Time course of CYP3A activity during and after metamizole (dipyrone) in healthy volunteers
Mareile H. Breithaupt, Evelyn Krohmer, Lenka A. Taylor, Eva Körner, Torsten Hoppe‐Tichy, Jürgen Burhenne, Kathrin I. Foerster, Markus Dachtler, Gerald Huber, Rakesh Venkatesh, Karin Eggenreich, David Czock, Gerd Mikus, Antje Blank, Walter E. Haefeli
Abstract
Aims In patients of all ages, metamizole is a frequently used analgesic. Recently, metamizole has been identified as an inducer of, among others, cytochrome P450 (CYP) 3A activity, but the time course of this interaction has not been evaluated. Methods Using repeated oral microdoses (30 μg) of the CYP3A index substrate midazolam, we assessed changes in midazolam pharmacokinetics (area under the concentration–time curve from 2–4 h: AUC 2–4 and estimated partial metabolic clearance: eCl met ) before, at steady‐state, and after discontinuation of 3 × 1000 mg metamizole/day orally for 8 days. Results Significant changes in pharmacokinetic parameters were detected already 3 days after start of metamizole treatment. At the steady‐state of enzyme induction, the geometric mean ratio of midazolam AUC 2–4 was substantially reduced to 0.18 (90% confidence interval: 0.14–0.24) with a corresponding 5.43‐fold (4.15–7.10) increase of eCl met . After discontinuation of metamizole, the changes slowly recovered, but were still significant at the end of the observation period on the fifth day after discontinuation of metamizole therapy (AUC 2–4 reduced to 0.50 [0.41–0.63] and eCl met 1.99‐fold increased [1.60–2.47, P < 0.05]). Conclusion Metamizole acts as a strong inducer of CYP3A already few days after start of metamizole administration and, thus, should be avoided in patients using drugs with narrow therapeutic index and major clearance via CYP3A. If their administration is essential, close monitoring and dose adjustment of comedication should be performed as early as the first week after the initiation and after discontinuation of metamizole therapy.