Exam 1 Flashcards
Volume of distribution
Amount of drug in the body/plasma drug concentration
High volume of distribution
Means that the drug is not highly protein bound
Clearance of a drug
0.693(Vd)/half life
Bioavailability
How much of the drug will reach the blood after metabolism
What form of drug route will have greatest bioavailability
IV and sublingual
Fastest route of absorption
Inhalation
What will make urine more acidic
Cranberry juice, vitamin C, NH4Cl
What will make urine more basic
Aspirin
What types of drugs will cross placenta and blood brain barrier
Small, lipid soluble, non-protein bound
Inhibition of CYP450 leads to
Drug toxicity
General inducers of CYP450
GPCRABS
Glucocorticoids, phenytoin, carbamazepine, rifampin, alcohol, barbiturates, st johns wort
General inhibitors of CYP450
GPACMANS
Grapefruit, protease inhibitors, proton pump inhibitors, azoles, cimetidine, macrolides, amiodarone, non-dihydropyridines, SSRIs
Drugs that undergo zero order elimination
Phenytoin, salicylates, aspirin, alcohol
Drugs that have a small therapeutic index
Have a higher chance of toxicity–need to monitor drug levels
Water percentage in neonates
75-80%, less body fat
When do kidneys and liver reach maturation in infants
2 years old
Before this, drug toxicity can occur more frequently
When does gastric output levels reach adult levels in children
2 years old
Gastric emptying in infants/children
prolonged
Pulmonary absorption in children
Decreased due to increased RR and larger tidal volume
Volume of distribution in children
Larger due to increased total body water and less albumin
Body water and fat in elderly
Less body water and more body fat
Half life of drugs may increase if higher volume of distribution
Drugs that have increased CNS effects in elderly
Anticholinergics, TCAs, antihistamines, antispasmodics, benzodiazepines, analgesics
Allosteric site
A binding site for substrates not active in initiating a response; may induce a conformational change in the structure of the active site, rendering it more or less susceptible to response from a substrate
Downregulation
Decreased availability of drug receptors