Does BUPROPION\NALTREXONE Cause Product administration error? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Product administration error have been filed in association with BUPROPION\NALTREXONE. This represents 0.1% of all adverse event reports for BUPROPION\NALTREXONE.
9
Reports of Product administration error with BUPROPION\NALTREXONE
0.1%
of all BUPROPION\NALTREXONE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product administration error From BUPROPION\NALTREXONE?
Of the 9 reports, 2 (22.2%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUPROPION\NALTREXONE. However, 9 reports have been filed with the FAERS database.
What Other Side Effects Does BUPROPION\NALTREXONE Cause?
Nausea (1,857)
Headache (1,054)
Dizziness (986)
Vomiting (646)
Constipation (602)
Feeling abnormal (550)
Fatigue (474)
Anxiety (378)
Insomnia (367)
Diarrhoea (350)
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 BUPROPION\NALTREXONE Alternatives Have Lower Product administration error Risk?
BUPROPION\NALTREXONE vs BUROSUMAB
BUPROPION\NALTREXONE vs BUROSUMAB-TWZA
BUPROPION\NALTREXONE vs BUSPIRONE
BUPROPION\NALTREXONE vs BUSULFAN
BUPROPION\NALTREXONE vs BUSULFEX