How are Amiodarone adverse event reports trending over time?
This graph shows volume of adverse events submitted to the FDA by quarter for Amiodarone, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Amiodarone is flagged as the suspect drug causing the adverse event.
What are the most common Amiodarone adverse events reported to the FDA?
Drug Interaction | 962 (2.38%) |
Dyspnoea | 627 (1.55%) |
Atrial Fibrillation | 608 (1.5%) |
Bradycardia | 486 (1.2%) |
Hyperthyroidism | 482 (1.19%) |
Interstitial Lung Disease | 421 (1.04%) |
International Normalised Ratio Incr... | 413 (1.02%) |
Asthenia | 378 (.94%) |
Ventricular Tachycardia | 358 (.89%) |
Hypothyroidism | 350 (.87%) |
Electrocardiogram Qt Prolonged | 347 (.86%) |
![]() |
Share/Embed Graph
Export Data
This graph shows the top adverse events submitted to the FDA for Amiodarone, as well as related generic and/or brandname drugs containing the same primary active ingredients, from Q1 2004 to Q3 2012. Adverse events are counted if Amiodarone is flagged as a suspect drug causing the adverse event. For each adverse event listed, percent (%) represents percentage of the adverse event to all adverse events reported for the drug. Percent does not represent a rate related to drug utilization.
What are the most common Amiodarone adverse events reported to the FDA?
Cardiac Arrhythmias | 3585 (8.87%) |
Respiratory | 2040 (5.05%) |
Lower Respiratory Tract Disorders | 1897 (4.69%) |
Neurological | 1889 (4.67%) |
Therapeutic And Nontherapeutic Effe... | 1391 (3.44%) |
Cardiac And Vascular Investigations | 1304 (3.23%) |
Hepatic And Hepatobiliary | 1293 (3.2%) |
Epidermal And Dermal Conditions | 1124 (2.78%) |
Hematology Investigations | 1007 (2.49%) |
Thyroid Gland | 1007 (2.49%) |
Renal Disorders | 943 (2.33%) |
![]() |
Share/Embed Graph
Export Data
This graph shows the top categories of adverse events submitted to the FDA for Amiodarone, as well as related generic and/or brandname drugs containing the same primary active ingredients, from Q1 2004 to Q3 2012. Adverse events are counted if Amiodarone is flagged as a suspect drug causing the adverse event. For each adverse event listed, percent (%) represents percentage of the adverse event to all adverse events reported for the drug. Percent does not represent a rate related to drug utilization.
Why are people taking Amiodarone, according to those reporting adverse events to the FDA?
Atrial Fibrillation | 4122 |
Arrhythmia | 1255 |
Drug Use For Unknown Indication | 1030 |
Product Used For Unknown Indication | 869 |
Ventricular Tachycardia | 604 |
Atrial Flutter | 378 |
![]() |
Label | Labeler | Effective |
---|---|---|
Amiodarone Hydrochloride | Bedford Laboratories | 22-OCT-09 |
Amiodarone Hydrochloride | Bedford Laboratories | 22-OCT-09 |
Amiodarone Hydrochloride | McKesson Packaging Services Business Unit of McKesson Corporation | 21-JUN-10 |
Amiodarone Hydrochloride | Physicians Total Care, Inc. | 22-AUG-10 |
Amiodarone Hydrochloride | Sagent Pharmaceuticals | 30-SEP-10 |
Pacerone | Physicians Total Care, Inc. | 19-JAN-11 |
Amiodarone Hydrochloride | Cardinal Health | 08-APR-11 |
Amiodarone Hydrochloride | REMEDYREPACK INC. | 12-APR-11 |
Amiodarone Hydrochloride | Rebel Distributors Corp | 13-APR-11 |
Amiodarone Hydrochloride | Cadila Healthcare Limited | 20-APR-11 |
Amiodarone Hydrochloride | Zydus Pharmaceuticals (USA) Inc. | 20-APR-11 |
Amiodarone Hydrochloride | Golden State Medical Supply, Inc. | 01-JUL-11 |
Amiodarone Hydrochloride | American Health Packaging | 18-JUL-11 |
Amiodarone Hydrochloride | Hospira, Inc. | 22-AUG-11 |
Nexterone | Baxter Healthcare Corporation | 09-JAN-12 |
Amiodarone Hydrochloride | McKesson Contract Packaging | 11-JAN-12 |
Amiodarone Hydrochloride | Taro Pharmaceuticals U.S.A., Inc. | 12-JAN-12 |
Amiodarone Hydrochloride | APP Pharmaceuticals, LLC | 25-JAN-12 |
Pacerone | Cardinal Health | 26-JAN-12 |
Amiodarone Hydrochloride | General Injectables & Vaccines, Inc. | 07-MAR-12 |
Amiodarone Hydrochloride | Physicians Total Care, Inc. | 08-MAR-12 |
Amiodarone Hydrochloride | Mylan Institutional Inc. | 09-MAR-12 |
Pacerone | Aphena Pharma Solutions - Tennessee, Inc. | 28-MAR-12 |
Pacerone | Upsher-Smith Laboratories, Inc. | 31-AUG-12 |
Pacerone | Upsher-Smith Laboratories, Inc. | 31-AUG-12 |
Amiodarone Hydrochloride | Mylan Institutional LLC | 31-AUG-12 |
Amiodarone Hydrochloride | Teva Pharmaceuticals USA Inc | 11-SEP-12 |
Amiodarone Hydrochloride | Cardinal Health | 18-SEP-12 |
Amiodarone Hydrochloride | NCS HealthCare of KY, Inc dba Vangard Labs | 17-OCT-12 |
Amiodarone Hcl | Cantrell Drug Company | 24-OCT-12 |
Amiodarone Hydrochloride | Wockhardt Limited | 06-NOV-12 |
Amiodarone Hydrochloride | West-ward Pharmaceutical Corp | 04-DEC-12 |
Amiodarone Hydrochloride | General Injectables & Vaccines, Inc | 19-DEC-12 |
Amiodarone Hcl | Libertas Pharma, Inc. | 24-DEC-12 |
Cordarone | Wyeth Pharmaceuticals Company, a subsidiary of Pfizer Inc. | 15-JAN-13 |
Amiodarone Hydrochloride | Eon Labs, Inc. | 07-FEB-13 |
What Amiodarone safety concerns are being reported by doctors and researchers in the medical literature?
This report contains aggregated drug side effects and adverse events for Amiodarone. The data has been pulled from the United States Food and Drug Administration's (US FDA) Adverse Event Reporting System (AERS), a database containing more than 4,000,000 adverse event reports.
DrugCite expands your query using the Unified Medical Language System (UMLS) to include generic drugs and primary active ingredients. While the core of DrugCite's advanced drug filtering algorithm is based on the industry standard UMLS, DrugCite's proprietary filtering system also includes dozens of additional steps to reconcile malformed drug names in the FDA's data.
DrugCite only counts a drug if the submitter of the adverse event indicates that the drug is suspected to have caused the adverse event.
Depending on how the data is aggregated, different counts may occur. When someone submits an adverse event to the FDA, the submitter can attribute multiple adverse events to one or more drugs. For example, an individual taking Paxil could submit the adverse events "anxiety" and "suicidal ideation" for the same individual safety report (ISR). This means when DrugCite aggregates by adverse event, two distinct adverse events are counted in the adverse event graph; once for "anxiety" and again for "suicidal ideation". However, when DrugCite aggregates by individual safety reports irrespective of the details of the adverse events contained within the safety report, the report is only counted once.
Share your experience with Amiodarone.