Does AGOMELATINE Cause Intentional product use issue? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Intentional product use issue have been filed in association with AGOMELATINE. This represents 0.6% of all adverse event reports for AGOMELATINE.
5
Reports of Intentional product use issue with AGOMELATINE
0.6%
of all AGOMELATINE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Intentional product use issue From AGOMELATINE?
Of the 5 reports, 2 (40.0%) required hospitalization, and 1 (20.0%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AGOMELATINE. However, 5 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which AGOMELATINE Alternatives Have Lower Intentional product use issue Risk?
AGOMELATINE vs ALAWAY
AGOMELATINE vs ALBENDAZOLE
AGOMELATINE vs ALBIGLUTIDE
AGOMELATINE vs ALBUMIN
AGOMELATINE vs ALBUMIN HUMAN