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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 · 871 Präparate · 48256 Quellenpassagen · 124 strukturierte Aussagen. Automatisch aktualisiert, ohne menschliche Freigabe.

Quellenpassagen (14)

Wechselwirkungen · Epivir

Epivir 150 mg film-coated tablets Epivir 300 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 6

HOS-085834 · Präparat HOS-083204

The possibility of interactions with other medicinal products administered concurrently should be considered, particularly when the main route of elimination is active renal secretion via the organic cationic transport system e.g. trimethoprim. Other medicinal products (e.g. ranitidine, cimetidine) are eliminated only in part by this mechanism and were shown not to interact with lamivudine. The nucleoside analogues (e.g. didanosine) like zidovudine, are not eliminated by this mechanism and are unlikely to interact with lamivudine.

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): trimethoprim (HOS-085184) ranitidine (HOS-085660) cimetidine (HOS-085835) didanosine (HOS-085836) zidovudine (HOS-085837)

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Version 2026-08-20T14:36:00Z · SHA-256 dda482a8b09324ebc742f0589dd9c287ef99dfaee8f30a2889bc848f23ef2100 · Passage f95f33741513a03415ee49d3475d877bb6b9081af94776eebfc6141682077199 · Zeichen 851–1387 im Abschnitt

Wechselwirkungen · Epivir

Epivir 10 mg/mL oral solution · Abschnitt 4.5 · PDF-Seite 21

HOS-085872 · Präparat HOS-083204

The possibility of interactions with other medicinal products administered concurrently should be considered, particularly when the main route of elimination is active renal secretion via the organic cationic transport system e.g. trimethoprim. Other medicinal products (e.g. ranitidine, cimetidine) are eliminated only in part by this mechanism and were shown not to interact with lamivudine. The nucleoside analogues (e.g. didanosine) like zidovudine, are not eliminated by this mechanism and are unlikely to interact with lamivudine.

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): didanosine (HOS-085836) zidovudine (HOS-085837) trimethoprim (HOS-085184) ranitidine (HOS-085660) cimetidine (HOS-085835)

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Version 2026-08-20T14:36:00Z · SHA-256 dda482a8b09324ebc742f0589dd9c287ef99dfaee8f30a2889bc848f23ef2100 · Passage f95f33741513a03415ee49d3475d877bb6b9081af94776eebfc6141682077199 · Zeichen 851–1387 im Abschnitt

Wechselwirkungen · Combivir

Combivir 150 mg/300 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 7

HOS-088512 · Präparat HOS-083663

Drugs by Therapeutic Area Interaction Recommendation Geometric mean change (%) concerning co- (Possible mechanism) administration ANTIRETROVIRAL MEDICINAL PRODUCTS Didanosine/Lamivudine Interaction not studied. No dosage adjustment necessary. Didanosine /Zidovudine Interaction not studied. Stavudine/Lamivudine Interaction not studied. Combination not Stavudine/Zidovudine In vitro antagonism of anti-HIV recommended. activity between stavudine and zidovudine could result in decreased efficacy of both drugs. ANTI-INFECTIVE PRODUCTS Atovaquone/Lamivudine Interaction not studied. As only limited data available Atovaquone/Zidovudine Zidovudine AUC 33% the clinical significance is (750 mg twice daily with Atovaquone AUC  unknown. food/200 mg thrice daily) Clarithromycin/Lamivudine Interaction not studied. Separate administration of Clarithromycin/Zidovudine Zidovudine AUC 12% Combivir and clarithromycin (500 mg twice daily/100 mg by at least 2 hours every 4 hours) Trimethoprim/sulfamethoxazole Lamivudine: AUC 40% No Combivir dosage (Co-trimoxazole)/Lamivudine adjustment necessary, unless (160 mg/800 mg once daily for Trimethoprim: AUC  patient has renal impairment 5 days/300 mg single dose) Sulfamethoxazole: AUC  (See Section 4.2).

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): didanosine (HOS-085836) stavudine (HOS-088080) atovaquone (HOS-086266) clarithromycin (HOS-084517) trimethoprim (HOS-085184) sulfamethoxazole (HOS-084533)

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Version 2022-08-29T01:24:00Z · SHA-256 4660d55c0813c2571a95614bba44492fff03e6854bbe956eb43509fe476e679d · Passage ef0dd78ec8fb1f808137e8f5128b1cd7fa4540efa9cc39a15103836ffbdd97d9 · Zeichen 1146–3116 im Abschnitt

Wechselwirkungen · Trizivir

TRIZIVIR 300 mg/150 mg/300 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 8

HOS-108560 · Präparat HOS-093047

Drugs by Therapeutic Area Interaction Recommendation Geometric mean change concerning co- (%) administration (Possible mechanism) ANTIRETROVIRAL MEDICINAL PRODUCTS Didanosine/Abacavir Interaction not studied. No dosage adjustment Didanosine/Lamivudine Interaction not studied. necessary. Didanosine/Zidovudine Interaction not studied. Stavudine/Abacavir Interaction not studied. Combination not Stavudine/Lamivudine Interaction not studied. recommended.

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): didanosine (HOS-085836) stavudine (HOS-088080)

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Version 2026-01-19T14:10:00Z · SHA-256 0fa44d429f9cace08dce2fd9d8c4f2ed838fc8cb0ed1b7cfc79bd6b9caa26349 · Passage 25e2eda4712b7995d43a3cb14050be9aa438e6a4898bdc14db6c4e7477aa31e8 · Zeichen 1694–2450 im Abschnitt

Wechselwirkungen · Reyataz

REYATAZ 200 mg hard capsules REYATAZ 300 mg hard capsules · Abschnitt 4.5 · PDF-Seite 11

HOS-112069 · Präparat HOS-093615

The mechanism of interaction between atazanavir and ritonavir is CYP3A4 inhibition. Indinavir Indinavir is associated with indirect Co-administration of REYATAZ unconjugated hyperbilirubinaemia due to and indinavir is not recommended inhibition of UGT. (see section 4.4). Nucleoside/nucleotide reverse transcriptase inhibitors (NRTIs) Lamivudine 150 mg twice daily No significant effect on lamivudine and Based on these data and because + zidovudine 300 mg twice daily zidovudine concentrations was observed. ritonavir is not expected to have a (atazanavir 400 mg once daily) significant impact on the pharmacokinetics of NRTIs, the co- administration of these medicinal products and REYATAZ is not expected to significantly alter the exposure of the co-administered medicinal products. Abacavir The co-administration of abacavir and REYATAZ is not expected to significantly alter the exposure of abacavir. Didanosine (buffered tablets) Atazanavir, simultaneous administration Didanosine should be taken at the 200 mg/stavudine 40 mg, both with ddI+d4T (fasted) fasted state 2 hours after single dose Atazanavir AUC: ↓87% (↓92% ↓79%) REYATAZ taken with food. The (atazanavir 400 mg single dose) Atazanavir Cmax: ↓89% (↓94% ↓82%) co-administration of stavudine with Atazanavir Cmin: ↓84% (↓90% ↓73%) REYATAZ is not expected to significantly alter the exposure of Atazanavir, dosed 1 hr after ddI+d4T stavudine. (fasted) Atazanavir AUC: ↔3% (↓36% ↑67%) Atazanavir Cmax: ↑12% (↓33% ↑18%) Atazanavir Cmin: ↔3% (↓39% ↑73%)

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): ritonavir (HOS-084521) indinavir (HOS-084518) lamivudine (HOS-085829) zidovudine (HOS-085837) abacavir (HOS-088077) didanosine (HOS-085836) stavudine (HOS-088080)

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Version 2026-06-29T13:00:00Z · SHA-256 ff5481974bd7c752b73fa0c147cf3e96fc892edc735359fa71817833db471beb · Passage e16bb7b3c75a72e29e2846a95fde7bf075f1035a1823dc0170957041762fa37d · Zeichen 9816–12649 im Abschnitt

Wechselwirkungen · Kivexa

Kivexa 600 mg/300 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 7

HOS-113477 · Präparat HOS-093937

Drugs by Therapeutic Area Interaction Recommendation concerning Geometric mean change (%) co-administration (Possible mechanism) ANTIRETROVIRAL MEDICINAL PRODUCTS Didanosine /Abacavir Interaction not studied. No dosage adjustment Didanosine/Lamivudine Interaction not studied. necessary. Zidovudine/Abacavir Interaction not studied Zidovudine/Lamivudine Lamivudine: AUC  Zidovudine 300 mg single dose Zidovudine : AUC  Lamivudine 150 mg single dose Emtricitabine/Lamivudine Due to similarities, Kivexa should not be administered concomitantly with other cytidine analogues, such as emtricitabine. ANTI-INFECTIVE PRODUCTS Trimethoprim/sulfamethoxazole Interaction not studied. No Kivexa dosage adjustment (Co-trimoxazole)/Abacavir necessary. Trimethoprim/sulfamethoxazole Lamivudine: AUC 40% (Co-trimoxazole)/Lamivudine When concomitant (160 mg/800 mg once daily for Trimethoprim: AUC  administration with 5 days/300 mg single dose) Sulfamethoxazole: AUC  co-trimoxazole is warranted,

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): didanosine (HOS-085836) zidovudine (HOS-085837) emtricitabine (HOS-085840) trimethoprim (HOS-085184) sulfamethoxazole (HOS-084533)

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Version 2026-01-19T12:00:00Z · SHA-256 014b022d5230b58f7efa74f9573b1c2e42d28f6a3d171aa8848bc0f8c92c1380 · Passage 3b23f2886f7d80d744304e64283fcb23c64e14afd5a52f5e8622a5373e4f7cc1 · Zeichen 1544–3217 im Abschnitt

Wechselwirkungen · Prezista

PREZISTA 100 mg/ml oral suspension · Abschnitt 4.5 · PDF-Seite 11–12

HOS-116342 · Präparat HOS-094447

11 Raltegravir Some clinical studies suggest raltegravir At present the effect of raltegravir may cause a modest decrease in on darunavir plasma darunavir plasma concentrations. concentrations does not appear to be clinically relevant. Boosted PREZISTA and raltegravir can be used without dose adjustments. Nucleo(s/t)ide reverse transcriptase inhibitors (NRTIs) Didanosine didanosine AUC ↓ 9% Boosted PREZISTA and 400 mg once daily didanosine Cmin ND didanosine can be used without didanosine Cmax ↓ 16% dose adjustments. darunavir AUC ↔ Didanosine is to be administered darunavir Cmin ↔ on an empty stomach, thus it darunavir Cmax ↔ should be administered 1 hour before or 2 hours after boosted PREZISTA given with food. Tenofovir disoproxil tenofovir AUC ↑ 22% Monitoring of renal function may 245 mg once daily‡ tenofovir Cmin ↑ 37% be indicated when boosted tenofovir Cmax ↑ 24% PREZISTA is given in # darunavir AUC ↑ 21% combination with tenofovir # darunavir Cmin ↑ 24% disoproxil, particularly in patients # with underlying systemic or renal darunavir Cmax ↑ 16% disease, or in patients taking (↑ tenofovir from effect on MDR-1 nephrotoxic agents. transport in the renal tubules) PREZISTA co-administered with cobicistat lowers the creatinine clearance. Refer to section 4.4 if creatinine clearance is used for dose adjustment of tenofovir disoproxil. Emtricitabine/tenofovir Tenofovir alafenamide ↔ The recommended dose of alafenamide Tenofovir ↑ emtricitabine/tenofovir alafenamide is 200/10 mg once daily when used with boosted PREZISTA. Abacavir Not studied. Based on the different Boosted PREZISTA can be used Emtricitabine elimination pathways of the other NRTIs with these NRTIs without dose Lamivudine zidovudine, emtricitabine, stavudine, adjustment. Stavudine lamivudine, that are primarily renally Zidovudine excreted, and abacavir for which PREZISTA co-administered with metabolism is not mediated by CYP450, cobicistat lowers the creatinine no interactions are expected for these clearance. Refer to section 4.4 if medicinal compounds and boosted creatinine clearance is used for PREZISTA. dose adjustment of emtricitabine or lamivudine.

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): emtricitabine (HOS-085840) tenofovir alafenamide (HOS-110476) creatinine (HOS-086273) raltegravir (HOS-086187) didanosine (HOS-085836) tenofovir disoproxil (HOS-108843) tenofovir (HOS-088083) cobicistat (HOS-088111) abacavir (HOS-088077) lamivudine (HOS-085829) zidovudine (HOS-085837) stavudine (HOS-088080)

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Version 2024-07-26T09:44:00Z · SHA-256 457dafbe8b3b9cee45b9ca7b46919ded598e0d0cd16715525d161e54f80b9117 · Passage 512d9066057a9fd93eb4b013c0f43af18ef8a6621ab7ae5b2a63872300e65b37 · Zeichen 8755–13360 im Abschnitt

Wechselwirkungen · Prezista

PREZISTA 75 mg film-coated tablets PREZISTA 150 mg film-coated tablets PREZISTA 600 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 53–54

HOS-116511 · Präparat HOS-094447

53 Nucleo(s/t)ide reverse transcriptase inhibitors (NRTIs) Didanosine didanosine AUC ↓ 9% PREZISTA co-administered with 400 mg once daily didanosine Cmin ND low dose ritonavir and didanosine didanosine Cmax ↓ 16% can be used without dose darunavir AUC ↔ adjustments. darunavir Cmin ↔ Didanosine is to be administered darunavir Cmax ↔ on an empty stomach, thus it should be administered 1 hour before or 2 hours after PREZISTA/ritonavir given with food. Tenofovir disoproxil tenofovir AUC ↑ 22% Monitoring of renal function may 245 mg once daily‡ tenofovir Cmin ↑ 37% be indicated when PREZISTA tenofovir Cmax ↑ 24% co-administered with low dose # darunavir AUC ↑ 21% ritonavir is given in combination # darunavir Cmin ↑ 24% with tenofovir disoproxil, # particularly in patients with darunavir Cmax ↑ 16% underlying systemic or renal (↑ tenofovir from effect on MDR-1 disease, or in patients taking transport in the renal tubules) nephrotoxic agents. Emtricitabine/tenofovir Tenofovir alafenamide ↔ The recommended dose of alafenamide Tenofovir ↑ emtricitabine/tenofovir alafenamide is 200/10 mg once daily when used with PREZISTA with low dose ritonavir. Abacavir Not studied. Based on the different PREZISTA co-administered with Emtricitabine elimination pathways of the other NRTIs low dose ritonavir can be used Lamivudine zidovudine, emtricitabine, stavudine, with these NRTIs without dose Stavudine lamivudine, that are primarily renally adjustment. Zidovudine excreted, and abacavir for which metabolism is not mediated by CYP450, no interactions are expected for these medicinal compounds and PREZISTA co-administered with low dose ritonavir. Non-nucleo(s/t)ide reverse transcriptase inhibitors (NNRTIs) Efavirenz efavirenz AUC ↑ 21% Clinical monitoring for central 600 mg once daily efavirenz Cmin ↑ 17% nervous system toxicity associated efavirenz Cmax ↑ 15% with increased exposure to # darunavir AUC ↓ 13% efavirenz may be indicated when # darunavir Cmin ↓ 31% PREZISTA co-administered with # low dose ritonavir is given in darunavir Cmax ↓ 15% combination with efavirenz. (↑ efavirenz from CYP3A inhibition) (↓ darunavir from CYP3A induction) Efavirenz in combination with PREZISTA/ritonavir 800/100 mg once daily may result in sub-optimal darunavir Cmin. If efavirenz is to be used in combination with PREZISTA/ritonavir, the PREZISTA/ritonavir 600/100 mg twice daily regimen should be used (see section 4.4). Etravirine etravirine AUC ↓ 37% PREZISTA co-administered with 100 mg twice daily etravirine Cmin ↓ 49% low dose ritonavir and etravirine etravirine Cmax ↓ 32% 200 mg twice daily can be used darunavir AUC ↑ 15% without dose adjustments. darunavir Cmin ↔ darunavir Cmax ↔

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): abacavir (HOS-088077) lamivudine (HOS-085829) zidovudine (HOS-085837) stavudine (HOS-088080) tenofovir alafenamide (HOS-110476) didanosine (HOS-085836) ritonavir (HOS-084521) tenofovir disoproxil (HOS-108843) tenofovir (HOS-088083) emtricitabine (HOS-085840) efavirenz (HOS-087947) etravirine (HOS-088088)

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Version 2024-07-26T09:44:00Z · SHA-256 457dafbe8b3b9cee45b9ca7b46919ded598e0d0cd16715525d161e54f80b9117 · Passage f8ead3f953777de3c19f091bf055bc5528212e16095144f2b7b3940946af839d · Zeichen 6411–12375 im Abschnitt

Wechselwirkungen · Intelence

INTELENCE 25 mg tablets INTELENCE 100 mg tablets INTELENCE 200 mg tablets · Abschnitt 4.5 · PDF-Seite 7

HOS-119733 · Präparat HOS-095005

Table 2: Interactions and dose recommendations with other medicinal products Medicinal products by Effects on drug levels Recommendations therapeutic areas Least Squares Mean Ratio concerning (90% CI; 1.00 = No effect) co-administration ANTI-INFECTIVES Antiretrovirals NRTIs Didanosine didanosine No significant effect on 400 mg once daily AUC ↔ 0.99 (0.79-1.25) didanosine and etravirine PK Cmin ND parameters is seen. Cmax ↔ 0.91 (0.58-1.42) INTELENCE and didanosine etravirine can be used without dose AUC ↔ 1.11 (0.99-1.25) adjustments. Cmin ↔ 1.05 (0.93-1.18) Cmax ↔ 1.16 (1.02-1.32) Tenofovir disoproxil tenofovir No significant effect on 245 mg once dailyb AUC ↔ 1.15 (1.09-1.21) tenofovir and etravirine PK Cmin ↑ 1.19 (1.13-1.26) parameters is seen. Cmax ↑ 1.15 (1.04-1.27) INTELENCE and tenofovir etravirine can be used without dose AUC ↓ 0.81 (0.75-0.88) adjustments. Cmin ↓ 0.82 (0.73-0.91) Cmax ↓ 0.81 (0.75-0.88) Other NRTIs Not studied, but no interaction expected based INTELENCE can be used on the primary renal elimination route for other with these NRTIs without NRTIs (e.g., abacavir, emtricitabine, dose adjustment. lamivudine, stavudine and zidovudine).

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 disoproxil (HOS-108843) tenofovir (HOS-088083) abacavir (HOS-088077) emtricitabine (HOS-085840) lamivudine (HOS-085829) stavudine (HOS-088080) zidovudine (HOS-085837) didanosine (HOS-085836)

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Version 2024-08-13T16:37:00Z · SHA-256 b6b2c3fd3d600c0f1fd17ddc8f6c1da50bcb8b2181089113d0397c5ec46864c4 · Passage f29152615b96440b7358c56a91ccfc38d2ce96481ae99b250502680fed6f7a18 · Zeichen 1742–3928 im Abschnitt

Wechselwirkungen · Triumeq

Triumeq 50 mg/600 mg/300 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 10

HOS-129249 · Präparat HOS-096703

Emtricitabine, didanosine, Interaction not studied Triumeq is not recommended for use in stavudine, zidovudine. combination with emtricitabine containing products, since both lamivudine (in Triumeq) and emtricitabine are cytidine analogues (i.e. risk for intracellular interactions, (see section 4.4)) Protease inhibitors Atazanavir/Dolutegravir Dolutegravir ↑ No dose adjustment is necessary. AUC ↑ 91% Cmax ↑ 50% Cτ ↑ 180%

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): emtricitabine (HOS-085840) didanosine (HOS-085836) stavudine (HOS-088080) zidovudine (HOS-085837) protease (HOS-085623) atazanavir (HOS-086180)

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Version 2026-06-15T14:46:00Z · SHA-256 b49ac3bee235cd6ac4023cc2bbeb8b80e01234448e4e420209ba281a1edf7209 · Passage 3bf10bb4dbff2b9e9a1f2913477a1a9b99c0f91eb5eef71b2dcdb54e9afc81f8 · Zeichen 10865–11769 im Abschnitt

Wechselwirkungen · Triumeq

Triumeq 5 mg/60 mg/30 mg dispersible tablets · Abschnitt 4.5 · PDF-Seite 47

HOS-129348 · Präparat HOS-096703

Emtricitabine, didanosine, Interaction not studied Triumeq is not recommended for use in stavudine, zidovudine. combination with emtricitabine containing products, since both lamivudine (in Triumeq) and emtricitabine are cytidine analogues (i.e. risk for intracellular interactions, (see section 4.4)) Protease inhibitors Atazanavir/Dolutegravir Dolutegravir ↑ No dose adjustment is necessary. AUC ↑ 91% Cmax ↑ 50% Cτ ↑ 180%

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): emtricitabine (HOS-085840) didanosine (HOS-085836) stavudine (HOS-088080) zidovudine (HOS-085837) protease (HOS-085623) atazanavir (HOS-086180)

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Version 2026-06-15T14:46:00Z · SHA-256 b49ac3bee235cd6ac4023cc2bbeb8b80e01234448e4e420209ba281a1edf7209 · Passage 3bf10bb4dbff2b9e9a1f2913477a1a9b99c0f91eb5eef71b2dcdb54e9afc81f8 · Zeichen 9175–10079 im Abschnitt

Wechselwirkungen · Darunavir Viatris (previously Darunavir Mylan)

Darunavir Viatris 75 mg film-coated tablets Darunavir Viatris 150 mg film-coated tablets Darunavir Viatris 300 mg film-coated tablets Darunavir Viatris 600 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 10

HOS-134477 · Präparat HOS-097580

INTERACTIONS AND DOSE RECOMMENDATIONS WITH OTHER MEDICINAL PRODUCTS Medicinal products by Interaction Geometric mean change Recommendations concerning co- therapeutic areas (%) administration HIV ANTIRETROVIRALS Integrase strand transfer inhibitors Dolutegravir dolutegravir AUC ↓ 22% dolutegravir Darunavir co-administered with low C24h ↓ 38% dolutegravir Cmax ↓ 11% dose ritonavir and dolutegravir can darunavir ↔* be used without dose adjustment. * Using cross-study comparisons to historical pharmacokinetic data Raltegravir Some clinical studies suggest At present the effect of raltegravir raltegravir may cause a modest on darunavir plasma concentrations decrease in darunavir plasma does not appear to be clinically concentrations. relevant. Darunavir co-administered with low dose ritonavir and raltegravir can be used without dose adjustments. Nucleo(s/t)ide reverse transcriptase inhibitors (NRTIs) Didanosine didanosine AUC ↓ 9% Darunavir co-administered with low 400 mg once daily didanosine Cmin ND dose ritonavir and didanosine can didanosine Cmax ↓ 16% be used without dose adjustments. darunavir AUC ↔ Didanosine is to be administered on darunavir Cmin ↔ an empty stomach, thus it should be darunavir Cmax ↔ administered 1 hour before or 2 hours after darunavir/ritonavir given with food. Tenofovir disoproxil tenofovir AUC ↑ 22% Monitoring of renal function may 245 mg once daily‡ tenofovir Cmin ↑ 37% be indicated when darunavir co- tenofovir Cmax ↑ 24% administered with low dose # darunavir AUC ↑ 21% ritonavir is given in combination # darunavir Cmin ↑ 24% with tenofovir disoproxil, # darunavir Cmax ↑ 16% particularly in patients with underlying systemic or renal (↑ tenofovir from effect on MDR-1 disease, or in patients taking transport in the renal tubules) nephrotoxic agents. Emtricitabine/tenofovir Tenofovir alafenamide ↔ The recommended dose of alafenamide Tenofovir ↑ emtricitabine/tenofovir alafenamide is 200/10 mg once daily when used with darunavir with low dose ritonavir. Abacavir Not studied. Based on the different Darunavir co-administered with low Emtricitabine elimination pathways of the other dose ritonavir can be used with Lamivudine NRTIs zidovudine, emtricitabine, these NRTIs without dose Stavudine stavudine, lamivudine, that are adjustment. Zidovudine primarily renally excreted, and abacavir for which metabolism is not mediated by CYP450, no interactions are expected for these medicinal compounds and darunavir co- administered with low dose ritonavir.

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 alafenamide (HOS-110476) tenofovir disoproxil (HOS-108843) abacavir (HOS-088077) tenofovir (HOS-088083) lamivudine (HOS-085829) emtricitabine (HOS-085840) dolutegravir (HOS-089992) ritonavir (HOS-084521) raltegravir (HOS-086187) didanosine (HOS-085836) zidovudine (HOS-085837) stavudine (HOS-088080)

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Version 2026-10-20T12:32:00Z · SHA-256 50f4771a683f17214737463c6df88a158b1e699bbb9916413602e547e369e804 · Passage ccba4214faa97b5376d4e4a8ce74635a775924857bc2c674b7028ff519f04d29 · Zeichen 4790–9569 im Abschnitt

Wechselwirkungen · Darunavir Viatris (previously Darunavir Mylan)

Darunavir Viatris 400 mg film-coated tablets Darunavir Viatris 800 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 50–51

HOS-134609 · Präparat HOS-097580

50 INTERACTIONS AND DOSE RECOMMENDATIONS WITH OTHER MEDICINAL PRODUCTS Medicinal products by Interaction Recommendations concerning co- therapeutic areas Geometric mean change (%) administration Nucleo(s/t)ide reverse transcriptase inhibitors (NRTIs) Didanosine didanosine AUC ↓ 9% Boosted darunavir and didanosine 400 mg once daily didanosine Cmin ND can be used without dose didanosine Cmax ↓ 16% adjustments. darunavir AUC ↔ Didanosine is to be administered on darunavir Cmin ↔ an empty stomach, thus it should be darunavir Cmax ↔ administered 1 hour before or 2 hours after boosted darunavir given with food. Tenofovir disoproxil 245 mg tenofovir AUC ↑ 22% Monitoring of renal function may be once daily‡ tenofovir Cmin ↑ 37% indicated when boosted darunavir is tenofovir Cmax ↑ 24% given in combination with tenofovir # darunavir AUC ↑ 21% disoproxil, particularly in patients # darunavir Cmin ↑ 24% with underlying systemic or renal # darunavir Cmax ↑ 16% disease, or in patients taking nephrotoxic agents. (↑ tenofovir from effect on MDR-1 transport in the renal tubules) Darunavir co-administered with cobicistat lowers the creatinine clearance. Refer to section 4.4 if creatinine clearance is used for dose adjustment of tenofovir disoproxil. Emtricitabine/tenofovir Tenofovir alafenamide ↔ The recommended dose of alafenamide Tenofovir ↑ emtricitabine/tenofovir alafenamide is 200/10 mg once daily when used with boosted darunavir. Abacavir Not studied. Based on the different Boosted darunavir can be used with Emtricitabine elimination pathways of the other these NRTIs without dose Lamivudine NRTIs zidovudine, emtricitabine, adjustment. Stavudine stavudine, lamivudine, that are Zidovudine primarily renally excreted, and Darunavir co-administered with abacavir for which metabolism is cobicistat lowers the creatinine not mediated by CYP450, no clearance. Refer to section 4.4 if interactions are expected for these creatinine clearance is used for dose medicinal compounds and boosted adjustment of emtricitabine or darunavir. lamivudine.

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): emtricitabine (HOS-085840) tenofovir alafenamide (HOS-110476) didanosine (HOS-085836) tenofovir disoproxil (HOS-108843) tenofovir (HOS-088083) cobicistat (HOS-088111) creatinine (HOS-086273) abacavir (HOS-088077) lamivudine (HOS-085829) zidovudine (HOS-085837) stavudine (HOS-088080)

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Version 2026-10-20T12:32:00Z · SHA-256 50f4771a683f17214737463c6df88a158b1e699bbb9916413602e547e369e804 · Passage 12f10221f64cd5bd996c35b7dbe8c441b3a4283b2a2e058c57f14f12c78125d7 · Zeichen 9327–13171 im Abschnitt

Wechselwirkungen · Dovato

Dovato 50 mg/300 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 7–8

HOS-142822 · Präparat HOS-098886

7 Nevirapine/Dolutegravir Dolutegravir  The recommended dose of dolutegravir (Not studied, a similar is 50 mg twice daily when reduction in exposure as co-administered with nevirapine. As observed with efavirenz is Dovato is a fixed-dose tablet, an expected, due to additional 50 mg tablet of dolutegravir induction) should be administered, approximately 12 hours after Dovato for the duration of the nevirapine co-administration (a separate formulation of dolutegravir is available for this dose adjustment, see section 4.2). Rilpivirine/Dolutegravir Dolutegravir  No dose adjustment is necessary. AUC  12% Cmax  13% Cτ  22% Rilpivirine  Nucleoside reverse transcriptase inhibitors (NRTIs) Tenofovir disoproxil Dolutegravir  No dose adjustment is necessary when AUC  1% Dovato is combined with tenofovir, Cmax  3% didanosine, stavudine or zidovudine. Cτ  8% Tenofovir  Dovato is not recommended for use in combination with emtricitabine containing products, since both Emtricitabine, didanosine, Interaction not studied lamivudine (in Dovato) and stavudine, tenofovir emtricitabine are cytidine analogues (i.e. alafenamide, zidovudine risk for intracellular interactions), see section 4.4. Protease inhibitors Atazanavir/Dolutegravir Dolutegravir  No dose adjustment is necessary. AUC  91% Cmax  50% C  180%

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): emtricitabine (HOS-085840) protease (HOS-085623) atazanavir (HOS-086180) didanosine (HOS-085836) stavudine (HOS-088080) zidovudine (HOS-085837) nevirapine (HOS-088064) efavirenz (HOS-087947) rilpivirine (HOS-088090) tenofovir disoproxil (HOS-108843) tenofovir (HOS-088083)

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Version 2025-11-14T01:22:00Z · SHA-256 9ebb38c4be2b7abc7ba2934afb44e75aa1d6b86e46ecc069e568b333119de792 · Passage 3a54b7ec17f478707f317729fc54112d075d89e9ca126df050e9dd9dc88cd6d2 · Zeichen 7977–10650 im Abschnitt

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