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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does FLUOXYMESTERONE Cause Product use in unapproved indication? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product use in unapproved indication have been filed in association with FLUOXYMESTERONE. This represents 19.4% of all adverse event reports for FLUOXYMESTERONE.

6
Reports of Product use in unapproved indication with FLUOXYMESTERONE
19.4%
of all FLUOXYMESTERONE reports
0
Deaths
5
Hospitalizations

How Dangerous Is Product use in unapproved indication From FLUOXYMESTERONE?

Of the 6 reports, 5 (83.3%) 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 FLUOXYMESTERONE. However, 6 reports have been filed with the FAERS database.

What Other Side Effects Does FLUOXYMESTERONE Cause?

Drug abuse (16) Intentional product misuse (13) Autoimmune thyroiditis (9) Diabetes mellitus (9) Secondary hypogonadism (9) Hepatic neoplasm (8) Multiple organ dysfunction syndrome (8) Haematocrit increased (7) Intra-abdominal haemorrhage (7) Performance enhancing product use (7)

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)

Related Pages

FLUOXYMESTERONE Full Profile All Product use in unapproved indication Reports All Drugs Causing Product use in unapproved indication FLUOXYMESTERONE Demographics