Does CELECOXIB Cause Product administration error? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Product administration error have been filed in association with CELECOXIB (Celecoxib). This represents 0.0% of all adverse event reports for CELECOXIB.
11
Reports of Product administration error with CELECOXIB
0.0%
of all CELECOXIB reports
1
Deaths
1
Hospitalizations
How Dangerous Is Product administration error From CELECOXIB?
Of the 11 reports, 1 (9.1%) resulted in death, 1 (9.1%) required hospitalization, and 5 (45.5%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CELECOXIB. However, 11 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 error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which CELECOXIB Alternatives Have Lower Product administration error Risk?
CELECOXIB vs CELIPROLOL
CELECOXIB vs CELLCEPT
CELECOXIB vs CEMIPLIMAB
CELECOXIB vs CEMIPLIMAB-RWLC
CELECOXIB vs CENEGERMIN-BKBJ