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Review of Pharmacology - 9E (2015)

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<strong>Review</strong> <strong>of</strong> <strong>Pharmacology</strong><br />

82. Ans. (b) Physostigmine (Ref: KDT 6/e p113, 114)<br />

Being tertiary amine, physostigmine can reverse CNS manifestations <strong>of</strong> belladona (source <strong>of</strong> atropine) poisoning. It is<br />

therefore, preferred as an antidote for this type <strong>of</strong> poisoning.<br />

83. Ans. (d) Hyperthermia (Ref: KDT 6/e p113)<br />

Atropa belladona contains anticholinergic principles like atropine and hyoscine. Atropine is contra-indicated in children due<br />

to the risk <strong>of</strong> hyperthermia.<br />

84. Ans. (c) Reversible antagonist at muscarinic receptors (Ref: KDT 6/e p109)<br />

85. Ans. (a) Hypertension (Ref: KDT 6/e p112, 113)<br />

86. Ans. (a) Eye (Ref: KDT 6/e p111)<br />

87. Ans. (b) Tropicamide (Ref: Katzung 11/e p124)<br />

Atropine is longest acting (5-6 days) whereas tropicamide is the shortest acting (15-60 min) mydriatic.<br />

88. Ans. (c) Muscarinic receptor inhibition (Ref: KDT 6/e p111)<br />

• Oxybutynin is a synthetic anticholinergic agent.<br />

89. Ans. (a) Increase bowel sound (Ref: KDT 6/e p107)<br />

• Atropine is an anticholinergic drug. It decreases bowel sounds.<br />

90. Ans. (c) Excessive salivation (Ref: KDT 6/e p113)<br />

Atropine is an anticholinergic drug. Its toxicity causes:<br />

Autonomic Nervous System<br />

• Dry mouth (and not excessive salivation)<br />

• Hot skin<br />

• Dilated pupil and photophobia<br />

• Excitement<br />

• Flushing <strong>of</strong> skin<br />

• Hypotension → cardiovascular collapse<br />

• Convulsions and coma<br />

91. Ans. (a) Hyoscine (Ref: KDT 6/e p113)<br />

Hyoscine is used for the prophylaxis<strong>of</strong> motion sickness whereas other drugs listed in the question are used for the treatment<br />

<strong>of</strong> vomiting.<br />

92. Ans. (d) Increased bowel sounds (Ref: KDT 6/e p107)<br />

Atropine is an anticholinergic drug. It will decrease GI motility. Atropine flushing is seen in overdose, the exact mechanism<br />

<strong>of</strong> which is not known.<br />

93. Ans. (a) Mydriasis is required without cycloplegia (Ref: KDT 6/e p127)<br />

94. Ans. (d) Physostigmine (Ref: KDT 6/e p104)<br />

95. Ans. (d) Tropicamide (Ref: KDT 6/e p111)<br />

96. Ans. (d) Pirenzepine (Ref: KDT 6/e p111)<br />

97. Ans. (d) Amphetamine (Ref: KDT 6/e p126)<br />

98. Ans. (d) Phenylepherine (Ref: KDT 6/e p130)<br />

99. Ans. (b) Inhibition <strong>of</strong> sweating (Ref: KDT 6/e p108)<br />

100. Ans. (a) Muscarinic (Ref: KDT 6/e p111)<br />

101. Ans. (d) Noradrenaline (Ref: KDT 7/e p130)<br />

• Dobutamine is selective beta 1 agonist, fenoldopam is selective D1 agonist whereas phenylephrine acts only on<br />

alpha1. NA can act on alpha1, alpha2 and beta1 receptors<br />

102. Ans. (c) Obstructive sleep apnea (Ref: www.fda.gov; KDT 6/e p470-471)<br />

• Modafinil is a sympathomimetic drug and is alpha and beta agonist in brain. The drug also acts upon several other<br />

receptors. It has brain activating properties and is the drug <strong>of</strong> choice for narcolepsy.<br />

• Modafinil can also be used for sleep disorders in shift workers.<br />

• Recently, FDA has approved modafinil as an adjunctive treatment for obstructive sleep apnea. Remember, continous<br />

positive airway pressure (cPAP) is the treatment <strong>of</strong> choice for this disorder. Modafinil is approved only as adjunctive<br />

treatment.<br />

100<br />

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