Does NALTREXONE Cause Product dose omission? 278 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 278 reports of Product dose omission have been filed in association with NALTREXONE (NALTREXONE HYDROCHLORIDE). This represents 1.1% of all adverse event reports for NALTREXONE.
278
Reports of Product dose omission with NALTREXONE
1.1%
of all NALTREXONE reports
20
Deaths
17
Hospitalizations
How Dangerous Is Product dose omission From NALTREXONE?
Of the 278 reports, 20 (7.2%) resulted in death, 17 (6.1%) required hospitalization, and 2 (0.7%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NALTREXONE. However, 278 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 dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which NALTREXONE Alternatives Have Lower Product dose omission Risk?
NALTREXONE vs NAPHAZOLINE\PHENIRAMINE
NALTREXONE vs NAPROXEN
NALTREXONE vs NAPROXEN\NAPROXEN
NALTREXONE vs NAPROXEN\PSEUDOEPHEDRINE
NALTREXONE vs NAPROXEN\SUMATRIPTAN