Does NALTREXONE Cause Product physical consistency issue? 64 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 64 reports of Product physical consistency issue have been filed in association with NALTREXONE (NALTREXONE HYDROCHLORIDE). This represents 0.3% of all adverse event reports for NALTREXONE.
64
Reports of Product physical consistency issue with NALTREXONE
0.3%
of all NALTREXONE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product physical consistency issue From NALTREXONE?
Of the 64 reports, 2 (3.1%) required hospitalization.
Is Product physical consistency issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NALTREXONE. However, 64 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 physical consistency issue?
LEUPROLIDE (926)
CLASCOTERONE (317)
BUPRENORPHINE (242)
MINOXIDIL (171)
CHOLESTYRAMINE (141)
NAPROXEN (117)
TESTOSTERONE (113)
RUXOLITINIB (103)
DEVICE (85)
CLOBETASOL (76)
Which NALTREXONE Alternatives Have Lower Product physical consistency issue Risk?
NALTREXONE vs NAPHAZOLINE\PHENIRAMINE
NALTREXONE vs NAPROXEN
NALTREXONE vs NAPROXEN\NAPROXEN
NALTREXONE vs NAPROXEN\PSEUDOEPHEDRINE
NALTREXONE vs NAPROXEN\SUMATRIPTAN