শুধুমাত্র তথ্যমূলক — চিকিৎসা পরামর্শ নয়। সর্বদা লাইসেন্সপ্রাপ্ত স্বাস্থ্যসেবা প্রদানকারীর পরামর্শ নিন।

Shasthya স্বাস্থ্য · সহজে স্বাস্থ্যসেবা
EN
কমিউনিটি ডেটা হালনাগাদ হয়েছে 2 মাস আগে
T

Tocimab

Rx

200 mg/10 ml • আইভি ইনফিউশন

🌐 View in English
যে রূপে পাওয়া যায়: 200 mg/10 ml · 10 ml vial

ইঙ্গিত ও ব্যবহার

Tocimab এর জন্য নির্দেশিত:

ডোজ নির্দেশিকা

শুধুমাত্র নির্দেশিকা তথ্য

প্রদর্শিত ডোজগুলি সরকারি উৎসের সাধারণ নির্দেশিকা। ব্যক্তিগতকৃত ডোজের জন্য সর্বদা আপনার ডাক্তার বা ফার্মাসিস্টের পরামর্শ নিন।

প্রাপ্তবয়স্ক:

Interruption of dosing may be needed for management of dose-related laboratory abnormalities including elevated liver enzymes, neutropenia, and thrombocytopenia.Rheumatoid Arthritis: Tocilizumab may be used as monotherapy or concomitantly with methotrexate or other non-biologic DMARDs as an intravenous infusion.Recommended Intravenous Dosage Regimen: The recommended dosage of Tocilizumab for adult patients given as a 60-minute single intravenous drip infusion is 4 mg per kg of body weight every 4 weeks followed by an increase to 8 mg per kg of body weight every 4 weeks based on clinical response. Reduction of dose from 8 mg per kg of body weight to 4 mg per kg of body weight is recommended for management of certain dose-related laboratory changes including elevated liver enzymes, neutropenia, and thrombocytopenia Doses exceeding 800 mg per infusion are not recommended in RA patients Polyarticular Juvenile Idiopathic Arthritis: Tocilizumab may be used as an intravenous infusion or as asubcutaneous injection alone or in combination with methotrexate. Do not change dose based solely on a single body weight measurement, as weight may fluctuate.Recommended Intravenous Dosage Regimen: The recommended dosage of Tocilizumab for PJIA patients given once every 4 weeks as a 60-minute single intravenous drip infusion is: Patients less than 30 kg weight: 10 mg per kg of body weight Patients at or above 30 kg weight: 8 mg per kg of body weight Systemic Juvenile Idiopathic Arthritis: Tocilizumab may be used as an intravenous infusion or as a subcutaneous injection alone or in combination with methotrexate. Do not change a dose based solely on a single body weight measurement, as weight may fluctuate.Recommended Intravenous Dosage Regimen: The recommended dose of Tocilizumab for SJIA patients givenonce every 2 weeks as a 60-minute single intravenous drip infusion is: Patients less than 30 kg weight: 12 mg per kg of body weight Patients at or above 30 kg weight: 8 mg per kg of body weight Coronavirus Disease 2019: The recommended dosage of Tocilizumab is a single 60-minuteintravenous infusion as follows: Patients less than 30 kg weight: 12 mg per kg of body weight Patients at or above 30 kg weight: 8 mg per kg of body weight If clinical signs or symptoms worsen or do not improve after the first dose, one additional infusion of Tocilizumab may be administered at least 8 hours after the initial infusion. Maximum dosage in COVID-19 patients is 800 mg per infusion. Cytokine Release Syndrome: Use only the intravenous route for treatment of CRS. The recommended dose of Tocilizumab for treatment of CRS given as a 60-minute intravenous infusion is:Recommended Intravenous CRS Dosage Patients less than 30 kg weight: 12 mg per kg of body weight Alone or in combination with corticosteroids. Patients at or above 30 kg weight: 8 mg per kg of body weight Alone or in combination with corticosteroids. If no clinical improvement in the signs and symptoms of CRS occurs after the first dose, up to 3 additional doses of Tocilizumab may be administered. The interval between consecutive doses should be at least 8 hours. Doses exceeding 800 mg per infusion are not recommended in CRS patients.Giant Cell Arteritis: The recommended dosage of Tocilizumab for adult patients given as a 60-minute single intravenous drip infusion is 6 mg per kg of body weight every 4 weeks in combination with a tapering course of glucocorticoids. Tocilizumab can be used alone following discontinuation of glucocorticoids Doses exceeding 600 mg per infusion are not recommended in GCA patients Systemic Sclerosis-Associated Interstitial Lung Disease: The recommended dose of Tocilizumab for adult patients with SSc-ILD is 162 mg given once every week as a subcutaneous injection. Intravenous administration is not approved for SSc-ILD Administration of Intravenous Formulation: For adults with RA, GCA, CRS, PJIA and SJIA patients at or above 30 kg, dilute to 100 mL in 0.9% or 0.45% Sodium Chloride Injection, USP for intravenous infusion using aseptic technique For PJIA, SJIA and CRS patients less than 30 kg, dilute to 50 mL in 0.9% or 0.45% Sodium Chloride Injection, USP for intravenous infusion using aseptic technique Administer as a single intravenous drip infusion over 1 hour; do not administer as bolus or push.

পার্শ্বপ্রতিক্রিয়া

Most common adverse reactions [incidence of at least 5%): upper respiratory tract infections, nasopharyngitis, headache, hypertension, increased ALT, injection site reactions. Most common adverse reactions in COVID-19 (incidence >3%) are constipation, anxiety, diarrhea, insomnia, hypertension and nausea.

সতর্কতা ও নিষেধাজ্ঞা

সতর্কতা ও সাবধানতা

Serious Infections: Do not administer Tocimab during an active infection, including localized infections. If a serious infection develops, interrupt Tocimab until the infection is controlledTuberculosis: Evaluate patients for tuberculosis risk factors and test for latent infection prior to initiating TocimabGastrointestinal Perforation: Use with caution in patients who may be at increased riskHepatotoxicity: Monitor patients for signs and symptoms of hepatic injury. Modify or discontinue Tocimab if abnormal liver tests persist or worsen or if clinical signs and symptoms of liver disease developLaboratory Monitoring: Recommended due to potential consequences of treatment-related changes in neutrophils, platelets, lipids, and liver function testsHypersensitivity reactions, including anaphylaxis and death have occurredLive Vaccines: Avoid use with TocimabAvoid using Tocimab with biological DMARDs.It is recommended that Tocimab not be initiated in patients with an absolute neutrophil count (ANC) below 2000 per mm3 , platelet count below 100,000 per mm3 , or who have ALT or AST above 1.5 times the upper limit of normal (ULN)

নিষেধাজ্ঞা

Tocilizumab is contraindicated in patients with known hypersensitivity to Tocilizumab.

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