Does DILTIAZEM Cause Recalled product? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Recalled product have been filed in association with DILTIAZEM (Cardizem CD). This represents 0.0% of all adverse event reports for DILTIAZEM.
6
Reports of Recalled product with DILTIAZEM
0.0%
of all DILTIAZEM reports
0
Deaths
0
Hospitalizations
How Dangerous Is Recalled product From DILTIAZEM?
Of the 6 reports.
Is Recalled product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DILTIAZEM. However, 6 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 Recalled product?
PARATHYROID HORMONE (900)
ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT (80)
CALCITRIOL (68)
CALCIUM (66)
REMDESIVIR (36)
LEVOTHYROXINE\LIOTHYRONINE (34)
TESTOSTERONE (32)
VALSARTAN (32)
CHLORHEXIDINE (28)
ALCOHOL (26)
Which DILTIAZEM Alternatives Have Lower Recalled product Risk?
DILTIAZEM vs DIMENHYDRINATE
DILTIAZEM vs DIMETHICONE
DILTIAZEM vs DIMETHICONE\LOPERAMIDE
DILTIAZEM vs DIMETHINDENE
DILTIAZEM vs DIMETHYL