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a) Ganglion-blockers
b) Atropine-similar drugs
c) Neuromuscular junction blockers
d) Both a and c
a) In the myocardium
b) In sympathetic postganglionic neurons
c) On effector cell membranes of glandular and smooth muscle cells
d) On the motor end plates
a) Atropine
b) Benztropine
c) Hexamethonium
d) Succinylcholine
a) Scopolamine
b) Pipecuronium
c) Trimethaphan
d) Pilocarpine
a) Homatropine
b) Hexamethonium
c) Rapacuronium
d) Edrophonium
a) Vencuronium
b) Scopolamine
c) Succinylcholine
d) Hexamethonium
a) Pancuronium
b) Succinylcholine
c) Hexamethonium
d) Scopolamine
a) Atropine
b) Scopolamine
c) Homatropine
d) Ipratropium
a) Eye
b) Heart
c) Smooth muscle organs
d) Glands
a) Competitive ganglion blockade
b) Competitive muscarinic blockade
c) Competitive neuromuscular blockade
d) Noncompetitive neuromuscular blockade
a) The salivary, bronchial and sweat glands
b) The gastric parietal cells
c) Smooth muscle and autonomic effectors
d) The heart
a) M1 receptor subtype
b) M2 receptor subtype
c) M3 receptor subtype
d) All of the above
a) Atropine
b) Ipratropium
c) Scopolamine
d) Homatropine
a) Miosis, a reduction in intraocular pressure and cyclospasm
b) Mydriasis, a rise in intraocular pressure and cycloplegia
c) Miosis, a rise in intraocular pressure and cycloplegia
d) Mydriasis, a rise in intraocular pressure and cyclospasm
a) Atropine
b) Hexamethonium
c) Pilocarpine
d) Carbachol
a) Atria
b) Sinoatrial node
c) Atrioventricular node
d) Ventricle
a) Bradycardia, hypotension and bronchoconstriction
b) Tachycardia, little effect on blood pressure and bronchodilation
c) Decrease in contractile strength, conduction velocity through the AV node
d) Tachycardia, hypertensive crisis and bronchodilation
a) Muscle tone
b) Secretions
c) Nausea and vomiting
d) All of the above
a) Slow gastric empting and prolongation of the exposure of the ulcer bed to acid
b) Low efficiency and necessity of large doses
c) Adverse effects
d) All of the above
a) Atropine
b) Scopolamine
c) Pirenzepine
d) Homatropine
a) Spasmolitic activity
b) Intestinal hypermotility
c) Stimulation of contraction in the gut
d) Stimulation of secretory activity
a) Carbachol
b) Vecuronium
c) Atropine
d) Edrophonium
a) In adults
b) In pregnant women
c) In infants and children
d) All of the above
a) Hexamethonium
b) Atropine
c) Succinylcholine
d) Pilocarpine
a) More marked central effect
b) Less potent in decreasing bronchial, salivary and sweat gland secretion
c) More potent in producing mydriasis and cycloplegia
d) Lower effects on the heart, bronchial muscle and intestines
a) Benztropine
b) Edrophonium
c) Succinylcholine
d) Hexamethonium
a) Pilocarpine
b) Neostigmine
c) Homatropine
d) Ipratropium
a) Atropine
b) Ipratropium
c) Lobeline
d) Homatropine
a) Suscinilcholine
b) Pralidoxime
c) Pirenzepine
d) Propiverine
a) Pralidoxime
b) Pilocarpine
c) Homatropine
d) Atropine
a) Motion sickness
b) Glaucoma
c) Hyperhidrosis
d) Asthma
a) Mydriasis, cycloplegia
b) Hyperthermia, dry mouth, hot and flushed skin
c) Agitation and delirium
d) Bradicardia, orthostatic hypotension
a) Neostigmine
b) Hexametonium
c) Homatropine
d) Acetylcholine
a) Glaucoma
b) Myasthenia
c) Bronchial asthma
d) Paralytic ileus and atony of the urinary bladder
a) Muscarinic receptor site
b) Neuromuscular junction
c) Autonomic ganglia
d) Axonal transmission
a) Orthostatic hypotension
b) Lack of selectivity
c) Homeostatic reflexes block
d) Respiratory depression
a) Homatropine
b) Trimethaphane
c) Hexamethonium
d) Pancuronium
a) Mecamylamine
b) Scopolamine
c) Trimethaphane
d) Vecocuronium
a) Reduction of both peripheral vascular resistance and venous return
b) Partial mydriasis and loss of accommodation
c) Constipation and urinary retention
d) Stimulation of thermoregulatory sweating
a) Hypertensive crises
b) Controlled hypotension
c) Cardiovascular collapse
d) Pulmonary edema
a) Interaction of acetylcholine with cholinergic receptors
b) Release of acetylcholine from prejunctional membrane
c) Packaging of acetylcholine into synaptic vesicles
d) Reuptake of acetylcholine into the nerve ending
a) Nicotinic acethylcholine receptors
b) Muscarinic acethylcholine receptors
c) The motor end plate
d) Contractile apparatus
a) Block acetylcholine reuptake
b) Prevent access of the transmitter to its receptor and depolarization
c) Block transmission by an excess of a depolarizing agonist
d) All of the above
a) Rocuronium
b) Carbachol
c) Atracurium
d) Succylcholine
a) Rapacuronium
b) Mivacurium
c) Tubocurarine
d) Rocuronium
a) Vecuronium
b) Tubocurarine
c) Pancuronium
d) Rapacuronium
a) Succinylcholine
b) Rapacuronium
c) Pancuronium
d) Tubocurarine
seizures:
a) Pancuronium
b) Succinylcholine
c) Tubocurarine
d) Atracurium
a) Atracurium
b) Succinylcholine
c) Pipecuronium
d) Doxacurium
a) Succinylcholine
b) Tubocurarine
c) Mivacurium
d) Pancuronium
a) Mivacurium
b) Rapacuronium
c) Rocuronium
d) Succinylcholine
a) Renal failure
b) An abnormal variant of plasma cholinesterase
c) Hepatic disease
d) Both b and c
a) Interact with nicotinic receptor to compete with acetylcholine without receptor activation
b) React with the nicotinic receptor to open the channel and cause depolarisation of the end plate
c) Cause desensitization, noncompetive block manifested by flaccid paralysis
d) Cholinesterase inhibitors do not have the ability to reverse the blockade
a) Mivacurium
b) Pancuronium
c) Succinylcholine
d) Tubocurarine
a) Hand
b) Leg
c) Neck
d) Diaphragm
a) Succylcholine
b) Tubocurarine
c) Pancuronium
d) Rocuronium
a) Vecuronium
b) Succinylcholine
c) Tubocurarine
d) Rapacuronium
a) Tubocurarine
b) Atracurium
c) Pancuronium
d) Succinylcholine
a) Vecuronium
b) Tubocurarine
c) Rapacuronium
d) Succinylcholine
a) Hypercaliemia
b) A decrease in intraocular pressure
c) Emesis
d) Muscle pain
a) Tubocurarine
b) Succinylcholine
c) Pancuronium
d) Gallamine
a) Pipecuronium
b) Succinylcholine
c) Atracurium
d) Rapacuronium
a) Aminoglycosides
b) Antiarrhythmic drugs
c) Nondepolarizing blockers
d) Local anesthetics
a) Myasthenia gravis
b) Burns
c) Asthma
d) Parkinsonism
a) Atropine
b) Neostigmine
c) Acetylcholine
d) Pralidoxime