Does VERAPAMIL Cause Wrong patient received product? 15 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Wrong patient received product have been filed in association with VERAPAMIL (Verapamil Hydrochloride). This represents 0.2% of all adverse event reports for VERAPAMIL.
15
Reports of Wrong patient received product with VERAPAMIL
0.2%
of all VERAPAMIL reports
11
Deaths
3
Hospitalizations
How Dangerous Is Wrong patient received product From VERAPAMIL?
Of the 15 reports, 11 (73.3%) resulted in death, 3 (20.0%) required hospitalization, and 3 (20.0%) 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 VERAPAMIL. However, 15 reports have been filed with the FAERS database.
What Other Side Effects Does VERAPAMIL Cause?
Completed suicide (1,274)
Toxicity to various agents (1,048)
Drug ineffective (917)
Hypotension (897)
Bradycardia (690)
Off label use (578)
Dyspnoea (563)
Dizziness (548)
Drug interaction (521)
Nausea (506)
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 VERAPAMIL Alternatives Have Lower Wrong patient received product Risk?
VERAPAMIL vs VERICIGUAT
VERAPAMIL vs VERTEPORFIN
VERAPAMIL vs VESICARE
VERAPAMIL vs VFEND
VERAPAMIL vs VIAGRA