Does NALTREXONE Cause Product compounding quality issue? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product compounding quality issue have been filed in association with NALTREXONE (NALTREXONE HYDROCHLORIDE). This represents 0.0% of all adverse event reports for NALTREXONE.
5
Reports of Product compounding quality issue with NALTREXONE
0.0%
of all NALTREXONE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product compounding quality issue From NALTREXONE?
Of the 5 reports.
Is Product compounding quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NALTREXONE. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does NALTREXONE Cause?
Injection site reaction (4,360)
Injection site pain (2,990)
Alcoholism (1,928)
Injection site mass (1,849)
Nausea (1,782)
Fatigue (1,486)
Pain (1,348)
Drug dependence (1,334)
Drug ineffective (1,250)
Feeling abnormal (1,241)
What Other Drugs Cause Product compounding quality issue?
TRIAMCINOLONE (23)
EXENATIDE (20)
VORICONAZOLE (20)
SODIUM (14)
SEMAGLUTIDE (12)
DEXTROSE (8)
POTASSIUM (8)
TIRZEPATIDE (8)
CALCIUM (7)
MAGNESIUM (7)
Which NALTREXONE Alternatives Have Lower Product compounding quality issue Risk?
NALTREXONE vs NAPHAZOLINE\PHENIRAMINE
NALTREXONE vs NAPROXEN
NALTREXONE vs NAPROXEN\NAPROXEN
NALTREXONE vs NAPROXEN\PSEUDOEPHEDRINE
NALTREXONE vs NAPROXEN\SUMATRIPTAN