Does CELECOXIB Cause Maternal exposure timing unspecified? 160 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 160 reports of Maternal exposure timing unspecified have been filed in association with CELECOXIB (Celecoxib). This represents 0.5% of all adverse event reports for CELECOXIB.
160
Reports of Maternal exposure timing unspecified with CELECOXIB
0.5%
of all CELECOXIB reports
152
Deaths
156
Hospitalizations
How Dangerous Is Maternal exposure timing unspecified From CELECOXIB?
Of the 160 reports, 152 (95.0%) resulted in death, 156 (97.5%) required hospitalization, and 159 (99.4%) 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 CELECOXIB. However, 160 reports have been filed with the FAERS database.
What Other Side Effects Does CELECOXIB Cause?
Drug ineffective (8,188)
Drug hypersensitivity (5,314)
Pain (4,248)
Rheumatoid arthritis (3,789)
Off label use (3,782)
Arthralgia (3,766)
Nausea (3,497)
Fatigue (3,235)
Condition aggravated (3,060)
Diarrhoea (3,017)
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 CELECOXIB Alternatives Have Lower Maternal exposure timing unspecified Risk?
CELECOXIB vs CELIPROLOL
CELECOXIB vs CELLCEPT
CELECOXIB vs CEMIPLIMAB
CELECOXIB vs CEMIPLIMAB-RWLC
CELECOXIB vs CENEGERMIN-BKBJ