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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 2026-10-26 · 1181 Präparate · 62955 Quellenpassagen · 167 strukturierte Aussagen. Automatisch aktualisiert, ohne menschliche Freigabe.

Quellenpassagen (1)

Wechselwirkungen · Symtuza

Symtuza 800 mg/150 mg/200 mg/10 mg film-coated tablets Symtuza 675 mg/150 mg/200 mg/10 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 12–13

HOS-138486 · Präparat HOS-098200

12 ANTIMALARIALS Artemether/Lumefantrine Based on theoretical considerations Symtuza and DRV/COBI is expected to increase artemether/lumefantrine can be lumefantrine plasma used without dose adjustments; concentrations. however, due to the increase in (CYP3A inhibition) lumefantrine exposure, the combination should be used with caution. ANTIMYCOBACTERIALS Rifampicin Based on theoretical considerations The combination of rifampicin rifampicin is expected to decrease and Symtuza is contraindicated darunavir and/or cobicistat and/or (see section 4.3). tenofovir alafenamide plasma concentrations. (CYP3A and/or P-gp induction) Rifabutin Based on theoretical considerations Co-administration of Symtuza Rifapentine these antimycobacterials are with rifabutin and rifapentine is expected to decrease darunavir not recommended. If the and/or cobicistat and/or tenofovir combination is needed, the alafenamide plasma recommended dose of rifabutin is concentrations. 150 mg 3 times per week on set (CYP3A and/or P-gp induction) days (for example Monday-Wednesday-Friday). Increased monitoring for rifabutin associated adverse reactions including neutropenia and uveitis is warranted due to an expected increase in exposure to rifabutin. Further dose reduction of rifabutin has not been studied. It should be kept in mind that the twice weekly dose of 150 mg may not provide an optimal exposure to rifabutin thus leading to a risk of rifamycin resistance and a treatment failure. Consideration should be given to official guidance on the appropriate treatment of tuberculosis in HIV infected patients.

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): tenofovir (HOS-088083) lumefantrine (HOS-114826) artemether (HOS-116383) rifabutin (HOS-086262) rifapentine (HOS-116386)

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Quellennachweis

Version 2026-09-16T11:21:00Z · SHA-256 542f840b29cc7afaff9940b20511550e8d35031b33d95efd774fd49f70f7819d · Passage 37b1a8ed5fbc959e0c62ff07b54b15ba0df2d2ba1c8eeefb033338da5eac50e7 · Zeichen 18477–21949 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.