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Aratac (Amiodarone)

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Aratac is one of the most commonly used anti-arrhythmic drugs. While the United States FDA has labeled Aratac for the treatment of life-threatening ventricular arrhythmias. Aratac is commonly used off-label to treat supraventricular tachyarrhythmias such as atrial fibrillation as well as for the prevention of ventricular tachyarrhythmias (VTs) in high-risk patients.

Other names for this medication:
Amiocar, Amiodacore, Amiodarex, Amiodarona, Amiodarone, Amiohexal, Amiokordin, Amirone, Ancoron, Angoten, Aratac, Braxan, Cardilor, Cordalin, Cordan, Cordarex, Coronax, Coronovo, Daritmin, Daronal, Diarona, Keritmon, Miocor, Miodar, Miodrone, Nodis, Novarona, Opacorden, Rhythmiodarone, Rithmik, Tiaryt, Trangorex

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Also known as: Amiodarone


Amiodarone is used to treat life-threatening heart rhythm problems called ventricular arrhythmias. This medicine is used in patients who have already been treated with other medicines that did not work well.

Amiodarone belongs to the group of medicines known as antiarrhythmics. It works directly on the heart tissue and will slow the nerve impulses in the heart. This helps keep your heart rhythm normal.

This medicine is available only with your doctor's prescription.


This section provides information on the proper use of a number of products that contain amiodarone. It may not be specific to Aratac. 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.


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


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 Aratac are:

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Appropriate studies have not been performed on the relationship of age to the effects of amiodarone injection in the pediatric population. Safety and efficacy have not been established.

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Fatal acute hemorrhage and activity of serum and erythrocyte cholinesterase. Extraction and HPLC protocols were optimized and validated for the quantification of 9 phenolic and 3 methylxanthine compounds to examine inter- and intra-variation in white and green tea types and subtypes. Included randomized controlled trials (RCTs), prospective cohort studies, case-control studies, pre-post studies, and case reports that assessed pharmacologic and nonpharmacologic intervention for the management of OH in patients with SCI. Although target-contact and activity both participated in the induction of secretory modifications in neuron B19, target-mediated changes did not involve retrograde effects on presynaptic neuronal excitability. Samples were processed to detect Th17 cells and natural Treg cells by flow cytometry, and related gene expression was assessed by real-time reverse transcription-polymerase chain reaction. The present study sought to extend these findings by studying the inferior colliculus potential (ICP) in unanesthetized chinchillas. In the palliative treatment setting, less toxicity and longer survival may be more significant than response rate. On the nature of self-monitoring: construct explication with Q-sort ratings.

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