Does CELECOXIB Cause Product dose omission in error? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Product dose omission in error have been filed in association with CELECOXIB (Celecoxib). This represents 0.0% of all adverse event reports for CELECOXIB.
12
Reports of Product dose omission in error with CELECOXIB
0.0%
of all CELECOXIB reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product dose omission in error From CELECOXIB?
Of the 12 reports.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CELECOXIB. However, 12 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 dose omission in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
Which CELECOXIB Alternatives Have Lower Product dose omission in error Risk?
CELECOXIB vs CELIPROLOL
CELECOXIB vs CELLCEPT
CELECOXIB vs CEMIPLIMAB
CELECOXIB vs CEMIPLIMAB-RWLC
CELECOXIB vs CENEGERMIN-BKBJ