Does OXYBUTYNIN Cause Product administration error? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Product administration error have been filed in association with OXYBUTYNIN (Oxybutynin Chloride). This represents 0.2% of all adverse event reports for OXYBUTYNIN.
12
Reports of Product administration error with OXYBUTYNIN
0.2%
of all OXYBUTYNIN reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product administration error From OXYBUTYNIN?
Of the 12 reports, 2 (16.7%) required hospitalization, and 2 (16.7%) 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 OXYBUTYNIN. However, 12 reports have been filed with the FAERS database.
What Other Side Effects Does OXYBUTYNIN Cause?
Drug ineffective (1,784)
Dry mouth (519)
Application site erythema (395)
Off label use (385)
Constipation (379)
Product adhesion issue (336)
Headache (334)
Erythema (315)
Nausea (308)
Application site pruritus (289)
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 OXYBUTYNIN Alternatives Have Lower Product administration error Risk?
OXYBUTYNIN vs OXYBUTYNIN\OXYBUTYNIN
OXYBUTYNIN vs OXYCODONE
OXYBUTYNIN vs OXYCODONE TEREPHTHALATE
OXYBUTYNIN vs OXYCODONE\OXYCODONE
OXYBUTYNIN vs OXYCONTIN