Does AREDIA Cause Hyperkeratosis? 19 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 19 reports of Hyperkeratosis have been filed in association with AREDIA. This represents 11.5% of all adverse event reports for AREDIA.
19
Reports of Hyperkeratosis with AREDIA
11.5%
of all AREDIA reports
0
Deaths
17
Hospitalizations
How Dangerous Is Hyperkeratosis From AREDIA?
Of the 19 reports, 17 (89.5%) required hospitalization.
Is Hyperkeratosis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AREDIA. However, 19 reports have been filed with the FAERS database.
What Other Side Effects Does AREDIA Cause?
Osteonecrosis of jaw (151)
Pain (128)
Anxiety (122)
Spinal osteoarthritis (114)
Osteoarthritis (113)
Dyspnoea (107)
Arthralgia (102)
Osteomyelitis (95)
Anaemia (89)
Atelectasis (89)
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 AREDIA Alternatives Have Lower Hyperkeratosis Risk?
AREDIA vs ARFORMOTEROL
AREDIA vs ARGATROBAN
AREDIA vs ARGININE
AREDIA vs ARGININE\LYSINE
AREDIA vs ARIMIDEX