Uses
What the official label says Amiodarone is used for
The FDA label for Amiodarone states:
Amiodarone hydrochloride tablets are indicated for the treatment of documented, life-threatening recurrent ventricular fibrillation and life-threatening recurrent hemodynamically unstable tachycardia in adults who have not responded to adequate doses of other available antiarrhythmics or when alternative agents cannot be tolerated. Amiodarone hydrochloride tablets is an antiarrhythmic indicated for: Recurrent ventricular fibrillation. ( 1 ) Recurrent hemodynamically unstable ventricular tachycardia. ( 1 )
Read the label's “Indications and usage” section (verbatim)
Amiodarone hydrochloride tablets are indicated for the treatment of documented, life-threatening recurrent ventricular fibrillation and life-threatening recurrent hemodynamically unstable tachycardia in adults who have not responded to adequate doses of other available antiarrhythmics or when alternative agents cannot be tolerated. Amiodarone hydrochloride tablets is an antiarrhythmic indicated for: Recurrent ventricular fibrillation. ( 1 ) Recurrent hemodynamically unstable ventricular tachycardia. ( 1 )
Names & forms
Brand names, forms and strengths
Brand names (from RxNorm; not every brand is still sold): Nexterone, Pacerone.
Generic name: amiodarone · RxNorm ID (RxCUI): 703
| Form | Strengths listed in RxNorm |
|---|---|
| Injectable Solution | 50 MG/ML |
| Injection | 1.5 MG/ML, 1.8 MG/ML, 50 MG/ML |
| Oral Tablet | 100 MG, 200 MG, 300 MG, 400 MG |
| Prefilled Syringe | 50 MG/ML |
Strengths are listed so you can recognise a product — not as dosing information. Only your prescriber can decide what is right for you.
Read the label's “Dosage forms and strengths” section (verbatim)
100 mg tablets: round, flat-faced, beveled-edge white tablets debossed with "m" on the upper portion and "154" on the lower half on one side of the tablet, and plain on the other. 200 mg tablets: round, flat-faced, beveled-edge, scored white tablets debossed with "m" on the upper portion and "155" on the lower half on one side of the tablet with a score mark between and plain on the other. 400 mg tablets: oval-shaped, convex, scored yellow tablets debossed with "m" on the left and "156" on the right with a score mark between on one side, and plain on the other. Tablets, 100 mg, 200 mg, and 400 mg. ( 3 )
Appearance
What Amiodarone looks like
amiodarone hydrochloride 100 mg
Dr. Reddy's Labratories Inc.
amiodarone hydrochloride 200 mg
Dr. Reddy's Labratories Inc.
amiodarone hydrochloride 400 mg
Dr. Reddy's Labratories Inc.
amiodarone hydrochloride 100 mg
Sun Pharmaceutical Industries, Inc.
amiodarone hydrochloride 200 mg
Sun Pharmaceutical Industries, Inc.
amiodarone hydrochloride 400 mg
Sun Pharmaceutical Industries, Inc.
| Strength | Form | Colour | Shape | Size | Imprint | Score | Labeler |
|---|---|---|---|---|---|---|---|
| amiodarone hydrochloride 100 mg | tablet | white | round | 8 mm | m · 154 | 1 | Dr. Reddy's Labratories Inc. |
| amiodarone hydrochloride 200 mg | tablet | white | round | 10 mm | m · 155 | 2 | Dr. Reddy's Labratories Inc. |
| amiodarone hydrochloride 400 mg | tablet | yellow | oval | 16 mm | m · 156 | 2 | Dr. Reddy's Labratories Inc. |
| amiodarone hydrochloride 100 mg | tablet | white | round | 8 mm | TARO · 55 | 1 | Sun Pharmaceutical Industries, Inc. |
| amiodarone hydrochloride 200 mg | tablet | orange“Light orange” | round | 11 mm | TARO · 56 | 2 | Sun Pharmaceutical Industries, Inc. |
| amiodarone hydrochloride 400 mg | tablet | yellow“Light yellow” | round | 13 mm | TARO · 59 | 2 | Sun Pharmaceutical Industries, Inc. |
| amiodarone hydrochloride 300 mg | tablet | orange“Peach” | round | 12 mm | TARO · 58 | 2 | Sun Pharmaceutical Industries, Inc. |
| amiodarone hydrochloride 200 mg | tablet | white“White to Off-white” | round | 11 mm | 8 · 4 · A | 2 | Aurobindo Pharma Limited |
| amiodarone hydrochloride 100 mg | tablet | yellow | round | 7 mm | AS · 100 | 1 | Chartwell RX, LLC |
| amiodarone hydrochloride 200 mg | tablet | yellow | round | 10 mm | AS · 200 | 2 | Chartwell RX, LLC |
| amiodarone hydrochloride 400 mg | tablet | yellow | oval | 16 mm | AS · 400 | 2 | Chartwell RX, LLC |
From the product data in each manufacturer's label on DailyMed. Many companies make Amiodarone, so your medicine may look different from any shown here. If a pill looks unfamiliar, ask your pharmacist before taking it.
Read the label's “How supplied” section (verbatim)
Amiodarone hydrochloride tablets, USP are available as follows: 100 mg, white, round, flat-faced, beveled-edge tablet. Debossed with "m" on the upper portion and "154" on the lower half on one side of the tablet, and plain on the other. Bottles of 30 tablets NDC 75907-005-30 200 mg, white, round, flat-faced, beveled-edge, scored tablet. Debossed with "m" on the upper portion and "155" on the lower half on one side of the tablet with a score mark between and plain on the other. Bottles of 60 tablets NDC 75907-006-60 Bottles of 90 tablets NDC 75907-006-90 Bottles of 500 tablets NDC 75907-006-05 400 mg, Oval-shaped, convex, yellow, scored tablet. Debossed with "m" on the left and "156" on the right with a score mark between on one side, and plain on the other. Bottles of 30 tablets NDC 75907-007-30 Keep tightly closed. Store at Controlled Room Temperature, 20° to 25°C (68° to 77°F). Protect from light. Dispense in a light-resistant, tight container.
Safety
Important warnings for Amiodarone
Boxed warning (verbatim from the FDA label)
PULMONARY, HEPATIC and CARDIAC TOXICITY Amiodarone hydrochloride tablets is intended for use only in patients with the indicated life-threatening arrhythmias because its use is accompanied by substantial toxicity [see Indications and Usage (1) ]. Amiodarone hydrochloride tablets can cause pulmonary toxicity (hypersensitivity pneumonitis or interstitial/alveolar pneumonitis) that has resulted in clinically manifest disease at rates as high as 17% in some series of patients. Pulmonary toxicity has been fatal about 10% of the time . Obtain a baseline chest X-ray and pulmonary-function tests, including diffusion capacity, when amiodarone hydrochloride tablets therapy is initiated. Repeat history, physical exam, and chest X-ray every 3 to 6 months [see Warnings and Precautions 5.2) ]. Amiodarone hydrochloride tablets can cause hepatoxicity, which can be fatal. Obtain baseline and periodic liver transaminases and discontinue or reduce dose if the increase exceeds three times normal, or doubles in a patient with an elevated baseline. Discontinue amiodarone hydrochloride tablets if the patient experiences signs or symptoms of clinical liver injury [see Warnings and Precautions (5.3) ]. Amiodarone hydrochloride tablets can exacerbate arrhythmias. Initiate amiodarone hydrochloride tablets in a clinical setting where continuous electrocardiograms and cardiac resuscitation are available [see Warnings and Precautions (5.4) ]. WARNING: PULMONARY, HEPATIC, and CARDIAC TOXICITY See full prescribing information for complete boxed warning . Reserve amiodarone hydrochloride tablets for patients with the indicated life-threatening arrhythmias because its use is accompanied by substantial toxicity, some also life-threatening. Utilize alternative agents first. ( 1 ) Amiodarone hydrochloride tablets life-threatening toxicities include pulmonary ( 5.2 ), hepatic ( 5.3 ), and proarrhythmic ( 5.4 ). Initiate under hospital or specialist supervision. ( 5 )
Contraindications — who should not use it (verbatim)
Cardiogenic shock. Sick sinus syndrome, second- or third-degree atrioventricular block, bradycardia leading to syncope without a functioning pacemaker. Known hypersensitivity to the drug or to any of its components, including iodine. Amiodarone hydrochloride tablets are contraindicated in patients with ( 4 ): Cardiogenic shock. Sick sinus syndrome, second- or third-degree AV block, bradycardia leading to syncope without a functioning pacemaker. Known hypersensitivity to the drug or any of its components.
Warnings and precautions (verbatim excerpt)
Persistence of Adverse Effects: Adverse reactions and drug interaction can persist for several weeks following discontinuation. ( 5.1 ) Impaired Vision: Corneal microdeposits (common; reversible), optic neuropathy/neuritis (rare; may lead to blindness). ( 5.5 ) Thyroid Abnormalities: Hyperthyroidism or hypothyroidism. ( 5.6 ) 5.1 Persistence of Adverse Effects Because of the long half-life of amiodarone (15 to 142 days) and its active metabolite desethylamiodarone (14 to 75 days), adverse reactions and drug interactions can persist for several weeks following amiodarone discontinuation [see Clinical Pharmacology (12.3) ] . 5.2 Pulmonary Toxicity Amiodarone hydrochloride tablets may cause a clinical syndrome of cough and progressive dyspnea accompanied by functional, radiographic, gallium-scan, and pathological data consistent with pulmonary toxicity. Pulmonary toxicity secondary to amiodarone hydrochloride tablets may result from either indirect or direct toxicity as represented by hypersensitivity pneumonitis (including eosinophilic pneumonia) or interstitial/alveolar pneumonitis, respectively. Rates of pulmonary toxicity have been reported to be as high as 17% and is fatal in about 10% of cases. Obtain a baseline chest X-ray and pulmonary-function tests, including diffusion capacity, when amiodarone hydrochloride tablets therapy is initiated. Repeat history, physical exam, and chest X-ray every 3 to 6 months or if symptoms occur. Consider alternative antiarrhythmic therapy if the patient experiences signs or symptoms of pulmonary toxicity. Prednisone 40 to 60 mg/day tapered over several weeks may be helpful in treating pulmonary toxicity. Adult Respiratory Distress Syndrome (ARDS) Postoperatively, occurrences of ARDS have been reported in patients receiving amiodarone hydrochloride tablets therapy who have undergone either cardiac or noncardiac surgery. Although patients usually respond well to vigorous respiratory therapy, in rare instances the outcome has been fatal. 5.3 Hepatic Injury Asymptomatic elevations of hepatic enzyme levels are seen frequently, but amiodarone hydrochloride tablets can cause life-threatening hepatic injury. Histology has resembled that of alcoholic hepatitis or cirrhosis. Obtain baseline and periodic liver transaminases. If transaminases exceed three times normal, or doubles in a patient with an elevated baseline, discontinue or reduce dose of amiodarone hydrochloride tablets, obtain follow-up tests and treat appropriately. 5.4 Worsened Arrhythmia Amiodarone hydrochloride tablets can exacerbate the presenting arrhythmia in about 2 to 5% of patients or cause new ventricular fibrillation, incessant ventricular tachycardia, increased resistance to cardioversion, and polymorphic ventricular tachycardia associated with QTc prolongation (Torsade de Pointes [TdP]). Correct hypokalemia, hypomagnesemia, and hypocalcemia before initiating treatment with amiodarone hydrochloride tablets, as these disorders can exaggerate the degree of QTc prolongation and increase the potential for TdP. Give special attention to electrolyte and acid-base balance in patients experiencing severe or prolonged diarrhea or receiving drugs affecting electrolyte levels, such as diuretics, laxatives, systemic corticosteroids, or amphotericin B. 5.5 Visual Impairment and Loss of Vision Optic Neuropathy and Optic Neuritis Cases of optic neuropathy and optic neuritis, usually resulting in visual impairment and sometimes permanent blindness, have been reported in patients treated with amiodarone and may occur at any time during therapy. If symptoms of visual impairment appear, such as changes in visual acuity and decreases in peripheral vision, consider discontinuing amiodarone hydrochloride tablets and promptly refer for ophthalmic examination. Regular ophthalmic examination, including funduscopy and slit-lamp examination, is recommended during administration of amiodarone hydrochloride tablets [see Adverse Reactions (6.1) ] . Corneal Microdeposits Corneal microdeposits appear in the majority of adults treated with amiodarone hydrochloride tablets. They are usually discernible only by slit-lamp examination, but give rise to symptoms such as visual halos or blurred vision in as many as 10% of patients. Corneal microdeposits are reversible upon reduction of dose or termination of treatment. Asymptomatic microdeposits alone are not a reason to reduce dose or discontinue treatment [see Adverse Reactions (6.1) ] . 5.6 Thyroid Abnormalities Amiodarone hydrochloride tablets inhibits peripheral conversion of thyroxine (T 4 ) to triiodothyronine (T 3 ) and may cause increased thyroxine levels, decreased T 3 levels, and increased levels of inactive reverse T 3 (rT 3 ) in clinically euthyroid patients. Amiodarone hydrochloride tablets can cause either hypothyroidism (reported in up to 10% of patients) or hyperthyroidism (occurring in about 2% of patients). Monitor thyroid function prior to treatment and periodically thereafter, particularly in elderly patients, and in any patient with a history of thyroid nodules, goiter, or other thyroid dysfunction. Hyperthyroidism may induce arrhythmia breakthrough. If any new signs of arrhythmia appear, the possibility of hyperthyroidism should be considered. Antithyroid drugs, β-adrenergic blockers, temporary corticosteroid therapy may be necessary to treat the symptoms of hyperthyroidism. The action of antithyroid drugs may be delayed in amiodarone-induced thyrotoxicosis because of substantial quantities of preformed thyroid hormones stored in the gland. Radioactive iodine therapy is contraindicated because of the low radioiodine uptake associated with amiodarone-induced hyperthyroidism. Amiodarone hydrochloride tablets-induced hyperthyroidism may be followed by a transient period of hypothyroidism. Hypothyrodism may be primary or subsequent to resolution of preceding amiodarone-induced hyperthyroidism. …
Side effects — opening of the label's adverse reactions section
The following serious adverse reactions are described in more detail in other sections of the prescribing information: Pulmonary Toxicity [see Warnings and Precautions (5.2) ] Hepatic Injury [see Warnings and Precautions (5.3) ] Worsened Arrhythmia [see Warnings and Precautions (5.4) ] Visual Impairment and Loss of Vision [see Warnings and Precautions (5.5) ] Thyroid Abnormalities [see Warnings and Precautions (5.6) ] Bradycardia [see Warnings and Precautions (5.7) ] Peripheral Neuropathy [see Warnings and Precautions (5.10) ] Photosensitivity and Skin Discoloration [see Warnings and Precautions (5.11) ] The most common reactions (>1%) leading to discontinuation of amiodarone hydrochloride tablets include pulmonary toxicity, paroxysmal ventricular tachycardia, congestive heart failure, and elevation of liver enzymes. ( 6 ) To report SUSPECTED ADVERSE REACTIONS, contact Dr. …
Drug interactions — opening of the label's section
Because of amiodarone's long half-life, expect drug interactions to persist for weeks to months after discontinuation of amiodarone. Drug interactions with amiodarone are described in Table 1 below. Table 1: Amiodarone Drug Interactions Concomitant Drug Class/Name Examples Clinical Comment Pharmacodynamic Interactions QT Prolonging Drugs class I and III antiarrhythmics, lithium, certain phenothiazines, tricyclic antidepressants, certain fluoroquinolone and macrolide antibiotics, azole antifungals, halogenated inhalation anesthetic agents Increased risk of Torsade de Pointes. Avoid concomitant use. Negative Chronotropes digoxin, beta blockers, verapamil, diltiazem, clonidine, ivabradine Potentiates the electrophysiologic and hemodynamic effects of amiodarone, resulting in bradycardia, sinus arrest, and AV block. Monitor heart rate. …
This is not a complete list of warnings or side effects. Read the full label and talk to your prescriber or pharmacist. To report a side effect to the FDA, use MedWatch.
Resources
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