Zum Inhalt

HealthOSArzneimittel

Arbeitsbereiche

Nachschlagen

Wirkstoffe & Arzneimittelsicherheit

Exakte Wirkstoffkennungen und zitierbare Passagen zu Wechselwirkungen, Gegenanzeigen und Nebenwirkungen.

Ein Paarvergleich findet Originalpassagen, die den anderen Wirkstoff wörtlich nennen. Aussagen gelten für das jeweilige Präparat und seine Formulierung. Klassenbegriffe und abweichende Synonyme können fehlen. Kein Treffer bedeutet nicht, dass keine Wechselwirkung besteht.

RxNorm 05-Oct-2026 · geprüft 2026-10-25 · 1009 Präparate · 54812 Quellenpassagen · 148 strukturierte Aussagen. Automatisch aktualisiert, ohne menschliche Freigabe.

Quellenpassagen (1)

Wechselwirkungen · Tivicay

Tivicay 10 mg film-coated tablets Tivicay 25 mg film-coated tablets Tivicay 50 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 8–9

HOS-129163 · Präparat HOS-096689

8 Darunavir/ritonavir Dolutegravir  No dose adjustment is necessary. AUC  22% Cmax  11% C24  38% (induction of UGT1A1 and CYP3A enzymes) Lopinavir/ritonavir Dolutegravir  No dose adjustment is necessary. AUC  4% Cmax  0% C24  6% Other Antiviral agents Daclatasvir Dolutegravir  Daclatasvir did not change dolutegravir plasma AUC  33% concentration to a clinically relevant extent. Cmax  29% Dolutegravir did not change daclatasvir plasma C  45% concentration. No dose adjustment is necessary. Daclatasvir  Other agents Potassium channel blocker Fampridine (also Fampridine  Co-administration of dolutegravir has the potential known as to cause seizures due to increased fampridine dalfampridine) plasma concentration via inhibition of OCT2 transporter; co-administration has not been studied. Fampridine co-administration with dolutegravir is contraindicated. Anticonvulsants Carbamazepine Dolutegravir  The recommended adult dose of dolutegravir is 50 AUC  49% mg twice daily when co-administered with Cmax  33% carbamazepine. In paediatric patients the weight- C  73% based once daily dose should be administered twice daily. Alternatives to carbamazepine should be used where possible for INI resistant patients. Oxcarbazepine Dolutegravir  The recommended adult dose of dolutegravir is 50 Phenytoin (Not studied, decrease mg twice daily when co-administered with these Phenobarbital expected due to induction of metabolic inducers. In paediatric patients the UGT1A1 and CYP3A weight-based once daily dose should be enzymes, a similar reduction administered twice daily. Alternative in exposure as observed combinations that do not include these metabolic with carbamazepine is inducers should be used where possible in INI- expected) resistant patients. Azole anti-fungal agents Ketoconazole Dolutegravir  No dose adjustment is necessary. Based on data Fluconazole (Not studied) from other CYP3A4 inhibitors, a marked increase Itraconazole is not expected. Posaconazole Voriconazole Herbal products St. John’s wort Dolutegravir  The recommended adult dose of dolutegravir is 50 (Not studied, decrease mg twice daily when co-administered with St. expected due to induction of John’s wort. In paediatric patients the weight- UGT1A1 and CYP3A based once daily dose should be administered enzymes, a similar reduction twice daily. Alternative combinations that do not in exposure as observed include St. John’s wort should be used where with carbamazepine is possible in INI-resistant patients. expected) Antacids and supplements

Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.

RxNorm-Namen im Text (wörtliche Treffer, Rolle nicht bewertet): lopinavir (HOS-086269) daclatasvir (HOS-119742) phenobarbital (HOS-085617) ketoconazole (HOS-084513) carbamazepine (HOS-085618) voriconazole (HOS-084524) itraconazole (HOS-084516) dalfampridine (HOS-124191) fluconazole (HOS-087945) darunavir (HOS-086181) oxcarbazepine (HOS-110224) ritonavir (HOS-084521) potassium (HOS-086929) phenytoin (HOS-084531) posaconazole (HOS-085622)

Vollständigen Kontext in der EMA-Fachinformation lesen →
Quellennachweis

Version 2025-11-14T16:54:00Z · SHA-256 49ffb99144edc826feca26a0b941946b69a295b5c67e5f5fd79358277916c087 · Passage 7146ae3c08ab0159cbd699143845d13f9721ca0ad65d42e769709558e2d4148f · Zeichen 9118–13250 im Abschnitt

This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product.