Does NALTREXONE Cause Product solubility abnormal? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Product solubility abnormal have been filed in association with NALTREXONE (NALTREXONE HYDROCHLORIDE). This represents 0.1% of all adverse event reports for NALTREXONE.
12
Reports of Product solubility abnormal with NALTREXONE
0.1%
of all NALTREXONE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product solubility abnormal From NALTREXONE?
Of the 12 reports.
Is Product solubility abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NALTREXONE. However, 12 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 solubility abnormal?
BUPRENORPHINE (498)
BUPRENORPHINE\NALOXONE (274)
POLYETHYLENE GLYCOL 3350 (220)
CHOLESTYRAMINE (193)
PATIROMER (107)
LEVOTHYROXINE (100)
SOMATROPIN (98)
EXENATIDE (97)
ESTRADIOL (94)
NITROGLYCERIN (81)
Which NALTREXONE Alternatives Have Lower Product solubility abnormal Risk?
NALTREXONE vs NAPHAZOLINE\PHENIRAMINE
NALTREXONE vs NAPROXEN
NALTREXONE vs NAPROXEN\NAPROXEN
NALTREXONE vs NAPROXEN\PSEUDOEPHEDRINE
NALTREXONE vs NAPROXEN\SUMATRIPTAN