chapter 4 part 2 Flashcards
Indirect interactions
Drug A alters the endogenous levels and affects Drug B
- diuretics decrease K+ plasma conc, and enhance digoxin and glycoside toxicity.
2.MAO I- inhibit metabolism of Ne AND SO Ne WILL INCREASE in levels, tyramine and ephedrine
- H-1 receptors antagonists mepyramine, which causes drowsiness and if taken with alcohol can lead to accidents
Age on drug response :
Drug responses can vary due to: DIMINISHED CARDIAC OUTPUT (heart attack)
- diminish hepatic metabolism
-can prolong the duration of the drug action
-Increasing body fat will increase Vd levels, and decrease plasma protein binding. this promotes the accumulation of highly lipid-soluble agents : diazepam (valium) and thiopental (pentothal).
age
neonates immature organs: reduced hepatic metabolism and renal excretion
elders: difference in Vd, renal clearance, absorption, hepatic metabolism
CYP3A4 (inhibitor)
Grapefruit juice are potent inhibitors of this in the intestine wall of mucosa
CYP1A2(inducer)
VEGETABLES LIKE brussel sprouts, cabbage, califlower and hydropcarbons in broiled meat
tetracyclines and fluoroquinolone antibiotics
calcium in dairy products can chelate these drugs
cigarette smokers have rapid metabolism compared to nonsmokers
b/c of enzyme inducer CYP1A
industrial workers exposed to pesticides will
metabolize certain drugs rapidly
drug-drug interactions
at the same time, one drug will affect and produce a pharmacological response
pharmacokinetics and pharmadynamic interactions
pharmadynamic interactions
direct interaction - drug A blocks drug b target site and diminishes or antagonizes drug b effect
ex; B-adrenoreceptors antagonists diminishes B-receptor agonists (propranolol salbutamol and terbutaline)
indirect interactions - drug A alters the endogenous levels of actions of Drug B
ex. diuretics will decrease k concentrations and enhance glycoside toxicity and digoxin
ex. MAO inhibitors will inhibit NE metabolism and increase NE levels like ephedrine and tyramine
ex. H-1 receptors antagonists like mepyramine cause drowsiness and when mixed with alcohol leads to accidents
pharmacokinetic interactions-clinically relevant
drug response cure is STEEP
therapeutic range is NARROW
EX. anti convulsions, antiarrhythmics, antithrombotics, antineoplastics, immunosuppressants, lithium
in vitro drug interactions
one drug interacts in vitro with another drug can inactive one or both drug
ex. thiopentone and suxamethonium - not in the same syringe but a complex is formed
ex. heparin is highly charged and interacts with basic drugs like this
absorption
gi absorption is slowed when drug inhibits emptying of gastric (Atropine and opiates)
gi absorption is accelerated by drugs like metoclopramide
calcium and iron with tetracycline will cause an insoluble complex which decreases absorption
cholestyramine is a bile acid binding resin used to treat hypercholesteremia and binds with warfarin and dioxin to prevent absorptions
epinephrine and anesthetic causes vasoconstriction and slows the anesthetic absportions
distributions
displacement of drug from binding site and increase conc of free drug
then an increase excretion produces a new steady state of drug conc in plasma is decrease but free drug conc is the same as before displacing drug
toxicity from displacement can occur BEFORE NEW steady state
displacing agents
aspirin and sulfonamides like hydrate choral because of tight/strong binding to plasma albumin
ex aspirin displaces warfarin and valproate