chap 8 Flashcards
Genetic polymorphisms account for differences in metabolism, including:
- Poor metabolizers, who lack a working enzyme
- Intermediate metabolizers, who have one working, wild-type allele and one mutant allele
- Extensive metabolizers, with two normally functioning alleles
- All of the above
- All of the above
Up to 21% of Asians are ultra-rapid 2D6 metabolizers, leading to:
- A need to monitor drugs metabolized by 2D6 for toxicity
- Increased dosages needed of drugs metabolized by 2D6, such as the selective serotonin reuptake inhibitors
- Decreased conversion of codeine to morphine by CYP 2D6
- The need for lowered dosages of drugs, such as beta blockers
- Increased dosages needed of drugs metabolized by 2D6, such as the selective serotonin reuptake inhibitors
Rifampin is a nonspecific CYP450 inducer that may:
- Lead to toxic levels of rifampin and must be monitored closely
- Cause toxic levels of drugs, such as oral contraceptives, when coadministered
- Induce the metabolism of drugs, such as oral contraceptives, leading to therapeutic failure
- Cause nonspecific changes in drug metabolism
- Induce the metabolism of drugs, such as oral contraceptives, leading to therapeutic failure
Inhibition of P-glycoprotein by a drug such as quinidine may lead to:
- Decreased therapeutic levels of quinidine
- Increased therapeutic levels of quinidine
- Decreased levels of a coadministered drug, such as digoxin, that requires P-glycoprotein for absorption and elimination
- Increased levels of a coadministered drug, such as digoxin, that requires P-glycoprotein for absorption and elimination
- Increased levels of a coadministered drug, such as digoxin, that requires P-glycoprotein for absorption and elimination
Genetic testing for VCORC1 mutation to assess potential warfarin resistance is required prior to prescribing warfarin.
- True
- False
- false
Pharmacogenetic testing is required by the U.S. Food and Drug Administration prior to prescribing:
- Erythromycin
- Digoxin
- Cetuximab
- Rifampin
- Cetuximab
Carbamazepine has a Black Box Warning recommending testing for the HLA-B*1502 allele in patients with Asian ancestry prior to starting therapy due to:
- Decreased effectiveness of carbamazepine in treating seizures in Asian patients with the HLA-B*1502 allele
- Increased risk for drug interactions in Asian patients with the HLA-B*1502 allele
- Increased risk for Stevens-Johnson syndrome in Asian patients with HLA-B*1502 allele
- Patients who have the HLA-B*1502 allele being more likely to have a resistance to carbamazepine
- Increased risk for Stevens-Johnson syndrome in Asian patients with HLA-B*1502 allele
A genetic variation in how the metabolite of the cancer drug irinotecan SN-38 is inactivated by the body may lead to:
- Decreased effectiveness of irinotecan in the treatment of cancer
- Increased adverse drug reactions, such as neutropenia
- Delayed metabolism of the prodrug irinotecan into the active metabolite SN-38
- Increased concerns for irinotecan being carcinogenic
- Increased adverse drug reactions, such as neutropenia
Patients who have a poor metabolism phenotype will have:
- Slowed metabolism of a prodrug into an active drug, leading to accumulation of prodrug
- Accumulation of inactive metabolites of drugs
- A need for increased dosages of medications
- Increased elimination of an active drug
- Slowed metabolism of a prodrug into an active drug, leading to accumulation of prodrug
Ultra-rapid metabolizers of drugs may have:
- To have dosages of drugs adjusted downward to prevent drug accumulation
- Active drug rapidly metabolized into inactive metabolites, leading to potential therapeutic failure
- Increased elimination of active, nonmetabolized drug
- Slowed metabolism of a prodrug into an active drug, leading to an accumulation of prodrug
- Active drug rapidly metabolized into inactive metabolites, leading to potential therapeutic failure
A provider may consider testing for CYP2D6 variants prior to starting tamoxifen for breast cancer to:
- Ensure the patient will not have increased adverse drug reactions to the tamoxifen
- Identify potential drug-drug interactions that may occur with tamoxifen
- Reduce the likelihood of therapeutic failure with tamoxifen treatment
- Identify poor metabolizers of tamoxifen
- Reduce the likelihood of therapeutic failure with tamoxifen treatment