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Glatiramer acetate treatment

Kipnis J, Schwartz M (2002) Dnal action of glatiramer acetate (Cop-1) in the treatment of CNS antoimmnne and neurodegenerative disorders. Trends Mol Med 8 319-323. [Pg.427]

Most common adverse effects in controlled trials include injection site reactions, vasodilatation, chest pain, asthenia, infection, pain, nausea, arthralgia, anxiety, and hypertonia. About 10% of patients experience an immediate post-injection reaction (flushing, chest pain, palpitations, anxiety, dyspnea, throat constriction, and urticaria). The symptoms are transient and self-limited, and usually do not require specific treatment. Transient chest pain was noted in 21% of Copaxone patients versus 11% in the placebo group with no long-term sequelae. Unlike therapy with the IFNps, glatiramer acetate is not associated with flu-like symptoms. [Pg.596]

Khan OA, Tslis AC, Kamholz JA, Garbem JY, Lewis RA, Lisak RP (2001b) A prospective open-label treatment trial to compare the effect of IFN beta-la (Avonex), IFN beta-lb (Betaseron) and glatiramer acetate (Copaxone) on the relapse rate in relapsing-remit-ting multiple sclerosis Results after 18 months of therapy. Mult Scler 7 349-353. [Pg.601]

Treatment with interferon-/ or glatiramer acetate (Avonex, Betaseron, Copaxone, and Rebif, or ABC-R, therapy) can reduce annual relapse rate, slow progression of disability, slow cognitive decline, and slow changes seen on the brain MRIs. [Pg.1007]

Patients suffering from MS frequently will have symptoms such as spasticity, bladder dysfunction, fatigue, pain, and depression that may require treatment. Patients must be counseled thattherapies such as interferon-/ and glatiramer acetate will not relieve these symptoms. [Pg.1007]

Nicolau syndrome (embolia cutis medicamentosa) has been described in a 39-year-old woman with multiple sclerosis after subcutaneous treatment with glatiramer acetate for 2 years [55 ]. Continuation of treatment with glatiramer acetate at other injection sites was recommended, and further injections were well tolerated. The lesion healed within 10 weeks without any residual effects. [Pg.618]

Bains SN, Hsieh FH, Rensel MR, Radojicic C, Katz HT, Inamdar SR, Lang DM. Glatiramer acetate successful desensitization for treatment of multiple sclerosis. Ann Allergy Asthma Immunol 2010 104(4) 321-5. [Pg.643]


See other pages where Glatiramer acetate treatment is mentioned: [Pg.70]    [Pg.359]    [Pg.187]    [Pg.594]    [Pg.637]    [Pg.652]    [Pg.594]    [Pg.637]    [Pg.641]    [Pg.642]    [Pg.652]    [Pg.1007]    [Pg.1012]    [Pg.1015]    [Pg.463]    [Pg.256]    [Pg.618]    [Pg.6396]    [Pg.45]    [Pg.179]   
See also in sourсe #XX -- [ Pg.1721 ]




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