Does DILTIAZEM Cause Wrong patient received product? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Wrong patient received product have been filed in association with DILTIAZEM (Cardizem CD). This represents 0.1% of all adverse event reports for DILTIAZEM.
13
Reports of Wrong patient received product with DILTIAZEM
0.1%
of all DILTIAZEM reports
9
Deaths
0
Hospitalizations
How Dangerous Is Wrong patient received product From DILTIAZEM?
Of the 13 reports, 9 (69.2%) resulted in death.
Is Wrong patient received product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DILTIAZEM. However, 13 reports have been filed with the FAERS database.
What Other Side Effects Does DILTIAZEM Cause?
Completed suicide (1,696)
Toxicity to various agents (1,663)
Hypotension (1,550)
Dyspnoea (1,436)
Drug ineffective (1,315)
Fall (1,262)
Pain (1,169)
Dizziness (1,091)
Fatigue (1,054)
Headache (874)
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 DILTIAZEM Alternatives Have Lower Wrong patient received product Risk?
DILTIAZEM vs DIMENHYDRINATE
DILTIAZEM vs DIMETHICONE
DILTIAZEM vs DIMETHICONE\LOPERAMIDE
DILTIAZEM vs DIMETHINDENE
DILTIAZEM vs DIMETHYL