Does BUPRENORPHINE\NALOXONE Cause Product administration error? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Product administration error have been filed in association with BUPRENORPHINE\NALOXONE. This represents 0.1% of all adverse event reports for BUPRENORPHINE\NALOXONE.
16
Reports of Product administration error with BUPRENORPHINE\NALOXONE
0.1%
of all BUPRENORPHINE\NALOXONE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product administration error From BUPRENORPHINE\NALOXONE?
Of the 16 reports, 2 (12.5%) required hospitalization, and 1 (6.3%) 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 BUPRENORPHINE\NALOXONE. However, 16 reports have been filed with the FAERS database.
What Other Side Effects Does BUPRENORPHINE\NALOXONE Cause?
Drug dependence (4,755)
Drug withdrawal syndrome (3,167)
Pain (2,472)
Off label use (1,946)
Nausea (1,899)
Overdose (1,749)
Emotional distress (1,696)
Vomiting (1,370)
Foetal exposure during pregnancy (1,309)
Anxiety (1,307)
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 BUPRENORPHINE\NALOXONE Alternatives Have Lower Product administration error Risk?
BUPRENORPHINE\NALOXONE vs BUPROPION
BUPRENORPHINE\NALOXONE vs BUPROPION HYDROBROMIDE
BUPRENORPHINE\NALOXONE vs BUPROPION\DEXTROMETHORPHAN HYDROBROMIDE
BUPRENORPHINE\NALOXONE vs BUPROPION\NALTREXONE
BUPRENORPHINE\NALOXONE vs BUROSUMAB