Quest for the right Drug
ווקבריה זריקה VOCABRIA INJECTION (CABOTEGRAVIR)
תרופה במרשם
תרופה בסל
נרקוטיקה
ציטוטוקסיקה
צורת מתן:
תוך-שרירי : I.M
צורת מינון:
אין פרטים : PROLONGED RELEASE SUSPENSION FOR INJECTION
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
Posology : מינונים
4.2 Posology and method of administration Vocabria should be prescribed by physicians experienced in the management of HIV infection. Each injection should be administered by a healthcare professional. Vocabria injection is indicated for the treatment of HIV-1 in combination with rilpivirine injection, therefore, the prescribing information for rilpivirine injection should be consulted for recommended dosing. Prior to starting Vocabria injection, healthcare professionals should have carefully selected patients who agree to the required injection schedule and counsel patients about the importance of adherence to scheduled dosing visits to help maintain viral suppression and reduce the risk of viral rebound and potential development of resistance with missed doses. Following discontinuation of Vocabria and rilpivirine injection, it is essential to adopt an alternative, fully suppressive antiretroviral regimen no later than one month after the final injection of Vocabria when dosed monthly and no later than two months after the final injection of Vocabria when dosed every 2 months (see section 4.4). The healthcare provider and patient may decide to use cabotegravir tablets as an oral lead-in prior to the initiation of Vocabria injection to assess tolerability to cabotegravir (see Table 1) or may proceed directly to Vocabria injections (see Table 2 for monthly and Table 3 for every 2 month dosing recommendations). Posology Adults Oral lead-in When used for oral lead-in, oral cabotegravir together with oral rilpivirine should be taken for approximately one month (at least 28 days) to assess tolerability to cabotegravir and rilpivirine (see section 4.4). One cabotegravir 30 mg tablet should be taken with one rilpivirine 25 mg tablet, once daily. When administered with rilpivirine, cabotegravir tablets should be taken with a meal (see cabotegravir tablet prescribing information). Table 1 Oral Lead-in Dosing Schedule in Adults ORAL LEAD-IN Medicinal For one month (at least 28 days), followed by the Initiation Injectiona product Cabotegravir 30 mg once daily Rilpivirine 25 mg once daily a see Table 2 for monthly injection dosing schedule and Table 3 for every 2 month dosing schedule. Monthly dosing Initiation injection (600 mg corresponding to 3 mL dose) On the final day of current antiretroviral therapy or oral lead-in therapy, the recommended initial dose of Vocabria injection in adults is a single 600 mg intramuscular injection. Vocabria injection and rilpivirine injection should be administered at separate gluteal injection sites at the same visit. Continuation injection (400 mg corresponding to 2 mL dose) After the initiation injection, the continuation injection dose of Vocabria in adults is a single 400 mg monthly intramuscular injection. Vocabria injection and rilpivirine injection should be administered at separate gluteal injection sites at the same visit. Patients may be given injections up to 7 days before or after the date of the monthly 400 mg injection schedule. Table 2 Recommended monthly intramuscular dosing schedule in adults INITIATION CONTINUATION INJECTION INJECTION Medicinal product Direct to injection: One month after initiation month 1 injection and monthly onwards or Following oral lead-in: month 2 Vocabria 600 mg 400 mg Rilpivirine 900 mg 600 mg Every 2 Month Dosing Initiation Injections – one month apart (600 mg) On the final day of current antiretroviral therapy or oral lead-in therapy, the recommended initial Vocabria injection in adults is a single 600 mg intramuscular injection. One month later, a second Vocabria 600 mg intramuscular injection should be administered. Patients may be given the second 600 mg initiation injection up to 7 days before or after the scheduled dosing date. Vocabria injection and rilpivirine injection should be administered at separate gluteal injection sites at the same visit. Continuation Injections – 2 months apart (600 mg) After the initiation injections, the recommended Vocabria continuation injection dose in adults is a single 600 mg intramuscular injection administered every 2 months. Vocabria injection and rilpivirine injection should be administered at separate gluteal injection sites at the same visit. Patients may be given injections up to 7 days before or after the date of the every 2 month, 600 mg injection schedule. Table 3 Recommended every 2 month intramuscular dosing schedule in adults INITIATION CONTINUATION INJECTIONS INJECTIONS Medicinal Direct to Two months after final product injection: initiation injection and months 1 and 2 every 2 months onwards or Following oral lead-in: months 2 and 3 Vocabria 600 mg 600 mg Rilpivirine 900 mg 900 mg Dosing recommendations when switching from monthly to every 2 month injections Patients switching from a monthly continuation injection schedule to an every 2 month continuation injection schedule should receive a single 600 mg intramuscular injection of cabotegravir one month after the last 400 mg continuation injection dose and then 600 mg every 2 months thereafter. Dosing recommendations when switching from every 2 month to monthly injections Patients switching from an every 2 month continuation injection schedule to a monthly continuation dosing schedule should receive a single 400 mg intramuscular injection of cabotegravir 2 months after the last 600 mg continuation injection dose and then 400 mg monthly thereafter. Missed doses Patients who miss a scheduled injection visit should be clinically reassessed to ensure resumption of therapy remains appropriate. See Tables 4 and 5 for dosing recommendations after a missed injection. Missed monthly injection If a patient plans to miss a scheduled injection visit by more than 7 days, oral therapy (one 30 mg cabotegravir tablet and one 25 mg rilpivirine tablet once daily) may be used to replace up to 2 consecutive monthly injection visits. For oral therapy durations greater than two months, an alternative oral regimen is recommended. The first dose of oral therapy should be taken one month (+/- 7 days) after the last injection doses of Vocabria and rilpivirine. Injection dosing should be resumed on the day oral dosing completes, as recommended in Table 4. Table 4 Vocabria injection dosing recommendations after missed injections or oral therapy for patients on monthly injection dosing Time since last Recommendation injection ≤2 months: Continue with the monthly 400 mg injection schedule as soon as possible >2 months: Re-initiate the patient on the 600 mg dose, and then continue to follow the monthly 400 mg injection schedule. Missed 2 month injection If a patient plans to miss a scheduled Vocabria injection visit by more than 7 days, oral therapy (one 30 mg cabotegravir tablet and one 25 mg rilpivirine tablet, once daily) may be used to replace one, 2- monthly injection visit. For oral therapy durations greater than two months, an alternative oral regimen is recommended. The first dose of oral therapy should be taken two months (+/- 7 days) after the last injection doses of cabotegravir and rilpivirine. Injection dosing should be resumed on the day oral dosing completes, as recommended in Table 5. Table 5 Vocabria injection dosing recommendations after missed injections or oral therapy for patients on every 2 month injection dosing Missed Injection Time since last Recommendation (all injections are 3 mL) Visit injection Injection 2 ≤2 months Resume with 600 mg injection as soon as possible and then continue with the every 2 month injection schedule. >2 months Re-initiate the patient on the 600 mg dose, followed by a second 600 mg initiation injection one month later. Then follow the every 2 month injection schedule. Injection 3 or ≤3 months Resume with 600 mg injection as soon as possible later and then continue with the every 2 month injection schedule. >3 months Re-initiate the patient on the 600 mg dose, followed by a second 600 mg initiation injection one month later. Then follow the every 2 month injection schedule. Elderly No dose adjustment is required in elderly patients. There are limited data available on the use of cabotegravir in patients aged 65 years and over (see section 5.2). Renal impairment No dosage adjustment is required in patients with mild to severe renal impairment (CrCl <30 mL/min and not on dialysis [see section 5.2]). Cabotegravir has not been studied in patients with end-stage renal disease on renal replacement therapy. As cabotegravir is greater than 99% protein bound, dialysis is not expected to alter exposures of cabotegravir. If administered in a patient on renal replacement therapy, cabotegravir should be used with caution. Hepatic impairment No dosage adjustment is required in patients with mild or moderate hepatic impairment (Child-Pugh score A or B). Cabotegravir has not been studied in patients with severe hepatic impairment (Child- Pugh score C, [see section 5.2]). If administered in a patient with severe hepatic impairment, cabotegravir should be used with caution. Paediatric population The safety and efficacy of Vocabria in children and adolescents aged under 18 years have not been established. No data are available. Method of administration For intramuscular use. Care should be taken to avoid inadvertent injection into a blood vessel. Vocabria injection should be administered by a healthcare professional. For instructions on administration, see “Instructions for Use” in the package leaflet. Carefully follow these instructions when preparing the suspension for injection to avoid leakage. Vocabria injection should always be co-administered with rilpivirine injection. The order of injections is not important. The prescribing information for rilpivirine injection should be consulted for recommended dosing. When administering Vocabria injection, healthcare professionals should take into consideration the Body Mass Index (BMI) of the patient to ensure that the needle length is sufficient to reach the gluteus muscle. Hold the vial firmly and vigorously shake for a full 10 seconds. Invert the vial and check the resuspension. It should look uniform. If the suspension is not uniform, shake the vial again. It is normal to see small air bubbles. Injections must be administered to the ventrogluteal (recommended) or the dorsogluteal sites.
פרטי מסגרת הכללה בסל
א. התרופה האמורה תינתן לטיפול בנשאי HIV המדוכאים וירולוגית במשטר טיפול אנטירטרוויראלי קבוע.ב. הטיפול יינתן בשילוב עם Rilpivirine. ג. מתן התרופה ייעשה לפי מרשם של מנהל מרפאה לטיפול באיידס, במוסד רפואי שהמנהל הכיר בו כמרכז AIDS.ד. משטר הטיפול בתרופה יהיה כפוף להנחיות המנהל, כפי שיעודכנו מזמן לזמן על פי המידע העדכני בתחום הטיפול במחלה.
שימוש לפי פנקס קופ''ח כללית 1994
לא צוין
תאריך הכללה מקורי בסל
03/02/2022
הגבלות
תרופה מוגבלת לרישום ע'י רופא מומחה או הגבלה אחרת
ATC
מידע נוסף
עלון מידע לצרכן
14.08.22 - עלון לצרכן אנגלית 14.08.22 - עלון לצרכן עברית 14.08.22 - עלון לצרכן ערבית 12.10.22 - עלון לצרכן עברית 29.11.22 - עלון לצרכן אנגלית 29.11.22 - עלון לצרכן עברית 29.11.22 - עלון לצרכן ערבית 07.06.23 - עלון לצרכן אנגלית 07.05.23 - עלון לצרכן עברית 07.06.23 - עלון לצרכן ערבית 09.01.24 - עלון לצרכן עברית 14.02.24 - עלון לצרכן אנגלית 14.02.24 - עלון לצרכן עברית 14.02.24 - עלון לצרכן ערבית 08.05.24 - עלון לצרכן עברית 11.07.24 - עלון לצרכן אנגלית 11.07.24 - עלון לצרכן עברית 11.07.24 - עלון לצרכן ערבית 07.05.23 - החמרה לעלון 09.01.24 - החמרה לעלון 08.05.24 - החמרה לעלוןלתרופה במאגר משרד הבריאות
ווקבריה זריקה