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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does CELECOXIB Cause Intentional dose omission? 36 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 36 reports of Intentional dose omission have been filed in association with CELECOXIB (Celecoxib). This represents 0.1% of all adverse event reports for CELECOXIB.

36
Reports of Intentional dose omission with CELECOXIB
0.1%
of all CELECOXIB reports
0
Deaths
5
Hospitalizations

How Dangerous Is Intentional dose omission From CELECOXIB?

Of the 36 reports, 5 (13.9%) required hospitalization.

Is Intentional dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CELECOXIB. However, 36 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 dose omission?

DUPILUMAB (2,269) CERTOLIZUMAB PEGOL (1,253) ADALIMUMAB (845) TOFACITINIB (845) INFLIXIMAB (815) ABALOPARATIDE (623) ETANERCEPT (615) AMBRISENTAN (595) SODIUM OXYBATE (580) CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)

Which CELECOXIB Alternatives Have Lower Intentional dose omission Risk?

CELECOXIB vs CELIPROLOL CELECOXIB vs CELLCEPT CELECOXIB vs CEMIPLIMAB CELECOXIB vs CEMIPLIMAB-RWLC CELECOXIB vs CENEGERMIN-BKBJ

Related Pages

CELECOXIB Full Profile All Intentional dose omission Reports All Drugs Causing Intentional dose omission CELECOXIB Demographics