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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 FOTEMUSTINE Cause Product use in unapproved indication? 23 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Product use in unapproved indication have been filed in association with FOTEMUSTINE. This represents 8.7% of all adverse event reports for FOTEMUSTINE.

23
Reports of Product use in unapproved indication with FOTEMUSTINE
8.7%
of all FOTEMUSTINE reports
1
Deaths
12
Hospitalizations

How Dangerous Is Product use in unapproved indication From FOTEMUSTINE?

Of the 23 reports, 1 (4.3%) resulted in death, 12 (52.2%) required hospitalization, and 7 (30.4%) were considered life-threatening.

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 FOTEMUSTINE. However, 23 reports have been filed with the FAERS database.

What Other Side Effects Does FOTEMUSTINE Cause?

Off label use (66) Disease progression (38) Acute myeloid leukaemia (30) Thrombocytopenia (29) Mucosal inflammation (25) Neutropenia (24) Platelet count decreased (22) Neutrophil count decreased (20) Septic shock (20) White blood cell count decreased (20)

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)

Which FOTEMUSTINE Alternatives Have Lower Product use in unapproved indication Risk?

FOTEMUSTINE vs FRAMYCETIN FOTEMUSTINE vs FREMANEZUMAB FOTEMUSTINE vs FREMANEZUMAB-VFRM FOTEMUSTINE vs FROVATRIPTAN FOTEMUSTINE vs FRUCTOSE

Related Pages

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