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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 Wrong patient received product? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Wrong patient received product have been filed in association with MELATONIN (Melatonin 1527). This represents 0.2% of all adverse event reports for MELATONIN.

7
Reports of Wrong patient received product with MELATONIN
0.2%
of all MELATONIN reports
1
Deaths
2
Hospitalizations

How Dangerous Is Wrong patient received product From MELATONIN?

Of the 7 reports, 1 (14.3%) resulted in death, 2 (28.6%) required hospitalization.

Is Wrong patient received product Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for MELATONIN. However, 7 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 Wrong patient received product?

INSULIN LISPRO (334) CLOZAPINE (198) RISPERIDONE (176) OXAZEPAM (152) BISOPROLOL (150) LEVETIRACETAM (126) ACETAMINOPHEN (123) METFORMIN (116) INSULIN GLARGINE (114) CLONAZEPAM (112)

Which MELATONIN Alternatives Have Lower Wrong patient received product 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 Wrong patient received product Reports All Drugs Causing Wrong patient received product MELATONIN Demographics