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searching for Severe cutaneous adverse reactions 8 found (20 total)

alternate case: severe cutaneous adverse reactions

HLA-B58 (451 words) [view diff] exact match in snippet view article find links to article

Stevens–Johnson syndrome. Allopurinol is a frequent cause of severe cutaneous adverse reactions, including drug-hypersensitivity syndrome, Stevens–Johnson

List of adverse effects of paroxetine (1,309 words) [view diff] exact match in snippet view article find links to article

sometimes associated with jaundice and/or liver failure) Priapism Severe cutaneous adverse reactions (including erythema multiforme, Stevens–Johnson syndrome and

Yuan-Tsong Chen (1,179 words) [view diff] exact match in snippet view article find links to article

(15 March 2005). "HLA-B*5801 allele as a genetic marker for severe cutaneous adverse reactions caused by allopurinol". Proceedings of the National Academy

Allopurinol (2,755 words) [view diff] exact match in snippet view article find links to article

HLA-B*5801 allele is a genetic marker for allopurinol-induced severe cutaneous adverse reactions, including Stevens-Johnson syndrome (SJS) and toxic epidermal

HLA-B (1,889 words) [view diff] exact match in snippet view article find links to article

(March 2005). "HLA-B*5801 allele as a genetic marker for severe cutaneous adverse reactions caused by allopurinol". Proceedings of the National Academy

Carbamazepine (3,052 words) [view diff] exact match in snippet view article find links to article

PMID 16876011. Kaniwa N, Saito Y (June 2013). "Pharmacogenomics of severe cutaneous adverse reactions and drug-induced liver injury". Journal of Human Genetics

P-i mechanism (4,156 words) [view diff] case mismatch in snippet view article find links to article

symptoms: survey conducted by the Asian Research Committee on Severe Cutaneous Adverse Reactions (ASCAR)". The Journal of Dermatology. 42 (3): 276–282. doi:10

Modafinil (15,639 words) [view diff] exact match in snippet view article find links to article

and January 2007, the FDA received reports of six cases of severe cutaneous adverse reactions, including erythema multiforme, Stevens–Johnson syndrome,