Active Ingredient: Adalimumab
Adalimumab is indicated for the treatment of non-infectious intermediate, posterior and panuveitis in adult patients who have had an inadequate response to corticosteroids, in patients in need of corticosteroidsparing, or in whom corticosteroid treatment is inappropriate.
For this indication, competent medicine agencies globally authorize below treatments:
Subcutaneous
40 - 80 mg
From 40 To 80 mg once every 14 day(s)
80 mg
40 mg
The recommended dose of adalimumab for adult patients with uveitis is an initial dose of 80 mg, followed by 40 mg given every other week starting one week after the initial dose.
There is limited experience in the initiation of treatment with adalimumab alone. Treatment with adalimumab can be initiated in combination with corticosteroids and/or with other non-biologic immunomodulatory agents. Concomitant corticosteroids may be tapered in accordance with clinical practice starting two weeks after initiating treatment with adalimumab.
It is recommended that the benefit and risk of continued long-term treatment should be evaluated on a yearly basis.
Adalimumab may be available in other strengths and/or presentations depending on the individual treatment needs.
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