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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 RAMELTEON 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 RAMELTEON (Ramelteon). This represents 0.8% of all adverse event reports for RAMELTEON.

7
Reports of Adverse event with RAMELTEON
0.8%
of all RAMELTEON reports
0
Deaths
3
Hospitalizations

How Dangerous Is Adverse event From RAMELTEON?

Of the 7 reports, 3 (42.9%) required hospitalization, and 1 (14.3%) were considered life-threatening.

Is Adverse event Listed in the Official Label?

Yes, Adverse event is listed as a known adverse reaction in the official FDA drug label for RAMELTEON.

What Other Side Effects Does RAMELTEON Cause?

Drug ineffective (160) Somnolence (61) Off label use (58) Intentional overdose (45) No adverse event (41) Toxicity to various agents (41) Dizziness (38) Insomnia (30) Wrong technique in product usage process (30) Overdose (28)

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 RAMELTEON Alternatives Have Lower Adverse event Risk?

RAMELTEON vs RAMIPRIL RAMELTEON vs RAMUCIRUMAB RAMELTEON vs RANEXA RAMELTEON vs RANIBIZUMAB RAMELTEON vs RANIMUSTINE

Related Pages

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