Pharmacology Flashcards
This measure relates the dose of the drug required to produce a desired effect to that which produces an undesired effect.
therapeutic index
This is the fraction of unchanged drug reaching the systemic circulation following administration by any route:
Bioavailability
In this clinical phase of drug development, the drug is studied in patients with the target disease to determine its efficacy.
phase 2
This is an irreversible inhibitor of GABA aminotransferase and is useful in the treatment of partial seizures and WEST syndrome:
vigabatrin
Action of Insulin in the liver:
increase storage of glucose as glycogen
Most common adverse effect of insulin:
hypoglycemia
Effect of digitalis in the AV node during arrythmias:
AV blockade
Immediate metabolic precursor of dopamine that penetrates the blood-brain barrier:
levodopa
The following are true of phenoxybenzamine:
B. blocks catecholamine-induced vasoconstriction / D. stimulates histamine (H1) acetylcholine and serotonin receptors
Antiarrhythmic drugs that prolong effective refractory period by prolonging action potential duration:
Bretylium
Antiarrhytmic of choice for suppression of recurrences of ventricular tachycardia & fibrillation after termination of the arrhythmia by cardioversion:
Lidocaine
The most serious toxic reaction to local anesthetics is:
tonic-clonic convulsions
Lithium’s most common side effect/s
polyuria and subclinical hypothyrodism
Most important unwanted effect of anti-psychotics secondary to relative choline deficiency.
Tardive dyskinesia
Blocks norepinephrine & serotonin reuptake pumps-the “the off switches” of amine transmission
tricyclics
Drug interaction of older MAO inhibitor with tyramine ingested in food:
Hypertensive reactions
The following are sites of the major classes of anti-hypertensive drugs, except:
Hypothalamus
The following statements regarding selection of anti-hypertensive drugs are correct, except:
A. ACE inhibitors are particularly useful in diabetic patients with evidence of renal disease. / B. White race responds better to diuretics and calcium channel blockers than to ß-blockers and ACE inhibitors.* / C. Beta-blockers or calcium channel blockers are useful in patients who have angina. / D. Diuretics or ACE inhibitors are useful who also have CHF
The following are the determinants of vascular tone, except:
a.Increasing cGMP / b.Increasing cAMP in the vascular cells / c.Decreasing intracellular calcium* / d.Stabilizing or preventing depolarization of the vascular smooth muscle cell membrane
The following are the pharmacodynamics of nitroglycerine, except:
A. Smooth muscle relaxation / B. Decreased ventricular preload / C. Responsible for a decrease in platelet aggregation / D. Increased cardiac output*
The following are the pharmacodynamics of NSAIDs, except:
A. Mediated chiefly through inhibition of biosynthesis of prostaglandins / B. All NSAIDs inhibit platelet aggregation* / C. All NSAIDs are anagesic, anti-inflammatory and antipyretic / D. They are all gastric irritants as well
The following are disease-modifying antirheumatic drugs, except:
a. Methotrexate / b. Cyclosporins / c. Corticosteroids* / d. Azathioprine
This agent inhibits cell wall synthesis by binding firmly to the D-Ala-D-Ala terminus of nascent peptidoglycan pentapeptide. It inhibits the transglycosylase, preventing further elongation of peptidoglycan and cross-linking.
Vancomycin
This agent is a potent inhibitor of microbial protein synthesis. It binds reversibly to the 50 S subunit of the bacterial ribosome and inhibits peptidyl transferase step of protein synthesis. This agent is active against rickettsiae but not chlamydiae:
Chloramphenicol