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Braxan (Amiodarone)
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Braxan

Braxan is a class III antiarrhythmic indicated for the treatment of recurrent hemodynamically unstable ventricular tachycardia and recurrent ventricular fibrillation. The FDA approved indications for Braxan are recurrent ventricular fibrillation (VF) and recurrent hemodynamically unstable ventricular tachycardia (VT). Off-label indications include atrial fibrillation and supraventricular tachycardia.

Other names for this medication:
Amiodacore, Amiodaronum, Amiodura, Amiogamma, Amiokordin, Amiotach, Amirone, Ancaron, Angoron, Angoten, Aratac, Asulblan, Braxan, Cardilor, Cardiodarone, Cardiron, Cordalin, Cordan, Cornaron, Coronax, Coronovo, Diarona, Eurythmic, Kendaron, Nexterone, Rhythmiodarone, Rivodarone, Tiaryt, Trangorex

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Also known as: Amiodarone

Description

Braxan is an antiarrhythmic. It works by stabilizing the heart rhythm in conditions in which the heart is beating too fast or in an irregular rhythm. Generic name of Braxan is Amiodarone. Braxan is also known as Amiodarone, Pacerone. Brand name of Braxan is Braxan.

Dosage

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

You will receive your first dose of this medicine in the hospital. Your doctor will watch you closely after you take this medicine to make sure you do not have any serious side effects.

Take this medicine exactly as directed by your doctor. Do not take more of it, do not take it more often, and do not take it for a longer time than your doctor ordered. Do not miss any doses. It may also take 1 to 3 weeks before your body responds to this medicine.

This medicine should come with a Medication Guide. Read and follow these instructions carefully. Ask your doctor if you have any questions.

You may take this medicine with or without food, but take it the same way each time.

The dose of this medicine 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 this medicine. 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 form (tablets): For ventricular arrhythmias: Adults—At first, 800 to 1600 milligrams (mg) per day taken in divided doses. Your doctor may adjust your dose as needed and tolerated. Children—Use and dose must be determined by your doctor.

Overdose

If you overdose Braxan and you don't feel good you should visit your doctor or health care provider immediately.

Storage

Store at room temperature between 20 and 25 degrees C (68 and 77 degrees F) away from moisture, light and heat. Keep container tightly closed. Throw away any unused medicine after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Braxan are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.

Contraindications

Tell your doctor if you have ever had any unusual or allergic reaction to this medicine or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.

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Correlation between transport capacity and growth rate in chemostat cultures. Reduced dietary diversity is a strong predictor of stunting in rural Bangladesh. Myopic development and progression is biomechanical and dominated by axial elongation. Report 1: effects of manual-focus LVES on visual acuity and contrast sensitivity. The single-leg hop for distance and the lower extremity functional test, when administered to Division III athletes during the preseason, may help identify those at risk for a time-loss low back or lower extremity injury. None of the patients was receiving corticosteroid or immunosuppressive treatment. To assess frequencies of reimbursements for antihypertensive, lipid-lowering and antidiabetic medications in France among national health insurance beneficiaries in 2010 and their associations according to age, sex, French regions, level deprivation and the presence of certain CVD. We observed transcription-related defects when regions of Rtf1 that mediate histone modification or association with active genes were deleted, but disruption of the physical association between Rtf1 and other Paf1 complex subunits caused only subtle mutant phenotypes.

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