Does TEMOZOLOMIDE Cause Product use in unapproved indication? 1,353 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,353 reports of Product use in unapproved indication have been filed in association with TEMOZOLOMIDE (TEMOZOLOMIDE). This represents 8.0% of all adverse event reports for TEMOZOLOMIDE.
1,353
Reports of Product use in unapproved indication with TEMOZOLOMIDE
8.0%
of all TEMOZOLOMIDE reports
82
Deaths
80
Hospitalizations
How Dangerous Is Product use in unapproved indication From TEMOZOLOMIDE?
Of the 1,353 reports, 82 (6.1%) resulted in death, 80 (5.9%) required hospitalization, and 36 (2.7%) 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 TEMOZOLOMIDE. However, 1,353 reports have been filed with the FAERS database.
What Other Side Effects Does TEMOZOLOMIDE Cause?
Disease progression (1,562)
Death (1,403)
Off label use (1,357)
Thrombocytopenia (1,300)
Drug ineffective (1,131)
Nausea (1,071)
Neutropenia (809)
Malignant neoplasm progression (779)
Fatigue (766)
Vomiting (697)
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 TEMOZOLOMIDE Alternatives Have Lower Product use in unapproved indication Risk?
TEMOZOLOMIDE vs TEMSIROLIMUS
TEMOZOLOMIDE vs TENAMFETAMINE
TEMOZOLOMIDE vs TENAPANOR
TEMOZOLOMIDE vs TENECTEPLASE
TEMOZOLOMIDE vs TENELIGLIPTIN