Does NALTREXONE Cause Product dose omission issue? 359 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 359 reports of Product dose omission issue have been filed in association with NALTREXONE (NALTREXONE HYDROCHLORIDE). This represents 1.4% of all adverse event reports for NALTREXONE.
359
Reports of Product dose omission issue with NALTREXONE
1.4%
of all NALTREXONE reports
11
Deaths
28
Hospitalizations
How Dangerous Is Product dose omission issue From NALTREXONE?
Of the 359 reports, 11 (3.1%) resulted in death, 28 (7.8%) required hospitalization, and 1 (0.3%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NALTREXONE. However, 359 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 issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which NALTREXONE Alternatives Have Lower Product dose omission issue Risk?
NALTREXONE vs NAPHAZOLINE\PHENIRAMINE
NALTREXONE vs NAPROXEN
NALTREXONE vs NAPROXEN\NAPROXEN
NALTREXONE vs NAPROXEN\PSEUDOEPHEDRINE
NALTREXONE vs NAPROXEN\SUMATRIPTAN