Zum Inhalt

HealthOSArzneimittel

Arbeitsbereiche

Nachschlagen

Wirkstoffe & Arzneimittelsicherheit

Exakte Wirkstoffkennungen und zitierbare Passagen zu Wechselwirkungen, Gegenanzeigen und Nebenwirkungen.

Ein Paarvergleich findet Originalpassagen, die den anderen Wirkstoff wörtlich nennen. Aussagen gelten für das jeweilige Präparat und seine Formulierung. Klassenbegriffe und abweichende Synonyme können fehlen. Kein Treffer bedeutet nicht, dass keine Wechselwirkung besteht.

RxNorm 05-Oct-2026 · geprüft 2026-10-25 · 1009 Präparate · 54812 Quellenpassagen · 148 strukturierte Aussagen. Automatisch aktualisiert, ohne menschliche Freigabe.

Quellenpassagen (19)

Wechselwirkungen · Diacomit

Diacomit 250 mg hard capsules · Abschnitt 4.5 · PDF-Seite 5

HOS-115320 · Präparat HOS-094267

As stiripentol inhibited CYP2D6 in vitro at concentrations that are achieved clinically in plasma, substances that are metabolized by this isoenzyme like: beta-blockers (propranolol, carvedilol, timolol), antidepressants (fluoxetine, paroxetine, sertraline, imipramine, clomipramine), antipsychotics (haloperidol), analgesics (codeine, dextromethorphan, tramadol) may be subject to metabolic interactions with stiripentol. A dose-adjustment may be necessary for substances metabolised by CYP2D6 and that are individually dose titrated.

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): paroxetine (HOS-086246) codeine (HOS-090544) carvedilol (HOS-115322) imipramine (HOS-085907) clomipramine (HOS-085906) sertraline (HOS-086247) fluoxetine (HOS-085946) haloperidol (HOS-085602) propranolol (HOS-084529) dextromethorphan (HOS-109265) timolol (HOS-090571) tramadol (HOS-112871)

Vollständigen Kontext in der EMA-Fachinformation lesen →
Quellennachweis

Version 2026-10-19T15:31:00Z · SHA-256 b075bfe26e1e2e48d4d17e44e4cfe0a1e4c38681d9170c43ecb8af51f184b9ab · Passage a21431794e1268b71b022189130a03e98fd764c99d14f6721c85c72fca8b9c3b · Zeichen 2843–3378 im Abschnitt

Wechselwirkungen · Diacomit

Diacomit 500 mg hard capsules · Abschnitt 4.5 · PDF-Seite 16

HOS-115384 · Präparat HOS-094267

As stiripentol inhibited CYP2D6 in vitro at concentrations that are achieved clinically in plasma, substances that are metabolized by this isoenzyme like: beta-blockers (propranolol, carvedilol, timolol), antidepressants (fluoxetine, paroxetine, sertraline, imipramine, clomipramine), antipsychotics (haloperidol), analgesics (codeine, dextromethorphan, tramadol) may be subject to metabolic interactions with stiripentol. A dose-adjustment may be necessary for substances metabolised by CYP2D6 and that are individually dose titrated.

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): paroxetine (HOS-086246) codeine (HOS-090544) carvedilol (HOS-115322) imipramine (HOS-085907) clomipramine (HOS-085906) sertraline (HOS-086247) fluoxetine (HOS-085946) haloperidol (HOS-085602) propranolol (HOS-084529) dextromethorphan (HOS-109265) timolol (HOS-090571) tramadol (HOS-112871)

Vollständigen Kontext in der EMA-Fachinformation lesen →
Quellennachweis

Version 2026-10-19T15:31:00Z · SHA-256 b075bfe26e1e2e48d4d17e44e4cfe0a1e4c38681d9170c43ecb8af51f184b9ab · Passage a21431794e1268b71b022189130a03e98fd764c99d14f6721c85c72fca8b9c3b · Zeichen 2840–3375 im Abschnitt

Wechselwirkungen · Diacomit

Diacomit 250 mg powder for oral suspension in sachet · Abschnitt 4.5 · PDF-Seite 27

HOS-115418 · Präparat HOS-094267

As stiripentol inhibited CYP2D6 in vitro at concentrations that are achieved clinically in plasma, substances that are metabolized by this isoenzyme like: beta-blockers (propranolol, carvedilol, timolol), antidepressants (fluoxetine, paroxetine, sertraline, imipramine, clomipramine), antipsychotics (haloperidol), analgesics (codeine, dextromethorphan, tramadol) may be subject to metabolic interactions with stiripentol. A dose-adjustment may be necessary for substances metabolised by CYP2D6 and that are individually dose titrated.

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): paroxetine (HOS-086246) codeine (HOS-090544) carvedilol (HOS-115322) imipramine (HOS-085907) clomipramine (HOS-085906) sertraline (HOS-086247) fluoxetine (HOS-085946) haloperidol (HOS-085602) propranolol (HOS-084529) dextromethorphan (HOS-109265) timolol (HOS-090571) tramadol (HOS-112871)

Vollständigen Kontext in der EMA-Fachinformation lesen →
Quellennachweis

Version 2026-10-19T15:31:00Z · SHA-256 b075bfe26e1e2e48d4d17e44e4cfe0a1e4c38681d9170c43ecb8af51f184b9ab · Passage a21431794e1268b71b022189130a03e98fd764c99d14f6721c85c72fca8b9c3b · Zeichen 2847–3382 im Abschnitt

Wechselwirkungen · Diacomit

Diacomit 500 mg powder for oral suspension in sachet · Abschnitt 4.5 · PDF-Seite 38

HOS-115453 · Präparat HOS-094267

As stiripentol inhibited CYP2D6 in vitro at concentrations that are achieved clinically in plasma, substances that are metabolized by this isoenzyme like: beta-blockers (propranolol, carvedilol, timolol), antidepressants (fluoxetine, paroxetine, sertraline, imipramine, clomipramine), antipsychotics (haloperidol), analgesics (codeine, dextromethorphan, tramadol) may be subject to metabolic interactions with stiripentol. A dose-adjustment may be necessary for substances metabolised by CYP2D6 and that are individually dose titrated.

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): paroxetine (HOS-086246) codeine (HOS-090544) carvedilol (HOS-115322) imipramine (HOS-085907) clomipramine (HOS-085906) sertraline (HOS-086247) fluoxetine (HOS-085946) haloperidol (HOS-085602) propranolol (HOS-084529) dextromethorphan (HOS-109265) timolol (HOS-090571) tramadol (HOS-112871)

Vollständigen Kontext in der EMA-Fachinformation lesen →
Quellennachweis

Version 2026-10-19T15:31:00Z · SHA-256 b075bfe26e1e2e48d4d17e44e4cfe0a1e4c38681d9170c43ecb8af51f184b9ab · Passage a21431794e1268b71b022189130a03e98fd764c99d14f6721c85c72fca8b9c3b · Zeichen 2848–3383 im Abschnitt

Wechselwirkungen · Prezista

PREZISTA 100 mg/ml oral suspension · Abschnitt 4.5 · PDF-Seite 19–20

HOS-116394 · Präparat HOS-094447

19 ANTIPSYCHOTICS/NEUROLEPTICS Quetiapine Not studied. Boosted PREZISTA is Concomitant administration of expected to increase these antipsychotic boosted PREZISTA and quetiapine plasma concentrations. is contraindicated as it may (CYP3A inhibition) increase quetiapine-related toxicity. Increased concentrations of quetiapine may lead to coma (see section 4.3). Perphenazine Not studied. Boosted PREZISTA is A dose decrease may be needed for Risperidone expected to increase these antipsychotic these drugs when co-administered Thioridazine plasma concentrations. with boosted PREZISTA. (CYP3A, CYP2D6 and/or P-gp Lurasidone inhibition) Concomitant administration of Pimozide boosted PREZISTA and Sertindole lurasidone, pimozide or sertindole is contraindicated (see section 4.3). β-BLOCKERS Carvedilol Not studied. Boosted PREZISTA is Clinical monitoring is Metoprolol expected to increase these β-blocker recommended when Timolol plasma concentrations. co-administering boosted (CYP2D6 inhibition) PREZISTA with β-blockers. A lower dose of the β-blocker should be considered. CALCIUM CHANNEL BLOCKERS Amlodipine Not studied. Boosted PREZISTA can be Clinical monitoring of therapeutic Diltiazem expected to increase the plasma and adverse effects is Felodipine concentrations of calcium channel recommended when these Nicardipine blockers. medicines are concomitantly Nifedipine (CYP3A and/or CYP2D6 inhibition) administered with boosted Verapamil PREZISTA. CORTICOSTEROIDS Corticosteroids primarily Fluticasone: in a clinical study where Concomitant use of boosted metabolised by CYP3A ritonavir 100 mg capsules twice daily PREZISTA and corticosteroids (all (including were co-administered with 50 g routes of administration) that are betamethasone, intranasal fluticasone propionate (4 times metabolised by CYP3A may budesonide, fluticasone, daily) for 7 days in healthy subjects, increase the risk of development of mometasone, prednisone, fluticasone propionate plasma systemic corticosteroid effects, triamcinolone) concentrations increased significantly, including Cushing’s syndrome and whereas the intrinsic cortisol levels adrenal suppression. decreased by approximately 86% (90% CI 82-89%). Greater effects may be Co-administration with CYP3A- expected when fluticasone is inhaled. metabolised corticosteroids is not Systemic corticosteroid effects including recommended unless the potential Cushing’s syndrome and adrenal benefit to the patient outweighs the suppression have been reported in risk, in which case patients should patients receiving ritonavir and inhaled or be monitored for systemic intranasally administered fluticasone. The corticosteroid effects. effects of high fluticasone systemic exposure on ritonavir plasma levels are Alternative corticosteroids which unknown. are less dependent on CYP3A metabolism e.g. beclomethasone Other corticosteroids: interaction not should be considered, particularly studied. Plasma concentrations of these for long term use. medicinal products may be increased when co-administered with boosted PREZISTA, resulting in reduced serum cortisol concentrations. Dexamethasone Not studied. Dexamethasone may Systemic dexamethasone should (systemic) decrease plasma concentrations of be used with caution when darunavir. combined with boosted (CYP3A induction) PREZISTA.

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): sertindole (HOS-085601) quetiapine (HOS-086150) diltiazem (HOS-086288) triamcinolone (HOS-086333) nifedipine (HOS-086289) fluticasone (HOS-108914) nicardipine (HOS-090619) felodipine (HOS-108908) fluticasone propionate (HOS-086331) carvedilol (HOS-115322) risperidone (HOS-086280) amlodipine (HOS-086287) thioridazine (HOS-086281) perphenazine (HOS-116395) calcium (HOS-085615) betamethasone (HOS-090066) dexamethasone (HOS-084535) lead (HOS-085592) budesonide (HOS-086332) pimozide (HOS-085600) mometasone (HOS-114048) ritonavir (HOS-084521) beclomethasone (HOS-086334) lurasidone (HOS-086148) prednisone (HOS-084526) metoprolol (HOS-090094) timolol (HOS-090571) verapamil (HOS-090602)

Vollständigen Kontext in der EMA-Fachinformation lesen →
Quellennachweis

Version 2024-07-26T09:44:00Z · SHA-256 457dafbe8b3b9cee45b9ca7b46919ded598e0d0cd16715525d161e54f80b9117 · Passage 06bb26e6737c57cc3c74485aceb2076b3feb5ff5bad566ac99081f05e0924029 · Zeichen 52002–57572 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 61–62

HOS-116527 · Präparat HOS-094447

61 Perphenazine Not studied. PREZISTA is expected to A dose decrease may be needed for Risperidone increase these antipsychotic plasma these drugs when co-administered Thioridazine concentrations. with PREZISTA co-administered (CYP3A, CYP2D6 and/or P-gp with low dose ritonavir. inhibition) Lurasidone Concomitant administration of Pimozide PREZISTA with low dose Sertindole ritonavir and lurasidone, pimozide or sertindole is contraindicated (see section 4.3). β-BLOCKERS Carvedilol Not studied. PREZISTA is expected to Clinical monitoring is Metoprolol increase these β-blocker plasma recommended when Timolol concentrations. co-administering PREZISTA with (CYP2D6 inhibition) β-blockers. A lower dose of the β-blocker should be considered. CALCIUM CHANNEL BLOCKERS Amlodipine Not studied. PREZISTA co-administered Clinical monitoring of therapeutic Diltiazem with low dose ritonavir can be expected and adverse effects is Felodipine to increase the plasma concentrations of recommended when these Nicardipine calcium channel blockers. medicines are concomitantly Nifedipine (CYP3A and/or CYP2D6 inhibition) administered with PREZISTA with Verapamil low dose ritonavir. CORTICOSTEROIDS Corticosteroids primarily Fluticasone: in a clinical study where Concomitant use of PREZISTA metabolised by CYP3A ritonavir 100 mg capsules twice daily with low dose ritonavir and (including were co-administered with 50 g corticosteroids (all routes of betamethasone, intranasal fluticasone propionate (4 times administration) that are budesonide, fluticasone, daily) for 7 days in healthy subjects, metabolised by CYP3A may mometasone, prednisone, fluticasone propionate plasma increase the risk of development of triamcinolone) concentrations increased significantly, systemic corticosteroid effects, whereas the intrinsic cortisol levels including Cushing’s syndrome and decreased by approximately 86% (90% adrenal suppression. CI 82-89%). Greater effects may be expected when fluticasone is inhaled. Co-administration with CYP3A- Systemic corticosteroid effects including metabolised corticosteroids is not Cushing’s syndrome and adrenal recommended unless the potential suppression have been reported in benefit to the patient outweighs the patients receiving ritonavir and inhaled or risk, in which case patients should intranasally administered fluticasone. The be monitored for systemic effects of high fluticasone systemic corticosteroid effects. exposure on ritonavir plasma levels are unknown. Alternative corticosteroids which are less dependent on CYP3A Other corticosteroids: interaction not metabolism e.g. beclomethasone studied. Plasma concentrations of these should be considered, particularly medicinal products may be increased for long term use. when co-administered with PREZISTA with low dose ritonavir, resulting in reduced serum cortisol concentrations. Dexamethasone Not studied. Dexamethasone may Systemic dexamethasone should (systemic) decrease plasma concentrations of be used with caution when darunavir. combined with PREZISTA (CYP3A induction) 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): sertindole (HOS-085601) diltiazem (HOS-086288) triamcinolone (HOS-086333) nifedipine (HOS-086289) fluticasone (HOS-108914) nicardipine (HOS-090619) felodipine (HOS-108908) fluticasone propionate (HOS-086331) carvedilol (HOS-115322) risperidone (HOS-086280) amlodipine (HOS-086287) thioridazine (HOS-086281) perphenazine (HOS-116395) calcium (HOS-085615) betamethasone (HOS-090066) dexamethasone (HOS-084535) budesonide (HOS-086332) pimozide (HOS-085600) mometasone (HOS-114048) ritonavir (HOS-084521) beclomethasone (HOS-086334) lurasidone (HOS-086148) prednisone (HOS-084526) metoprolol (HOS-090094) timolol (HOS-090571) verapamil (HOS-090602)

Vollständigen Kontext in der EMA-Fachinformation lesen →
Quellennachweis

Version 2024-07-26T09:44:00Z · SHA-256 457dafbe8b3b9cee45b9ca7b46919ded598e0d0cd16715525d161e54f80b9117 · Passage 8b9ea54ec289adeef1a2f9f81165d44d84f0b8d5433cec6f77b7df8c89fd8286 · Zeichen 43290–48378 im Abschnitt

Wechselwirkungen · Prezista

PREZISTA 400 mg film-coated tablets PREZISTA 800 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 101–102

HOS-116617 · Präparat HOS-094447

101 ANTIPSYCHOTICS/NEUROLEPTICS Quetiapine Not studied. Boosted PREZISTA is Concomitant administration of expected to increase these antipsychotic boosted PREZISTA and quetiapine plasma concentrations. is contraindicated as it may (CYP3A inhibition) increase quetiapine-related toxicity. Increased concentrations of quetiapine may lead to coma (see section 4.3). Perphenazine Not studied. Boosted PREZISTA is A dose decrease may be needed for Risperidone expected to increase these antipsychotic these drugs when co-administered Thioridazine plasma concentrations. with boosted PREZISTA. (CYP3A, CYP2D6 and/or P-gp Lurasidone inhibition) Concomitant administration of Pimozide boosted PREZISTA and Sertindole lurasidone, pimozide or sertindole is contraindicated (see section 4.3). β-BLOCKERS Carvedilol Not studied. Boosted PREZISTA is Clinical monitoring is Metoprolol expected to increase these β-blocker recommended when Timolol plasma concentrations. co-administering boosted (CYP2D6 inhibition) PREZISTA with β-blockers. A lower dose of the β-blocker should be considered. CALCIUM CHANNEL BLOCKERS Amlodipine Not studied. Boosted PREZISTA can be Clinical monitoring of therapeutic Diltiazem expected to increase the plasma and adverse effects is Felodipine concentrations of calcium channel recommended when these Nicardipine blockers. medicines are concomitantly Nifedipine (CYP3A and/or CYP2D6 inhibition) administered with boosted Verapamil PREZISTA. CORTICOSTEROIDS Corticosteroids primarily Fluticasone: in a clinical study where Concomitant use of boosted metabolised by CYP3A ritonavir 100 mg capsules twice daily PREZISTA and corticosteroids (all (including were co-administered with 50 g routes of administration) that are betamethasone, intranasal fluticasone propionate (4 times metabolised by CYP3A may budesonide, fluticasone, daily) for 7 days in healthy subjects, increase the risk of development of mometasone, prednisone, fluticasone propionate plasma systemic corticosteroid effects, triamcinolone) concentrations increased significantly, including Cushing’s syndrome and whereas the intrinsic cortisol levels adrenal suppression. decreased by approximately 86% (90% CI 82-89%). Greater effects may be Co-administration with CYP3A- expected when fluticasone is inhaled. metabolised corticosteroids is not Systemic corticosteroid effects including recommended unless the potential Cushing’s syndrome and adrenal benefit to the patient outweighs the suppression have been reported in risk, in which case patients should patients receiving ritonavir and inhaled or be monitored for systemic intranasally administered fluticasone. The corticosteroid effects. effects of high fluticasone systemic exposure on ritonavir plasma levels are Alternative corticosteroids which unknown. are less dependent on CYP3A metabolism e.g. beclomethasone Other corticosteroids: interaction not should be considered, particularly studied. Plasma concentrations of these for long term use. medicinal products may be increased when co-administered with boosted PREZISTA, resulting in reduced serum cortisol concentrations. Dexamethasone Not studied. Dexamethasone may Systemic dexamethasone should (systemic) decrease plasma concentrations of be used with caution when darunavir. combined with boosted (CYP3A induction) PREZISTA.

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): sertindole (HOS-085601) quetiapine (HOS-086150) diltiazem (HOS-086288) triamcinolone (HOS-086333) nifedipine (HOS-086289) fluticasone (HOS-108914) nicardipine (HOS-090619) felodipine (HOS-108908) fluticasone propionate (HOS-086331) carvedilol (HOS-115322) risperidone (HOS-086280) amlodipine (HOS-086287) thioridazine (HOS-086281) perphenazine (HOS-116395) calcium (HOS-085615) betamethasone (HOS-090066) dexamethasone (HOS-084535) lead (HOS-085592) budesonide (HOS-086332) pimozide (HOS-085600) mometasone (HOS-114048) ritonavir (HOS-084521) beclomethasone (HOS-086334) lurasidone (HOS-086148) prednisone (HOS-084526) metoprolol (HOS-090094) timolol (HOS-090571) verapamil (HOS-090602)

Vollständigen Kontext in der EMA-Fachinformation lesen →
Quellennachweis

Version 2024-07-26T09:44:00Z · SHA-256 457dafbe8b3b9cee45b9ca7b46919ded598e0d0cd16715525d161e54f80b9117 · Passage ccb6e0bf9fbd4db134b19a5c68f5c32c6656fffa35e00c9b9b966f86c2226743 · Zeichen 51473–57044 im Abschnitt

Wechselwirkungen · Fampyra

Fampyra 10 mg prolonged-release tablets · Abschnitt 4.5 · PDF-Seite 4

HOS-124199 · Präparat HOS-095817

Fampridine is eliminated mainly via the kidneys with active renal secretion accounting for about 60% (see section 5.2). OCT2 is the transporter responsible for the active secretion of fampridine. Thus, the concomitant use of fampridine with medicinal products that are inhibitors of OCT2 for example, cimetidine are contraindicated (see section 4.3) and concomitant use of fampridine with medicinal products that are substrates of OCT2 for example, carvedilol, propranolol and metformin is cautioned (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): cimetidine (HOS-085835) carvedilol (HOS-115322) propranolol (HOS-084529) metformin (HOS-091032)

Vollständigen Kontext in der EMA-Fachinformation lesen →
Quellennachweis

Version 2025-08-21T09:21:00Z · SHA-256 6b1c569f97c0d64fb05b1fbf79a364d26b495f50374a291d2e13abe546b06f2c · Passage e6bb3e54180e624f7880863f0825e0b67195889ea64a475bc6e4b38f288962ae · Zeichen 187–705 im Abschnitt

Wechselwirkungen · Entresto

Entresto 24 mg/26 mg film-coated tablets Entresto 49 mg/51 mg film-coated tablets Entresto 97 mg/103 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 9

HOS-134381 · Präparat HOS-097566

No clinically meaningful interaction was observed when sacubitril/valsartan was co-administered with digoxin, warfarin, hydrochlorothiazide, amlodipine, omeprazole, carvedilol or a combination of levonorgestrel/ethinyl estradiol.

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): carvedilol (HOS-115322) levonorgestrel (HOS-089677) hydrochlorothiazide (HOS-086937) amlodipine (HOS-086287) digoxin (HOS-086172) ethinyl estradiol (HOS-088135) warfarin (HOS-085950) omeprazole (HOS-085912)

Vollständigen Kontext in der EMA-Fachinformation lesen →
Quellennachweis

Version 2026-01-13T10:33:00Z · SHA-256 63effd0dd78bf1b11f8cfe5ae77efc68b2653de13ba467bbf4e48289e340b97e · Passage cbb24f63824a014ba2c4c0a6554c663395ca6d0333d113ff55379662f9349148 · Zeichen 5775–6004 im Abschnitt

Wechselwirkungen · Entresto

Entresto 6 mg/6 mg granules in capsules for opening Entresto 15 mg/16 mg granules in capsules for opening · Abschnitt 4.5 · PDF-Seite 29

HOS-134419 · Präparat HOS-097566

No clinically meaningful interaction was observed when sacubitril/valsartan was co-administered with digoxin, warfarin, hydrochlorothiazide, amlodipine, omeprazole, carvedilol or a combination of levonorgestrel/ethinyl estradiol.

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): carvedilol (HOS-115322) levonorgestrel (HOS-089677) hydrochlorothiazide (HOS-086937) amlodipine (HOS-086287) digoxin (HOS-086172) ethinyl estradiol (HOS-088135) warfarin (HOS-085950) omeprazole (HOS-085912)

Vollständigen Kontext in der EMA-Fachinformation lesen →
Quellennachweis

Version 2026-01-13T10:33:00Z · SHA-256 63effd0dd78bf1b11f8cfe5ae77efc68b2653de13ba467bbf4e48289e340b97e · Passage cbb24f63824a014ba2c4c0a6554c663395ca6d0333d113ff55379662f9349148 · Zeichen 5719–5948 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 17–18

HOS-134507 · Präparat HOS-097580

17 INTERACTIONS AND DOSE RECOMMENDATIONS WITH OTHER MEDICINAL PRODUCTS Medicinal products by Interaction Geometric mean change Recommendations concerning co- therapeutic areas (%) administration Perphenazine Not studied. Darunavir is expected to A dose decrease may be needed for Risperidone increase these antipsychotic plasma these drugs when co-administered Thioridazine concentrations. with darunavir co-administered with (CYP3A, CYP2D6 and/or P-gp low dose ritonavir. inhibition) Lurasidone Pimozide Concomitant administration of Sertindole darunavir with low dose ritonavir and lurasidone, pimozide or sertindole is contraindicated (see section 4.3). β-BLOCKERS Carvedilol Not studied. Darunavir is expected to Clinical monitoring is Metoprolol increase these β-blocker plasma recommended when co- Timolol concentrations. administering darunavir with β- (CYP2D6 inhibition) blockers. A lower dose of the β- blocker should be considered. CALCIUM CHANNEL BLOCKERS Amlodipine Not studied. Darunavir co-administered Clinical monitoring of therapeutic Diltiazem with low dose ritonavir can be and adverse effects is recommended Felodipine expected to increase the plasma when these medicines are Nicardipine concentrations of calcium channel concomitantly administered with Nifedipine blockers. darunavir with low dose ritonavir. Verapamil (CYP3A and/or CYP2D6 inhibition) CORTICOSTEROIDS Corticosteroids primarily Fluticasone: in a clinical study where Concomitant use of darunavir with metabolised by CYP3A ritonavir 100 mg capsules twice daily low dose ritonavir and (including betamethasone, were co-administered with 50 μg corticosteroids (all routes of budesonide, fluticasone, intranasal fluticasone propionate (4 administration) that are metabolised mometasone, prednisone, times daily) for 7 days in healthy by CYP3A may increase the risk of triamcinolone) subjects, fluticasone propionate plasma development of systemic concentrations increased significantly, corticosteroid effects, including whereas the intrinsic cortisol levels Cushing’s syndrome and adrenal decreased by approximately 86% (90% suppression. CI 82-89%). Greater effects may be expected when fluticasone is inhaled. Co-administration with CYP3A- Systemic corticosteroid effects metabolised corticosteroids is not including Cushing’s syndrome and recommended unless the potential adrenal suppression have been reported benefit to the patient outweighs the in patients receiving ritonavir and risk, in which case patients should inhaled or intranasally administered be monitored for systemic fluticasone. The effects of high corticosteroid effects. fluticasone systemic exposure on ritonavir plasma levels are unknown. Alternative corticosteroids which are less dependent on CYP3A Other corticosteroids: interaction not metabolism e.g. beclomethasone studied. Plasma concentrations of these should be considered, particularly medicinal products may be increased for long term use. when co-administered with darunavir with low dose ritonavir, resulting in reduced serum cortisol concentrations. Dexamethasone (systemic) Not studied. Dexamethasone may Systemic dexamethasone should be decrease plasma concentrations of used with caution when combined darunavir. (CYP3A induction) with 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): sertindole (HOS-085601) diltiazem (HOS-086288) triamcinolone (HOS-086333) nifedipine (HOS-086289) fluticasone (HOS-108914) nicardipine (HOS-090619) felodipine (HOS-108908) fluticasone propionate (HOS-086331) carvedilol (HOS-115322) risperidone (HOS-086280) amlodipine (HOS-086287) thioridazine (HOS-086281) perphenazine (HOS-116395) calcium (HOS-085615) betamethasone (HOS-090066) dexamethasone (HOS-084535) budesonide (HOS-086332) pimozide (HOS-085600) mometasone (HOS-114048) ritonavir (HOS-084521) beclomethasone (HOS-086334) lurasidone (HOS-086148) prednisone (HOS-084526) metoprolol (HOS-090094) timolol (HOS-090571) verapamil (HOS-090602)

Vollständigen Kontext in der EMA-Fachinformation lesen →
Quellennachweis

Version 2026-10-20T12:32:00Z · SHA-256 50f4771a683f17214737463c6df88a158b1e699bbb9916413602e547e369e804 · Passage 4d699252eaa8e454816efcf834725c875d4dc8037df504e7418d309238a96785 · Zeichen 43154–48076 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 59–60

HOS-134627 · Präparat HOS-097580

59 INTERACTIONS AND DOSE RECOMMENDATIONS WITH OTHER MEDICINAL PRODUCTS Medicinal products by Interaction Recommendations concerning co- therapeutic areas Geometric mean change (%) administration Perphenazine Not studied. Boosted darunavir is A dose decrease may be needed for Risperidone expected to increase these these drugs when co-administered Thioridazine antipsychotic plasma with boosted darunavir. concentrations. (CYP3A, CYP2D6 and/or P-gp inhibition) Lurasidone Concomitant administration of Pimozide boosted darunavir and lurasidone, Sertindole pimozide or sertindole is contraindicated (see section 4.3). β-BLOCKERS Carvedilol Not studied. Boosted darunavir is Clinical monitoring is recommended Metoprolol expected to increase these β-blocker when co-administering boosted Timolol plasma concentrations. darunavir with β-blockers. A lower (CYP2D6 inhibition) dose of the β-blocker should be considered. CALCIUM CHANNEL BLOCKERS Amlodipine Not studied. Boosted darunavir can Clinical monitoring of therapeutic Diltiazem be expected to increase the plasma and adverse effects is recommended Felodipine concentrations of calcium channel when these medicines are Nicardipine blockers. concomitantly administered with Nifedipine (CYP3A and/or CYP2D6 boosted darunavir. Verapamil inhibition) CORTICOSTEROIDS Corticosteroids primarily Fluticasone: in a clinical study Concomitant use of boosted metabolised by CYP3A where ritonavir 100 mg capsules darunavir and corticosteroids (all (including betamethasone, twice daily were co-administered routes of administration) that are budesonide, fluticasone, with 50 μg intranasal fluticasone metabolised by CYP3A may increase mometasone, prednisone, propionate (4 times daily) for 7 the risk of development of systemic triamcinolone) days in healthy subjects, fluticasone corticosteroid effects, including propionate plasma concentrations Cushing’s syndrome and adrenal increased significantly, whereas the suppression. intrinsic cortisol levels decreased by approximately 86% (90% CI 82- Co-administration with CYP3A- 89%). Greater effects may be metabolised corticosteroids is not expected when fluticasone is recommended unless the potential inhaled. Systemic corticosteroid benefit to the patient outweighs the effects including Cushing's risk, in which case patients should be syndrome and adrenal suppression monitored for systemic corticosteroid have been reported in patients effects. receiving ritonavir and inhaled or intranasally administered Alternative corticosteroids which are fluticasone. The effects of high less dependent on CYP3A fluticasone systemic exposure on metabolism ritonavir plasma levels are e.g. beclomethasone should be unknown. considered, particularly for long term use. Other corticosteroids: interaction not studied. Plasma concentrations of these medicinal products may be increased when co-administered with boosted darunavir, resulting in reduced serum cortisol concentrations. Dexamethasone (systemic) Not studied. Dexamethasone may Systemic dexamethasone should be decrease plasma concentrations of used with caution when combined darunavir. with boosted darunavir. (CYP3A induction)

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): sertindole (HOS-085601) diltiazem (HOS-086288) triamcinolone (HOS-086333) nifedipine (HOS-086289) fluticasone (HOS-108914) nicardipine (HOS-090619) felodipine (HOS-108908) carvedilol (HOS-115322) risperidone (HOS-086280) amlodipine (HOS-086287) thioridazine (HOS-086281) perphenazine (HOS-116395) calcium (HOS-085615) betamethasone (HOS-090066) dexamethasone (HOS-084535) budesonide (HOS-086332) pimozide (HOS-085600) mometasone (HOS-114048) propionate (HOS-108915) ritonavir (HOS-084521) beclomethasone (HOS-086334) lurasidone (HOS-086148) prednisone (HOS-084526) metoprolol (HOS-090094) timolol (HOS-090571) verapamil (HOS-090602)

Vollständigen Kontext in der EMA-Fachinformation lesen →
Quellennachweis

Version 2026-10-20T12:32:00Z · SHA-256 50f4771a683f17214737463c6df88a158b1e699bbb9916413602e547e369e804 · Passage 5be93392fc9daddc5a4bddcaf5177effda2055057fdf350b6c14c2d3c31e17fc · Zeichen 49576–54404 im Abschnitt

Wechselwirkungen · Neparvis

Neparvis 24 mg/26 mg film-coated tablets Neparvis 49 mg/51 mg film-coated tablets Neparvis 97 mg/103 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 9

HOS-138104 · Präparat HOS-098142

No clinically meaningful interaction was observed when sacubitril/valsartan was co-administered with digoxin, warfarin, hydrochlorothiazide, amlodipine, omeprazole, carvedilol or a combination of levonorgestrel/ethinyl estradiol.

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): carvedilol (HOS-115322) levonorgestrel (HOS-089677) hydrochlorothiazide (HOS-086937) amlodipine (HOS-086287) digoxin (HOS-086172) ethinyl estradiol (HOS-088135) warfarin (HOS-085950) omeprazole (HOS-085912)

Vollständigen Kontext in der EMA-Fachinformation lesen →
Quellennachweis

Version 2026-01-13T16:33:00Z · SHA-256 08c9e21821039ca07b73a73e3ade3e3cdcfc16fa2da815f0f3e25e38fa083f2e · Passage cbb24f63824a014ba2c4c0a6554c663395ca6d0333d113ff55379662f9349148 · Zeichen 5776–6005 im Abschnitt

Wechselwirkungen · Neparvis

Neparvis 6 mg/6 mg granules in capsules for opening Neparvis 15 mg/16 mg granules in capsules for opening · Abschnitt 4.5 · PDF-Seite 28

HOS-138139 · Präparat HOS-098142

No clinically meaningful interaction was observed when sacubitril/valsartan was co-administered with digoxin, warfarin, hydrochlorothiazide, amlodipine, omeprazole, carvedilol or a combination of levonorgestrel/ethinyl estradiol.

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): carvedilol (HOS-115322) levonorgestrel (HOS-089677) hydrochlorothiazide (HOS-086937) amlodipine (HOS-086287) digoxin (HOS-086172) ethinyl estradiol (HOS-088135) warfarin (HOS-085950) omeprazole (HOS-085912)

Vollständigen Kontext in der EMA-Fachinformation lesen →
Quellennachweis

Version 2026-01-13T16:33:00Z · SHA-256 08c9e21821039ca07b73a73e3ade3e3cdcfc16fa2da815f0f3e25e38fa083f2e · Passage cbb24f63824a014ba2c4c0a6554c663395ca6d0333d113ff55379662f9349148 · Zeichen 5719–5948 im Abschnitt

Wechselwirkungen · Symtuza

Symtuza 800 mg/150 mg/200 mg/10 mg film-coated tablets Symtuza 675 mg/150 mg/200 mg/10 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 14

HOS-138490 · Präparat HOS-098200

Lurasidone The combination of lurasidone, Pimozide pimozide, quetiapine or sertindole Quetiapine and Symtuza is contraindicated Sertindole (see section 4.3). β-BLOCKERS Carvedilol Based on theoretical considerations Clinical monitoring is Metoprolol DRV/COBI is expected to increase recommended when Timolol these beta-blocker plasma co-administering Symtuza with concentrations. beta-blockers and a lower dose of (CYP2D6 inhibition) the beta-blocker should be considered. CALCIUM CHANNEL BLOCKERS Amlodipine Based on theoretical considerations Clinical monitoring is Diltiazem DRV/COBI is expected to increase recommended when these Felodipine these calcium channel blocker medicinal products are Nicardipine plasma concentrations. co-administered with Symtuza. Nifedipine (CYP3A inhibition) Verapamil CORTICOSTEROIDS Corticosteroids primarily Based on theoretical considerations Concomitant use of Symtuza and metabolised by CYP3A DRV/COBI is expected to increase corticosteroids (all routes of (including betamethasone, these corticosteroid plasma administration) that are budesonide, fluticasone, concentrations. metabolised by CYP3A may mometasone, prednisone, (CYP3A inhibition) increase the risk for development triamcinolone) of systemic corticosteroid effects, including Cushing’s syndrome and adrenal suppression.

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): sertindole (HOS-085601) quetiapine (HOS-086150) diltiazem (HOS-086288) triamcinolone (HOS-086333) nifedipine (HOS-086289) fluticasone (HOS-108914) nicardipine (HOS-090619) felodipine (HOS-108908) carvedilol (HOS-115322) amlodipine (HOS-086287) calcium (HOS-085615) betamethasone (HOS-090066) budesonide (HOS-086332) pimozide (HOS-085600) mometasone (HOS-114048) lurasidone (HOS-086148) prednisone (HOS-084526) metoprolol (HOS-090094) timolol (HOS-090571) verapamil (HOS-090602)

Vollständigen Kontext in der EMA-Fachinformation lesen →
Quellennachweis

Version 2026-09-16T11:21:00Z · SHA-256 542f840b29cc7afaff9940b20511550e8d35031b33d95efd774fd49f70f7819d · Passage 93d51832ca83543fafde6c13b4aad3650a78fd53d8dfafa10a844085355fa52e · Zeichen 24581–26821 im Abschnitt

Wechselwirkungen · Talzenna

Talzenna 0.1 mg hard capsules Talzenna 0.25 mg hard capsules Talzenna 0.35 mg hard capsules Talzenna 0.5 mg hard capsules Talzenna 1 mg hard capsules · Abschnitt 4.5 · PDF-Seite 7

HOS-140563 · Präparat HOS-098546

Concomitant use of strong P-gp inhibitors (including but not limited to amiodarone, carvedilol, clarithromycin, cobicistat, darunavir, dronedarone, erythromycin, indinavir, itraconazole, ketoconazole, lapatinib, lopinavir, propafenone, quinidine, ranolazine, ritonavir, saquinavir, telaprevir, tipranavir, and verapamil) should be avoided. If co-administration with a strong P-gp inhibitor is unavoidable, the Talzenna dose should be reduced (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): indinavir (HOS-084518) lopinavir (HOS-086269) propafenone (HOS-084530) dronedarone (HOS-086144) ketoconazole (HOS-084513) carvedilol (HOS-115322) cobicistat (HOS-088111) quinidine (HOS-085593) telaprevir (HOS-090618) lapatinib (HOS-122565) itraconazole (HOS-084516) saquinavir (HOS-084522) clarithromycin (HOS-084517) erythromycin (HOS-084514) darunavir (HOS-086181) ritonavir (HOS-084521) amiodarone (HOS-085596) ranolazine (HOS-086141) tipranavir (HOS-086184) verapamil (HOS-090602)

Vollständigen Kontext in der EMA-Fachinformation lesen →
Quellennachweis

Version 2025-07-18T15:15:00Z · SHA-256 ed4d297943838ad90546bb310100bb9880e0b3c9833c452b88d5862d4841e255 · Passage 234ecfeab8722ea5160a874b4a7240829c7b65e708ad9e195210f3f70d12f3a4 · Zeichen 1803–2263 im Abschnitt

Wechselwirkungen · Xospata

Xospata 40 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 6

HOS-141410 · Präparat HOS-098642

CYP3A, P-gp and/or BCRP inhibitors Strong inhibitors of CYP3A, P-gp and/or BCRP (e.g., voriconazole, itraconazole, posaconazole, clarithromycin, erythromycin, captopril, carvedilol, ritonavir, azithromycin) can increase gilteritinib plasma concentrations. A single, 10 mg dose of gilteritinib co-administered with itraconazole (200 mg once daily for 28 days), a strong CYP3A, P-gp and BCRP inhibitor, to healthy subjects resulted in an approximate 20% increase in mean Cmax and 2.2-fold increase in mean AUCinf relative to subjects administered a single dose of gilteritinib alone. Gilteritinib exposure increased approximately 1.5-fold in patients with relapsed or refractory AML when co-administered with a strong CYP3A, P-gp and/or BCRP inhibitor (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): captopril (HOS-085478) carvedilol (HOS-115322) azithromycin (HOS-088112) voriconazole (HOS-084524) itraconazole (HOS-084516) clarithromycin (HOS-084517) erythromycin (HOS-084514) ritonavir (HOS-084521) posaconazole (HOS-085622)

Vollständigen Kontext in der EMA-Fachinformation lesen →
Quellennachweis

Version 2024-07-09T15:12:00Z · SHA-256 c553334e12e70f11f6e5ebf231d99102b822bac3002cf0bd26bc31c72e26836b · Passage 41d2074bca95d47bf686b06bba6001dbcad79c2302143c825f3f7dbca7701f26 · Zeichen 710–1478 im Abschnitt

Wechselwirkungen · Jyseleca

Jyseleca 100 mg film-coated tablets Jyseleca 200 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 8

HOS-144360 · Präparat HOS-099170

Filgotinib is primarily metabolised by carboxylesterase 2 (CES2), which can be inhibited in vitro by medicinal products such as fenofibrate, carvedilol, diltiazem or simvastatin. The clinical relevance of this interaction is unknown.

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): diltiazem (HOS-086288) carvedilol (HOS-115322) fenofibrate (HOS-123816) simvastatin (HOS-086158)

Vollständigen Kontext in der EMA-Fachinformation lesen →
Quellennachweis

Version 2025-06-10T15:54:00Z · SHA-256 4442cfcdd2007795a9b4a5f2ba8b8acde0a07629686c5967414dd017b37ddace · Passage ae8da9b53328b1a7ea6afa2729cbc6051986e88af0169289777c2e2ceee4dc63 · Zeichen 50–283 im Abschnitt

Wechselwirkungen · Orgovyx

Orgovyx 120 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 6

HOS-146539 · Präparat HOS-099534

Antihypertensives carvedilol, verapamil.

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): carvedilol (HOS-115322) verapamil (HOS-090602)

Vollständigen Kontext in der EMA-Fachinformation lesen →
Quellennachweis

Version 2026-10-02T16:34:00Z · SHA-256 83d5275c068e4da33497bf48ce37dfa4eca293d7cd335add5247289a5323daa8 · Passage 4a6c4b6cd5f394d2a04e4a81a6c2e83d04cda758b5c1428c4762298ce996b5cb · Zeichen 5479–5521 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.