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mabura-40mg

PRODUCT DETAILS

Trade name : Mabura
Active ingredient : Adalimumab
Strength availability : 40MG/0.8ML
Manufactured by : Hetero Drugs Ltd
Package : one prefilled syringe/injection
Category : Anti-rheumatoid, Immuno suppressive agent
Route : Subcutaneous use

for MORE INFORMATION !!!

Mabura is an anti-rheumatoid arthritis and Ankylosing spondylitis. Mabura is used alone or combined with methotrexate. Mabura is a prescription medicine, used by the patients who are all having a valid prescription only under the knowledge of medical practitioner. Mabura containing Adalimumab has various activities like; Tumor necrosis factor inhibitory activity Anti-inflammatory activity Immuno suppressive activity Anti-rheumatoid activity (disease modifying) Monoclonal antibody

USED FOR

Mabura injection is used in various conditions like; Rheumatoid arthritis used alone or combine with methotrexate Juvenile idiopathic arthritis in pediatric Psoriasis arthritis Adult crohn’s disease Ankylosing spondylitis Plaque psoriasis Ulcerative colitis All these conditions, Mabura are used to reduce the symptoms and provide better heal.

Mabura WORKS AS

Mabura is used to inhibit the tumor necrosis factor which is commonly originating cytidine responsible for inflammatory and immunity response. Rheumatoid arthritis is a condition, in which TNF level gets elevated and accumulated in synovial fluid causes inflammation of joints. Mabura containing Adalimumab expels its activity by certainly binds to TNF alpha and complicated in stoppage of association of TNH alpha with its receptors such as p55 & p75 cell surface TNF receptors. Mabura is also experienced in lysis of surface TNF expose cells in vitro in the presence of complement.

ADME

Absorption :
The peak plasma concentration time of Mabura is occurs at 131 ± 56 hours and maximum serum concentration reaches as 4.7 ± 1.6mcg/ml The mean bioavailability of Mabura is reaches at 64%
Distribution :
The volume of distribution of Mabura is 4.7 to 6.0L
Metabolism :
Metabolism of Mabura occur hepatically using microsomal enzymes, because of elevation of TNF levels in chronic inflammation which may diminish the production of CYP isoenzymes, the contrariety of TNF activity by Mabura may distribute the formation of CYP isoenzymes
Excretion :
The systemic clearance of Adalimumab is relatively occurs as 12ml/hr The mean terminal half life period of Adalimumab is relatively occurs as 2 weeks ranging from 10 to 20 days

DOSAGE

In rheumatoid arthritis, psoriasis arthritis & Ankylosing spondylitis (RA, PA, & AS) : The usual prescribed dosage of Mabura for these conditions, 40mg should be given for every other week through subcutaneously. Methotrexate, NSAIDS, glucocorticoid, salicylates, analgesics, or DMARDs may be carrying out during the therapy with Mabura if required. In some conditional patients, methotrexate should not be used in combination. In this condition the frequency of dosage of Mabura is increases to 40mg for every week.
In adult crohn’s : The usual recommended dosage of Mabura is 160mg initiate at day 1 (administered as four 40mg in a day or two 40mg per day for two successive days) following with 80mg two weeks later (day 15). Later two weeks, day 29 initiates with maintenance dose of 40mg should be given for every other week. Aminosalicylates, corticosteroids, or Immuno modulatory agents may be used during the therapy with Mabura
For pediatrics :
6 years & older : 17kg to less than 40kg: The initial dose is 80mg given subcutaneous on day 1 followed by 40mg two weeks later, then 20mg SC every other week 40kg or greater: The recommended dosage 160mg of Mabura should be given subcutaneous on day 1, respectively 80mg SC for two weeks later, then 40mg SC every other week.
In juvenile idiopathic arthritis : The usual recommended dose of Mabura is suitable for the age of 4 to 17 years with polyarticular JIA is calculated on the basis of body weight of the patients. 2 years and older pediatric patients Mabura is suggested. Methotrexate, NSAIDS, glucocorticoid, salicylates or analgesics may be used in combination. • In 10kg to less than 15kg: 10mg dose should be recommended • In 15 kg to <30kg: 20mg of dose should be given for every other week • ≥30kg: 40mg of dose should be given for every other week In ulcerative colitis: The prescribed dosage of Mabura is 160mg initially given at day 1 (administered as four 40mg in a day or two 40mg per day for two successive days) following with 80mg two weeks later (day 15). After two weeks, day 29 starts with continuance dose of 40mg every other week. Plaque psoriasis: The recommended dosage of Mabura is starting with 80mg, which is followed by 40mg for every other week, initiate one week after the initial dose

WARNING & SAFETY MEASURES

While using Mabura some adverse effects occur : Active or latent tuberculosis, Lymphoma and other malignancy, Hepatosplenic T-cell lymphoma, Various viral, fungal & bacterial infections occur, Increased the risk of infections. To reduce these conditions :
Avoid concurrent use of methotrexate with Mabura Before initiate the treatment with Mabura, patients must counsel about the adverse effects acquired by Mabura Risk factors :
Viral, fungal or bacterial infections History of patient already having opportunistic infection Exposure of tuberculosis Serious or intermittent infections
Other adverse effects :
Neurological reactions, Hematological problems, HBV reoccurrence. Risk of non-melanoma skin carcinoma : Discontinuation of treatment with Mabura Hepatosplenic T-cell lymphoma in pediatric patients: Stop the therapy immediately Hypersensitivity reactions occurs, to prevent this reactions avoid concomitant use of Mabura with other immunosuppressant agents.

DRUG INTERACTION

Avoid the concomitant use of Mabura with live vaccines. Anakinra, a interleukin 1 antagonist while combining with Mabura causes serious infection associated to anakinra, to avoid this problem concomitant use of Mabura with anakinra should not be recommended. Mabura concurrently used with methotrexate, in rheumatoid arthritis may causes diminishing apparent clearance of Mabura.

CONTRAINDICATION

Mabura has no contraindications Hypersensitivity reactions present, if patients are contraindicated to the ingredient of Mabura

MISSED DOSE

Mabura is used by the patients having serious rheumatoid arthritis, no self medication occur. If patient fail to take the dose of Mabura must consult with physician and follow the instruction given by medical adviser or skip the missed dose and follow the regular dosing schedule.

OVERDOSAGE

Once over dose occurs in the patients receiving Mabura, must monitored the signs and manifestation due to overdose of Mabura. Patient should be provided with safety measures.

SIDE EFFECTS

Severe infections :
Malignancies, Erythema, Back pain, Hypertension, Thrombocytopenia, Anaphylaxis, Angioneurotic edema, Interstitial lung disease like pulmonary fibrosis, Cutaneous vasculitis, psoriasis, Erythema multiforme, Systemic vasculitis, Itching, Hemorrhage, Pain, swelling, Rash, Pneumonia, Tuberculosis, Lupus like syndrome, Sinusitis, Flu like syndrome, Respiratory tract infection, Abdominal pain, Nausea, Injection site pain, Headache, Lab values abnormalities : • Hematuria
• Elevation of alkaline phosphatase
• Hypercholesterolemia
• Hyperlipidaemia.

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