Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
46 Cards in this Set
- Front
- Back
To reduce the tachycardia characteristic of paroxysmal atrial tachycardia, which of the following drugs would bring your heart rate back to "normal" through its actions outside the heart?
|
B. Methoxamine
|
|
You have a dry mouth, dilated pupils, and a high heart rate. From these symptoms you conclude that u have received an overdose of:
|
A. Atropine
|
|
Albuterol:
|
B. Activates non innervated Beta2 receptors to dilate blood vessels of skeletal muscle
|
|
Atracurium
|
A. Is used as a muscle relaxant in surgical procedures
|
|
The therapeutic threshold concentration (aka minimal effective conc.) of a drug:
|
D. Is the minimum plasma concentration of the drug which is required to induce the desired therapeutic response
|
|
An expected side effect when using systemically administered Bethanechol to treat atony of the urinary bladder after childbirth:
|
E. A and C
A. Decreased heart rate (bradycardia) C. Decreased blood pressure resulting from vasodilation of some blood vessels |
|
A pharmacological antagonist at a particular type of receptor
|
E. A and C
A. will bind but not activate those receptors C. Will have physiological or clinical efficacy (based on its activity at those receptors |
|
Norepinephrine
|
D. Is the neurotransmitter at most postganglionic neuron - effector cell syn apses in the sympathetic nervous system
|
|
An appropriate drug to reverse the effects of atropine overdose:
|
A. Physostigmine
|
|
All of the following routes of administration are classified as parenteral except:
|
B. Oral
|
|
You are salivating excessively and your muscle strength seems less than normal. From these symptoms, you conclude that you have received an overdose of:
|
A. Neostigmine
|
|
Uses of anticholinesterases in therapy include administration by appropriate routes to:
|
C. Restore urinary bladder function in individuals with urinary bladder atony
|
|
Figure of response vs dose
|
E. A and C
|
|
Glycopyrrolate is administered with a general anesthetic in many instances because glycopyrrolate will:
|
E. A and C
A. Reverse general anesthesia induced bradycardia and block of conduction through AV node C. Reduce bronchoconstriction |
|
The idea of spare receptors comes from evidence that:
|
D. For full agonists, EC50 is less than KD50
|
|
Activation of the sympathetic nervous system
|
A. increases heart rate
|
|
Figure of response vs dose with antagonists
|
B. For the receptor activated by the full agonsist, antagonist t has a higher affinity than ant S
|
|
Phenylephrine will increase pressure by
|
A. Activation of a1 adrenoreceptors on blood vessels of the skin and mesentary
|
|
A drug which might be expected to reduce blood pressure through effects on receptor on blood vessels but which has no direct effect on cardiac output
|
B. Prazosin
|
|
Edrophonium is preferred over other drugs to differentially diagnose cholinergic cris and myasthenia gravis because:
|
D. Edrophonium is a short acting cholinesterase inhibitor
|
|
A drug which mimics acetylcholine at cholinergic receptors in autonomic ganglia but is not a choline ester:
|
E. Nicotine
|
|
Drug A is administered repeatedly with a constant interval between consecutive doses and with a constant dose. The mean plasma concentration of drug A is measured. This concentration:
|
B. 1 and 3 are correct
|
|
A drug which has high affinity for a1 adrenoreceptors and very low affinity for other adrenoreceptors and which is an agonist at a1 adrenoreceptors:
|
A will be useful as a nasal decongestant
|
|
Atenolol and propanolol can both be used to treat hypertension. Atenolol may be preferred over propranolol for this purpose because, as a side effect, propranolol:
|
D. Can cause coronary artery constriction
|
|
A drug which when adminstered intravenously does not enter the Central nervous system rapidly, increases gastrointestinal motility but does not affect skeletal muscle contraction
|
A. Bethanechol
|
|
A drug that activates receptors and initiates a series of cellular reactions that result in a less than maximal response by the cell/tissue/organ, even when it binds 100% of those receptors is:
|
A. a partial agonist
|
|
Trimethaphan
|
C. is an antagonist at nicotinic receptors in autonomic ganglia
|
|
A drug which is a substrate for cholinesterases, increases salivary secretion, and will increase binding of acetylcholone released from motor neurons to cholinergic receptors on skeletal muscle
|
D. physostigmine
|
|
Dobutamine:
|
D. Mimics the effects of isoproterenol to alter heart rate and contractility of heart muscle
|
|
Epinephrine:
|
C. Causes hypoglycemia by inducing insulin secretion from the pancreas
|
|
Clondine
|
B. Activates adrenoreceptors on axon terminals of neuroepinephrine-secreting neurons
|
|
A drug which reduces contraction of the uterus in pregnant women:
|
B. Terbutaline
|
|
Dopamine:
|
E. A and C
A, Activates B1 Adrenoreceptors in the heart C. INduces vasodilation through activation of vascular dopamine receptors |
|
A drug which induces miosis when applied to the eye but has a different mechanism of action than pilocarpine
|
D. Physostigmine
|
|
Epinephrine decreases diastolic blood pressure by
|
A. Activation of B2 adrenoreceptors on the blood vessels of skeletal muscle
|
|
The liver enzyme Z metabolizes Drug A. If Drug A is administered repeatedly, then the amount of Enzyme Z in the liver is increases. Consequently...
|
A. The halflife of the drug A will be decreased
|
|
The direct actions of atropine in the heart:
|
A. Include increased heart rate
|
|
Pilocarpine is administered topically to the eye to treat glaucoma because systematically administered pilocarpine would have the undesired effect of
|
A. Decreased heart rate
|
|
A drug which is a cholinomimetic and a choline ester but has no effect at the skeletal neuromuscular junction
|
E. Bethanechol
|
|
Pralidoxime is useful to treat overdose by
|
B. Parathion
|
|
Tacrine is used in the treatment of Alzheimer's disease. Tacrine:
|
A. Is a cholinesterase inhibitor
|
|
Renin Secretion:
|
E. A and C
A. Increases renal Na and water retention and increases blood pressure C. Increases total peripheral resistance due to angiotensin II induced vasoconstriction |
|
Tropicamide:
|
B. is used as a mydriatic
|
|
A drug which has inotropic effects in the heart via B1 adrenoreceptors and also induces bronchodilation but does not produce vasoconstriction:
|
D. Isoproterenol
|
|
Two drugs with the same affinity for a receptor:
|
C. May produce different effects after binding to the receptor
|
|
You are given the same oral dose of a drug every 24 hours. by the sixth day, the drug seems to have a reduced effectiveness (compared to its effect on the first couple of days). This reduced effectiveness could be the result of
|
A. Increased rate of elimination
|