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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 AGOMELATINE Cause Adverse event? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Adverse event have been filed in association with AGOMELATINE. This represents 0.8% of all adverse event reports for AGOMELATINE.

7
Reports of Adverse event with AGOMELATINE
0.8%
of all AGOMELATINE reports
1
Deaths
6
Hospitalizations

How Dangerous Is Adverse event From AGOMELATINE?

Of the 7 reports, 1 (14.3%) resulted in death, 6 (85.7%) required hospitalization.

Is Adverse event Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for AGOMELATINE. However, 7 reports have been filed with the FAERS database.

What Other Side Effects Does AGOMELATINE Cause?

Fall (229) Insomnia (215) Coma (207) Tachycardia (206) Arthralgia (204) Diarrhoea (204) Dizziness (204) Fatigue (204) Pruritus (203) Dyspnoea (202)

What Other Drugs Cause Adverse event?

ABATACEPT (4,028) APIXABAN (3,871) ETANERCEPT (3,096) LENALIDOMIDE (2,426) INFLIXIMAB (2,269) ADALIMUMAB (2,121) METHOTREXATE (1,846) LEFLUNOMIDE (1,476) RIVAROXABAN (1,465) ALENDRONATE (1,462)

Which AGOMELATINE Alternatives Have Lower Adverse event Risk?

AGOMELATINE vs ALAWAY AGOMELATINE vs ALBENDAZOLE AGOMELATINE vs ALBIGLUTIDE AGOMELATINE vs ALBUMIN AGOMELATINE vs ALBUMIN HUMAN

Related Pages

AGOMELATINE Full Profile All Adverse event Reports All Drugs Causing Adverse event AGOMELATINE Demographics