Does CELECOXIB Cause Product substitution issue? 396 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 396 reports of Product substitution issue have been filed in association with CELECOXIB (Celecoxib). This represents 1.3% of all adverse event reports for CELECOXIB.
396
Reports of Product substitution issue with CELECOXIB
1.3%
of all CELECOXIB reports
2
Deaths
6
Hospitalizations
How Dangerous Is Product substitution issue From CELECOXIB?
Of the 396 reports, 2 (0.5%) resulted in death, 6 (1.5%) required hospitalization, and 4 (1.0%) were considered life-threatening.
Is Product substitution issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CELECOXIB. However, 396 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 substitution issue?
AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE (2,832)
BUPROPION (1,578)
METHYLPHENIDATE (1,408)
CLONAZEPAM (1,288)
LAMOTRIGINE (979)
ALBUTEROL (864)
LEVOTHYROXINE (803)
DULOXETINE (766)
ESTRADIOL (692)
SERTRALINE (636)
Which CELECOXIB Alternatives Have Lower Product substitution issue Risk?
CELECOXIB vs CELIPROLOL
CELECOXIB vs CELLCEPT
CELECOXIB vs CEMIPLIMAB
CELECOXIB vs CEMIPLIMAB-RWLC
CELECOXIB vs CENEGERMIN-BKBJ