N02AJ06 - Codeine and Paracetamol |
Propably not porphyrinogenic |
PNP |
Rationale
Paracetamol: Low extent of oxidative metabolism. Inducer of CYP 3A4. Three references consider it safe. Occasional patient reports of suspected porphyrinogenicity, but vast and significant clinical experience of non-porphyrinogenicity. Codeine: Opioid substrate for 2D6 and 3A4. Several references consider it safe for use.
Chemical description
Paracetamol: Anilide (acetaminophen) derivative metabolized by conjugation with glucuronic acid and sulfate. A small part (<4%) is oxidatively metabolized by CYPs and excreted as cysteine and mercapto conjugates. At low concentrations inducer of CYP 3A4, increasing activity and content. Australian list: safe. South African list: use French list: avoid, known to have precipitated an acute attack Thunell; patient inquiry: tolerated (n=28), possibly not tolerated (n=2 C. Andersson; patient inquiry: used without illeffecs (n=18). Used in Swedish porphyria ward. Codeine: Opioide with analgetic and antitussive properties. Demetylated by CYP 2D6 and 3A4. Inhibitor of 2D6. EPI-list: safe South African list: use French list: authorized.
IPNet drug reports
Paracetamol: Uneventful use reported in 430 patients with acute porphyria. Codeine: Uneventful use reported in 27 patients with acute porphyria.
Similar drugs
References
# | Citation details | PMID |
---|---|---|
* | Scientific articles | |
1. | Effects of antihypertensive drugs on hepatic heme synthesis.
Anderson KE Biochem. Biophys. Acta 543:313, 1978. |
708789 |
2. | The paradoxical effect of acetaminophen on CYP3A4 activity and content in transfected HepG2 cells
Feierman DE, Melnikov Z, Zhang J Arch Biochem Biophys. 2002 Feb 1;398(1):109-17. |
11811955 |
3. | Drugs in the acute porphyrias - toxicogenetic diseases.
Moore MR, Hift RJ Cell Mol Biol (Noisy-le-grand). 1997 Feb;43(1):89-94 |
9074793 |
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