Skip to main content

Mabtas 500mg INJECTION ( Intas) | Rituximab | Apple pharmaceuticals

Mabtas 500mg

         Mabtas 500mg is a anticancer medicine which prevents the growth and spread of cancer cells in the body, the main ingredient which is used as rituximab. Mabtas 500mg will help to prevent the Non- Hodgkins lymphoma or chronic lymphocytic and with combination with another anticancer drugs like methotrexate is used for rheumatoid arthritis symptoms in adult treatment. Mabtas 500mg with steroid regimen combination is given for the treatment of some rare disorders which cause blood vessels and other tissues inflammation in the body.


INDICATION

        Mabtas 500mg and hyaluronidase human injection are given alone or combination with another drugs to treat certain types of non-Hodgkin's lymphoma and chronic lymphocytic leukemia (cancer start in WBC). Mabtas 500mg injection combination with methotrexate (Otrexup, Rasuvo, Xatmep, others) is also indicated for the treatment rheumatoid arthritis symptoms in adults that have been already treated with a some type of regimen knowns as tumor necrosis factor (TNF) inhibitor. Mabtas 500mg is a type in a classification of drugs called monoclonal antibodies. Mabtas 500mg is used to killing cancer cells to treat NHL , CLL, rheumatoid arthritis, granulomatosis with polyangiitis, and microscopic polyangiitis by inhibiting the activity of the immune system parts that can injury the joints, veins, and other blood vessels and cause organs (heart and lungs) damage.


MISSED DOSE

       If a dose missed then have the drug soon you remembered, if next dose time reach then leave the missed dose and follow the normal schedule. Do not have 2 dose at a same time. Please consult with doctor for further details.

BEFORE EACH INFUSION THE DRUG IS PREMEDICATE :

First infusion: Starting treatment rate of 50 mg/hr is administer , in not showing infusion toxicity, rate raised up to 50 mg/hr increments at intervals of 30 min and max of 400 mg/hr. Successive infusion: initial at rate of 100 mg/hr, in not showing infusion toxicity, rate raised upto 100 mg/hr increments at intervals of 30 min and max of 400 mg/hr. While combination with CHOP chemotherapy the injection Mabtas has not been given. Hence Premedication with corticosteroids must be considered.

LOW GRADE OR FOLLICULAR NON-HODGKINS LYMPHOMA :

The drug Dose is 375 mg/m2 as an IV infusion. Once weeks for 4 or 8 doses administrated for Relapsed treatment Once weekly for 4 doses administrated for Retreatment for relapsed. Previously untreated: administer on day 1 of each cycle of chemotherapy, up to 8 doses. In complete or partial response of patient, start with 8 weeks for maintenance following Mabtas 500mg in combination with chemotherapy completed then administer 8weeks for 12 doses as a single agent. Once weekly for 4 doses at intervals of 6 months and max of 16 dose for Non – progression (following CVP chemotherapy completion 6 – 8 cycles): On day 1 each cycle of chemotherapy up to 8 infusions for Diffuse large B- cell NHL

CHRONIC LYMPHOCYTIC LEUKEMIA :

Before starting of FC chemotherapy, dose recommended is 375 mg/m2 followed 500 mg/m2 on day 1 of 2-6 cycles every 28 days.

mabtas 500mg
mabtas 500mg

PHARMACOKINETICS


Absorption: Not available
Distribution: volume of distribution is 3.1 L There are no human plasma level
Metabolism: Mabtas 500mg metabolized by human antimurine antibody production.
Elimination: not available The drug elimination of half life of NHL is 22 days and for RA is 18.0 days, GPA and microscopic polyangitis is 23 days.


MECHANISM OF ACTION


Mabtas 500mg is a type of class called as monoclonal antibody. A new type of "targeted" cancer treatment and an integral part of the body's immune system. Naturally the body fused to antibodies in along with an antigen which has entered the body and attack the antigen for destruction by the immune system. Monoclonal antibiotics which only targeted by an essential cells only, they may cause less toxicity to healthy cell and it is prescribed treatment given only for cancers in which antigens (and the respective antibodies) have been already identified. Mabtas injection works by linking to the CD20 antigen on normal and malignant B-cells. Hence natural immune security of body are initiated to attach and kill the marked B-cells. Young cells (stem cells) in the bone marrow which will develop into the various cell types and do not have the CD20 antigen. After treatment CD20 antigen allows healthy B-cells to multiply.


ADMINISTRATION

Take an amount Mabtas injection is administer and diluted to final concentration of 1 mg/ml upto 4 mg/ml as infusion (containing either 0.9% Nacl or 5% dextrose in water). Gently Invert the bag and mix the solution. Discard unused drug left in vial. OVERDOSAGE: If over dose occurs seek immediately to the emergency department or poison control help line. please consult the doctor for further clarification.

DOSAGE


COMPONENT OF ZEVALIN FOR TREATMENT OF NHL :

The dose 250 mg/m2 of Mabtas injection within 4 hours prior to the administration of Indium-111-(In-111-) Zevalin and Yttrium-90- (Y-90-) Zevalin. 7–9 days before to Rituxan and Y-90- Zevalin administrate Rituxan and In-111-Zevalin.

RHEUMATOID ARTHRITIS :

When combination of Mabtas injection with methotrexate is administrated. Mabtas injection given as two dose of 100mg IV infusion 2 weeks separated. When glucocorticoids administered as methylprednisolone 100mg IV Subsequent course based on clinical evaluation must administer every 24 weeks, but not early than every 16 weeks.

GRANULOMATOSIS POLYANGITIS AND MICROSCOPIC POLYANGITIS : 

Mabtas injection administer Dose of 375 mg/m2 IV infusion weekly once for 4 weeks. When Glucocorticoids given with methylprednisolone by dose of 1000 mg IV/ day for 1- 3 days and purse by oral prednisone 1 mg/kg/day are recommended for the treatment of symptoms of serious vacuities This drug should initiate within 14 days before or with the starting of Mabtas injection and may continue during and after the 4 week course with treatment of Mabtas injection drug. Safety and not established for subsequent infusion.

mabtass 500mg injection
mabtass 500mg injection

PRECAUTIONS

Allgeric condition against Mabtas 500mg or any other medication inform your doctor. Information about past medical history used which include in prescription, non-prescription, vitamins &supplements , nutritional products just inform the doctor. While using Mabtas 500mg do not take any vaccination or immunization without taking advice from doctors. Avoid use of Mabtas 500mg if you are pregnant. It will harm the baby unborn, while using Mabtas 500mguse correct birth control to prevent pregnancy and for at least 2 weeks after your treatment ends. Mabtas 500mg may affect the ability to have children in women. Inform your doctor if you planning to pregnant. It is unknown whether Mabtas 500mg passes into breast milk , avoid breast-feed while on Mabtas 500mg treatment.

CONTRAINDICATION

Hypersensitivity or murine proteins. Active severe infectons in rheumatoid arthritis Uncontrolled cardiac disease.

DRUG INTERACTION


Mabtas 500mg drug interaction has limited data is available at present. Interation with fludarabine or cyclophosphamide have no effects in pharmacokinetics in CLL patients. Mabtas combination with methotrexate had no effects in pharmacokinetics.

STORAGE


Store the drug at 2℃ – 3℃ Keep away from the childerns Use the drug before expiry date Protected from direct sunlight and Do not freeze or shake. Discard the unused drug by asking the advice from doctor or pharmacist.

SIDE EFFECTS


Common effects: fever and chills (flu lik symptoms)
Less common side effects: Weakness; 
  • nausea ; 
  • headache;
  •  cough ;
  •  dyspnea ;
  •  pharyngitis

Phone Number

+91-9987711567
URL

Email ID

applepharmaceutical@gmail.com
info@myapplepharma.com

Comments

Popular posts from this blog

Comprar Tagrisso 80mg | Precio Tagrisso 80mg medicina

DESCRIPCIÓN Una tableta de Tagrisso de 80 mg contiene un principio activo conocido como Osimeritinib, que antes se conocía como Mereletinib.Tagrisso 80 mg está considerado como medicamento de tercera generación, que está disponible en forma de tableta.Tagrisso 80 mg es un inhibidor inevitable del receptor del factor de crecimiento epidérmico, desviado de manera selectiva, que contiene actividad anticancerígena. La categoría farmacológica de Tagrisso 80mg es tirosina quinasa prohibitor. INDICACIÓN Un comprimido de Tagrisso 80 mg (osimertinib) está ampliamente indicado como tratamiento de primera línea para el cáncer de pulmón no microcítico avanzado con pacientes con mutación EGFR positiva.Tagrisso 40mgi s también se utiliza para el tratamiento de pacientes afectados con una mutación positiva de EGFR T792M NSCLC, la enfermedad ha avanzado en o después del tratamiento con inhibidores de la tirosina quinasa.Usos en Embarazo, lactancia, pediatría: No se asigna la categoría de embara

Trastuzumab - Biceltis 440mg injection online | Myapplepharma

Biceltis 440 mg Injection             Biceltis 440mg is a group of medicines which belongs to anti neoplastic medication. Biceltis is a chemotherapy drug. It is recommended that Biceltis 440mg be administered under the guidance of a qualified physician experienced in the use of cancer chemotherapeutic agents. USES           The injection Biceltis 440mg is used alone or combination with other medicine for the treatment in patients who suffering from metastatic breast cancer.           The drug also indicated with combination of other medicine for the treatment of certain types of stomach or esophagus cancer in some persons. WORK AS         Different type of breast cancer cells has a higher than normal level of a protein called HER2 (human epidermal growth factor receptor 2) on their surface. These HER2 receptors get signals which stimulate the tumor cells to develop and reproduce. But breast cancer cells with too many HER2 receptors can Choice too many growth signa

Купить Erlonat 150 | Erlonat 150 цена 150 $

ОПИСАНИЕ Erlonat 150мг  таблетки состоят из активных ингредиентов, известных как Erlotinib (Generic Tarceva) , который считается производным хиназолина и противораковые агенты, которые отвечают как ингибиторы протеинкиназы на EGFR, связанные с тирозинкиназой. Erlonat 150мг в основном используется в лечение немелкоклеточного рака легких и рака поджелудочной железы, а также участие в лечении различных видов рака. Эрлонат особенно нацелен эпидермальный фактор роста, рецепторная тирозинкиназа. ИСПОЛЬЗОВАНИЕ Erlonat Немелкоклеточный рак легких: Эрлонат показан в качестве продолжения терапии у пациентов с длительной или метастазирующей немелкоклеточной карциномой легкого, чье заболевание имеет не получить аванс после четырех циклов терапии с использованием первой линии на основе платины. Erlonat используется в этом состоянии только после отказа одного из предыдущих режим химиотерапии. При использовании Erlonat 150мг с такими соединениями на основе платины, как карбоплатин, гемцитаби