Monday 25 October 2010

Diltia XT 24-Hour Sustained-Release Capsules


Pronunciation: dil-TYE-a-zem
Generic Name: Diltiazem
Brand Name: Examples include Diltia XT and Dilt-XR


Diltia XT 24-Hour Sustained-Release 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.


Diltia XT 24-Hour Sustained-Release 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 Diltia XT 24-Hour Sustained-Release Capsules if:


  • you are allergic to any ingredient in Diltia XT 24-Hour Sustained-Release 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 Diltia XT 24-Hour Sustained-Release Capsules:


Some medical conditions may interact with Diltia XT 24-Hour Sustained-Release 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 Diltia XT 24-Hour Sustained-Release 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 Diltia XT 24-Hour Sustained-Release Capsules's side effects, such as heart rhythm problems

  • 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 Diltia XT 24-Hour Sustained-Release Capsules

  • Moricizine or rifamycins (eg, rifampin) because they may decrease Diltia XT 24-Hour Sustained-Release Capsules's effectiveness

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


Use Diltia XT 24-Hour Sustained-Release Capsules as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • Take Diltia XT 24-Hour Sustained-Release Capsules by mouth on an empty stomach at least 1 hour before or 2 hours after eating.

  • Swallow Diltia XT 24-Hour Sustained-Release Capsules whole. Do not open, break, crush, or chew before swallowing.

  • Taking Diltia XT 24-Hour Sustained-Release Capsules at the same time each day will help you remember to take it.

  • Continue to take Diltia XT 24-Hour Sustained-Release Capsules even if you feel well. Do not miss any doses.

  • If you miss a dose of Diltia XT 24-Hour Sustained-Release 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 Diltia XT 24-Hour Sustained-Release Capsules.



Important safety information:


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

  • Diltia XT 24-Hour Sustained-Release 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.

  • Diltia XT 24-Hour Sustained-Release Capsules may cause you to become sunburned more easily. Avoid the sun, sunlamps, or tanning booths until you know how you react to Diltia XT 24-Hour Sustained-Release 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 Diltia XT 24-Hour Sustained-Release Capsules. Your condition may get worse if you suddenly stop taking it. If you need to stop Diltia XT 24-Hour Sustained-Release Capsules or add a new medicine, your doctor will gradually lower your dose.

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

  • Be sure to have your blood pressure checked regularly while taking Diltia XT 24-Hour Sustained-Release Capsules.

  • Lab tests, including blood pressure, electrocardiogram (ECG), and heart rate, may be performed while you use Diltia XT 24-Hour Sustained-Release 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 Diltia XT 24-Hour Sustained-Release 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.

  • Diltia XT 24-Hour Sustained-Release Capsules should be used with extreme caution in CHILDREN; safety and effectiveness 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 Diltia XT 24-Hour Sustained-Release Capsules while you are pregnant. Diltia XT 24-Hour Sustained-Release Capsules are found in breast milk. Do not breast-feed while taking Diltia XT 24-Hour Sustained-Release Capsules.


Possible side effects of Diltia XT 24-Hour Sustained-Release 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; mental or mood changes; personality changes; reddened, blistered, or swollen skin; severe or persistent dizziness, lightheadedness, nausea, or vomiting; shortness of 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: Diltia XT 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 Diltia XT 24-Hour Sustained-Release Capsules:

Store Diltia XT 24-Hour Sustained-Release Capsules at room temperature, between 59 and 77 degrees F (15 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Diltia XT 24-Hour Sustained-Release Capsules out of the reach of children and away from pets.


General information:


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

  • Diltia XT 24-Hour Sustained-Release 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 Diltia XT 24-Hour Sustained-Release 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 Diltia XT resources


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


Compare Diltia XT with other medications


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  • Heart Failure
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  • Raynaud's Syndrome
  • Supraventricular Tachycardia

Saturday 23 October 2010

Fluconazol Mayrhofer




Fluconazol Mayrhofer may be available in the countries listed below.


Ingredient matches for Fluconazol Mayrhofer



Fluconazole

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


  • Austria

International Drug Name Search

Friday 22 October 2010

Methacholine




In the US, Methacholine (methacholine systemic) is a member of the drug class miscellaneous uncategorized agents and is used to treat Diagnosis and Investigation.

US matches:

  • Methacholine Solution

CAS registry number (Chemical Abstracts Service)

0000055-92-5

Chemical Formula

C8-H18N-O2

Molecular Weight

160

Therapeutic Category

Parasympathomimetic agent, direct acting

Chemical Names

1-Propanaminium, 2-(acetyloxy)-N,N,N-trimethyl-

1-Propanaminium, 2-(acetyloxy)-N,N,N-trimethyl-, chloride

Foreign Names

  • Methacholin (German)
  • Méthacholine (French)
  • Metacolina (Spanish)

Generic Names

  • Mecholine (IS)
  • Metacolina cloruro (OS: DCIT)
  • Méthacholine (chlorure de) (OS: DCF)
  • Methacholiniumchlorid (IS)
  • Metacolina cloruro (PH: F.U. IX)
  • Methacholinchlorid (PH: Ph. Helv. 10)
  • Méthacholine (chlorure de) (PH: Ph. Franç. Xe édit)
  • Methacholine Chloride (PH: USP 32)
  • Methacholini chloridum (PH: Ph. Helv. 10)

Brand Names

  • Metacolina Lofarma
    Lofarma, Italy


  • Provocholine
    Diater, Spain; Methapharm, Canada; Methapharm, United States

International Drug Name Search

Glossary

DCFDénomination Commune Française
DCITDenominazione Comune Italiana
ISInofficial Synonym
OSOfficial Synonym
PHPharmacopoeia Name

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

Tuesday 12 October 2010

Pivalone compositum




Pivalone compositum may be available in the countries listed below.


Ingredient matches for Pivalone compositum



Neomycin

Neomycin sulfate (a derivative of Neomycin) is reported as an ingredient of Pivalone compositum in the following countries:


  • Switzerland

Tixocortol

Tixocortol 21-pivalate (a derivative of Tixocortol) is reported as an ingredient of Pivalone compositum in the following countries:


  • Switzerland

International Drug Name Search

Monday 11 October 2010

Nexotensil




Nexotensil may be available in the countries listed below.


Ingredient matches for Nexotensil



Amlodipine

Amlodipine besilate (a derivative of Amlodipine) is reported as an ingredient of Nexotensil in the following countries:


  • Argentina

International Drug Name Search

Friday 8 October 2010

Bicalutamid Billix




Bicalutamid Billix may be available in the countries listed below.


Ingredient matches for Bicalutamid Billix



Bicalutamide

Bicalutamide is reported as an ingredient of Bicalutamid Billix in the following countries:


  • Germany

International Drug Name Search

Cipronex




Cipronex may be available in the countries listed below.


Ingredient matches for Cipronex



Ciprofloxacin

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


  • Georgia

  • Latvia

  • Poland

International Drug Name Search

Sunday 3 October 2010

Bromhist Pediatric Drops


Pronunciation: brome-fen-EER-ah-meen/soo-doe-eh-FED-rin
Generic Name: Brompheniramine/Pseudoephedrine
Brand Name: Bromhist Pediatric


Bromhist Pediatric Drops are used for:

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


Bromhist Pediatric Drops are an antihistamine and decongestant combination. The antihistamine works by blocking the action of histamine, which helps reduce symptoms such as watery eyes and sneezing. The decongestant promotes sinus and nasal drainage, which relieves congestion and pressure.


Do NOT use Bromhist Pediatric Drops if:


  • you are allergic to any ingredient in Bromhist Pediatric Drops

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

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

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



Before using Bromhist Pediatric Drops:


Some medical conditions may interact with Bromhist Pediatric Drops. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:


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

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

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

  • if you have a fast, slow, or irregular heartbeat; heart blood vessel problems; or other heart problems

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

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


  • Beta-blockers (eg, propranolol), COMT inhibitors (eg, tolcapone), furazolidone, indomethacin, MAO inhibitors (eg, phenelzine), sodium oxybate (GHB), or tricyclic antidepressants (eg, amitriptyline) because side effects of Bromhist Pediatric Drops may be increased

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

  • Bromocriptine or hydantoins (eg, phenytoin) because side effects may be increased by Bromhist Pediatric Drops

  • Guanadrel, guanethidine, methyldopa, mecamylamine, or reserpine because effectiveness may be decreased by Bromhist Pediatric Drops

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


Use Bromhist Pediatric Drops as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • Bromhist Pediatric Drops may be taken with or without food.

  • Use the dropper that comes with Bromhist Pediatric Drops to measure your dose. Ask your pharmacist for help if you are unsure of how to measure your dose.

  • If you miss a dose of Bromhist Pediatric Drops, 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 Bromhist Pediatric Drops.



Important safety information:


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

  • Do not take diet or appetite control medicines while you are taking Bromhist Pediatric Drops without checking with your doctor.

  • Bromhist Pediatric Drops contains pseudoephedrine. Before you begin taking any new prescription or nonprescription medicine, read the ingredients to see if it also contains pseudoephedrine. If it does or if you are uncertain, contact your doctor or pharmacist.

  • Do NOT exceed the recommended dose or take Bromhist Pediatric Drops for longer than prescribed without checking with your doctor.

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

  • Bromhist Pediatric Drops may cause increased sensitivity to the sun. Avoid exposure to the sun, sunlamps, or tanning booths until you know how you react to Bromhist Pediatric Drops. Use a sunscreen or protective clothing if you must be outside for a prolonged period.

  • If you are scheduled for allergy skin testing, do not take Bromhist Pediatric Drops for several days before the test because it may decrease your response to the skin tests.

  • Before you have any medical or dental treatments, emergency care, or surgery, tell the doctor or dentist that you are using Bromhist Pediatric Drops.

  • Use Bromhist Pediatric Drops with caution in the ELDERLY because they may be more sensitive to its effects.

  • Caution is advised when using Bromhist Pediatric Drops in CHILDREN because they may be more sensitive to its effects.

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


Possible side effects of Bromhist Pediatric Drops:


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



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



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

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



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


See also: Bromhist Pediatric side effects (in more detail)


If OVERDOSE is suspected:


Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include blurred vision; confusion; hallucinations; seizures; severe dizziness, lightheadedness, or headache; severe drowsiness; unusually fast, slow, or irregular heartbeat; vomiting.


Proper storage of Bromhist Pediatric Drops:

Store Bromhist Pediatric Drops at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Bromhist Pediatric Drops out of the reach of children and away from pets.


General information:


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

  • Bromhist Pediatric Drops 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 Bromhist Pediatric Drops. 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 Bromhist Pediatric resources


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


  • Bromhist Pediatric Drops Concise Consumer Information (Cerner Multum)

  • B-Vex PD Concise Consumer Information (Cerner Multum)

  • Dimaphen Concise Consumer Information (Cerner Multum)



Compare Bromhist Pediatric with other medications


  • Hay Fever
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