Does AMIODARONE Cause Product prescribing error? 81 Reports in FDA Database
Lower Your Cholesterol — The Natural Way
The Oxidized Cholesterol Strategy: a science-backed plan for heart health.
According to the FDA Adverse Event Reporting System (FAERS), 81 reports of Product prescribing error have been filed in association with AMIODARONE (Amiodarone Hydrochloride). This represents 0.3% of all adverse event reports for AMIODARONE.
81
Reports of Product prescribing error with AMIODARONE
0.3%
of all AMIODARONE reports
14
Deaths
43
Hospitalizations
How Dangerous Is Product prescribing error From AMIODARONE?
Of the 81 reports, 14 (17.3%) resulted in death, 43 (53.1%) required hospitalization, and 39 (48.1%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AMIODARONE. However, 81 reports have been filed with the FAERS database.
What Other Side Effects Does AMIODARONE Cause?
Drug ineffective (2,223)
Dyspnoea (2,182)
Off label use (1,608)
Drug interaction (1,589)
Asthenia (1,452)
Interstitial lung disease (1,421)
Hyperthyroidism (1,410)
Fatigue (1,269)
Bradycardia (1,261)
Atrial fibrillation (1,211)
What Other Drugs Cause Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which AMIODARONE Alternatives Have Lower Product prescribing error Risk?
AMIODARONE vs AMISULPRIDE
AMIODARONE vs AMITRIPTYLINE
AMIODARONE vs AMITRIPTYLINE\PERPHENAZINE
AMIODARONE vs AMIVANTAMAB
AMIODARONE vs AMIVANTAMAB-VMJW