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 · Advagraf
Advagraf 0.5 mg prolonged-release hard capsules Advagraf 1 mg prolonged-release hard capsules Advagraf 3 mg prolonged-release hard capsules Advagraf 5 mg prolonged-release hard capsules · Abschnitt 4.5 · PDF-Seite 10–11
HOS-116802 · Präparat HOS-094481
10
Drug/Substance Class or Drug interaction effect Recommendations concerning
Name co-administration
Strong CYP3A4 inhibitors: May increase tacrolimus whole It is recommended that
antifungal agents (e.g., blood trough concentrations and concomitant use should be
ketoconazole, itraconazole, increase the risk of serious adverse avoided. If co-administration
posaconazole, voriconazole), reactions (e.g., nephrotoxicity, of a strong CYP3A4 inhibitor
the macrolide antibiotics neurotoxicity, QT prolongation) is unavoidable, consider
(e.g., telithromycin, which requires close monitoring omitting the dose of tacrolimus
troleandomycin, [see section 4.4]. the day the strong CYP3A4
clarithromycin, josamycin), Rapid and sharp increases in inhibitor is initiated. Reinitiate
HIV protease inhibitors tacrolimus levels may occur, as tacrolimus the next day at a
(e.g., ritonavir, nelfinavir, early as within 1-3 days after co- reduced dose based on
saquinavir), HCV protease administration, despite immediate tacrolimus blood
inhibitors (e.g., telaprevir, reduction of tacrolimus dose. concentrations. Changes in
boceprevir, and the Overall tacrolimus exposure may both tacrolimus dose and/or
combination of ombitasvir increase > 5 fold. When ritonavir dosing frequency should be
and paritaprevir with combinations are co-administered, individualized and adjusted as
ritonavir, when used with tacrolimus exposure may increase needed based on tacrolimus
and without dasabuvir), > 50 fold. Nearly all patients may trough concentrations, which
nefazodone, the require a reduction in tacrolimus should be assessed at initiation,
pharmacokinetic enhancer dose and temporary interruption of monitored frequently
cobicistat, and the kinase tacrolimus may also be necessary. throughout (starting within the
inhibitors idelalisib, The effect on tacrolimus blood first few days) and re-
ceritinib. concentrations may remain for evaluated on and after
Strong interactions have also several days after co-administration completion of the CYP3A4
been observed with the is completed. inhibitor. Upon completion,
macrolide antibiotic appropriate dose and dosing
erythromycin frequency of tacrolimus should
be guided by tacrolimus blood
concentrations. Monitor renal
function, ECG for QT
prolongation, and other side
effects closely.
Moderate or weak CYP3A4 May increase tacrolimus whole Monitor tacrolimus whole
inhibitors: blood trough concentrations and blood trough concentrations
antifungal agents (e.g., increase the risk of serious adverse frequently, starting within the
fluconazole, isavuconazole, reactions (e.g., neurotoxicity, QT first few days of co-
clotrimazole, miconazole), prolongation) [see section 4.4]. A administration. Reduce
the macrolide antibiotics rapid increase in tacrolimus level tacrolimus dose if needed [see
(e.g., azithromycin), calcium may occur. section 4.2]. Monitor renal
channel blockers (e.g., function, ECG for QT
nifedipine, nicardipine, prolongation, and other side
diltiazem, verapamil), effects closely.
amiodarone, danazol,
ethinylestradiol,
lansoprazole, omeprazole,
the HCV antivirals
elbasvir/grazoprevir and
glecaprevir/pibrentasvir, the
CMV antiviral letermovir,
and the tyrosine kinase
inhibitors nilotinib,
crizotinib and imatinib and
(Chinese) herbal remedies
containing extracts of
Schisandra sphenanthera
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): lansoprazole (HOS-085166) letermovir (HOS-090621) ceritinib (HOS-086215) josamycin (HOS-113844) diltiazem (HOS-086288) nefazodone (HOS-084519) elbasvir (HOS-108814) isavuconazole (HOS-085186) nifedipine (HOS-086289) nelfinavir (HOS-084520) nicardipine (HOS-090619) protease (HOS-085623) ketoconazole (HOS-084513) pibrentasvir (HOS-086298) crizotinib (HOS-116818) cobicistat (HOS-088111) glecaprevir (HOS-086297) azithromycin (HOS-088112) clotrimazole (HOS-090574) calcium (HOS-085615) imatinib (HOS-110212) dasabuvir (HOS-110302) voriconazole (HOS-084524) telaprevir (HOS-090618) telithromycin (HOS-084523) grazoprevir (HOS-108815) itraconazole (HOS-084516) saquinavir (HOS-084522) danazol (HOS-085473) fluconazole (HOS-087945) ombitasvir (HOS-110300) boceprevir (HOS-090617) clarithromycin (HOS-084517) erythromycin (HOS-084514) troleandomycin (HOS-090575) ritonavir (HOS-084521) amiodarone (HOS-085596) paritaprevir (HOS-110301) tyrosine (HOS-108875) posaconazole (HOS-085622) nilotinib (HOS-086218) miconazole (HOS-115630) idelalisib (HOS-116811) omeprazole (HOS-085912) verapamil (HOS-090602)
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Wechselwirkungen · Modigraf
Modigraf 0.2 mg granules for oral suspension Modigraf 1 mg granules for oral suspension · Abschnitt 4.5 · PDF-Seite 10–11
HOS-209742 · Präparat HOS-154375
10
Medicinal products which have effects on tacrolimus
Drug/Substance Class or Drug interaction effect Recommendations concerning co-
Name administration
Grapefruit or grapefruit juice May increase tacrolimus Avoid grapefruit or grapefruit
whole blood trough juice.
concentrations and increase
the risk of serious adverse
reactions (e.g., neurotoxicity,
QT prolongation) [see
section 4.4].
Ciclosporin May increase tacrolimus The simultaneous use of
whole blood trough ciclosporin and tacrolimus should
concentrations. In addition, be avoided [see section 4.4].
synergistic/additive
nephrotoxic effects can
occur.
Products known to have May enhance nephrotoxic or Concurrent use of tacrolimus with
nephrotoxic or neurotoxic neurotoxic effects of drugs known to have nephrotoxic
effects: tacrolimus. effects should be avoided. When
aminoglycosides, gyrase co-administration cannot be
inhibitors, vancomycin, avoided, monitor renal function
sulfamethoxazole + and other side effects and adjust
trimethoprim, NSAIDs, tacrolimus dose if needed.
ganciclovir, acyclovir,
amphotericin B, ibuprofen
cidofovir, foscarnet
Strong CYP3A4 inhibitors: May increase tacrolimus It is recommended that
antifungal agents (e.g., whole blood trough concomitant use should be
ketoconazole, itraconazole, concentrations and increase avoided. If co-administration of a
posaconazole, voriconazole), the risk of serious adverse strong CYP3A4 inhibitor is
the macrolide antibiotics reactions (e.g., unavoidable, consider omitting
(e.g., telithromycin, nephrotoxicity, the dose of tacrolimus the day the
troleandomycin, neurotoxicity, QT strong CYP3A4 inhibitor is
clarithromycin, josamycin), prolongation) which requires initiated. Reinitiate tacrolimus the
HIV protease inhibitors (e.g., close monitoring [see next day at a reduced dose based
ritonavir, nelfinavir, section 4.4]. on tacrolimus blood
saquinavir), HCV protease Rapid and sharp increases in concentrations. Changes in both
inhibitors (e.g., telaprevir, tacrolimus levels may occur, tacrolimus dose and/or dosing
boceprevir, and the as early as within 1-3 days frequency should be
combination of ombitasvir after co-administration, individualized and adjusted as
and paritaprevir with despite immediate reduction needed based on tacrolimus
ritonavir, when used with and of tacrolimus dose. Overall trough concentrations, which
without dasabuvir), tacrolimus exposure may should be assessed at initiation,
nefazodone, the increase > 5 fold. When monitored frequently throughout
pharmacokinetic enhancer ritonavir combinations are (starting within the first few days)
cobicistat and the kinase co-administered, tacrolimus and re-evaluated on and after
inhibitors idelalisib, ceritinib. exposure may increase > 50 completion of the CYP3A4
Strong interactions have also fold. inhibitor. Upon completion,
been observed with the Nearly all patients may appropriate dose and dosing
macrolide antibiotic require a reduction in frequency of tacrolimus should be
erythromycin tacrolimus dose and guided by tacrolimus blood
temporary interruption of concentrations. Monitor renal
tacrolimus may also be function, ECG for QT
necessary. prolongation, and other side
effects closely.
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): foscarnet (HOS-110484) sulfamethoxazole (HOS-084533) ceritinib (HOS-086215) josamycin (HOS-113844) nefazodone (HOS-084519) nelfinavir (HOS-084520) ibuprofen (HOS-087884) protease (HOS-085623) amphotericin B (HOS-109312) trimethoprim (HOS-085184) ketoconazole (HOS-084513) cobicistat (HOS-088111) cidofovir (HOS-110482) grapefruit juice (HOS-088787) dasabuvir (HOS-110302) voriconazole (HOS-084524) telaprevir (HOS-090618) telithromycin (HOS-084523) itraconazole (HOS-084516) saquinavir (HOS-084522) ombitasvir (HOS-110300) boceprevir (HOS-090617) clarithromycin (HOS-084517) vancomycin (HOS-110486) erythromycin (HOS-084514) troleandomycin (HOS-090575) ritonavir (HOS-084521) ganciclovir (HOS-085194) paritaprevir (HOS-110301) acyclovir (HOS-088527) posaconazole (HOS-085622) idelalisib (HOS-116811)
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Gegenanzeigen · Zydelig
Zydelig 100 mg film-coated tablets Zydelig 150 mg film-coated tablets · Abschnitt 4.3 · PDF-Seite 4
HOS-132090 · Präparat HOS-097192
Hypersensitivity to the active substance or to any of the excipients listed in section 6.1.
Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.
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Wechselwirkungen · Zydelig
Zydelig 100 mg film-coated tablets Zydelig 150 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 6
HOS-132091 · Präparat HOS-097192
Idelalisib is metabolised primarily via aldehyde oxidase, and to a lesser extent via CYP3A and
glucuronidation (UGT1A4). Its primary metabolite is GS-563117, which is not pharmacologically
active. Idelalisib and GS-563117 are substrates of P-gp and BCRP.
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
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Wechselwirkungen · Zydelig
Zydelig 100 mg film-coated tablets Zydelig 150 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 6–7
HOS-132092 · Präparat HOS-097192
6
Effect of other medicinal products on idelalisib pharmacokinetics
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 2024-10-21T17:52:00Z · SHA-256 f55f90ba278a87ef1c8e7162344ed4bd66ac7180deaf4c8fda3eca5bbf8e87e5 · Passage 2b05e79cb3c510d7ce3b288a4f64ce0dd6cf486ca70711856053e3e164848fc0 · Zeichen 306–374 im Abschnitt
Wechselwirkungen · Zydelig
Zydelig 100 mg film-coated tablets Zydelig 150 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 7
HOS-132093 · Präparat HOS-097192
CYP3A inducers
A clinical drug interaction study found that co-administration of a single dose of 150 mg idelalisib
with rifampicin (a strong CYP3A inducer) resulted in a ~75% reduction in idelalisib AUCinf.
Co-administration of Zydelig with moderate or strong CYP3A inducers such as rifampicin, phenytoin,
St. John’s wort, or carbamazepine should be avoided as this may result in decreased efficacy.
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) phenytoin (HOS-084531)
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Wechselwirkungen · Zydelig
Zydelig 100 mg film-coated tablets Zydelig 150 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 7
HOS-132094 · Präparat HOS-097192
CYP3A/P-gp inhibitors
A clinical drug interaction study found that co-administration of a single dose of 400 mg idelalisib
with 400 mg once daily ketoconazole (a strong CYP3A, P-gp and BCRP inhibitor) resulted in a 26%
increase in Cmax and a 79% increase in AUCinf of idelalisib. No initial dose adjustment of idelalisib is
considered necessary when administered with CYP3A/P-gp inhibitors, but an intensified monitoring of
adverse reactions is 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): ketoconazole (HOS-084513)
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Wechselwirkungen · Zydelig
Zydelig 100 mg film-coated tablets Zydelig 150 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 7
HOS-132095 · Präparat HOS-097192
Effect of idelalisib on the pharmacokinetics of other medicinal products
Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.
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Wechselwirkungen · Zydelig
Zydelig 100 mg film-coated tablets Zydelig 150 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 7
HOS-132096 · Präparat HOS-097192
CYP3A substrates
The primary metabolite of idelalisib, GS-563117, is a strong CYP3A inhibitor. A clinical drug
interaction study found that co-administration of idelalisib with midazolam (a sensitive CYP3A
substrate) resulted in a ~140% increase in Cmax and a ~440% increase in AUCinf of midazolam due to
the CYP3A inhibition by GS-563117. Co-administration of idelalisib with CYP3A substrates may
increase their systemic exposures and increase or prolong their therapeutic activity and adverse
reactions. In vitro, the CYP3A4 inhibition was irreversible, and return to normal enzyme activity is
therefore expected to take several days after stopping idelalisib administration.
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): midazolam (HOS-086167)
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Wechselwirkungen · Zydelig
Zydelig 100 mg film-coated tablets Zydelig 150 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 7
HOS-132097 · Präparat HOS-097192
Potential interactions between idelalisib and co-administered medicinal products that are CYP3A
substrates are listed in Table 1 (increase is indicated as “↑”). This list is not exhaustive and is intended
to serve as guidance only. In general, the SmPC for the other product must be consulted for the
recommendations regarding co-administration with CYP3A4 inhibitors (see section 4.4).
Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.
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Wechselwirkungen · Zydelig
Zydelig 100 mg film-coated tablets Zydelig 150 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 7
HOS-132098 · Präparat HOS-097192
Table 1: Interactions between idelalisib and other medicinal products that are CYP3A
substrates
Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.
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Wechselwirkungen · Zydelig
Zydelig 100 mg film-coated tablets Zydelig 150 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 7
HOS-132099 · Präparat HOS-097192
Medicinal product Expected effect of Clinical recommendation upon
idelalisib on medicinal co-administration with idelalisib
product levels
ALPHA-1 ADRENORECEPTOR ANTAGONISTS
Alfuzosin ↑ serum concentrations Idelalisib should not be
co-administered with alfuzosin.
ANALGESICS
Fentanyl, alfentanil, methadone, ↑ serum concentrations Careful monitoring of adverse
buprenorphine/naloxone reactions (e.g., respiratory depression,
sedation) is recommended.
ANTIARRHYTHMICS
Amiodarone, quinidine ↑ serum concentrations Idelalisib should not be
co-administered with amiodarone or
quinidine.
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) alfuzosin (HOS-086139) methadone (HOS-086198) quinidine (HOS-085593) buprenorphine (HOS-086193) naloxone (HOS-109490) fentanyl (HOS-086196) amiodarone (HOS-085596)
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Wechselwirkungen · Zydelig
Zydelig 100 mg film-coated tablets Zydelig 150 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 7
HOS-132100 · Präparat HOS-097192
Bepridil, disopyramide, ↑ serum concentrations Clinical monitoring is recommended.
lidocaine
ANTI-CANCER AGENTS
Tyrosine kinase inhibitors such ↑ serum concentrations Careful monitoring of the tolerance to
as dasatinib and nilotinib, also these anti-cancer agents is
vincristine and vinblastine 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): dasatinib (HOS-086217) lidocaine (HOS-108866) vinblastine (HOS-086220) bepridil (HOS-085612) vincristine (HOS-086219) disopyramide (HOS-085595) tyrosine (HOS-108875) nilotinib (HOS-086218)
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Wechselwirkungen · Zydelig
Zydelig 100 mg film-coated tablets Zydelig 150 mg film-coated tablets · Abschnitt 4.5 · PDF-Seite 7–8
HOS-132102 · Präparat HOS-097192
7
Medicinal product Expected effect of Clinical recommendation upon
idelalisib on medicinal co-administration with idelalisib
product levels
ANTICOAGULANTS
Warfarin ↑ serum concentrations It is recommended that the
international normalised ratio (INR)
be monitored upon co-administration
and following ceasing treatment with
idelalisib.
ANTICONVULSANTS
Carbamazepine ↑ serum concentrations Anticonvulsant medicinal product
levels should be monitored.
ANTIDEPRESSANTS
Trazodone ↑ serum concentrations Careful dose titration of the
antidepressant and monitoring for
antidepressant response is
recommended.
ANTI-GOUT
Colchicine ↑ serum concentrations Dose reductions of colchicine may be
required. Idelalisib should not be
co-administered with colchicine to
patients with renal or hepatic
impairment.
ANTI-HYPERTENSIVES
Amlodipine, diltiazem, ↑ serum concentrations Clinical monitoring of therapeutic
felodipine, nifedipine, effect and adverse reactions is
nicardipine recommended.
ANTI-INFECTIVES
Antifungals
Ketoconazole, itraconazole, ↑ serum concentrations Clinical monitoring is recommended.
posaconazole, voriconazole
Antimycobacterials
Rifabutin ↑ serum concentrations Increased monitoring for rifabutin-
associated adverse reactions including
neutropenia and uveitis is
recommended.
HCV protease inhibitors
Boceprevir, telaprevir ↑ serum concentrations Clinical monitoring is recommended.
Macrolide antibiotics
Clarithromycin, telithromycin ↑ serum concentrations No dose adjustment of clarithromycin
is required for patients with normal
renal function or mild renal
impairment (creatinine clearance
[CrCl] 60-90 mL/min). Clinical
monitoring is recommended for
patients with CrCl < 90 mL/min. For
patients with CrCl < 60 mL/min,
alternative antibacterials should be
considered.
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) nifedipine (HOS-086289) nicardipine (HOS-090619) protease (HOS-085623) ketoconazole (HOS-084513) felodipine (HOS-108908) carbamazepine (HOS-085618) rifabutin (HOS-086262) amlodipine (HOS-086287) creatinine (HOS-086273) voriconazole (HOS-084524) telaprevir (HOS-090618) telithromycin (HOS-084523) itraconazole (HOS-084516) trazodone (HOS-086251) boceprevir (HOS-090617) clarithromycin (HOS-084517) colchicine (HOS-086147) warfarin (HOS-085950) posaconazole (HOS-085622)
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Version 2024-10-21T17:52:00Z · SHA-256 f55f90ba278a87ef1c8e7162344ed4bd66ac7180deaf4c8fda3eca5bbf8e87e5 · Passage 5f9a56fd2cd08a1553975154a7af1dc43198c97641aafb1794cd76642177c219 · Zeichen 4000–7499 im Abschnitt
Wechselwirkungen · Zydelig
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HOS-132104 · Präparat HOS-097192
Clinical monitoring is recommended
for telithromycin.
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): telithromycin (HOS-084523)
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Version 2024-10-21T17:52:00Z · SHA-256 f55f90ba278a87ef1c8e7162344ed4bd66ac7180deaf4c8fda3eca5bbf8e87e5 · Passage 155ba289e7c26bfc08e68ff1cff32fd6c5ba7439d6048e545c31792e2638fde5 · Zeichen 7559–7670 im Abschnitt
Wechselwirkungen · Zydelig
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HOS-132105 · Präparat HOS-097192
8
Medicinal product Expected effect of Clinical recommendation upon
idelalisib on medicinal co-administration with idelalisib
product levels
ANTI-PSYCHOTICS/NEUROLEPTICS
Quetiapine, pimozide ↑ serum concentrations Idelalisib should not be
co-administered with quetiapine or
pimozide.
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): quetiapine (HOS-086150) pimozide (HOS-085600)
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Version 2024-10-21T17:52:00Z · SHA-256 f55f90ba278a87ef1c8e7162344ed4bd66ac7180deaf4c8fda3eca5bbf8e87e5 · Passage 790a848c95a0bb1b7b5c26608fa26cdabe9825fe87ebb9198f842fffce365364 · Zeichen 7721–8212 im Abschnitt
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HOS-132106 · Präparat HOS-097192
Alternative medicinal products, such
as olanzapine, may be considered.
ENDOTHELIN RECEPTOR ANTAGONISTS
Bosentan ↑ serum concentrations Caution should be exercised and
patients closely observed for bosentan-
related toxicity.
ERGOT ALKALOIDS
Ergotamine, dihydroergotamine ↑ serum concentrations Idelalisib should not be
co-administered with ergotamine or
dihydroergotamine.
GASTROINTESTINAL MOTILITY AGENTS
Cisapride ↑ serum concentrations Idelalisib should not be
co-administered with cisapride.
GLUCOCORTICOIDS
Inhaled/nasal corticosteroids:
Budesonide, fluticasone ↑ serum concentrations Clinical monitoring is 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): olanzapine (HOS-085937) fluticasone (HOS-108914) cisapride (HOS-085610) ergot alkaloids (HOS-108807) budesonide (HOS-086332) ergotamine (HOS-086154) bosentan (HOS-086291) dihydroergotamine (HOS-086152)
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Version 2024-10-21T17:52:00Z · SHA-256 f55f90ba278a87ef1c8e7162344ed4bd66ac7180deaf4c8fda3eca5bbf8e87e5 · Passage 3bc5dd16d11d17191775a3e4049c2785427ec9be009ef5c94fd6d9a10a26f310 · Zeichen 8272–9312 im Abschnitt
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HOS-132107 · Präparat HOS-097192
Oral budesonide ↑ serum concentrations Clinical monitoring is recommended
for increased signs/symptoms of
corticosteroid effects.
HMG CO-A REDUCTASE INHIBITORS
Lovastatin, simvastatin ↑ serum concentrations Idelalisib should not be
co-administered with lovastatin or
simvastatin.
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): lovastatin (HOS-086157) simvastatin (HOS-086158) budesonide (HOS-086332)
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Version 2024-10-21T17:52:00Z · SHA-256 f55f90ba278a87ef1c8e7162344ed4bd66ac7180deaf4c8fda3eca5bbf8e87e5 · Passage 3536af7eddfa7b781b757454c00c55ec649f5b73d703a40f2f7ae63a9d806cad · Zeichen 9314–9855 im Abschnitt
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HOS-132108 · Präparat HOS-097192
Atorvastatin ↑ serum concentrations Clinical monitoring is recommended
and a lower starting dose of
atorvastatin may be considered.
Alternatively, switching to pravastatin,
rosuvastatin, or pitavastatin may be
considered.
IMMUNOSUPPRESSANTS
Ciclosporin, sirolimus, ↑ serum concentrations Therapeutic monitoring is
tacrolimus recommended.
INHALED BETA AGONIST
Salmeterol ↑ serum concentrations Concurrent administration of
salmeterol and idelalisib is not
recommended. The combination may
result in increased risk of
cardiovascular adverse events
associated with salmeterol, including
QT prolongation, palpitations, and
sinus tachycardia.
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): atorvastatin (HOS-086304) rosuvastatin (HOS-086307) salmeterol (HOS-086285) tacrolimus (HOS-085202) sirolimus (HOS-085172) pravastatin (HOS-086306) pitavastatin (HOS-125743)
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Version 2024-10-21T17:52:00Z · SHA-256 f55f90ba278a87ef1c8e7162344ed4bd66ac7180deaf4c8fda3eca5bbf8e87e5 · Passage 605a8be7dd70dff78b919a26f1676d15c94c8048045977153eff24af0e81463e · Zeichen 9857–11294 im Abschnitt
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HOS-132110 · Präparat HOS-097192
9
Medicinal product Expected effect of Clinical recommendation upon
idelalisib on medicinal co-administration with idelalisib
product levels
PHOSPHODIESTERASE INHIBITORS
For pulmonary arterial hypertension:
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 2024-10-21T17:52:00Z · SHA-256 f55f90ba278a87ef1c8e7162344ed4bd66ac7180deaf4c8fda3eca5bbf8e87e5 · Passage 81315523aa175e05e48ca1826ca6049cace062aa970792bcbe4edea92044abf4 · Zeichen 11346–11715 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.