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    Adalimumab Injection, API Form : Liquid

    • API FormLiquid
    • ApplicationUsed to Reduce Pain and Swelling Due to Certain Types of Arthritis (such as Rheumatoid, Psoriatic
    • DosageAs per Doctor's Prescription
    • StorageCool and Dry Place
    • Best Before36 Months from Manufacturing
    • Supply TypeExporter, Supplier
    • Preferred Buyer Location All over the world
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    • calendar Member Since 3 Years
    • building Nature of Business Exporter
    • gst icon GST No. 07ABEFM6994Q2Z7

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    • API FormLiquid
    • ApplicationUsed to Reduce Pain and Swelling Due to Certain Types of Arthritis (such as Rheumatoid, Psoriatic
    • DosageAs per Doctor's Prescription
    • StorageCool and Dry Place
    • Best Before36 Months from Manufacturing

    Adalimumab is used to reduce pain and swelling due to certain types of arthritis (such as rheumatoid, psoriatic, juvenile idiopathic, ankylosing spondylitis). This medication is also used to treat certain skin disorders (such as plaque-type psoriasis, hidradenitis suppurativa). It works by blocking a protein (tumor necrosis factor or TNF) found in the body’s immune system that causes joint swelling and damage in arthritis as well as red scaly patches in psoriasis. Adalimumab belongs to a class of drugs known as TNF blockers. By reducing joint swelling, this medication helps to reduce further joint damage and preserve joint function. Adalimumab is also used to treat certain bowel conditions (Crohn’s disease, ulcerative colitis) and a certain eye disease (uveitis). Adalimumab Syringe Kit – GENERIC NAME: ADALIMUMAB

     

    Adalimumab, sold under the brand name Humira, among others, is a monoclonal antibody used to treat rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, Crohn’s disease, ulcerative colitis, plaque psoriasis, hidradenitis suppurativa, uveitis, and juvenile idiopathic arthritis. It is administered by injection under the skin.

     

    Adalimumab is a disease-modifying antirheumatic drug (DMARD) and monoclonal antibody that works by inactivating tumor necrosis factor-alpha (TNFα).

     

    Adalimumab was approved for medical use in the United States in 2002. It is on the World Health Organization’s List of Essential Medicines. It is available as a biosimilar medication. In 2019, it was the 152nd most commonly prescribed medication in the United States, with more than 4 million prescriptions.


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