Does DRONEDARONE Cause Product dose omission? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Product dose omission have been filed in association with DRONEDARONE (Multaq). This represents 0.4% of all adverse event reports for DRONEDARONE.
11
Reports of Product dose omission with DRONEDARONE
0.4%
of all DRONEDARONE reports
0
Deaths
5
Hospitalizations
How Dangerous Is Product dose omission From DRONEDARONE?
Of the 11 reports, 5 (45.5%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DRONEDARONE. However, 11 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 dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which DRONEDARONE Alternatives Have Lower Product dose omission Risk?
DRONEDARONE vs DROPERIDOL
DRONEDARONE vs DROSPIRENONE
DRONEDARONE vs DROSPIRENONE\ESTETROL
DRONEDARONE vs DROSPIRENONE\ESTRADIOL
DRONEDARONE vs DROSPIRENONE\ETHINYL ESTRADIOL