Quest for the right Drug
ליבטנסיטי LIVTENCITY (MARIBAVIR)
תרופה במרשם
תרופה בסל
נרקוטיקה
ציטוטוקסיקה
צורת מתן:
פומי : PER OS
צורת מינון:
טבליות מצופות פילם : FILM COATED TABLETS
עלון לרופא
מינוניםPosology התוויות
Indications תופעות לוואי
Adverse reactions התוויות נגד
Contraindications אינטראקציות
Interactions מינון יתר
Overdose הריון/הנקה
Pregnancy & Lactation אוכלוסיות מיוחדות
Special populations תכונות פרמקולוגיות
Pharmacological properties מידע רוקחי
Pharmaceutical particulars אזהרת שימוש
Special Warning עלון לרופא
Physicians Leaflet
Interactions : אינטראקציות
7 DRUG INTERACTIONS 7.1 Reduced Antiviral Activity When Coadministered with Ganciclovir or Valganciclovir LIVTENCITY is not recommended to be coadministered with valganciclovir/ganciclovir (vGCV/GCV). LIVTENCITY may antagonize the antiviral activity of ganciclovir and valganciclovir by inhibiting human CMV pUL97 kinase, which is required for activation/phosphorylation of ganciclovir and valganciclovir [see Warnings and Precautions (5.1) and Microbiology (12.4)]. 7.2 Potential for Other Drugs to Affect LIVTENCITY Maribavir is a substrate of CYP3A4. Coadministration of LIVTENCITY with strong inducers of CYP3A4 is not recommended, except for selected anticonvulsants [see Dosage and Administration (3.2) and Drug Interactions (7.3)]. 7.3 Potential for LIVTENCITY to Affect Other Drugs Maribavir is a weak inhibitor of CYP3A4, and an inhibitor of P-gp and breast cancer resistance protein (BCRP). Coadministration of LIVTENCITY with drugs that are sensitive substrates of CYP3A, P-gp and BCRP may result in a clinically relevant increase in plasma concentrations of these substrates (see Table 4). Table 4 provides a list of established or potentially clinically significant drug interactions, based on either clinical drug interaction studies or predicted interactions due to the expected magnitude of interaction and potential for serious adverse events or decrease in efficacy [see Warnings and Precautions (5.3) and Clinical Pharmacology (12.3)]. Table 4: Established and Other Potentially Significant Drug Interactionsa Effect on Concomitant Drug Class: Drug Name Clinical Comments Concentration Antiarrhythmics Use caution when LIVTENCITY and digoxin are coadministered. Digoxinb ↑ Digoxin Monitor serum digoxin concentrations. The dose of digoxin may need to be reduced when coadministered with LIVTENCITY.c Anticonvulsants A dose adjustment of LIVTENCITY to 800 mg twice daily is Carbamazepine ↓ Maribavir recommended when coadministered with carbamazepine. A dose adjustment of LIVTENCITY to 1,200 mg twice daily is Phenobarbital ↓ Maribavir recommended when coadministration with phenobarbital. A dose adjustment of LIVTENCITY to 1,200 mg twice daily is Phenytoin ↓ Maribavir recommended when coadministration with phenytoin. Antimycobacterials Coadministration of LIVTENCITY and rifabutin is not recommended Rifabutin ↓ Maribavir due to potential for a decrease in efficacy of LIVTENCITY. Coadministration of LIVTENCITY and rifampin is not recommended Rifampinb ↓ Maribavir due to potential for a decrease in efficacy of LIVTENCITY. Herbal Products Coadministration of LIVTENCITY and St. John’s wort is not St. John’s wort ↓ Maribavir recommended due to potential for a decrease in efficacy of LIVTENCITY. HMG-CoA Reductase Inhibitors The patient should be closely monitored for rosuvastatin-related Rosuvastatinc ↑ Rosuvastatin events, especially the occurrence of myopathy and rhabdomyolysis.c Immunosuppressants Frequently monitor cyclosporine levels throughout treatment with Cyclosporine ↑ Cyclosporine LIVTENCITY, especially following initiation and after discontinuation of LIVTENCITY and adjust dose, as needed.c Frequently monitor everolimus levels throughout treatment with Everolimus ↑ Everolimus LIVTENCITY, especially following initiation and after discontinuation of LIVTENCITY and adjust dose, as needed.c Frequently monitor sirolimus levels throughout treatment with Sirolimus ↑ Sirolimus LIVTENCITY, especially following initiation and after discontinuation of LIVTENCITY and adjust dose, as needed.c Frequently monitor tacrolimus levels throughout treatment with Tacrolimusb ↑ Tacrolimus LIVTENCITY, especially following initiation and after discontinuation of LIVTENCITY and adjust dose, as needed.c ↓=decrease, ↑=increase. a This table is not all inclusive. b The interaction between LIVTENCITY and the concomitant drug was evaluated in a clinical study [see Clinical Pharmacology (12.3)]. c Refer to the respective prescribing information. 7.4 Drugs without Clinically Significant Interactions with LIVTENCITY No clinically significant interactions were observed in clinical drug-drug interaction studies of LIVTENCITY and ketoconazole, antacid, caffeine, warfarin, voriconazole, dextromethorphan, or midazolam [see Clinical Pharmacology (12.3)].
פרטי מסגרת הכללה בסל
א. התרופה תינתן לטיפול במבוגרים וילדים בני 12 שנים ומעלה עם זיהום או מחלה על רקע CMV (Cytomegalovirus), אשר פיתחו עמידות לטיפול קודם (עם או ללא עמידות גנוטיפית) (לעניין זה עמידות לטיפול קודם תוגדר כעמידות שהתפתחה לטיפול באחד מאלה – Cidofovir, Foscarnet, Valganciclovir), לאחר השתלת איברים סולידיים (SOT) או השתלת מח עצם (SCT/HSCT).ב. הטיפול בתכשיר יעשה לפי מרשם של רופא מומחה במחלות זיהומיות או רופא מומחה בהמטולוגיה או רופא מומחה העובד ביחידת השתלות.התוויות מפורטות למתן הטיפול מפורטות בחוזר חטיבת טכנולוגיות רפואיות, מידע ומחקר (נספח ג' לחוזר זה).
שימוש לפי פנקס קופ''ח כללית 1994
לא צוין
תאריך הכללה מקורי בסל
17/03/2024
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