Presentation: Entyvio intravenous (IV): 300 mg powder for concentrate for solution for infusion. Indication: Adult patients with moderately to severely active ulcerative colitis (UC)/Crohn’s disease (CD) who have had an inadequate response with, lost response to, or were intolerant to either conventional therapy or a tumour necrosis factor-alpha (TNFα) antagonist. Adult patients with moderately to severely active chronic pouchitis, who have undergone proctocolectomy and ileal pouch anal anastomosis for UC and have had an inadequate response with or lost response to antibiotic therapy. Dosage and administration: UC: Recommended dose regimen 300 mg administered by IV infusion over 30 minutes at 0, 2, 6 weeks and every 8 weeks thereafter. Discontinue treatment if no evidence of therapeutic benefit by week 10. If patients experience a decrease in response, they may benefit from increased dosage frequency to 300 mg every 4 weeks. Corticosteroids may be reduced/discontinued in patients who respond to treatment with Entyvio. If therapy is interrupted and needs to be restarted, Entyvio dosing every 4 weeks may be considered. CD: Recommended dose regimen is 300 mg administered by IV infusion over 30 minutes at 0, 2, 6 weeks and every 8 weeks thereafter. Patients who have not shown evidence of therapeutic benefit may benefit from a dose at week 10. Continue therapy every 8 weeks from week 14 in responding patients. Therapy should be discontinued if no evidence of therapeutic benefit is observed by week 14. If therapy is interrupted and needs to be restarted, Entyvio dosing every 4 weeks may be considered. Pouchitis: Recommended dose regimen is 300 mg administered by IV infusion at 0, 2 and 6 weeks and then every 8 weeks thereafter. Treatment should be initiated in parallel with standard of care antibiotic (e.g., four-week of ciprofloxacin). Therapy discontinuation should be considered if no evidence of therapeutic benefit is observed by week 14. There are no retreatment data available if therapy is interrupted and needs to be restarted. Elderly patients: No dosage adjustment required. Renal or hepatic impairment: Entyvio has not been studied in these populations. No dose recommendation can be given. Paediatric populations: No data available in children aged 0-17 years. Contraindications: Hypersensitivity to Entyvio or any of the excipients. Active severe infections such as tuberculosis (TB), sepsis, cytomegalovirus, listeriosis and opportunistic infections such as Progressive Multifocal Leukoencephalopathy (PML). Warnings and precautions: Patients should be observed continuously during infusions for signs/symptoms of hypersensitivity reactions. Patients should continue to be observed for two hours following infusion completion for the first two infusions and one hour for subsequent infusions. Infusion-related reactions (IRR): Hypersensitivity reactions have been reported, the majority were of mild to moderate severity. Discontinue treatment if anaphylaxis or other serious allergic reactions occur and initiate appropriate treatment. In mild to moderate IRR, slow or interrupt infusion. Consideration for pre-treatment with antihistamine, hydrocortisone and/or paracetamol should be given prior to next infusion, for patients with history of mild/moderate IRR to Entyvio. Infections: Not to be initiated in patients with active, severe infections until infections are controlled. Consider withholding in patients who develop severe infection while on treatment with Entyvio. Before initiating treatment, patients must be screened for TB. If latent TB is diagnosed, anti-tuberculosis appropriate treatment must be initiated prior to Entyvio treatment. John Cunningham (JC) virus infection resulting in PML . Monitor patients for any new or worsening neurological signs/symptoms. Malignancy: Increased risk of malignancy in UC and CD. Immunomodulatory products may increase risk. Prior and concurrent use of biological products: No clinical data available for Entyvio use in patients previously treated with natalizumab or rituximab. Patients previously exposed to natalizumab should wait at least 12 weeks prior to initiating Entyvio therapy. Entyvio not recommended for concomitant use with biologic immunosuppressants Live and oral vaccines:Patients may continue to receive non-live vaccines. Patients recommended to be up-to-date with all appropriate immunisations prior to initiating Entyvio. Live vaccines may be administered concurrently only if benefit clearly outweighs risk. Interactions: No interaction studies performed. UC and CD: Concomitant administration of corticosteroids, immunomodulators (azathioprine, 6-mercaptopurine, and methotrexate) and aminosalicylates did not have a clinically meaningful effect on Entyvio pharmacokinetics. Pouchitis: co-administered with antibiotics have been observed. The effect on the pharmacokinetics of commonly co-administered medicinal compounds has not been studied. Fertility, pregnancy and lactation: There are no data on the effects of vedolizumab on human fertility. Women of childbearing potential should use adequate contraception and continue for at least 18 weeks after last Entyvio treatment. Preferable to avoid use of Entyvio during pregnancy unless benefits clearly outweigh potential risk to both the mother and foetus. Entyvio has been detected in human milk. The effects on breast-fed infants and milk production are unknown. Use of Entyvio in lactating women should consider the benefit of therapy against potential risks to the infant. Undesirable effects: Very Common (≥1/10): nasopharyngitis, headache, arthralgia. Common (≥1/100, <1/10): pneumonia, clostridium difficile infection bronchitis, gastroenteritis, upper respiratory tract infection, influenza, sinusitis, pharyngitis, herpes zoster, paraesthesia, hypertension, oropharyngeal pain, nasal congestion, cough, anal abscess, anal fissure, nausea, dyspepsia, constipation, abdominal distension, flatulence, haemorrhoids, rectal haemorrhage*, rash, pruritus, eczema, erythema, night sweats, acne, muscle spasms, back pain, muscular weakness, fatigue, pain in extremity, pyrexia, infusion related reaction (asthenia and chest discomfort), infusion site reaction (including: Infusion site pain and Infusion site irritation), Uncommon (≥ 1/1,000 to < 1/100): respiratory tract infection, vulvovaginal candidiasis, oral candidiasis, herpes zoster, folliculitis, infusion site reaction (including infusion site pain and irritation), infusion related reaction, chills, feeling cold. Very rare (< 1/10,000): pneumonia, anaphylactic reaction, anaphylactic shock, blurred vision.
For detailed information, please consult full prescribing information.
For reporting suspected adverse events (AE) and special situation reports (SSRs) for Takeda products: AE.HongKong@takeda.com
Medical Information and other Inquiries for Takeda Products at medinfohk@takeda.com
|
|
Takeda Pharmaceuticals (Hong Kong) Limited |
