MDS PREP
Which one of the following drugs increases gastrointestinal motility?
1) Glycopyrrolate.
2) Atropine.
3) Neostigmine.
4) Fentanyl.
Pharmacology Answer: 3
Synthetic opioids, sharing properties of opium and morphine, include meperidine, propoxyphene, diphenoxylate, fentanyl, buprenorphine, methadone, and pentazocine. Various opiate effects are analgesia, respiratory depression, constipation, and euphoria.
Fentanyl (80 to 100 times more powerful than morphine) is especially dangerous.
Atropine blocks the muscarinic receptors. Atropine decreases gastrointestinal tract motility and secretion and causes constipation.
Although various derivatives and congeners of atropine (such as propantheline, isopropamide, and glycopyrrolate) have been advocated in patients with peptic ulcer or with diarrheal syndromes
Neostigmine is Cholinesterase inhibitors that enhance the effects of parasympathetic stimulation and leads to reversal of intoxication by agents with a anticholinergic action
Which of the following statements is not true regarding sulfonamides:
1) Sulfasalazine is absorbed well from GIT
2) Crystalluria can occur with sulfonamide administration
3) Sulfonamide administration to Newborn may cause Kernicterus
4) Sulfonamides are of value in treatment of infections due to Norcardia species
Pharmacology Answer: 1
Sulfasalazine is absorbed well from GIT
Sulfasalazine is poorly absorbed (10-20%) from the GIT .
Syncope may be treated with any of the following drug except
1) Phenylephrine
2) Oxygen
3) Ephedrine
4) Isoproterenol
Pharmacology Answer: 4
Isoproterenol is used in the management of bronchospasm during anesthesia;
adjunctive treatment for shock.
Following drug interact with cefotaxime?
1) Digoxin
2) Paracetamol
3) Loop diuretics
4) Nifedipine
Pharmacology Answer: 3
Nephrotoxicity of cephalosporins is accentuated by concurrent administration of loop diuretics.
Which drug is most effective in reducing mortality in patients with left ventricular systolic dysfunction ?
1) Enalapril
2) Aspirin
3) Digoxin
4) Frusemide
Pharmacology Answer: 1
ACE inhibition has a beneficial impact on survival rates, functional status, and hemodynamics in patients with left ventricular systolic dysfunction.
In the renin-angiotensin system, a fall in perfusion pressure stimulates the juxtaglomerular cells in the kidney to release the enzyme renin.
Renin cleaves the decapeptide angiotensin I from angiotensinogen, a glycoprotein synthesized in the liver.
The octapeptide angiotensin II is formed by the action of ACE on angiotensin I.
Angiotensin II is a potent vasoconstrictor and stimulates the release of aldosterone and norepinephrine.
The main excitatory neuro transmitter in CNS is
1) Glycine
2) Acetyl choline
3) Aspartate
4) Glutamate
Pharmacology Answer: 2
The chemical compound acetylcholine (ACh) is a neurotransmitter in both the peripheral nervous system (PNS)and central nervous system (CNS) in many organisms including humans. Acetylcholine is one of many neurotransmitters in the autonomic nervous system (ANS) and the only neurotransmiter used in the somatic nervous system.
Dry mouth during antidepressant therapy is caused by blockade of:
1) Muscarinic acetylcholine receptors.
2) Serotonergic receptors.
3) Dopaminergic receptors.
4) GABA receptors.
Pharmacology Answer: 1
Anticholinergic side effect of antidepressant leads to dry mouth in the patients on these drugs.
Dry mouth is due to the Muscarinic acetylcholine receptor antagonism of these drugs.
Permanent auditory nerve deafness is frequently associated with use of
1. tetracycline
2. penicillin
3. bacitracin
4. streptomycin
Pharmacology
Answer: 4
Permanent auditory nerve deafness is frequently associated with use of streptomycin