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

Quellenpassagen (1)

Wechselwirkungen · Viread

Viread 123 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 9

HOS-110490 · Präparat HOS-093385

Medicinal product by Effects on drug levels Recommendation concerning therapeutic areas Mean percent change in AUC, co-administration with 245 mg (dose in mg) Cmax, Cmin tenofovir disoproxil ANTI-INFECTIVES Antiretrovirals Protease inhibitors Atazanavir/Ritonavir Atazanavir: No dose adjustment is (300 q.d./100 q.d.) AUC: ↓ 25% recommended. The increased Cmax: ↓ 28% exposure of tenofovir could Cmin: ↓ 26% potentiate tenofovir-associated Tenofovir: adverse events, including renal AUC: ↑ 37% disorders. Renal function should Cmax: ↑ 34% be closely monitored Cmin: ↑ 29% (see section 4.4). Lopinavir/Ritonavir Lopinavir/ritonavir: No dose adjustment is (400 b.i.d./100 b.i.d.) No significant effect on recommended. The increased lopinavir/ritonavir PK exposure of tenofovir could parameters. potentiate tenofovir-associated Tenofovir: adverse events, including renal AUC: ↑ 32% disorders. Renal function should Cmax: ↔ be closely monitored Cmin: ↑ 51% (see section 4.4). Darunavir/Ritonavir Darunavir: No dose adjustment is (300/100 b.i.d.) No significant effect on recommended. The increased darunavir/ritonavir PK exposure of tenofovir could parameters. potentiate tenofovir-associated Tenofovir: adverse events, including renal AUC: ↑ 22% disorders. Renal function should Cmin: ↑ 37% be closely monitored (see section 4.4). NRTIs Didanosine Co-administration of tenofovir Co-administration of tenofovir disoproxil and didanosine results disoproxil and didanosine is not in a 40-60% increase in systemic recommended (see section 4.4). exposure to didanosine. Increased systemic exposure to didanosine may increase didanosine related adverse reactions. Rarely, pancreatitis and lactic acidosis, sometimes fatal, have been reported. Co-administration of tenofovir disoproxil and didanosine at a dose of 400 mg daily has been associated with a significant decrease in CD4 cell count, possibly due to an intracellular interaction increasing phosphorylated (i.e. active) didanosine. A decreased dosage of 250 mg didanosine co-administered with tenofovir disoproxil therapy has been associated with reports of high rates of virological failure within several tested combinations for the treatment of HIV-1 infection.

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) lopinavir (HOS-086269) atazanavir (HOS-086180) protease (HOS-085623) didanosine (HOS-085836) darunavir (HOS-086181) ritonavir (HOS-084521)

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Quellennachweis

Version 2024-02-29T16:34:00Z · SHA-256 ab427f9266bbb81991653ebf14729e0d885f7cb9014fd47e3b3ee4fc69589ee0 · Passage 2da8a9413a0cdf6c2adfbb5e8a3514645ef92df343ae795985c6e470290e6c16 · Zeichen 1811–6985 im Abschnitt

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