Does CELECOXIB Cause Product quality issue? 538 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 538 reports of Product quality issue have been filed in association with CELECOXIB (Celecoxib). This represents 1.7% of all adverse event reports for CELECOXIB.
538
Reports of Product quality issue with CELECOXIB
1.7%
of all CELECOXIB reports
434
Deaths
366
Hospitalizations
How Dangerous Is Product quality issue From CELECOXIB?
Of the 538 reports, 434 (80.7%) resulted in death, 366 (68.0%) required hospitalization, and 390 (72.5%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CELECOXIB. However, 538 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 quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which CELECOXIB Alternatives Have Lower Product quality issue Risk?
CELECOXIB vs CELIPROLOL
CELECOXIB vs CELLCEPT
CELECOXIB vs CEMIPLIMAB
CELECOXIB vs CEMIPLIMAB-RWLC
CELECOXIB vs CENEGERMIN-BKBJ