Does IDEBENONE Cause Product use in unapproved indication? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product use in unapproved indication have been filed in association with IDEBENONE. This represents 9.6% of all adverse event reports for IDEBENONE.
5
Reports of Product use in unapproved indication with IDEBENONE
9.6%
of all IDEBENONE reports
1
Deaths
0
Hospitalizations
How Dangerous Is Product use in unapproved indication From IDEBENONE?
Of the 5 reports, 1 (20.0%) resulted in death.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IDEBENONE. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does IDEBENONE Cause?
Cholestasis (14)
Fatigue (12)
Thrombocytopenia (10)
Activated partial thromboplastin time prolonged (9)
Cataract nuclear (9)
Hepatic encephalopathy (9)
Vomiting (9)
Decreased appetite (8)
Hepatitis acute (8)
Jaundice (8)
What Other Drugs Cause Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)