Wednesday, 27 January 2010

Sinvastatina Bluepharma




Sinvastatina Bluepharma may be available in the countries listed below.


Ingredient matches for Sinvastatina Bluepharma



Simvastatin

Simvastatin is reported as an ingredient of Sinvastatina Bluepharma in the following countries:


  • Portugal

International Drug Name Search

Monday, 25 January 2010

Diflucan Intravenous



Generic Name: fluconazole (Intravenous route)

floo-KON-a-zole

Commonly used brand name(s)

In the U.S.


  • Diflucan IV

In Canada


  • Diflucan

Available Dosage Forms:


  • Solution

  • Injectable

Therapeutic Class: Antifungal


Chemical Class: Triazole


Uses For Diflucan


Fluconazole injection is used to treat serious fungal or yeast infections, such as vaginal candidiasis, oropharyngeal candidiasis (thrush, oral thrush), esophageal candidiasis (candida esophagitis), other candida infections (including urinary tract infections, peritonitis [inflammation of the lining of the abdomen or stomach], and infections that may occur in different parts of the body), or fungal (cryptococcal) meningitis. This medicine works by killing the fungus or yeast, or preventing its growth.


Fluconazole injection is also used to prevent candidiasis in patients having bone marrow transplants, who receive cancer or radiation treatment.


This medicine is to be given only by or under the direct supervision of a doctor.


Before Using Diflucan


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


Appropriate studies performed to date have not demonstrated pediatric-specific problems that would limit the usefulness of fluconazole injection in children 6 months to 13 years of age. However, safety and efficacy have not been established in infants younger than 6 months of age.


Geriatric


Appropriate studies performed to date have not demonstrated geriatric-specific problems that would limit the usefulness of fluconazole injection in the elderly. However, elderly patients are more likely to have age-related kidney problems, which may require an adjustment in the dose for patients receiving fluconazole injection.


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


Studies in women suggest that this medication poses minimal risk to the infant when used during 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 receiving 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.


  • Alfuzosin

  • Astemizole

  • Bepridil

  • Cisapride

  • Clozapine

  • Crizotinib

  • Dasatinib

  • Dronedarone

  • Granisetron

  • Lapatinib

  • Levomethadyl

  • Lumefantrine

  • Mesoridazine

  • Nilotinib

  • Ondansetron

  • Pimozide

  • Quetiapine

  • Salmeterol

  • Sorafenib

  • Sparfloxacin

  • Sunitinib

  • Terfenadine

  • Thioridazine

  • Vardenafil

  • Ziprasidone

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.


  • Acenocoumarol

  • Ajmaline

  • Alprazolam

  • Amiodarone

  • Amisulpride

  • Amitriptyline

  • Amoxapine

  • Anisindione

  • Apomorphine

  • Aprindine

  • Arsenic Trioxide

  • Asenapine

  • Atorvastatin

  • Azithromycin

  • Bretylium

  • Cerivastatin

  • Chloral Hydrate

  • Chloroquine

  • Chlorpromazine

  • Ciprofloxacin

  • Citalopram

  • Clarithromycin

  • Clomipramine

  • Clopidogrel

  • Colchicine

  • Desipramine

  • Dibenzepin

  • Dicumarol

  • Dihydroergotamine

  • Disopyramide

  • Dofetilide

  • Dolasetron

  • Doxepin

  • Droperidol

  • Enflurane

  • Eplerenone

  • Ergoloid Mesylates

  • Ergonovine

  • Ergotamine

  • Erythromycin

  • Everolimus

  • Fentanyl

  • Flecainide

  • Fluoxetine

  • Foscarnet

  • Gatifloxacin

  • Gemifloxacin

  • Halofantrine

  • Haloperidol

  • Halothane

  • Hydroquinidine

  • Ibutilide

  • Iloperidone

  • Imipramine

  • Isoflurane

  • Isradipine

  • Levofloxacin

  • Lidoflazine

  • Lopinavir

  • Lorcainide

  • Lovastatin

  • Mefloquine

  • Methylergonovine

  • Moxifloxacin

  • Nevirapine

  • Nitrofurantoin

  • Norfloxacin

  • Nortriptyline

  • Octreotide

  • Ofloxacin

  • Paliperidone

  • Pazopanib

  • Pentamidine

  • Perflutren Lipid Microsphere

  • Phenindione

  • Phenprocoumon

  • Pirmenol

  • Posaconazole

  • Prajmaline

  • Probucol

  • Procainamide

  • Prochlorperazine

  • Promethazine

  • Propafenone

  • Protriptyline

  • Quinidine

  • Quinine

  • Ranolazine

  • Rifabutin

  • Risperidone

  • Sertindole

  • Simvastatin

  • Sirolimus

  • Sodium Phosphate

  • Sodium Phosphate, Dibasic

  • Sodium Phosphate, Monobasic

  • Solifenacin

  • Sotalol

  • Spiramycin

  • Sulfamethoxazole

  • Sultopride

  • Telavancin

  • Telithromycin

  • Tetrabenazine

  • Tolvaptan

  • Toremifene

  • Trazodone

  • Triazolam

  • Trifluoperazine

  • Trimethoprim

  • Trimipramine

  • Vandetanib

  • Vasopressin

  • Vemurafenib

  • Voriconazole

  • Warfarin

  • Zolmitriptan

  • Zotepine

Using this medicine with any of the following medicines may cause an increased risk of certain side effects, but using both drugs may be the best treatment for you. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines.


  • Alfentanil

  • Amlodipine

  • Atevirdine

  • Carbamazepine

  • Celecoxib

  • Cyclosporine

  • Etravirine

  • Felodipine

  • Fosphenytoin

  • Glimepiride

  • Losartan

  • Methadone

  • Midazolam

  • Nicardipine

  • Nifedipine

  • Omeprazole

  • Phenytoin

  • Prednisone

  • Ramelteon

  • Rifampin

  • Rifapentine

  • Rosuvastatin

  • Saquinavir

  • Tacrolimus

  • Tipranavir

  • Tretinoin

  • Trimetrexate

  • Valdecoxib

  • Vincristine

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:


  • Electrolyte problems (mineral imbalance) or

  • Heart disease—Use with caution. These conditions may increase your chance of having heart rhythm problems and make the effects of this medicine worse.

  • Heart rhythm problems (e.g., QT prolongation) or

  • Liver disease—Use with caution. May make these conditions worse.

  • Kidney disease—Use with caution. The effects may be increased because of slower removal of the medicine from the body.

Proper Use of fluconazole

This section provides information on the proper use of a number of products that contain fluconazole. It may not be specific to Diflucan. Please read with care.


A nurse or other trained health professional will give you or your child this medicine. This medicine is given through a needle placed in one of your veins.


Your doctor will give you or your child a few doses of this medicine until your condition improves, and then switch you to an oral medicine that works the same way. If you have any concerns about this, talk to your doctor.


Precautions While Using Diflucan


It is very important that your doctor check the progress of you or your child at regular visits to make sure this medicine is working properly. Blood tests may be needed to check for unwanted effects.


If your or your child's symptoms do not improve, or if they become worse, check with your doctor. You may need to use this medicine for several months before your infection gets better.


You or your child should not use astemizole (Hismanal®), cisapride (Propulsid®), pimozide (Orap®), quinidine (Cardioquin®), or terfenadine (Seldane®) while receiving this medicine because of the risk of unwanted side effects.


Using this medicine for a long time or using it too much while you are pregnant (especially during the first trimester) can harm your unborn baby. Use an effective form of birth control to keep from getting pregnant. If you think you have become pregnant while using this medicine, tell your doctor right away.


This medicine may rarely cause serious liver problems. Stop using this medicine and check with your doctor right away if you or your child are having more than one of these symptoms: abdominal or stomach pain or tenderness; clay-colored stools; dark urine; decreased appetite; fever; headache; itching; loss of appetite; nausea and vomiting; skin rash; swelling of the feet or lower legs; unusual tiredness or weakness; or yellow eyes or skin.


This medicine may rarely cause a serious type of allergic reaction called anaphylaxis. Anaphylaxis can be life-threatening and requires immediate medical attention. Tell your doctor right away if you or your child have a rash; itching; swelling of the face, tongue, and throat; trouble breathing; or chest pain after you receive the medicine.


Serious skin reactions can occur in certain people during treatment with this medicine. Check with your doctor right away if you or your child start having a skin rash, itching, or any other skin changes while you are using this medicine.


This medicine may rarely cause a heart rhythm problem called QT prolongation. It may change the way your heart beats and cause fainting or serious side effects in some patients. Check with your doctor right away if you or your child have any symptoms of heart rhythm problems, such as fast, pounding, or irregular heartbeats.


This medicine may cause some people to become dizzy, drowsy, or less alert than they are normally. Make sure you know how you react to this medicine before you drive, use machines, or do anything else that could be dangerous if you are dizzy or not alert.


Do not take other medicines unless they have been discussed with your doctor. This includes prescription or nonprescription (over-the-counter [OTC]) medicines and herbal or vitamin supplements.


Diflucan 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 or nurse immediately if any of the following side effects occur:


Rare
  • Abdominal or stomach pain

  • chills

  • clay-colored stools

  • cough

  • dark urine

  • diarrhea

  • difficulty with swallowing

  • dizziness

  • fast heartbeat

  • fever

  • general feeling of tiredness or weakness

  • headache

  • hives

  • itching

  • large, hive-like swelling on the face, eyelids, lips, tongue, throat, hands, legs, feet, or sex organs

  • light-colored stools

  • loss of appetite

  • nausea and vomiting

  • puffiness or swelling of the eyelids or around the eyes, face, lips, or tongue

  • shortness of breath

  • skin rash

  • stomach pain, continuing

  • tightness in the chest

  • unpleasant breath odor

  • unusual tiredness or weakness

  • upper right abdominal or stomach pain

  • vomiting of blood

  • wheezing

  • yellow eyes and skin

Incidence not known
  • Black, tarry stools

  • blistering, peeling, or loosening of the skin

  • chest pain or discomfort

  • convulsions

  • decreased urine

  • dry mouth

  • fainting

  • hoarseness

  • increased thirst

  • irregular or slow heart rate

  • joint or muscle pain

  • loss of bladder control

  • lower back or side pain

  • mood changes

  • muscle pain or cramps

  • muscle spasm or jerking of all extremities

  • numbness or tingling in the hands, feet, or lips

  • painful or difficult urination

  • pale skin

  • red skin lesions, often with a purple center

  • red, irritated eyes

  • sore throat

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

  • sudden loss of consciousness

  • swollen glands

  • unusual bleeding or bruising

Get emergency help immediately if any of the following symptoms of overdose occur:


Symptoms of overdose
  • Fearfulness, suspiciousness, or other mental changes

  • seeing, hearing, or feeling things that are not there

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
  • Acid or sour stomach

  • belching

  • change in taste or bad, unusual, or unpleasant (after) taste

  • heartburn

  • indigestion

  • stomach discomfort or upset

Incidence not known
  • Hair loss or thinning of the hair

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: Diflucan Intravenous 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 Diflucan Intravenous resources


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


Compare Diflucan Intravenous with other medications


  • Blastomycosis
  • Bone Marrow Transplantation
  • Candida Infections, Systemic
  • Candida Urinary Tract Infection
  • Chronic Mucocutaneous Candidiasis
  • Coccidioidomycosis
  • Coccidioidomycosis, Meningitis
  • Cryptococcal Meningitis, Immunocompetent Host
  • Cryptococcal Meningitis, Immunosuppressed Host
  • Cryptococcosis
  • Esophageal Candidiasis
  • Fungal Infection Prophylaxis
  • Fungal Infection, Internal and Disseminated
  • Fungal Peritonitis
  • Fungal Pneumonia
  • Histoplasmosis
  • Onychomycosis, Fingernail
  • Onychomycosis, Toenail
  • Oral Thrush
  • Tinea Versicolor
  • Vaginal Yeast Infection

Saturday, 23 January 2010

Zopitin




Zopitin may be available in the countries listed below.


Ingredient matches for Zopitin



Eszopiclone

Zopiclone is reported as an ingredient of Zopitin in the following countries:


  • Czech Republic

  • Estonia

  • Finland

  • Latvia

  • Lithuania

  • Poland

  • Slovakia

International Drug Name Search

Dapsone




In the US, Dapsone (dapsone systemic) is a member of the drug class leprostatics and is used to treat Bullous Pemphigoid, Dermatitis Herpetiformis, Leprosy, Leprosy - Lepromatous, Leprosy - Tuberculoid, Leukocytoclastic Vasculitis, Pemphigoid, Pemphigus, Pneumocystis Pneumonia, Pneumocystis Pneumonia Prophylaxis and Toxoplasmosis - Prophylaxis.

US matches:

  • Dapsone

  • Dapsone Gel

  • Dapsone topical

Scheme

Rec.INN

ATC (Anatomical Therapeutic Chemical Classification)

D10AX05,J04BA02

CAS registry number (Chemical Abstracts Service)

0000080-08-0

Chemical Formula

C12-H12-N2-O2-S

Molecular Weight

248

Therapeutic Category

Antileprotic agent

Chemical Name

Benzenamine, 4,4'-sulfonylbis-

Foreign Names

  • Dapsonum (Latin)
  • Dapson (German)
  • Dapsone (French)
  • Dapsona (Spanish)

Generic Names

  • Dapsone (OS: BAN, USAN, DCIT, DCF)
  • DADPS (IS)
  • DDS (IS)
  • Diaphenylsulfon (IS)
  • Diaphénylsulfone (IS)
  • Diphenason (IS)
  • F 1358 (IS)
  • NSC 6091 (IS)
  • Dapson (PH: Ph. Eur. 6)
  • Dapsone (PH: BP 2010, Ph. Int. 4, USP 32, Ph. Eur. 6)
  • Dapsonum (PH: Ph. Int. 4, Ph. Eur. 6)

Brand Names

  • Aczone
    Allergan, United States


  • Avlosulfon
    AstraZeneca, Ethiopia


  • Daps
    Pfizer, Argentina


  • Dapsoderm-X
    Mex-América, Mexico


  • Dapson PCH
    Pharmachemie, Netherlands


  • Dapson ratiopharm
    ratiopharm, Netherlands


  • Dapson Scanpharm
    Scanpharm, Denmark


  • Dapson
    Weifa, Norway


  • Dapsone
    Actavis, United Kingdom; Jacobus, Canada; Jacobus, United States; Link, Australia; Link, New Zealand


  • Dapson-Fatol
    Riemser, Germany


  • Disulone (Dapsone and Ferrous Oxalate)
    Aventis, Slovakia; Sanofi-Aventis, France


  • Lectisol
    Tanabe Mitsubishi, Japan


  • Lennon-Dapsone
    Aspen Pharmacare, South Africa


  • Protogen
    Tanabe Mitsubishi, Japan


  • Sulfona Zimaia
    Zimaia, Portugal


  • Sulfona
    Orsade, Spain

International Drug Name Search

Glossary

BANBritish Approved Name
DCFDénomination Commune Française
DCITDenominazione Comune Italiana
ISInofficial Synonym
OSOfficial Synonym
PHPharmacopoeia Name
Rec.INNRecommended International Nonproprietary Name (World Health Organization)
USANUnited States Adopted Name

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

Brompheniramine/Pseudoephedrine Sustained-Release Tablets


Pronunciation: brome-fen-EER-ah-meen/soo-doe-eh-FED-rin
Generic Name: Brompheniramine/Pseudoephedrine
Brand Name: Examples include Bidhist-D and Lodrane 12D


Brompheniramine/Pseudoephedrine Sustained-Release Tablets are used for:

Relieving symptoms of sinus congestion, pressure, runny nose, and sneezing due to colds, upper respiratory infections, and allergies. It may also be used for other conditions as determined by your doctor.


Brompheniramine/Pseudoephedrine Sustained-Release Tablets are an antihistamine and decongestant combination. The antihistamine works by blocking the action of histamine, which helps reduce symptoms such as watery eyes and sneezing. The decongestant promotes sinus and nasal drainage, which relieves congestion and pressure.


Do NOT use Brompheniramine/Pseudoephedrine Sustained-Release Tablets if:


  • you are allergic to any ingredient in Brompheniramine/Pseudoephedrine Sustained-Release Tablets

  • you have severe high blood pressure, severe heart blood vessel disease, rapid heartbeat, or severe heart problems

  • you take sodium oxybate (GHB) or if you have taken furazolidone or a monoamine oxidase (MAO) inhibitor (eg, phenelzine) within the last 14 days

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



Before using Brompheniramine/Pseudoephedrine Sustained-Release Tablets:


Some medical conditions may interact with Brompheniramine/Pseudoephedrine Sustained-Release Tablets. 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 fast, slow, or irregular heartbeat; heart blood vessel problems; or other heart problems

  • if you have a history of asthma; lung problems (eg, emphysema); adrenal gland problems (eg, adrenal gland tumor); high blood pressure; diabetes; stroke; glaucoma; a blockage of your stomach, bladder, or intestines; ulcers; trouble urinating; an enlarged prostate; seizures; or an overactive thyroid

Some MEDICINES MAY INTERACT with Brompheniramine/Pseudoephedrine Sustained-Release Tablets. Tell your health care provider if you are taking any other medicines, especially any of the following:


  • Beta-blockers (eg, propranolol), COMT inhibitors (eg, tolcapone), furazolidone, indomethacin, MAO inhibitors (eg, phenelzine), sodium oxybate (GHB), or tricyclic antidepressants (eg, amitriptyline) because side effects of Brompheniramine/Pseudoephedrine Sustained-Release Tablets may be increased

  • Digoxin or droxidopa because the risk of irregular heartbeat or heart attack may be increased

  • Bromocriptine or hydantoins (eg, phenytoin) because side effects may be increased by Brompheniramine/Pseudoephedrine Sustained-Release Tablets

  • Guanadrel, guanethidine, methyldopa, mecamylamine, or reserpine because effectiveness may be decreased by Brompheniramine/Pseudoephedrine Sustained-Release Tablets

This may not be a complete list of all interactions that may occur. Ask your health care provider if Brompheniramine/Pseudoephedrine Sustained-Release Tablets 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 Brompheniramine/Pseudoephedrine Sustained-Release Tablets:


Use Brompheniramine/Pseudoephedrine Sustained-Release Tablets as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • Brompheniramine/Pseudoephedrine Sustained-Release Tablets may be taken with or without food.

  • Swallow Brompheniramine/Pseudoephedrine Sustained-Release Tablets whole. Do not break, crush, or chew before swallowing. Some brands of Brompheniramine/Pseudoephedrine Sustained-Release Tablets may be broken in half before they are taken. If you have difficulty swallowing the whole tablet, ask your pharmacist if your brand may be broken in half.

  • If you miss a dose of Brompheniramine/Pseudoephedrine Sustained-Release Tablets, 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 Brompheniramine/Pseudoephedrine Sustained-Release Tablets.



Important safety information:


  • Brompheniramine/Pseudoephedrine Sustained-Release Tablets may cause dizziness, drowsiness, or blurred vision. Do not drive, operate machinery, or do anything else that could be dangerous until you know how you react to Brompheniramine/Pseudoephedrine Sustained-Release Tablets. Using Brompheniramine/Pseudoephedrine Sustained-Release Tablets alone, with certain other medicines, or with alcohol may lessen your ability to drive or perform other potentially dangerous tasks.

  • Do not take diet or appetite control medicines while you are taking Brompheniramine/Pseudoephedrine Sustained-Release Tablets without checking with your doctor.

  • Brompheniramine/Pseudoephedrine Sustained-Release Tablets contains pseudoephedrine. Before you begin taking any new prescription or nonprescription medicine, read the ingredients to see if it also contains pseudoephedrine. If it does or if you are uncertain, contact your doctor or pharmacist.

  • Do NOT exceed the recommended dose or take Brompheniramine/Pseudoephedrine Sustained-Release Tablets for longer than prescribed without checking with your doctor.

  • If your symptoms do not improve within 5 to 7 days or if they become worse, check with your doctor.

  • Brompheniramine/Pseudoephedrine Sustained-Release Tablets may cause increased sensitivity to the sun. Avoid exposure to the sun, sunlamps, or tanning booths until you know how you react to Brompheniramine/Pseudoephedrine Sustained-Release Tablets. Use a sunscreen or protective clothing if you must be outside for a prolonged period.

  • If you are scheduled for allergy skin testing, do not take Brompheniramine/Pseudoephedrine Sustained-Release Tablets for several days before the test because it may decrease your response to the skin tests.

  • Before you have any medical or dental treatments, emergency care, or surgery, tell the doctor or dentist that you are using Brompheniramine/Pseudoephedrine Sustained-Release Tablets.

  • Use Brompheniramine/Pseudoephedrine Sustained-Release Tablets with caution in the ELDERLY because they may be more sensitive to its effects.

  • Caution is advised when using Brompheniramine/Pseudoephedrine Sustained-Release Tablets in CHILDREN because they may be more sensitive to its effects.

  • PREGNANCY and BREAST-FEEDING: If you become pregnant while taking Brompheniramine/Pseudoephedrine Sustained-Release Tablets, discuss with your doctor the benefits and risks of using Brompheniramine/Pseudoephedrine Sustained-Release Tablets during pregnancy. It is unknown if Brompheniramine/Pseudoephedrine Sustained-Release Tablets are excreted in breast milk. Do not breast-feed while taking Brompheniramine/Pseudoephedrine Sustained-Release Tablets.


Possible side effects of Brompheniramine/Pseudoephedrine Sustained-Release Tablets:


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



Constipation; diarrhea; dizziness; drowsiness; excitability; headache; loss of appetite; nausea; nervousness or anxiety; trouble sleeping; upset stomach; vomiting; weakness.



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

Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); difficulty urinating or inability to urinate; fast or irregular heartbeat; hallucinations; seizures; severe dizziness, lightheadedness, or headache; tremor; trouble sleeping; vision changes.



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


See also: Brompheniramine/Pseudoephedrine 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 blurred vision; confusion; hallucinations; seizures; severe dizziness, lightheadedness, or headache; severe drowsiness; unusually fast, slow, or irregular heartbeat; vomiting.


Proper storage of Brompheniramine/Pseudoephedrine Sustained-Release Tablets:

Store Brompheniramine/Pseudoephedrine Sustained-Release Tablets at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Brompheniramine/Pseudoephedrine Sustained-Release Tablets out of the reach of children and away from pets.


General information:


  • If you have any questions about Brompheniramine/Pseudoephedrine Sustained-Release Tablets, please talk with your doctor, pharmacist, or other health care provider.

  • Brompheniramine/Pseudoephedrine Sustained-Release Tablets are 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 Brompheniramine/Pseudoephedrine Sustained-Release Tablets. 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 Brompheniramine/Pseudoephedrine resources


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


Compare Brompheniramine/Pseudoephedrine with other medications


  • Hay Fever
  • Nasal Congestion

Sunday, 17 January 2010

bexarotene


Generic Name: bexarotene (beks AIR oh teen)

Brand Names: Targretin


What is bexarotene ?

The exact way bexarotene works is unknown, but it is believed to inhibit the growth of tumor cells.


Bexarotene is used to treat skin lesions of cutaneous T-cell lymphoma (CTCL) in patients who have not responded to or not tolerated other therapies.


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


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


Avoid prolonged exposure to sunlight or artificial ultraviolet light (e.g. sunlamps). Bexarotene may increase the sensitivity of your skin to sunlight. Use a sunscreen and wear protective clothing when exposure to the sun is unavoidable. Do not take bexarotene if you are pregnant or if you could become pregnant. Bexarotene is in the FDA pregnancy category X. This means that bexarotene will cause birth defects in an unborn baby. You must take a pregnancy test and have negative results within one week before starting treatment with bexarotene, and a pregnancy test should be repeated monthly during treatment. Bexarotene should be started on the second or third day of a normal menstrual period. Also, you will need to use two reliable forms of birth control at the same time for one month before starting treatment with bexarotene, during treatment with bexarotene, and for at least 1 month following the end of your treatment. If you become pregnant, stop using birth control, or miss your menstrual period, immediately stop taking bexarotene and notify your doctor. Men taking bexarotene with sexual partners who are pregnant, possibly pregnant, or who could become pregnant, must use condoms during sexual intercourse while using bexarotene and for at least one month after the last dose of bexarotene. Swallow each capsule whole. Do not chew them, dissolve them in liquid, or allow them to dissolve in your mouth.

Your doctor will want to monitor the levels of lipids (triglycerides and cholesterol) and thyroid hormones in your blood periodically during treatment with bexarotene. Treatment may be necessary if your cholesterol or triglyceride levels become elevated, or if your thyroid hormone levels are low.


Grapefruit and grapefruit juice may interact with bexarotene. The interaction could have potentially dangerous effects. Discuss the use of grapefruit and grapefruit juice with your doctor. Do not increase or decrease the amount of grapefruit products in your diet without first talking to your doctor.

What should I discuss with my healthcare provider before using bexarotene?


Do not take bexarotene without first talking to your doctor if you

  • are allergic to other retinoids such as isotretinoin (Accutane), acitretin (Soriatane), etretinate (Tegison), or tretinoin (Vesinoid);




  • have or ever have had pancreatitis (inflammation of the pancreas);




  • have high triglyceride levels in your blood;




  • have diabetes mellitus;




  • have or ever have had gall bladder disease;




  • have or ever have had liver disease;




  • regularly drink alcohol;




  • are taking gemfibrozil (Lopid);




  • are taking any prescription medication especially for fungal infections, bacterial infections, diabetes, or seizures; or,




  • eat grapefruit or drink grapefruit juice.



You may not be able to take bexarotene, or you may require a dosage adjustment or special monitoring during treatment if you have any of the conditions, or are taking any of the medications listed above.


Do not take bexarotene if you are pregnant or if you could become pregnant. Bexarotene is in the FDA pregnancy category X. This means that bexarotene will cause birth defects in an unborn baby. You must take a pregnancy test and have negative results within one week before starting treatment with bexarotene, and a pregnancy test should be repeated monthly during treatment. Bexarotene should be started on the second or third day of a normal menstrual period. Also, you will need to use two reliable forms of birth control at the same time for one month before starting treatment with bexarotene, during treatment with bexarotene, and for at least 1 month following the end of your treatment. If you become pregnant, stop using birth control, or miss your menstrual period, immediately stop taking bexarotene and notify your doctor. Men taking bexarotene with sexual partners who are pregnant, possibly pregnant, or who could become pregnant, must use condoms during sexual intercourse while using bexarotene and for at least one month after the last dose of bexarotene. It is not known whether bexarotene passes into breast milk. Do not take bexarotene without first talking to your doctor if you are breast-feeding a baby.

How should I use bexarotene ?


Take bexarotene exactly as directed by your doctor. If you do not understand these instructions, ask your pharmacist, nurse, or doctor to explain them to you.


Your doctor will tell you how many bexarotene capsules to take each day. Take your daily dose of bexarotene all at once. Take bexarotene once a day with or immediately following a meal. Swallow each capsule whole. Do not chew them, dissolve them in liquid, or allow them to dissolve in your mouth. Do not take any bexarotene capsules after the expiration date printed on the label.

If any bexarotene capsules are broken or leaking, do not touch the capsules or the contents and notify your pharmacist immediately. If the contents of a broken capsule get on your skin, immediately wash the area with soap and water and notify your physician.


Your doctor will want to monitor the levels of lipids (triglycerides and cholesterol) and thyroid hormones in your blood periodically during treatment with bexarotene. Treatment may be necessary if your cholesterol or triglyceride levels become elevated, or if your thyroid hormone levels are low.


It may take many weeks of treatment to see the effects of this drug. Do not stop taking bexarotene if you do not see results immediately. Some patients treated with bexarotene see improvement within the first several weeks of treatment, however most patients require several months or more of treatment to improve.


Store bexarotene at room temperature away from moisture and heat. Keep this product out of the reach of children.

What happens if I miss a dose?


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


What happens if I overdose?


Seek emergency medical attention.

Symptoms of a bexarotene overdose are unknown.


What should I avoid while using bexarotene ?


Avoid prolonged exposure to sunlight or artificial ultraviolet light (e.g. sunlamps). Bexarotene may increase the sensitivity of your skin to sunlight. Use a sunscreen and wear protective clothing when exposure to the sun is unavoidable.

Vitamin A may increase side effects when taking bexarotene. Limit your use of vitamin A supplements to not more than the recommended daily allowance (RDA) of 4000 to 5000 International Units (IU) a day. If you take vitamins, check the label to see how much vitamin A they contain. If you are not sure, ask your doctor or pharmacist.


Grapefruit and grapefruit juice may interact with bexarotene. The interaction could have potentially dangerous effects. Discuss the use of grapefruit and grapefruit juice with your doctor. Do not increase or decrease the amount of grapefruit products in your diet without first talking to your doctor.

Bexarotene side effects


If you experience any of the following serious side effects, stop taking bexarotene and seek emergency medical attention:

  • an allergic reaction (difficulty breathing; closing of your throat; swelling of your lips, tongue, or face; or hives); or




  • symptoms of pancreatitis (inflammation of the pancreas) such as persistent nausea, vomiting, and abdominal or back pain.



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



  • an increase in fats in the blood (blood lipids) such as cholesterol or triglycerides (blood tests will detect this);




  • a underactive thyroid (blood tests will detect this);




  • blood problems;




  • headache;




  • fatigue;




  • weakness or loss of strength;




  • swelling;




  • rash;




  • dry skin;




  • infections;




  • nausea; or




  • diarrhea.



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. You may report side effects to FDA at 1-800-FDA-1088.


Bexarotene Dosing Information


Usual Adult Dose for Cutaneous T-cell Lymphoma:

Initial Dose: 300 mg/m2 orally once a day with a meal.

Bexarotene therapy may be continued for as long as the patient is deriving benefit.


What other drugs will affect bexarotene ?


Vitamin A may increase side effects when taking bexarotene. Limit your use of vitamin A supplements to not more than the recommended daily allowance (RDA) of 4000 to 5000 International Units (IU) a day. If you take vitamins, check the label to see how much vitamin A they contain. If you are not sure, ask your doctor or pharmacist.


Do not take bexarotene without first talking to your doctor if you are taking any of the following drugs:

  • gemfibrozil (Lopid);




  • ketoconazole (Nizoral) or itraconazole (Sporanox);




  • erythromycin (E.E.S., E-Mycin, Eryc, Ery-Tab, Ilosone, others);




  • rifampin (Rifadin, Rimactane);




  • phenobarbital (Luminal, Solfoton);




  • phenytoin (Dilantin, others); or




  • a diabetes medicine such as insulin, glipizide (Glucotrol), glyburide (Diabeta, Micronase, Glynase), chlorpropamide (Diabinese), tolbutamide (Orinase), tolazamide (Tolinase), glimepiride (Amaryl), rosiglitazone (Avandia), pioglitazone (Actos), metformin (Glucophage), and others.



You may not be able to take bexarotene, or you may require a dosage adjustment or special monitoring during treatment if you are taking any of the medicines listed above.


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



More bexarotene resources


  • Bexarotene Dosage
  • Bexarotene Use in Pregnancy & Breastfeeding
  • Bexarotene Drug Interactions
  • Bexarotene Support Group
  • 0 Reviews for Bexarotene - Add your own review/rating


  • bexarotene Advanced Consumer (Micromedex) - Includes Dosage Information

  • Bexarotene Professional Patient Advice (Wolters Kluwer)

  • Bexarotene Monograph (AHFS DI)

  • Bexarotene MedFacts Consumer Leaflet (Wolters Kluwer)

  • Targretin Prescribing Information (FDA)



Compare bexarotene with other medications


  • Cutaneous T-cell Lymphoma


Where can I get more information?


  • Your pharmacist has additional information about bexarotene written for health professionals that you may read.


Thursday, 14 January 2010

Letynol




Letynol may be available in the countries listed below.


Ingredient matches for Letynol



Cefotaxime

Cefotaxime sodium salt (a derivative of Cefotaxime) is reported as an ingredient of Letynol in the following countries:


  • Greece

International Drug Name Search

Monday, 11 January 2010

Sucralfato Pliva




Sucralfato Pliva may be available in the countries listed below.


Ingredient matches for Sucralfato Pliva



Sucralfate

Sucralfate is reported as an ingredient of Sucralfato Pliva in the following countries:


  • Italy

International Drug Name Search

Monday, 4 January 2010

Sulphasalazine




Sulphasalazine may be available in the countries listed below.


Ingredient matches for Sulphasalazine



Sulfasalazine

Sulfasalazine is reported as an ingredient of Sulphasalazine in the following countries:


  • Cyprus

International Drug Name Search

Bystolic



Generic Name: nebivolol (ne BIV oh lol)

Brand Names: Bystolic


What is nebivolol?

Nebivolol is in a group of drugs called beta-blockers. Beta-blockers affect the heart and circulation (blood flow through arteries and veins).


Nebivolol is used to treat hypertension (high blood pressure).


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


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


Do not skip doses or stop taking nebivolol without first talking to your doctor. Stopping suddenly may make your condition worse or cause other serious heart problems such as severe chest pain or heart attack. You may need to use less and less before you stop the medication completely. If you need surgery, tell the surgeon ahead of time that you are using nebivolol. Nebivolol may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert.

Nebivolol is only part of a complete program of treatment that also includes diet, exercise, and weight control. Follow your diet, medication, and exercise routines very closely.


Keep using this medicine as directed, even if you feel well. High blood pressure often has no symptoms. You may need to use blood pressure medication for the rest of your life.


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


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

  • severe liver disease; or




  • a heart problem such as heart block, sick sinus syndrome, slow heart rate, or heart failure.



If you have any of these other conditions, you may need a nebivolol dose adjustment or special tests:



  • asthma, bronchitis, emphysema;




  • liver or kidney disease;




  • diabetes;




  • a thyroid disorder;




  • a history of allergies;




  • problems with circulation (such as Raynaud's syndrome);




  • pheochromocytoma (tumor of the adrenal gland); or




  • if you have recently had a heart attack.




FDA pregnancy category C. It is not known whether nebivolol 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 nebivolol 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 nebivolol?


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.


Take nebivolol at the same time every day. You may take the medication with or without food.


Do not skip doses or stop taking nebivolol without first talking to your doctor. Stopping suddenly may make your condition worse or cause other serious heart problems such as severe chest pain or heart attack. You may need to use less and less before you stop the medication completely.

Your blood pressure will need to be checked often. Visit your doctor regularly.


If you need surgery, tell the surgeon ahead of time that you are using nebivolol.

Nebivolol is only part of a complete program of treatment that also includes diet, exercise, and weight control. Follow your diet, medication, and exercise routines very closely.


Keep using this medicine as directed, even if you feel well. High blood pressure often has no symptoms. You may need to use blood pressure medication for the rest of your life.


Store at room temperature away from moisture and heat.

See also: Bystolic dosage (in more detail)

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 slow heart rate, dizziness, vomiting, trouble breathing, or feeling like you might pass out.


What should I avoid while taking nebivolol?


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

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

  • feeling short of breath, even with mild exertion;




  • swelling of your ankles or feet;




  • slow or uneven heartbeats; or




  • numbness or cold feeling in your hands and feet.



Less serious side effects may include:



  • headache;




  • tired feeling;




  • nausea, stomach pain;




  • diarrhea; or




  • sleep problems (insomnia).



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 nebivolol?


Tell your doctor about all other medicines you use, especially:



  • digitalis (digoxin, Lanoxin);




  • clonidine (Catapres);




  • reserpine;




  • a heart or blood pressure medication such as diltiazem (Cartia, Cardizem), felodipine (Plendil), nifedipine (Nifedical, Procardia), verapamil (Calan, Covera, Isoptin, Verelan), and others;




  • heart rhythm medicine such as amiodarone (Cordarone, Pacerone), quinidine (Quin-G), procainamide (Pronestyl), disopyramide (Norpace), flecaininde (Tambocor), mexiletine (Mexitil), propafenone, (Rythmol), and others;




  • an antidepressant such as fluoxetine (Prozac), paroxetine (Paxil), and others; or




  • another beta-blocker such as atenolol (Tenormin, Tenoretic), carvedilol (Coreg), labetalol (Normodyne, Trandate), metoprolol (Lopressor, Toprol), nadolol (Corgard), propranolol (Inderal, InnoPran), sotalol (Betapace), and others.



This list is not complete and other drugs may interact with nebivolol. 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 Bystolic resources


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


  • Bystolic Prescribing Information (FDA)

  • Bystolic Monograph (AHFS DI)

  • Bystolic Advanced Consumer (Micromedex) - Includes Dosage Information

  • Bystolic Consumer Overview

  • Bystolic MedFacts Consumer Leaflet (Wolters Kluwer)

  • Nebivolol Professional Patient Advice (Wolters Kluwer)



Compare Bystolic with other medications


  • High Blood Pressure
  • Mitral Valve Prolapse


Where can I get more information?


  • Your pharmacist can provide more information about nebivolol.

See also: Bystolic side effects (in more detail)


Saturday, 2 January 2010

Venlafaxin Krewel




Venlafaxin Krewel may be available in the countries listed below.


Ingredient matches for Venlafaxin Krewel



Venlafaxine

Venlafaxine hydrochloride (a derivative of Venlafaxine) is reported as an ingredient of Venlafaxin Krewel in the following countries:


  • Germany

International Drug Name Search