Wechselwirkungen · Vyndaqel
Vyndaqel 20 mg soft capsules · Abschnitt 4.5 · PDF-Seite 4
HOS-125087 · Präparat HOS-095993
Likewise, tafamidis inhibits the uptake transporters OAT1 and OAT3 (organic anion transporters) with IC50=2.9 µM and IC50=2.36 µM, respectively, and may cause drug-drug interactions at clinically relevant concentrations with substrates of these transporters (e.g. non-steroidal anti-inflammatory drugs, bumetanide, furosemide, lamivudine, methotrexate, oseltamivir, tenofovir, ganciclovir, adefovir, cidofovir, zidovudine, zalcitabine). Based on in vitro data, the maximal predicted changes in AUC of OAT1 and OAT3 substrates were determined to be less than 1.25 for the tafamidis meglumine 20 mg dose, therefore, inhibition of OAT1 or OAT3 transporters by tafamidis is not expected to result in clinically significant interactions.
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RxNorm-Namen im Text (wörtliche Treffer, Rolle nicht bewertet): oseltamivir (HOS-110021) tenofovir (HOS-088083) furosemide (HOS-089060) adefovir (HOS-088122) cidofovir (HOS-110482) zalcitabine (HOS-125095) lamivudine (HOS-085829) zidovudine (HOS-085837) bumetanide (HOS-125088) ganciclovir (HOS-085194) methotrexate (HOS-087522) tafamidis meglumine (HOS-125083)
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Version 2026-08-27T10:46:00Z · SHA-256 7fde249f53e9cf92633a9107a5bb5d809aebe75c0b5a520f64d9b84810531536 · Passage 60a0d15b7135628afbac37e9955ce41a97a4f199f269c4989eb45adbb15fbf2f · Zeichen 832–1564 im Abschnitt