Does METHYLPREDNISOLONE Cause Hyperkeratosis? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Hyperkeratosis have been filed in association with METHYLPREDNISOLONE (Medroloan II SUIK). This represents 0.0% of all adverse event reports for METHYLPREDNISOLONE.
8
Reports of Hyperkeratosis with METHYLPREDNISOLONE
0.0%
of all METHYLPREDNISOLONE reports
2
Deaths
5
Hospitalizations
How Dangerous Is Hyperkeratosis From METHYLPREDNISOLONE?
Of the 8 reports, 2 (25.0%) resulted in death, 5 (62.5%) required hospitalization, and 1 (12.5%) were considered life-threatening.
Is Hyperkeratosis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for METHYLPREDNISOLONE. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does METHYLPREDNISOLONE Cause?
Off label use (10,364)
Drug ineffective (9,959)
Product use in unapproved indication (4,115)
Condition aggravated (3,784)
Headache (3,419)
Fatigue (3,250)
Pyrexia (3,226)
Pain (3,165)
Nausea (3,105)
Pneumonia (3,006)
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 METHYLPREDNISOLONE Alternatives Have Lower Hyperkeratosis Risk?
METHYLPREDNISOLONE vs METHYLPREDNISOLONE ACEPONATE
METHYLPREDNISOLONE vs METHYLPREDNISOLONE HEMISUCCINATE
METHYLPREDNISOLONE vs METILDIGOXIN
METHYLPREDNISOLONE vs METOCLOPRAMIDE
METHYLPREDNISOLONE vs METOLAZONE