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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 SERTINDOLE Cause Product use in unapproved indication? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product use in unapproved indication have been filed in association with SERTINDOLE. This represents 11.5% of all adverse event reports for SERTINDOLE.

7
Reports of Product use in unapproved indication with SERTINDOLE
11.5%
of all SERTINDOLE reports
0
Deaths
7
Hospitalizations

How Dangerous Is Product use in unapproved indication From SERTINDOLE?

Of the 7 reports, 7 (100.0%) 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 SERTINDOLE. However, 7 reports have been filed with the FAERS database.

What Other Side Effects Does SERTINDOLE Cause?

Drug ineffective (16) Weight increased (16) Fatigue (13) Anxiety (11) Electrocardiogram qt prolonged (11) Insomnia (11) Hyperprolactinaemia (10) Hallucination, auditory (9) Tremor (8) Hypotension (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

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