The paracetamol (acetaminophen) formed is CYP3A4 inducer, but gives rise only to a low hepatic oxidative load. Occasional patient reports of suspected porphyrinogenicity but vast and significant clinical experience of non-porphyrinogenicity.

Moderatly strong analgesic and antipyretic for intravenous administration. At the end of the infusion 99% of propacetamol is hydrolyzed in plasma to paracetamol and di-ethylglycine. The paracetamol metabolite is excreted in urine as sulfate and glucuronide conjugates. Less than 4% metabolized by CYPs. At low concentrations paracetamol is inducer of CYP3A4, increasing activity and content.