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 · Kaletra
Kaletra (80 mg + 20 mg) / ml oral solution · Abschnitt 4.5 · PDF-Seite 23–24
HOS-108925 · Präparat HOS-093083
23
Glecaprevir/pibrentasvir Serum concentrations may be Concomitant administration of
increased due to P-glycoprotein, glecaprevir/pibrentasvir and
BCRP and OATP1B inhibition by Kaletra is not recommended due
lopinavir/ritonavir. to an increased risk of ALT
elevations associated with
increased glecaprevir exposure.
Sofosbuvir/velpatasvir/ Serum concentrations of It is not recommended to
voxilaprevir sofosbuvir, velpatasvir and coadminister Kaletra and
voxilaprevir may be increased due sofosbuvir/velpatasvir/
to P-glycoprotein, BCRP and voxilaprevir.
OATP1B1/3 inhibition by
lopinavir/ritonavir. However,
only the increase in voxilaprevir
exposure is considered clinically
relevant.
HCV protease inhibitors
Simeprevir 200 mg daily Simeprevir: It is not recommended to
(ritonavir 100 mg BID) AUC: ↑ 7.2-fold co-administer Kaletra and
Cmax: ↑ 4.7-fold simeprevir.
Cmin: ↑ 14.4-fold
Herbal products
St John’s wort (Hypericum Lopinavir: Herbal preparations containing St
perforatum) Concentrations may be reduced John’s wort must not be combined
due to induction of CYP3A by the with lopinavir and ritonavir. If a
herbal preparation St John’s wort. patient is already taking St John’s
wort, stop St John’s wort and if
possible check viral levels.
Lopinavir and ritonavir levels may
increase on stopping
St John’s wort. The dose of
Kaletra may need adjusting. The
inducing effect may persist for at
least 2 weeks after cessation of
treatment with St John’s wort (see
section 4.3). Therefore, Kaletra
can be started safely 2 weeks after
cessation of St John's wort.
Immunosuppressants
Cyclosporin, Sirolimus Cyclosporin, Sirolimus More frequent therapeutic
(rapamycin), and (rapamycin), Tacrolimus: concentration monitoring is
Tacrolimus Concentrations may be increased recommended until plasma levels
due to CYP3A inhibition by of these products have been
lopinavir/ritonavir. stabilised.
Lipid lowering agents
Lovastatin and Simvastatin Lovastatin, Simvastatin: Since increased concentrations of
Markedly increased plasma HMG-CoA reductase inhibitors
concentrations due to CYP3A may cause myopathy, including
inhibition by lopinavir/ritonavir. rhabdomyolysis, the combination
of these agents with Kaletra is
contraindicated (see section 4.3).
Lipid-modifying agents
Lomitapide CYP3A4 inhibitors increase the Concomitant use of Kaletra with
exposure of lomitapide, with lomitapide is contraindicated (see
strong inhibitors increasing prescribing information for
exposure approximately 27-fold. lomitapide) (see section 4.3).
Due to CYP3A inhibition by
lopinavir/ritonavir, concentrations
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): sofosbuvir (HOS-108928) protease (HOS-085623) lovastatin (HOS-086157) pibrentasvir (HOS-086298) lomitapide (HOS-086160) simvastatin (HOS-086158) glecaprevir (HOS-086297) voxilaprevir (HOS-108930) tacrolimus (HOS-085202) velpatasvir (HOS-108929) simeprevir (HOS-086302) sirolimus (HOS-085172)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2025-12-02T16:00:00Z · SHA-256 441d9e5f9e4b42d645e4bd802abc892cef6574b0be5b3f18d2a96678774ae365 · Passage d661859df9e7416124e84f058321f8363c31c96c6c3cbfadb04946272feb4ff7 · Zeichen 52766–57555 im Abschnitt
Wechselwirkungen · Kaletra
Kaletra 200 mg/50 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 59
HOS-109021 · Präparat HOS-093083
Lopinavir: ↔
Glecaprevir/pibrentasvir Serum concentrations may be Concomitant administration of
increased due to P-glycoprotein, glecaprevir/pibrentasvir and Kaletra
BCRP and OATP1B inhibition by is not recommended due to an
lopinavir/ritonavir. increased risk of ALT elevations
associated with increased glecaprevir
exposure.
Sofosbuvir/velpatasvir/ Serum concentrations of It is not recommended to
voxilaprevir sofosbuvir, velpatasvir and coadminister Kaletra and
voxilaprevir may be increased due sofosbuvir/velpatasvir/ voxilaprevir.
to P-glycoprotein, BCRP and
OATP1B1/3 inhibition by
lopinavir/ritonavir. However, only
the increase in voxilaprevir
exposure is considered clinically
relevant.
HCV protease inhibitors
Simeprevir 200 mg Simeprevir: It is not recommended to
daily (ritonavir 100 mg AUC: ↑ 7.2-fold co-administer Kaletra and simeprevir.
BID) Cmax: ↑ 4.7-fold
Cmin: ↑ 14.4-fold
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): sofosbuvir (HOS-108928) protease (HOS-085623) pibrentasvir (HOS-086298) glecaprevir (HOS-086297) voxilaprevir (HOS-108930) velpatasvir (HOS-108929) simeprevir (HOS-086302)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2025-12-02T16:00:00Z · SHA-256 441d9e5f9e4b42d645e4bd802abc892cef6574b0be5b3f18d2a96678774ae365 · Passage a7ffd699710dfcc905a1f28162df38c655a626dd6695d2536a15fef3b5c330fb · Zeichen 50777–52256 im Abschnitt
Wechselwirkungen · Kaletra
Kaletra 100 mg/25 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 94–95
HOS-109100 · Präparat HOS-093083
94
Sofosbuvir/velpatasvir/ Serum concentrations of It is not recommended to
voxilaprevir sofosbuvir, velpatasvir and coadminister Kaletra and
voxilaprevir may be increased due sofosbuvir/velpatasvir/
to P-glycoprotein, BCRP and voxilaprevir.
OATP1B1/3 inhibition by
lopinavir/ritonavir. However, only
the increase in voxilaprevir
exposure is considered clinically
relevant.
HCV protease inhibitors
Simeprevir 200 mg Simeprevir: It is not recommended to
daily (ritonavir 100 mg AUC: ↑ 7.2-fold co-administer Kaletra and
BID) Cmax: ↑ 4.7-fold simeprevir.
Cmin: ↑ 14.4-fold
Herbal products
St John’s wort Lopinavir: Herbal preparations containing St
(Hypericum perforatum) Concentrations may be reduced John’s wort must not be combined
due to induction of CYP3A by the with lopinavir and ritonavir. If a
herbal preparation St John’s wort. patient is already taking St John’s
wort, stop St John’s wort and if
possible check viral levels.
Lopinavir and ritonavir levels may
increase on stopping St John’s wort.
The dose of Kaletra may need
adjusting. The inducing effect may
persist for at least 2 weeks after
cessation of treatment with St
John’s wort (see section 4.3).
Therefore, Kaletra can be started
safely 2 weeks after cessation of St
John's wort.
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): sofosbuvir (HOS-108928) protease (HOS-085623) voxilaprevir (HOS-108930) velpatasvir (HOS-108929) simeprevir (HOS-086302)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2025-12-02T16:00:00Z · SHA-256 441d9e5f9e4b42d645e4bd802abc892cef6574b0be5b3f18d2a96678774ae365 · Passage ee23650cbabf756b8993f6c87d5c69ed1f0fde54c3889133693585c6c3314a93 · Zeichen 52603–55069 im Abschnitt
Gegenanzeigen · Evra
EVRA 203 micrograms/24 hours + 33.9 micrograms/24 hours transdermal patch · Abschnitt 4.3 · PDF-Seite 5–6
HOS-110299 · Präparat HOS-093363
5
• Presence or risk of arterial thromboembolism (ATE)
• Arterial thromboembolism – current arterial thromboembolism, history of arterial
thromboembolism (e.g. myocardial infarction) or prodromal condition (e.g. angina
pectoris);
• Cerebrovascular disease – current stroke, history of stroke or prodromal condition
(e.g. transient ischaemic attack, TIA);
• Known hereditary or acquired predisposition for arterial thromboembolism, such as
hyperhomocysteinaemia and antiphospholipid-antibodies (anticardiolipin-antibodies,
lupus anticoagulant);
• History of migraine with focal neurological symptoms;
• A high risk of arterial thromboembolism due to multiple risk factors (see section 4.4) or
to the presence of one serious risk factor such as:
- diabetes mellitus with vascular symptoms
- severe hypertension
- severe dyslipoproteinaemia
• Hypersensitivity to the active substances or to any of the excipients listed in section 6.1
• Known or suspected carcinoma of the breast
• Carcinoma of the endometrium or other known or suspected oestrogen-dependent neoplasia
• Abnormal liver function related to acute or chronic hepatocellular disease
• Hepatic adenomas or carcinomas
• Undiagnosed abnormal genital bleeding
• Concomitant use with the medicinal products containing ombitasvir/paritaprevir/ritonavir and
dasabuvir, medicinal products containing glecaprevir/pibrentasvir or
sofosbuvir/velpatasvir/voxilaprevir (see section 4.5).
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): sofosbuvir (HOS-108928) pibrentasvir (HOS-086298) glecaprevir (HOS-086297) dasabuvir (HOS-110302) voxilaprevir (HOS-108930) ombitasvir (HOS-110300) velpatasvir (HOS-108929) ritonavir (HOS-084521) paritaprevir (HOS-110301)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2025-04-22T17:22:00Z · SHA-256 08ee5b4a9562d12725bc2847cb5a881102ab4ddbaaf7c1a2e28b65b78fd2ab5d · Passage 0b84b4ce379340aec479b3699d0b67d6f02d4b453bb9a5e3d40b02692d6515fc · Zeichen 895–2550 im Abschnitt
Wechselwirkungen · Evra
EVRA 203 micrograms/24 hours + 33.9 micrograms/24 hours transdermal patch · Abschnitt 4.5 · PDF-Seite 11
HOS-110304 · Präparat HOS-093363
Pharmacodynamic interactions
During clinical trials with patients treated for hepatitis C virus infections (HCV) with medicinal
products containing ombitasvir/paritaprevir/ritonavir and dasabuvir with or without ribavirin,
transaminase (ALT) elevations higher than 5 times the upper limit of normal (ULN) occurred
significantly more frequently in women using ethinyl estradiol-containing medications such as
combined hormonal contraceptives (CHCs). Additionally, also in patients treated with
glecaprevir/pibrentasvir or sofosbuvir/velpatasvir/voxilaprevir, ALT elevations were observed in
women using ethinyl estradiol-containing medications such as CHCs (see section 4.3).
Therefore, EVRA-users must switch to an alternative method of contraception (e.g., progestagen-only
contraception or non-hormonal methods) prior to starting therapy with these combination drug
regimens. EVRA can be restarted 2 weeks following completion of treatment with these combination
drug regimens.
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): sofosbuvir (HOS-108928) pibrentasvir (HOS-086298) glecaprevir (HOS-086297) hepatitis C virus (HOS-108813) ribavirin (HOS-088127) dasabuvir (HOS-110302) voxilaprevir (HOS-108930) ombitasvir (HOS-110300) velpatasvir (HOS-108929) ritonavir (HOS-084521) paritaprevir (HOS-110301)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2025-04-22T17:22:00Z · SHA-256 08ee5b4a9562d12725bc2847cb5a881102ab4ddbaaf7c1a2e28b65b78fd2ab5d · Passage a2c9d2476ababdf6aa70cd37d7f709e3b0de8b4455edc5193e41c8ca51311e4e · Zeichen 125–1104 im Abschnitt
Wechselwirkungen · Viread
Viread 123 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 13–14
HOS-110514 · Präparat HOS-093385
13
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 a352840ea53b0c7aa2c2c1477faa3502b999395202d25ef8a0192525e4dfa26d · Zeichen 18217–19800 im Abschnitt
Wechselwirkungen · Viread
Viread 123 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 14–15
HOS-110518 · Präparat HOS-093385
14
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 737e46afeb9439dde410899a01dd79d8a2f0e067b384f6b1c089de70a2e4dede · Zeichen 20772–22354 im Abschnitt
Wechselwirkungen · Viread
Viread 123 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 15–16
HOS-110522 · Präparat HOS-093385
15
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 26c0232f6e9aca312defaa3abb7db0177d9af751e67aef58f622af58ce0b6a51 · Zeichen 23322–24904 im Abschnitt
Wechselwirkungen · Viread
Viread 123 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 16–17
HOS-110525 · Präparat HOS-093385
16
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: No dose adjustment is
(400 mg/100 mg q.d.) + AUC: ↔ recommended. The increased
Raltegravir Cmax: ↔ exposure of tenofovir could
(400 mg b.i.d) + potentiate adverse reactions
Emtricitabine/Tenofovir disoproxil GS-3310072: associated with tenofovir
(200 mg/245 mg q.d.) AUC: ↔ disoproxil, including renal
Cmax: ↔ disorders. Renal function should
Cmin: ↔ be closely monitored (see
section 4.4).
Velpatasvir:
AUC: ↔
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) velpatasvir (HOS-108929) raltegravir (HOS-086187) emtricitabine (HOS-085840)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2024-02-29T16:34:00Z · SHA-256 ab427f9266bbb81991653ebf14729e0d885f7cb9014fd47e3b3ee4fc69589ee0 · Passage 966a3427a78d47bcc95eb523705319fb15c2f308fe708ed9b5a99fd363633252 · Zeichen 25864–27187 im Abschnitt
Wechselwirkungen · Viread
Viread 123 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 17
HOS-110527 · Präparat HOS-093385
Tenofovir:
AUC: ↑ 40%
Cmax: ↑ 46%
Cmin: ↑ 70%
Sofosbuvir/Velpatasvir Sofosbuvir: Concomitant administration of
(400 mg/100 mg q.d.) + AUC: ↔ sofosbuvir/velpatasvir and
Efavirenz/Emtricitabine/Tenofovir Cmax: ↑ 38% efavirenz is expected to decrease
disoproxil plasma concentrations of
(600 mg/200 mg/245 mg q.d.) GS-3310072: velpatasvir. Co-administration of
AUC: ↔ sofosbuvir/velpatasvir with
Cmax: ↔ efavirenz-containing regimens is
Cmin: ↔ not 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): tenofovir (HOS-088083) sofosbuvir (HOS-108928) velpatasvir (HOS-108929) efavirenz (HOS-087947) emtricitabine (HOS-085840)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2024-02-29T16:34:00Z · SHA-256 ab427f9266bbb81991653ebf14729e0d885f7cb9014fd47e3b3ee4fc69589ee0 · Passage 19af9fb82c372f5c469cbedf4451efbe959c7dc1bb44317e7ac3acbbd33aaeea · Zeichen 27602–28530 im Abschnitt
Wechselwirkungen · Viread
Viread 123 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 17
HOS-110528 · Präparat HOS-093385
Velpatasvir:
AUC: ↓ 53%
Cmax: ↓ 47%
Cmin: ↓ 57%
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): velpatasvir (HOS-108929)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2024-02-29T16:34:00Z · SHA-256 ab427f9266bbb81991653ebf14729e0d885f7cb9014fd47e3b3ee4fc69589ee0 · Passage 9c54a520a26ffac986ee2757f7d253f80b8bd75bac6b7305d1641ab8bfbc7d0c · Zeichen 28569–28727 im Abschnitt
Wechselwirkungen · Viread
Viread 123 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 17–18
HOS-110531 · Präparat HOS-093385
17
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: No dose adjustment is
(400 mg/100 mg q.d.) + AUC: ↔ recommended. The increased
Emtricitabine/Rilpivirine/Tenofovir Cmax: ↔ exposure of tenofovir could
disoproxil potentiate adverse reactions
(200 mg/25 mg/245 mg q.d.) GS-3310072: associated with tenofovir
AUC: ↔ disoproxil, including renal
Cmax: ↔ disorders. Renal function should
Cmin: ↔ be closely monitored (see
section 4.4).
Velpatasvir:
AUC: ↔
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) velpatasvir (HOS-108929) rilpivirine (HOS-088090) emtricitabine (HOS-085840)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2024-02-29T16:34:00Z · SHA-256 ab427f9266bbb81991653ebf14729e0d885f7cb9014fd47e3b3ee4fc69589ee0 · Passage 7b3ecba6da2d284d03b65e52edaa2021f453243f80887fa3055792f01dde485f · Zeichen 29352–30691 im Abschnitt
Wechselwirkungen · Viread
Viread 123 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 18–19
HOS-110533 · Präparat HOS-093385
18
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 d550c8d9097fb86a9733da7c544c1bce662495bf9924cb0e60e96c3044614d33 · Zeichen 31330–33402 im Abschnitt
Wechselwirkungen · Viread
Viread 163 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 53–54
HOS-110611 · Präparat HOS-093385
53
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: ↔ 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 97e1bc9f3b6c03c77c7d04d94f760c7fbda9ec9eabb9eb670e2965f8b6ad20d7 · Zeichen 20449–22870 im Abschnitt
Wechselwirkungen · Viread
Viread 163 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 54–55
HOS-110613 · Präparat HOS-093385
54
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: ↓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 e6335f4176b98a52989a9f36192d67ce8031012747a37072e892d128b679320b · Zeichen 23244–25660 im Abschnitt
Wechselwirkungen · Viread
Viread 163 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 55–56
HOS-110615 · Präparat HOS-093385
55
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 f429fcd15aa6871cb839634b36d3ad1413e88ea18aacf119f35aa295ac448c15 · Zeichen 26038–28373 im Abschnitt
Wechselwirkungen · Viread
Viread 163 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 56–57
HOS-110618 · Präparat HOS-093385
56
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: No dose adjustment is
(400 mg/100 mg q.d.) + AUC: ↔ recommended. The increased
Raltegravir Cmax: ↔ exposure of tenofovir could
(400 mg b.i.d) + potentiate adverse reactions
Emtricitabine/Tenofovir GS-3310072: associated with tenofovir
disoproxil AUC: ↔ disoproxil, including renal
(200 mg/245 mg q.d.) Cmax: ↔ disorders. Renal function
Cmin: ↔ should be closely monitored
(see section 4.4).
Velpatasvir:
AUC: ↔
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) velpatasvir (HOS-108929) raltegravir (HOS-086187) emtricitabine (HOS-085840)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2024-02-29T16:34:00Z · SHA-256 ab427f9266bbb81991653ebf14729e0d885f7cb9014fd47e3b3ee4fc69589ee0 · Passage d918ad90182808eeef28bb54c14d0388e927f2cef6a5d62eb2c8a06c36441ce9 · Zeichen 28716–30128 im Abschnitt
Wechselwirkungen · Viread
Viread 163 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 57
HOS-110620 · Präparat HOS-093385
Tenofovir:
AUC: ↑ 40%
Cmax: ↑ 46%
Cmin: ↑ 70%
Sofosbuvir/Velpatasvir Sofosbuvir: Concomitant administration
(400 mg/100 mg q.d.) + AUC: ↔ of sofosbuvir/velpatasvir and
Efavirenz/Emtricitabine/ Cmax: ↑ 38% efavirenz is expected to
Tenofovir disoproxil decrease plasma
(600 mg/200 mg/245 mg q.d.) GS-3310072: concentrations of velpatasvir.
AUC: ↔ Co-administration of
Cmax: ↔ sofosbuvir/velpatasvir with
Cmin: ↔ efavirenz-containing regimens
is not recommended.
Velpatasvir:
AUC: ↓ 53%
Cmax: ↓ 47%
Cmin: ↓ 57%
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) velpatasvir (HOS-108929) efavirenz (HOS-087947) emtricitabine (HOS-085840)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2024-02-29T16:34:00Z · SHA-256 ab427f9266bbb81991653ebf14729e0d885f7cb9014fd47e3b3ee4fc69589ee0 · Passage 5c1b9efc7fc481ee581edaae4980803e3c398b4914c4390d9d33b745fa667f83 · Zeichen 30480–31650 im Abschnitt
Wechselwirkungen · Viread
Viread 163 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 57–58
HOS-110623 · Präparat HOS-093385
57
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: No dose adjustment is
(400 mg/100 mg q.d.) + AUC: ↔ recommended. The increased
Emtricitabine/Rilpivirine/ Cmax: ↔ exposure of tenofovir could
Tenofovir disoproxil potentiate adverse reactions
(200 mg/25 mg/245 mg q.d.) GS-3310072: associated with tenofovir
AUC: ↔ disoproxil, including renal
Cmax: ↔ disorders. Renal function
Cmin: ↔ should be closely monitored
(see section 4.4).
Velpatasvir:
AUC: ↔
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) velpatasvir (HOS-108929) rilpivirine (HOS-088090) emtricitabine (HOS-085840)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2024-02-29T16:34:00Z · SHA-256 ab427f9266bbb81991653ebf14729e0d885f7cb9014fd47e3b3ee4fc69589ee0 · Passage eb4a0e126258305565110ef9c38aa7f37d72ebe07f355d3b96b3093f20504945 · Zeichen 32184–33579 im Abschnitt
Wechselwirkungen · Viread
Viread 163 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 58–59
HOS-110627 · Präparat HOS-093385
58
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 8f90c3405a909c8e9cd0f1c3dec1c93cb05981de545d195f7ffe4f8d2624fc77 · Zeichen 34101–36770 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.