Does METOCLOPRAMIDE Cause Incorrect product administration duration? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Incorrect product administration duration have been filed in association with METOCLOPRAMIDE (metoclopramide hydrochloride). This represents 0.2% of all adverse event reports for METOCLOPRAMIDE.
16
Reports of Incorrect product administration duration with METOCLOPRAMIDE
0.2%
of all METOCLOPRAMIDE reports
0
Deaths
12
Hospitalizations
How Dangerous Is Incorrect product administration duration From METOCLOPRAMIDE?
Of the 16 reports, 12 (75.0%) required hospitalization, and 1 (6.3%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for METOCLOPRAMIDE. However, 16 reports have been filed with the FAERS database.
What Other Side Effects Does METOCLOPRAMIDE Cause?
Nausea (1,080)
Drug ineffective (927)
Off label use (926)
Drug hypersensitivity (751)
Vomiting (672)
Dyspnoea (525)
Headache (499)
Diarrhoea (481)
Hypersensitivity (473)
Tardive dyskinesia (465)
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 METOCLOPRAMIDE Alternatives Have Lower Incorrect product administration duration Risk?
METOCLOPRAMIDE vs METOLAZONE
METOCLOPRAMIDE vs METOPIMAZINE
METOCLOPRAMIDE vs METOPROLOL
METOCLOPRAMIDE vs METRELEPTIN
METOCLOPRAMIDE vs METRONIDAZOLE