Does PROPIOMAZINE Cause Incorrect product administration duration? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Incorrect product administration duration have been filed in association with PROPIOMAZINE. This represents 0.5% of all adverse event reports for PROPIOMAZINE.
9
Reports of Incorrect product administration duration with PROPIOMAZINE
0.5%
of all PROPIOMAZINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Incorrect product administration duration From PROPIOMAZINE?
Of the 9 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 PROPIOMAZINE. However, 9 reports have been filed with the FAERS database.
What Other Side Effects Does PROPIOMAZINE Cause?
Intentional overdose (1,568)
Intentional self-injury (1,470)
Fatigue (368)
Depressed level of consciousness (306)
Tachycardia (243)
Toxicity to various agents (207)
Somnolence (139)
Suicide attempt (108)
Loss of consciousness (94)
Dysarthria (73)
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 PROPIOMAZINE Alternatives Have Lower Incorrect product administration duration Risk?
PROPIOMAZINE vs PROPOFOL
PROPIOMAZINE vs PROPOXYPHENE
PROPIOMAZINE vs PROPOXYPHENE/ACETAMINOPHEN
PROPIOMAZINE vs PROPRANOLOL
PROPIOMAZINE vs PROPRANOLOL\PROPRANOLOL