Does DILTIAZEM Cause Intentional product misuse? 92 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 92 reports of Intentional product misuse have been filed in association with DILTIAZEM (Cardizem CD). This represents 0.6% of all adverse event reports for DILTIAZEM.
92
Reports of Intentional product misuse with DILTIAZEM
0.6%
of all DILTIAZEM reports
60
Deaths
48
Hospitalizations
How Dangerous Is Intentional product misuse From DILTIAZEM?
Of the 92 reports, 60 (65.2%) resulted in death, 48 (52.2%) required hospitalization, and 30 (32.6%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DILTIAZEM. However, 92 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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which DILTIAZEM Alternatives Have Lower Intentional product misuse Risk?
DILTIAZEM vs DIMENHYDRINATE
DILTIAZEM vs DIMETHICONE
DILTIAZEM vs DIMETHICONE\LOPERAMIDE
DILTIAZEM vs DIMETHINDENE
DILTIAZEM vs DIMETHYL