Does DILTIAZEM Cause Maternal exposure timing unspecified? 51 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 51 reports of Maternal exposure timing unspecified have been filed in association with DILTIAZEM (Cardizem CD). This represents 0.4% of all adverse event reports for DILTIAZEM.
51
Reports of Maternal exposure timing unspecified with DILTIAZEM
0.4%
of all DILTIAZEM reports
49
Deaths
51
Hospitalizations
How Dangerous Is Maternal exposure timing unspecified From DILTIAZEM?
Of the 51 reports, 49 (96.1%) resulted in death, 51 (100.0%) required hospitalization, and 51 (100.0%) were considered life-threatening.
Is Maternal exposure timing unspecified Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DILTIAZEM. However, 51 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 Maternal exposure timing unspecified?
RITUXIMAB (402)
METHOTREXATE (350)
ADALIMUMAB (343)
DICLOFENAC (331)
TOCILIZUMAB (327)
HYDROXYCHLOROQUINE (309)
FOLIC ACID (304)
INFLIXIMAB (303)
LEFLUNOMIDE (302)
SECUKINUMAB (301)
Which DILTIAZEM Alternatives Have Lower Maternal exposure timing unspecified Risk?
DILTIAZEM vs DIMENHYDRINATE
DILTIAZEM vs DIMETHICONE
DILTIAZEM vs DIMETHICONE\LOPERAMIDE
DILTIAZEM vs DIMETHINDENE
DILTIAZEM vs DIMETHYL