Does NALTREXONE Cause Product administration error? 211 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 211 reports of Product administration error have been filed in association with NALTREXONE (NALTREXONE HYDROCHLORIDE). This represents 0.8% of all adverse event reports for NALTREXONE.
211
Reports of Product administration error with NALTREXONE
0.8%
of all NALTREXONE reports
3
Deaths
21
Hospitalizations
How Dangerous Is Product administration error From NALTREXONE?
Of the 211 reports, 3 (1.4%) resulted in death, 21 (10.0%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NALTREXONE. However, 211 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 administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which NALTREXONE Alternatives Have Lower Product administration error Risk?
NALTREXONE vs NAPHAZOLINE\PHENIRAMINE
NALTREXONE vs NAPROXEN
NALTREXONE vs NAPROXEN\NAPROXEN
NALTREXONE vs NAPROXEN\PSEUDOEPHEDRINE
NALTREXONE vs NAPROXEN\SUMATRIPTAN