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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 Product administration interrupted? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Product administration interrupted have been filed in association with CELECOXIB (Celecoxib). This represents 0.0% of all adverse event reports for CELECOXIB.

8
Reports of Product administration interrupted with CELECOXIB
0.0%
of all CELECOXIB reports
0
Deaths
2
Hospitalizations

How Dangerous Is Product administration interrupted From CELECOXIB?

Of the 8 reports, 2 (25.0%) required hospitalization.

Is Product administration interrupted Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CELECOXIB. However, 8 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 administration interrupted?

CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (1,446) SODIUM OXYBATE (1,272) CANNABIDIOL (511) ISOTRETINOIN (503) APREMILAST (314) TREPROSTINIL (295) EPOPROSTENOL (205) LENALIDOMIDE (146) ETANERCEPT (142) INTERFERON BETA-1A (115)

Which CELECOXIB Alternatives Have Lower Product administration interrupted Risk?

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

Related Pages

CELECOXIB Full Profile All Product administration interrupted Reports All Drugs Causing Product administration interrupted CELECOXIB Demographics