Does THIOPENTAL Cause Product use in unapproved indication? 63 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 63 reports of Product use in unapproved indication have been filed in association with THIOPENTAL. This represents 6.0% of all adverse event reports for THIOPENTAL.
63
Reports of Product use in unapproved indication with THIOPENTAL
6.0%
of all THIOPENTAL reports
24
Deaths
37
Hospitalizations
How Dangerous Is Product use in unapproved indication From THIOPENTAL?
Of the 63 reports, 24 (38.1%) resulted in death, 37 (58.7%) required hospitalization, and 7 (11.1%) 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 THIOPENTAL. However, 63 reports have been filed with the FAERS database.
What Other Side Effects Does THIOPENTAL Cause?
Drug ineffective (266)
Off label use (150)
Status epilepticus (93)
Hypotension (82)
Maternal exposure during pregnancy (74)
Foetal exposure during pregnancy (70)
Exposure during pregnancy (64)
Diabetes insipidus (55)
Drug hypersensitivity (45)
Loss of consciousness (44)
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 THIOPENTAL Alternatives Have Lower Product use in unapproved indication Risk?
THIOPENTAL vs THIORIDAZINE
THIOPENTAL vs THIOTEPA
THIOPENTAL vs THIOTHIXENE
THIOPENTAL vs THROMBIN
THIOPENTAL vs THROMBIN HUMAN