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.
Gegenanzeigen · Ketoconazole Esteve (previously Ketoconazole HRA)
Ketoconazole Esteve 200 mg tablets · Abschnitt 4.3 · PDF-Seite 4
HOS-132828 · Präparat HOS-097310
- Hypersensitivity to the active substance or to any of the excipients listed in section 6.1;
- Hypersensitivity to any imidazole antifungal medicinal product;
- Acute or chronic liver disease and/or if pre-treatment liver enzymes levels are above 2 times the upper
limit of normal (see sections 4.2 and 4.4):
- Pregnancy (see section 4.6);
- Breastfeeding (see section 4.6);
- Congenital or documented acquired QTc prolongation ;
- Concomitant therapy with any of the following medicinal products which may interact and result in
potentially life-threatening adverse reactions (see section 4.5):
o CYP3A4 metabolised HMG-CoA reductase inhibitors (e.g. simvastatin, atorvastatin and
lovastatin) due to an increased risk of skeletal muscle toxicity including rhabdomyolysis;
o eplerenone due to an increased risk of hyperkalemia and hypotension;
o substances that may have their plasma concentrations increased and have QT prolonging potential:
methadone, disopyramide, quinidine, dronedarone, pimozide, sertindole, saquinavir
(saquinavir/ritonavir 1000/100 mg bid), ranolazine, mizolastine, halofantrine;
o dabigatran due to an increased bleeding risk;
o triazolam, oral midazolam and alprazolam due to potential for prolonged or increased sedation and
respiratory depression;
o ergot alkaloids (eg dihydroergotamine, ergometrine (ergonovine), ergotamine and
methylergometrine (methylergonovine) due to an increased risk of ergotism and other serious
vasospastic adverse reactions;
o lurasidone;
o quetiapine due to an increased risk of toxicity;
o telithromycin and clarithromycin in patients with severe renal impairment due to an increased risk
of hepatotoxicity and QT interval prolongation;
o felodipine, nisoldipine due to an increased risk of oedema and congestive heart failure;
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) methylergonovine (HOS-086155) dronedarone (HOS-086144) methadone (HOS-086198) lovastatin (HOS-086157) eplerenone (HOS-089050) atorvastatin (HOS-086304) felodipine (HOS-108908) alprazolam (HOS-086171) halofantrine (HOS-085606) simvastatin (HOS-086158) quinidine (HOS-085593) dabigatran (HOS-112096) ergot alkaloids (HOS-108807) imidazole (HOS-117862) disopyramide (HOS-085595) telithromycin (HOS-084523) saquinavir (HOS-084522) clarithromycin (HOS-084517) pimozide (HOS-085600) nisoldipine (HOS-114251) ergotamine (HOS-086154) ritonavir (HOS-084521) lurasidone (HOS-086148) ranolazine (HOS-086141) ergonovine (HOS-086153) triazolam (HOS-086168) dihydroergotamine (HOS-086152) midazolam (HOS-086167) mizolastine (HOS-085609)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2025-05-05T12:00:00Z · SHA-256 1463d2e081bcaa454cdfd6129ad3b8e03e3df9233f9d0704cfceba71c89c59b5 · Passage f9d16641f2e5b06b321fa0c79f0dacdfede818d20585398b4d37ddb19dad6a14 · Zeichen 0–2044 im Abschnitt
Gegenanzeigen · Ketoconazole Esteve (previously Ketoconazole HRA)
Ketoconazole Esteve 200 mg tablets · Abschnitt 4.3 · PDF-Seite 4–5
HOS-132835 · Präparat HOS-097310
4
o colchicine in patients with renal impairment due to an increased risk of severe adverse reactions;
o irinotecan due to an alteration of the metabolism of this medicinal product;
o everolimus, sirolimus (also known as rapamycin) due to an increase of the plasma concentrations
of these medicinal products;
o vardenafil in men older than 75-years due to increased risk of adverse reactions;
o paritaprevir/ombitasvir (ritonavir) due to increased risk of adverse reactions;
o fesoterodine and solifenacin in patients with renal impairment;
o tolvaptan used for a specific disease called “syndrome of inappropriate antidiuretic hormone
secretion”.
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): solifenacin (HOS-116433) tolvaptan (HOS-109429) ombitasvir (HOS-110300) colchicine (HOS-086147) everolimus (HOS-086310) fesoterodine (HOS-116432) sirolimus (HOS-085172) ritonavir (HOS-084521) paritaprevir (HOS-110301) irinotecan (HOS-112102) vardenafil (HOS-086163)
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Version 2025-05-05T12:00:00Z · SHA-256 1463d2e081bcaa454cdfd6129ad3b8e03e3df9233f9d0704cfceba71c89c59b5 · Passage faff2553122d6c384dc8d1a2a28fb45dbf0f436b1bcaa7a98bc5fee989b1cf04 · Zeichen 2103–2872 im Abschnitt
Gegenanzeigen · Ketoconazole Esteve (previously Ketoconazole HRA)
Ketoconazole Esteve 200 mg tablets · Abschnitt 4.3 · PDF-Seite 5
HOS-132840 · Präparat HOS-097310
The list above is not an inclusive list of compounds that may interact with ketoconazole and result in
potentially life-threatening reactions.
Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2025-05-05T12:00:00Z · SHA-256 1463d2e081bcaa454cdfd6129ad3b8e03e3df9233f9d0704cfceba71c89c59b5 · Passage a842ba17bd46fe6b36909c37467baa6188580fa256f65ccce8bce0b9df875fe9 · Zeichen 2874–3016 im Abschnitt
Wechselwirkungen · Ketoconazole Esteve (previously Ketoconazole HRA)
Ketoconazole Esteve 200 mg tablets · Abschnitt 4.5 · PDF-Seite 7
HOS-132841 · Präparat HOS-097310
Concomitant therapy with medicinal products that are contraindicated during treatment with ketoconazole
and resulting in potentially life-threatening adverse reactions :
Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2025-05-05T12:00:00Z · SHA-256 1463d2e081bcaa454cdfd6129ad3b8e03e3df9233f9d0704cfceba71c89c59b5 · Passage 1b985485228a6982c8f130d7695cba516bb54c83cc9821a0d1c0dc0281876aac · Zeichen 0–169 im Abschnitt
Wechselwirkungen · Ketoconazole Esteve (previously Ketoconazole HRA)
Ketoconazole Esteve 200 mg tablets · Abschnitt 4.5 · PDF-Seite 7
HOS-132842 · Präparat HOS-097310
o CYP3A4 metabolised HMG-CoA reductase inhibitors (e.g. simvastatin, atorvastatin and lovastatin)
due to an increased risk of skeletal muscle toxicity including rhabdomyolysis;
o eplerenone due to an increased risk of hyperkalemia and hypotension;
o substances that may have their plasma concentrations increased and have QT prolonging potential :
methadone, disopyramide, quinidine, dronedarone, pimozide, sertindole, saquinavir (saquinavir/ritonavir
1000/100 mg bid), ranolazine, mizolastine, halofantrine;
o dabigatran due to an increased bleeding risk;
o triazolam, oral midazolam and alprazolam due to potential for prolonged or increased sedation and
respiratory depression;
o ergot alkaloids (eg dihydroergotamine, ergometrine (ergonovine), ergotamine and methylergometrine
(methylergonovine) due to an increased risk of ergotism and other serious vasospastic adverse
reactionsevents
o lurasidone;
o quetiapine due to an increased risk of toxicity;
o telithromycin and clarithromycin in patients with severe renal impairment due to an increased risk of
hepatotoxicity and QT interval prolongation;
o felodipine, nisoldipine due to an increased risk of oedema and congestive heart failure;
o colchicine in patients with renal impairment due to an increased risk of severe adverse reactions;
o irinotecan due to an alteration of the metabolism of this medicinal product;
o everolimus, sirolimus (also known as rapamycin) due to an increase of the plasma concentrations of
these medicinal products;
o vardenafil in men older than 75-years due to increased risk of adverse reactions
o paritaprevir/ombitasvir (ritonavir) due to increased risk of adverse reactions;
o fesoterodine and solifenacin in patients with renal impairment;
o tolvaptan used for a specific disease called “syndrome of inappropriate antidiuretic hormone
secretion”.
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) solifenacin (HOS-116433) methylergonovine (HOS-086155) dronedarone (HOS-086144) methadone (HOS-086198) lovastatin (HOS-086157) eplerenone (HOS-089050) atorvastatin (HOS-086304) felodipine (HOS-108908) alprazolam (HOS-086171) halofantrine (HOS-085606) simvastatin (HOS-086158) quinidine (HOS-085593) dabigatran (HOS-112096) tolvaptan (HOS-109429) ergot alkaloids (HOS-108807) disopyramide (HOS-085595) telithromycin (HOS-084523) saquinavir (HOS-084522) ombitasvir (HOS-110300) clarithromycin (HOS-084517) pimozide (HOS-085600) nisoldipine (HOS-114251) colchicine (HOS-086147) everolimus (HOS-086310) fesoterodine (HOS-116432) sirolimus (HOS-085172) ergotamine (HOS-086154) ritonavir (HOS-084521) paritaprevir (HOS-110301) lurasidone (HOS-086148) ranolazine (HOS-086141) irinotecan (HOS-112102) ergonovine (HOS-086153) triazolam (HOS-086168) dihydroergotamine (HOS-086152) midazolam (HOS-086167) mizolastine (HOS-085609) vardenafil (HOS-086163)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2025-05-05T12:00:00Z · SHA-256 1463d2e081bcaa454cdfd6129ad3b8e03e3df9233f9d0704cfceba71c89c59b5 · Passage 0b65d259964c6f340994be44a864bad55b31283e3fc412d0d5a47323a792d889 · Zeichen 171–2105 im Abschnitt
Wechselwirkungen · Ketoconazole Esteve (previously Ketoconazole HRA)
Ketoconazole Esteve 200 mg tablets · Abschnitt 4.5 · PDF-Seite 7
HOS-132843 · Präparat HOS-097310
The list above is not an inclusive list of compounds that may interact with ketoconazole and result in
potentially life-threatening reactions.
Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2025-05-05T12:00:00Z · SHA-256 1463d2e081bcaa454cdfd6129ad3b8e03e3df9233f9d0704cfceba71c89c59b5 · Passage a842ba17bd46fe6b36909c37467baa6188580fa256f65ccce8bce0b9df875fe9 · Zeichen 2107–2249 im Abschnitt
Wechselwirkungen · Ketoconazole Esteve (previously Ketoconazole HRA)
Ketoconazole Esteve 200 mg tablets · Abschnitt 4.5 · PDF-Seite 7
HOS-132844 · Präparat HOS-097310
Medicinal products affecting the absorption of ketoconazole
Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2025-05-05T12:00:00Z · SHA-256 1463d2e081bcaa454cdfd6129ad3b8e03e3df9233f9d0704cfceba71c89c59b5 · Passage a130e09f31f391b4e3a2f0835c03eb23d67d74242b52942e1fe02189bf3e62b1 · Zeichen 2251–2310 im Abschnitt
Wechselwirkungen · Ketoconazole Esteve (previously Ketoconazole HRA)
Ketoconazole Esteve 200 mg tablets · Abschnitt 4.5 · PDF-Seite 7
HOS-132845 · Präparat HOS-097310
Medicinal products affecting gastric acidity impair the absorption of ketoconazole (see section 4.4).
Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2025-05-05T12:00:00Z · SHA-256 1463d2e081bcaa454cdfd6129ad3b8e03e3df9233f9d0704cfceba71c89c59b5 · Passage 4866cc3aba39f22b349c54509913abc311baeaf0286440c798b3c59488451911 · Zeichen 2312–2413 im Abschnitt
Wechselwirkungen · Ketoconazole Esteve (previously Ketoconazole HRA)
Ketoconazole Esteve 200 mg tablets · Abschnitt 4.5 · PDF-Seite 7
HOS-132846 · Präparat HOS-097310
Effects of other medicinal products on the metabolism of ketoconazole
Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2025-05-05T12:00:00Z · SHA-256 1463d2e081bcaa454cdfd6129ad3b8e03e3df9233f9d0704cfceba71c89c59b5 · Passage 8e5f358dfa74710f8b8a73799560d430e3102daf8f23a52a7855111fd8edb7c8 · Zeichen 2415–2484 im Abschnitt
Wechselwirkungen · Ketoconazole Esteve (previously Ketoconazole HRA)
Ketoconazole Esteve 200 mg tablets · Abschnitt 4.5 · PDF-Seite 7
HOS-132847 · Präparat HOS-097310
Ketoconazole is mainly metabolised by cytochrome CYP3A4.
Enzyme-inducing medicinal products such as rifampicin, rifabutin, carbamazepine, isoniazid, nevirapine,
mitotane and phenytoin may significantly reduce the bioavailability of ketoconazole. Use of ketoconazole with
potent enzyme inducers is 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): carbamazepine (HOS-085618) rifabutin (HOS-086262) mitotane (HOS-112479) nevirapine (HOS-088064) isoniazid (HOS-088590) phenytoin (HOS-084531)
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Version 2025-05-05T12:00:00Z · SHA-256 1463d2e081bcaa454cdfd6129ad3b8e03e3df9233f9d0704cfceba71c89c59b5 · Passage 8438e2557ee1bbba4af94523b7f8fd21331bb2f8e99ca2dc95c8883b5c86c5e8 · Zeichen 2486–2799 im Abschnitt
Wechselwirkungen · Ketoconazole Esteve (previously Ketoconazole HRA)
Ketoconazole Esteve 200 mg tablets · Abschnitt 4.5 · PDF-Seite 7–8
HOS-132849 · Präparat HOS-097310
7
Potent inhibitors of CYP3A4 (e.g. antivirals such as ritonavir, ritonavir-boosted darunavir and ritonavir-
boosted fosamprenavir) may increase the bioavailability of ketoconazole, these medicinal products should be
used with caution when co-administered with ketoconazole and patients should be monitored closely for signs
and symptoms of adrenal insuficiency. Ketoconazole dose should be adjusted accordingly.
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): darunavir (HOS-086181) fosamprenavir (HOS-086182) ritonavir (HOS-084521)
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Version 2025-05-05T12:00:00Z · SHA-256 1463d2e081bcaa454cdfd6129ad3b8e03e3df9233f9d0704cfceba71c89c59b5 · Passage 5b3140c4dc780b3a88698cba0baeea875f455d5586c5dd66ff2202ef1cee7835 · Zeichen 2856–3269 im Abschnitt
Wechselwirkungen · Ketoconazole Esteve (previously Ketoconazole HRA)
Ketoconazole Esteve 200 mg tablets · Abschnitt 4.5 · PDF-Seite 8
HOS-132850 · Präparat HOS-097310
Effects of ketoconazole on the metabolism of the other medicinal products
Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2025-05-05T12:00:00Z · SHA-256 1463d2e081bcaa454cdfd6129ad3b8e03e3df9233f9d0704cfceba71c89c59b5 · Passage c96cf2790b5aad95c271b7adb863e5bf9553c5eb973fc67571586e73bb5f2f7e · Zeichen 3271–3344 im Abschnitt
Wechselwirkungen · Ketoconazole Esteve (previously Ketoconazole HRA)
Ketoconazole Esteve 200 mg tablets · Abschnitt 4.5 · PDF-Seite 8
HOS-132851 · Präparat HOS-097310
- Ketoconazole is a potent inhibitor of CYP3A4 and can inhibit the metabolism of medicinal products
metabolised by this enzyme. This can result in an increase and/or prolongation of their effects, including
adverse reactions.
- In vitro data indicate that ketoconazole is an inhibitor of CYP1A2 and does not significantly inhibit CYP
2A6 and 2E1. At clinically relevant concentrations inhibition of CYP2B6, 2C9/C8, 2C19 and 2D6 by
ketoconazole cannot be excluded.
- Ketoconazole can inhibit the transport of medicinal products by P-gp, which may result in an increased
plasma concentration of these medicinal products.
- Ketoconazole inhibits BCRP (Breast Cancer Resistance Protein) in in vitro studies. Data of inhibition
indicate that risk of interaction with BCRP substrates cannot be excluded at the systemic level with very
high doses of ketoconazole. However, ketoconazole may be an inhibitor of BCRP at the intestinal level at
clinically relevant concentrations. Considering the rapid absorption of ketoconazole, intake of BCRP
substrates should be postponed for 2 hours after ketoconazole intake.
Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.
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Version 2025-05-05T12:00:00Z · SHA-256 1463d2e081bcaa454cdfd6129ad3b8e03e3df9233f9d0704cfceba71c89c59b5 · Passage 08cf46cecfbfd47dd7db2431b6f70ede9c27dde3799daa13e28f0ded7d8d2184 · Zeichen 3346–4520 im Abschnitt
Wechselwirkungen · Ketoconazole Esteve (previously Ketoconazole HRA)
Ketoconazole Esteve 200 mg tablets · Abschnitt 4.5 · PDF-Seite 8
HOS-132852 · Präparat HOS-097310
Table 1 Interactions and recommendations for co-administration.
Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2025-05-05T12:00:00Z · SHA-256 1463d2e081bcaa454cdfd6129ad3b8e03e3df9233f9d0704cfceba71c89c59b5 · Passage d4418a33bdb025192f9d8f7076ccb651272a4b32e1c847cfde5f60ad04c1df10 · Zeichen 4522–4585 im Abschnitt
Wechselwirkungen · Ketoconazole Esteve (previously Ketoconazole HRA)
Ketoconazole Esteve 200 mg tablets · Abschnitt 4.5 · PDF-Seite 8
HOS-132853 · Präparat HOS-097310
Interactions between ketoconazole and other medicinal products are listed in the table below (increase is
indicated as “↑”, decrease as “↓”, an no change as “↔”). The degrees of interaction mentioned below are not
absolute values and may be dependent on the ketoconazole dose given, i.e. many results are reported following
a ketoconazole dose of 200 mg and a stronger interaction may be expected at a higher dose and/or shorter
dosing interval. The following list is not an inclusive list of interactions between ketoconazole and other
medicinal products
Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2025-05-05T12:00:00Z · SHA-256 1463d2e081bcaa454cdfd6129ad3b8e03e3df9233f9d0704cfceba71c89c59b5 · Passage 617eb8ea7e3a7860493aa5abfa24de9d08ea6321a6b4863035b117d56cbcf4df · Zeichen 4587–5142 im Abschnitt
Wechselwirkungen · Ketoconazole Esteve (previously Ketoconazole HRA)
Ketoconazole Esteve 200 mg tablets · Abschnitt 4.5 · PDF-Seite 8
HOS-132854 · Präparat HOS-097310
Medicinal product by Expected effect on drug levels Recommendation for co-
therapeutic area administration
Analgesic opioid
Methadone Potential ↑ in plasma concentrations of Contraindicated due to the increased
methadone risk of serious cardiovascular events
including QT prolongation and
torsade de pointes, or respiratory or
CNS depression (see section 4.3).
Buprenorphine IV and Buprenorphine: Careful monitoring.
sublingual AUC: ↑ 1.5-fold The buprenorphine dose should be
Cmax: ↑1.7-fold adjusted.
Alfentanil, fentanyl Potential ↑in plasma concentrations of Careful monitoring of adverse
alfentanil and fentanyl reactions (respiratory depression,
sedation) is recommended. It may be
necessary to lower the dose of
alfentanil and fentanyl.
Oxycodone ↑in plasma concentrations of oxycodone Careful monitoring.
have been observed The oxycodone dose may be
adjusted.
Antiarrhythmics
Disopyramide Potential ↑in plasma concentrations of Contraindicated due to the risk of
Quinidine disopyramide and quinidine serious cardiovascular events
including QT prolongation (see
Dronedarone Repeated doses of 200 mg ketoconazole section 4.3).
daily resulted in a 17-fold increase in
dronedarone exposure
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): alfentanil (HOS-109375) dronedarone (HOS-086144) methadone (HOS-086198) oxycodone (HOS-109487) quinidine (HOS-085593) buprenorphine (HOS-086193) disopyramide (HOS-085595) fentanyl (HOS-086196)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2025-05-05T12:00:00Z · SHA-256 1463d2e081bcaa454cdfd6129ad3b8e03e3df9233f9d0704cfceba71c89c59b5 · Passage a1dd81238eab9495ccc07c3bae05807a0a25b388887cce3d7c2818dcf0cb8b03 · Zeichen 5148–7488 im Abschnitt
Wechselwirkungen · Ketoconazole Esteve (previously Ketoconazole HRA)
Ketoconazole Esteve 200 mg tablets · Abschnitt 4.5 · PDF-Seite 8–9
HOS-132855 · Präparat HOS-097310
8
Medicinal product by Expected effect on drug levels Recommendation for co-
therapeutic area administration
Digoxin Potential ↑in plasma concentrations of Careful monitoring of digoxin levels
digoxine is recommended.
Anticoagulants and
antiplatelet drugs
Dabigatran Dabigatran: Contraindicated due to an increased
AUC: ↑ 2.6-fold bleeding risk (see section 4.3).
Cmax: ↑2.5-fold
Rivaroxaban Rivaroxaban: Not recommended due to an
AUC: ↑ 2.6-fold increased bleeding risk.
Cmax: ↑1.7-fold
Apixaban Apixaban Not recommended due to an
AUC: ↑ 2-fold increased bleeding risk.
Cmax: ↑1.6-fold
Cilostazol Cilostazol: Careful monitoring
AUC: ↑ 2.2 fold A cilostazol dose of 50 mg twice
daily is recommended in combination
The overall pharmacological activity of with ketoconazole.
cilostazol increases 35% when co-
administered with ketoconazole.
Warfarin and other Potential ↑in plasma concentrations of Careful monitoring
coumarin-like drugs warfarin INR (international normalised ratio)
monitoring recommended.
Edoxaban AUC: ↑ 1.8-fold Dose of edoxaban needs to be
Cmax: ↑ 1.8-fold reduced when used concomitantly,
please consult edoxaban SmPC.
Anticonvulsants
Carbamazepine Potential ↑in plasma concentrations of Not recommended.
Phenytoin carbamazepine and phenytoin (See also “Effects of other medicinal
products on the metabolism of
Potential ↓ in plasma concentrations of Ketoconazole Esteve ”).
ketoconazole are expected.
(CYP3A enzyme induction)
Antidiabetics
Repaglinide Repaglinide: Careful monitoring.
AUC: ↑ 1.2-fold Dose adjustement of repaglinide may
Cmax: ↑ 1.2-fold be required.
Saxagliptin Saxagliptin: Careful monitoring.
AUC: ↑ 2.5-fold Dose adjustment of saxagliptin may
Cmax: ↑ 1.6-fold be required.
Associated with a decrease in
corresponding values for the active
metabolite
Tolbutamide Tolbutamide: Careful monitoring.
AUC: ↑ 1.7-fold Dose adjustment of tolbutamide may
be required.
Anti-infectives
Rifabutin Potential ↑ in plasma concentrations of Not recommended. (See also “Effects
Rifampicin rifabutine. of other medicinal products on the
Isoniazid Potencial ↓ in plasma concentrations of metabolism of Ketoconazole Esteve
ketoconazole are expected. ”)
(CYP3A4 enzyme 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): cilostazol (HOS-111550) saxagliptin (HOS-121455) carbamazepine (HOS-085618) rifabutin (HOS-086262) digoxin (HOS-086172) dabigatran (HOS-112096) rivaroxaban (HOS-086236) edoxaban (HOS-086234) apixaban (HOS-112091) isoniazid (HOS-088590) phenytoin (HOS-084531) warfarin (HOS-085950) repaglinide (HOS-086935) tolbutamide (HOS-086568)
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Version 2025-05-05T12:00:00Z · SHA-256 1463d2e081bcaa454cdfd6129ad3b8e03e3df9233f9d0704cfceba71c89c59b5 · Passage 24d8b798c2e9f588393126dccbf62410ab1c9fc1c2be502385d6b5856457931a · Zeichen 7545–11521 im Abschnitt
Wechselwirkungen · Ketoconazole Esteve (previously Ketoconazole HRA)
Ketoconazole Esteve 200 mg tablets · Abschnitt 4.5 · PDF-Seite 9–10
HOS-132857 · Präparat HOS-097310
9
Medicinal product by Expected effect on drug levels Recommendation for co-
therapeutic area administration
Telithromycin Telithromycine: Not recommended.
Clarithromycin AUC: ↑ 2-fold Contraindicated in patients with
Cmax: ↑1.5-fold severe renal impairment due to the
Potential ↑in plasma concentrations of risk of QT interval prolongation and
clarithromycin serious hepatic adverse reactions (see
section 4.3).
Isavuconazole AUC: ↑ 5-fold Not recommended due to increased
Cmax: ↑ 1.1 -fold risk of isavuconazole adverse
reactions, please consult
isavuconazole SmPC
Praziquantel ↑in plasma concentrations of Careful monitoring.
praziquantel have been observed Dose adjustment of praziquantel
may be required.
Antimigraine Drugs
Ergots alkaloids such as Potential ↑in plasma concentrations of Contraindicated due to the increased
dihydroergotamine, ergot alkaloids risk of ergotism and other serious
ergometrine vasospastic adverse reactions (see
(ergonovine), section 4.3).
ergotamine,
methylergometrine
(methylergonovine)
Eletriptan Eletriptan: Not recommended.
AUC: ↑ 5.9-fold
Cmax: ↑ 2.7-fold
Antineoplastics
Irinotecan Irinotecan: Contraindicated due to an alteration
AUC: ↑ 2.1-fold of the metabolism of this medicinal
product (see section 4.3).
Sunitinib Sunitinib Not recommended due to the risk of
Dasatinib AUC: ↑ 1.5-fold increased exposure to these medicinal
Lapatinib Cmax: ↑ 1.5-fold products and QT prolongation.
Nilotinib Lapatinib:
Erlotinib AUC: ↑ 3.6-fold
Dabrafenib Nilotinib:
Cabozantinib AUC: ↑ 3.0-fold
Erlotinib:
AUC: ↑ 1.9-fold
Cmax: ↑ 1.7-fold
Dasatinib
↑in plasma concentrations of
Dasatinib have been observed
Dabrafenib
AUC: ↑ 1.7-fold
Cmax: ↑ 1.3-fold
Cabozantinib
AUC: ↑ 1.4-fold
Cmax: ↔
Ibrutinib Ibrutinib: Not recommended as it may increase
AUC: ↑ 24-fold ibrutinib-related toxicity.
Cmax: ↑ 29-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): praziquantel (HOS-132858) dasatinib (HOS-086217) isavuconazole (HOS-085186) methylergonovine (HOS-086155) dabrafenib (HOS-109452) ergot alkaloids (HOS-108807) telithromycin (HOS-084523) lapatinib (HOS-122565) clarithromycin (HOS-084517) erlotinib (HOS-113527) eletriptan (HOS-132859) sunitinib (HOS-109453) ergotamine (HOS-086154) irinotecan (HOS-112102) ergonovine (HOS-086153) cabozantinib (HOS-109450) nilotinib (HOS-086218) dihydroergotamine (HOS-086152) ibrutinib (HOS-086226)
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Version 2025-05-05T12:00:00Z · SHA-256 1463d2e081bcaa454cdfd6129ad3b8e03e3df9233f9d0704cfceba71c89c59b5 · Passage 03def5869df8cb542da23a60d098a55dd2a7a8fe93c7c4d29a7dfa3bc81a0b64 · Zeichen 11575–15074 im Abschnitt
Wechselwirkungen · Ketoconazole Esteve (previously Ketoconazole HRA)
Ketoconazole Esteve 200 mg tablets · Abschnitt 4.5 · PDF-Seite 10–11
HOS-132860 · Präparat HOS-097310
10
Medicinal product by Expected effect on drug levels Recommendation for co-
therapeutic area administration
Crizotinib Crizotinib Not recommended due to the risk of
AUC: ↑ 3.2-fold QT interval prolongation and serious
Cmax: ↑ 1.4-fold hepatic adverse reactions.
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): crizotinib (HOS-116818)
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2025-05-05T12:00:00Z · SHA-256 1463d2e081bcaa454cdfd6129ad3b8e03e3df9233f9d0704cfceba71c89c59b5 · Passage 91ac6130f3f7657d11df1aae49ac3cd31ba5b3839fb590262ba64cf623d2a901 · Zeichen 15129–15599 im Abschnitt
Wechselwirkungen · Ketoconazole Esteve (previously Ketoconazole HRA)
Ketoconazole Esteve 200 mg tablets · Abschnitt 4.5 · PDF-Seite 11–12
HOS-132861 · Präparat HOS-097310
Monitoring of QT-prolongation if
used concomitantly.
Bortezomib Bortezomib: Careful monitoring.
Busulfan AUC: ↑ 1.4-fold Dose adjustment of each medicinal
Docetaxel Imatinib: product may be required.
Imatinib AUC: ↑ 1.4-fold
Cabazitaxel Cmax: ↑ 1.3-fold
↑in plasma concentrations of
docetaxel have been observed
Potential ↑in plasma concentrations of
busulfan
Cabazitaxel
AUC: ↑ 1.3-fold
Paclitaxel Paclitaxel: Careful monitoring.
No change in plasma concentration were Dose adjustment of paclitaxel
shown with paclitaxel concentrate. No may be required.
studies were performed with albumin
bound nanoparticules.
Vincristine, vinblastine Potential ↑in plasma concentrations of Careful monitoring as it may cause
(vinca alkaloids) vinca alkaloids. an earlier onset and/or an increased
severity of side-effects.
Antipsychotics,
Anxiolytics and
Hypnotics
Triazolam AUC: ↑ have been observed Contraindicated due to the risk of
Alprazolam Cmax: ↑ have been observed potentially prolonged or increased
Midazolam oral sedation and respiratory depression
(see section 4.3).
Lurasidone Lurasidone: Contraindicated due to the increased
AUC: ↑ 9 fold risk of adverse reactions (see section
Cmax: ↑ 6 fold 4.3).
Pimozide Potential ↑in plasma concentrations of Contraindicated due to the risk of
pimozide. serious cardiovascular events
including QT prolongation (see
section 4.3).
Sertindole Potential ↑in plasma concentrations of Contraindicated due to the risk of QT
sertindole. prolongation (see section 4.3).
Quetiapine Quetiapine: Contraindicated as it may increase
AUC: ↑ 6.2-fold quetiapine-related toxicity (see
Cmax: ↑ 3.4-fold section 4.3).
Haloperidol Potential ↑in plasma concentrations of Not recommended due to the
haloperidol. increased risk of QT prolongation
and extrapyramidal symptoms. It
may be necessary to reduce
haloperidol dosage.
Reboxetine Reboxetine: Not recommended because of
AUC: ↑ 1.5-fold of both enantiomers reboxetine narrow’s therapeutic
margin.
Midazolam IV Midazolam: Careful monitoring.
AUC: ↑ 1.6-fold Dose adjustment of midazolam IV
may be required.
11
Medicinal product by Expected effect on drug levels Recommendation for co-
therapeutic area administration
Buspirone Potential ↑in plasma concentrations of Careful monitoring.
buspirone. Dose adjustement of buspirone
may be required.
Aripiprazole Aripiprazole Careful monitoring.
AUC: ↑ 1.6-fold Aripiprazole dose should be reduced
Cmax: ↑ 1.4-fold to approximatively one-half of its
prescribed dose.
Risperidone Potential ↑in AUC of risperidone: Careful monitoring. Dose adjustment
of risperidone may be required.
Antivirals products
Saquinavir Saquinavir: Contraindicated due to the risk of QT
(saquinavir/ritonavir AUC: ↔ prolongation (see section 4.3).
1000/100 mg bid) Cmax: ↔
Ketoconazole
AUC: ↑ 2.7-fold
Cmax:↑ 1.5-fold
(CYP3A4 enzyme inhibition by
ritonavir)
Paritaprevir: Contraindicated due to the increased
AUC: ↑2.2-fold risk of adverse reactions (see section
Cmax: ↑1.7-fold 4.3).
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): aripiprazole (HOS-129408) sertindole (HOS-085601) quetiapine (HOS-086150) busulfan (HOS-115553) reboxetine (HOS-132863) alprazolam (HOS-086171) vinblastine (HOS-086220) risperidone (HOS-086280) vincristine (HOS-086219) imatinib (HOS-110212) docetaxel (HOS-084505) saquinavir (HOS-084522) bortezomib (HOS-110227) pimozide (HOS-085600) cabazitaxel (HOS-124028) buspirone (HOS-086325) paclitaxel (HOS-087959) haloperidol (HOS-085602) ritonavir (HOS-084521) paritaprevir (HOS-110301) lurasidone (HOS-086148) triazolam (HOS-086168) midazolam (HOS-086167)
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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.