Does DRONEDARONE Cause Product prescribing issue? 8 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), 8 reports of Product prescribing issue have been filed in association with DRONEDARONE (Multaq). This represents 0.3% of all adverse event reports for DRONEDARONE.
8
Reports of Product prescribing issue with DRONEDARONE
0.3%
of all DRONEDARONE reports
1
Deaths
2
Hospitalizations
How Dangerous Is Product prescribing issue From DRONEDARONE?
Of the 8 reports, 1 (12.5%) resulted in death, 2 (25.0%) required hospitalization.
Is Product prescribing issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DRONEDARONE. However, 8 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 issue?
DUPILUMAB (1,715)
POLYETHYLENE GLYCOL 3350 (1,439)
LENALIDOMIDE (948)
OXYCODONE (646)
RIVAROXABAN (359)
ACETAMINOPHEN\OXYCODONE (347)
ETONOGESTREL (311)
ACETAMINOPHEN\HYDROCODONE (298)
CERTOLIZUMAB PEGOL (297)
CABOZANTINIB S-MALATE (294)
Which DRONEDARONE Alternatives Have Lower Product prescribing issue Risk?
DRONEDARONE vs DROPERIDOL
DRONEDARONE vs DROSPIRENONE
DRONEDARONE vs DROSPIRENONE\ESTETROL
DRONEDARONE vs DROSPIRENONE\ESTRADIOL
DRONEDARONE vs DROSPIRENONE\ETHINYL ESTRADIOL