Does NALTREXONE Cause Product preparation error? 120 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 120 reports of Product preparation error have been filed in association with NALTREXONE (NALTREXONE HYDROCHLORIDE). This represents 0.5% of all adverse event reports for NALTREXONE.
120
Reports of Product preparation error with NALTREXONE
0.5%
of all NALTREXONE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product preparation error From NALTREXONE?
Of the 120 reports, 3 (2.5%) required hospitalization.
Is Product preparation error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NALTREXONE. However, 120 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 preparation error?
ONABOTULINUMTOXINA (3,593)
EVOLOCUMAB (2,785)
DUPILUMAB (2,707)
BUPRENORPHINE\NALOXONE (777)
ABOBOTULINUMTOXINA (751)
ALBIGLUTIDE (691)
ALBUTEROL (520)
PEGFILGRASTIM (473)
ALIROCUMAB (402)
LEUPROLIDE (400)
Which NALTREXONE Alternatives Have Lower Product preparation error Risk?
NALTREXONE vs NAPHAZOLINE\PHENIRAMINE
NALTREXONE vs NAPROXEN
NALTREXONE vs NAPROXEN\NAPROXEN
NALTREXONE vs NAPROXEN\PSEUDOEPHEDRINE
NALTREXONE vs NAPROXEN\SUMATRIPTAN