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Pharmacogenomics_Paediatric v0.50 CYP2C9 David Metz edited their review of gene: CYP2C9: Changed phenotypes: Phenytoin metabolism - increased risk toxicities
Pharmacogenomics_Paediatric v0.50 CYP2C9 David Metz changed review comment from: 25099164
Reduced phenytoin metabolism, increased risk phenytoin-induced SJS/TEN
If CYP2C9 IM or PM and phenytoin naive, avoid phenytoin.; to: 25099164
If CYP2C9 IM, consider 25% reduction starting dose (moderate recommendation).
If CYP2C9 PM, consider 50% reduction starting dose phenytoin (strong recommendation).
Pharmacogenomics_Paediatric v0.50 CYP2C9 David Metz edited their review of gene: CYP2C9: Added comment: 25099164
Reduced phenytoin metabolism, increased risk phenytoin-induced SJS/TEN
If CYP2C9 IM or PM and phenytoin naive, avoid phenytoin.; Changed publications: 18406467, 25099164; Changed phenotypes: Increased risk phenytoin-induced SJS/TEN
Pharmacogenomics_Paediatric v0.33 CYP2C9 David Metz changed review comment from: (32189324)
Note poor metabolizer status has increased exposure (and possible sensitivity) to certain NSAIDs.
"Alternative therapies not primarily metabolized by CYP2C9 include aspirin, ketorolac, naproxen, and sulindac. Selection of
therapy will depend on individual patient treatment goals and risks for toxicity."
Probably not sufficient evidence to test for CYP2C9 alone, however if information available may be worth noting.; to: (32189324)
Note poor metabolizer status has increased exposure (and possible sensitivity) to certain NSAIDs.
"Alternative therapies not primarily metabolized by CYP2C9 include aspirin, ketorolac, naproxen, and sulindac. Selection of therapy will depend on individual patient treatment goals and risks for toxicity."
Probably not sufficient evidence to test for CYP2C9 alone, however if information available may be worth noting.
Pharmacogenomics_Paediatric v0.33 CYP2C9 David Metz commented on gene: CYP2C9: (32189324)
Note poor metabolizer status has increased exposure (and possible sensitivity) to certain NSAIDs.
"Alternative therapies not primarily metabolized by CYP2C9 include aspirin, ketorolac, naproxen, and sulindac. Selection of
therapy will depend on individual patient treatment goals and risks for toxicity."
Probably not sufficient evidence to test for CYP2C9 alone, however if information available may be worth noting.
Pharmacogenomics_Paediatric v0.33 CYP2C9 David Metz reviewed gene: CYP2C9: Rating: ; Mode of pathogenicity: None; Publications: 18406467; Phenotypes: ; Mode of inheritance: None
Pharmacogenomics_Paediatric v0.31 CYP2C9 Zornitza Stark Publications for gene: CYP2C9 were set to 25099164
Pharmacogenomics_Paediatric v0.30 CYP2C9 Zornitza Stark edited their review of gene: CYP2C9: Changed publications: 25099164, 21900891, 28198005
Pharmacogenomics_Paediatric v0.29 CYP2C9 Zornitza Stark Publications for gene: CYP2C9 were set to
Pharmacogenomics_Paediatric v0.28 CYP2C9 Zornitza Stark edited their review of gene: CYP2C9: Changed publications: 25099164
Pharmacogenomics_Paediatric v0.19 CYP2C9 Zornitza Stark edited their review of gene: CYP2C9: Added comment: Activity levels of CYP2C9 are at 1-2% of adult values in the fetus during the first trimester. These levels gradually increase to 30% of adult values at term. There is a high variability in these levels during the first 5 months of life, with levels eventually approaching adult values somewhere between 5 months and 2 years of age.; Changed phenotypes: Warfarin sensitivity, MIM# 122700, Phenytoin
Pharmacogenomics_Paediatric v0.8 CYP2C9 Zornitza Stark Marked gene: CYP2C9 as ready
Pharmacogenomics_Paediatric v0.8 CYP2C9 Zornitza Stark Gene: cyp2c9 has been classified as Green List (High Evidence).
Pharmacogenomics_Paediatric v0.8 CYP2C9 Zornitza Stark Classified gene: CYP2C9 as Green List (high evidence)
Pharmacogenomics_Paediatric v0.8 CYP2C9 Zornitza Stark Gene: cyp2c9 has been classified as Green List (High Evidence).
Pharmacogenomics_Paediatric v0.7 CYP2C9 Zornitza Stark gene: CYP2C9 was added
gene: CYP2C9 was added to Pharmacogenomics_Paediatric. Sources: Expert list
Mode of inheritance for gene: CYP2C9 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: CYP2C9 were set to Warfarin sensitivity, MIM# 122700; Phenytoin
Review for gene: CYP2C9 was set to GREEN
Added comment: Sources: Expert list