Does NALOXONE\TILIDINE Cause Hyperkeratosis? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Hyperkeratosis have been filed in association with NALOXONE\TILIDINE. This represents 0.8% of all adverse event reports for NALOXONE\TILIDINE.
5
Reports of Hyperkeratosis with NALOXONE\TILIDINE
0.8%
of all NALOXONE\TILIDINE reports
0
Deaths
5
Hospitalizations
How Dangerous Is Hyperkeratosis From NALOXONE\TILIDINE?
Of the 5 reports, 5 (100.0%) required hospitalization.
Is Hyperkeratosis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NALOXONE\TILIDINE. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does NALOXONE\TILIDINE Cause?
Fall (186)
Dizziness (126)
Pain (98)
Nausea (83)
Constipation (80)
Fatigue (77)
General physical health deterioration (76)
Vomiting (71)
Arthralgia (69)
Abdominal pain upper (56)
What Other Drugs Cause Hyperkeratosis?
CABOZANTINIB S-MALATE (411)
ADALIMUMAB (332)
SUNITINIB MALATE (170)
ETANERCEPT (168)
SORAFENIB (150)
METHOTREXATE (149)
VEMURAFENIB (145)
REGORAFENIB (136)
RIPRETINIB (124)
RITUXIMAB (121)
Which NALOXONE\TILIDINE Alternatives Have Lower Hyperkeratosis Risk?
NALOXONE\TILIDINE vs NALTREXONE
NALOXONE\TILIDINE vs NAPHAZOLINE\PHENIRAMINE
NALOXONE\TILIDINE vs NAPROXEN
NALOXONE\TILIDINE vs NAPROXEN\NAPROXEN
NALOXONE\TILIDINE vs NAPROXEN\PSEUDOEPHEDRINE