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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 THIOPENTAL Cause Off label use? 150 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 150 reports of Off label use have been filed in association with THIOPENTAL. This represents 14.3% of all adverse event reports for THIOPENTAL.

150
Reports of Off label use with THIOPENTAL
14.3%
of all THIOPENTAL reports
52
Deaths
93
Hospitalizations

How Dangerous Is Off label use From THIOPENTAL?

Of the 150 reports, 52 (34.7%) resulted in death, 93 (62.0%) required hospitalization, and 35 (23.3%) were considered life-threatening.

Is Off label use Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for THIOPENTAL. However, 150 reports have been filed with the FAERS database.

What Other Side Effects Does THIOPENTAL Cause?

Drug ineffective (266) Status epilepticus (93) Hypotension (82) Maternal exposure during pregnancy (74) Foetal exposure during pregnancy (70) Exposure during pregnancy (64) Product use in unapproved indication (63) Diabetes insipidus (55) Drug hypersensitivity (45) Loss of consciousness (44)

What Other Drugs Cause Off label use?

RITUXIMAB (39,751) INFLIXIMAB (34,801) DENOSUMAB (34,612) METHOTREXATE (24,020) VEDOLIZUMAB (21,017) ETANERCEPT (20,178) TOCILIZUMAB (18,256) PREDNISONE (17,867) LENALIDOMIDE (17,017) ADALIMUMAB (16,417)

Which THIOPENTAL Alternatives Have Lower Off label use Risk?

THIOPENTAL vs THIORIDAZINE THIOPENTAL vs THIOTEPA THIOPENTAL vs THIOTHIXENE THIOPENTAL vs THROMBIN THIOPENTAL vs THROMBIN HUMAN

Related Pages

THIOPENTAL Full Profile All Off label use Reports All Drugs Causing Off label use THIOPENTAL Demographics