Friday 31 December 2010

Precipitated Calcium Carbonate




Precipitated Calcium Carbonate may be available in the countries listed below.


Ingredient matches for Precipitated Calcium Carbonate



Calcium Carbonate

Precipitated Calcium Carbonate (JAN) is known as Calcium Carbonate in the US.

International Drug Name Search

Glossary

JANJapanese Accepted Name

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

Tuesday 28 December 2010

Isosorbide mononitraat Mylan




Isosorbide mononitraat Mylan may be available in the countries listed below.


Ingredient matches for Isosorbide mononitraat Mylan



Isosorbide Mononitrate

Isosorbide Mononitrate is reported as an ingredient of Isosorbide mononitraat Mylan in the following countries:


  • Netherlands

International Drug Name Search

Saturday 18 December 2010

Maxit




Maxit may be available in the countries listed below.


Ingredient matches for Maxit



Diclofenac

Diclofenac potassium salt (a derivative of Diclofenac) is reported as an ingredient of Maxit in the following countries:


  • Sri Lanka

International Drug Name Search

Thursday 16 December 2010

Ambasept




Ambasept may be available in the countries listed below.


Ingredient matches for Ambasept



Ambazone

Ambazone is reported as an ingredient of Ambasept in the following countries:


  • Romania

International Drug Name Search

DDAVP




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


In the US, DDAVP (desmopressin systemic) is a member of the drug class antidiuretic hormones and is used to treat Diabetes Insipidus, Hemophilia A, Primary Nocturnal Enuresis and von Willebrand's Disease.

US matches:

  • DDAVP

  • DDAVP Solution

  • DDAVP Spray (Non-refrigerated)

  • DDAVP Tube

  • DDAVP Rhinal Tube nasal

  • DDAVP injection

  • DDAVP nasal

  • DDAVP Rhinal Tube

  • DDAVP Nasal Spray

  • DDAVP Tablets

UK matches:

  • DDAVP/Desmopressin Injection
  • DDAVP Melt 60mcg, 120mcg and 240mcg oral lyophilisate (SPC)
  • DDAVP Tablets 0.1mg (SPC)
  • DDAVP Tablets 0.2mg (SPC)
  • DDAVP/Desmopressin Injection (SPC)
  • DDAVP/Desmopressin Intranasal Solution (SPC)

Ingredient matches for DDAVP



Desmopressin

Desmopressin is reported as an ingredient of DDAVP in the following countries:


  • Greece

  • Portugal

Desmopressin acetate (a derivative of Desmopressin) is reported as an ingredient of DDAVP in the following countries:


  • Canada

  • Chile

  • South Africa

  • United Kingdom

  • United States

International Drug Name Search

Glossary

SPC Summary of Product Characteristics (UK)

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

Wednesday 15 December 2010

Torbugesic




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

Ingredient matches for Torbugesic



Butorphanol

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


  • Australia

  • France

  • Germany

  • Ireland

  • New Zealand

  • United Kingdom

  • United States

International Drug Name Search

Anastrozol Teva




Anastrozol Teva may be available in the countries listed below.


Ingredient matches for Anastrozol Teva



Anastrozole

Anastrozole is reported as an ingredient of Anastrozol Teva in the following countries:


  • Latvia

  • Lithuania

  • Poland

  • Slovakia

  • Slovenia

  • Switzerland

International Drug Name Search

Monday 13 December 2010

Timolol T




Timolol T may be available in the countries listed below.


Ingredient matches for Timolol T



Timolol

Timolol maleate (a derivative of Timolol) is reported as an ingredient of Timolol T in the following countries:


  • Japan

International Drug Name Search

Saturday 11 December 2010

Giafen




Giafen may be available in the countries listed below.


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

Ingredient matches for Giafen



Guaifenesin

Guaifenesin is reported as an ingredient of Giafen in the following countries:


  • Australia

  • New Zealand

International Drug Name Search

Friday 3 December 2010

Gynostatin




Gynostatin may be available in the countries listed below.


Ingredient matches for Gynostatin



Nystatin

Nystatin is reported as an ingredient of Gynostatin in the following countries:


  • Peru

International Drug Name Search

Saturday 27 November 2010

Ginedermofix Vaginal




Ginedermofix Vaginal may be available in the countries listed below.


Ingredient matches for Ginedermofix Vaginal



Sertaconazole

Sertaconazole nitrate (a derivative of Sertaconazole) is reported as an ingredient of Ginedermofix Vaginal in the following countries:


  • Spain

International Drug Name Search

Friday 26 November 2010

Wipeout




Wipeout may be available in the countries listed below.


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

Ingredient matches for Wipeout



Deltamethrin

Deltamethrin is reported as an ingredient of Wipeout in the following countries:


  • New Zealand

International Drug Name Search

Sunday 21 November 2010

Limonata




Limonata may be available in the countries listed below.


Ingredient matches for Limonata



Magnesium Carbonate

Magnesium Carbonate is reported as an ingredient of Limonata in the following countries:


  • Greece

International Drug Name Search

Monday 8 November 2010

Gluconate de Calcium Lavoisier




Gluconate de Calcium Lavoisier may be available in the countries listed below.


Ingredient matches for Gluconate de Calcium Lavoisier



Calcium Glucoheptonate

Calcium Glucoheptonate is reported as an ingredient of Gluconate de Calcium Lavoisier in the following countries:


  • France

Calcium Gluconate

Calcium Gluconate is reported as an ingredient of Gluconate de Calcium Lavoisier in the following countries:


  • France

International Drug Name Search

Sunday 7 November 2010

Goserelin Acetate




Goserelin Acetate may be available in the countries listed below.


Ingredient matches for Goserelin Acetate



Goserelin

Goserelin Acetate (BANM, JAN) is known as Goserelin in the US.

International Drug Name Search

Glossary

BANMBritish Approved Name (Modified)
JANJapanese Accepted Name

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

Saturday 6 November 2010

Dodorest




Dodorest may be available in the countries listed below.


Ingredient matches for Dodorest



Zolpidem

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


  • Luxembourg

International Drug Name Search

Monday 1 November 2010

Benemide




Benemide may be available in the countries listed below.


Ingredient matches for Benemide



Probenecid

Probenecid is reported as an ingredient of Benemide in the following countries:


  • France

International Drug Name Search

Sunday 31 October 2010

Insulin Actrapid




Insulin Actrapid may be available in the countries listed below.


Ingredient matches for Insulin Actrapid



Insulin Injection, Soluble

Insulin Injection, Soluble human (a derivative of Insulin Injection, Soluble) is reported as an ingredient of Insulin Actrapid in the following countries:


  • Bahrain

  • Czech Republic

  • Finland

  • Iceland

  • Israel

  • Romania

  • Russian Federation

  • Serbia

  • Sri Lanka

Insulin Injection, Soluble porcine or bovine (a derivative of Insulin Injection, Soluble) is reported as an ingredient of Insulin Actrapid in the following countries:


  • India

International Drug Name Search

Thursday 28 October 2010

Cefazolina Biocrom




Cefazolina Biocrom may be available in the countries listed below.


Ingredient matches for Cefazolina Biocrom



Cefazolin

Cefazolin is reported as an ingredient of Cefazolina Biocrom in the following countries:


  • Argentina

International Drug Name Search

Lomotil




In the US, Lomotil (atropine/diphenoxylate systemic) is a member of the drug class antidiarrheals and is used to treat Diarrhea.

US matches:

  • Lomotil

  • Lomotil Solution

  • Lomotil

UK matches:

  • Lomotil tablets (SPC)

Ingredient matches for Lomotil



Atropine

Atropine sulfate (a derivative of Atropine) is reported as an ingredient of Lomotil in the following countries:


  • Australia

  • Canada

  • Colombia

  • Ethiopia

  • Ghana

  • Hong Kong

  • India

  • Ireland

  • Nigeria

  • Oman

  • Singapore

  • South Africa

  • Thailand

  • Turkey

  • United Kingdom

  • United States

Diphenoxylate

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


  • Australia

  • Canada

  • Colombia

  • Ethiopia

  • Ghana

  • Hong Kong

  • India

  • Ireland

  • Nigeria

  • Oman

  • Singapore

  • South Africa

  • Thailand

  • Turkey

  • United Kingdom

  • United States

  • Venezuela

Loperamide

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


  • Mexico

  • Philippines

International Drug Name Search

Glossary

SPC Summary of Product Characteristics (UK)

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

Tuesday 26 October 2010

Chuben




Chuben may be available in the countries listed below.


Ingredient matches for Chuben



Albendazole

Albendazole is reported as an ingredient of Chuben in the following countries:


  • Bangladesh

International Drug Name Search

Monday 25 October 2010

Follistim AQ


Follistim AQ is a brand name of follicle stimulating hormone, approved by the FDA in the following formulation(s):


FOLLISTIM AQ (follitropin alfa/beta - injectable; subcutaneous)



  • Manufacturer: ORGANON USA INC

    Approval date: March 23, 2004

    Strength(s): 300 IU/0.36ML [RLD], 600 IU/0.72ML [RLD]


  • Manufacturer: ORGANON USA INC

    Approval date: February 11, 2005

    Strength(s): 900 IU/1.08ML [RLD]


  • Manufacturer: ORGANON USA INC

    Approval date: August 26, 2005

    Strength(s): 150 IU/0.5ML [RLD], 75 IU/0.5ML [RLD]

Has a generic version of Follistim AQ been approved?


No. There is currently no therapeutically equivalent version of Follistim AQ available.


Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Follistim AQ. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents


Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.




  • Recombinant heterodimeric human fertility hormones, and methods, cells, and vectors and DNA for the production thereof
    Patent 5,767,251
    Issued: June 16, 1998
    Inventor(s): Reddy; Vermuri B. & Hsiung; Nancy & Beck; Anton K. & Bernstine; Edward George
    Assignee(s): Genzyme Corporation
    Biologically active heterodimeric human fertility hormones composed of two different subunits, each subunit being synthesized in the same cell transformed by at least one cell expression vector having heterologous DNA encoding each subunit with each subunit being controlled by a separate promoter. Preferred human fertility hormones include hCG, hLH and hFSH.
    Patent expiration dates:

    • June 16, 2015
      ✓ 
      Drug substance




  • Liquid gonadotropin containing formulations
    Patent 5,929,028
    Issued: July 27, 1999
    Inventor(s): Skrabanja; Arnold Titus Philip & van den Oetelaar; Petrus Johannes Maria
    Assignee(s): Akzo Nobel, N.V.
    The invention concerns a liquid gonadotropin-containing formulation characterised in that the formulation comprises a gonadotropin and stabilising amounts of a polycarboxylic acid or a salt thereof and of a thioether compound. The particular proteins (e.g. LH, TSH, FSH, or HCG) are in admixture with the particular stabilizers in an aqueous solution. The preparations contain a sufficient amount of the polycarboxylic acid or a salt thereof, preferably sodium citrate, and a sufficient amount of the thioether compound, preferably methionine, to stabilize the protein. The preparations preferably also include a nonreducing disaccharide like sucrose, and a non-ionic surfactant.
    Patent expiration dates:

    • January 14, 2018
      ✓ 
      Patent use: METHOD OF TREATING INFERTILITY
      ✓ 
      Drug product




  • FSH formulation
    Patent 7,446,090
    Issued: November 4, 2008
    Inventor(s): Hoffmann; James Arthur & Lu; Jirong
    Assignee(s): Ares Trading S.A.
    This invention relates to FSH or a FSH variant containing an alpha and beta subunit contained in formulations, and articles of manufacture. The invention provides advantageous new proteins and nucleic acids, multi-use pharmaceutical solutions, formulations and products of said proteins and nucleic acids where none approved for commercial use had previously existed having such extended use indications. These products are particularly useful in therapeutic regimens for increasing serum levels of FSH or a FSH variant over a period of treatment. Thus, inter alia, the invention fills the need for convenient products of FSH or from a FSH variant.
    Patent expiration dates:

    • August 23, 2019
      ✓ 
      Drug product




  • FSH and FSH variant formulations, products and methods
    Patent 7,563,763
    Issued: July 21, 2009
    Inventor(s): Hoffmann; James Arthur & Lu; Jirong
    Assignee(s): Ares Trading S.A.
    This invention relates to FSH or a FSH variant containing an alpha and beta subunit contained in formulations, and articles of manufacture. The invention provides advantageous new proteins and nucleic acids, multi-use pharmaceutical solutions, formulations and products of said proteins and nucleic acids where none approved for commercial use had previously existed having such extended use indications. These products are particularly useful in therapeutic regimens for increasing serum levels of FSH or a FSH variant over a period of treatment. Thus, inter alia, the invention fills the need for convenient products of FSH or from a FSH variant.
    Patent expiration dates:

    • August 23, 2019
      ✓ 
      Patent use: METHOD OF TREATING INFERTILITY


    • August 23, 2019
      ✓ 
      Patent use: A METHOD FOR ADMINISTERING FOLLICLE STIMULATING HORMONE (FSH) FOR OVARIAN FOLLICLE OR TESTICULAR STIMULATION IN THE HUMAN



Related Exclusivities

Exclusivity is exclusive marketing rights granted by the FDA upon approval of a drug and can run concurrently with a patent or not. Exclusivity is a statutory provision and is granted to an NDA applicant if statutory requirements are met.

  • Exclusivity expiration dates:
    • June 28, 2013 - INDUCTION OF SPERMATOGENESIS IN MEN WITH PRIMARY AND SECONDARY HYPOGONADOTROPIC HYPOGONADISM IN WHOM THE CAUSE OF INFERTILITY IS NOT DUE TO PRIMARY TESTICULAR FAILURE

    • August 22, 2014 - NEW EFFICACY DATA AND DOSING REGIMEN FOR PREGNANCY IN NORMAL OVULATORY WOMEN UNDERGOING CONTROLLED OVARIAN STIMULATION AS PART OF AN IVF OR INTRACYTOPLASMIC SPERM INJECTION (ICSI) CYCLE

See also...

  • Follistim AQ Consumer Information (Drugs.com)
  • Follistim AQ Consumer Information (Wolters Kluwer)
  • Follistim AQ Consumer Information (Cerner Multum)
  • Follistim AQ Advanced Consumer Information (Micromedex)
  • Follitropin Alfa Powder Consumer Information (Wolters Kluwer)
  • Follitropin Alfa Solution Consumer Information (Wolters Kluwer)
  • Follitropin Beta Consumer Information (Wolters Kluwer)
  • Follicle stimulating hormone Consumer Information (Cerner Multum)
  • Follitropin alfa Subcutaneous Advanced Consumer Information (Micromedex)
  • Follitropin beta Subcutaneous Advanced Consumer Information (Micromedex)

Sunday 24 October 2010

Saltos




Saltos may be available in the countries listed below.


Ingredient matches for Saltos



Salbutamol

Salbutamol is reported as an ingredient of Saltos in the following countries:


  • Russian Federation

International Drug Name Search

Saturday 23 October 2010

Nortan




Nortan may be available in the countries listed below.


Ingredient matches for Nortan



Atenolol

Atenolol is reported as an ingredient of Nortan in the following countries:


  • Turkey

International Drug Name Search

Friday 22 October 2010

Raxide




Raxide may be available in the countries listed below.


Ingredient matches for Raxide



Ranitidine

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


  • Philippines

International Drug Name Search

Spironolactone Altizide Biogaran




Spironolactone Altizide Biogaran may be available in the countries listed below.


Ingredient matches for Spironolactone Altizide Biogaran



Altizide

Altizide is reported as an ingredient of Spironolactone Altizide Biogaran in the following countries:


  • France

Spironolactone

Spironolactone is reported as an ingredient of Spironolactone Altizide Biogaran in the following countries:


  • France

International Drug Name Search

Tuesday 19 October 2010

Fluconazol-GRY




Fluconazol-GRY may be available in the countries listed below.


Ingredient matches for Fluconazol-GRY



Fluconazole

Fluconazole is reported as an ingredient of Fluconazol-GRY in the following countries:


  • Germany

International Drug Name Search

Thursday 14 October 2010

Opipramol-neuraxpharm




Opipramol-neuraxpharm may be available in the countries listed below.


Ingredient matches for Opipramol-neuraxpharm



Opipramol

Opipramol dihydrochloride (a derivative of Opipramol) is reported as an ingredient of Opipramol-neuraxpharm in the following countries:


  • Germany

International Drug Name Search

Saturday 9 October 2010

Inderalici




Inderalici may be available in the countries listed below.


Ingredient matches for Inderalici



Propranolol

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


  • Mexico

International Drug Name Search

Friday 8 October 2010

Cefotim




Cefotim may be available in the countries listed below.


Ingredient matches for Cefotim



Cefotaxime

Cefotaxime is reported as an ingredient of Cefotim in the following countries:


  • Tunisia

International Drug Name Search

Monday 4 October 2010

brompheniramine/carbetapentane/phenylephrine


Generic Name: brompheniramine/carbetapentane/phenylephrine (brome fen IR a meen, kar be ta PEN tane, fen il EF rin)

Brand names: BetaTan, Pulmari, VazoTan, Seradex, V-Cof, Trexbrom


What is brompheniramine, carbetapentane and phenylephrine?

Carbetapentane is a cough suppressant.


Brompheniramine is an antihistamine. It blocks the effects of the naturally occurring chemical histamine in the body. Histamine can produce allergy symptoms such as sneezing, runny nose, and watery eyes.


Phenylephrine is a decongestant that shrinks blood vessels in the nasal passages. Dilated blood vessels can cause nasal congestion (stuffy nose).


The combination of brompheniramine, carbetapentane and phenylephrine is used to treat cough and nasal congestion associated with allergies or the common cold.


Brompheniramine, carbetapentane and phenylephrine may also be used for purposes other than those listed in this medication guide.


What is the most important information I should know about brompheniramine, carbetapentane and phenylephrine?


Do not use brompheniramine, carbetapentane and phenylephrine if you have used an MAO inhibitor such as isocarboxazid (Marplan), phenelzine (Nardil), rasagiline (Azilect), selegiline (Eldepryl, Emsam), or tranylcypromine (Parnate) within the past 14 days. Serious, life-threatening side effects can occur if you take brompheniramine, carbetapentane and phenylephrine before the MAO inhibitor has cleared from your body. This medication can cause side effects that may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be awake and alert. Avoid drinking alcohol. It can increase some of the side effects of brompheniramine, carbetapentane and phenylephrine. Do not use any other over-the-counter cough, cold, or allergy medications without first asking your doctor or pharmacist. Brompheniramine or phenylephrine are contained in many medicines available over the counter. If you take certain products together you may accidentally take too much of a certain drug. Read the label of any other medicine you are using to see if it contains brompheniramine, carbetapentane, or phenylephrine.

Avoid using other medicines that make you sleepy (such as cold medicine, pain medication, muscle relaxers, and medicine for seizures, depression or anxiety). They can add to sleepiness caused by brompheniramine, carbetapentane, and phenylephrine.


What should I discuss with my healthcare provider before taking brompheniramine, carbetapentane and phenylephrine?


Do not use brompheniramine, carbetapentane and phenylephrine if you have used an MAO inhibitor such as isocarboxazid (Marplan), phenelzine (Nardil), rasagiline (Azilect), selegiline (Eldepryl, Emsam), or tranylcypromine (Parnate) within the past 14 days. Serious, life-threatening side effects can occur if you take brompheniramine, carbetapentane and phenylephrine before the MAO inhibitor has cleared from your body. Do not take this medication if you are allergic to brompheniramine, carbetapentane, or phenylephrine. These medications are contained in many cough, cold, and allergy medications.

Before taking this medication, tell your doctor if you are allergic to any drugs, or if you have:



  • a history of head injury or seizure disorder;




  • sleep apnea (periods of not breathing during sleep);




  • thyroid problems;




  • asthma, emphysema, or chronic obstructive pulmonary disease (COPD);




  • gallbladder disease;




  • Addison's disease;




  • diabetes;




  • glaucoma;




  • an ulcer or an obstruction in the stomach;




  • bladder problems or difficulty urinating;



  • an enlarged prostate;


  • high blood pressure, irregular heartbeats, or any type of heart disease;



  • kidney disease; or

  • liver disease.

If you have any of these conditions, you may not be able to use brompheniramine, carbetapentane, and phenylephrine, or you may need a dosage adjustment or special tests during treatment.


This medication may be harmful to an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant during treatment. Brompheniramine, carbetapentane and phenylephrine can pass into breast milk and may harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby. Older adults may be more likely to have side effects from this medication.

How should I take brompheniramine, carbetapentane and phenylephrine?


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


Shake the oral suspension (liquid) well just before you measure a dose. To be sure you get the correct dose, measure the liquid with a marked measuring spoon or medicine cup, not with a regular table spoon. If you do not have a dose-measuring device, ask your pharmacist for one.

Call your doctor if your symptoms do not improve, if they get worse, or if you develop a fever.


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

See also: Brompheniramine/carbetapentane/phenylephrine dosage (in more detail)

What happens if I miss a dose?


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


What happens if I overdose?


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

Symptoms of a brompheniramine, carbetapentane and phenylephrine overdose may include dry mouth, large pupils, warmth or tingling under the skin, nausea, vomiting, restless feeling, or hallucinations.


What should I avoid while taking brompheniramine, carbetapentane and phenylephrine?


This medication can cause side effects that may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be awake and alert. Avoid drinking alcohol. It can increase some of the side effects of brompheniramine, carbetapentane and phenylephrine. Do not use any other over-the-counter cough, cold, or allergy medications without first asking your doctor or pharmacist. Brompheniramine or phenylephrine are contained in many medicines available over the counter. If you take certain products together you may accidentally take too much of a certain drug. Read the label of any other medicine you are using to see if it contains brompheniramine, carbetapentane, or phenylephrine.

Avoid using other medicines that make you sleepy (such as cold medicine, pain medication, muscle relaxers, and medicine for seizures, depression or anxiety). They can add to sleepiness caused by brompheniramine, carbetapentane, and phenylephrine.


Brompheniramine, carbetapentane and phenylephrine side effects


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

Less serious side effects are more likely to occur with this medication, such as:



  • dryness of the eyes, nose, or mouth;




  • drowsiness or dizziness;




  • blurred vision;




  • difficulty urinating; or




  • excitation (in children).



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.


Brompheniramine/carbetapentane/phenylephrine Dosing Information


Usual Adult Dose for Allergic Rhinitis:

brompheniramine/carbetapentane/phenylephrine 4 mg-30 mg-7.5 mg/5 mL or brompheniramine/carbetapentane/phenylephrine 6 mg-25 mg-10 mg/5 mL oral suspension: 5 to 10 mL orally every 12 hours.
brompheniramine/carbetapentane/phenylephrine 6 mg-30 mg-10 mg/5 mL oral suspension: 5 mL orally every 6 hours. Not to exceed 4 doses in 24 hours.

Usual Adult Dose for Cold Symptoms:

brompheniramine/carbetapentane/phenylephrine 4 mg-30 mg-7.5 mg/5 mL or brompheniramine/carbetapentane/phenylephrine 6 mg-25 mg-10 mg/5 mL oral suspension: 5 to 10 mL orally every 12 hours.
brompheniramine/carbetapentane/phenylephrine 6 mg-30 mg-10 mg/5 mL oral suspension: 5 mL orally every 6 hours. Not to exceed 4 doses in 24 hours.

Usual Adult Dose for Cough and Nasal Congestion:

brompheniramine/carbetapentane/phenylephrine 4 mg-30 mg-7.5 mg/5 mL or brompheniramine/carbetapentane/phenylephrine 6 mg-25 mg-10 mg/5 mL oral suspension: 5 to 10 mL orally every 12 hours.
brompheniramine/carbetapentane/phenylephrine 6 mg-30 mg-10 mg/5 mL oral suspension: 5 mL orally every 6 hours. Not to exceed 4 doses in 24 hours.

Usual Pediatric Dose for Allergic Rhinitis:

brompheniramine/carbetapentane/phenylephrine 4 mg-30 mg-7.5 mg/5 mL oral suspension:
12 yrs or older: 5 to 10 mL orally every 12 hours.
6 yrs to 11 yrs: 2.5 to 5 mL orally every 12 hours.
2 yrs to 5 yrs: 1.25 to 2.5 mL orally every 12 hours.

brompheniramine/carbetapentane/phenylephrine 6 mg-25 mg-10 mg/5 mL oral suspension:
12 yrs or older: 5 to 10 mL orally every 12 hours.
6 yrs to 11 yrs: 5 mL orally every 12 hours.
2 yrs to 5 yrs: 2.5 mL orally every 12 hours.

brompheniramine/carbetapentane/phenylephrine 6 mg-30 mg-10 mg/5 mL oral suspension:
12 yrs or older: 5 mL orally every 6 hours. Not to exceed 4 doses in 24 hours.
6 yrs to 11 yrs: 2.5 mL orally every 6 hours. Not to exceed 4 doses in 24 hours.

Usual Pediatric Dose for Cold Symptoms:

brompheniramine/carbetapentane/phenylephrine 4 mg-30 mg-7.5 mg/5 mL oral suspension:
12 yrs or older: 5 to 10 mL orally every 12 hours.
6 yrs to 11 yrs: 2.5 to 5 mL orally every 12 hours.
2 yrs to 5 yrs: 1.25 to 2.5 mL orally every 12 hours.

brompheniramine/carbetapentane/phenylephrine 6 mg-25 mg-10 mg/5 mL oral suspension:
12 yrs or older: 5 to 10 mL orally every 12 hours.
6 yrs to 11 yrs: 5 mL orally every 12 hours.
2 yrs to 5 yrs: 2.5 mL orally every 12 hours.

brompheniramine/carbetapentane/phenylephrine 6 mg-30 mg-10 mg/5 mL oral suspension:
12 yrs or older: 5 mL orally every 6 hours. Not to exceed 4 doses in 24 hours.
6 yrs to 11 yrs: 2.5 mL orally every 6 hours. Not to exceed 4 doses in 24 hours.

Usual Pediatric Dose for Cough and Nasal Congestion:

brompheniramine/carbetapentane/phenylephrine 4 mg-30 mg-7.5 mg/5 mL oral suspension:
12 yrs or older: 5 to 10 mL orally every 12 hours.
6 yrs to 11 yrs: 2.5 to 5 mL orally every 12 hours.
2 yrs to 5 yrs: 1.25 to 2.5 mL orally every 12 hours.

brompheniramine/carbetapentane/phenylephrine 6 mg-25 mg-10 mg/5 mL oral suspension:
12 yrs or older: 5 to 10 mL orally every 12 hours.
6 yrs to 11 yrs: 5 mL orally every 12 hours.
2 yrs to 5 yrs: 2.5 mL orally every 12 hours.

brompheniramine/carbetapentane/phenylephrine 6 mg-30 mg-10 mg/5 mL oral suspension:
12 yrs or older: 5 mL orally every 6 hours. Not to exceed 4 doses in 24 hours.
6 yrs to 11 yrs: 2.5 mL orally every 6 hours. Not to exceed 4 doses in 24 hours.


What other drugs will affect brompheniramine, carbetapentane and phenylephrine?


There may be other drugs not listed that can affect brompheniramine, carbetapentane, and phenylephrine. Tell your doctor about all the prescription and over-the-counter medications you use. This includes vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start using a new medication without telling your doctor.



More brompheniramine/carbetapentane/phenylephrine resources


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


  • Brompheniramine/Carbetapentane/Phenylephrine Liquid MedFacts Consumer Leaflet (Wolters Kluwer)

  • BetaTan Suspension MedFacts Consumer Leaflet (Wolters Kluwer)

  • BetaTan Consumer Overview

  • Trexbrom Prescribing Information (FDA)



Compare brompheniramine/carbetapentane/phenylephrine with other medications


  • Cold Symptoms
  • Cough and Nasal Congestion
  • Hay Fever


Where can I get more information?


  • Your pharmacist has information about brompheniramine, carbetapentane and phenylephrine written for health professionals that you may read.

See also: brompheniramine/carbetapentane/phenylephrine side effects (in more detail)


Sunday 3 October 2010

Tilhasan




Tilhasan may be available in the countries listed below.


Ingredient matches for Tilhasan



Diltiazem

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


  • Vietnam

International Drug Name Search

Clozapine Mylan




Clozapine Mylan may be available in the countries listed below.


Ingredient matches for Clozapine Mylan



Clozapine

Clozapine is reported as an ingredient of Clozapine Mylan in the following countries:


  • France

International Drug Name Search

Saturday 2 October 2010

Kanrenol




Kanrenol may be available in the countries listed below.


Ingredient matches for Kanrenol



Potassium Canrenoate

Potassium Canrenoate is reported as an ingredient of Kanrenol in the following countries:


  • Italy

International Drug Name Search

Monday 27 September 2010

Dacarbazine DBL




Dacarbazine DBL may be available in the countries listed below.


Ingredient matches for Dacarbazine DBL



Dacarbazine

Dacarbazine is reported as an ingredient of Dacarbazine DBL in the following countries:


  • Hong Kong

  • Indonesia

  • Malaysia

International Drug Name Search

Monday 20 September 2010

Dicyclomine Syrup



Pronunciation: dye-SYE-kloe-meen
Generic Name: Dicyclomine
Brand Name: Bentyl


Dicyclomine Syrup is used for:

Treatment of the symptoms of irritable bowel syndrome. It may also be used for other conditions as determined by your doctor.


Dicyclomine Syrup is an anticholinergic. It works by blocking a chemical in the smooth muscle of the stomach and intestines causing them to relax, which reduces cramping.


Do NOT use Dicyclomine Syrup if:


  • you are allergic to any ingredient in Dicyclomine Syrup

  • you have blockage of the esophagus, stomach, intestine, or urinary tract

  • you have heart problems due to severe bleeding

  • you have glaucoma

  • you have inflammation of the esophagus due to acid reflux, loss of strength in the intestinal muscles, or chronic inflammation and ulceration of the bowels

  • you have myasthenia gravis (a condition in which the muscles become progressively paralyzed)

  • you are breast-feeding

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



Before using Dicyclomine Syrup:


Some medical conditions may interact with Dicyclomine Syrup. 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 chronic inflammation or ulcers of the bowel, diarrhea, enlargement of the prostate, hiatal hernia, kidney or liver disease, nerve problems or disease, overactive thyroid, or urinary blockage or retention

  • if you have heart disease, heart failure, a history of rapid or irregular heartbeat, or high blood pressure

  • if you are at risk for glaucoma

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


  • Amantadine, antiarrhythmics (eg, quinidine), antihistamines (eg, diphenhydramine), benzodiazepines (eg, diazepam), monoamine oxidase inhibitors (MAOIs) (eg, phenelzine), narcotic pain medicine (eg, meperidine), nitrates (eg, nitroglycerin, isosorbide), nitrites (eg, sodium nitrite), phenothiazines (eg, chlorpromazine), sympathomimetics (eg, pseudoephedrine), or tricyclic antidepressants (eg, amitriptyline) because they may increase the risk of Dicyclomine Syrup's side effects

  • Metoclopramide or phenothiazines (eg, chlorpromazine) because their effectiveness may be decreased by Dicyclomine Syrup

  • Digoxin because the risk of its side effects may be increased by Dicyclomine Syrup

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


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


  • Take Dicyclomine Syrup by mouth with or without food.

  • Use a measuring device marked for medicine dosing. Ask your pharmacist for help if you are unsure of how to measure your dose.

  • If you are also taking antacids, you may need to separate them from Dicyclomine Syrup. Ask your doctor or pharmacist for more information.

  • Take Dicyclomine Syrup on a regular schedule around the clock, unless your doctor tells you otherwise.

  • If you miss a dose of Dicyclomine Syrup, 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 Dicyclomine Syrup.



Important safety information:


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

  • Check with your doctor before you drink alcohol or use medicines that may cause drowsiness (eg, sleep aids, muscle relaxers) while you are using Dicyclomine Syrup; it may add to their effects. Ask your pharmacist if you have questions about which medicines may cause drowsiness.

  • Do not become overheated in hot weather or while you are being active; heatstroke may occur.

  • Dicyclomine Syrup may make your eyes more sensitive to sunlight. It may help to wear sunglasses.

  • Use Dicyclomine Syrup with caution in the ELDERLY; they may be more sensitive to its effects.

  • Dicyclomine Syrup should not be used in CHILDREN younger than 6 months old; safety and effectiveness in these children have not been confirmed.

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


Possible side effects of Dicyclomine Syrup:


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:



Blurred vision; constipation; decreased sweating; difficulty sleeping; dizziness; drowsiness; dry mouth; headache; lightheadedness; loss of taste; nausea; nervousness.



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

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); agitation; confusion; diarrhea; difficulty focusing your eyes; difficulty moving; difficulty speaking; difficulty urinating; disorientation; exaggerated sense of well-being; fainting; hallucinations; pounding in the chest; rapid heartbeat; short-term memory loss; unusual weakness; vomiting.



This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects at http://www.fda.gov/medwatch .


See also: Dicyclomine 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 convulsions (seizures); difficulty breathing; dilated pupils; disorientation; excessive thirst; flushed, hot, dry skin; hallucinations or unusual behavior; muscle weakness; nausea; rapid heartbeat and breathing; restlessness; severe dizziness or drowsiness; severe dry mouth; vomiting.


Proper storage of Dicyclomine Syrup:

Store at room temperature, below 86 degrees F (30 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Dicyclomine Syrup out of the reach of children and away from pets.


General information:


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

  • Dicyclomine Syrup 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 Dicyclomine Syrup. 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 Dicyclomine resources


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


Compare Dicyclomine with other medications


  • Colitis
  • Irritable Bowel Syndrome

Monday 13 September 2010

Cetoros




Cetoros may be available in the countries listed below.


Ingredient matches for Cetoros



Piracetam

Piracetam is reported as an ingredient of Cetoros in the following countries:


  • Indonesia

International Drug Name Search

Saturday 11 September 2010

Cuterpès




Cuterpès may be available in the countries listed below.


Ingredient matches for Cuterpès



Ibacitabine

Ibacitabine is reported as an ingredient of Cuterpès in the following countries:


  • France

  • Tunisia

International Drug Name Search

Isosorbide Mononitrate




In the US, Isosorbide Mononitrate (isosorbide mononitrate systemic) is a member of the drug class antianginal agents and is used to treat Angina Pectoris Prophylaxis, Esophageal Spasm and Heart Failure.

US matches:

  • Isosorbide Mononitrate

  • Isosorbide Mononitrate Sustained-Release Tablets

  • Isosorbide Mononitrate Extended Release

UK matches:

  • Isosorbide Mononitrate Tablets 10mg, 20mg, 40mg (Actavis UK Ltd)
  • Isosorbide mononitrate 20mg tablets (SPC)
  • Isosorbide Mononitrate 40mg (SPC)
  • Isosorbide Mononitrate Tablets 40mg (SPC)

Ingredient matches for Isosorbide Mononitrate



Isosorbide Mononitrate

Isosorbide Mononitrate (BAN, JAN, USAN) is known as Isosorbide Mononitrate in the US.



Isosorbide

Isosorbide is reported as an ingredient of Isosorbide Mononitrate in the following countries:


  • United States

International Drug Name Search

Glossary

BANBritish Approved Name
JANJapanese Accepted Name
SPC Summary of Product Characteristics (UK)
USANUnited States Adopted Name

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

Friday 10 September 2010

Miotens




Miotens may be available in the countries listed below.


Ingredient matches for Miotens



Thiocolchicoside

Thiocolchicoside is reported as an ingredient of Miotens in the following countries:


  • Italy

International Drug Name Search

Tradil




Tradil may be available in the countries listed below.


Ingredient matches for Tradil



Dexibuprofen

Dexibuprofen is reported as an ingredient of Tradil in the following countries:


  • Sweden

International Drug Name Search

Friday 3 September 2010

Toricam Gel




Toricam Gel may be available in the countries listed below.


Ingredient matches for Toricam Gel



Piroxicam

Piroxicam is reported as an ingredient of Toricam Gel in the following countries:


  • Taiwan

International Drug Name Search

Friday 27 August 2010

Sylvie




Sylvie may be available in the countries listed below.


Ingredient matches for Sylvie



Ethinylestradiol

Ethinylestradiol is reported as an ingredient of Sylvie in the following countries:


  • Poland

Gestodene

Gestodene is reported as an ingredient of Sylvie in the following countries:


  • Poland

International Drug Name Search

Ichtholan




Ichtholan may be available in the countries listed below.


Ingredient matches for Ichtholan



Ichthammol

Ichthammol is reported as an ingredient of Ichtholan in the following countries:


  • Ethiopia

  • Germany

  • Switzerland

Ichthammol decolorized (a derivative of Ichthammol) is reported as an ingredient of Ichtholan in the following countries:


  • Austria

International Drug Name Search

Thursday 19 August 2010

Oxycyclin




Oxycyclin may be available in the countries listed below.


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

Ingredient matches for Oxycyclin



Oxytetracycline

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


  • Austria

International Drug Name Search

Ibuprofeno All Pro




Ibuprofeno All Pro may be available in the countries listed below.


Ingredient matches for Ibuprofeno All Pro



Ibuprofen

Ibuprofen is reported as an ingredient of Ibuprofeno All Pro in the following countries:


  • Argentina

International Drug Name Search

Wednesday 18 August 2010

Nitroglycerinum




Nitroglycerinum may be available in the countries listed below.


Ingredient matches for Nitroglycerinum



Nitroglycerin

Nitroglycerin is reported as an ingredient of Nitroglycerinum in the following countries:


  • Lithuania

  • Poland

International Drug Name Search

Sunday 15 August 2010

Burgerstein Beta-Carotin




Burgerstein Beta-Carotin may be available in the countries listed below.


Ingredient matches for Burgerstein Beta-Carotin



Betacarotene

Betacarotene is reported as an ingredient of Burgerstein Beta-Carotin in the following countries:


  • Switzerland

International Drug Name Search

Saturday 7 August 2010

Isothipendyl




Scheme

Rec.INN

ATC (Anatomical Therapeutic Chemical Classification)

D04AA22,R06AD09

CAS registry number (Chemical Abstracts Service)

0000482-15-5

Chemical Formula

C16-H19-N3-S

Molecular Weight

285

Therapeutic Categories

Antiallergic agent

Histamine, H₁-receptor antagonist

Chemical Name

10H-Pyrido[3,2-b][1,4]benzothiazine-10-ethanamine, N,N,α-trimethyl-

Foreign Names

  • Isothipendylum (Latin)
  • Isothipendyl (German)
  • Isothipendyl (French)
  • Isotipendilo (Spanish)

Generic Names

  • Isothipendyl (OS: BAN, DCF)
  • Isotipendile (OS: DCIT)

Brand Names

  • Actapront
    Purissimus, Argentina


  • Andantol
    Deutsche Pharma, Peru; Aché, Brazil; Sanfer, Mexico; Transfarma Medica Indah, Indonesia


  • Apaisyl
    Merck Médication Familiale, France


  • Apaisylgel
    Merck Médication Familiale, France


  • Calmogel
    Sanofi-Aventis, Italy


  • Sedermyl
    Cooper, France


  • Thiodantol
    Rekah, Israel

International Drug Name Search

Glossary

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

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

Friday 6 August 2010

Irritos




Irritos may be available in the countries listed below.


Ingredient matches for Irritos



Dextromethorphan

Dextromethorphan is reported as an ingredient of Irritos in the following countries:


  • Peru

Dextromethorphan hydrobromide (a derivative of Dextromethorphan) is reported as an ingredient of Irritos in the following countries:


  • Spain

Phenylpropanolamine

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


  • Spain

International Drug Name Search

Tuesday 3 August 2010

Pulmicort Turbuhaler




In the US, Pulmicort Turbuhaler (budesonide systemic) is a member of the drug class inhaled corticosteroids and is used to treat Asthma, Maintenance.

US matches:

  • Pulmicort Turbuhaler Powder

  • Pulmicort Turbuhaler

Ingredient matches for Pulmicort Turbuhaler



Budesonide

Budesonide is reported as an ingredient of Pulmicort Turbuhaler in the following countries:


  • Aruba

  • Bahamas

  • Barbados

  • Bermuda

  • Brazil

  • China

  • Czech Republic

  • France

  • Haiti

  • Iceland

  • Jamaica

  • Netherlands Antilles

  • New Zealand

  • Norway

  • Romania

  • Russian Federation

  • Slovenia

  • Spain

  • Sweden

  • Thailand

  • Trinidad & Tobago

International Drug Name Search

Monday 26 July 2010

Furomex




Furomex may be available in the countries listed below.


Ingredient matches for Furomex



Furosemide

Furosemide is reported as an ingredient of Furomex in the following countries:


  • Bahrain

  • Egypt

  • Jordan

  • Kuwait

  • Lebanon

  • United Arab Emirates

International Drug Name Search

Sunday 25 July 2010

Estradiol Apotex




Estradiol Apotex may be available in the countries listed below.


Ingredient matches for Estradiol Apotex



Estradiol

Estradiol hemihydrate (a derivative of Estradiol) is reported as an ingredient of Estradiol Apotex in the following countries:


  • Netherlands

International Drug Name Search

Copper Oxide




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

CAS registry number (Chemical Abstracts Service)

0001317-38-0

Chemical Formula

Cu-O

Molecular Weight

79

Chemical Name

Copper(II) oxide (IUPAC)

Foreign Names

  • Cuprum oxydatum (Latin)
  • Kupferoxid (German)

Generic Names

  • Black Copper Oxide (IS)
  • C.I. 77403 (IS)
  • C.I. Pigment Black 15 (IS)
  • Cupric oxide (IS)
  • Cuprioxyd (IS)
  • NSC 83537 (IS)
  • UNII-V1XJQ704R4 (IS)

Brand Name

  • Bayer Copper Capsules 4 Grams (veterinary use)
    Bayer Animal, New Zealand

International Drug Name Search

Glossary

IUPACInternational Union of Pure and Applied Chemistry
ISInofficial Synonym

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

Saturday 24 July 2010

bromocriptine


broe-moe-KRIP-teen


Commonly used brand name(s)

In the U.S.


  • Cycloset

  • Parlodel

Available Dosage Forms:


  • Tablet

  • Capsule

Therapeutic Class: Antiparkinsonian


Pharmacologic Class: Dopamine Agonist


Uses For bromocriptine


Bromocriptine belongs to the group of medicines known as ergot alkaloids. Bromocriptine blocks release of a hormone called prolactin from the pituitary gland. Prolactin affects the menstrual cycle and milk production. Bromocriptine is used to treat certain menstrual problems or to stop milk production in some women or men who have abnormal milk leakage. It is also used to treat infertility in both men and women that occurs because the body made too much prolactin.


Bromocriptine is also used to treat some people who have Parkinson's disease. It works by stimulating certain parts of the brain and nervous system that are involved in this disease.


Bromocriptine is also used to treat acromegaly (overproduction of growth hormone) and pituitary prolactinomas (tumors of the pituitary gland).


Bromocriptine is also used together with proper diet and exercise to treat high blood sugar levels in patients with type 2 diabetes.


Bromocriptine may also be used for other conditions as determined by your doctor.


bromocriptine is available only with your doctor's prescription.


Once a medicine has been approved for marketing for a certain use, experience may show that it is also useful for other medical problems. Although these uses are not included in product labeling, bromocriptine is used in certain patients with the following medical conditions:


  • To stop milk production after an abortion or miscarriage or in women after a delivery who should not breast-feed for medical reasons.

  • Neuroleptic malignant syndrome.

Before Using bromocriptine


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 bromocriptine, the following should be considered:


Allergies


Tell your doctor if you have ever had any unusual or allergic reaction to bromocriptine 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 have not been performed on the relationship of age to the effects of bromocriptine in the pediatric population. Safety and efficacy have not been established.


bromocriptine has been tested in a limited number of teenagers 15 years of age and older. In effective doses, the medicine has not been shown to cause different side effects or problems than it does in adults. Appropriate studies have not been done in teenagers younger than 15 years of age, and there is no specific information comparing use of bromocriptine in these teenagers with use in other age groups.


Geriatric


Appropriate studies performed to date have not demonstrated geriatric-specific problems that would limit the usefulness of bromocriptine in the elderly.


Confusion, hallucinations, or uncontrolled body movements may be more likely to occur in elderly patients, who are usually more sensitive than younger adults to the effects of bromocriptine.


Pregnancy








Pregnancy CategoryExplanation
All TrimestersBAnimal studies have revealed no evidence of harm to the fetus, however, there are no adequate studies in pregnant women OR animal studies have shown an adverse effect, but adequate studies in pregnant women have failed to demonstrate a risk to the fetus.

Breast Feeding


Studies suggest that this medication may alter milk production or composition. If an alternative to this medication is not prescribed, you should monitor the infant for side effects and adequate milk intake.


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 bromocriptine, 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 bromocriptine 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.


  • Isometheptene

  • Phenylpropanolamine

Using bromocriptine 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.


  • Bromperidol

  • Clarithromycin

  • Cyclosporine

  • Kava

  • Thioridazine

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 bromocriptine. Make sure you tell your doctor if you have any other medical problems, especially:


  • Diabetic ketoacidosis (ketones in the blood) or

  • Syncopal (fainting) migraine headaches or

  • Type I diabetes—Should not be used in patients with these conditions.

  • Fever or

  • Infection or

  • Surgery or

  • Trauma—These conditions may cause temporary problems with blood sugar control and your doctor may want to treat you temporarily with insulin.

  • High blood pressure, or history of or

  • Pregnancy-induced high blood pressure, history of—Rarely, bromocriptine can make the high blood pressure worse.

  • Hypotension (low blood pressure) or

  • Mental problems (e.g., psychotic disorder)—May make these conditions worse.

  • Liver disease—Toxic effects of bromocriptine may occur in patients with liver disease because the body is not able to remove bromocriptine from the bloodstream as it normally would.

Proper Use of bromocriptine


bromocriptine comes with a patient information insert. Read and follow the instructions in the insert carefully. Ask your doctor if you have any questions.


Follow carefully the special meal plan your doctor gave you. This is the most important part of controlling your condition, and is necessary if the medicine is to work properly. Also, exercise regularly and test for sugar in your blood or urine as directed.


If bromocriptine upsets your stomach, it may be taken with meals or milk. Also, taking the dose at bedtime may help to lessen nausea if it occurs. If stomach upset continues, check with your doctor. Your doctor may recommend that you take the first doses vaginally.


Dosing


The dose of bromocriptine 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 bromocriptine. If your dose is different, do not change it unless your doctor tells you to do so.


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


  • For oral dosage forms (capsules and tablets):
    • For infertility, male hormone problem (male hypogonadism), starting the menstrual cycle (amenorrhea), or stopping abnormal milk secretion from nipples (galactorrhea):
      • Adults and teenagers 15 years of age or older—At first, 1.25 to 2.5 milligrams (mg) once a day taken at bedtime with a snack. Then your doctor may change your dose by 2.5 mg every three to seven days as needed. Doses greater than 5 mg a day are taken in divided doses with meals or at bedtime with a snack.

      • Teenagers less than 15 years of age and children—Use and dose must be determined by your doctor.


    • For lowering growth hormone (acromegaly):
      • Adults and teenagers 15 years of age or older—At first, 1.25 to 2.5 milligrams (mg) once a day taken at bedtime with a snack for three days. Then your doctor may change your dose by 1.25 or 2.5 mg every three to seven days as needed. Doses greater than 5 mg are divided into smaller doses and taken with meals or at bedtime with a snack.

      • Teenagers younger than 15 years of age and children—Use and dose must be determined by your doctor.


    • For Parkinson's disease:
      • Adults and teenagers 15 years of age or older—At first, 1.25 milligrams (mg) one or two times a day taken with meals or at bedtime with a snack. Then your doctor may change your dose over several weeks as needed.

      • Teenagers younger than 15 years of age and children—Use and dose must be determined by your doctor.


    • For pituitary tumors:
      • Adults and teenagers 15 years of age or older—At first, 1.25 milligrams (mg) two or three times a day taken with meals. Then your doctor may change your dose over several weeks as needed.

      • Teenagers younger than 15 years of age and children—Use and dose must be determined by your doctor.


    • For type 2 diabetes:
      • Adults—At first, 0.8 milligram (mg) once a day, taken within two hours after waking up in the morning. Your doctor may increase your dose as needed. However, the dose is usually not more than 4.8 mg per day.

      • Children—Use and dose must be determined by your doctor.



Missed Dose


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


Storage


Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing.


Keep out of the reach of children.


Do not keep outdated medicine or medicine no longer needed.


Ask your healthcare professional how you should dispose of any medicine you do not use.


Precautions While Using bromocriptine


It is important that your doctor check your progress at regular visits to make sure that bromocriptine is working properly. Blood tests may be needed to check for unwanted effects.


It is very important to follow carefully any instructions from your health care team about:


  • Counseling—Other family members need to learn how to prevent side effects or help with side effects if they occur. Also, patients with diabetes may need special counseling about diabetes medicine dosing changes that might occur because of lifestyle changes, such as changes in exercise and diet. Furthermore, counseling on contraception and pregnancy may be needed because of the problems that can occur in patients with diabetes during pregnancy.

  • Travel—Keep your recent prescription and your medical history with you. Be prepared for an emergency as you would normally. Make allowances for changing time zones and keep your meal times as close as possible to your usual meal times.

  • In case of emergency—There may be a time when you need emergency help for a problem caused by your diabetes. You need to be prepared for these emergencies. It is a good idea to wear a medical identification (ID) bracelet or neck chain at all times. Also, carry an ID card in your wallet or purse that says you have diabetes and a list of all of your medicines.

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


Dizziness, lightheadedness, or fainting may occur, especially when you get up from a lying or sitting position suddenly. These symptoms are more likely to occur when you begin taking bromocriptine, or when the dose is increased.


Too much bromocriptine can cause low blood sugar (hypoglycemia) when it is used under certain conditions. Symptoms of low blood sugar must be treated before they lead to unconsciousness (passing out). Different people may feel different symptoms of low blood sugar. It is important that you learn which symptoms of low blood sugar you usually have so that you can treat it quickly and call someone on your health care team right away when you need advice.


Symptoms of hypoglycemia (low blood sugar) include anxiety; behavior change similar to being drunk; blurred vision; cold sweats; confusion; cool, pale skin; difficulty in thinking; drowsiness; excessive hunger; fast heartbeat; headache (continuing); nausea; nervousness; nightmares; restless sleep; shakiness; slurred speech; or unusual tiredness or weakness.


If symptoms of low blood sugar occur, eat glucose tablets or gel, corn syrup, honey, or sugar cubes; or drink fruit juice, non-diet soft drink, or sugar dissolved in water. Also, check your blood for low blood sugar. Glucagon is used in emergency situations when severe symptoms such as seizures (convulsions) or unconsciousness occur. Have a glucagon kit available, along with a syringe or needle, and know how to use it. Members of your household also should know how to use it.


High blood sugar may occur if you do not exercise as much as usual, have a fever or infection, do not take enough or skip a dose of your diabetes medicine, or overeat or do not follow your meal plan.


If symptoms of high blood sugar occur, check your sugar level and then call your doctor for instructions.


Dizziness is more likely to occur after the first dose of bromocriptine. Taking the first dose at bedtime or when you are able to lie down may lessen problems. It may also be helpful if you get up slowly from a lying or sitting position. Your doctor may also recommend that you take the first dose vaginally.


Bromocriptine may cause dryness of the mouth. For temporary relief, use sugarless candy or gum, melt bits of ice in your mouth, or use a saliva substitute. However, if dry mouth continues for more than 2 weeks, check with your medical doctor or dentist. Continuing dryness of the mouth may increase the chance of dental disease, including tooth decay, gum disease, and fungus infections.


It may take several weeks for bromocriptine to work. Do not stop taking bromocriptine or reduce the amount you are taking without first checking with your doctor.


Drinking alcohol while you are taking bromocriptine may cause you to have a certain reaction. Avoid alcoholic beverages until you have discussed this with your doctor. Some of the symptoms you may have if you drink any alcohol while you are taking bromocriptine are blurred vision, chest pain, confusion, fast or pounding heartbeat, flushing or redness of the face, nausea, severe weakness, sweating, throbbing headache, or vomiting.


For females who are able to bear children and who are taking bromocriptine for menstrual or infertility problems, to stop milk production, or to treat acromegaly or pituitary tumors:


  • It is best to use some type of birth control while you are taking bromocriptine. However, do not use oral contraceptives (“the Pill”) since they may prevent bromocriptine from working. For women using bromocriptine for infertility, tell your doctor when your normal menstrual cycle returns. If you wish to become pregnant, you and your doctor should decide on the best time for you to stop using birth control. Tell your doctor right away if you think you have become pregnant while taking bromocriptine. You and your doctor should discuss whether or not you should continue to take bromocriptine during pregnancy.

  • Check with your doctor right away if you develop blurred vision, a sudden headache, or severe nausea and vomiting.

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.


bromocriptine 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.


Some serious side effects have occurred during the use of bromocriptine to stop milk flow after pregnancy or abortion. These side effects have included strokes, seizures (convulsions), and heart attacks. Some deaths have also occurred. You should discuss with your doctor the good that bromocriptine will do as well as the risks of using it.


Check with your doctor immediately if any of the following side effects occur:


More common
  • Dizziness or lightheadedness, especially when getting up from a lying or sitting position

  • nausea

Less common—reported more often in patients with Parkinson's disease
  • Confusion

  • hallucinations (seeing, hearing, or feeling things that are not there)

  • uncontrolled movements of the body, such as the face, tongue, arms, hands, head, and upper body

Rare—reported more often in patients taking large doses
  • Abdominal or stomach pain (continuing or severe)

  • increased frequency of urination

  • loss of appetite (continuing)

  • lower back pain

  • runny nose (continuing)

  • weakness

Rare
  • Black, tarry stools

  • bloody vomit

  • chest pain (severe)

  • convulsions (seizures)

  • fainting

  • fast heartbeat

  • headache (unusual)

  • increased sweating

  • nausea and vomiting (continuing or severe)

  • nervousness

  • shortness of breath (unexplained)

  • vision changes (such as blurred vision or temporary blindness)

  • weakness (sudden)

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

  • diarrhea

  • drowsiness or tiredness

  • dry mouth

  • leg cramps at night

  • loss of appetite

  • mental depression

  • stomach pain

  • stuffy nose

  • tingling or pain in the fingers and toes when exposed to cold

  • vomiting

Some side effects may be more likely to occur in patients who are taking bromocriptine for Parkinson's disease, acromegaly, or pituitary tumors since they may be taking larger doses.


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: bromocriptine side effects (in more detail)



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More bromocriptine resources


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