Does CELECOXIB Cause Intentional product use issue? 1,395 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,395 reports of Intentional product use issue have been filed in association with CELECOXIB (Celecoxib). This represents 4.4% of all adverse event reports for CELECOXIB.
1,395
Reports of Intentional product use issue with CELECOXIB
4.4%
of all CELECOXIB reports
839
Deaths
934
Hospitalizations
How Dangerous Is Intentional product use issue From CELECOXIB?
Of the 1,395 reports, 839 (60.1%) resulted in death, 934 (67.0%) required hospitalization, and 917 (65.7%) 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 CELECOXIB. However, 1,395 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 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 CELECOXIB Alternatives Have Lower Intentional product use issue Risk?
CELECOXIB vs CELIPROLOL
CELECOXIB vs CELLCEPT
CELECOXIB vs CEMIPLIMAB
CELECOXIB vs CEMIPLIMAB-RWLC
CELECOXIB vs CENEGERMIN-BKBJ