Does MELATONIN Cause Incorrect product administration duration? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Incorrect product administration duration have been filed in association with MELATONIN (Melatonin 1527). This represents 0.3% of all adverse event reports for MELATONIN.
12
Reports of Incorrect product administration duration with MELATONIN
0.3%
of all MELATONIN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Incorrect product administration duration From MELATONIN?
Of the 12 reports.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MELATONIN. However, 12 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which MELATONIN Alternatives Have Lower Incorrect product administration duration Risk?
MELATONIN vs MELOXICAM
MELATONIN vs MELPERONE
MELATONIN vs MELPHALAN
MELATONIN vs MEMANTINE
MELATONIN vs MENINGOCOCCAL GROUP B VACCINE