Does MESTEROLONE Cause Product use in unapproved indication? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Product use in unapproved indication have been filed in association with MESTEROLONE. This represents 21.1% of all adverse event reports for MESTEROLONE.
8
Reports of Product use in unapproved indication with MESTEROLONE
21.1%
of all MESTEROLONE reports
1
Deaths
7
Hospitalizations
How Dangerous Is Product use in unapproved indication From MESTEROLONE?
Of the 8 reports, 1 (12.5%) resulted in death, 7 (87.5%) required hospitalization.
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 MESTEROLONE. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does MESTEROLONE Cause?
Drug abuse (19)
Secondary hypogonadism (10)
Autoimmune thyroiditis (9)
Diabetes mellitus (9)
Off label use (8)
Haematocrit increased (7)
Performance enhancing product use (7)
Blood glucose increased (6)
Glucose tolerance decreased (6)
Intentional product misuse (6)
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)