Does NIFEDIPINE Cause Intentional product use issue? 21 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Intentional product use issue have been filed in association with NIFEDIPINE (Nifedipine). This represents 0.3% of all adverse event reports for NIFEDIPINE.
21
Reports of Intentional product use issue with NIFEDIPINE
0.3%
of all NIFEDIPINE reports
2
Deaths
7
Hospitalizations
How Dangerous Is Intentional product use issue From NIFEDIPINE?
Of the 21 reports, 2 (9.5%) resulted in death, 7 (33.3%) required hospitalization, and 1 (4.8%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NIFEDIPINE. However, 21 reports have been filed with the FAERS database.
What Other Side Effects Does NIFEDIPINE Cause?
Foetal exposure during pregnancy (927)
Drug ineffective (883)
Premature baby (791)
Maternal exposure during pregnancy (704)
Premature delivery (555)
Exposure during pregnancy (524)
Hypotension (505)
Off label use (474)
Drug hypersensitivity (459)
Completed suicide (431)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which NIFEDIPINE Alternatives Have Lower Intentional product use issue Risk?
NIFEDIPINE vs NILOTINIB
NIFEDIPINE vs NIMESULIDE
NIFEDIPINE vs NIMODIPINE
NIFEDIPINE vs NINTEDANIB
NIFEDIPINE vs NINTEDANIB ESYLATE