Does CLOMIPRAMINE Cause Wrong patient received product? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Wrong patient received product have been filed in association with CLOMIPRAMINE (Clomipramine Hydrochloride). This represents 0.2% of all adverse event reports for CLOMIPRAMINE.
6
Reports of Wrong patient received product with CLOMIPRAMINE
0.2%
of all CLOMIPRAMINE reports
4
Deaths
2
Hospitalizations
How Dangerous Is Wrong patient received product From CLOMIPRAMINE?
Of the 6 reports, 4 (66.7%) resulted in death, 2 (33.3%) required hospitalization.
Is Wrong patient received product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CLOMIPRAMINE. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does CLOMIPRAMINE Cause?
Drug ineffective (561)
Toxicity to various agents (427)
Suicide attempt (375)
Off label use (271)
Coma (262)
Intentional overdose (237)
Weight increased (214)
Akathisia (204)
Obsessive-compulsive disorder (187)
Therapeutic product effect incomplete (184)
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 CLOMIPRAMINE Alternatives Have Lower Wrong patient received product Risk?
CLOMIPRAMINE vs CLONAZEPAM
CLOMIPRAMINE vs CLONIDINE
CLOMIPRAMINE vs CLOPIDOGREL
CLOMIPRAMINE vs CLOPIDOGREL BESILATE
CLOMIPRAMINE vs CLOPIDOGREL BISULFATE