Does DILTIAZEM Cause Wrong technique in product usage process? 62 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 62 reports of Wrong technique in product usage process have been filed in association with DILTIAZEM (Cardizem CD). This represents 0.4% of all adverse event reports for DILTIAZEM.
62
Reports of Wrong technique in product usage process with DILTIAZEM
0.4%
of all DILTIAZEM reports
1
Deaths
13
Hospitalizations
How Dangerous Is Wrong technique in product usage process From DILTIAZEM?
Of the 62 reports, 1 (1.6%) resulted in death, 13 (21.0%) required hospitalization, and 3 (4.8%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DILTIAZEM. However, 62 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which DILTIAZEM Alternatives Have Lower Wrong technique in product usage process Risk?
DILTIAZEM vs DIMENHYDRINATE
DILTIAZEM vs DIMETHICONE
DILTIAZEM vs DIMETHICONE\LOPERAMIDE
DILTIAZEM vs DIMETHINDENE
DILTIAZEM vs DIMETHYL