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Review of Pharmacology - 9E (2015)

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

• No beta lactam antibiotic is effective against MRSA.<br />

• In high concentration, imipenem-cilastatin combination can result in seizures.<br />

Chemotherapy A: General Considerations and Non-specific...<br />

50. Ans. (c) They have acquired penicillin binding protein which has low affinity for β -lactam antibiotic <br />

(Ref: KDT 6/e p700)<br />

• Resistance to most penicillins is due to elaboration <strong>of</strong> beta-lactamase.<br />

• Methicillin is most resistant penicillin to β-lactamase.<br />

• Staphylococcus aureus develops resistance to methicillins by acquisition <strong>of</strong> altered penicillin binding proteins.<br />

51. Ans. (a) Benzathine penicillin (Ref: KDT 6/e p697)<br />

52. Ans. (a) Methicillin resistant Staph aureus (Ref: KDT 6/e p702, 703)<br />

• Staphylococcus aureus develops resistance to methicillin by acquiring altered penicillin binding proteins that have low<br />

affinity. No β-lactam antibiotic is effective against MRSA.<br />

• Clavulanic acid is an inhibitor <strong>of</strong> β-lactamase. It can restore the sensitivity <strong>of</strong> penicillins against the organisms who<br />

have developed penicillinases.<br />

53. Ans. (b) It acts by inhibiting bacterial protein synthesis (Ref: KDT 6/e p732)<br />

• Vancomycin is a glycopeptide that acts by inhibiting bacterial cell wall synthesis. It is a bactericidal drug (like other<br />

cell wall synthesis inhibitors).<br />

• It is the drug <strong>of</strong> choice for MRSA and enterococci resistant to penicillins.<br />

• Nephrotoxicity, ototoxicity and red man syndrome are prominent adverse effects <strong>of</strong> vancomycin.<br />

54. Ans. (c) It is not susceptible to penicillinases (Ref: KDT 6/e p732)<br />

• Vancomycin is a glycopeptide bactericidal antibiotic that is administered by parenteral route.<br />

• It is penicillinase resistant, thus can be used in MRSA infections.<br />

• It is also used for the treatment <strong>of</strong> pseudomembranous colitis.<br />

• Vancomycin is ineffective against pseudomonas.<br />

55. Ans. (c) Piperacillin (Ref: KDT 6/e p702)<br />

• Piperacillin can be combined with beta-lactamase inhibitor, tazobactam.<br />

• Vancomycin is NOT effective against pseudomonas.<br />

• All β-lactams except aztreonam are contra-indicated if severe allergic reaction develops to any β-lactam antibiotic.<br />

56. Ans. (b) Aztreonam (Ref: KDT 6/e p708)<br />

In patient with severe sensitivity to penicillin, all beta lactams except monobactams are contraindicated. Both aztreonam<br />

and imipenem are effective for gram negative infections but because imipenem causes seizures as serious adverse effect,<br />

aztreonam is preferred in such a patient.<br />

57. Ans. (d) Given twice daily orally (Ref: KDT 6/e p707)<br />

• Cefepime is a a 4th generation cephalosporin.<br />

• Due to high potency and extended spectrum, it is effective in many serious infections like hospital acquired<br />

pneumonia, febrile neutropenia, bacteremia, septicemia etc.<br />

• All β-lactam antibiotics act by inhibiting the enzyme transpeptidase.<br />

• Cefepime is given by i.v. route as it is not effctive orally.<br />

58. Ans. (a) Cephalexin (Ref: KDT 6/e p704-705; Goodman & Gilman 10/e p1209)<br />

Cephalexin is an orally effective first generation cephalosporin active against gram positive but not against gram negative<br />

organisms like pseudomonas.<br />

59. Ans. (a) Imipenem (Ref: KDT 6/e p708)<br />

60. Ans. (c) Ceftazidime (Ref: KDT 6/e p706)<br />

61. Ans. (b) Benzathine penicillin is short acting penicillin (Ref: KDT 6/e p697, 699, 700)<br />

Benzathine penicillin is the longest acting penicillin.<br />

62. Ans. (a) Inhibition <strong>of</strong> cell wall synthesis (Ref: KDT 6/e p668)<br />

63. Ans. (a) Effective in pseudomonas infection (Ref: KDT 6/e p702)<br />

• Carbenicillin is a penicillin congener effective against pseudomonas and indole positive proteus which are not<br />

inhibited by penicillin G or ampicillin/amoxicillin.<br />

• It is inactive orally and excreted rapidly in urine. It is sensitive to penicillinase and acid, so administered parenterally<br />

as sodium salt.<br />

562<br />

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