Does DILTIAZEM Cause Poor quality product administered? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Poor quality product administered have been filed in association with DILTIAZEM (Cardizem CD). This represents 0.1% of all adverse event reports for DILTIAZEM.
9
Reports of Poor quality product administered with DILTIAZEM
0.1%
of all DILTIAZEM reports
5
Deaths
0
Hospitalizations
How Dangerous Is Poor quality product administered From DILTIAZEM?
Of the 9 reports, 5 (55.6%) resulted in death, and 5 (55.6%) were considered life-threatening.
Is Poor quality product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DILTIAZEM. However, 9 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 Poor quality product administered?
ONABOTULINUMTOXINA (495)
ICOSAPENT ETHYL (452)
MINOXIDIL (428)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (376)
ADALIMUMAB (239)
TESTOSTERONE CYPIONATE (235)
SOMATROPIN (234)
POLYETHYLENE GLYCOL 3350 (223)
IBUPROFEN (222)
INSULIN GLARGINE (133)
Which DILTIAZEM Alternatives Have Lower Poor quality product administered Risk?
DILTIAZEM vs DIMENHYDRINATE
DILTIAZEM vs DIMETHICONE
DILTIAZEM vs DIMETHICONE\LOPERAMIDE
DILTIAZEM vs DIMETHINDENE
DILTIAZEM vs DIMETHYL