Does AMIODARONE Cause Wrong product administered? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Wrong product administered have been filed in association with AMIODARONE (Amiodarone Hydrochloride). This represents 0.1% of all adverse event reports for AMIODARONE.
13
Reports of Wrong product administered with AMIODARONE
0.1%
of all AMIODARONE reports
3
Deaths
2
Hospitalizations
How Dangerous Is Wrong product administered From AMIODARONE?
Of the 13 reports, 3 (23.1%) resulted in death, 2 (15.4%) required hospitalization, and 1 (7.7%) were considered life-threatening.
Is Wrong product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AMIODARONE. However, 13 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 Wrong product administered?
INSULIN LISPRO (337)
INSULIN GLARGINE (226)
RISPERIDONE (141)
QUETIAPINE (137)
ACETAMINOPHEN (133)
INSULIN ASPART (112)
CLOZAPINE (106)
INSULIN HUMAN (104)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104)
IBUPROFEN (102)
Which AMIODARONE Alternatives Have Lower Wrong product administered Risk?
AMIODARONE vs AMISULPRIDE
AMIODARONE vs AMITRIPTYLINE
AMIODARONE vs AMITRIPTYLINE\PERPHENAZINE
AMIODARONE vs AMIVANTAMAB
AMIODARONE vs AMIVANTAMAB-VMJW