Oscar-winning director, a major star, a survival saga that makes Heart of Darkness look like a pleasure cruise. and all anyone wants to talk about is the bear attack.

And in fact, it's hard not to start there. It comes about comes 24 minutes in. Fur-trapper Hugh Glass, played by a hirsute, bundled-up Leonardo DiCaprio, has helped his fellow trappers escape a harrowing Arikara massacre. In most movies that would be the scene everyone's talking about — arrows piercing vocal cords in mid-cry, death raining down from trees.

But a few men get away, and are hellbent on getting to the comparative safety of a far-off fort before winter hits. Glass, separated from the others, has spotted two bear cubs in the woods. He raises his rifle, then hears a loud snuffling behind him: Mama bear. who has correctly figured out what Glass has in mind for her cubs, charges before he can swing his rifle around. In one horrifying, continuous take, she knocks him down, claws, bites, stomps, and shakes his body, ripping his flesh, breaking his bones.

Only when Glass is motionless after a long, long mauling does she pause in her attack — sizing him up, stepping on his head, sniffing his skin until the call of her cubs distracts her.

And you think it's over.

By the time Glass' son Hawk (Forrest Goodluck) and the other trappers come upon him, Glass is barely clinging to life. Carrying him over rough terrain as winter approaches will doom them all, realizes Captain Andrew Henry (Domhnall Gleeson). He offers a bit of extra pay to two men who will stay to watch over him and then bury him when the time comes.

A young trapper about Hawk's age volunteers to stay, as does John Fitzgerald (Tom Hardy), who's been grousing about Glass and his son (whose mother was Pawnee) since the Indian attack. Alas, Fitzgerald is not someone you want in your corner. Once the others have moved on, he stabs Hawk, all but buries Glass alive, then leaves them to the elements.

At which point a survival/revenge saga begins that's every bit as breathtaking to behold as it is punishing to watch. Filmmaker Alejandro Gonzalez Inarritu, fresh off the Oscar-winning Birdman . and working with the same cinematographer who made Birdman's long continuous camera takes so fluid, spent eight winter months in the Canadian and Argentine wilderness with a cast that didn't have to fake being freezing or exhausted. DiCaprio in particular, gets swept over waterfalls, rides his horse off cliffs, drags himself by his fingernails across icy landscapes, and endures Indian attacks, mostly in natural light, ice in his beard, the camera getting so close to him that his breath fogs the lens.

What elevates this standard, if relentless, plot line is that The Revenant feels like high-wire work without a net. Audiences have gotten used to seeing actors doing what look like dangerous things, but in the full knowledge that those actors are not actually in danger. that they're on a soundstage somewhere in front of a green screen.

To shoot The Revenant DiCaprio, aided by the occasional stuntman, actually dragged himself against genuinely frozen ground, and plunged into a raging river with ice in it, and I don't care how advanced the wetsuit is that was hidden under his clothes, that makes a difference you can feel. He's exposed, at the mercy of the elements in a cruelly brutal way, and so is the storytelling.

Yes, there's some digital work here. The filmmakers did not actually turn a grizzly loose on one of the most valuable talents in Hollywood. But the effects are used to make things more real, not more fantastic, and that, also makes a difference.

The dictionary definition of "revenant" is "one who returns after death or a long absence." Applies to the main character obviously. But watching The Revenant . you're aware that a kind of filmmaking — raw and visceral — is returning after a long absence, too.

Weijiexin, Weijiexin

Vantin is used for treating mild to moderate infections caused by certain bacteria. Vantin is a cephalosporin antibiotic. It works by interfering with the formation of the bacteria's cell wall so that the wall ruptures, resulting in the death of the bacteria.

Use Vantin as directed by your doctor.

Take Vantin by mouth with food.

Vantin works best if it is taken at the same time each day.

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

Vantin should not be given within 2 hours of antacids or H 2 antagonists (eg, famotidine).

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

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

Store Vantin at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Brief storage at temperatures between 59 to 86 degrees F (15 to 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Vantin out of the reach of children and away from pets.

Active Ingredient: Cefpodoxime proxetil.

Do NOT use Vantin if:

you are allergic to any ingredient in Vantin or to any other cephalosporin antibiotic (eg, cephalexin, cefprozil).

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

Tell your health care provider if you have any medical conditions, especially if any of the following apply to you:

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

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

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

if you have diarrhea, a stomach or intestinal infection, or a blood clotting problem

if you have had a severe allergic reaction (eg, severe rash, hives, difficulty breathing, dizziness) to a penicillin antibiotic (eg, amoxicillin) or other beta-lactam antibiotic (eg, imipenem).

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

Aminoglycosides (eg, gentamicin), cyclosporine, or diuretics (eg, furosemide, hydrochlorothiazide) because the risk of side effects on the kidney may be increased.

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

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

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

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

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

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

Pregnancy and breast-feeding: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Vantin while you are pregnant. The medicine is found in breast milk. Do not breastfeed while taking Vantin.

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:

Diarrhea; headache; loose stools; nausea; upset stomach; vomiting.

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

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); bloody stools; seizures; severe diarrhea; skin rash; stomach pain/cramps; vaginal irritation or discharge.

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.

Vantin is used for treating mild to moderate infections caused by certain bacteria. Vantin is a cephalosporin antibiotic. It works by interfering with the formation of the bacteria's cell wall so that the wall ruptures, resulting in the death of the bacteria.

Use Vantin as directed by your doctor.

Take Vantin by mouth with food.

Vantin works best if it is taken at the same time each day.

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

Vantin should not be given within 2 hours of antacids or H 2 antagonists (eg, famotidine).

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

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

Store Vantin at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Brief storage at temperatures between 59 to 86 degrees F (15 to 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Vantin out of the reach of children and away from pets.

Active Ingredient: Cefpodoxime proxetil.

Do NOT use Vantin if:

you are allergic to any ingredient in Vantin or to any other cephalosporin antibiotic (eg, cephalexin, cefprozil).

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

Tell your health care provider if you have any medical conditions, especially if any of the following apply to you:

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

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

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

if you have diarrhea, a stomach or intestinal infection, or a blood clotting problem

if you have had a severe allergic reaction (eg, severe rash, hives, difficulty breathing, dizziness) to a penicillin antibiotic (eg, amoxicillin) or other beta-lactam antibiotic (eg, imipenem).

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

Aminoglycosides (eg, gentamicin), cyclosporine, or diuretics (eg, furosemide, hydrochlorothiazide) because the risk of side effects on the kidney may be increased.

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

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

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

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

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

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

Pregnancy and breast-feeding: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Vantin while you are pregnant. The medicine is found in breast milk. Do not breastfeed while taking Vantin.

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:

Diarrhea; headache; loose stools; nausea; upset stomach; vomiting.

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

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); bloody stools; seizures; severe diarrhea; skin rash; stomach pain/cramps; vaginal irritation or discharge.

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.

Antibiotics - Weijiexin (Brand name: vantin)

Vantin is used for treating mild to moderate infections caused by certain bacteria. Vantin is a cephalosporin antibiotic. It works by interfering with the formation of the bacteria's cell wall so that the wall ruptures, resulting in the death of the bacteria.

Use Vantin as directed by your doctor.

Take Vantin by mouth with food.

Vantin works best if it is taken at the same time each day.

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

Vantin should not be given within 2 hours of antacids or H 2 antagonists (eg, famotidine).

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

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

Store Vantin at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Brief storage at temperatures between 59 to 86 degrees F (15 to 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Vantin out of the reach of children and away from pets.

Active Ingredient: Cefpodoxime proxetil.

Do NOT use Vantin if:

you are allergic to any ingredient in Vantin or to any other cephalosporin antibiotic (eg, cephalexin, cefprozil).

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

Tell your health care provider if you have any medical conditions, especially if any of the following apply to you:

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

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

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

if you have diarrhea, a stomach or intestinal infection, or a blood clotting problem

if you have had a severe allergic reaction (eg, severe rash, hives, difficulty breathing, dizziness) to a penicillin antibiotic (eg, amoxicillin) or other beta-lactam antibiotic (eg, imipenem).

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

Aminoglycosides (eg, gentamicin), cyclosporine, or diuretics (eg, furosemide, hydrochlorothiazide) because the risk of side effects on the kidney may be increased.

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

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

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

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

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

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

Pregnancy and breast-feeding: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Vantin while you are pregnant. The medicine is found in breast milk. Do not breastfeed while taking Vantin.

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:

Diarrhea; headache; loose stools; nausea; upset stomach; vomiting.

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

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); bloody stools; seizures; severe diarrhea; skin rash; stomach pain/cramps; vaginal irritation or discharge.

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.

Amotid Forte Tablet - Uses, Side-Effects, Reviews, Composition, Interactions, Precautions, Substitut

Amotid Forte Tablet

Amotid Forte Tablet - Uses, Composition, Side Effects and Reviews

Amotid Forte Tablet is indicated for the treatment of bacterial infections of respiratory tract, bacterial infections of urinary tract, bacterial infections of skin, bacterial infections of heart, bacterial infections of gums, bacterial infections of ear and other conditions. Amotid Forte Tablet contains the following active ingredients: Amoxicillin. It is available in tablet form. Kaptab Pharma manufactures Amotid Forte Tablet. Detailed information related to Amotid Forte Tablet's uses, composition, dosage, side effects and reviews is listed below:

Amotid Forte Tablet Uses

Amotid Forte Tablet is used in the treatment, control, prevention, & improvement of the following diseases, conditions and symptoms:

Bacterial infections of respiratory tract

Bacterial infections of urinary tract

Bacterial infections of skin

Bacterial infections of heart

Bacterial infections of gums

Bacterial infections of ear

Learn more: Uses (in more detail)

Amotid Forte Tablet Working, Mechanism of Action and Pharmacology

Amotid Forte Tablet improves the patient's condition by performing the following functions:

Amotid Forte Tablet Composition and Active Ingredients

Amotid Forte Tablet is composed of the following active ingredients (salts)

Please note that this medicine may be available in various strengths for each active ingredient listed above.

Amotid Forte Tablet Side-effects

The following is a list of possible side effects that may occur from all constituting ingredients of Amotid Forte Tablet. This is not a comprehensive list. These side effects are possible, but do not always occur. Some of the side effects may be rare but serious. Consult your doctor if you observe any of the following side effects, especially if they do not go away.

Nausea

Skin rash

Severe skin allergies

Pain

Irritation at the site of injection

Vomiting

If you notice other side effects not listed above, contact your doctor for medical advice. You may also report side effects to your local food and drug administration authority.

Learn more: Side-effects (in more detail)

Amotid Forte Tablet Precautions & How to Use

Before using this drug, inform your doctor about your current list of medications, over the counter products (e. g. vitamins, herbal supplements, etc.), allergies, pre-existing diseases, and current health conditions (e. g. pregnancy, upcoming surgery, etc.). Some health conditions may make you more susceptible to the side effects of the drug. Take as directed by your doctor or follow the direction printed on the product insert. Dosage is based on your condition. Tell your doctor if your condition persists or worsens. Important counseling points are listed below.

Do not take it for more than 2 weeks

Do periodic assessment of renal, hepatic or hematopoietic functions

Keep taking medicine until treatment is finished

Space the doses evenly during the day

Take the medicine with food

Learn more: Precautions & How to Use (in more detail)

Amotid Forte Tablet Frequently asked Questions

Can Amotid Forte Tablet be used for Bacterial infections of respiratory tract and Bacterial infections of urinary tract?

Yes, bacterial infections of respiratory tract and bacterial infections of urinary tract are among the most common reported uses for Amotid Forte Tablet. Please do not use Amotid Forte Tablet for bacterial infections of respiratory tract and bacterial infections of urinary tract without consulting first with your doctor. Click here to find out what other patients report as common uses for Amotid Forte Tablet.

Is it safe to drive or operate heavy machinery when consuming?

If you experience drowsiness, dizziness, hypotension or headache as side-effects when eating Amotid Forte Tablet medicine then it maybe not be safe to drive a vehicle or operate heavy machinery. One should not drive a vehicle if eating the medicine makes you drowsy, dizzy or lowers your blood-pressure extensively. Pharmacists also advise patients not to drink alcohol with medicines as alcohol intensifies drowsiness side-effects. Please check for these effects on your body when using Amotid Forte Tablet. Always consult with your doctor for recommendations specific to your body and health conditions.

Is this medicine or product addictive or habit forming?

Most medicines don't come with a potential for addiction or abuse. Usually, government's categorizes medicines that can be addictive as controlled substances. Examples include schedule H or X in India and schedule II-V in the US. Please consult the product package to make sure that the medicine does not belong to such special categorizations of medicines. Lastly, do not self-medicate and increase your body's dependence to medicines without the advice of a doctor.

Can it be stopped immediately or do I have to slowly ween off consumption?

Some medicines need to be tapered or cannot be stopped immediately because of rebound effects. Please consult with your doctor for recommendations specific to your body, health and other medications that you may be using.

Is Amotid Forte Tablet safe to consume or apply when pregnant?

Please consult with your doctor for case-specific recommendations.

Is Amotid Forte Tablet safe while breastfeeding?

Please discuss the risks and benefits with your doctor.

Consumer Survey: Amotid Forte Tablet

The following are the results of on-going survey on TabletWise. com for Amotid Forte Tablet. These results only indicate the perceptions of the website users. Please base your medical decisions only on the advice of a doctor or a registered medical professional.

Uses, Effectiveness and Side-effects

Following are the uses, perceived effectiveness and perceived side-effects incidence information reported by website visitor for Amotid Forte Tablet:

User reported uses

No data has been collected for this survey

User reported time for results

No data has been collected for this survey

Caverject (Alprostadil Injection) Side Effects, Interactions, Warning, Dosage & Uses, Prostadil

DRUG DESCRIPTION

CAVERJECT Sterile Powder contains alprostadil as the naturally occurring form of prostaglandin E 1 (PGE 1 ) and is designated chemically as (11α,13E,15S)-11,15dihydroxy-9-oxoprost-13-en-1-oic acid. The molecular weight is 354.49.

Alprostadil is a white to off-white crystalline powder with a melting point between 115° and 116° C. Its solubility at 35° C is 8000 micrograms per 100 milliliter double distilled water. CAVERJECT is available as a sterile freeze-dried powder for intracavernosal use in four sizes: 5, 10, 20 and 40 micrograms per vial — When reconstituted as directed with 1 milliliter of bacteriostatic water for injection or sterile water, both preserved with benzyl alcohol 0.945% w/v, gives 1.13 milliliters of reconstituted solution. Each milliliter of CAVERJECT contains 5.4, 10.5, 20.5 or 41.1 micrograms of alprostadil depending on vial strength, 172 milligrams of lactose, 47 micrograms of sodium citrate and 8.4 milligrams of benzyl alcohol. The deliverable amount of alprostadil is 5, 10, 20 or 40 micrograms per milliliter because approximately 0.4 microgram for the 5 microgram strength, 0.5 microgram for the 10 and 20 microgram strengths and 1.1 microgram for the 40 microgram strength is lost due to adsorption to the vial and syringe. When necessary, the pH of alprostadil for injection was adjusted with hydrochloric acid and/or sodium hydroxide before lyophilization .

The structural formula of alprostadil is represented below:

What are the possible side effects of alprostadil (Caverject, Caverject Impulse, Edex, Muse)?

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

Stop using alprostadil and call your doctor at once if you have a serious side effect such as:

feeling light-headed, fainting;

trouble urinating, blood in your urine;

bleeding, bruising, or swelling where you injected the medication;

a painful erection that lasts 4 hours or longer;

severe pain or irritation of your penis or urethra;.

What are the precautions when taking alprostadil injection (Caverject)?

Before using alprostadil, tell your doctor or pharmacist if you are allergic to it; or if you have any other allergies. This product may contain inactive ingredients, which can cause allergic reactions or other problems. Talk to your pharmacist for more details.

Before using this medication, tell your doctor or pharmacist your medical history, especially of: penis conditions (e. g. angulation, fibrosis/scarring, Peyronie's disease), blood system cancers (e. g. leukemia, multiple myeloma), sickle cell anemia.

Use of this drug does not protect against sexually transmitted diseases (e. g. HIV, hepatitis B, gonorrhea, syphilis). To decrease your risk of infection, always use an effective barrier method such as a latex or polyurethane condom during all sexual activity. Consult.

Last reviewed on RxList: 5/16/2016 This monograph has been modified to include the generic and brand name in many instances.

Contact - A, Arudein

Contact

A. RUDIN – Los Angeles Pacific Design Center 8687 Melrose Avenue Suite G172 Los Angeles, CA 90069 T 310. 659. 2388 F 310. 659. 1304 sales@arudin. com

A. RUDIN – San Francisco Galleria Design Center 101 Henry Adams Street Suite 140 San Francisco, CA 94103 T 415. 431. 5021 F 415. 431. 7940 salessf@arudin. com

A. RUDIN – Chicago Chicago Merchandise Mart 200 World Trade Center Suite 6-169 Chicago, IL 60654 T 312. 494. 9300 F 312. 494. 9310 saleschi@arudin. com

A. RUDIN – New York D&D Building 979 Third Avenue Suite 1201 New York, NY 10022 T 212. 644. 3766 F 212. 644. 3776 salesny@arudin. com

A. RUDIN – Corp. Office 6062 Alcoa Avenue Los Angeles, CA 90058 T 323. 589. 5547 F 323. 589. 8611

ARIZONA Town Arizona Design Center 2716 North 68th St Suite 7 Scottsdale, AZ 85257 T 480. 214. 4792 F 602. 297. 6821 W townstudio. com

COLORADO Town Denver Design Center 601 South Broadway Suite A Denver CO 80209 T 303. 282. 8696 F 303. 282. 8697 W townstudio. com

MASSACHUSETTS The M-Geough Company One Design Center Place Suite 410 Boston, MA 02210 T 617. 451. 1412 F 617. 451. 0065 W m-geough. com

MINNESOTA Scherping Westphal Market Square 275 Market Street Suite 209 Minneapolis, MN 55405 T 612. 822. 2700 F 612. 822. 2332 W scherpingwestphal. com

TEXAS E. C. Dicken Dallas Design Center 1025 North Stemmons Suite 260 Dallas, TX 75207 T 214. 742. 4801 F 214. 651. 7369 W ecdicken. com

WASHINGTON Trammell-Gagne, LLC Seattle Design Center 5701 Sixth Avenue, South Suite 105 Seattle, WA 98108 T 206. 762. 1511 F 206. 762. 1611 W tgshowroom. com

WASHINGTON D. C. Michael-Cleary 1099 4th St SW Suite 350 Washington, DC 20005 T 202. 488. 9787 F 202. 488. 9789

ATLANTA Paul Plus Atlanta 351 Peachtree Hills Ave. Suite 121 Atlanta, GA 30305 T 404. 261. 1820 F 404. 233. 1988 W paulplusatlanta. com

Generlac (Lactulose Oral) Medical Facts From, Genlac

Generlac

Lactulose is a type of sugar. It is broken down in the large intestine into mild acids that draw water into the colon, which helps soften the stools.

Lactulose is used to treat chronic constipation.

Lactulose is sometimes used to treat or prevent certain conditions of the brain that are caused by liver failure, which can lead to confusion, problems with memory or thinking, behavior changes, tremors, feeling irritable, sleep problems, loss of coordination, and loss of consciousness.

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

What is the most important information I should know about lactulose?

You should not use this medication if you are on a special diet low in galactose (milk sugar).

Before taking lactulose, tell your doctor if you have diabetes or if you need to have any type of intestinal test using a scope (such as a colonoscopy).

It may take up to 48 hours before you have a bowel movement after taking lactulose.

Stop using lactulose and call your doctor at once if you have severe or ongoing diarrhea.

The liquid form of lactulose may become slightly darker in color, but this is a harmless effect. However, do not use the medicine if it becomes very dark, or if it gets thicker or thinner in texture.

If you use lactulose over a long period of time, your doctor may want you to have occasional blood tests. Do not miss any scheduled appointments.

What should I discuss with my healthcare provider before taking lactulose?

You should not use this medication if you are on a special diet low in galactose (milk sugar).

To make sure you can safely take lactulose, tell your doctor if you have other medical conditions, especially:

if you need to have any type of intestinal test using a scope (such as a colonoscopy).

FDA pregnancy category B. This medication 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 lactulose 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 lactulose?

Take exactly as prescribed by your doctor. Do not take in larger or smaller amounts or for longer than recommended. Follow the directions on your prescription label.

Measure liquid medicine with a special dose-measuring spoon or cup, not a regular table spoon. If you do not have a dose-measuring device, ask your pharmacist for one.

The liquid form of lactulose may become slightly darker in color, but this is a harmless effect. However, do not use the medicine if it becomes very dark, or if it gets thicker or thinner in texture.

Lactulose powder should be mixed with at least 4 ounces of water. You may also use fruit juice or milk to make the medication taste better.

It may take up to 48 hours before you have a bowel movement after taking lactulose.

If you use lactulose over a long period of time, your doctor may want you to have occasional blood tests. Do not miss any scheduled appointments.

Store lactulose at room temperature away from moisture and heat.

What happens if I miss a dose?

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

What happens if I overdose?

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

Overdose symptoms may include confusion, uneven heart rate, extreme thirst, increased urination, leg discomfort, and muscle weakness or limp feeling.

What should I avoid while taking lactulose?

Avoid using antacids without your doctor's advice. Use only the type of antacid your doctor recommends. Some antacids can make it harder for your body to absorb lactulose.

Lactulose side effects

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

Stop using lactulose and call your doctor at once if you have severe or ongoing diarrhea.

Less serious side effects may include:

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 lactulose?

There may be other drugs that can interact with lactulose. 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.

More about Generlac (lactulose)

Consumer resources

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Related treatment guides

Where can I get more information?

Your pharmacist can provide more information about lactulose.

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

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

Copyright 1996-2012 Cerner Multum, Inc. Version: 2.01. Revision Date: 2012-09-11, 1:35:03 PM.

Drug Status

Article Page, Zantidon

Ranitidine

Richard Jewell

University of Southampton School of Medicine, Southampton, UK

Available online 8 January 2008.

Ranitidine is a competitive histamine H 2 receptor antagonist, used clinically for the treatment of peptic ulceration …

Name of the Clinical Form

Related Names Source: EMTREE

Aciloc; Acloral; Aducin; AH-19065; Alquen; Antagon; Antagonin; Antak; Alter-H 2 ; Alvidina; Anistal; Antanidina; Apozan; Apoprin; Artonil; Ausran; Avintac; Azantac; Azuranit; Baroxal; Cauteridol; Coralen; Credaxol; d 14951; Danitin; Denulcer; Digestosan; Dinaxin; EINECS266-332-5; Esofex; Fagus; Galidrin; Gastran; Gastrec; Gastridina; Gastrolav; Gastrulcer; Gasyran; Histac; Histak; HSDB 3925; Indigestion Relief; Inside; Iqfadina; Katalem; Kuracid; Label; Lake; Logat; Lumaren; Melfax; Meticel; Microdit; Microtid; Neugal; Noctone; Novo-Ranidine; Nu-Rantit; Pep-Rani; Peptic Relief; Ppetab; Pertifar; Quantor; Quardin; Radan; Radine; Radyn; Ran; Ran H2; Ranacid; Ranaps; Ranepal; Rani; Rani 2; Raniben; Raniberi; Ranibeta; Ranibloc; Ranic; Ranicodan; Ranicur; Ranicux; Ranidil; Ranidin; Ranidine; Ranidura; Ranidura T; Ranifarma; Ranifur; Ranigast; Ranihexal; Ranikur; Ranil; Ranilonga; Ranimed; Ranimerck; Ranimex; Rani-nerton; Raniplex; Raniprotect; Rani-Q; Ranisan; Ranisen; Ranitic; Ranitidina; Ranitidine; Ranitidine hydrochloride; Ranitidinum; Ranitil; Ranitine; Ranivel; Ranix; Ranixal; Ran Lich; Ranoxyl; Rantec; Ranteen; Ranuber; Ranulin; Ranzil; Rantag; Ratic; Ratica; Raudil; Redacid; Regalil; Rubiulcer; Serranit; Serviradine; Simetac; Sinhcloran; Sirani; Sostril; Stacer; Suronit; Syntidine; Tanidina; Taural; Terposen; Toriol; Trigger; Ulcaid; Ulcecur; Ulcedin; Ulceran; Ulcerol; Ulcex; Ulcidine; Ulcirex; Ulcolind Rani; Ulcoren; Ulcocur; Ulkodin; Ulsal; Ulsavin; Ultidine; Ultran; Xanidine; Zadine; Zaedoc; Zanidex; Zanidin; Zanamet; Zantab; Zantac; Zantac 75; Zantic; Zantidon; Zendhin; Zerandin; Zidac; Zinetac; Zoran; Zylium; Zantac (trade); aciloc; ah 19065; ah19065; antagonin; azantac; baroxal; coralen; d14951; gastran; histac; lumaren; n [2 [[5 [(dimethylamino)methyl]furfuryl]thio]ethyl] n' methyl 2 nitro 1,1 ethenediamine; ranidil; ranidura; ranigast; raniplex; ranisan; ranitidin; ranitidine hydrochloride; ranitine; ranuber; retamin; sostril; toriol; ulceran; ulcocur; ulsal; ultidine; zantac; zantac 75; zantic; zinetac

N-[2-[[[-5-[(Dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]-N'-methyl-2-nitro-1,1-ethenediaminehydrochloride; n [2 [[5 [(dimethylamino)methyl]furfuryl]thio]ethyl] n' methyl2 nitro 1,1 ethenediamine; NN-Dimethyl-5-[2-(1-methylamino-2-nitrovinylamino)ethylthiomethyl]furfurylamine

Preis Rosalox - $, Rosalox

Flagyl ER is used for treating certain bacterial infections of the vagina (bacterial vaginosis). Flagyl ER is an oral antiprotozoal and antibacterial. It is thought to work by entering the bacterial cell, acting on some components of the cell, and destroying the bacteria.

Use Flagyl ER as directed by your doctor.

Take Flagyl ER by mouth on an empty stomach at least 1 hour before or 2 hours after eating.

Swallow Flagyl ER whole. Do not break, crush, or chew before swallowing.

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

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

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

Store Flagyl ER at 77 degrees F (25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Flagyl ER out of the reach of children and away from pets.

Active Ingredient: Metronidazole.

Do NOT use Flagyl ER if:

you are allergic to any ingredient in Flagyl ER or to another nitroimidazole (eg, tinidazole)

you are in the first trimestr of pregnancy

you are taking busulfan, an ergot alkaloid (eg, ergotamine), or you have taken disulfiram within the past 2 weeks

you are taking an HIV protease inhibitor that contains alcohol (eg, amprenavir solution); check with your pharmacist if you are unsure if the medicine contains alcohol

you drink alcohol.

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

Some medical conditions may interact with Flagyl ER. 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 nerve, brain, or blood problems; Crohn disease; or a history of liver problems or seizures.

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

Disulfiram because side effects, such as mental or mood changes, may occur

Amiodarone because the risk of irregular heartbeat may be increased

Barbiturates (eg, phenobarbital) or phenytoin because they may decrease Flagyl ER's effectiveness

Anticoagulants (eg, warfarin), busulfan, cyclosporine, ergot alkaloids (eg, ergotamine), HIV protease inhibitors containing alcohol (eg, amprenavir solution ), lithium, or macrolide immunosuppressants (eg, tacrolimus) because the risk of their side effects may be increased by Flagyl ER.

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

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

Do not drink alcohol while you are taking Flagyl ER and for at least 3 days after the last dose.

Contact your doctor right away if stomach pain or cramps, severe diarrhea, or bloody stools occur. Do not treat diarrhea without first checking with your doctor.

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

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

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

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

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

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

Flagyl ER 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 Flagyl ER while you are pregnant. Do not use Flagyl ER in the first 3 months of pregnancy. Flagyl ER is found in breast milk. Do not breastfeed while taking Flagyl ER.

Buy Akne Bp - Benzoyl, Peroxide - Online Without Prescriptions, Akne Bp

Benzac (Akne bp)

Benzoyl peroxide has an antibacterial effect. It also has a mild drying effect, which allows excess oils and dirt to be easily washed away from the skin.

Use 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. Wash your hands before and after applying this medication. Shake the lotion well just before each use.

Clean and pat dry the skin to be treated. Apply benzoyl peroxide in a thin layer and rub in gently. Do not cover the treated skin area unless your doctor has told you to.

Benzoyl peroxide topical is usually applied one to three times daily. Follow your doctor's instructions.

Benzoyl peroxide may bleach hair or fabrics. Avoid allowing this medication to come into contact with your hair or clothing.

It may take several weeks before your symptoms improve. Keep using the medication as directed and tell your doctor if your symptoms do not improve.

If you miss a dose - use the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not use extra medicine to make up the missed dose.

Store this medicine at room temperature in a tightly-closed container, away from heat and light.

Avoid getting this medication in your mouth or eyes. If it does get into any of these areas, rinse with water. Do not use benzoyl peroxide topical on sunburned, windburned, dry, chapped, irritated, or broken skin. Also avoid using benzoyl peroxide topical on wounds or on areas of eczema. Wait until these conditions have healed before using this medication.

Avoid using skin products that can cause irritation, such as harsh soaps, shampoos, or skin cleansers, hair coloring or permanent chemicals, hair removers or waxes, or skin products with alcohol, spices, astringents, or lime. Do not use other medicated skin products unless your doctor has told you to.

Do not use benzoyl peroxide topical while you are also using tretinoin (Altinac, Avita, Renova, Retin-A, Tretin-X). Using these medications together could cause severe skin irritation. FDA pregnancy category C. It is not known whether benzoyl peroxide topical will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medication. It is not known whether benzoyl peroxide 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.

Benzoyl peroxide may bleach hair or fabrics. Avoid allowing this medication to come into contact with your hair or clothing.

Do NOT use Benzac if you are allergic to any ingredient in Benzac.

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

Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Stop using benzoyl peroxide and call your doctor at once if you have severe stinging or burning of your skin.

Less serious side effects may include:

mild stinging or burning;

itching or tingly feeling;

skin dryness, peeling, or flaking; or

redness or other irritation.

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects.

Customers who bought this product also bought

Nitrolingual, Nitrolingual Duo Pack, Nitromist, Nitrostat, Nitro-Time (Nitroglycerin (Oral, Nitro-Ti

Brand Names: Nitrolingual, Nitrolingual Duo Pack, Nitromist, Nitrostat, Nitro-Time

Generic Name: nitroglycerin (oral/sublingual) (Pronunciation: NYE troe GLI ser in (OR al/sub LIN gwal))

What is nitroglycerin (Nitrolingual, Nitrolingual Duo Pack, Nitromist, Nitrostat, Nitro-Time)?

Nitroglycerin is in a group of drugs called nitrates. Nitroglycerin dilates (widens) blood vessels, making it easier for blood to flow through them and easier for the heart to pump.

Nitroglycerin is used to treat or prevent attacks of chest pain (angina ).

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

Nitroglycerin 2.5 mg ER_EON

clear/purple, imprinted with E5174

Nitroglycerin 2.5 mg-ETH

clear/purple, imprinted with ETHEX, 004

Nitroglycerin 6.5 mg ER-EON

blue/yellow, imprinted with E1235

Nitroglycerin 6.5 mg-ETH

blue/yellow, imprinted with ETHEX, 005

Nitroglycerin 9 mg ER-EON

green/yellow, imprinted with E1217

Nitroglycerin ER 9 mg-ETH

clear, imprinted with ETHEX, 006

Nitroquick 0.3 mg-ETH

oval, white, imprinted with 3, ETH

Nitroquick 0.4 mg-ETH

oval, white, imprinted with 4, ETH

Nitroquick 0.6 mg

oval, white, imprinted with 6, ETH

Nitrostat 0.3 mg

round, white, imprinted with 3, N

Nitrostat 0.4 mg

round, white, imprinted with 4, N

What are the possible side effects of nitroglycerin (Nitrolingual, Nitrolingual Duo Pack, Nitromist, Nitrostat, Nitro-Time)?

Get emergency medical help if you have any of these signs of an allergic reaction: 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:

fast, slow, pounding, or uneven heart rate;

blurred vision or dry mouth;

nausea, vomiting, sweating, pale skin, feeling like you might pass out; or

fever. sore throat. and headache with a severe blistering, peeling, and red skin rash .

Less serious side effects may include:

mild burning or tingling with the tablet in your mouth;

warmth, redness, or tingly feeling under your skin; or

feeling weak or dizzy.

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 is the most important information I should know about nitroglycerin (Nitrolingual, Nitrolingual Duo Pack, Nitromist, Nitrostat, Nitro-Time)?

Do not use nitroglycerin if you are taking sildenafil (Viagra, Revatio), tadalafil (Cialis), or vardenafil (Levitra). Serious, life-threatening side effects can occur if you take nitroglycerin while you are using sildenafil.

Nitroglycerin can cause severe headaches, especially when you first start using it. These headaches may gradually become less severe as you continue to use nitroglycerin. Do not stop taking the medication. Ask your doctor before using any headache pain medication.

Medical Dictionary

Osteocare Masticabil, Calciu Masticabil

Osteocare masticabil

Osteocare masticabil - 30 tablete masticabile

Aroma naturala de portocala si menta.

Osteocare masticabil este un supliment alimentar. Osteocare masticabil nu trebuie sa inlocuiasca un regim alimentar variat si echilibrat.

Mod de administrare:

copii (4-12 ani) 1 tableta pe zi

adulti 1 tableta de 2 ori pe zi

A nu se administra copiilor sub 4 ani! Aceste tablete masticabile nu sunt concepute pentru a putea fi inghitite intregi. A nu se depasi doza zilnica recomandata. Ingrediente: carbonat de calciu, hidroxid de magneziu, dextroza, zaharoza, arome: naturala de portocala (accelerator: maltodextrina, antioxidant: acetat de d-alfa tocoferol*) si menta, agenti de ingrosare: acid stearic, dioxid de siliciu si stearat de magneziu, oxid de zinc, borat de sodiu, sulfat de cupru, vitamina D(colecalciferol, [acceleratori: guma arabica, zaharoza, amidon de porumb, lant mediu de trigliceride, antioxidant: DL-alpha tocoferol]), sulfat de magneziu, indulcitori:sucraloza, selenat de sodiu. *din Soia

Contine zahar si indulcitori. A nu se consuma daca aveti alergie la soia.

Nu contine: gluten, lactoza, sare, colorant sau conservant artificial.

Produsul nu este testat pe animale.

A nu se lasa la indemana copiilor.

A se consuma de preferinta, inaintea datei de: vezi cutie

Produs notificat la Ministerul Sanatatii (nr 1870 / 07.06.2012) Producator: VitabioticsLtd, Anglia

Importator/Distribuitor: Vavian Pharma, Romania, Bucuresti, B-dul Basarabia nr.256, sector 3.Tel 021-317.2505, www. vavianpharma. ro, office@vavianpharma. ro

Septra (Trimethoprim And Sulfamethoxazole) Side Effects, Interactions, Warning, Dosage & Uses, Sertr

To reduce the development of drug-resistant bacteria and maintain the effectiveness of SEPTRA and other antibacterial drugs, SEPTRA should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria.

DRUG DESCRIPTION

SEPTRA (trimethoprim and sulfamethoxazole) is a synthetic antibacterial combination product. Each SEPTRA Tablet contains 80 mg trimethoprim and 400 mg sulfamethoxazole and the inactive ingredients docusate sodium (0.4 mg per tablet), FD&C Red No. 40, magnesium stearate, povidone, and sodium starch glycolate.

Each SEPTRA DS (double strength) Tablet contains 160 mg trimethoprim and 800 mg sulfamethoxazole and the inactive ingredients docusate sodium (0.8 mg per tablet), FD&C Red No. 40, magnesium stearate, povidone, and sodium starch glycolate.

Each teaspoonful (5 mL) of SEPTRA Suspension contains 40 mg trimethoprim and 200 mg sulfamethoxazole and the inactive ingredients alcohol 0.26%, methylparaben 0.1% and sodium benzoate 0.1% (added as preservatives), carboxymethylcellulose sodium, citric acid, FD&C Red No. 40 and Yellow No. 6, flavor, glycerin, microcrystalline cellulose, polysorbate 80, saccharin sodium, and sorbitol. Each teaspoonful (5 mL) of SEPTRA Grape Suspension contains 40 mg trimethoprim and 200 mg sulfamethoxazole and the inactive ingredients alcohol 0.26%, methylparaben 0.1%, and sodium benzoate 0.1% (added as preservatives), carboxymethylcellulose sodium, citric acid, FD&C Red No. 40 and Blue No. 1, flavor, glycerin, microcrystalline cellulose, polysorbate 80, saccharin sodium, and sorbitol. Both tablet and suspension forms are for oral administration.

Trimethoprim is 5-[(3,4,5-trimeth-oxyphenyl)methyl]-2,4- pyrimidinediamine. It is a white to light yellow, odorless, bitter compound with a molecular weight of 290.32, and the molecular formula C 14 H 18 N 4 O 3 . The structural formula is:

Sulfamethoxazole is 4-amino-N-(5-methyl-3-isoxazolyl)benzenesulfonamide. It is an almost white, odorless, tasteless compound with a molecular weight of 253.28, and the molecular formula C 10 H 11 N 3 O 3 S. The structural formula is:

What are the possible side effects of sulfamethoxazole and trimethoprim?

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

Call your doctor at once if you have a serious side effect such as:

diarrhea that is watery or bloody;

fever, chills, swollen glands, body aches, flu symptoms, sores in your mouth and throat;

new or worsening cough;

pale skin, feeling light-headed, rapid heart rate, trouble concentrating;

easy bruising, unusual bleeding (nose, mouth, vagina, or rectum), purple or red.

What are the precautions when taking trimethoprim and sulfamethoxazole (Septra)?

Before taking sulfamethoxazole with trimethoprim, tell your doctor or pharmacist if you are allergic to sulfa medications or trimethoprim; or if you have any other allergies. This product may contain inactive ingredients, which can cause allergic reactions or other problems. Talk to your pharmacist for more details.

Before using this medication, tell your doctor or pharmacist your medical history, especially of: kidney disease, liver disease, certain blood disorders (such as porphyria, anemia due to folate vitamin deficiency), history of blood disorders caused by trimethoprim or sulfa medications, vitamin deficiency (folate or folic acid), severe allergies, asthma, decreased bone marrow function (bone marrow suppression), a certain metabolic disorder (G6PD deficiency).

Last reviewed on RxList: 10/30/2013 This monograph has been modified to include the generic and brand name in many instances.

Ther - News And Analysis, Ther

Theranos halts new Zika test

SA Editor Yoel Minkoff

• SA Editor Yoel Minkoff

In yet another setback for Theranos (Private:THER ), the company withdrew its request for emergency clearance of a Zika-virus blood test after federal regulators found it didn't include proper patient safeguards, WSJ reports .

Meanwhile, Singapore has confirmed another 26 locally-transmitted Zika cases, bringing the total to 82, with some new victims being identified outside of the previously-affected areas.

Theranos to appeal CMS sanctions

08/26/16 • SA Editor Douglas W. House

• SA Editor Douglas W. House

Embattled blood testing start-up Theranos (Private:THER ) announces that it intends to appeal the CMS sanctions on its Newark, CA lab. It says it has made substantial progress in correcting the deficiencies cited including installing new lab leadership, beefing up its clinical policies and procedures and retooling its training programs. Patient testing at the site has been suspended as dictated by the regulator.

Previously: Theranos founder Holmes banned from lab business for two years (July 8)

Theranos presents new product plans

08/02/16 • SA Editor Yoel Minkoff

• SA Editor Yoel Minkoff

Embattled Theranos (Private:THER ) founder Elizabeth Holmes announced a new blood-testing device at an academic conference on Monday, but didn’t address issues found with the company's earlier machines as it wasn't the "appropriate" forum to discuss the problems.

Theranos' new device, called miniLab, can run a broad range of blood tests on a single desktop machine, including a diagnostic for the Zika virus.

Previously: Theranos looks to to restore credibility (Aug. 01 2016)

Theranos looks to to restore credibility

08/01/16 • SA Editor Yoel Minkoff

• SA Editor Yoel Minkoff

Theranos (Private:THER ) founder Elizabeth Holmes is scheduled to speak today at the annual meeting of the AACC in Philadelphia, where she is expected to share the first data about the secretive company's technology.

Government regulators have already barred Holmes from owning or operating a clinical laboratory for two years and Walgreens recently closed the Theranos testing centers in its drugstores.

Theranos employees not immune to Holmes' spin

07/11/16 • SA Editor Douglas W. House

• SA Editor Douglas W. House

Theranos (Private:THER ) Founder and CEO Elizabeth Holmes' relentless sales pitch about the supposed wondrous progress of the company's technology now extends to company employees. According to a report by the Wall Street Journal . Ms. Holmes made a presentation to staffers last month during which she said the company has developed 304 tests for use on its Edison device despite the fact that most of these experiments haven't progressed beyond laboratory research. An unnamed attendee said her egregious spin and tightly controlled secrecy has further eroded trust between her and the people working there.

The company is mired in lawsuits related to its botched lab operations and failure to address the problems cited by regulators. Ms. Holmes was recently barred from owning or operating a clinical lab for two years.

Despite the avalanche of problems, she remains undeterred. She recently hired Academy Award-winning director Errol Morris to film videos of herself and others for the company's website. In a presentation at a tech conference last month, she took issue with the Journal's reporting, calling it "inaccurate" with elements taken "completely out of context." She is also supposedly talking with Jason Blum, executive producer of HBO's "The Jinx: The Life and Deaths of Robert Durst," about a documentary on her life and career.

Theranos founder Holmes banned from lab business for two years

07/08/16 • SA Editor Douglas W. House

• SA Editor Douglas W. House

The fall-out for troubled diagnostics upstart Theranos (Private:THER ) has almost run its course. The U. S. Centers for Medicare & Medicaid Services (CMS) has notified founder Elizabeth Holmes that she has been banned from owning or operating a diagnostic laboratory for two years. In addition, the company has been fined an undisclosed amount and has lost its eligibility to receive payments from federal health insurance programs for lab services due to losing its CLIA certification (all specialties except hematology) for its Newark, CA lab.

The revocation will not take effect for 60 days, but patient testing at Newark will cease immediately. All work will be performed at its Arizona facility until the issues with CMS are resolved.

Update . On August 25, the company announced that it will appeal the CMS sanctions on its Newark lab.

Walgreens formally ends Theranos relationship

06/12/16 • SA Editor Stephen Alpher

• SA Editor Stephen Alpher

With regulators circling Theranos (Private:THER ), Walgreens (NASDAQ:WBA ) announces its intention to terminate its relationship with the blood-testing startup, and immediately close all 40 Theranos Wellness Centers at its stores.

It's yet another blow to Theranos, as those centers are the company's primary source of revenue.

WSJ: Craving growth, Walgreens dismissed doubts about Theranos

05/26/16 • SA Editor Stephen Alpher

• SA Editor Stephen Alpher

Walgreens (NASDAQ:WBA ) made a deal including plans to put Theranos (Private:THER ) blood-testing centers in thousands of its stores despite never fully validating the startup's technology, according to a WSJ report .

Before announcing the deal in 2013, some Walgreens executives and outside advisors had their doubts, but when pushed for answers, Theranos - in a way that went beyond Silicon Valley's endemic secrecy - provided few answers. Nevertheless, Walgreens moved forward anyway, in part because management felt Theranos might choose a different drugstore chain partner.

Walgreens doesn't expect to recoup any of its at least $50M investment in Theranos.

Theranos voids two years of Edison blood test results

05/19/16 • SA Editor Yoel Minkoff

• SA Editor Yoel Minkoff

Troubled biotech startup Theranos (Private:THER ) has told federal health regulators that it voided two years of results from the blood tests that it once staked its future on, WSJ reports .

All results taken from its Edison blood-testing devices in 2014 and 2015 were thrown out and updated reports sent to doctors.

The Edison blood test was considered disruptive because they relied on a drop of blood from a finger prick, and was one of the main reasons Theranos achieved a $9B valuation in 2014.

Theranos expands board, reorganizes structure; COO retiring

05/11/16 • Jason Aycock

Theranos (Private:THER ) tonight says it's expanding its board by three members, and that President and Chief Operating Officer Sunny Balwani is retiring, adding yet another executive spot to fill.

The company is also reorganizing to create dedicated units for Technology and Clinical Operations.

Dr. Fabrizio Bonanni, a veteran of Amgen and Baxter International, is joining the board and working in a special capacity with management as it looks to expand its executive team.

Dr. William Foege (formerly of CDC) and Richard Kovacevich (former Wells Fargo CEO) are joining the board from Theranos' Board of Counselors.

Now read Study Throws Down The Gauntlet To Theranos »

Theranos under investigation by SEC, U. S. attorneys

04/18/16 • Jason Aycock

Blood-testing start-up Theranos (Private:THER ) says it's being probed by the SEC as well as U. S. attorneys -- a criminal investigation that is following up on previous additional scrutiny from healthcare regulators.

The company acknowledged the investigations in a memo it gave to partner firms, including Walgreens Boots Alliance.

The agencies are seeking documents and Theranos is cooperating fully, it says, adding that previous inquiries by the FDA and state health departments in Pennsylvania and California are closed.

In March, a Centers for Medicare and Medicaid Services report found that the company's blood-testing devices failed to meet Theranos' own standards for accuracy. This week, the agency said it's pursuing a two-year ban for founder Elizabeth Holmes from owning or operating a clinical lab.

Now read Study Throws Down The Gauntlet To Theranos »

Report: Theranos tests failed company's own accuracy standards

03/31/16 • Jason Aycock

A government report has found that the Edison blood-testing devices of Theranos (Private:THER ) failed to meet the company's own standards for accuracy on a range of tests.

The full report, reviewed by The Wall Street Journal, shows the first outside look at Theranos' own performance records for its proprietary testing devices. Centers for Medicare and Medicaid Services inspected the company's lab in Newark, Calif. last fall to generate the new report.

Erratic quality-control tests were frequent in July 2014, and from February 2015 to June 2015, the report said. In February 2015, a test to measure a hormone that affects testosterone levels failed 87% of checks.

Inspectors cited the lab for doing tests with unqualified personnel, storing blood samples at incorrect temperatures, and delaying notifying patients of flawed results. Theranos has submitted a "plan of correction," but CMS reportedly finds the plan inadequate and expects to impose sanctions on the company.

On Monday, a study from Mount Sinai Hospital found Theranos results to be highly abnormal compared to competitors.

Now read Study Throws Down The Gauntlet To Theranos »

Study Throws Down The Gauntlet To Theranos

03/29/16 • EP Vantage

Vitaxicam, Vitaxicam

Vitaxicam

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

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Piroxicam

Click for further information on drug naming conventions and International Nonproprietary Names .

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

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Buy Lidomex Kowa Online Without Prescriptions, Lidomex Kowa

Prednisolone is used for treating allergies, arthritis, breathing problems (eg, asthma), certain blood disorders, collagen diseases (eg, lupus), certain eye diseases (eg, keratitis), cancer (eg, leukemia), endocrine problems (eg, adrenocortical insufficiency), intestinal problems (eg, ulcerative colitis), swelling due to certain conditions, or skin conditions (eg, psoriasis). Prednisolone is a corticosteroid. It works by modifying the body's immune response to various conditions and decreasing inflammation.

Use Prednisolone as directed by your doctor.

Take Prednisolone by mouth with food.

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

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

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

Do NOT use Prednisolone if:

you are allergic to any ingredient in Prednisolone

you have a systemic fungal infection, a certain type of malaria, inflammation of the optic nerve, or herpes infection of the eye

you are scheduled to have a live or attenuated live vaccination (eg, smallpox)

you are taking mifepristone.

Contact your doctor right away if any of these apply to you.

Some medical conditions may interact with Prednisolone. 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 heart problems (eg, congestive heart failure), heart attack, high blood pressure, kidney problems, liver problems, diabetes, seizures, an underactive thyroid, adrenal gland problems, fluid retention (eg, swelling of the hands, ankles, or feet), or any mental or mood problems

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

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

if you have any stomach problems (eg, ulcers), intestinal problems (eg, blockage, perforation, or 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 a recent vaccination (eg, smallpox).

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

Clarithromycin, cyclosporine, estrogens (eg, estradiol), oral contraceptives (eg, birth control pills), or ketoconazole because they may increase the risk of Prednisolone's side effects

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

Anticholinesterases (eg, pyridostigmine), aspirin, diuretics (eg, hydrochlorothiazide, furosemide), methotrexate, mifepristone, quinolone antibiotics (eg, ciprofloxacin), ritodrine, or live or attenuated live vaccines because the risk of their side effects may be increased by Prednisolone

Anticoagulants (eg, warfarin), hydantoins (eg, phenytoin), or killed or inactivated vaccines because their effectiveness may be decreased by Prednisolone.

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

Avoid alcohol while you are using Prednisolone.

Prednisolone 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.

If you are taking Prednisolone regularly over a long period of time, carry an ID card at all times that says you take Prednisolone.

Do not receive a live vaccine (eg, measles, mumps, smallpox) while you are taking Prednisolone. Talk with your doctor before you receive any vaccine.

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

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

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

Caution is advised when using Prednisolone in children; they may be more sensitive to its effects.

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

Pregnancy and breast-feeding: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Prednisolone while you are pregnant. Prednisolone is found in breast milk. If you are or will be breast-feeding while you use Prednisolone, check with your doctor. Discuss any possible risks to your baby.

If you are on long-term or high dosage therapy and you suddenly stop taking Prednisolone, you may have withdrawal symptoms, including fever, vomiting, appetite loss, diarrhea, nausea, dizziness, weight loss, weakness, general body discomfort, joint or muscle pain.

Buy Hakuserin - Clotrimazole - Online Without Prescriptions, Hakuserin

Mycelex-g (Hakuserin)

Mycelex-G (Clotrimazole) is an antifungal medication. It prevents fungus from growing.

Clotrimazole vaginal is used to treat vaginal candida (yeast) infections.

Clotrimazole vaginal may also be used for purposes other than those listed in this medication guide.

Use Mycelex-G exactly as directed by your doctor, or follow the directions that accompany the package. If you do not understand these instructions, ask your pharmacist, nurse, or doctor to explain them to you.

Wash your hands before and after using this medication.

Insert the tablet, suppository, or cream into the vagina using the applicator as directed.

Use this medication continuously for the prescribed amount of time, even during your menstrual period.

You can use a sanitary napkin to prevent the medication from staining your clothing but do not use a tampon.

If the infection does not clear up after you have finished one course of therapy, or if it appears to get worse, see your doctor. You may have another type of infection.

Avoid getting this medication in your eyes, nose, or mouth. Store clotrimazole vaginal at room temperature away from moisture and heat.

Active ingredient: Clotrimazole

Clotrimazole is an antifungal medication. It prevents fungus from growing.

Clotrimazole vaginal is used to treat vaginal candida (yeast) infections.

It also may be used for purposes other than those listed in this medication guide.

Do not use clotrimazole vaginal if you have ever had an allergic reaction to it.

If this is the first time that you have ever had symptoms of a vaginal yeast infection, consult your doctor before using this medication.

Do not use clotrimazole vaginal if you have a fever, abdominal pain, foul-smelling discharge, diabetes, HIV, or AIDS. Consult your doctor. Do not use this medication without first talking to your doctor if you are pregnant. Do not use clotrimazole vaginal without first talking to your doctor if you are breast-feeding a baby. Do not use this medication if you are younger than 12 years of age.

Important safety information

Use this medication for the full amount of time prescribed by your doctor or recommended in the package even if you begin to feel better. Your symptoms may improve before the infection is completely healed.

Avoid wearing tight-fitting, synthetic clothing (e. g. panty hose) that does not allow air circulation. Wear loose-fitting clothing made of cotton and other natural fibers until the infection is healed. Avoid getting this medication in your eyes, nose, or mouth.

Stop using clotrimazole vaginal and seek emergency medical attention if you experience an allergic reaction (shortness of breath; closing of your throat; swelling of your lips, face, or tongue; or hives).

Other, less serious side effects may be more likely to occur. These include burning, itching, irritation of the skin, and an increased need to urinate.

Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome.

Avoid using other vaginal creams or douches at the same time as clotrimazole unless your doctor approves.

Drugs other than those listed here may also interact with clotrimazole vaginal. Talk to your doctor and pharmacist before taking any prescription or over the counter medicines.

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Diavista-M Drug & Pharmaceuticals, Diavista

Medication: Diavista-M

Diavista-M consists of Metformin . Pioglitazone .

Metformin - Diavista-M (Metformin) is a biguanide antihyperglycemic agent used for treating non-insulin-dependent diabetes mellitus (NIDDM). It improves glycemic control by decreasing hepatic glucose production, decreasing glucose absorption and increasing insulin-mediated glucose uptake. Diavista-M (Metformin) is the only oral antihyperglycemic agent that is not associated with weight gain. Diavista-M (Metformin) may induce weight loss and is the drug of choice for obese NIDDM patients. When used alone, Diavista-M (Metformin) does not cause hypoglycemia; however, it may potentiate the hypoglycemic effects of sulfonylureas and insulin. Its main side effects are dyspepsia, nausea and diarrhea. Dose titration and/or use of smaller divided doses may decrease side effects. Diavista-M (Metformin) should be avoided in those with severely compromised renal function (creatinine clearance < 30 ml/min), acute/decompensated heart failure, severe liver disease and for 48 hours after the use of iodinated contrast dyes due to the risk of lactic acidosis. Lower doses should be used in the elderly and those with decreased renal function. Diavista-M (Metformin) decreases fasting plasma glucose, postprandial blood glucose and glycosolated hemoglobin (HbA1c) levels, which are reflective of the last 8-10 weeks of glucose control. Diavista-M (Metformin) may also have a positive effect on lipid levels.

Indication: For use as an adjunct to diet and exercise in adult patients (18 years and older) with NIDDM. May also be used for the management of metabolic and reproductive abnormalities associated with polycystic ovary syndrome (PCOS).

Diavista-M (Metformin) is an oral antihyperglycemic agent that improves glucose tolerance in patients with NIDDM, lowering both basal and postprandial plasma glucose. Diavista-M (Metformin) is not chemically or pharmacologically related to any other class of oral antihyperglycemic agents. Unlike sulfonylureas, Diavista-M (Metformin) does not produce hypoglycemia in either patients with NIDDM or healthy subjects and does not cause hyperinsulinemia. Diavista-M (Metformin) does not affect insulin secretion.

Pioglitazone - Diavista-M (Pioglitazone) is used for the treatment of diabetes mellitus type 2. Diavista-M (Pioglitazone) selectively stimulates nuclear receptor peroxisone proliferator-activated receptor gamma (PPAR-gamma). It modulates the transcription of the insulin-sensitive genes involved in the control of glucose and lipid metabolism in the lipidic, muscular tissues and in the liver.

Indication: Treatment of Type II diabetes mellitus

Diavista-M (Pioglitazone), a member of the drug group known as the thiazolidinediones or "insulin sensitizers", is not chemically or functionally related to the alpha-glucosidase inhibitors, the biguanides, or the sulfonylureas. Diavista-M (Pioglitazone) targets insulin resistance and, hence, is used alone or in combination with insulin, metformin, or asulfonylurea as an antidiabetic agent.

Pharmaceutical active ingredients containing related brand and generic drugs, medications or other health care products:

Diavista-m available forms, composition, doses:

Norofulvin Equine Paste 70g - Vet Meds Online, Norofulvin

Norofulvin equine paste 70g

Oral treatment of ringworm for equines, A white viscous paste containing 33.3% w/w Griseofulvin Ph. Eur. in a 70g dial-a-dose syringe. Norofulvin Equine Paste is an oral antifungal antibiotic effective in the treatment of ringworm in horses.

A white viscous paste containing 33.3% w/w Griseofulvin Ph. Eur. in a 70g dial-a-dose syringe. Norofulvin Equine Paste is an oral antifungal antibiotic effective in the treatment of ringworm in horses caused by Trichophyton and Microsporum spp. After absorption from the gastro-intestinal tract the antifungal antibiotic is concentrated in the newly formed keratin enabling the cells of the skin and hair to resist fungal attack.

For oral administration using a dial-a-dose syringe, 10 mg Griseofulvin/kg bodyweight daily for 7 consecutive days. The following is the dosing regimen recommended for each of the 7 days dosing period. LIVEWEIGHT DOSE (Expressed as no. of dial turns) Horses 150 kg 1 300 kg 2 450 kg 3 600 kg 4 Where the animals weight is other than above weight, ?, ?, or ? turns of the dial may be given where appropriate. PROPHYLACTIC ADMINISTRATION OF NOROFULVIN EQUINE PASTE IS ADVISABLE FOR IN-CONTACT ANIMALS ONLY.

Concurrent administration of substances such as Phenylbutazone and sedatives which induce drug-metabolizing enzymes may result in impaired efficacy of Norofulvin. Norofulvin is not recommended for use in pregnant mares. Do not use in horses intended for human consumption. Other systemic fungal infections including Candida albicans and Aspergillis spp do not respond to Griseofulvin therapy. Norofulvin Equine Paste must not be handled by women of child bearing potential. Protective gloves should be worn when using this product. Take care to avoid skin contact. In the case of skin contact wash affected area thoroughly. If irritation occurs/persists seek medical advice. Take care to avoid accidental eye contact. In case of accidental eye contact flush thoroughly with clean water and seek medical advice. Ingestion: If accidentally swallowed, seek medical attention and show product label and/or pack insert to the doctor. Wash hands thoroughly after using this product. Dispose of any unused product and empty containers in accordance with guidance from your local waste regulation authority. Do not store above 25?C. Keep out of the reach of children.

POM-V 70g dial-a-dose syringe. Norbrook Laboratories Ltd Vm 02000/4055 The normal seven day course is recommended. Stables occupied by infected horses should be thoroughly disinfected and cleaned; all equipment used during the treatment should also be cleaned and disinfected. These measures will minimize the risk of cross infection.

A white viscous paste containing 33.3% w/w Griseofulvin Ph. Eur. in a 70g dial-a-dose syringe. Norofulvin Equine Paste is an oral antifungal antibiotic effective in the treatment of ringworm in horses caused by Trichophyton and Microsporum spp. After absorption from the gastro-intestinal tract the antifungal antibiotic is concentrated in the newly formed keratin enabling the cells of the skin and hair to resist fungal attack.

For oral administration using a dial-a-dose syringe, 10 mg Griseofulvin/kg bodyweight daily for 7 consecutive days. The following is the dosing regimen recommended for each of the 7 days dosing period. LIVEWEIGHT DOSE (Expressed as no. of dial turns) Horses 150 kg 1 300 kg 2 450 kg 3 600 kg 4 Where the animals weight is other than above weight, ?, ?, or ? turns of the dial may be given where appropriate. PROPHYLACTIC ADMINISTRATION OF NOROFULVIN EQUINE PASTE IS ADVISABLE FOR IN-CONTACT ANIMALS ONLY.

Concurrent administration of substances such as Phenylbutazone and sedatives which induce drug-metabolizing enzymes may result in impaired efficacy of Norofulvin. Norofulvin is not recommended for use in pregnant mares. Do not use in horses intended for human consumption. Other systemic fungal infections including Candida albicans and Aspergillis spp do not respond to Griseofulvin therapy. Norofulvin Equine Paste must not be handled by women of child bearing potential. Protective gloves should be worn when using this product. Take care to avoid skin contact. In the case of skin contact wash affected area thoroughly. If irritation occurs/persists seek medical advice. Take care to avoid accidental eye contact. In case of accidental eye contact flush thoroughly with clean water and seek medical advice. Ingestion: If accidentally swallowed, seek medical attention and show product label and/or pack insert to the doctor. Wash hands thoroughly after using this product. Dispose of any unused product and empty containers in accordance with guidance from your local waste regulation authority. Do not store above 25?C. Keep out of the reach of children.

POM-V 70g dial-a-dose syringe. Norbrook Laboratories Ltd Vm 02000/4055 The normal seven day course is recommended. Stables occupied by infected horses should be thoroughly disinfected and cleaned; all equipment used during the treatment should also be cleaned and disinfected. These measures will minimize the risk of cross infection.

Ery-Sol Medical Facts From, Erysol

Ery-Sol

What other drugs will affect Ery-Sol (erythromycin topical)?

It is not likely that other drugs you take orally or inject will have an effect on topically applied erythromycin. But many drugs can interact with each other. Tell your doctor about all your prescription and over-the-counter medications, vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start a new medication without telling your doctor.

Where can I get more information?

Your pharmacist can provide more information about erythromycin topical.

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

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

Copyright 1996-2006 Cerner Multum, Inc. Version: 1.06. Revision Date: 04/01/2008 10:44:05 AM.

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Digoxin Dosage Guide With Precautions, Digoxinum

Digoxin Dosage

Usual Pediatric Dose for:

Additional dosage information:

Usual Adult Dose for Congestive Heart Failure

Rapid Digitalization with a Loading Dose : Peak digoxin body stores of 8 to 12 mcg/kg generally provide a therapeutic effect with minimum risk of toxicity in most patients with heart failure and normal sinus rhythm.

The loading dose should be administered in several fractions, with approximately half the total given as the first dose. Additional fractions of the total dose may be given at 6 to 8 hour intervals. Careful assessment of the patient's clinical response should be considered before each additional dose. If the patient's response necessitates a change from the calculated loading dose of digoxin, then calculation of the maintenance dose should be based upon the amount actually given.

Tablets : Initial: 500 to 750 mcg usually produces a detectable effect in 0.5 to 2 hours with a maximal effect in 2 to 6 hours. Additional doses of 125 to 375 mcg may be given at 6 to 8 hour intervals until clinical evidence of an adequate effect is noted. The usual amount of digoxin tablets that a 70 kg patient requires to achieve 8 to 12 mcg/kg peak body stores is 750 to 1250 mcg.

Capsules : Initial: 400 to 600 mcg of digoxin capsules generally produces a detectable effect in 0.5 to 2 hours with a maximal effect in 2 to 6 hours. Additional doses of 100 to 300 mcg may be given cautiously at 6 to 8 hour intervals until clinical evidence of an adequate effect is noted. The usual amount of digoxin capsules that a 70 kg patient requires to achieve 8 to 12 mcg/kg peak body stores is 600 to 1000 mcg.

Injection: Initial: 400 to 600 mcg of digoxin intravenously usually produces a detectable effect in 5 to 30 minutes with a maximal effect in 1 to 4 hours. Additional doses of 100 to 300 mcg may be given cautiously at 6 to 8 hour intervals until clinical evidence of an adequate effect is noted. The usual amount of digoxin injection that a 70 kg patient requires to achieve 8 to 12 mcg/kg peak body stores is 600 to 1000 mcg. The injectable route is frequently used to achieve rapid digitalization, with conversion to digoxin tablets or digoxin capsules for maintenance therapy.

Maintenance Dose : The doses of digoxin tablets used in controlled trials in patients with heart failure have ranged from 125 to 500 mcg once daily. In these studies, the digoxin dose has been generally titrated according to the patient's age, lean body weight, and renal function. Therapy is generally initiated at a dose of 250 mcg once daily in patients under age 70 with good renal function.

Usual Adult Dose for Atrial Fibrillation

Peak digoxin body stores larger than the 8 to 12 mcg/kg required for most patients with heart failure and normal sinus rhythm have been used for control of ventricular rate in patients with atrial fibrillation. Doses of digoxin used for the treatment of chronic atrial fibrillation should be titrated to the minimum dose that achieves the desired ventricular rate control without causing undesirable side effects.

Usual Pediatric Dose for Atrial Fibrillation

Do not give full total digitalizing dose at once. Administer loading doses in several portions, give roughly half the total as the first dose. Give additional fractions of the total dose at 6 to 8 hour intervals (oral) or 4 to 8 hour intervals (parenteral). Divided daily dosing is recommended for infants and young children under 10 years of age.

Parenteral administration should be used only when the need for rapid digitalization is urgent or when the drug cannot be taken orally. Intravenous administration is preferred over intramuscular injection as it can lead to severe pain at the injection site. If it is necessary to administer the drug by the intramuscular route, it should be injected deep into the muscle followed by massage. No more than 500 mcg should be injected into a single site.

Calculated doses should be based on lean body weight.

Premature : Digitalizing (Loading) dose: Oral elixir: 20 to 30 mcg/kg; Intravenous: 15 to 25 mcg/kg Maintenance dose: oral 5 to 7.5 mcg/kg; intravenous 4 to 6 mcg/kg

Full Term : Digitalizing (Loading) dose: Oral elixir: 25 to 35 mcg/kg; Intravenous: 20 to 30 mcg/kg Maintenance dose: oral 6 to 10 mcg/kg; intravenous 5 to 8 mcg/kg

1-24 months : Digitalizing (Loading) dose: Oral elixir: 35 to 60 mcg/kg; Intravenous: 30 to 50 mcg/kg Maintenance dose: 10 to 15 mcg/kg oral; intravenous 7.5 to 12 mcg/kg

3 to 5 years : Digitalizing (Loading) dose: Oral elixir: 30 to 40 mcg/kg; Intravenous: 25 to 35 mcg/kg Maintenance dose: oral 7.5 to 10 mcg/kg; intravenous 6 to 9 mcg/kg

6 to 10 years : Digitalizing (Loading) dose: Oral elixir: 20 to 35 mcg/kg; Intravenous: 15 to 30 mcg/kg Maintenance dose: oral 5 to 10 mcg/kg; intravenous 4 to 8 mcg/kg

11 years and older : Digitalizing (Loading) dose: Oral elixir: 10 to 15 mcg/kg; Intravenous: 8 to 12 mcg/kg Maintenance dose: oral 2.5 to 5 mcg/kg; intravenous 2 to 3 mcg/kg

Renal Dose Adjustments

CrCl <10 mL/min: Loading dose: Generally reduced by 50%. Maintenance dose: Can be administered as 10% to 25% of maintenance dose or the interval increased to every 48 hours.

CrCl 10 to 50 mL/min: Total digitalizing dose: 0.5 to 1 mg (the initial dose is usually one-half of the total digitalizing dose, followed by 1/4 of the digitalizing dose in each of two subsequent doses at 6 and 12 hour intervals). Maintenance dose: 25% to 75% of the normal daily dose or administer normal dose every 36 hours.

In general, a maintenance dose of 125 mcg orally once daily is recommended in patients with impaired renal function, and at a dose of 62.5 mcg is recommended in patients with marked renal impairment. Doses may be increased every 2 weeks according to clinical response.

Because of altered digoxin distribution and elimination, projected peak body stores for patients with renal insufficiency should be conservative (i. e. 6 to 10 mcg/kg).

Liver Dose Adjustments

No adjustment recommended

Dose Adjustments

If patients are switched from intravenous to oral formulations, allowances must be made for differences in bioavailability when calculating maintenance dosages. When changing from oral formulations to IM or IV therapy, dosage should be reduced by 20% to 25%.

Lanoxicaps (gelatin capsules) have greater bioavailability than standard tablets, and the recommended oral doses are only 80% of those for tablets and elixir. Therefore, the 0.2 mg capsule is equivalent to 0.25 mg tablets; the 0.1 mg capsule is equivalent to 0.125 mg tablets; and the 0.05 mg capsule is equivalent to 0.0625 mg. Divided dosage of the capsule formulation is preferred in patients that require a daily dose greater than 300 mcg, those with a previous history of digitalis toxicity, and in patients who may be more likely to become toxic.

Hyperthyroid patients generally require a slightly higher loading dose (10%). Hypothyroid patients generally require a slightly lower loading dose (10%).

Dialysis

Digoxin is not removed by hemo - or peritoneal dialysis.

Other Comments

Calculated doses should be based on lean body weight.

While most patients with signs and symptoms of toxicity have serum digoxin levels greater than 2.0 ng/mL, there is a somewhat poor correlation between levels, effect and toxicity. Therefore, serum level monitoring is usually only recommended to assess patient compliance, to evaluate clinical deterioration following an initially good response, to evaluate unsuspected toxicity, and to assess patients who are at a higher risk of toxicity. Such patients may include individuals with underlying renal or cardiopulmonary disease, thyroid disease, and electrolyte imbalances such as hypokalemia, hypomagnesemia, or hypercalcemia. Patients > 65 years of age are also at higher risk for toxicity. The best time to sample a trough serum digoxin level is just before a dose 7 to 14 days after initiation of therapy. If the patient is also taking quinidine when serum digoxin levels are needed, the blood sample may be drawn just before both drugs are given. A common mistake is checking serum digoxin levels immediately after a loading or maintenance dose. Because digoxin distributes slowly into peripheral tissues over at least 6 hours, assays performed before this period do not indicate steady-state levels.

Intramuscular injection is extremely painful and offers no advantages unless other routes of administration are contraindicated.

A post-hoc analysis of a large study (DIG trial) involving patients with chronic heart failure (HF) receiving long-term digoxin therapy, revealed that discontinuation of digoxin was associated with a significant increase in all-cause hospitalization and hospitalization for HF, but had no effect on all-cause mortality. In contrast, continuation of digoxin at low serum concentrations (0.5 to 0.9 ng/mL) was associated with a reduction in all-cause mortality, all-cause hospitalizations, and hospitalizations for HF. In addition, heart failure guideline recommendations include that if a patient with HF is already receiving digoxin but not an ACEI or beta-blocker, treatment with digoxin should not be discontinued.

Propepsa, Propepsa

Propepsa

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

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Aciclin, Aciclin

Aciclovir

Click for further information on drug naming conventions and International Nonproprietary Names .

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

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Drugs. com Mobile Apps

The easiest way to lookup drug information, identify pills, check interactions and set up your own personal medication records. Available for Android and iOS devices.

Aciclin

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

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Imitrex - Pain Relief, Finigraine

Imitrex is indicated for the acute treatment of migraine attacks with or without aura in adults. Imitrex is a headache medicine that narrows blood vessels around the brain. Imitrex also reduces substances in the body that can trigger headache pain, nausea, sensitivity to light and sound, and other migraine symptoms.

Use Imitrex exactly as prescribed by your doctor. Do not use in larger or smaller amounts or for longer than recommended. Follow the directions on your prescription label. Overuse of migraine headache medicine can actually make your headaches worse.

Use Imitrex as soon as you notice headache symptoms, or after an attack has already begun.

Your doctor may want to give your first dose of this medicine in a hospital or clinic setting to see if you have any serious side effects.

Take one Imitrex tablet whole with a full glass of water. Do not split the tablet.

After taking a tablet: If your headache does not completely go away, or goes away and comes back, take a second tablet two (2) hours after the first. Do not take more than 200 mg of sumatriptan oral tablets in 24 hours. If your symptoms have not improved, contact your doctor before taking any more tablets.

Since Imitrex is used as needed, it does not have a daily dosing schedule. Call your doctor promptly if your symptoms do not improve after using this medicine.

After taking a Imitrex tablet, you must wait two (2) hours before taking a second tablet. Do not take more than 200 mg of sumatriptan tablets in 24 hours.

After using Imitrex nasal spray, you must wait two (2) hours before using a second spray. Do not use more than 40 mg of nasal spray in 24 hours.

Contact your doctor if you have more than four headaches in one month (30 days).

In controlled clinical trials, single doses of 25, 50, or 100 mg of IMITREX Tablets were effective for the acute treatment of migraine in adults. There is evidence that doses of 50 and 100 mg may provide a greater effect than 25 mg.

The choice of dose should therefore be made on an individual basis, weighing the possible benefit of a higher dose with the potential for a greater risk of adverse events.

If the headache returns or the patient has a partial response to the initial dose, the dose may be repeated after 2 hours, not to exceed a total daily dose of 200 mg.

Store Imitrex at room temperature away from moisture, heat, and light.

Do not use Imitrex within 24 hours before or after using another migraine headache medicine, including:

sumatriptan injection, almotriptan (Axert), eletriptan (Relpax), frovatriptan (Frova), naratriptan (Amerge), rizatriptan (Maxalt, Maxalt-MLT), or zolmitriptan (Zomig); or

ergot medicine such as dihydroergotamine (D. H.E. 45, Migranal), ergotamine (Ergomar, Cafergot, Migergot), dihydroergotamine (D. H.E. 45, Migranal), or methylergonovine (Methergine).

Imitrex may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert.

You should not use Imitrex if you are allergic to sumatriptan, or if you have:

coronary heart disease, angina (chest pain), blood circulation problems, lack of blood supply to the heart;

a history of heart disease, heart attack, or stroke, including "mini-stroke";

severe or uncontrolled high blood pressure;

severe liver disease;

ischemic bowel disease; or

a headache that seems different from your usual migraine headaches.

Do not use Imitrex if you have used an MAO inhibitor such as furazolidone (Furoxone), isocarboxazid (Marplan), phenelzine (Nardil), rasagiline (Azilect), selegiline (Eldepryl, Emsam, Zelapar), or tranylcypromine (Parnate) in the last 14 days.

To make sure you can safely use Imitrex, tell your doctor if you have any of these other conditions:

liver disease;

kidney disease;

epilepsy or other seizure disorder;

high blood pressure, a heart rhythm disorder; or

coronary heart disease (or risk factors such as diabetes, menopause, smoking, being overweight, having high cholesterol, having a family history of coronary artery disease, being older than 40 and a man, or being a woman who has had a hysterectomy).

FDA pregnancy category C. It is not known whether Imitrex will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medication. Sumatriptan can pass into breast milk and may harm a nursing baby. Do not breast-feed within 12 hours after using Imitrex. If you use a breast pump during this time, throw out any milk you collect. Do not feed it to your baby. Imitrex should not be given to anyone under 18 or over 65 years of age.

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

feeling of pain or tightness in your jaw, neck, or throat;

chest pain or heavy feeling, pain spreading to the arm or shoulder, nausea, sweating, general ill feeling;

sudden numbness or weakness, especially on one side of the body;

sudden severe headache, confusion, problems with vision, speech, or balance;

sudden and severe stomach pain and bloody diarrhea;

seizure (convulsions);

numbness or tingling and a pale or blue-colored appearance in your fingers or toes; or

(if you are also taking an antidepressant) - agitation, hallucinations, fever, fast heart rate, overactive reflexes, nausea, vomiting, diarrhea, loss of coordination, fainting.

Less serious Imitrex side effects may include:

mild headache (not a migraine);

pressure or heavy feeling in any part of your body;

feeling hot or cold;

dizziness, spinning sensation;

drowsiness;

nausea, vomiting, drooling;

unusual taste in your mouth after using the nasal spray;

burning, numbness, pain or other irritation in your nose or throat after using the nasal spray; or

warmth, redness, or mild tingling under your skin.

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects.

Imitrex is indicated for the acute treatment of migraine attacks with or without aura in adults. Imitrex is a headache medicine that narrows blood vessels around the brain. Imitrex also reduces substances in the body that can trigger headache pain, nausea, sensitivity to light and sound, and other migraine symptoms.

Use Imitrex exactly as prescribed by your doctor. Do not use in larger or smaller amounts or for longer than recommended. Follow the directions on your prescription label. Overuse of migraine headache medicine can actually make your headaches worse.

Use Imitrex as soon as you notice headache symptoms, or after an attack has already begun.

Your doctor may want to give your first dose of this medicine in a hospital or clinic setting to see if you have any serious side effects.

Take one Imitrex tablet whole with a full glass of water. Do not split the tablet.

After taking a tablet: If your headache does not completely go away, or goes away and comes back, take a second tablet two (2) hours after the first. Do not take more than 200 mg of sumatriptan oral tablets in 24 hours. If your symptoms have not improved, contact your doctor before taking any more tablets.

Since Imitrex is used as needed, it does not have a daily dosing schedule. Call your doctor promptly if your symptoms do not improve after using this medicine.

After taking a Imitrex tablet, you must wait two (2) hours before taking a second tablet. Do not take more than 200 mg of sumatriptan tablets in 24 hours.

After using Imitrex nasal spray, you must wait two (2) hours before using a second spray. Do not use more than 40 mg of nasal spray in 24 hours.

Contact your doctor if you have more than four headaches in one month (30 days).

In controlled clinical trials, single doses of 25, 50, or 100 mg of IMITREX Tablets were effective for the acute treatment of migraine in adults. There is evidence that doses of 50 and 100 mg may provide a greater effect than 25 mg.

The choice of dose should therefore be made on an individual basis, weighing the possible benefit of a higher dose with the potential for a greater risk of adverse events.

If the headache returns or the patient has a partial response to the initial dose, the dose may be repeated after 2 hours, not to exceed a total daily dose of 200 mg.

Store Imitrex at room temperature away from moisture, heat, and light.

Do not use Imitrex within 24 hours before or after using another migraine headache medicine, including:

sumatriptan injection, almotriptan (Axert), eletriptan (Relpax), frovatriptan (Frova), naratriptan (Amerge), rizatriptan (Maxalt, Maxalt-MLT), or zolmitriptan (Zomig); or

ergot medicine such as dihydroergotamine (D. H.E. 45, Migranal), ergotamine (Ergomar, Cafergot, Migergot), dihydroergotamine (D. H.E. 45, Migranal), or methylergonovine (Methergine).

Imitrex may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert.

You should not use Imitrex if you are allergic to sumatriptan, or if you have:

coronary heart disease, angina (chest pain), blood circulation problems, lack of blood supply to the heart;

a history of heart disease, heart attack, or stroke, including "mini-stroke";

severe or uncontrolled high blood pressure;

severe liver disease;

ischemic bowel disease; or

a headache that seems different from your usual migraine headaches.

Do not use Imitrex if you have used an MAO inhibitor such as furazolidone (Furoxone), isocarboxazid (Marplan), phenelzine (Nardil), rasagiline (Azilect), selegiline (Eldepryl, Emsam, Zelapar), or tranylcypromine (Parnate) in the last 14 days.

To make sure you can safely use Imitrex, tell your doctor if you have any of these other conditions:

liver disease;

kidney disease;

epilepsy or other seizure disorder;

high blood pressure, a heart rhythm disorder; or

coronary heart disease (or risk factors such as diabetes, menopause, smoking, being overweight, having high cholesterol, having a family history of coronary artery disease, being older than 40 and a man, or being a woman who has had a hysterectomy).

FDA pregnancy category C. It is not known whether Imitrex will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medication. Sumatriptan can pass into breast milk and may harm a nursing baby. Do not breast-feed within 12 hours after using Imitrex. If you use a breast pump during this time, throw out any milk you collect. Do not feed it to your baby. Imitrex should not be given to anyone under 18 or over 65 years of age.

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

feeling of pain or tightness in your jaw, neck, or throat;

chest pain or heavy feeling, pain spreading to the arm or shoulder, nausea, sweating, general ill feeling;

sudden numbness or weakness, especially on one side of the body;

sudden severe headache, confusion, problems with vision, speech, or balance;

sudden and severe stomach pain and bloody diarrhea;

seizure (convulsions);

numbness or tingling and a pale or blue-colored appearance in your fingers or toes; or

(if you are also taking an antidepressant) - agitation, hallucinations, fever, fast heart rate, overactive reflexes, nausea, vomiting, diarrhea, loss of coordination, fainting.

Less serious Imitrex side effects may include:

mild headache (not a migraine);

pressure or heavy feeling in any part of your body;

feeling hot or cold;

dizziness, spinning sensation;

drowsiness;

nausea, vomiting, drooling;

unusual taste in your mouth after using the nasal spray;

burning, numbness, pain or other irritation in your nose or throat after using the nasal spray; or

warmth, redness, or mild tingling under your skin.

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects.

Zyrtec (Cetirizine) Dosing, Indications, Interactions, Adverse Effects, And More, Zyrtec4

cetirizine (Rx, OTC) Brand and Other Names: Zyrtec, Zyrtec Allergy, more. Children's Zyrtec Allergy, Children's Zyrtec Hives Relief, PediaCare Children's 24 Hour Allergy, Aller-Tec, Wal-Zyr

Allergies/Hay Fever/Urticaria

Perennial and seasonal allergic and vasomotor rhinitis

<2 years: Safety and efficacy not established

2-6 years: 2.5 mg (0.5 teaspoon) oral solution PO qDay; can increase to 5 mg PO qDay or 2.5 mg PO twice daily; not to exceed 5 mg qDay

>6 years: 5-10 mg PO qDay, depending on severity of symptoms; not to exceed 10 mg qDay

Dosing Modifications

GFR ?30 mL/min/1.73 m?: Dose adjustment not necessary

GFR 10-29 mL/min/1.73 m?: Decrease dose by 50%

GFR < 10 mL/min/1.73 m?: Not recommended

Intermittent hemodialysis or peritoneal dialysis: Decrease dose by 50%

Dose adjustment not provided by manufacturer's label

Administration

May be taken with or without food

5 mg PO qDay; may increase to 10 mg/day mazimum, depending on severity of symptoms; not to exceed 5 mg qDay in patients >77 years

To view formulary information first create a list of plans. Your list will be saved and can be edited at any time.

Adding plans allows you to:

View the formulary and any restrictions for each plan.

Manage and view all your plans together – even plans in different states.

Compare formulary status to other drugs in the same class.

Access your plan list on any device – mobile or desktop.

The above information is provided for general informational and educational purposes only. Individual plans may vary and formulary information changes. Contact the applicable plan provider for the most current information.

View explanations for tiers and restrictions

This drug is available at the lowest co-pay. Most commonly, these are generic drugs.

This drug is available at a middle level co-pay. Most commonly, these are "preferred" (on formulary) brand drugs.

This drug is available at a higher level co-pay. Most commonly, these are "non-preferred" brand drugs.

This drug is available at a higher level co-pay. Most commonly, these are "non-preferred" brand drugs or specialty prescription products.

This drug is available at a higher level co-pay. Most commonly, these are "non-preferred" brand drugs or specialty prescription products.

This drug is available at a higher level co-pay. Most commonly, these are "non-preferred" brand drugs or specialty prescription products.

NOT COVERED – Drugs that are not covered by the plan.

Prior Authorization Drugs that require prior authorization. This restriction requires that specific clinical criteria be met prior to the approval of the prescription.

Quantity Limits Drugs that have quantity limits associated with each prescription. This restriction typically limits the quantity of the drug that will be covered.

Step Therapy Drugs that have step therapy associated with each prescription. This restriction typically requires that certain criteria be met prior to approval for the prescription.

Other Restrictions Drugs that have restrictions other than prior authorization, quantity limits, and step therapy associated with each prescription.

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Acquistare Convulsofin (Depakote) Senza Ricetta, Convulsofin

Convulsofin (Depakote) Acquistare Online senza Ricetta

Convulsofin (Depakote) Spiegazione

Il farmaco e in realta un trattamento ideale all'interno di battaglia verso i problemi di grippaggio.

Il farmaco funziona mediante la coltivazione della quantita di un materiale organico particolare all'interno della mente.

Il farmaco puo essere indicato anche come Valproato semisodico, sale Divalproex, valproico acidita, Divaa.

E 'davvero anticonvulsivante.

titolo generale associato con Convulsofin Divalproex e in realta Salt.

Marche associati Convulsofin tendono ad essere Convulsofin, Convulsofin Emergeny CAMERA, Convulsofin Sprinkles.

Convulsofin (Depakote) dosaggio

Il farmaco e disponibile in:

125 mg Lower Dose materiale di attrito

250 mg Dose normale materiale di attrito

500mg migliorata Dose materiale di attrito

Ottenere Convulsofin pillole per bocca insieme con i pasti.

Ottenere Convulsofin allo stesso tempo ogni giorno con acqua potabile.

Di solito non frantumare o masticare questo.

Se volete ottenere migliori risultati di solito non smettere di usare Convulsofin tutto ad un tratto.

Convulsofin (Depakote) manca associato a dosaggio

Di solito non si ottiene doppia dose. Nel caso in cui si salta il dosaggio e necessario portare una volta di tenere a mente per quanto riguarda al tuo carente. Quando e il momento per il dosaggio e necessario per portare avanti la propria normale routine di dosaggio.

Convulsofin (Depakote) Overdose

In caso di overdose Convulsofin e anche di evitare grandi e necessario controllare il vostro medico o anche il medico immediatamente. Associata con Convulsofin sovradosaggio: superficiale, inspirazione ed espirazione, battito cardiaco indebolito, sonnolenza, sensazione di sonnolenza, mancanza di consapevolezza.

Convulsofin (Depakote) spazio di archiviazione

Shop a temperature spaziali tra i 10 ei 30 livelli D (59 e ottantasei livelli F) di umidita e la temperatura. Mantenere testo saldamente chiuso. Rafforzare qualsiasi tipo di farmaco intatto successivo al giorno di scadenza. Mantenere posto sicuro fuori del modo di bambini.

Convulsofin (Depakote) Effetti negativi

Il farmaco offre gli effetti negativi. Il piu tipico tendono ad essere:

materiale di attrito diarrea

Materiale coprostasis di attrito

fatica del materiale di attrito

disturbi depressivi attrito Materiale

Materiale ansia di attrito

problemi mestruali materiale di attrito

tette piu grandi del materiale di attrito

tremante materiale di attrito

materiale di attrito calvicie

Materiale modifiche di peso corporeo di attrito

sapore insolito o addirittura a disagio sui denti materiale di attrito

sensazione materiale di attrito sonno

un po ' materiale di debolezza di attrito

modifiche psicologiche materiale di attrito materiale

modifiche alla vista di attrito

molto meno tipico e gravi effetti negativi in ??tutto con Convulsofin:

le risposte di reazione allergiche (orticaria, inspirando ed espirando problemi, allergie, cosi come eruzione) materiale di attrito

vomitare materiale di attrito

incomprensioni svenimento materiale di attrito

semplice perdita di sangue materiale di attrito

materiale di attrito caldo

materiale brividi attrito

intero dolori del corpo materiale di attrito

segni di influenza e sintomi materiale di attrito

pipi in normali materiale di attrito materiale

allucinazioni attrito

destrezza sufficiente materiale di attrito

doppia vista materiale d'attrito

le azioni indietro e indietro dal materiale di attrito occhio

un po 'di materiale di debolezza di attrito

urti semplice materiale di attrito

flusso sanguigno all'interno del vostro pipi materiale di attrito

materiale di attrito sonno

Gli effetti negativi sono indicazioni si basano su farmaci che si potrebbero utilizzare ma in aggiunta si basano sulla sua condizione di benessere e altri aspetti.

Convulsofin (Depakote) Controindicazioni

Di solito non si ottiene Convulsofin nel caso in cui siete sensibili al fine di Convulsofin elementi.

Di solito non si ottiene Convulsofin nel caso in cui si aspettano, andando a rimanere incinta, e / o l'allattamento al seno.

Di solito non si ottiene farmaci che possono provocare sonnolenza.

Siate cauti nel caso in cui si utilizza qualsiasi tipo di medico le ha prescritto o farmaco anche senza ricetta medica, la preparazione naturale, o addirittura supplemento.

Siate cauti con Convulsofin nel caso in cui si e afflitti da e hanno una breve storia associata a vomitare, grave affaticamento e frustrazione; attacchi associati a incomprensioni e mancanza di capacita di credere e comprehend, particolarmente durante la gravidanza o subito dopo il parto; coma (perdita associata con la consapevolezza nel corso di un periodo associato con il tempo); problemi di corrispondenza vostre azioni; essere patogeno dell'immunodeficienza umana (HIV); citomegalovirus (CMV, l'agente patogeno che puo provocare segni e sintomi che gli individui che hanno indebolito i sistemi di difesa); trigliceridi (superiore rispetto alla quantita normale di grasso corporeo nel sangue); o malattia anche renale, problemi periodo di urea, ritardo psicologico.

Siate cauti con Convulsofin per l'aspirina, barbiturici per esempio fenobarbitale e diluenti flusso sanguigno Seconal per esempio Coumadin, Ciclosporina (Sandimmune, Neoral), nortriptilina (Pamelor), clonazepam (Klonopin), etosuccimide (Zarontin). felbamato (Felbatol), lamotrigina (Lamictal), fenitoina (Dilantin), cosi come Primidone Mysoline), rifampicina (Rifater, Rimactane), Riposo aiuta ad esempio Halcion, tolbutamide (Orinase), Tranquillanti per esempio Valium e Xanax, zidovudina (Retrovir), amitriptilina (Elavil), carbamazepina (Tegretol), Merrem 4 (meropenem per quanto riguarda l'iniezione).

Nel caso in cui si verificano sonnolenza e affaticamento durante l'utilizzo Convulsofin e necessario per evitare qualsiasi tipo di azioni, ad esempio in viaggio o anche attrezzature da lavoro.

Evitare le bevande alcoliche durante l'utilizzo Convulsofin.

Evitare di diventare disidratazione.

Se si desidera avere un trattamento chirurgico, essere cauti con Convulsofin.

Puo essere dannoso per prevenire Convulsofin utilizzando tutto ad un tratto.

Convulsofin (Depakote) Domande generali

Queen: Che cosa e esattamente Convulsofin?

Il: Convulsofin e davvero una medicina eccellente che si consuma in un certo numero di rimediare of00 problemi sequestro. E 'davvero anticonvulsant. A

Queen: Che cosa e esattamente concentrarsi su Convulsofin?

Il: focus su Convulsofin e davvero una battaglia verso il sequestro problems. A

Queen: Cosi come fa esattamente la funzione Convulsofin?

Il: Il farmaco funziona mediante la coltivazione della quantita di un materiale organico particolare all'interno del mind. A

Queen: Esattamente quello che devo FAG situazione associata a dosaggio manca?

Nel caso di dosaggio priva e necessario per pillola piu rapidamente possibile. Di solito non si ottiene doppia dose. E quando e davvero il momento piu felice per dose e necessario per portare avanti la propria normale routine associata con Convulsofin using. A

Queen: non dobbiamo davvero sfruttare Convulsofin?

Il: Di solito non si ottiene Convulsofin nel caso in cui siete sensibili al fine di Convulsofin elementi. Di solito non si ottiene Convulsofin nel caso in cui ci si aspetta, andando a rimanere incinta, e / o l'allattamento al feeding. A

Queen: May Convulsofin innescare attacco allergico?

Il: infatti, puo. Risposte di reazione allergiche Convulsofin tendono ad essere eccema, inspirando ed espirando problemi, allergie, cosi come eruption. A

acquistare Convulsofin (Depakote) on-line, Convulsofin (Depakote) acquistare online senza ricetta, Convulsofin (Depakote) acquistare senza ricetta, acquistare a buon mercato Convulsofin (Depakote), Convulsofin (Depakote) comprare senza prescrizione medica, acquistare Convulsofin (Depakote) dal Canada, acquistare Convulsofin (Depakote) Canada, Convulsofin (Depakote) ordine on-line, Convulsofin (Depakote) on line ordine senza prescrizione, Convulsofin (Depakote) ordine senza prescrizione, Pillola orale Convulsofin (Depakote)

Ricerca

La Gente Cerca Anche

Nufalev Dosis Obat, Nufalev

nufalev

Ini adalah review terhadap obat dengan merk nufalev. di bagian akhir review ini juga disertakan tautan untuk mengetahui merk obat-obat lain dengan kandungan yang sama dengan nufalev.

golongan . obat keras

kemasan . strip 10 tablet

komposisi . levofloxacin hemihidrat setara levofloxacin anhidrat 500 mg

Sekilas tentang zat aktif (nama generik)

levofloksasin (levofloxacin) adalah antibiotik golongan fluorokuinolon yang mempunyai spektrum luas, aktif terhadap bakteri gram negatif maupun gram positif. levofloksasin (levofloxacin) adalah levo isomer dari ofloksasina. seperti semua kuinolon, levofloksasin (levofloxacin) bekerja dengan cara menghambat dua tipe enzim II topoisomerase yaitu DNA Gyrase dan topoisomerase IV. topoisomerase IV memerlukan DNA terpisah yang telah direplikasi sebelum pembelahan sel bakteri. Dengan DNA yang tidak dipisahkan, proses terhenti dan bakteri tidak bisa membagi. Sedangkan DNA gyrase bertanggungjawab untuk supercoil DNA sehingga akan cocok di dalam sel yang baru terbentuk. kombinasi dari dua mekanisme di atas akan membunuh bakteri sehingga levofloksasin (levofloxacin) digolongkan sebagai bakterisida.

Indikasi nufalev

Kegunaan nufalev (levofloxacin) adalah untuk pengobatan infeksi maksilaris sinusitis akut, eksaserbasi bakteri akut bronkitis kronik, pneumonia komunitas, kulit dan struktur kulit yang kompleks, infeksi saluran kemih, pieloneritis dan infeksi lain yang disebabkan kuman peka terhadap nufalev (levofloxacin).

kontra indikasi

nufalev (levofloxacin) harus dihindari pada pasien dengan hipersensitivitas terhadap nufalev (levofloxacin) atau antibiotik golongan kuinolon lainnya. nufalev (levofloxacin) juga kontra indikasi pada pasien dengan epilepsi atau gangguan kejang lainnya. dan pada pasien yang memiliki riwayat pemakaian kuinolon terkait tendon pecah .

Efek Samping nufalev

Kebanyakan efek samping nufalev (levofloxacin) bersifat ringan sampai sedang. Namun, efek samping serius kadang terjadi. Efek samping yang paling umum seperti gangguan gastrointestinal. mual, muntah, dan sembelit. nufalev (levofloxacin) juga menyebabkan intoksifikasi pernafasan, darah dan kelainan hormonal serta kardiovaskuler. efek samping yang yang kadang terjadi meskipun jarang adalah tremor, kegelisahan, ansietas, sakit kepala ringan, kebingungan, halusinasi, paranoid, depresi, mimpi buruk, insomnia.

perhatian

hati-hati pemberian nufalev (levofloxacin) pada pasien dengan penyakit hati. efektivitas dan keamanan pemakaian pada anak-anak, wanita hamil dan menyusui belum terbukti.

Toleransi terhadap kehamilan

penelitian pada reproduksi hewan menunjukkan levofloxacin memberikan efek buruk pada janin. Tidak ada studi yang memadai dan terkendali dengan baik pada manusia. tetapi jika manfaat potensial terhadap ibu lebih besar daripada risiko pada janin maka obat ini bisa diberikan.

interaksi obat

penggunaan nufalev (levofloxacin) bersama antasida yang mengandung magnesium hidroksida atau aluminium hidroksida, menurunkan penyerapan nufalev (levofloxacin) oleh usus. Hal yang sama terjadi jika diberikan bersamaan dengan suplemen zat besi dan multi-vitamin yang mengandung zinc. nufalev (levofloxacin) menunjukkan potensi untuk memblokir pemecahan warfarin dan phenprocoumon. Hal ini dapat meningkatkan kerja obat seperti warfarin, sehingga menyebabkan efek samping yang lebih potensial, seperti perdarahan. Dalam dosis tinggi, penggunaan nufalev (levofloxacin) bersamaan dengan anti inflamasi non steroid (NSAID) dapat menyebabkan kejang.

Dosis nufalev

nufalev (levofloxacin) diberikan dengan dosis. dosis oral sama dengan dosis parenteral. pemberian melalui infus dilakukan secara perlahan-lahan. sinusitis maksilaris akut. 500 mg tiap 24 jam selama 10-14 hari. eksaserbasi akut bronkitis kronis. 500 mg tiap 24 jam selama 7 hari; community acquired pneumonia . 500 mg tiap 24 jam selama 7-14 hari. infeksi saluran kemih terkomplikasi, pieloneritis akut. 250 mg tiap 24 jam selama 10 hari. infeksi kulit dan struktur kulit tidak terkomplikasi. 500 mg tiap 24 jam selama 7-10 hari.

Terkait

Dilaudid (Hydromorphone Hydrochloride) Side Effects, Interactions, Warning, Dosage & Uses, Dilucid

DILAUDID ORAL LIQUID AND DILAUDID TABLETS CONTAIN HYDROMORPHONE, WHICH IS A POTENT SCHEDULE II CONTROLLED OPIOID AGONIST. SCHEDULE II OPIOID AGONISTS, INCLUDING MORPHINE, OXYMORPHONE, OXYCODONE, FENTANYL, AND METHADONE, HAVE THE HIGHEST POTENTIAL FOR ABUSE AND RISK OF PRODUCING RESPIRATORY DEPRESSION. ALCOHOL, OTHER OPIOIDS AND CENTRAL NERVOUS SYSTEM DEPRESSANTS (SEDATIVE-HYPNOTICS) POTENTIATE THE RESPIRATORY DEPRESSANT EFFECTS OF HYDROMORPHONE, INCREASING THE RISK OF RESPIRATORY DEPRESSION THAT MIGHT RESULT IN DEATH.

DRUG DESCRIPTION

DILAUDID (hydromorphone hydrochloride), a hydrogenated ketone of morphine, is an opioid analgesic .

The chemical name of DILAUDID (hydromorphone hydrochloride) is 4,5α-epoxy-3-hydroxy-17- methylmorphinan-6-one hydrochloride. The structural formula is:

Each 5 mL (1 teaspoon ) of DILAUDID ORAL LIQUID contains 5 mg of hydromorphone hydrochloride. In addition, other ingredients include purified water, methylparaben, propylparaben, sucrose, and glycerin. DILAUDID ORAL LIQUID may contain traces of sodium metabisulfite.

Color Coded Tablets (for Oral Administration) Contain:

2 mg hydromorphone hydrochloride (orange tablet) and D&C red #30 Lake dye, D&C yellow #10 Lake dye, lactose, and magnesium stearate. DILAUDID 2 mg TABLET may contain traces of sodium metabisulfite.

4 mg hydromorphone hydrochloride (yellow tablet) and D&C yellow #10 Lake dye, lactose, and magnesium stearate. DILAUDID 4 mg TABLET may contain traces of sodium metabisulfite.

8 mg hydromorphone hydrochloride (white tablet) and lactose anhydrous, and magnesium stearate. DILAUDID 8 mg TABLET may contain traces of sodium metabisulfite.

What are the possible side effects of hydromorphone (Dilaudid, Dilaudid-5, Exalgo)?

Get emergency medical help if you have any of these signs of an allergic reaction: 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:

weak or shallow breathing;

pounding heartbeats or fluttering in your chest;

wheezing, chest tightness, trouble breathing;

seizure (convulsions);

confusion, severe weakness or drowsiness; or

feeling like you might pass out.

Less serious side effects are more likely to.

What are the precautions when taking hydromorphone hydrochloride (Dilaudid)?

Before taking hydromorphone, tell your doctor or pharmacist if you are allergic to it; or to hydrocodone; or if you have any other allergies. This product may contain inactive ingredients (such as sulfites), which can cause allergic reactions or other problems. Talk to your pharmacist for more details.

Before using this medication, tell your doctor or pharmacist your medical history, especially of: brain disorders (such as head injury, tumor, seizures), breathing problems (such as asthma, sleep apnea, chronic obstructive pulmonary disease-COPD), kidney disease, liver disease, mental/mood disorders (such as confusion, depression), personal or family history of regular use/abuse of drugs/alcohol, stomach/intestinal problems (such as blockage, constipation, diarrhea due to.

Last reviewed on RxList: 7/16/2015 This monograph has been modified to include the generic and brand name in many instances.

Diflucan - Anti Fungal, Figalol

Product Description Common use Diflucan is an anti-fungal antibiotic which is used to treat fungal infections called candidiasis. This medication is prescribed for the treatment of such type of infections as vaginal, throat and fungal infections, infections of the urinary tract, peritonitis, and pneumonia. Diflucan works by killing sensitive fungi by interfering with the formation of the fungal cell membrane.

Dosage and direction Take it orally once a day, with or without food using the measuring spoon. Take it at the same time each day with a full glass of water if you want to get the best result. Diflucan make you feel better after 24 hours. However, your symptoms will go away completely just after few days. If there is no change in your health after a few days consult your doctor immediately. The dosage for adults may vary from type of infection: 1) Genital thrush - 150mg as a single dose 2) Mucosal thrush - dose depends on where the infection is located 50mg once daily during month. 3)Fungal skin infections - 50mg once daily for 2-4 weeks ; 4) Internal fungal infections 400mg on the first day then 200-400mg once daily for 6-8 weeks or longer if needed. 5) To stop you from getting fungal infections - 50-400mg once daily while you have risk to get an infection; 6) To stop infection caused by Cryptococcus from coming back - 100-200mg once daily indefinitely The dosage for children 4 weeks to 15 years old may also vary from type of infection: 1) mucosal infections - 3mg/kg once daily; 2)internal fungal infections - 6-12mg/kg once daily; 3)prevention of fungal infections - 3-12mg/kg once daily while at risk of getting an infection. For children 2-4 weeks old it is same dose as above but given once every 2 days. A maximum dose of 12mg/kg every 2 days. For children less than 2 weeks old it is same dose as above but given once every 3 days. Do not give more then 12mg/kg every 3 days. Note: this instruction presented here is just for review. It's very necessary to consult your doctor before using. It will help you to get best results.

For vaginal yeast infections, doctors usually prescribe a single dose of Diflucan. If the yeast infection does not improve after 5 days, contact your doctor as soon as possible. Be careful with this medication if your medical history include liver disease or kidney disease. Although uncommon, this drug may make you dizzy, so be more attentive while you are driving or using machinery. Limit alcohol intake. Diflucan should not be used during pregnancy, lactation or if you plan to become pregnant without a doctor's advice. Do not use before breast-feeding without a doctor's advice.

Contraindications Diflucan is not allowed to people who have hypersensitivity to Fluconazole or other anti fungal azole preparations, eg clotrimazole, ketoconazole, itraconazole and other. Also Diflucan contraindicated in: Kidney and liver disorders; Cardiovascular diseases including heart diseases(heart rate or rhythm disturbances); Low blood levels of calcium, magnesium or potassium.

Possible side effect

They may include an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Also the most possible side effects include: nausea, stomach pain, low fever, loss of appetite, dark urine, clay-colored stools, jaundice (yellowing of the skin or eyes); fever, chills, body aches, flu symptoms; severe blistering, peeling, and red skin rash; easy bruising or bleeding, unusual weakness; or seizure (convulsions). Less serious include: mild nausea, vomiting, diarrhea, or upset stomach; headache; dizziness; unusual or unpleasant taste in your mouth; or skin rash or itching. If you experience one of them stop using Diflucan and tell your doctor as soon as possible. Also consult your doctor about any side effect that seems unusual.

Drug interaction Diflucan interact with such medication as: a blood thinner such as warfarin (Coumadin) cyclosporine (Gengraf, Sandimmune, Neoral); an oral diabetes medicine such as glipizide (Glucotrol), glyburide (Diabeta, Micronase, Glynase), tolbutamide (Orinase), tolazamide (Tolinase), chlorpropamide (Diabinese), and others; rifabutin (Mycobutin) or rifampin (Rifadin, Rifater, Rifamate, Rimactane); a sedative such as diazepam (Valium), lorazepam (Ativan), alprazolam (Xanax), or midazolam (Versed); seizure medication such as phenytoin (Dilantin) or valproic acid (Depakene); tacrolimus ((Prograf); theophylline (Theo-Dur, Theolair, Theochron, Elixophyllin, Slo-Phyllin, others). Also note that interaction between two medications does not always mean that you must stop taking one of them. Usually it affects the the effect of drugs, so consult your doctor about the way these interactions are being managed or should be managed.

Missed dose If you forgot to take your dose in time, please do it as soon as you remember. But do not take if it is too late or almost time for your next dose. Do not take double or extra doses. Take your usual dose next day in the same time.

Overdose Symptoms of Diflucan overdose may include: confusion or unusual thoughts or behavior. If you experience one of them call your doctor immediately.

Storage Store at room temperature between 59-77 degrees F (15-25 degrees C) away from light and moisture, kids and pets. Do not use after expiration term.

Disclaimer We provide only general information about medications which does not cover all directions, possible drug integrations, or precautions. Information on 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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