Kemstro was originally designed in 1960 to treat epilepsy. However, the result was not satisfactory. Kemstro was then reintroduced in 1971 when it was found to treat muscle spasticity and has seen wide use since. Kemstro is FDA-approved for the management of reversible spasticity, particularly for the relief of flexor spasms, clonus, and concomitant pain, common sequelae of spinal cord lesions and multiple sclerosis. However, for patients who experience intolerable adverse effects or who fail to respond to oral therapy, intrathecal Kemstro might be considered. Intrathecal Kemstro administration is FDA-approved for the management of spasticity of cerebral origins, such as traumatic brain injury or severe spasticity of spinal cord origin that is unresponsive to treatment with maximum doses of oral Kemstro, tizanidine, and/or dantrolene.
Other names for this medication:
Baclofen,
Lioresal,
Baclofene,
Baclofeno,
Baclon,
Baclopar,
Barambo,
Clofen,
Kemstro,
Liofen,
Lyflex,
Miorel,
Pacifen,
Similar Products:
Gantrisin,
Pantin,
Fuben,
Omezzol,
Mirtazapine,
Liondox,
Flutan,
Ciproxin,
Quetiapina,
Benoxil,
Gabapentina,
Cipro,
Vermazol,
Audazol,
Osiren,
Trifen,
Talpramin,
Depaxil,
Topina,
Zyntabac,
Ciriax,
Metrogel,
Gabatal,
Sievert,
Delak,
Lafigin,
Ulcosan,
Rispolux,
Tetraciclina,
Efavir,
Claneksi,
Ampliron,
Vivorax,
Antivir,
Duloren,
Neoset,
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