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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does DILTIAZEM Cause Condition aggravated? 811 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 811 reports of Condition aggravated have been filed in association with DILTIAZEM (Cardizem CD). This represents 5.5% of all adverse event reports for DILTIAZEM.

811
Reports of Condition aggravated with DILTIAZEM
5.5%
of all DILTIAZEM reports
352
Deaths
633
Hospitalizations

How Dangerous Is Condition aggravated From DILTIAZEM?

Of the 811 reports, 352 (43.4%) resulted in death, 633 (78.1%) required hospitalization, and 342 (42.2%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DILTIAZEM. However, 811 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 Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which DILTIAZEM Alternatives Have Lower Condition aggravated Risk?

DILTIAZEM vs DIMENHYDRINATE DILTIAZEM vs DIMETHICONE DILTIAZEM vs DIMETHICONE\LOPERAMIDE DILTIAZEM vs DIMETHINDENE DILTIAZEM vs DIMETHYL

Related Pages

DILTIAZEM Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated DILTIAZEM Demographics