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.
Other concomitant use
Specific interaction studies have shown no clinically significant effect of the following medicinal
products on pharmacokinetics and pharmacodynamics of ivabradine: proton pump inhibitors
(omeprazole, lansoprazole), sildenafil, HMG CoA reductase inhibitors (simvastatin), dihydropyridine
calcium channel blockers (amlodipine, lacidipine), digoxin and warfarin. In addition there was no
7
clinically significant effect of ivabradine on the pharmacokinetics of simvastatin, amlodipine,
lacidipine, on the pharmacokinetics and pharmacodynamics of digoxin, warfarin and on the
pharmacodynamics of aspirin.
In pivotal phase III clinical trials the following medicinal products were routinely combined with
ivabradine with no evidence of safety concerns: angiotensin converting enzyme inhibitors, angiotensin
II antagonists, beta-blockers, diuretics, anti-aldosterone agents, short and long acting nitrates, HMG
CoA reductase inhibitors, fibrates, proton pump inhibitors, oral antidiabetics, aspirin and other anti-
platelet medicinal products.
Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.
Other concomitant use
Specific interaction studies have shown no clinically significant effect of the following medicinal
products on pharmacokinetics and pharmacodynamics of ivabradine: proton pump inhibitors
(omeprazole, lansoprazole), sildenafil, HMG CoA reductase inhibitors (simvastatin), dihydropyridine
7
calcium channel blockers (amlodipine, lacidipine), digoxin and warfarin. In addition there was no
clinically significant effect of ivabradine on the pharmacokinetics of simvastatin, amlodipine,
lacidipine, on the pharmacokinetics and pharmacodynamics of digoxin, warfarin and on the
pharmacodynamics of aspirin.
In pivotal phase III clinical trials the following medicinal products were routinely combined with
ivabradine with no evidence of safety concerns: angiotensin converting enzyme inhibitors, angiotensin
II antagonists, beta-blockers, diuretics, anti-aldosterone agents, short and long acting nitrates, HMG
CoA reductase inhibitors, fibrates, proton pump inhibitors, oral antidiabetics, aspirin and other anti-
platelet medicinal products.
Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.
Weak CYP3A4 inhibitors are When administered with atorvastatin, the
expected to increase the exposure of dose of lomitapide should either be taken
lomitapide when taken 12 hours apart or be decreased by half (see
simultaneously. section 4.2). The dose of lomitapide should
be taken 12 hours apart from any other
When lomitapide 20 mg was concomitant weak CYP3A4 inhibitors.
co-administered simultaneously with Examples of weak CYP3A4 inhibitors
atorvastatin, a weak CYP3A4 include: alprazolam, amiodarone,
inhibitor, lomitapide AUC and Cmax amlodipine, atorvastatin, azithromycin,
increased approximately 2-fold. bicalutamide, cilostazol, cimetidine,
When the dose of lomitapide was ciclosporin, clotrimazole, fluoxetine,
taken 12 hours apart from fluvoxamine, fosaprepitant, ginkgo,
atorvastatin, no clinically meaningful goldenseal, isoniazid, ivacaftor, lacidipine,
increase in lomitapide exposure was lapatinib, linagliptin, nilotinib,
observed. oestrogen-containing oral contraceptives,
pazopanib, peppermint oil, propiverine,
When lomitapide 20 mg was co- ranitidine, ranolazine, roxithromycin, Seville
administered simultaneously or oranges, tacrolimus, ticagrelor and tolvaptan.
12 hours apart with ethinyl This list is not intended to be comprehensive
estradiol/norgestimate, a weak and prescribers should check the prescribing
CYP3A4 inhibitor, no clinically information of medicinal products to be co-
meaningful increase in lomitapide administered with Lojuxta for potential
exposure was observed. CYP3A4 mediated interactions.
Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.
Version 2026-06-25T14:24:00Z · SHA-256 56c36935b5cda4380e359902f1acbc5ec5bb081beeb96ca75e5ad86521fcd98c · Passage 714d59bc1bbe3ac0c5d4eeaa178f455a97b56caa11d4ced4ec39de50572ee7d0 · Zeichen 2870–5037 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.