Does METRONIDAZOLE Cause Incorrect product administration duration? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Incorrect product administration duration have been filed in association with METRONIDAZOLE (metronidazole). This represents 0.1% of all adverse event reports for METRONIDAZOLE.
14
Reports of Incorrect product administration duration with METRONIDAZOLE
0.1%
of all METRONIDAZOLE reports
0
Deaths
6
Hospitalizations
How Dangerous Is Incorrect product administration duration From METRONIDAZOLE?
Of the 14 reports, 6 (42.9%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for METRONIDAZOLE. However, 14 reports have been filed with the FAERS database.
What Other Side Effects Does METRONIDAZOLE Cause?
Drug ineffective (3,336)
Nausea (1,944)
Off label use (1,507)
Headache (1,167)
Vomiting (1,160)
Abdominal pain (1,076)
Pyrexia (1,048)
Diarrhoea (1,041)
Drug hypersensitivity (994)
Dizziness (900)
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 METRONIDAZOLE Alternatives Have Lower Incorrect product administration duration Risk?
METRONIDAZOLE vs METRONIDAZOLE\METRONIDAZOLE
METRONIDAZOLE vs METYRAPONE
METRONIDAZOLE vs MEXILETINE
METRONIDAZOLE vs MIANSERIN
METRONIDAZOLE vs MICAFUNGIN