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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 Hyperammonaemia? 14 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Hyperammonaemia have been filed in association with THIOPENTAL. This represents 1.3% of all adverse event reports for THIOPENTAL.

14
Reports of Hyperammonaemia with THIOPENTAL
1.3%
of all THIOPENTAL reports
0
Deaths
10
Hospitalizations

How Dangerous Is Hyperammonaemia From THIOPENTAL?

Of the 14 reports, 10 (71.4%) required hospitalization, and 3 (21.4%) were considered life-threatening.

Is Hyperammonaemia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for THIOPENTAL. However, 14 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) Product use in unapproved indication (63) Diabetes insipidus (55) Drug hypersensitivity (45)

What Other Drugs Cause Hyperammonaemia?

VALPROIC ACID (581) VALPROATE (328) FLUOROURACIL (263) DIVALPROEX (256) LEVETIRACETAM (192) TACROLIMUS (181) ACETAMINOPHEN (177) OXALIPLATIN (160) TOPIRAMATE (156) GLYCEROL PHENYLBUTYRATE (147)

Which THIOPENTAL Alternatives Have Lower Hyperammonaemia Risk?

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

Related Pages

THIOPENTAL Full Profile All Hyperammonaemia Reports All Drugs Causing Hyperammonaemia THIOPENTAL Demographics