Does TENIPOSIDE Cause Product use in unapproved indication? 53 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 53 reports of Product use in unapproved indication have been filed in association with TENIPOSIDE. This represents 16.7% of all adverse event reports for TENIPOSIDE.
53
Reports of Product use in unapproved indication with TENIPOSIDE
16.7%
of all TENIPOSIDE reports
5
Deaths
2
Hospitalizations
How Dangerous Is Product use in unapproved indication From TENIPOSIDE?
Of the 53 reports, 5 (9.4%) resulted in death, 2 (3.8%) required hospitalization, and 1 (1.9%) 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 TENIPOSIDE. However, 53 reports have been filed with the FAERS database.
What Other Side Effects Does TENIPOSIDE Cause?
Ototoxicity (71)
Off label use (61)
Leukopenia (25)
Bronchopulmonary aspergillosis (21)
Anaemia (20)
Histiocytosis haematophagic (18)
Left ventricular dysfunction (16)
Pancytopenia (16)
Alopecia (13)
Pneumocystis jirovecii pneumonia (13)
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 TENIPOSIDE Alternatives Have Lower Product use in unapproved indication Risk?
TENIPOSIDE vs TENOFOVIR
TENIPOSIDE vs TENOFOVIR ALAFENAMIDE
TENIPOSIDE vs TENOFOVIR DISOPROXIL
TENIPOSIDE vs TEPLIZUMAB-MZWV
TENIPOSIDE vs TEPOTINIB