Does DILTIAZEM Cause Intentional product use issue? 207 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 207 reports of Intentional product use issue have been filed in association with DILTIAZEM (Cardizem CD). This represents 1.4% of all adverse event reports for DILTIAZEM.
207
Reports of Intentional product use issue with DILTIAZEM
1.4%
of all DILTIAZEM reports
150
Deaths
185
Hospitalizations
How Dangerous Is Intentional product use issue From DILTIAZEM?
Of the 207 reports, 150 (72.5%) resulted in death, 185 (89.4%) required hospitalization, and 163 (78.7%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DILTIAZEM. However, 207 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 use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which DILTIAZEM Alternatives Have Lower Intentional product use issue Risk?
DILTIAZEM vs DIMENHYDRINATE
DILTIAZEM vs DIMETHICONE
DILTIAZEM vs DIMETHICONE\LOPERAMIDE
DILTIAZEM vs DIMETHINDENE
DILTIAZEM vs DIMETHYL