Sunday, 26 April 2009

Tiptipot Simicol




Tiptipot Simicol may be available in the countries listed below.


Ingredient matches for Tiptipot Simicol



Simeticone

Simeticone is reported as an ingredient of Tiptipot Simicol in the following countries:


  • Israel

International Drug Name Search

Nufex




Nufex may be available in the countries listed below.


Ingredient matches for Nufex



Cefalexin

Cefalexin is reported as an ingredient of Nufex in the following countries:


  • Bangladesh

  • India

International Drug Name Search

Friday, 24 April 2009

C.M.P.200




C.M.P.200 may be available in the countries listed below.


Ingredient matches for C.M.P.200



Carbamazepine

Carbamazepine is reported as an ingredient of C.M.P.200 in the following countries:


  • Argentina

International Drug Name Search

Thursday, 23 April 2009

Tolfine




Tolfine may be available in the countries listed below.


In some countries, this medicine may only be approved for veterinary use.

Ingredient matches for Tolfine



Tolfenamic Acid

Tolfenamic Acid is reported as an ingredient of Tolfine in the following countries:


  • Belgium

  • France

  • Netherlands

  • United Kingdom

International Drug Name Search

Monday, 20 April 2009

Detomo Vet




Detomo Vet may be available in the countries listed below.


In some countries, this medicine may only be approved for veterinary use.

Ingredient matches for Detomo Vet



Detomidine

Detomidine hydrochloride (a derivative of Detomidine) is reported as an ingredient of Detomo Vet in the following countries:


  • Australia

  • New Zealand

International Drug Name Search

Sunday, 19 April 2009

Depocyt


Generic Name: cytarabine liposome (Intrathecal route)


sye-TARE-a-been LYE-poh-some


Intrathecal route(Suspension)

In all clinical studies, chemical arachnoiditis, a syndrome manifested primarily by nausea, vomiting, headache, and fever was a common adverse event with cytarabine liposome. If left untreated, chemical arachnoiditis may be fatal. The incidence and severity of chemical arachnoiditis can be reduced by coadministration of dexamethasone and patients receiving cytarabine liposome should be treated concurrently with dexamethasone to mitigate the symptoms of chemical arachnoiditis .



Commonly used brand name(s)

In the U.S.


  • Depocyt

Available Dosage Forms:


  • Suspension

Therapeutic Class: Antineoplastic Agent


Pharmacologic Class: Antimetabolite


Uses For Depocyt


Liposomal cytarabine belongs to the group of medicines known as antineoplastics. It is used to treat cancer of the lymph system that has spread to the brain.


Liposomal cytarabine interferes with the growth of cancer cells, which are eventually destroyed. Since the growth of normal cells may also be affected by the medicine, other effects may also occur. Some of these may be serious and must be reported to your doctor. Some effects may occur after treatment with liposomal cytarabine has been stopped.


Before you begin treatment with liposomal cytarabine, you and your doctor should talk about the good this medicine will do as well as the risks of using it.


Liposomal cytarabine is to be administered only by or under the immediate supervision of your doctor.


Before Using Depocyt


In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For this medicine, the following should be considered:


Allergies


Tell your doctor if you have ever had any unusual or allergic reaction to this medicine or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.


Pediatric


Studies on this medicine have been done only in adult patients, and there is no specific information comparing use of liposomal cytarabine in children with use in other age groups.


Geriatric


Many medicines have not been studied specifically in older people. Therefore, it may not be known whether they work exactly the same way they do in younger adults or if they cause different side effects or problems in older people. There is no specific information comparing use of liposomal cytarabine in the elderly with use in other age groups.


Pregnancy








Pregnancy CategoryExplanation
All TrimestersDStudies in pregnant women have demonstrated a risk to the fetus. However, the benefits of therapy in a life threatening situation or a serious disease, may outweigh the potential risk.

Breast Feeding


There are no adequate studies in women for determining infant risk when using this medication during breastfeeding. Weigh the potential benefits against the potential risks before taking this medication while breastfeeding.


Interactions with Medicines


Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. When you are taking this medicine, it is especially important that your healthcare professional know if you are taking any of the medicines listed below. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive.


Using this medicine with any of the following medicines is not recommended. Your doctor may decide not to treat you with this medication or change some of the other medicines you take.


  • Rotavirus Vaccine, Live

Using this medicine with any of the following medicines is usually not recommended, but may be required in some cases. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines.


  • Adenovirus Vaccine Type 4, Live

  • Adenovirus Vaccine Type 7, Live

  • Bacillus of Calmette and Guerin Vaccine, Live

  • Influenza Virus Vaccine, Live

  • Measles Virus Vaccine, Live

  • Mumps Virus Vaccine, Live

  • Rotavirus Vaccine, Live

  • Rubella Virus Vaccine, Live

  • Smallpox Vaccine

  • Typhoid Vaccine

  • Varicella Virus Vaccine

  • Yellow Fever Vaccine

Interactions with Food/Tobacco/Alcohol


Certain medicines should not be used at or around the time of eating food or eating certain types of food since interactions may occur. Using alcohol or tobacco with certain medicines may also cause interactions to occur. Discuss with your healthcare professional the use of your medicine with food, alcohol, or tobacco.


Other Medical Problems


The presence of other medical problems may affect the use of this medicine. Make sure you tell your doctor if you have any other medical problems, especially:


  • Active meningitis—Use is not recommended

  • Blockage to cerebrospinal fluid flow— Increased risk of neurotoxicity

Proper Use of Depocyt


This medicine often causes nausea and vomiting. However, it is very important that you continue to receive the medicine, even if you begin to feel ill. Ask your health care professional for ways to lessen these effects.


Dosing


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


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


Precautions While Using Depocyt


It is very important that your doctor check your progress at regular visits to make sure that this medicine is working properly and to check for unwanted effects.


Depocyt Side Effects


Along with its needed effects, a medicine may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.


Check with your doctor as soon as possible if any of the following side effects occur:


More common
  • Back pain

  • fever

  • headache

  • nausea

  • neck pain or rigidity

  • sleepiness

  • vomiting

  • weakness

Less common
  • Black, tarry stools

  • blood in urine or stools

  • chills

  • cough or hoarseness

  • lower back or side pain

  • painful or difficult urination

  • pinpoint red spots on skin

  • sore throat

  • swelling of fingers, hands, arms, lower legs, or feet

  • unusual bleeding or bruising

Rare
  • Fast or irregular breathing

  • puffiness or swelling around the face

  • shortness of breath

  • sudden, severe decrease in blood pressure

  • unusual tiredness

Some side effects may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:


Less common
  • Constipation

  • urinary incontinence

Other side effects not listed may also occur in some patients. If you notice any other effects, check with your healthcare professional.


Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.

See also: Depocyt side effects (in more detail)



The information contained in the Thomson Reuters Micromedex products as delivered by Drugs.com is intended as an educational aid only. It is not intended as medical advice for individual conditions or treatment. It is not a substitute for a medical exam, nor does it replace the need for services provided by medical professionals. Talk to your doctor, nurse or pharmacist before taking any prescription or over the counter drugs (including any herbal medicines or supplements) or following any treatment or regimen. Only your doctor, nurse, or pharmacist can provide you with advice on what is safe and effective for you.


The use of the Thomson Reuters Healthcare products is at your sole risk. These products are provided "AS IS" and "as available" for use, without warranties of any kind, either express or implied. Thomson Reuters Healthcare and Drugs.com make no representation or warranty as to the accuracy, reliability, timeliness, usefulness or completeness of any of the information contained in the products. Additionally, THOMSON REUTERS HEALTHCARE MAKES NO REPRESENTATION OR WARRANTIES AS TO THE OPINIONS OR OTHER SERVICE OR DATA YOU MAY ACCESS, DOWNLOAD OR USE AS A RESULT OF USE OF THE THOMSON REUTERS HEALTHCARE PRODUCTS. ALL IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE OR USE ARE HEREBY EXCLUDED. Thomson Reuters Healthcare does not assume any responsibility or risk for your use of the Thomson Reuters Healthcare products.


More Depocyt resources


  • Depocyt Side Effects (in more detail)
  • Depocyt Use in Pregnancy & Breastfeeding
  • Depocyt Drug Interactions
  • Depocyt Support Group
  • 0 Reviews for Depocyt - Add your own review/rating


  • Cytarabine Liposomal Professional Patient Advice (Wolters Kluwer)

  • DepoCyt Prescribing Information (FDA)

  • DepoCyt Concise Consumer Information (Cerner Multum)

  • DepoCyt Monograph (AHFS DI)

  • DepoCyt MedFacts Consumer Leaflet (Wolters Kluwer)



Compare Depocyt with other medications


  • Meningitis, Lymphomatous

Monday, 13 April 2009

Givair




Givair may be available in the countries listed below.


Ingredient matches for Givair



Flunisolide

Flunisolide is reported as an ingredient of Givair in the following countries:


  • Italy

International Drug Name Search

Sunday, 12 April 2009

Dulera Inhalation Aerosol



Pronunciation: moe-MET-a-sone/for-MOE-ter-ol
Generic Name: Mometasone/Formoterol
Brand Name: Dulera

Long-acting beta-agonists such as one of the active ingredients in Dulera Inhalation Aerosol (formoterol) have been rarely associated with an increased risk of asthma-related death. They may also increase the risk of asthma-related hospitalizations in CHILDREN and TEENAGERS. Dulera Inhalation Aerosol should only be used to treat asthma patients who are not controlled by using other long-term asthma-control medicine. Dulera Inhalation Aerosol should not be used in patients whose asthma is well controlled by inhaled corticosteroids.





Dulera Inhalation Aerosol is used for:

Treating asthma in certain patients. It may also be used for other conditions as determined by your doctor.


Dulera Inhalation Aerosol is a combination of a corticosteroid and a long-acting beta-agonist bronchodilator. The corticosteroid works by decreasing inflammation in the lungs. The long-acting beta-agonist works by widening the airways in the lungs, which helps you breathe more easily.


Do NOT use Dulera Inhalation Aerosol if:


  • you are allergic to any ingredient in Dulera Inhalation Aerosol

  • you are using another medicine that has a long-acting beta-agonist (eg, salmeterol) in it

  • you are having an asthma attack (eg, sudden, severe onset or worsening of asthma symptoms such as wheezing, cough, chest tightness, shortness of breath)

  • you have asthma that is already well controlled with the use of a long-term asthma-control medicine (eg, inhaled corticosteroid)

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



Before using Dulera Inhalation Aerosol:


Some medical conditions may interact with Dulera Inhalation Aerosol. 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 diabetes, heart problems (eg, fast, slow or irregular heartbeat, heart blood vessel problems), high blood pressure, high blood acid levels (ketoacidosis), low blood potassium levels, seizures, tuberculosis, a weakened immune system, liver problems, or thyroid problems

  • if you have weakened bones (eg, osteoporosis), a family history of weakened bones, or have other risk factors of weak bones (eg, smoking, poor nutrition, you take certain medicines that weaken bones)

  • if you have a history of eye problems (eg, glaucoma, cataracts, increased eye pressure)

  • if you have diarrhea; a fungal, bacterial, or parasitic infection; a viral infection (eg, chickenpox, measles); herpes infection of the eye; or a lung infection (eg, pneumonia)

  • if you have recently been to an emergency room for asthma, have a history of frequent hospitalizations for asthma, or have ever had a life-threatening asthma attack

  • if you have had an unusual reaction to a sympathomimetic medicine (eg, albuterol, pseudoephedrine), such as fast or irregular heartbeat, overexcitement, or severe trouble sleeping

  • if you are taking a monoamine oxidase inhibitor (MAOI) (eg, phenelzine) or a tricyclic antidepressant (eg, amitriptyline), or if you have taken either of these medicines within the last 14 days

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


  • Beta-agonists (eg, albuterol), corticosteroids (eg, prednisone), diuretics (eg, furosemide, hydrochlorothiazide), or xanthines (eg, theophylline) because the risk of low blood potassium or irregular heartbeat may be increased

  • Azole antifungals (eg, itraconazole, ketoconazole), HIV protease inhibitors (eg, atazanavir, indinavir, ritonavir), linezolid, other long-acting beta-agonists (eg, salmeterol), macrolide antibiotics (eg, clarithromycin), monoamine oxidase inhibitors (MAOIs) (eg, phenelzine), nefazodone, telithromycin, or tricyclic antidepressants (eg, amitriptyline) because they may increase the risk of Dulera Inhalation Aerosol's side effects

  • Beta-blockers (eg, propranolol) because they may decrease Dulera Inhalation Aerosol's effectiveness or worsen your condition

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


How to use Dulera Inhalation Aerosol:


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


  • Dulera Inhalation Aerosol comes with an extra patient information sheet called a Medication Guide. Read it carefully. Read it again each time you get Dulera Inhalation Aerosol refilled.

  • You will need to prime the inhaler before using it for the first time, any time it has not been used for more than 5 days, or if it has been dropped. To prime the inhaler, point it away from you and others. Spray 4 times, shaking well before each spray.

  • Be sure that the canister is properly placed in the inhaler unit. Shake well before each use. Remove the mouthpiece cover. Check the mouthpiece for foreign objects. Breathe out slowly and completely. Place the mouthpiece between your lips and try to rest your tongue flat, unless your doctor has told you otherwise. Your doctor may have told you to hold the inhaler 1 or 2 inches (2 or 3 centimeters) away from the open mouth or to use a special spacing device. As you start to take a slow, deep breath, press the canister and mouthpiece together at exactly the same time. This will release a dose of Dulera Inhalation Aerosol. Continue breathing in slowly and deeply and hold for as long as comfortable up to 10 seconds, then breathe out slowly through your nose while keeping your lips closed. If more than 1 inhalation is to be used, wait at least 30 seconds and repeat the above steps. Keep the spray away from your eyes. Close the mouthpiece cover after each use.

  • Rinse your mouth with water after you finish using the medicine (do not swallow). This will help remove excess medicine and decrease your risk of developing an oral fungal infection.

  • Wipe the mouthpiece clean with a dry cloth at least once a week.

  • Use the new inhaler that comes with each refill. Do not reuse an old inhaler. Do not use Dulera Inhalation Aerosol with a different kind of inhaler.

  • Never wash the mouthpiece or any other part of the inhaler with water. Keep it dry and always store in a dry place. Do NOT try to take the inhaler apart.

  • This inhaler contains 124 sprays. A dose counter shows how many puffs are left in the inhaler. Do not use this inhaler after 124 sprays have been used (when the counter on the inhaler says "0"). The inhaler may not feel empty, but you will not get the correct amount of medicine with each spray if you continue to use it.

  • Continue to use Dulera Inhalation Aerosol even if you feel well. Do not miss any doses.

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

Ask your health care provider any questions you may have about how to use Dulera Inhalation Aerosol.



Important safety information:


  • Dulera Inhalation Aerosol is for oral inhalation only. Do not spray in the eyes. If you get Dulera Inhalation Aerosol in the eyes, rinse immediately with cool tap water. If eye redness and irritation continue, contact your doctor.

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

  • Some patients may have trouble using Dulera Inhalation Aerosol correctly. Some may also get mouth sores or a bad taste in the mouth after using it. If you have any of these problems, ask your health care provider if a spacing device may help.

  • The risk of serious heart problems (eg, irregular heartbeat) may be greater if you use Dulera Inhalation Aerosol in high doses. Do NOT use more than the recommended dose or use for longer than prescribed without checking with your doctor.

  • Dulera Inhalation Aerosol should be used to treat asthma only if your asthma is not well controlled while you are using a certain long-term asthma-control medicine (eg, inhaled corticosteroid) or if you have severe asthma. Contact your doctor if you have questions about this information.

  • Use caution if you switch from an oral steroid (eg, prednisone) to Dulera Inhalation Aerosol. It may take several months for your body to make enough natural steroids to handle events that cause physical stress. Such events may include injury, surgery, infection, loss of blood electrolytes, or a sudden asthma attack. These may be severe and sometimes fatal. Contact your doctor right away if any of these events occur. You may need to take an oral steroid (eg, prednisone) again. Carry a card at all times that says you may need an oral steroid (eg, prednisone) if any of these events occur.

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

  • If you have not had chickenpox, shingles, or measles, avoid contact with anyone who does. Tell your doctor right away if you are exposed to anyone who has these infections.

  • Do not receive a live vaccine (eg, measles, mumps) while you are taking Dulera Inhalation Aerosol. Talk with your doctor before you receive any vaccine.

  • Dulera Inhalation Aerosol will not stop an asthma attack once it has already started. Be sure to carry a short-acting bronchodilator inhaler (eg, albuterol) with you at all times to treat any breathing problems that may occur between doses of Dulera Inhalation Aerosol (eg, severe or sudden onset of wheezing or shortness of breath). If you have any questions about which medicines stop asthma attacks, check with your doctor or pharmacist.

  • If you have been regularly using a short-acting bronchodilator inhaler (eg, albuterol), talk with your doctor about how to use it with Dulera Inhalation Aerosol. Short-acting bronchodilators are normally only used with Dulera Inhalation Aerosol to treat breathing problems that may occur between doses.

  • Tell your doctor or dentist that you take Dulera Inhalation Aerosol before you receive any medical or dental care, emergency care, or surgery.

  • If your symptoms do not get better within 1 to 2 weeks of starting Dulera Inhalation Aerosol or if they get worse, contact your doctor right away.

  • Tell your doctor at once if you notice that your short-acting bronchodilator inhaler does not work as well, if you need to use it often (eg, 4 or more times a day for more than 2 days in a row, more than 1 canister in 8 weeks), or if you have a decrease in your peak flow meter results.

  • Contact your doctor or seek medical care right away if you have breathing problems that worsen quickly or if you use your short-acting bronchodilator and do not get relief.

  • Talk with your doctor or pharmacist about all of your asthma medicines and how to use them. Your doctor may make changes to your asthma-control medicines once your asthma is well controlled. Do not start, stop, or change the dose of any asthma medicine unless your doctor tells you to.

  • The medicine may sometimes cause breathing problems right after you use a dose. If this happens, use your short-acting bronchodilator. Contact your doctor or seek other medical care at once.

  • Lab tests, including lung function, blood pressure, and eye exams, may be performed while you use Dulera Inhalation Aerosol. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

  • Use Dulera Inhalation Aerosol with caution in the ELDERLY; they may be more sensitive to its effects, especially weakened bones.

  • Corticosteroids may affect the growth rate in CHILDREN and teenagers in some cases. They may need regular growth checks while they use Dulera Inhalation Aerosol.

  • Dulera Inhalation Aerosol should be used with extreme caution in CHILDREN younger than 12 years old; safety and effectiveness in these children have not been confirmed.

  • PREGNANCY and BREAST-FEEDING: It is not known if Dulera Inhalation Aerosol can cause harm to the fetus. If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Dulera Inhalation Aerosol while you are pregnant. It is not known if Dulera Inhalation Aerosol is found in breast milk. If you are or will be breast-feeding while you use Dulera Inhalation Aerosol, check with your doctor. Discuss any possible risks to your baby.


Possible side effects of Dulera Inhalation Aerosol:


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



Dizziness; dry mouth; headache; nausea; nervousness; stuffy nose; throat irritation; tiredness; tremor; trouble sleeping.



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

Severe allergic reactions (rash; hives; itching; difficulty breathing; flushing of the skin; tightness in the chest; swelling of the mouth, face, lips, tongue, or throat; unusual hoarseness); chest pain; fainting; fast or irregular heartbeat; fever, chills, or persistent sore throat; increased mucus production or change in color of mucus; muscle pain, weakness, or cramps; new or worsening asthma symptoms (eg, coughing, increased chest tightness, shortness of breath, wheezing); seizures; severe or persistent dizziness, headache, nervousness, or tremor; speech problems; vomiting; white patches in your mouth or throat.



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


See also: Dulera side effects (in more detail)


If OVERDOSE is suspected:


Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include chest pain; fainting; fast or irregular heartbeat; fatigue; headache; increased thirst or urination; muscle pain or cramps; nausea; nervousness; seizures; severe or persistent dizziness or dry mouth; symptoms of high blood sugar (eg, increased thirst, hunger, or urination; drowsiness; flushing of the skin; confusion; fruit-like breath odor); tremors; trouble sleeping; weakness.


Proper storage of Dulera Inhalation Aerosol:

Store Dulera Inhalation Aerosol at room temperature, between 68 and 77 degrees F (20 and 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 direct sunlight. Do not store in the bathroom. Do not puncture, break, or burn the canister even if it appears to be empty. Keep Dulera Inhalation Aerosol out of the reach of children and away from pets.


General information:


  • If you have any questions about Dulera Inhalation Aerosol, please talk with your doctor, pharmacist, or other health care provider.

  • Dulera Inhalation Aerosol is to be used only by the patient for whom it is prescribed. Do not share it with other people.

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

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

This information is a summary only. It does not contain all information about Dulera Inhalation Aerosol. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.



Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Dulera resources


  • Dulera Side Effects (in more detail)
  • Dulera Use in Pregnancy & Breastfeeding
  • Dulera Drug Interactions
  • Dulera Support Group
  • 6 Reviews for Dulera - Add your own review/rating


Compare Dulera with other medications


  • Asthma
  • Asthma, Maintenance

Saturday, 11 April 2009

Hobs-S




Hobs-S may be available in the countries listed below.


Ingredient matches for Hobs-S



Salicylic Acid

Salicylic Acid is reported as an ingredient of Hobs-S in the following countries:


  • India

Ulobetasol

Ulobetasol propionate (a derivative of Ulobetasol) is reported as an ingredient of Hobs-S in the following countries:


  • India

International Drug Name Search

Arcasin




Arcasin may be available in the countries listed below.


Ingredient matches for Arcasin



Phenoxymethylpenicillin

Phenoxymethylpenicillin potassium (a derivative of Phenoxymethylpenicillin) is reported as an ingredient of Arcasin in the following countries:


  • Germany

  • Kuwait

  • Lebanon

  • Qatar

  • Saudi Arabia

  • Syria

  • United Arab Emirates

International Drug Name Search

Friday, 10 April 2009

Actadol codeine 30 S




Actadol codeine 30 S may be available in the countries listed below.


Ingredient matches for Actadol codeine 30 S



Codeine

Codeine phosphate hemihydrate (a derivative of Codeine) is reported as an ingredient of Actadol codeine 30 S in the following countries:


  • Vietnam

Paracetamol

Paracetamol is reported as an ingredient of Actadol codeine 30 S in the following countries:


  • Vietnam

International Drug Name Search

Monday, 6 April 2009

Humulin 80 / 20




Humulin 80/20 may be available in the countries listed below.


Ingredient matches for Humulin 80/20



Insulin Injection, Biphasic Isophane

Insulin Injection, Biphasic Isophane human (a derivative of Insulin Injection, Biphasic Isophane) is reported as an ingredient of Humulin 80/20 in the following countries:


  • Aruba

  • Bahamas

  • Barbados

  • Bermuda

  • Cayman Islands

  • Haiti

  • Jamaica

  • Netherlands Antilles

  • Trinidad & Tobago

International Drug Name Search

Sunday, 5 April 2009

Pantoprazol Streuli




Pantoprazol Streuli may be available in the countries listed below.


Ingredient matches for Pantoprazol Streuli



Pantoprazole

Pantoprazole sodium (a derivative of Pantoprazole) is reported as an ingredient of Pantoprazol Streuli in the following countries:


  • Switzerland

International Drug Name Search

diphenhydramine


Generic Name: diphenhydramine (DYE fen HYE dra meen)

Brand names: Aler-Tab, Allergy, Allermax, Altaryl, Benadryl Allergy, Benadryl DF, Benadryl Dye Free Allergy, Benadryl Ultratab, Children's Allergy, Diphen Cough, Diphenhist, Dytuss, PediaCare Children's Allergy, Q-Dryl, Q-Dryl A/F, Siladryl, Siladryl Allergy, Silphen Cough, Simply Sleep, Sleep-ettes, Sleep-ettes D, Sominex Maximum Strength Caplet, Theraflu Thin Strips Multi Symptom, Triaminic Thin Strips Cough & Runny Nose, Unisom Sleepgels Maximum Strength, Valu-Dryl, ...show all 87 brand names.


What is diphenhydramine?

Diphenhydramine is an antihistamine. Diphenhydramine blocks the effects of the naturally occurring chemical histamine in the body.


Diphenhydramine is used to treat sneezing; runny nose; itching, watery eyes; hives; rashes; itching; and other symptoms of allergies and the common cold.


Diphenhydramine is also used to suppress coughs, to treat motion sickness, to induce sleep, and to treat mild forms of Parkinson's disease.


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


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


Use caution when driving, operating machinery, or performing other hazardous activities. Diphenhydramine may cause dizziness or drowsiness. If you experience dizziness or drowsiness, avoid these activities. Use alcohol cautiously. Alcohol may increase drowsiness and dizziness while taking diphenhydramine.

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


Do not take diphenhydramine if you have taken a monoamine oxidase inhibitor (MAOI) such as isocarboxazid (Marplan), phenelzine (Nardil), or tranylcypromine (Parnate) in the last 14 days. A very dangerous drug interaction could occur, leading to serious side effects.

Before taking this medication, tell your doctor if you have



  • glaucoma or increased pressure in the eye;




  • a stomach ulcer;




  • an enlarged prostate, bladder problems or difficulty urinating;




  • an overactive thyroid (hyperthyroidism);




  • hypertension or any type of heart problems; or




  • asthma.



You may not be able to take diphenhydramine, or you may require a lower dose or special monitoring during treatment if you have any of the conditions listed above.


Diphenhydramine is in the FDA pregnancy category B. This means that it is not expected to be harmful to an unborn baby. Do not take diphenhydramine without first talking to your doctor if you are pregnant. Infants are especially sensitive to the effects of antihistamines, and side effects could occur in a breast-feeding baby. Do not take diphenhydramine without first talking to your doctor if you are nursing a baby. If you are over 60 years of age, you may be more likely to experience side effects from diphenhydramine. You may require a lower dose of this medication.

How should I take diphenhydramine?


Take diphenhydramine exactly as directed on the package or as directed by your doctor. If you do not understand these directions, ask your pharmacist, nurse, or doctor to explain them to you.


Take each dose with a full glass of water.

Diphenhydramine can be taken with or without food.


For motion sickness, a dose is usually taken 30 minutes before motion, then with meals and at bedtime for the duration of exposure.


As a sleep aid, diphenhydramine should be taken approximately 30 minutes before bedtime.


To ensure that you get a correct dose, measure the liquid forms of diphenhydramine with a special dose-measuring spoon or cup, not with a regular tablespoon. If you do not have a dose-measuring device, ask your pharmacist where you can get one.


Never take more of this medication than is prescribed for you. The maximum amount of diphenhydramine that you should take in any 24-hour period is 300 mg.


Store diphenhydramine at room temperature away from moisture and heat.

What happens if I miss a dose?


Take the missed dose as soon as you remember. However, if it is almost time for the next dose, skip the missed dose and take only the next regularly scheduled dose. Do not take a double dose of this medication unless otherwise directed by your doctor.


What happens if I overdose?


Seek emergency medical attention if an overdose is suspected.

Symptoms of a diphenhydramine overdose include extreme sleepiness, confusion, weakness, ringing in the ears, blurred vision, large pupils, dry mouth, flushing, fever, shaking, insomnia, hallucinations, and possibly seizures.


What should I avoid while taking diphenhydramine?


Use caution when driving, operating machinery, or performing other hazardous activities. Diphenhydramine may cause dizziness or drowsiness. If you experience dizziness or drowsiness, avoid these activities. Use alcohol cautiously. Alcohol may increase drowsiness and dizziness while taking diphenhydramine.

Diphenhydramine side effects


Stop taking diphenhydramine and seek emergency medical attention if you experience an allergic reaction (difficulty breathing; closing of your throat; swelling of your lips, tongue, or face; or hives).

Other, less serious side effects may be more likely to occur. Continue to take diphenhydramine and talk to your doctor if you experience



  • sleepiness, fatigue, or dizziness;




  • headache;




  • dry mouth; or




  • difficulty urinating or an enlarged prostate.



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.


Diphenhydramine Dosing Information


Usual Adult Dose for Extrapyramidal Reaction:

Parenteral: 10 to 50 mg IV or IM as needed. May increase dose to 100 mg if required. Maximum daily dose 400 mg.

Oral: 25 to 50 mg orally every 6 to 8 hours.

Usual Adult Dose for Insomnia:

25 to 50 mg orally at bedtime.

Usual Adult Dose for Motion Sickness:

Parenteral: 10 to 50 mg IV or IM as needed. May increase dose to 100 mg if required. Maximum daily dose 400 mg.

Oral: 25 to 50 mg orally every 6 to 8 hours. Administer first dose 30 minutes before exposure to motion and repeat before meals and upon retiring for the duration of the journey.

Usual Adult Dose for Cough:

25 mg orally every 4 hours as needed, not to exceed 150 mg per day.

Usual Adult Dose for Cold Symptoms:

25 to 50 mg orally every 4 to 6 hours as needed, not to exceed 300 mg/24 hours.

Usual Adult Dose for Pruritus:

25 to 50 mg orally every 4 to 6 hours as needed, not to exceed 300 mg/24 hours.

Usual Adult Dose for Urticaria:

25 to 50 mg orally every 4 to 6 hours as needed, not to exceed 300 mg/24 hours.

Usual Pediatric Dose for Allergic Rhinitis:

Greater than or equal to 2 to less than 6 years: 6.25 mg orally every 4 to 6 hours, not to exceed 37.5 mg/24 hours.

Greater than or equal to 6 to less than 12 years: 12.5 to 25 mg orally every 4 to 6 hours, not to exceed 150 mg/24 hours.

Greater than or equal to 12 years: 25 to 50 mg orally every 4 to 6 hours, not to exceed 300 mg/24 hours.

Usual Pediatric Dose for Cold Symptoms:

Greater than or equal to 2 to less than 6 years: 6.25 mg orally every 4 to 6 hours, not to exceed 37.5 mg/24 hours.

Greater than or equal to 6 to less than 12 years: 12.5 to 25 mg orally every 4 to 6 hours, not to exceed 150 mg/24 hours.

Greater than or equal to 12 years: 25 to 50 mg orally every 4 to 6 hours, not to exceed 300 mg/24 hours.

Usual Pediatric Dose for Motion Sickness:

Greater than or equal to 2 to less than 6 years: 6.25 mg orally every 4 to 6 hours, not to exceed 37.5 mg/24 hours.

Greater than or equal to 6 to less than 12 years: 12.5 to 25 mg orally every 4 to 6 hours, not to exceed 150 mg/24 hours.

Greater than or equal to 12 years: 25 to 50 mg orally every 4 to 6 hours, not to exceed 300 mg/24 hours.

Usual Pediatric Dose for Insomnia:

Greater than or equal to 12 years: 25 to 50 mg orally at bedtime.

Usual Pediatric Dose for Cough:

Greater than or equal to 2 to less than 6 years: 6.25 mg orally every 4 hours, not to exceed 37.5 mg/24 hours.

Greater than or equal to 6 to less than 12 years: 12.5 mg orally every 4 hours, not to exceed 75 mg/24 hours.

Greater than or equal to 12 years: 25 mg orally every 4 hours, not to exceed 150 mg/24 hours.

Usual Pediatric Dose for Extrapyramidal Reaction:

In dystonic reactions: 1 to 2 mg/kg (max: 50 mg) IV or IM [Pediatric Advanced Life Support]

Usual Pediatric Dose for Allergic Reaction:

1 to 12 years: 5 mg/kg/day or 150 mg/m2/day administered orally, IM or IV, in equally divided doses every 6 to 8 hours, not to exceed 300 mg/24 hours.

In acute hypersensitivity reactions: 1 to 2 mg/kg IV or IM (max: 50 mg) [Advanced Pediatric Life Support]


What other drugs will affect diphenhydramine?


Do not take diphenhydramine if you have taken a monoamine oxidase inhibitor (MAOI) such as isocarboxazid (Marplan), phenelzine (Nardil), or tranylcypromine (Parnate) in the last 14 days. A very dangerous drug interaction could occur, leading to serious side effects.

Talk to your pharmacist before taking other over-the-counter cough, cold, allergy, or insomnia medications. These products may contain medicines similar to diphenhydramine, which could lead to an antihistamine overdose.


Before taking this medication, tell your doctor if you are taking any of the following medicines:



  • anxiety or sleep medicines such as alprazolam (Xanax), diazepam (Valium), chlordiazepoxide (Librium), temazepam (Restoril), or triazolam (Halcion);




  • medications for depression such as amitriptyline (Elavil), doxepin (Sinequan), nortriptyline (Pamelor), fluoxetine (Prozac), sertraline (Zoloft), or paroxetine (Paxil); or




  • any other medications that make you feel drowsy, sleepy, or relaxed.



Drugs other than those listed here may also interact with diphenhydramine. Talk to your doctor and pharmacist before taking any prescription or over-the-counter medicines, including vitamins, minerals, and herbal products.



More diphenhydramine resources


  • Diphenhydramine Use in Pregnancy & Breastfeeding
  • Drug Images
  • Diphenhydramine Drug Interactions
  • Diphenhydramine Support Group
  • 58 Reviews for Diphenhydramine - Add your own review/rating


  • Banophen MedFacts Consumer Leaflet (Wolters Kluwer)

  • Ben-Tann Suspension MedFacts Consumer Leaflet (Wolters Kluwer)

  • Benadryl Consumer Overview

  • Benadryl Cream MedFacts Consumer Leaflet (Wolters Kluwer)

  • Benadryl Allergy Chewable Tablets MedFacts Consumer Leaflet (Wolters Kluwer)

  • Children's Allergy Prescribing Information (FDA)

  • Diphen Advanced Consumer (Micromedex) - Includes Dosage Information

  • Diphenhydramine MedFacts Consumer Leaflet (Wolters Kluwer)

  • Diphenhydramine Prescribing Information (FDA)

  • Diphenhydramine Hydrochloride Monograph (AHFS DI)

  • Diphenoxylate Hydrochloride Monograph (AHFS DI)

  • Dytuss Elixir MedFacts Consumer Leaflet (Wolters Kluwer)

  • Simply Sleep MedFacts Consumer Leaflet (Wolters Kluwer)

  • Sominex MedFacts Consumer Leaflet (Wolters Kluwer)



Compare diphenhydramine with other medications


  • Allergic Reactions
  • Cold Symptoms
  • Cough
  • Extrapyramidal Reaction
  • Hay Fever
  • Insomnia
  • Motion Sickness
  • Nausea/Vomiting
  • Pruritus
  • Urticaria


Where can I get more information?


  • Your pharmacist can provide more information about diphenhydramine.


Saturday, 4 April 2009

Morzet




Morzet may be available in the countries listed below.


Ingredient matches for Morzet



Nicomorphine

Nicomorphine hydrochloride (a derivative of Nicomorphine) is reported as an ingredient of Morzet in the following countries:


  • Netherlands

International Drug Name Search

Thursday, 2 April 2009

Brondix




Brondix may be available in the countries listed below.


Ingredient matches for Brondix



Amoxicillin

Amoxicillin trihydrate (a derivative of Amoxicillin) is reported as an ingredient of Brondix in the following countries:


  • Spain

International Drug Name Search

Wednesday, 1 April 2009

Rivamer




Rivamer may be available in the countries listed below.


Ingredient matches for Rivamer



Rivastigmine

Rivastigmine tartrate (a derivative of Rivastigmine) is reported as an ingredient of Rivamer in the following countries:


  • Myanmar

International Drug Name Search