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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 Adulterated product? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Adulterated product have been filed in association with DILTIAZEM (Cardizem CD). This represents 0.0% of all adverse event reports for DILTIAZEM.

5
Reports of Adulterated product with DILTIAZEM
0.0%
of all DILTIAZEM reports
5
Deaths
0
Hospitalizations

How Dangerous Is Adulterated product From DILTIAZEM?

Of the 5 reports, 5 (100.0%) resulted in death.

Is Adulterated product Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DILTIAZEM. However, 5 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 Adulterated product?

LISDEXAMFETAMINE DIMESYLATE (31) THEOBROMINE (29) ACETAMINOPHEN (28) LIDOCAINE (28) COCAINE (27) CAFFEINE (24) CODEINE (23) THEOPHYLLINE (23) FENTANYL (22) MORPHINE (22)

Which DILTIAZEM Alternatives Have Lower Adulterated product Risk?

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

Related Pages

DILTIAZEM Full Profile All Adulterated product Reports All Drugs Causing Adulterated product DILTIAZEM Demographics