Does DILTIAZEM Cause Wrong product administered? 21 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Wrong product administered have been filed in association with DILTIAZEM (Cardizem CD). This represents 0.1% of all adverse event reports for DILTIAZEM.
21
Reports of Wrong product administered with DILTIAZEM
0.1%
of all DILTIAZEM reports
0
Deaths
1
Hospitalizations
How Dangerous Is Wrong product administered From DILTIAZEM?
Of the 21 reports, 1 (4.8%) required hospitalization.
Is Wrong product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DILTIAZEM. However, 21 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 product administered?
INSULIN LISPRO (337)
INSULIN GLARGINE (226)
RISPERIDONE (141)
QUETIAPINE (137)
ACETAMINOPHEN (133)
INSULIN ASPART (112)
CLOZAPINE (106)
INSULIN HUMAN (104)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104)
IBUPROFEN (102)
Which DILTIAZEM Alternatives Have Lower Wrong product administered Risk?
DILTIAZEM vs DIMENHYDRINATE
DILTIAZEM vs DIMETHICONE
DILTIAZEM vs DIMETHICONE\LOPERAMIDE
DILTIAZEM vs DIMETHINDENE
DILTIAZEM vs DIMETHYL