Does NALOXONE Cause Product prescribing issue? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Product prescribing issue have been filed in association with NALOXONE (Naloxone Hydrochloride). This represents 0.6% of all adverse event reports for NALOXONE.
16
Reports of Product prescribing issue with NALOXONE
0.6%
of all NALOXONE reports
10
Deaths
13
Hospitalizations
How Dangerous Is Product prescribing issue From NALOXONE?
Of the 16 reports, 10 (62.5%) resulted in death, 13 (81.3%) required hospitalization.
Is Product prescribing issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NALOXONE. However, 16 reports have been filed with the FAERS database.
What Other Side Effects Does NALOXONE Cause?
Toxicity to various agents (608)
Drug ineffective (462)
Overdose (381)
Drug withdrawal syndrome (192)
Drug dependence (189)
Death (137)
Drug abuse (134)
Vomiting (133)
Off label use (111)
Maternal exposure during pregnancy (110)
What Other Drugs Cause Product prescribing issue?
DUPILUMAB (1,715)
POLYETHYLENE GLYCOL 3350 (1,439)
LENALIDOMIDE (948)
OXYCODONE (646)
RIVAROXABAN (359)
ACETAMINOPHEN\OXYCODONE (347)
ETONOGESTREL (311)
ACETAMINOPHEN\HYDROCODONE (298)
CERTOLIZUMAB PEGOL (297)
CABOZANTINIB S-MALATE (294)
Which NALOXONE Alternatives Have Lower Product prescribing issue Risk?
NALOXONE vs NALOXONE\OXYCODONE
NALOXONE vs NALOXONE\TILIDINE
NALOXONE vs NALTREXONE
NALOXONE vs NAPHAZOLINE\PHENIRAMINE
NALOXONE vs NAPROXEN