Does PROMETHAZINE Cause Wrong patient received product? 34 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 34 reports of Wrong patient received product have been filed in association with PROMETHAZINE (Promethazine Hydrochloride). This represents 0.4% of all adverse event reports for PROMETHAZINE.
34
Reports of Wrong patient received product with PROMETHAZINE
0.4%
of all PROMETHAZINE reports
0
Deaths
16
Hospitalizations
How Dangerous Is Wrong patient received product From PROMETHAZINE?
Of the 34 reports, 16 (47.1%) required hospitalization, and 6 (17.6%) were considered life-threatening.
Is Wrong patient received product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PROMETHAZINE. However, 34 reports have been filed with the FAERS database.
What Other Side Effects Does PROMETHAZINE Cause?
Intentional overdose (3,193)
Intentional self-injury (2,869)
Toxicity to various agents (742)
Tachycardia (653)
Drug hypersensitivity (627)
Fatigue (617)
Depressed level of consciousness (522)
Somnolence (510)
Drug abuse (359)
Akathisia (343)
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 PROMETHAZINE Alternatives Have Lower Wrong patient received product Risk?
PROMETHAZINE vs PROMETHAZINE\PROMETHAZINE
PROMETHAZINE vs PROMETHAZINE\THIOUREA
PROMETHAZINE vs PROPAFENONE
PROMETHAZINE vs PROPARACAINE
PROMETHAZINE vs PROPECIA