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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 MELATONIN Cause Product prescribing error? 110 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 110 reports of Product prescribing error have been filed in association with MELATONIN (Melatonin 1527). This represents 2.7% of all adverse event reports for MELATONIN.

110
Reports of Product prescribing error with MELATONIN
2.7%
of all MELATONIN reports
5
Deaths
95
Hospitalizations

How Dangerous Is Product prescribing error From MELATONIN?

Of the 110 reports, 5 (4.5%) resulted in death, 95 (86.4%) required hospitalization, and 1 (0.9%) were considered life-threatening.

Is Product prescribing error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for MELATONIN. However, 110 reports have been filed with the FAERS database.

What Other Side Effects Does MELATONIN Cause?

Somnolence (642) Intentional overdose (640) Off label use (555) Intentional self-injury (463) Drug ineffective (458) Gastrooesophageal reflux disease (399) Nausea (377) Vomiting (341) Coma (336) Constipation (313)

What Other Drugs Cause Product prescribing error?

SOMATROPIN (1,123) SACUBITRIL\VALSARTAN (1,023) SECUKINUMAB (821) TOFACITINIB (805) DUPILUMAB (725) NIRMATRELVIR\RITONAVIR (611) PREGABALIN (476) METHOTREXATE (434) TORSEMIDE (352) METOPROLOL (325)

Which MELATONIN Alternatives Have Lower Product prescribing error Risk?

MELATONIN vs MELOXICAM MELATONIN vs MELPERONE MELATONIN vs MELPHALAN MELATONIN vs MEMANTINE MELATONIN vs MENINGOCOCCAL GROUP B VACCINE

Related Pages

MELATONIN Full Profile All Product prescribing error Reports All Drugs Causing Product prescribing error MELATONIN Demographics