Monday 28 December 2009

Salbutamol CF




Salbutamol CF may be available in the countries listed below.


Ingredient matches for Salbutamol CF



Salbutamol

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


  • Netherlands

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


  • Netherlands

International Drug Name Search

Friday 25 December 2009

Risperidona Merck




Risperidona Merck may be available in the countries listed below.


Ingredient matches for Risperidona Merck



Risperidone

Risperidone is reported as an ingredient of Risperidona Merck in the following countries:


  • Spain

International Drug Name Search

Saturday 19 December 2009

Azatioprina Asofarma




Azatioprina Asofarma may be available in the countries listed below.


Ingredient matches for Azatioprina Asofarma



Azathioprine

Azathioprine is reported as an ingredient of Azatioprina Asofarma in the following countries:


  • Argentina

International Drug Name Search

Friday 18 December 2009

Cefotaxim MIP




Cefotaxim MIP may be available in the countries listed below.


Ingredient matches for Cefotaxim MIP



Cefotaxime

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


  • Poland

International Drug Name Search

Terbasmin Turbuhaler Singad




Terbasmin Turbuhaler Singad may be available in the countries listed below.


Ingredient matches for Terbasmin Turbuhaler Singad



Terbutaline

Terbutaline sulfate (a derivative of Terbutaline) is reported as an ingredient of Terbasmin Turbuhaler Singad in the following countries:


  • Denmark

International Drug Name Search

Saturday 12 December 2009

dihydroergotamine injection


Generic Name: dihydroergotamine (injection) (dye HYE droe er GOT a meen)

Brand Names: D.H.E. 45


What is dihydroergotamine injection?

Dihydroergotamine is in a group of drugs called ergot alkaloids (ER-got AL-ka-loids). It works by narrowing the blood vessels around the brain and affects blood flow patterns that are associated with certain types of headaches.


Dihydroergotamine injection is used to treat a migraine or cluster headache attack. This medication will only treat a headache that has already begun. It will not prevent headaches or reduce the number of attacks.


Dihydroergotamine injection should not be used to treat common tension headaches or any headache that seems to be different from your usual migraine headaches. Dihydroergotamine is not for daily use.

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


What is the most important information I should know about dihydroergotamine injection?


This medication can harm an unborn baby or a nursing baby. Do not use if you are pregnant or breast-feeding. Using certain medications together with dihydroergotamine can cause even greater decreases in blood flow than dihydroergotamine used alone, which can lead to dangerous side effects. Tell your doctor about all other medications you are using.

Also tell your doctor about all of your medical conditions, especially breathing problems, high blood pressure, ischemic bowel disease, liver or kidney disease, or risk factors for heart disease.


Never use more than your prescribed dose of dihydroergotamine. An overdose can be fatal.

What should I discuss with my healthcare provider before using dihydroergotamine injection?


Do not use this medication if you are allergic to dihydroergotamine or other ergot medicine such as Ergomar, Cafergot, Migergot, Migranal, or Methergine. Do not use dihydroergotamine injection if you are pregnant or breast-feeding, or if you have:

  • a history of heart disease, angina (chest pain), blood circulation problems, or history of a heart attack or stroke;




  • coronary artery disease or "hardening of the arteries";




  • uncontrolled high blood pressure;




  • severe liver or kidney disease;




  • a serious infection called sepsis; or




  • if you have recently had heart or blood vessel surgery (such as bypass surgery).




Using certain medications together with dihydroergotamine can cause even greater decreases in blood flow than dihydroergotamine used alone, which can lead to dangerous side effects. Do not use dihydroergotamine if you are also using any of the following medications:

  • conivaptan (Vaprisol), imatinib (Gleevec), isoniazid (for treating tuberculosis), or nefazodone (an antidepressant);




  • diclofenac (Arthrotec, Cataflam, Voltaren, Flector Patch, Solareze);




  • clarithromycin (Biaxin), erythromycin (E.E.S., EryPed, Ery-Tab, Erythrocin), or telithromycin (Ketek);




  • clotrimazole (Mycelex Troche), itraconazole (Sporanox), ketoconazole (Extina, Ketozole, Nizoral, Xolegal), or voriconazole (Vfend);




  • heart or blood pressure medication such as diltiazem (Cardizem, Dilacor, Tiazac), nicardipine (Cardene), quinidine (Quin-G), or verapamil (Calan, Covera, Isoptin, Verelan); or




  • HIV/AIDS medicine such as atazanavir (Reyataz), delavirdine (Rescriptor), fosamprenavir (Lexiva), indinavir (Crixivan), nelfinavir (Viracept), saquinavir (Invirase, Fortovase), or ritonavir (Norvir).



Dihydroergotamine can cause rare but serious side effects on the heart, including heart attack or stroke. To make sure you can safely take dihdroergotamine, tell your doctor if you have any of these other conditions:



  • breathing problems;




  • high blood pressure;




  • ischemic bowel disease;




  • liver or kidney disease; or




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




FDA pregnancy category X. Dihydroergotamine can cause birth defects. Do not use if you are pregnant. Tell your doctor right away if you become pregnant during treatment. Use an effective form of birth control while you are using this medication. Dihydroergotamine can pass into breast milk and may harm a nursing baby. Dihydroergotamine may also decrease milk production. Do not use if you are breast-feeding a baby.

How should I use dihydroergotamine injection?


Use exactly as prescribed by your doctor. Never use more than your prescribed dose of dihydroergotamine. Tell your doctor if the medicine seems to stop working as well in treating your migraine attacks.


Dihydroergotamine is injected into a muscle. You may be shown how to use injections at home. Do not self-inject this medicine if you do not fully understand how to give the injection and properly dispose of used needles and syringes.


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


If your headache does not completely go away, you may use a second injection after 1 hour has passed, and a third injection if needed after another hour has passed (a total of 3 injections).


If you still have migraine symptoms after using 3 injections, call your doctor before using any more. If your headache goes away and then comes back, you may use the medication again if it has been at least 6 hours since your last injection.

Do not use more than a total of 3 injections of this medication in any 24-hour period. Do not use more than a total of 6 injections over a period of 7 days.


Dihydroergotamine injection should be clear and colorless. Do not use if the liquid has changed colors or has particles in it. Call your doctor for a new prescription.


If you use dihydroergotamine long-term, your doctor may want to check your heart function periodically using an electrocardiograph or ECG (sometimes called an EKG), a machine that measures electrical activity of the heart.


Store at room temperature away from moisture, heat, and light. Do not use if the expiration date on the label has passed.

What happens if I miss a dose?


Since dihydroergotamine is used on an as-needed basis, you are not likely to miss a dose. Do not use more than 3 injections of dihydroergotamine per day or more than 6 injections per week.


What happens if I overdose?


Seek emergency medical attention or call the Poison Help line at 1-800-222-1222. An overdose of dihydroergotamine can be fatal. Overdose symptoms may include some of the serious side effects listed in this medication guide.

What should I avoid while using dihydroergotamine injection?


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

  • another ergot medicine such as ergotamine (Ergomar, Cafergot, Migergot), dihydroergotamine (Migranal), or methylergonovine (Methergine); or




  • almotriptan (Axert), eletriptan (Relpax), frovatriptan (Frova), naratriptan (Amerge), sumatriptan (Imitrex), rizatriptan (Maxalt, Maxalt-MLT), or zolmitriptan (Zomig).



Grapefruit and grapefruit juice may interact with dihydroergotamine injection and lead to potentially dangerous effects. Discuss the use of grapefruit products with your doctor.


Dihydroergotamine injection side effects


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

  • fast or slow heart rate, swelling or itching in any part of your body;




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




  • sudden numbness or weakness, sudden headache, confusion, or problems with vision, speech, or balance;




  • leg weakness, muscle pain in your arms or legs;




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




  • stomach cramps, diarrhea that may be bloody;




  • cough with stabbing chest pain and trouble breathing; or




  • dangerously high blood pressure (severe headache, blurred vision, buzzing in your ears, anxiety, confusion, chest pain, shortness of breath).



Less serious side effects may include:



  • headache, dizziness, feeling anxious;




  • diarrhea;




  • sweating, mild skin rash, redness or tingly feeling under your skin.



This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.


Dihydroergotamine Dosing Information


Usual Adult Dose for Migraine:

IM or subcutaneous: Initial dose: 1 mg given as quickly as possible after the first symptom of headache. Additional 1 mg doses can be given hourly until the headache has stopped or a total dose of 3 mg has been reached. The total weekly dose should not exceed 6 mg.

IV: Initial dose: 1 mg given as quickly as possible after the first symptom of headache. Additional 1 mg doses can be given hourly until the headache has stopped or a total dose of 2 mg has been reached. The total weekly dose should not exceed 6 mg.

Intranasal: 1 spray (0.5 mg) into each nostril (total = 1 mg). Repeat if needed within 15 minutes to a maximum of 4 sprays (2 mg) per day. The total weekly dose should not exceed 8 sprays (4 mg).

Usual Adult Dose for Cluster Headache:

IM or subcutaneous: Initial dose: 1 mg given as quickly as possible after the first symptom of headache. Additional 1 mg doses can be given hourly until the headache has stopped or a total dose of 3 mg has been reached. The total weekly dose should not exceed 6 mg.

IV: Initial dose: 1 mg given as quickly as possible after the first symptom of headache. Additional 1 mg doses can be given hourly until the headache has stopped or a total dose of 2 mg has been reached. The total weekly dose should not exceed 6 mg.


What other drugs will affect dihydroergotamine injection?


Many drugs can interact with dihydroergotamine. Below is just a partial list. Tell your doctor if you are using:



  • zileuton (Zyflo);




  • nicotine (Nicoderm, Nicorette);




  • cold or allergy medications, diet pills, stimulants, or medication to treat ADHD (such as Ritalin or Adderall);




  • an antidepressant such fluoxetine (Prozac), sertraline (Zoloft), and others;




  • fluconazole (Diflucan) or other antifungal medication; or




  • heart or blood pressure medication such as atenolol (Tenormin), carvedilol (Coreg), metoprolol (Lopressor, Toprol), propranolol (Inderal, InnoPran), and others.



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


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


Compare dihydroergotamine with other medications


  • Cluster Headaches
  • Migraine


Where can I get more information?


  • Your pharmacist can provide more information about dihydroergotamine injection.

See also: dihydroergotamine side effects (in more detail)


Friday 11 December 2009

Diltiazem 24-Hour Extended-Release Beads Capsules



Pronunciation: dil-TYE-a-zem
Generic Name: Diltiazem
Brand Name: Examples include Taztia XT and Tiazac


Diltiazem 24-Hour Extended-Release Beads Capsules are used for:

Treating high blood pressure and chronic stable angina (chest pain). It may be used alone or in combination with other medicines. It may also be used for other conditions as determined by your doctor.


Diltiazem 24-Hour Extended-Release Beads Capsules are a calcium channel blocker. It works by relaxing (dilating) your blood vessels, lowering blood pressure, and decreasing heart rate, which lowers the workload of the heart. It also dilates coronary arteries, which increases blood flow to the heart.


Do NOT use Diltiazem 24-Hour Extended-Release Beads Capsules if:


  • you are allergic to any ingredient in Diltiazem 24-Hour Extended-Release Beads Capsules

  • you have certain heart problems (eg, sick sinus syndrome, second- or third-degree heart block) and do not have a pacemaker, you have very low blood pressure, or you have fluid buildup in the lungs during or soon after a heart attack

  • you are taking erythromycin

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



Before using Diltiazem 24-Hour Extended-Release Beads Capsules:


Some medical conditions may interact with Diltiazem 24-Hour Extended-Release Beads Capsules. 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 heart failure, a recent heart attack with lung congestion, heart block, a very slow heart rate, or other heart problems; low blood pressure; certain stomach or intestine problems (eg, narrowing); liver disease; or kidney problems

  • if you are taking other medicines for high blood pressure or heart conditions

Some MEDICINES MAY INTERACT with Diltiazem 24-Hour Extended-Release Beads Capsules. Tell your health care provider if you are taking any other medicines, especially any of the following:


  • Antiarrhythmics (eg, amiodarone, dronedarone), cimetidine, clonidine, HIV protease inhibitors (eg, atazanavir, indinavir), or tricyclic antidepressants (eg, amitriptyline), because they may increase the risk of Diltiazem 24-Hour Extended-Release Beads Capsules's side effects, such as heart rhythm problems

  • Moricizine or rifamycins (eg, rifampin) because they may decrease Diltiazem 24-Hour Extended-Release Beads Capsules's effectiveness

  • Benzodiazepines (eg, alprazolam), beta-blockers (eg, propranolol), buspirone, carbamazepine, cilostazol, cisapride, colchicine, corticosteroids (eg, hydrocortisone), cyclosporine, digoxin, everolimus, fentanyl, HMG-CoA reductase inhibitors (eg, simvastatin), hydantoins (eg, phenytoin), lurasidone, macrolide antibiotics (eg, erythromycin), macrolide immunosuppressants (eg, tacrolimus), nifedipine, quinidine, ranolazine, theophylline, or vasopressin antagonists (eg, tolvaptan) because the risk of their side effects, some potentially life-threatening, may be increased by Diltiazem 24-Hour Extended-Release Beads Capsules

This may not be a complete list of all interactions that may occur. Ask your health care provider if Diltiazem 24-Hour Extended-Release Beads Capsules 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 Diltiazem 24-Hour Extended-Release Beads Capsules:


Use Diltiazem 24-Hour Extended-Release Beads Capsules as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • Take Diltiazem 24-Hour Extended-Release Beads Capsules by mouth with or without food.

  • Swallow Diltiazem 24-Hour Extended-Release Beads Capsules whole. Do not break, crush, or chew before swallowing.

  • If you cannot swallow the capsule whole, you may open it and sprinkle the contents over a spoonful of applesauce. Do not divide your dose over more than 1 spoonful. The applesauce should not be hot and should be soft enough to be swallowed without chewing. Swallow the mixture right away, followed by a glass of water. Do not crush or chew the medicine before swallowing. Do not store the mixture for future use.

  • Taking Diltiazem 24-Hour Extended-Release Beads Capsules at the same time each day will help you remember to take it.

  • Continue to take Diltiazem 24-Hour Extended-Release Beads Capsules even if you feel well. Do not miss any doses.

  • If you miss a dose of Diltiazem 24-Hour Extended-Release Beads Capsules, 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 Diltiazem 24-Hour Extended-Release Beads Capsules.



Important safety information:


  • Diltiazem 24-Hour Extended-Release Beads Capsules may cause dizziness, lightheadedness, or drowsiness. These effects may be worse if you take it with alcohol or certain medicines. Use Diltiazem 24-Hour Extended-Release Beads Capsules with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.

  • Diltiazem 24-Hour Extended-Release Beads Capsules may cause dizziness, lightheadedness, or fainting; alcohol, hot weather, exercise, or fever may increase these effects. To prevent them, sit up or stand slowly, especially in the morning. Sit or lie down at the first sign of any of these effects.

  • Diltiazem 24-Hour Extended-Release Beads Capsules may cause you to become sunburned more easily. Avoid the sun, sunlamps, or tanning booths until you know how you react to Diltiazem 24-Hour Extended-Release Beads Capsules. Use a sunscreen or wear protective clothing if you must be outside for more than a short time.

  • Patients who take medicine for high blood pressure often feel tired or run down for a few weeks after starting treatment. Be sure to take your medicine even if you may not feel "normal." Tell your doctor if you develop any new symptoms.

  • Do not suddenly stop taking Diltiazem 24-Hour Extended-Release Beads Capsules. Your condition may get worse if you suddenly stop taking it. If you need to stop Diltiazem 24-Hour Extended-Release Beads Capsules or add a new medicine, your doctor will gradually lower your dose.

  • Tell your doctor or dentist that you take Diltiazem 24-Hour Extended-Release Beads Capsules before you receive any medical or dental care, emergency care, or surgery.

  • Be sure to have your blood pressure checked regularly while taking Diltiazem 24-Hour Extended-Release Beads Capsules.

  • Lab tests, including blood pressure, electrocardiogram (ECG), and heart rate, may be performed while you use Diltiazem 24-Hour Extended-Release Beads Capsules. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

  • Use Diltiazem 24-Hour Extended-Release Beads Capsules with caution in the ELDERLY; they may be more sensitive to its effects, especially swelling of the ankles, feet, or hands; dizziness; and slow heartbeat.

  • Diltiazem 24-Hour Extended-Release Beads Capsules should be used with extreme caution in CHILDREN; safety and effectiveness in children have not been confirmed.

  • PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of taking Diltiazem 24-Hour Extended-Release Beads Capsules while you are pregnant. Diltiazem 24-Hour Extended-Release Beads Capsules are found in breast milk. Do not breast-feed while taking Diltiazem 24-Hour Extended-Release Beads Capsules.


Possible side effects of Diltiazem 24-Hour Extended-Release Beads Capsules:


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; dizziness; facial flushing; headache; lightheadedness; tiredness; weakness.



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; unusual hoarseness); chest pain; fainting; fast, slow, or irregular heartbeat; fever, chills, or sore throat; hallucinations; mood or mental changes; personality changes; reddened, blistered, or swollen skin; severe or persistent dizziness, lightheadedness, nausea, or vomiting; shortness or breath; sudden weight gain; swelling of the feet, ankles, or hands; symptoms of liver problems (eg, dark urine, pale stools, yellowing of the skin or eyes); tender, bleeding, or swollen gums; unusual bleeding or bruising; unusual or persistent tiredness or weakness; 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: Diltiazem 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 confusion; difficulty breathing, especially when lying down; dizziness; drowsiness; fainting; lightheadedness, especially when standing; loss of consciousness; nausea; nervousness; slurred speech; unusual weakness; very slow heart rate.


Proper storage of Diltiazem 24-Hour Extended-Release Beads Capsules:

Store Diltiazem 24-Hour Extended-Release Beads Capsules at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Diltiazem 24-Hour Extended-Release Beads Capsules out of the reach of children and away from pets.


General information:


  • If you have any questions about Diltiazem 24-Hour Extended-Release Beads Capsules, please talk with your doctor, pharmacist, or other health care provider.

  • Diltiazem 24-Hour Extended-Release Beads Capsules 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 Diltiazem 24-Hour Extended-Release Beads Capsules. 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 Diltiazem resources


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


Compare Diltiazem with other medications


  • Angina Pectoris Prophylaxis
  • Atrial Fibrillation
  • Atrial Flutter
  • Heart Failure
  • High Blood Pressure
  • Raynaud's Syndrome
  • Supraventricular Tachycardia

Sunday 6 December 2009

Irinto




Irinto may be available in the countries listed below.


Ingredient matches for Irinto



Irinotecan

Irinotecan hydrochloride trihydrate (a derivative of Irinotecan) is reported as an ingredient of Irinto in the following countries:


  • Bulgaria

International Drug Name Search

Thursday 3 December 2009

Loperamid Domesco




Loperamid Domesco may be available in the countries listed below.


Ingredient matches for Loperamid Domesco



Loperamide

Loperamide is reported as an ingredient of Loperamid Domesco in the following countries:


  • Vietnam

International Drug Name Search

Dulcolax Suppositories



Pronunciation: bis-AK-oh-dil
Generic Name: Bisacodyl
Brand Name: Examples include Bisa-Lax and Dulcolax


Dulcolax Suppositories are used for:

Relieving occasional constipation and irregularity. It may also be used for other conditions as determined by your doctor.


Dulcolax Suppositories are a stimulant laxative. It acts directly on the bowels, stimulating the bowel muscles to cause a bowel movement.


Do NOT use Dulcolax Suppositories if:


  • you are allergic to any ingredient in Dulcolax Suppositories

  • you have severe stomach pain; appendicitis; severe constipation; stomach, intestinal, or rectal bleeding; or intestinal blockage

  • you are having abdominal surgery

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



Before using Dulcolax Suppositories:


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


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

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

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

  • if you have heart failure, abnormal levels of fluids or electrolytes in your body, nausea, vomiting, or undiagnosed stomach pain

Some MEDICINES MAY INTERACT with Dulcolax Suppositories. However, no specific interactions with Dulcolax Suppositories are known at this time.


Ask your health care provider if Dulcolax Suppositories 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 Dulcolax Suppositories:


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


  • Remove the wrapper from the suppository.

  • Insert suppository well up into the rectum as directed by your doctor or on the package labeling. Retain the suppository for 15 to 20 minutes.

  • If you have hemorrhoids, coat the tip of the suppository with petroleum jelly before inserting.

  • Drinking extra fluids while you are using Dulcolax Suppositories are recommended. Check with your doctor for instructions.

  • If you miss a dose of Dulcolax Suppositories and are using it regularly, use 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 use 2 doses at once.

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



Important safety information:


  • Do not use for longer than 1 week without checking with your doctor. Using Dulcolax Suppositories for a long time may result in loss of normal bowel function.

  • Do not take additional laxatives or stool softeners with Dulcolax Suppositories unless directed by your doctor.

  • Rectal bleeding or failure to have a bowel movement after use of a laxative may be a sign of a serious condition. Stop use and contact your doctor.

  • If you develop nausea, vomiting, or stomach pain, stop using Dulcolax Suppositories and check with your doctor.

  • If you notice a sudden change in bowel habits that lasts for 2 weeks or more, do not continue using Dulcolax Suppositories. Instead, check with your doctor.

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

  • Dulcolax Suppositories are not recommended for use in CHILDREN younger than 6 years 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 using Dulcolax Suppositories while pregnant. It is not known if Dulcolax Suppositories are found in breast milk. If you are or will be breast-feeding take Dulcolax Suppositories, check with your doctor. Discuss any possible risks to your baby.


Possible side effects of Dulcolax Suppositories:


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:



Cramps; faintness; stomach discomfort.



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).



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: Dulcolax 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 diarrhea; stomach cramps.


Proper storage of Dulcolax Suppositories:

Store Dulcolax Suppositories at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store in a tightly closed container away from heat, moisture, and light. Do not store in the bathroom. Keep Dulcolax Suppositories out of the reach of children and away from pets.


General information:


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

  • Dulcolax Suppositories 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 Dulcolax Suppositories. 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 Dulcolax resources


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


Compare Dulcolax with other medications


  • Bowel Preparation
  • Constipation

Tuesday 1 December 2009

Dibrolax




Dibrolax may be available in the countries listed below.


Ingredient matches for Dibrolax



Sodium Picosulfate

Sodium Picosulfate is reported as an ingredient of Dibrolax in the following countries:


  • Peru

International Drug Name Search