Does CELECOXIB Cause Incorrect product administration duration? 67 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 67 reports of Incorrect product administration duration have been filed in association with CELECOXIB (Celecoxib). This represents 0.2% of all adverse event reports for CELECOXIB.
67
Reports of Incorrect product administration duration with CELECOXIB
0.2%
of all CELECOXIB reports
62
Deaths
61
Hospitalizations
How Dangerous Is Incorrect product administration duration From CELECOXIB?
Of the 67 reports, 62 (92.5%) resulted in death, 61 (91.0%) required hospitalization, and 61 (91.0%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CELECOXIB. However, 67 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which CELECOXIB Alternatives Have Lower Incorrect product administration duration Risk?
CELECOXIB vs CELIPROLOL
CELECOXIB vs CELLCEPT
CELECOXIB vs CEMIPLIMAB
CELECOXIB vs CEMIPLIMAB-RWLC
CELECOXIB vs CENEGERMIN-BKBJ