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Multaq
Dronedarone
$495.00
400mg · 3 × 60 tablets · 3 months supply
Generic· By UniPharm
$165.00 per month
Brand or generic
Generic packs carry the same active ingredient at the same strength.
How long a supply?
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Annual cost
$1980a year at this pack size
Prescription required
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400mg
FDA boxed warningIncreased risk of death, stroke and heart failure in patients with decompensated heart failure or permanent atrial fibrillation
In patients with symptomatic heart failure and recent decompensation requiring hospitalization or NYHA Class IV heart failure, MULTAQ doubles the risk of death. MULTAQ is contraindicated in patients with symptomatic heart failure with recent decompensation requiring hospitalization or NYHA Class IV heart failure.
In patients with permanent atrial fibrillation, MULTAQ doubles the risk of death, stroke and hospitalization for heart failure. MULTAQ is contraindicated in patients in atrial fibrillation (AF) who will not or cannot be cardioverted into normal sinus rhythm.
MULTAQ is contraindicated in patients with symptomatic heart failure with recent decompensation requiring hospitalization or NYHA Class IV heart failure. MULTAQ doubles the risk of death in these patients.
MULTAQ is contraindicated in patients in atrial fibrillation (AF) who will not or cannot be cardioverted into normal sinus rhythm. In patients with permanent AF, MULTAQ doubles the risk of death, stroke, and hospitalization for heart failure.
About Multaq
Overview
Multaq contains dronedarone, an antiarrhythmic medicine supplied as tablets. It is used to reduce the risk of hospital admission for atrial fibrillation (AF) in people currently in a normal heart rhythm who have a history of intermittent or persistent AF. It has effects that help control heart rhythm, but exactly how it works is unknown.
What it treats
To reduce the risk of hospitalization for atrial fibrillation (AF) in people currently in normal heart rhythm who have a history of paroxysmal (intermittent) or persistent AF.
Safety information
Side effects
Common side effects include diarrhea, nausea, stomach pain, vomiting, indigestion, a slow heartbeat, weakness, and skin problems such as rash, itching, eczema or dermatitis. Contact your doctor if you develop new or worsening heart failure, liver injury, lung toxicity, low potassium or magnesium levels, or QT prolongation (a change in the heart’s electrical activity). These are serious safety concerns listed in the label. Heart rhythm, kidney function, and potassium and magnesium levels need monitoring during treatment. Multaq may harm an unborn baby. Use effective contraception during treatment if you could become pregnant.
FDA boxed warning
Increased risk of death, stroke and heart failure in patients with decompensated heart failure or permanent atrial fibrillation
In patients with symptomatic heart failure and recent decompensation requiring hospitalization or NYHA Class IV heart failure, MULTAQ doubles the risk of death. MULTAQ is contraindicated in patients with symptomatic heart failure with recent decompensation requiring hospitalization or NYHA Class IV heart failure.
In patients with permanent atrial fibrillation, MULTAQ doubles the risk of death, stroke and hospitalization for heart failure. MULTAQ is contraindicated in patients in atrial fibrillation (AF) who will not or cannot be cardioverted into normal sinus rhythm.
MULTAQ is contraindicated in patients with symptomatic heart failure with recent decompensation requiring hospitalization or NYHA Class IV heart failure. MULTAQ doubles the risk of death in these patients.
MULTAQ is contraindicated in patients in atrial fibrillation (AF) who will not or cannot be cardioverted into normal sinus rhythm. In patients with permanent AF, MULTAQ doubles the risk of death, stroke, and hospitalization for heart failure.
A boxed warning is the strongest warning the US Food and Drug Administration requires on a medicine label. Text is taken from the official label, with internal section references removed.
When to call your doctor
If symptoms are severe or getting worse quickly, seek emergency care rather than waiting.
Before taking this medicine
Do not take Multaq (dronedarone) if you have: • Permanent atrial fibrillation, meaning a normal heart rhythm will not or cannot be restored. • Heart failure with symptoms that recently worsened and required hospital treatment, or NYHA Class IV heart failure. • Second- or third-degree heart block or sick sinus syndrome, unless you have a functioning pacemaker. • A resting heart rate below 50 beats per minute. • Certain abnormal ECG measurements: a QTc interval above 500 milliseconds or a PR interval above 280 milliseconds. • Liver or lung damage caused by previous amiodarone treatment. • Severe liver impairment. • An allergy to dronedarone or any other ingredient in Multaq. Do not take Multaq with erythromycin or strong CYP3A inhibitors, including ketoconazole, itraconazole, voriconazole, cyclosporine, telithromycin, clarithromycin, nefazodone or ritonavir. It must also not be used with medicines or herbal products that prolong the QT interval and could cause a dangerous heart rhythm called torsade de pointes. These include certain antipsychotics, tricyclic antidepressants, some oral macrolide antibiotics, and Class I or III medicines for abnormal heart rhythms. Your heart rhythm should be checked at least every three months. If atrial fibrillation is detected, your clinician should stop Multaq or restore a normal rhythm through cardioversion. Appropriate treatment to prevent blood clots is needed before and throughout treatment. Multaq requires monitoring for liver, lung and kidney problems. Treatment should be stopped if liver injury is suspected or lung toxicity is confirmed. Kidney function should be checked periodically, and potassium and magnesium levels should remain within the normal range. Based on animal studies, Multaq may harm an unborn baby. If you could become pregnant, use effective contraception during treatment. Do not breastfeed while taking Multaq.
Interactions
Multaq can interact with other medicines. Tell your doctor about all medicines and supplements you take, particularly: • Class I or III medicines for abnormal heart rhythms: these must not be taken with Multaq. • Digoxin: your doctor may need to stop it or adjust your prescription and monitor digoxin levels. • Beta-blockers and calcium channel blockers: these may slow the heart rate too much or affect electrical conduction in the heart. Your doctor may need to adjust treatment and check an ECG. • Statins, including simvastatin: your doctor should review your treatment because specific restrictions apply. • Sirolimus and tacrolimus: monitoring and prescription adjustments may be needed. • Warfarin: your INR, a measure of blood clotting, should be checked after starting Multaq. • Medicines that increase the activity of the liver enzyme CYP3A: these should be avoided with Multaq. Ask your doctor or pharmacist to check your medicines. Avoid grapefruit juice while taking Multaq. Do not stop or change prescribed medicines without speaking to your doctor.
Using Multaq
Dosing
Dosing is set by your prescriber. Each health care professional may prescribe medication differently according to a patient's medical history and condition, so follow the directions on your prescription label and speak to your doctor or pharmacist before changing anything.
Storage
Store below 25°C in a dry place, in the original pack, away from direct light and moisture. Do not keep it in a bathroom. Keep all medicines out of the sight and reach of children.
Clinical information on this page is summarised from the US FDA label MULTAQ (DRONEDARONE) TABLET, FILM COATED [CARDINAL HEALTH 107, LLC] (DailyMed, retrieved 19 September 2026).
Patient information and references
Official and supporting information to read alongside advice from your prescriber or pharmacist.
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