Please provide your email address to receive an email when new articles are posted on . Stevens-Johnson syndrome is a mucocutaneous immune-mediated hypersensitivity reaction. It is often triggered by ...
We describe a patient with Stevens-Johnson syndrome (erythema multiforme major) associated with an increase in glipizide dosage administration. Glipizide is a second-generation sulfonylurea commonly ...
Most cases of SJS are probably a cell-mediated hypersensitivity reaction; in some cases monocytes and macrophages are present and auto-antibodies may be pathogenic. SJS is characterized by skin ...
Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) survivors encounter rare, life-threatening drug reactions and years of physical, emotional and social consequences long after ...
First identified by Stevens and Johnson in 1922, SJS and TEN are now recognized as disorders with a continuum of severity, from milder forms (SJS) to the most severe (TEN). SJS/TEN is associated with ...
Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) survivors encounter rare, life-threatening drug reactions and years of physical, emotional and social consequences long after ...
The presence of CKD among patients with SJS or TEN may influence the in-hospital mortality risk associated with analgesic and antipyretic therapies.
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