Wednesday, 10 August 2011

Disotate EDTA


Generic Name: edetate disodium (EDTA) (E de tate dye SOE dee um)

Brand Names: Disotate, Endrate


What is edetate disodium?

Edetate disodium (EDTA) is a chelating (KEE-late-ing) agent. A chelating agent is capable of removing a heavy metal, such as lead or mercury, from the blood.


EDTA is used to lower blood levels of calcium when they have become dangerously high. EDTA is also used to control heart rhythm disturbances caused by a heart medication called digitalis (digoxin, Lanoxin).


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


What is the most important information I should know about edetate disodium?


EDTA is given in a hospital or emergency setting. The medicine must be given slowly through a needle placed in your vein. The infusion can take at least 3 hours to complete.


If possible before you receive this medication, tell your caregivers if you have heart disease, congestive heart failure, a heart rhythm disorder, diabetes, low potassium (hypokalemia), or a history of seizures, brain tumor, or head injury.


In an emergency situation, it may not be possible before you are treated with EDTA to tell your caregivers about any health conditions you have or if you are pregnant or breast-feeding. However, make sure any doctor caring for your pregnancy or your baby knows that you have received this medication.


After treatment with EDTA, you will be watched to make sure the medication has been effective and you no longer have any effects of high calcium levels.


What should I discuss with my health care provider before receiving edetate disodium?


You should not receive this medication if you are unable to urinate, or if you have arteriosclerosis (hardening of the arteries).

If possible, before you receive EDTA, tell your doctor if you are allergic to any drugs, or if you have:



  • heart disease, congestive heart failure;




  • a heart rhythm disorder;




  • a history of seizures, brain tumor, or head injury;




  • diabetes;




  • low potassium levels (hypokalemia); or




  • if you take digitalis (digoxin, Lanoxin, Lanoxicaps).



If you have any of these conditions, you may not be able to receive EDTA, or you may need dosage adjustments or special tests during treatment.


FDA pregnancy category C. This medication may be harmful to an unborn baby. If possible, tell your doctor if you are pregnant before you receive EDTA. It is not known whether EDTA passes into breast milk or if it could harm a nursing baby. If possible, tell your doctor if you are breast-feeding a baby.

In an emergency situation, it may not be possible before you are treated with EDTA to tell your caregivers if you are pregnant or breast-feeding. However, make sure any doctor caring for your pregnancy or your baby knows that you have received this medication.


How is edetate disodium given?


EDTA is given as an injection through a needle placed into a vein. You will receive this injection in a hospital or emergency setting. The medicine must be given slowly through an IV infusion, and can take at least 3 hours to complete.


EDTA is usually given for 5 days in a row, followed by 1 day off the medicine. This schedule is then repeated for as long as needed until blood calcium levels are lowered to a safe level.


After you receive EDTA, you will need to remain lying down for a short time. Reversing high blood levels of calcium can cause a drop in your blood pressure. This can make you feel very light-headed or slow your breathing. You will need to be watched closely for these and other effects after you receive the medication.


To be sure this medication is helping your condition, your blood and urine will need to be tested often. This will help your doctor determine how long to treat you with EDTA.


What happens if I miss a dose?


Since EDTA is given by a healthcare provider, it is not likely that you will miss a dose.


What happens if I overdose?


Tell your caregivers right away if you think you have received too much of this medicine. Overdose symptoms may include feeling light-headed or fainting.


What should I avoid after receiving edetate disodium?


Avoid getting up too fast from a sitting or lying position, or you may feel dizzy. Get up slowly and steady yourself to prevent a fall.


Edetate disodium 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. Tell your caregivers at once if you have any of these serious side effects:

  • feeling like you might pass out; or




  • severe blistering, peeling, or red skin rash.



Less serious side effects include:



  • nausea, vomiting, diarrhea;




  • numbness or tingling (especially around your mouth);




  • headache; or




  • pain, redness, or swelling where the needle is placed.



This is not a complete list of side effects and others may occur. Tell your doctor about any unusual or bothersome side effect. You may report side effects to FDA at 1-800-FDA-1088.


What other drugs will affect edetate disodium?


There may be other drugs that can interact with EDTA. Tell your doctor about all your prescription and over-the-counter medications, vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start a new medication without telling your doctor.



More Disotate resources


  • Disotate Drug Interactions
  • Disotate Support Group
  • 0 Reviews for Disotate - Add your own review/rating


Compare Disotate with other medications


  • Hypercalcemia
  • Ventricular Arrhythmia


Where can I get more information?


  • Your doctor or pharmacist can provide more information about EDTA.


Monday, 8 August 2011

Chlorhexidine / Chlorobutanol Biogaran




Chlorhexidine/ Chlorobutanol Biogaran may be available in the countries listed below.


Ingredient matches for Chlorhexidine/ Chlorobutanol Biogaran



Chlorhexidine

Chlorhexidine digluconate (a derivative of Chlorhexidine) is reported as an ingredient of Chlorhexidine/ Chlorobutanol Biogaran in the following countries:


  • France

Chlorobutanol

Chlorobutanol is reported as an ingredient of Chlorhexidine/ Chlorobutanol Biogaran in the following countries:


  • France

International Drug Name Search

Saturday, 6 August 2011

Biltricide


Pronunciation: PRAZ-i-KWON-tel
Generic Name: Praziquantel
Brand Name: Biltricide


Biltricide is used for:

Treating certain worm infections (eg, schistosoma, liver flukes).


Biltricide is an anthelmintic agent. It works by killing sensitive worms.


Do NOT use Biltricide if:


  • you are allergic to any ingredient in Biltricide

  • you have certain worm infections of the eye (ocular cysticercosis)

  • you are breast-feeding

  • you are taking rifampin

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



Before using Biltricide:


Some medical conditions may interact with Biltricide. 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 liver, kidney, or heart problems, or worm infection of the brain (eg, cerebral cysticercosis)

  • if you have a history of seizures (eg, epilepsy)

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


  • Azole antifungals (eg, itraconazole, ketoconazole), cimetidine, or erythromycin because they may increase the risk of Biltricide's side effects

  • Anticonvulsants (eg, carbamazepine, phenobarbital, phenytoin), chloroquine, dexamethasone, or rifamycins (eg, rifampin) because they may decrease Biltricide's effectiveness

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


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


  • Take Biltricide with a full glass of water during meals.

  • Swallow Biltricide whole. Do not break, crush, or chew before swallowing.

  • Take your doses at least 4 hours apart but not more than 6 hours apart unless directed otherwise by your doctor.

  • If you miss a dose of Biltricide, take it as soon as possible. If it less than 4 hours until your next dose, contact your doctor to see if you need to establish a new dosing schedule.

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



Important safety information:


  • Biltricide may cause drowsiness or dizziness. These effects may be worse if you take it with alcohol or certain medicines. Use Biltricide with caution. Do not drive or perform other possibly unsafe tasks on the day that you use Biltricide and on the following day.

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

  • Use Biltricide with extreme caution in CHILDREN younger than 4 years of age; safety and effectiveness in children have not been confirmed.

  • PREGNANCY and BREAST-FEEDING: If you think you may be pregnant, contact your doctor. You will need to discuss the benefits and risks of using Biltricide while you are pregnant. Biltricide is found in breast milk. Do not breast-feed while taking Biltricide and for 72 hours after you have stopped taking Biltricide.


Possible side effects of Biltricide:


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



Dizziness; general feeling of being unwell; headache; nausea; stomach upset.



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); bloody diarrhea; fever; seizures; severe or persistent vomiting; slow or irregular heartbeat.



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: Biltricide 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.


Proper storage of Biltricide:

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


General information:


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

  • Biltricide 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 Biltricide. 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 Biltricide resources


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


  • Biltricide Prescribing Information (FDA)

  • Biltricide Advanced Consumer (Micromedex) - Includes Dosage Information

  • Biltricide Concise Consumer Information (Cerner Multum)

  • Biltricide Monograph (AHFS DI)

  • Praziquantel Professional Patient Advice (Wolters Kluwer)



Compare Biltricide with other medications


  • Cysticercus cellulosae
  • Dog Tapeworm
  • Echinococcus
  • Fasciolopsis buski, Intestinal Fluke
  • Fish Tapeworm Infection
  • Heterophyes heterophyes, Intestinal Fluke
  • Hymenolepis nana, Dwarf Tapeworm
  • Liver Fluke
  • Metagonimus yokogawai, Intestinal Fluke
  • Naophyetus salmincola
  • Opisthorchis viverrini, Liver Fluke
  • Paragonimus westermani, Lung Fluke
  • Schistosoma haematobium
  • Schistosoma japonicum
  • Schistosoma mansoni
  • Schistosoma mekongi
  • Taenia saginata, beef tapeworm
  • Taenia solium, pork tapeworm

Friday, 5 August 2011

Lepirudin




In the US, Lepirudin (lepirudin systemic) is a member of the drug class thrombin inhibitors and is used to treat Thrombocytopenia Drug Induced.

US matches:

  • Lepirudin

  • Lepirudin Intravenous

Scheme

Rec.INN

ATC (Anatomical Therapeutic Chemical Classification)

B01AE02

CAS registry number (Chemical Abstracts Service)

0138068-37-8

Chemical Formula

C287-H440-N80-O111-S6

Molecular Weight

6979

Therapeutic Category

Anticoagulant agent: Direct thrombin inhibitor

Chemical Name

1-L-Leucine-2-L-threonine-63-desulfohirudin (Hirudo medicinalisisoform HV1)

Foreign Names

  • Lepirudinum (Latin)
  • Lepirudin (German)
  • Lepirudine (French)
  • Lepirudina (Spanish)

Generic Names

  • Lepirudin (OS: BAN)
  • HBW 023 (IS: Chiron Behring)
  • rDNA-Hirudin (IS)

Brand Names

  • Refludan
    Bayer, Canada; Bayer, United States; Berlex, United States; Celgene, Belgium; Celgene, Switzerland; Celgene, Germany; Celgene, United Kingdom; Celgene, Sweden; Pharmion, Austria; Pharmion, Australia; Pharmion, France; Pharmion, Hungary; Pharmion, Ireland; Pharmion, Luxembourg; Pharmion, Netherlands; Pharmion, Norway; Schering, Italy


  • Refludin
    Key Oncologics, South Africa; Pharmion, Spain

International Drug Name Search

Glossary

BANBritish Approved Name
ISInofficial Synonym
OSOfficial Synonym
Rec.INNRecommended International Nonproprietary Name (World Health Organization)

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

Tuesday, 26 July 2011

Kelnac




Kelnac may be available in the countries listed below.


Ingredient matches for Kelnac



Plaunotol

Plaunotol is reported as an ingredient of Kelnac in the following countries:


  • Japan

International Drug Name Search

Monday, 25 July 2011

Gonilert




Gonilert may be available in the countries listed below.


Ingredient matches for Gonilert



Hyaluronic Acid

Hyaluronic Acid sodium salt (a derivative of Hyaluronic Acid) is reported as an ingredient of Gonilert in the following countries:


  • Greece

International Drug Name Search

Monday, 18 July 2011

Céliprolol Winthrop




Céliprolol Winthrop may be available in the countries listed below.


Ingredient matches for Céliprolol Winthrop



Celiprolol

Celiprolol hydrochloride (a derivative of Celiprolol) is reported as an ingredient of Céliprolol Winthrop in the following countries:


  • France

International Drug Name Search