MOSBY Flashcards
Which drugs tend to concentrate in body compartments of high pH?
A. Permanently charged drugs
B. Drugs that are not charged
C. Weak organic acids
D. Weak organic bases
E. Inorganic ions
C. Weak organic acids
Drug agonists having the same intrinsic activity also have the same _____.
A. Maximal effect
B. Potency
C. Receptor affinity
D. Therapeutic index
E. Aqueous solubility
A. Maximal effect
What receptor or signaling pathway is linked
most directly to a2-adrenoceptor stimulation?
A. Gi and a reduction in cAMP
B. Gs and an increase in cAMP
C. Gq and calcium
D. Sodium ion channel
E. Membrane receptor containing tyrosine kinase
A. Gi and a reduction in cAMP
What tissue or organ has many muscarinic
receptors but lacks innervation to those
receptors?
A. Heart
B. Parotid gland
C. Blood vessels
D. Sweat glands
E. Urinary bladder
C. Blood vessels
Which drug used in the therapy for Parkinsonism does not cross the blood–brain barrier?
A. Amantadine
B. Carbidopa
C. L-dopa
D. Selegiline
E. Tolcapone
B. Carbidopa
After an injection, which drug would be expected to have the longest duration of action? (Assume no vasoconstrictor was injected with the local anesthetic.)
A. Bupivacaine
B. Lidocaine
C. Mepivacaine
D. Prilocaine
E. Procaine
A. Bupivacaine
A very low blood:gas solubility coefficient (partition coefficient = 0.47), analgesic effect, and a drug that inhibits methionine synthase best describes which drug?
A. Ketamine
B. Nitrous oxide
C. Halothane
D. Isoflurane
E. Propofol
B. Nitrous oxide
Levonordefrin is added to certain cartridges containing mepivacaine. The desired effect of levonordefrin is due to what pharmacological effect?
A. Inhibition of nicotinic cholinergic receptors
B. Inhibition of muscarinic cholinergic receptors
C. Stimulation of α-adrenergic receptors
D. Stimulation of β-adrenergic receptors
E. Stimulation of dopamine receptors
C. Stimulation of α-adrenergic receptors
The analgesic effects of dextromethorphan are
due to what receptor effect?
A. Gamma aminobutyric acid (GABA) receptor
antagonism.
B. Dopamine receptor antagonism.
C. Nicotinic cholinergic receptor antagonism.
D. Mu (μ) opioid receptor antagonism.
E. N-methyl-D-aspartate (NMDA) receptor
antagonism.
E. N-methyl-D-aspartate (NMDA) receptor
antagonism.
Naloxone antagonizes the therapeutic and toxic
effects of which drug?
A. Acetaminophen
B. Aspirin
C. Carbamazepine
D. Fentanyl
E. Ibuprofen
D. Fentanyl
What is the mechanism of the analgesic action
of aspirin?
A. Stimulates μ opioid receptors
B. Blocks histamine H2
receptors
C. Inhibits cyclooxygenase
D. Inhibits lipoxygenase
E. Blocks sodium channels in nerves
C. Inhibits cyclooxygenase
What is the clinical setting for the use of
ketorolac by the oral route?
A. For severe pain
B. For initial treatment of pain
C. To continue therapy after an IV or IM dose of
ketorolac
D. Only in combination with an opioid
E. Only in combination with an NSAID
C. To continue therapy after an IV or IM dose of
ketorolac
The use of H2 histamine receptor blockers is
most clinically useful at what cell type?
A. Beta cells of the pancreas
B. Basophils
C. Mast cells
D. Juxtaglomerular cells
E. Parietal cells
E. Parietal cells
Which class of antihypertensive drug most effectively reduces the release of renin from the kidney?
A. β-adrenergic receptor blockers
B. ACE inhibitors
C. α-adrenergic receptor blockers
D. Calcium channel blockers
E. Angiotensin II receptor blockers
A. β-adrenergic receptor blockers
The administration of which compound will give “epinephrine reversal” (drop in blood pressure from epinephrine) if given prior to administration of epinephrine?
A. Guanethidine
B. Propranolol
C. Phenoxybenzamine
D. Tyramine
C. Phenoxybenzamine
What is the mechanism of action of enoxaparin?
A. Inhibition of synthesis of clotting factors II, VII, IX,
and X
B. Activation of antithrombin III with resulting
inhibition of clotting factor Xa
C. Indirect activation of tissue plasminogen activator
D. Direct inhibition of plasminogen with resulting
degradation of fibrin
E. Dilation of coronary blood vessels
B. Activation of antithrombin III with resulting
inhibition of clotting factor Xa
Oropharyngeal candidiasis is an adverse effect
most likely with which drug?
A. Inhaled salmeterol
B. Inhaled ipratropium
C. Inhaled nedocromil
D. Inhaled beclomethasone
E. Inhaled methacholine
D. Inhaled beclomethasone
Oral antacids are most likely to reduce the absorption of which drug when it is given orally?
A. Clarithromycin
B. Clindamycin
C. Metronidazole
D. Penicillin V
E. Tetracycline
E. Tetracycline
A decrease in glycogenolysis in the liver would
be expected from which drug?
A. Albuterol
B. Epinephrine
C. Glucagon
D. Insulin
E. Parathyroid hormone
D. Insulin
Nitrates and nitrites have what effect on blood
vessel smooth muscle?
A. Increase in the level of intracellular calcium
B. Increase in the level of cyclic guanosine
monophosphate (cGMP)
C. Antagonism at α1-adrenergic receptors
D. Antagonism at β-adrenergic receptors
E. Inhibition of L-type calcium channels
B. Increase in the level of cyclic guanosine
monophosphate (cGMP)
Clavulanic acid offers an advantage
therapeutically because it has what action?
A. It inhibits Streptococci at a low minimum
inhibitory concentration (MIC).
B. It inhibits transpeptidase.
C. It inhibits penicillinase.
D. It inhibits anaerobes at a low MIC.
E. It inhibits DNA gyrase.
C. It inhibits penicillinase.
Identify the enzyme whose inhibition is most
responsible for the cell wall synthesis inhibitory
effect of penicillin G.
A. β-lactamase
B. DNA gyrase
C. Nitro reductase
D. Transglycosylase
E. Transpeptidase
E. Transpeptidase
Which drug is often combined with sulfamethoxazole for the treatment of respiratory tract and urinary tract infections?
A. Amoxicillin
B. Ciprofloxacin
C. Clindamycin
D. Metronidazole
E. Trimethoprim
E. Trimethoprim