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Dimethylformamide metabolism following self-harm using a veterinary euthanasia product.
Philippe Hantson1, Antoine Villa, Anne-Cécile Galloy
1Intensive Care, Cliniques Saint-Luc, Avenue Hippocrate 10, Brussels, Belgium. philippe.hantson@uclouvain.be
Clinical Toxicology (Philadelphia, Pa.)
|September 21, 2010
Summary
Veterinary euthanasia drug T-61 self-poisoning caused mild liver injury in two veterinarians. N-acetylcysteine (NAC) did not clearly impact dimethylformamide (DMF) metabolite excretion, suggesting further research is needed.
Area of Science:
- Veterinary toxicology
- Clinical pharmacology
- Drug safety evaluation
Background:
- T-61, a veterinary euthanasia drug, contains embutramide, mebezonium, tetracaine, and dimethylformamide (DMF).
- Self-poisoning with T-61 can lead to severe toxicity, with delayed hepatotoxicity potentially linked to DMF.
- The efficacy of N-acetylcysteine (NAC) in mitigating T-61 toxicity is not well-established.
Observation:
- Two male veterinarians self-poisoned with T-61 via injection and ingestion.
- Both patients received N-acetylcysteine (NAC) treatment for varying durations.
- Urine samples were analyzed for dimethylformamide (DMF) and its metabolites, N-methylformamide (NMF) and N-acetyl-S-(N-methylcarbamoyl)cysteine (AMCC).
Findings:
- Both individuals experienced only mild liver injury despite T-61 exposure.
- Rapid urinary excretion of N-methylformamide (NMF) was observed, followed by slower excretion of AMCC.
- Dimethylformamide (DMF) and its metabolite elimination kinetics were slightly prolonged compared to occupational exposure data.
Implications:
- N-acetylcysteine (NAC) administration did not demonstrate a clear effect on the excretion of dimethylformamide (DMF) metabolites (NMF and AMCC).
- Favorable outcomes in these cases suggest T-61 toxicity may be manageable, but the role of NAC requires further investigation.
- Additional studies are warranted to elucidate the impact of NAC on DMF metabolite excretion kinetics and overall toxicity.

