Does CELECOXIB Cause Product prescribing error? 166 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 166 reports of Product prescribing error have been filed in association with CELECOXIB (Celecoxib). This represents 0.5% of all adverse event reports for CELECOXIB.
166
Reports of Product prescribing error with CELECOXIB
0.5%
of all CELECOXIB reports
6
Deaths
129
Hospitalizations
How Dangerous Is Product prescribing error From CELECOXIB?
Of the 166 reports, 6 (3.6%) resulted in death, 129 (77.7%) required hospitalization, and 1 (0.6%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CELECOXIB. However, 166 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 Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which CELECOXIB Alternatives Have Lower Product prescribing error Risk?
CELECOXIB vs CELIPROLOL
CELECOXIB vs CELLCEPT
CELECOXIB vs CEMIPLIMAB
CELECOXIB vs CEMIPLIMAB-RWLC
CELECOXIB vs CENEGERMIN-BKBJ