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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does DRONEDARONE Cause Condition aggravated? 47 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 47 reports of Condition aggravated have been filed in association with DRONEDARONE (Multaq). This represents 1.7% of all adverse event reports for DRONEDARONE.

47
Reports of Condition aggravated with DRONEDARONE
1.7%
of all DRONEDARONE reports
2
Deaths
12
Hospitalizations

How Dangerous Is Condition aggravated From DRONEDARONE?

Of the 47 reports, 2 (4.3%) resulted in death, 12 (25.5%) required hospitalization.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DRONEDARONE. However, 47 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 Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which DRONEDARONE Alternatives Have Lower Condition aggravated Risk?

DRONEDARONE vs DROPERIDOL DRONEDARONE vs DROSPIRENONE DRONEDARONE vs DROSPIRENONE\ESTETROL DRONEDARONE vs DROSPIRENONE\ESTRADIOL DRONEDARONE vs DROSPIRENONE\ETHINYL ESTRADIOL

Related Pages

DRONEDARONE Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated DRONEDARONE Demographics