Does BUPROPION\NALTREXONE Cause Product label issue? 18 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Product label issue have been filed in association with BUPROPION\NALTREXONE. This represents 0.2% of all adverse event reports for BUPROPION\NALTREXONE.
18
Reports of Product label issue with BUPROPION\NALTREXONE
0.2%
of all BUPROPION\NALTREXONE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product label issue From BUPROPION\NALTREXONE?
Of the 18 reports, 1 (5.6%) required hospitalization.
Is Product label issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUPROPION\NALTREXONE. However, 18 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 label issue?
RIVAROXABAN (379)
ACETAMINOPHEN (276)
GUSELKUMAB (177)
USTEKINUMAB (164)
DIMETHICONE\LOPERAMIDE (154)
CETIRIZINE (138)
IBUPROFEN (99)
GOLIMUMAB (76)
POLYETHYLENE GLYCOL 3350 (76)
FENTANYL (72)
Which BUPROPION\NALTREXONE Alternatives Have Lower Product label issue Risk?
BUPROPION\NALTREXONE vs BUROSUMAB
BUPROPION\NALTREXONE vs BUROSUMAB-TWZA
BUPROPION\NALTREXONE vs BUSPIRONE
BUPROPION\NALTREXONE vs BUSULFAN
BUPROPION\NALTREXONE vs BUSULFEX