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.
Wechselwirkungen · Viread
Viread 204 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 95–96
HOS-110705 · Präparat HOS-093385
95
Medicinal product by Effects on drug levels Recommendation
therapeutic areas Mean percent change in AUC, Cmax, Cmin concerning
(dose in mg) co-administration with
245 mg tenofovir disoproxil
Sofosbuvir/Velpatasvir Sofosbuvir: Increased plasma
(400 mg/100 mg q.d.) + AUC: ↓ 29% concentrations of tenofovir
Lopinavir/Ritonavir Cmax: ↓ 41% resulting from
(800 mg/200 mg q.d.) + co-administration of tenofovir
Emtricitabine/Tenofovir GS-3310072: disoproxil,
disoproxil AUC: ↔ sofosbuvir/velpatasvir and
(200 mg/245 mg q.d.) Cmax: ↔ lopinavir/ritonavir may
Cmin: ↔ increase adverse reactions
related to tenofovir disoproxil,
Velpatasvir: including renal disorders. The
AUC: ↔ safety of tenofovir disoproxil
Cmax: ↓ 30% when used with
Cmin: ↑ 63% sofosbuvir/velpatasvir and a
pharmacokinetic enhancer
Lopinavir: (e.g. ritonavir or cobicistat)
AUC: ↔ has not been established.
Cmax: ↔
Cmin: ↔ The combination should be
used with caution with
Ritonavir: frequent renal monitoring (see
AUC: ↔ section 4.4).
Cmax: ↔
Cmin: ↔
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) sofosbuvir (HOS-108928) cobicistat (HOS-088111) velpatasvir (HOS-108929) ritonavir (HOS-084521) emtricitabine (HOS-085840)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2024-02-29T16:34:00Z · SHA-256 ab427f9266bbb81991653ebf14729e0d885f7cb9014fd47e3b3ee4fc69589ee0 · Passage 6ae96ac05a5811e7e9c62d5d1a5ead4f456ef7ff416a2bb8d298cc66aa8cad12 · Zeichen 26038–28373 im Abschnitt
Wechselwirkungen · Viread
Viread 204 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 98–99
HOS-110717 · Präparat HOS-093385
98
Medicinal product by Effects on drug levels Recommendation
therapeutic areas Mean percent change in AUC, Cmax, Cmin concerning
(dose in mg) co-administration with
245 mg tenofovir disoproxil
Sofosbuvir/Velpatasvir/ Sofosbuvir: Increased plasma
Voxilaprevir (400 mg/100 mg/ AUC: ↔ concentrations of tenofovir
100 mg+100 mg q.d.)3 + Cmax: ↓ 30% resulting from co-
Darunavir (800 mg q.d.) + Cmin: N/A administration of tenofovir
Ritonavir (100 mg q.d.) + disoproxil,
Emtricitabine/Tenofovir GS-3310072: sofosbuvir/velpatasvir/voxilap
disoproxil (200 mg/245 mg q.d.) AUC: ↔ revir and darunavir/ritonavir
Cmax:↔ may increase adverse
Cmin: N/A reactions related to tenofovir
disoproxil, including renal
Velpatasvir: disorders.
AUC: ↔ The safety of tenofovir
Cmax: ↔ disoproxil when used with
Cmin: ↔ sofosbuvir/velpatasvir/voxilap
revir and a pharmacokinetic
Voxilaprevir: enhancer (e.g. ritonavir or
AUC: ↑ 143% cobicistat) has not been
Cmax:↑ 72% established.
Cmin: ↑ 300%
The combination should be
Darunavir: used with caution with
AUC: ↔ frequent renal monitoring (see
Cmax: ↔ section 4.4).
Cmin: ↓ 34%
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) sofosbuvir (HOS-108928) cobicistat (HOS-088111) voxilaprevir (HOS-108930) velpatasvir (HOS-108929) darunavir (HOS-086181) ritonavir (HOS-084521) emtricitabine (HOS-085840)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2024-02-29T16:34:00Z · SHA-256 ab427f9266bbb81991653ebf14729e0d885f7cb9014fd47e3b3ee4fc69589ee0 · Passage 08bfdc9714ebdae009fc223c2883980eb82fdcfb11046f8927ba2c44153bbf0d · Zeichen 34101–36770 im Abschnitt
Wechselwirkungen · Viread
Viread 245 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 131–132
HOS-110776 · Präparat HOS-093385
131
Medicinal product by Effects on drug levels Recommendation
therapeutic areas Mean percent change in AUC, Cmax, concerning
(dose in mg) Cmin co-administration with
245 mg tenofovir disoproxil
Entecavir AUC: ↔ No clinically significant
Cmax: ↔ pharmacokinetic interactions
when tenofovir disoproxil was
co-administered with
entecavir.
Hepatitis C virus antiviral agents
Ledipasvir/Sofosbuvir Ledipasvir: Increased plasma
(90 mg/400 mg q.d.) + AUC: ↑ 96% concentrations of tenofovir
Atazanavir/Ritonavir Cmax: ↑ 68% resulting from
(300 mg q.d./100 mg q.d.) + Cmin: ↑ 118% co-administration of tenofovir
Emtricitabine/Tenofovir disoproxil,
disoproxil Sofosbuvir: ledipasvir/sofosbuvir and
(200 mg/245 mg q.d.)1 AUC: ↔ atazanavir/ritonavir may
Cmax: ↔ increase adverse reactions
related to tenofovir disoproxil,
GS-3310072: including renal disorders. The
AUC: ↔ safety of tenofovir disoproxil
Cmax: ↔ when used with
Cmin: ↑ 42% ledipasvir/sofosbuvir and a
pharmacokinetic enhancer
Atazanavir: (e.g. ritonavir or cobicistat)
AUC: ↔ has not been established.
Cmax: ↔
Cmin: ↑ 63% The combination should be
used with caution with
Ritonavir: frequent renal monitoring, if
AUC: ↔ other alternatives are not
Cmax: ↔ available (see section 4.4).
Cmin: ↑ 45%
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) atazanavir (HOS-086180) sofosbuvir (HOS-108928) ledipasvir (HOS-110493) cobicistat (HOS-088111) entecavir (HOS-088124) hepatitis C virus (HOS-108813) ritonavir (HOS-084521) emtricitabine (HOS-085840)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2024-02-29T16:34:00Z · SHA-256 ab427f9266bbb81991653ebf14729e0d885f7cb9014fd47e3b3ee4fc69589ee0 · Passage a376c1607a42c4d6676b873fefa06418f25403bd43d4f4dc6508670201d13343 · Zeichen 8834–11900 im Abschnitt
Wechselwirkungen · Viread
Viread 245 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 132–133
HOS-110780 · Präparat HOS-093385
132
Medicinal product by Effects on drug levels Recommendation
therapeutic areas Mean percent change in AUC, Cmax, concerning
(dose in mg) Cmin co-administration with
245 mg tenofovir disoproxil
Ledipasvir/Sofosbuvir Ledipasvir: Increased plasma
(90 mg/400 mg q.d.) + AUC: ↔ concentrations of tenofovir
Darunavir/Ritonavir Cmax: ↔ resulting from
(800 mg q.d./100 mg q.d.) + Cmin: ↔ co-administration of tenofovir
Emtricitabine/Tenofovir disoproxil,
disoproxil Sofosbuvir: ledipasvir/sofosbuvir and
(200 mg/245 mg q.d.)1 AUC: ↓ 27% darunavir/ritonavir may
Cmax: ↓ 37% increase adverse reactions
related to tenofovir disoproxil,
GS-3310072: including renal disorders. The
AUC: ↔ safety of tenofovir disoproxil
Cmax: ↔ when used with
Cmin: ↔ ledipasvir/sofosbuvir and a
pharmacokinetic enhancer
Darunavir: (e.g. ritonavir or cobicistat)
AUC: ↔ has not been established.
Cmax: ↔
Cmin: ↔ The combination should be
used with caution with
Ritonavir: frequent renal monitoring, if
AUC: ↔ other alternatives are not
Cmax: ↔ available (see section 4.4).
Cmin: ↑ 48%
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) sofosbuvir (HOS-108928) ledipasvir (HOS-110493) cobicistat (HOS-088111) darunavir (HOS-086181) ritonavir (HOS-084521) emtricitabine (HOS-085840)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2024-02-29T16:34:00Z · SHA-256 ab427f9266bbb81991653ebf14729e0d885f7cb9014fd47e3b3ee4fc69589ee0 · Passage f7ee78d7e3dd95ae7870ba9cf2e0437b0a289c066c05c24f4220cb5788c7da78 · Zeichen 12310–14728 im Abschnitt
Wechselwirkungen · Viread
Viread 245 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 135–136
HOS-110792 · Präparat HOS-093385
135
Medicinal product by Effects on drug levels Recommendation
therapeutic areas Mean percent change in AUC, Cmax, concerning
(dose in mg) Cmin co-administration with
245 mg tenofovir disoproxil
Sofosbuvir/Velpatasvir Sofosbuvir: Increased plasma
(400 mg/100 mg q.d.) + AUC: ↔ concentrations of tenofovir
Atazanavir/Ritonavir Cmax: ↔ resulting from
(300 mg q.d./100 mg q.d.) + co-administration of tenofovir
Emtricitabine/Tenofovir GS-3310072: disoproxil,
disoproxil AUC: ↔ sofosbuvir/velpatasvir and
(200 mg/245 mg q.d.) Cmax: ↔ atazanavir/ritonavir may
Cmin: ↑ 42% increase adverse reactions
related to tenofovir disoproxil,
Velpatasvir: including renal disorders. The
AUC: ↑ 142% safety of tenofovir disoproxil
Cmax: ↑ 55% when used with
Cmin: ↑ 301% sofosbuvir/velpatasvir and a
pharmacokinetic enhancer
Atazanavir: (e.g. ritonavir or cobicistat)
AUC: ↔ has not been established.
Cmax: ↔
Cmin: ↑ 39% The combination should be
used with caution with
Ritonavir: frequent renal monitoring (see
AUC: ↔ section 4.4).
Cmax: ↔
Cmin: ↑ 29%
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) atazanavir (HOS-086180) sofosbuvir (HOS-108928) cobicistat (HOS-088111) velpatasvir (HOS-108929) ritonavir (HOS-084521) emtricitabine (HOS-085840)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2024-02-29T16:34:00Z · SHA-256 ab427f9266bbb81991653ebf14729e0d885f7cb9014fd47e3b3ee4fc69589ee0 · Passage 6bc11a6c70f3512e432da0db194c57ebcec0fff6cf72d6382df6c3518153a0cc · Zeichen 20851–23201 im Abschnitt
Wechselwirkungen · Viread
Viread 245 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 136–137
HOS-110794 · Präparat HOS-093385
136
Medicinal product by Effects on drug levels Recommendation
therapeutic areas Mean percent change in AUC, Cmax, concerning
(dose in mg) Cmin co-administration with
245 mg tenofovir disoproxil
Sofosbuvir/Velpatasvir Sofosbuvir: Increased plasma
(400 mg/100 mg q.d.) + AUC: ↓28% concentrations of tenofovir
Darunavir/Ritonavir Cmax: ↓ 38% resulting from
(800 mg q.d./100 mg q.d.) + co-administration of tenofovir
Emtricitabine/Tenofovir GS-3310072: disoproxil,
disoproxil AUC: ↔ sofosbuvir/velpatasvir and
(200 mg/245 mg q.d.) Cmax: ↔ darunavir/ritonavir may
Cmin: ↔ increase adverse reactions
related to tenofovir disoproxil,
Velpatasvir: including renal disorders. The
AUC: ↔ safety of tenofovir disoproxil
Cmax: ↓ 24% when used with
Cmin: ↔ sofosbuvir/velpatasvir and a
pharmacokinetic enhancer
Darunavir: (e.g. ritonavir or cobicistat)
AUC: ↔ has not been established.
Cmax: ↔
Cmin: ↔ The combination should be
used with caution with
Ritonavir: frequent renal monitoring (see
AUC: ↔ section 4.4).
Cmax: ↔
Cmin: ↔
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) sofosbuvir (HOS-108928) cobicistat (HOS-088111) velpatasvir (HOS-108929) darunavir (HOS-086181) ritonavir (HOS-084521) emtricitabine (HOS-085840)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2024-02-29T16:34:00Z · SHA-256 ab427f9266bbb81991653ebf14729e0d885f7cb9014fd47e3b3ee4fc69589ee0 · Passage 3cdab6913229040921e5a749beb676a28837206ae277d2ded2d72de9768f6154 · Zeichen 23575–25920 im Abschnitt
Wechselwirkungen · Viread
Viread 245 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 137–138
HOS-110796 · Präparat HOS-093385
137
Medicinal product by Effects on drug levels Recommendation
therapeutic areas Mean percent change in AUC, Cmax, concerning
(dose in mg) Cmin co-administration with
245 mg tenofovir disoproxil
Sofosbuvir/Velpatasvir Sofosbuvir: Increased plasma
(400 mg/100 mg q.d.) + AUC: ↓ 29% concentrations of tenofovir
Lopinavir/Ritonavir Cmax: ↓ 41% resulting from
(800 mg/200 mg q.d.) + co-administration of tenofovir
Emtricitabine/Tenofovir GS-3310072: disoproxil,
disoproxil AUC: ↔ sofosbuvir/velpatasvir and
(200 mg/245 mg q.d.) Cmax: ↔ lopinavir/ritonavir may
Cmin: ↔ increase adverse reactions
related to tenofovir disoproxil,
Velpatasvir: including renal disorders. The
AUC: ↔ safety of tenofovir disoproxil
Cmax: ↓ 30% when used with
Cmin: ↑ 63% sofosbuvir/velpatasvir and a
pharmacokinetic enhancer
Lopinavir: (e.g. ritonavir or cobicistat)
AUC: ↔ has not been established.
Cmax: ↔
Cmin: ↔ The combination should be
used with caution with
Ritonavir: frequent renal monitoring (see
AUC: ↔ section 4.4).
Cmax: ↔
Cmin: ↔
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) sofosbuvir (HOS-108928) cobicistat (HOS-088111) velpatasvir (HOS-108929) ritonavir (HOS-084521) emtricitabine (HOS-085840)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2024-02-29T16:34:00Z · SHA-256 ab427f9266bbb81991653ebf14729e0d885f7cb9014fd47e3b3ee4fc69589ee0 · Passage 522a7affd652cf50d480f8aefdfe1948990068c4336b6866ac10054e6ddc14d4 · Zeichen 26298–28589 im Abschnitt
Wechselwirkungen · Viread
Viread 245 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 140–141
HOS-110808 · Präparat HOS-093385
140
Medicinal product by Effects on drug levels Recommendation
therapeutic areas Mean percent change in AUC, Cmax, concerning
(dose in mg) Cmin co-administration with
245 mg tenofovir disoproxil
Sofosbuvir/Velpatasvir/ Sofosbuvir: Increased plasma
Voxilaprevir (400 mg/100 mg/ AUC: ↔ concentrations of tenofovir
100 mg+100 mg q.d.)3 + Cmax: ↓ 30% resulting from co-
Darunavir (800 mg q.d.) + Cmin: N/A administration of tenofovir
Ritonavir (100 mg q.d.) + disoproxil,
Emtricitabine/Tenofovir GS-3310072: sofosbuvir/velpatasvir/voxilap
disoproxil (200 mg/245 mg q.d.) AUC: ↔ revir and darunavir/ritonavir
Cmax:↔ may increase adverse
Cmin: N/A reactions related to tenofovir
disoproxil, including renal
Velpatasvir: disorders.
AUC: ↔ The safety of tenofovir
Cmax: ↔ disoproxil when used with
Cmin: ↔ sofosbuvir/velpatasvir/voxilap
revir and a pharmacokinetic
Voxilaprevir: enhancer (e.g. ritonavir or
AUC: ↑ 143% cobicistat) has not been
Cmax:↑ 72% established.
Cmin: ↑ 300%
The combination should be
Darunavir: used with caution with
AUC: ↔ frequent renal monitoring (see
Cmax: ↔ section 4.4).
Cmin: ↓ 34%
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) sofosbuvir (HOS-108928) cobicistat (HOS-088111) voxilaprevir (HOS-108930) velpatasvir (HOS-108929) darunavir (HOS-086181) ritonavir (HOS-084521) emtricitabine (HOS-085840)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2024-02-29T16:34:00Z · SHA-256 ab427f9266bbb81991653ebf14729e0d885f7cb9014fd47e3b3ee4fc69589ee0 · Passage 1b812f6615779168e7bbb1e66905e02e7c6a598c6d263941025e17b15f879d95 · Zeichen 34223–36815 im Abschnitt
Wechselwirkungen · Viread
Viread 33 mg/g granules · Abschnitt 4.5 · PDF-Seite 173–174
HOS-110865 · Präparat HOS-093385
173
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
Adefovir dipivoxil AUC: ↔ Tenofovir disoproxil should not be
Cmax: ↔ administered concurrently with
adefovir dipivoxil
(see section 4.4).
Entecavir AUC: ↔ No clinically significant
Cmax: ↔ pharmacokinetic interactions when
tenofovir disoproxil was
co-administered with entecavir.
Hepatitis C virus antiviral agents
Ledipasvir/Sofosbuvir Ledipasvir: Increased plasma concentrations
(90 mg/400 mg q.d.) + AUC: ↑ 96% of tenofovir resulting from
Atazanavir/Ritonavir Cmax: ↑ 68% co-administration of tenofovir
(300 mg q.d./100 mg q.d.) + Cmin: ↑ 118% disoproxil, ledipasvir/sofosbuvir
Emtricitabine/Tenofovir disoproxil and atazanavir/ritonavir may
(200 mg/245 mg q.d.)1 Sofosbuvir: increase adverse reactions related
AUC: ↔ to tenofovir disoproxil, including
Cmax: ↔ renal disorders. The safety of
tenofovir disoproxil when used
GS-3310072: with ledipasvir/sofosbuvir and a
AUC: ↔ pharmacokinetic enhancer (e.g.
Cmax: ↔ ritonavir or cobicistat) has not
Cmin: ↑ 42% been established.
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) adefovir dipivoxil (HOS-110478) atazanavir (HOS-086180) sofosbuvir (HOS-108928) ledipasvir (HOS-110493) cobicistat (HOS-088111) entecavir (HOS-088124) hepatitis C virus (HOS-108813) ritonavir (HOS-084521) emtricitabine (HOS-085840)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2024-02-29T16:34:00Z · SHA-256 ab427f9266bbb81991653ebf14729e0d885f7cb9014fd47e3b3ee4fc69589ee0 · Passage 5ef9605cacd3719bbe8a65be19e2de178afff577f46d271dfc383395175fe284 · Zeichen 7036–9416 im Abschnitt
Wechselwirkungen · Viread
Viread 33 mg/g granules · Abschnitt 4.5 · PDF-Seite 174–175
HOS-110870 · Präparat HOS-093385
174
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
Ledipasvir/Sofosbuvir Ledipasvir: Increased plasma concentrations
(90 mg/400 mg q.d.) + AUC: ↔ of tenofovir resulting from
Darunavir/Ritonavir Cmax: ↔ co-administration of tenofovir
(800 mg q.d./100 mg q.d.) + Cmin: ↔ disoproxil, ledipasvir/sofosbuvir
Emtricitabine/Tenofovir disoproxil and darunavir/ritonavir may
(200 mg/245 mg q.d.)1 Sofosbuvir: increase adverse reactions related
AUC: ↓ 27% to tenofovir disoproxil, including
Cmax: ↓ 37% renal disorders. The safety of
tenofovir disoproxil when used
GS-3310072: with ledipasvir/sofosbuvir and a
AUC: ↔ pharmacokinetic enhancer (e.g.
Cmax: ↔ ritonavir or cobicistat) has not
Cmin: ↔ been established.
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) sofosbuvir (HOS-108928) ledipasvir (HOS-110493) cobicistat (HOS-088111) darunavir (HOS-086181) ritonavir (HOS-084521) emtricitabine (HOS-085840)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2024-02-29T16:34:00Z · SHA-256 ab427f9266bbb81991653ebf14729e0d885f7cb9014fd47e3b3ee4fc69589ee0 · Passage 4ed85b31d5bd161eb6b921de946cdb215cbd28d4d15301ce59b479a32db6717b · Zeichen 10448–12029 im Abschnitt
Wechselwirkungen · Viread
Viread 33 mg/g granules · Abschnitt 4.5 · PDF-Seite 177–178
HOS-110883 · Präparat HOS-093385
177
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
Sofosbuvir/Velpatasvir Sofosbuvir: Increased plasma concentrations
(400 mg/100 mg q.d.) + AUC: ↔ of tenofovir resulting from
Atazanavir/Ritonavir Cmax: ↔ co-administration of tenofovir
(300 mg q.d./100 mg q.d.) + disoproxil, sofosbuvir/velpatasvir
Emtricitabine/Tenofovir disoproxil GS-3310072: and atazanavir/ritonavir may
(200 mg/245 mg q.d.) AUC: ↔ increase adverse reactions related
Cmax: ↔ to tenofovir disoproxil, including
Cmin: ↑ 42% renal disorders. The safety of
tenofovir disoproxil when used
Velpatasvir: with sofosbuvir/velpatasvir and a
AUC: ↑ 142% pharmacokinetic enhancer (e.g.
Cmax: ↑ 55% ritonavir or cobicistat) has not
Cmin: ↑ 301% been established.
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) atazanavir (HOS-086180) sofosbuvir (HOS-108928) cobicistat (HOS-088111) velpatasvir (HOS-108929) ritonavir (HOS-084521) emtricitabine (HOS-085840)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2024-02-29T16:34:00Z · SHA-256 ab427f9266bbb81991653ebf14729e0d885f7cb9014fd47e3b3ee4fc69589ee0 · Passage 8c5bfc7487f3120d6f6d4e1bd70dadd7df5fdcf39b1e407d38e2a8ce0c91ea11 · Zeichen 18608–20192 im Abschnitt
Wechselwirkungen · Viread
Viread 33 mg/g granules · Abschnitt 4.5 · PDF-Seite 178–179
HOS-110887 · Präparat HOS-093385
178
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
Sofosbuvir/Velpatasvir Sofosbuvir: Increased plasma concentrations
(400 mg/100 mg q.d.) + AUC: ↓28% of tenofovir resulting from
Darunavir/Ritonavir Cmax: ↓ 38% co-administration of tenofovir
(800 mg q.d./100 mg q.d.) + disoproxil, sofosbuvir/velpatasvir
Emtricitabine/Tenofovir disoproxil GS-3310072: and darunavir/ritonavir may
(200 mg/245 mg q.d.) AUC: ↔ increase adverse reactions related
Cmax: ↔ to tenofovir disoproxil, including
Cmin: ↔ renal disorders. The safety of
tenofovir disoproxil when used
Velpatasvir: with sofosbuvir/velpatasvir and a
AUC: ↔ pharmacokinetic enhancer (e.g.
Cmax: ↓ 24% ritonavir or cobicistat) has not
Cmin: ↔ been established.
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) sofosbuvir (HOS-108928) cobicistat (HOS-088111) velpatasvir (HOS-108929) darunavir (HOS-086181) ritonavir (HOS-084521) emtricitabine (HOS-085840)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2024-02-29T16:34:00Z · SHA-256 ab427f9266bbb81991653ebf14729e0d885f7cb9014fd47e3b3ee4fc69589ee0 · Passage 22c646a4fca2d85f7d7e8f3db628f4cc568f47de67ec24e4fb95329462c644d3 · Zeichen 21164–22747 im Abschnitt
Wechselwirkungen · Viread
Viread 33 mg/g granules · Abschnitt 4.5 · PDF-Seite 179–180
HOS-110891 · Präparat HOS-093385
179
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
Sofosbuvir/Velpatasvir Sofosbuvir: Increased plasma concentrations
(400 mg/100 mg q.d.) + AUC: ↓ 29% of tenofovir resulting from
Lopinavir/Ritonavir Cmax: ↓ 41% co-administration of tenofovir
(800 mg/200 mg q.d.) + disoproxil, sofosbuvir/velpatasvir
Emtricitabine/Tenofovir disoproxil GS-3310072: and lopinavir/ritonavir may
(200 mg/245 mg q.d.) AUC: ↔ increase adverse reactions related
Cmax: ↔ to tenofovir disoproxil, including
Cmin: ↔ renal disorders. The safety of
tenofovir disoproxil when used
Velpatasvir: with sofosbuvir/velpatasvir and a
AUC: ↔ pharmacokinetic enhancer (e.g.
Cmax: ↓ 30% ritonavir or cobicistat) has not
Cmin: ↑ 63% been established.
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) sofosbuvir (HOS-108928) cobicistat (HOS-088111) velpatasvir (HOS-108929) ritonavir (HOS-084521) emtricitabine (HOS-085840)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2024-02-29T16:34:00Z · SHA-256 ab427f9266bbb81991653ebf14729e0d885f7cb9014fd47e3b3ee4fc69589ee0 · Passage 403999cbf82d6706d8f63fb3ef0f3fd09bf8489b1b7d703dd61cc8174ad69373 · Zeichen 23715–25298 im Abschnitt
Wechselwirkungen · Viread
Viread 33 mg/g granules · Abschnitt 4.5 · PDF-Seite 182–183
HOS-110902 · Präparat HOS-093385
182
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
Sofosbuvir/Velpatasvir/ Sofosbuvir: Increased plasma concentrations
Voxilaprevir (400 mg/100 mg/ AUC: ↔ of tenofovir resulting from co-
100 mg+100 mg q.d.)3 + Darunavir Cmax: ↓ 30% administration of tenofovir
(800 mg q.d.) + Ritonavir (100 mg Cmin: N/A disoproxil,
q.d.) + Emtricitabine/Tenofovir sofosbuvir/velpatasvir/voxilaprevir
disoproxil (200 mg/245 mg q.d.) GS-3310072: and darunavir/ritonavir may
AUC: ↔ increase adverse reactions related
Cmax:↔ to tenofovir disoproxil, including
Cmin: N/A renal disorders.
The safety of tenofovir disoproxil
Velpatasvir: when used with
AUC: ↔ sofosbuvir/velpatasvir/voxilaprevir
Cmax: ↔ and a pharmacokinetic enhancer
Cmin: ↔ (e.g. ritonavir or cobicistat) has
not been established.
Voxilaprevir:
AUC: ↑ 143% The combination should be used
Cmax:↑ 72% with caution with frequent renal
Cmin: ↑ 300% monitoring (see section 4.4).
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) sofosbuvir (HOS-108928) cobicistat (HOS-088111) voxilaprevir (HOS-108930) velpatasvir (HOS-108929) darunavir (HOS-086181) ritonavir (HOS-084521) emtricitabine (HOS-085840)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2024-02-29T16:34:00Z · SHA-256 ab427f9266bbb81991653ebf14729e0d885f7cb9014fd47e3b3ee4fc69589ee0 · Passage f1e3a130c6292f9af5a597bb67ae8827c963cffc119eacc7b6e7c429321bc0da · Zeichen 31726–33799 im Abschnitt
Wechselwirkungen · Truvada
Truvada 200 mg/245 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 12
HOS-113726 · Präparat HOS-093961
Tenofovir:
AUC: ↓ 2% (↓ 5 to ↑ 0)
Cmax: ↓ 1% (↓ 7 to ↑ 6)
Cmin: NC
Hepatitis C virus (HCV) antiviral agents
Ledipasvir/Sofosbuvir Ledipasvir: Increased plasma concentrations
(90 mg/400 mg q.d.) + AUC: ↑ 96% (↑ 74 to ↑ 121) of tenofovir resulting from
Atazanavir/Ritonavir Cmax: ↑ 68% (↑ 54 to ↑ 84) co-administration of tenofovir
(300 mg q.d./100 mg q.d.) + Cmin: ↑ 118% (↑ 91 to ↑ 150) disoproxil, ledipasvir/sofosbuvir
Emtricitabine/Tenofovir disoproxil and atazanavir/ritonavir may
(200 mg/245 mg q.d.)1 Sofosbuvir: increase adverse reactions related
AUC: ↔ to tenofovir disoproxil, including
Cmax: ↔ renal disorders. The safety of
tenofovir disoproxil when used
GS-3310072: with ledipasvir/sofosbuvir and a
AUC: ↔ pharmacokinetic enhancer (e.g.
Cmax: ↔ ritonavir or cobicistat) has not
Cmin: ↑ 42% (↑ 34 to ↑ 49) been established.
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) atazanavir (HOS-086180) sofosbuvir (HOS-108928) ledipasvir (HOS-110493) cobicistat (HOS-088111) hepatitis C virus (HOS-108813) ritonavir (HOS-084521)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2024-02-29T18:10:00Z · SHA-256 c649f98085684f03838a5e69a1a4e7a871850d61dfdc001f745e6b31db212087 · Passage 036f429b643f0e27b6cbf765f88080762e068efbc27b6624fbf75c16b828aa67 · Zeichen 10432–11945 im Abschnitt
Wechselwirkungen · Truvada
Truvada 200 mg/245 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 12–13
HOS-113731 · Präparat HOS-093961
12
Medicinal product by Effects on drug levels Recommendation concerning
therapeutic areas Mean percent change in AUC, co-administration with Truvada
Cmax, Cmin with 90% confidence (emtricitabine 200 mg, tenofovir
intervals if available disoproxil 245 mg)
(mechanism)
Ledipasvir/Sofosbuvir Ledipasvir: Increased plasma concentrations
(90 mg/400 mg q.d.) + AUC: ↔ of tenofovir resulting from
Darunavir/Ritonavir Cmax: ↔ co-administration of tenofovir
(800 mg q.d./100 mg q.d.) + Cmin: ↔ disoproxil, ledipasvir/sofosbuvir
Emtricitabine/Tenofovir disoproxil and darunavir/ritonavir may
(200 mg/245 mg q.d.)1 Sofosbuvir: increase adverse reactions related
AUC: ↓ 27% (↓ 35 to ↓ 18) to tenofovir disoproxil, including
Cmax: ↓ 37% (↓ 48 to ↓ 25) renal disorders. The safety of
tenofovir disoproxil when used
GS-3310072: with ledipasvir/sofosbuvir and a
AUC: ↔ pharmacokinetic enhancer (e.g.
Cmax: ↔ ritonavir or cobicistat) has not
Cmin: ↔ been established.
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) sofosbuvir (HOS-108928) ledipasvir (HOS-110493) cobicistat (HOS-088111) darunavir (HOS-086181) ritonavir (HOS-084521)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2024-02-29T18:10:00Z · SHA-256 c649f98085684f03838a5e69a1a4e7a871850d61dfdc001f745e6b31db212087 · Passage 6bc6215033fa064ae3735ee2398ec0d40ede7e0675029804bac473c0b6ab2604 · Zeichen 13013–14783 im Abschnitt
Wechselwirkungen · Truvada
Truvada 200 mg/245 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 15–16
HOS-113745 · Präparat HOS-093961
15
Medicinal product by Effects on drug levels Recommendation concerning
therapeutic areas Mean percent change in AUC, co-administration with Truvada
Cmax, Cmin with 90% confidence (emtricitabine 200 mg, tenofovir
intervals if available disoproxil 245 mg)
(mechanism)
Sofosbuvir/Velpatasvir Sofosbuvir: Increased plasma concentrations
(400 mg/100 mg q.d.) + AUC: ↔ of tenofovir resulting from
Atazanavir/Ritonavir Cmax: ↔ co-administration of tenofovir
(300 mg q.d./100 mg q.d.) + disoproxil, sofosbuvir/velpatasvir
Emtricitabine/Tenofovir disoproxil GS-3310072: and atazanavir/ritonavir may
(200 mg/245 mg q.d.) AUC: ↔ increase adverse reactions related
Cmax: ↔ to tenofovir disoproxil, including
Cmin: ↑ 42% (↑ 37 to ↑ 49) renal disorders. The safety of
tenofovir disoproxil when used
Velpatasvir: with sofosbuvir/velpatasvir and a
AUC: ↑ 142% (↑ 123 to ↑ 164) pharmacokinetic enhancer (e.g.
Cmax: ↑ 55% (↑ 41 to ↑ 71) ritonavir or cobicistat) has not
Cmin: ↑ 301% (↑ 257 to ↑ 350) been established.
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) atazanavir (HOS-086180) sofosbuvir (HOS-108928) cobicistat (HOS-088111) velpatasvir (HOS-108929) ritonavir (HOS-084521)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2024-02-29T18:10:00Z · SHA-256 c649f98085684f03838a5e69a1a4e7a871850d61dfdc001f745e6b31db212087 · Passage 570eb1d908b5838404a6db78f9d34cf72a69c2c9b6bad76f351c948a5aab123f · Zeichen 21732–23470 im Abschnitt
Wechselwirkungen · Truvada
Truvada 200 mg/245 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 16–17
HOS-113749 · Präparat HOS-093961
16
Medicinal product by Effects on drug levels Recommendation concerning
therapeutic areas Mean percent change in AUC, co-administration with Truvada
Cmax, Cmin with 90% confidence (emtricitabine 200 mg, tenofovir
intervals if available disoproxil 245 mg)
(mechanism)
Sofosbuvir/Velpatasvir Sofosbuvir: Increased plasma concentrations
(400 mg/100 mg q.d.) + AUC: ↓ 28% (↓ 34 to ↓ 20) of tenofovir resulting from
Darunavir/Ritonavir Cmax: ↓ 38% (↓ 46 to ↓ 29) co-administration of tenofovir
(800 mg q.d./100 mg q.d.) + disoproxil, sofosbuvir/velpatasvir
Emtricitabine/Tenofovir disoproxil GS-3310072: and darunavir/ritonavir may
(200 mg/245 mg q.d.) AUC: ↔ increase adverse reactions related
Cmax: ↔ to tenofovir disoproxil, including
Cmin: ↔ renal disorders. The safety of
tenofovir disoproxil when used
Velpatasvir: with sofosbuvir/velpatasvir and a
AUC: ↔ pharmacokinetic enhancer (e.g.
Cmax: ↓ 24% (↓ 35 to ↓ 11) ritonavir or cobicistat) has not
Cmin: ↔ been established.
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) sofosbuvir (HOS-108928) cobicistat (HOS-088111) velpatasvir (HOS-108929) darunavir (HOS-086181) ritonavir (HOS-084521)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2024-02-29T18:10:00Z · SHA-256 c649f98085684f03838a5e69a1a4e7a871850d61dfdc001f745e6b31db212087 · Passage 98da0659d1b4f56022a84592fd6870d90e29bfa6968616439e8532c06ff20bf2 · Zeichen 24505–26242 im Abschnitt
Wechselwirkungen · Truvada
Truvada 200 mg/245 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 17–18
HOS-113753 · Präparat HOS-093961
17
Medicinal product by Effects on drug levels Recommendation concerning
therapeutic areas Mean percent change in AUC, co-administration with Truvada
Cmax, Cmin with 90% confidence (emtricitabine 200 mg, tenofovir
intervals if available disoproxil 245 mg)
(mechanism)
Sofosbuvir/Velpatasvir Sofosbuvir: Increased plasma concentrations
(400 mg/100 mg q.d.) + AUC: ↓ 29% (↓ 36 to ↓ 22) of tenofovir resulting from
Lopinavir/Ritonavir Cmax: ↓ 41% (↓ 51 to ↓ 29) co-administration of tenofovir
(800 mg/200 mg q.d.) + disoproxil, sofosbuvir/velpatasvir
Emtricitabine/Tenofovir disoproxil GS-3310072: and lopinavir/ritonavir may
(200 mg/245 mg q.d.) AUC: ↔ increase adverse reactions related
Cmax: ↔ to tenofovir disoproxil, including
Cmin: ↔ renal disorders. The safety of
tenofovir disoproxil when used
Velpatasvir: with sofosbuvir/velpatasvir and a
AUC: ↔ pharmacokinetic enhancer (e.g.
Cmax: ↓ 30% (↓ 41 to ↓ 17) ritonavir or cobicistat) has not
Cmin: ↑ 63% (↑ 43 to ↑ 85) been established.
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) sofosbuvir (HOS-108928) cobicistat (HOS-088111) velpatasvir (HOS-108929) ritonavir (HOS-084521)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2024-02-29T18:10:00Z · SHA-256 c649f98085684f03838a5e69a1a4e7a871850d61dfdc001f745e6b31db212087 · Passage da1320a696e4ce80fb3bdbf7eb388c83381f4c80390654f296710643bd0c1e8b · Zeichen 27258–28995 im Abschnitt
Wechselwirkungen · Truvada
Truvada 200 mg/245 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 20–21
HOS-113766 · Präparat HOS-093961
20
Medicinal product by Effects on drug levels Recommendation concerning
therapeutic areas Mean percent change in AUC, co-administration with Truvada
Cmax, Cmin with 90% confidence (emtricitabine 200 mg, tenofovir
intervals if available disoproxil 245 mg)
(mechanism)
Sofosbuvir/Velpatasvir/ Sofosbuvir: Increased plasma concentrations
Voxilaprevir (400 mg/100 mg/ AUC: ↔ of tenofovir resulting from
100 mg+100 mg q.d.)3 + Darunavir Cmax: ↓ 30% co-administration of tenofovir
(800 mg q.d.) + Ritonavir (100 mg Cmin: N/A disoproxil,
q.d.) + Emtricitabine/Tenofovir sofosbuvir/velpatasvir/voxilaprevir
disoproxil (200 mg/245 mg q.d.) GS-3310072: and darunavir/ritonavir may
AUC: ↔ increase adverse reactions related
Cmax:↔ to tenofovir disoproxil, including
Cmin: N/A renal disorders. The safety of
tenofovir disoproxil when used
Velpatasvir: with
AUC: ↔ sofosbuvir/velpatasvir/voxilaprevir
Cmax: ↔ and a pharmacokinetic enhancer
Cmin: ↔ (e.g. ritonavir or cobicistat) has
not been established.
Voxilaprevir:
AUC: ↑ 143% The combination should be used
Cmax:↑ 72% with caution with frequent renal
Cmin: ↑ 300% monitoring (see section 4.4).
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) sofosbuvir (HOS-108928) cobicistat (HOS-088111) voxilaprevir (HOS-108930) velpatasvir (HOS-108929) darunavir (HOS-086181) ritonavir (HOS-084521)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2024-02-29T18:10:00Z · SHA-256 c649f98085684f03838a5e69a1a4e7a871850d61dfdc001f745e6b31db212087 · Passage 6f74481580b8c90cf6fd65a3d6dad6640dce90b9ce96ade7696611e97706e566 · Zeichen 35883–38152 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.