Does DRONEDARONE Cause Product prescribing error? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product prescribing error have been filed in association with DRONEDARONE (Multaq). This represents 0.3% of all adverse event reports for DRONEDARONE.
7
Reports of Product prescribing error with DRONEDARONE
0.3%
of all DRONEDARONE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product prescribing error From DRONEDARONE?
Of the 7 reports.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DRONEDARONE. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does DRONEDARONE Cause?
Atrial fibrillation (309)
Dyspnoea (235)
Fatigue (206)
Off label use (189)
Drug interaction (176)
Nausea (151)
Diarrhoea (141)
Dizziness (136)
Drug ineffective (128)
Asthenia (101)
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 DRONEDARONE Alternatives Have Lower Product prescribing error Risk?
DRONEDARONE vs DROPERIDOL
DRONEDARONE vs DROSPIRENONE
DRONEDARONE vs DROSPIRENONE\ESTETROL
DRONEDARONE vs DROSPIRENONE\ESTRADIOL
DRONEDARONE vs DROSPIRENONE\ETHINYL ESTRADIOL