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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 Product use issue? 19 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 19 reports of Product use issue have been filed in association with AGOMELATINE. This represents 2.1% of all adverse event reports for AGOMELATINE.

19
Reports of Product use issue with AGOMELATINE
2.1%
of all AGOMELATINE reports
13
Deaths
10
Hospitalizations

How Dangerous Is Product use issue From AGOMELATINE?

Of the 19 reports, 13 (68.4%) resulted in death, 10 (52.6%) required hospitalization.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for AGOMELATINE. However, 19 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 Product use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Which AGOMELATINE Alternatives Have Lower Product use issue Risk?

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

Related Pages

AGOMELATINE Full Profile All Product use issue Reports All Drugs Causing Product use issue AGOMELATINE Demographics