ID Exam Practice 1

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Last updated 7:27 AM on 9/20/26
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52 Terms

1
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Which of the following correctly describes the bacterial cell wall structural difference between Gram-positive and Gram-negative organisms? A. Both Gram-positive and Gram-negative bacteria possess identical double-layered cell walls. B. Gram-positive bacteria have a double-layer membrane, while Gram-negative bacteria have a thick peptidoglycan wall. C. Gram-positive bacteria have a very thick cell membrane, while Gram-negative bacteria have a double-layer membrane. D. Gram-positive bacteria lack a cell wall, while Gram-negative bacteria have a thick cell wall.

C. Gram-positive bacteria have a very thick cell membrane, while Gram-negative bacteria have a double-layer membrane.

2
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Salt formation in penicillin structures occurs specifically at which functional group? A. The acyl side chain B. The thiazolidine sulfur C. The beta-lactam carbonyl D. The -COOH group

D. The -COOH group

3
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Beta-lactam hypersensitivity reactions are primarily caused by: A. Direct activation of IgE antibodies by intact beta-lactams B. Direct cytotoxicity to renal tubule cells C. Hapten formation between the host and beta-lactam breakdown products D. Chelation of beta-lactam structures with plasma proteins

C. Hapten formation between the host and beta-lactam breakdown products

4
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In which of the following clinical scenarios should penicillin skin testing be strictly avoided? (Select ALL that apply) A. History of mild maculopapular rash B. Toxic Epidermal Necrolysis (TEN) C. Stevens-Johnson Syndrome (SJS) D. Mild childhood urticaria

B, C โ€” Toxic Epidermal Necrolysis (TEN) and Stevens-Johnson Syndrome (SJS)

5
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Match the Penicillin R1 group modification to its primary effect. (Select ALL that apply) A. Ionizable groups โ†’ Improve dual Gram-positive/Gram-negative activity B. Lipophilic aromatic groups โ†’ Complete loss of Gram-positive activity C. Electron Withdrawing Groups (EWG) โ†’ Improve oral absorption/stability D. Ureido groups โ†’ Expand spectrum to broad-spectrum coverage

A, C, D โ€” Ionizable groups improve dual Gram-positive/Gram-negative activity; Electron Withdrawing Groups improve oral absorption/stability; Ureido groups expand spectrum to broad-spectrum coverage

6
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Adding steric hindering bulk to a penicillin structure provides stability in the acidic environment of the stomach primarily by: A. Blocking beta-lactamases B. Increasing renal clearance C. Enhancing active transport across the gut wall D. Preventing hepatic Phase I oxidation

A. Blocking beta-lactamases

7
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Strongly lipophilic antibacterial compounds are likely to possess which additional mechanism of action (MOA)? A. Blockade of folic acid synthesis B. Direct inhibition of DNA gyrase C. Inhibition of 50S ribosomal subunit D. Disruption of the cell membrane

D. Disruption of the cell membrane

8
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Compared to Penicillins, Cephalosporins exhibit: A. Higher ring strain and greater reactivity toward PBPs B. Reduced ring strain and less reactivity toward PBPs C. Equal reactivity toward PBPs with higher beta-lactamase susceptibility D. Complete loss of affinity for penicillin-binding proteins

B. Reduced ring strain and less reactivity toward PBPs

9
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Which structural element unique to cephalosporins contributes to specific unique adverse effects? A. The thiazolidine ring B. The R1 electron-withdrawing group C. The C3 "X" leaving group D. The beta-lactam carbonyl oxygen

C. The C3 "X" leaving group

10
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Which structural features are true regarding glycopeptides? (Select ALL that apply) A. Bottom part (R1 group) increases drug solubility B. Top part (R7 group) contains lipophilic groups C. Top part (R7 group) increases water solubility D. Bottom part (R1 group) is responsible for cell membrane insertion

A, B โ€” Bottom (R1) increases drug solubility; Top (R7) contains lipophilic groups

11
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Which option correctly pairs the metabolic reaction with its respective phase? A. Conjugation โ†’ Phase 1; Oxidation โ†’ Phase 2 B. Hydrolysis โ†’ Phase 2; Reduction โ†’ Phase 2 C. Conjugation โ†’ Phase 1; Reduction โ†’ Phase 1 D. Oxidation โ†’ Phase 1; Conjugation โ†’ Phase 2

D. Oxidation โ†’ Phase 1; Conjugation โ†’ Phase 2

12
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The enzyme dihydropteroate synthase (DHPS) catalyzes the conversion of which precursors? A. Dihydrofolic acid + Glutamate B. Tetrahydrofolate + Trimethoprim C. Pteridine + PABA D. Sulfamethoxazole + NADPH

C. Pteridine + PABA

13
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Which of the following adverse effects are specifically associated with Sulfamethoxazole (SMX)? (Select ALL that apply) A. Allergic reactions B. Crystalluria and nephrotoxicity C. Risk of kernicterus in neonates D. Hemolytic anemia in patients with G6PD deficiency

A, B, C, D โ€” All listed are valid Sulfamethoxazole adverse effects

14
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Clinical indications for the combination of Sulfamethoxazole/Trimethoprim (SMX/TMP) include which of the following? (Select ALL that apply) A. Urinary Tract Infections (UTIs) B. Skin and Soft Tissue Infections (SSTI) C. Pneumocystis jirovecii pneumonia (PJP) D. Toxoplasmosis

A, B, C, D โ€” UTIs, SSTI, PJP, and Toxoplasmosis

15
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What is the primary target and timing of action for DNA gyrase during bacterial DNA replication? A. Acts after replication; primary target in Gram-positive bacteria B. Acts during replication; primary target in Gram-negative bacteria C. Acts during replication; primary target in Gram-positive bacteria D. Acts after replication; primary target in Gram-negative bacteria

B. Acts during replication; primary target in Gram-negative bacteria

16
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What is the primary target and timing of action for Topoisomerase IV during bacterial DNA replication? A. Acts during replication; primary target in Gram-negative bacteria B. Acts during replication; primary target in Gram-positive bacteria C. Acts after replication; primary target in Gram-negative bacteria D. Acts after replication; primary target in Gram-positive bacteria

D. Acts after replication; primary target in Gram-positive bacteria

17
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First-generation quinolones are characterized by which features? (Select ALL that apply) A. Broad Gram-positive and anaerobic coverage B. Narrow spectrum (primarily Gram-negative urinary pathogens) C. Lack of a fluorine (F) substitution D. High oral bioavailability for systemic infections

B, C โ€” Narrow spectrum (primarily Gram-negative urinary pathogens) and lack of a fluorine substitution

18
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Which of the following fluoroquinolones belong to the 2nd Generation class? (Select ALL that apply) A. Gemifloxacin B. Norfloxacin C. Ofloxacin D. Ciprofloxacin

B, C, D โ€” Norfloxacin, Ofloxacin, and Ciprofloxacin

19
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Which fluoroquinolone exhibits the best activity against Pseudomonas aeruginosa? A. Moxifloxacin B. Gemifloxacin C. Ciprofloxacin D. Levofloxacin

C. Ciprofloxacin

20
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Which of the following fluoroquinolones are classified as 3rd Generation? (Select ALL that apply) A. Moxifloxacin B. Levofloxacin C. Gemifloxacin D. Ciprofloxacin

B, C โ€” Levofloxacin and Gemifloxacin

21
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Which fluoroquinolones belong to the 4th Generation class? (Select ALL that apply) A. Moxifloxacin B. Gatifloxacin C. Ofloxacin D. Norfloxacin

A, B โ€” Moxifloxacin and Gatifloxacin

22
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Fourth-generation quinolones uniquely contain a methoxy group at the R8 position to achieve which clinical effect? A. Eliminate renal clearance B. Prevent hepatic metabolism C. Enhance chelation with multivalent cations D. Increase Gram-positive and anaerobic activity

D. Increase Gram-positive and anaerobic activity

23
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Which fluoroquinolone does NOT reliably cover Pseudomonas aeruginosa? A. Levofloxacin B. Ofloxacin C. Moxifloxacin D. Ciprofloxacin

C. Moxifloxacin

24
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Which of the following are specific mechanisms of resistance developed against Fluoroquinolones (FQs)? (Select ALL that apply) A. Target mutations in DNA gyrase/topoisomerase B. Increased active efflux pumps C. Reduced entry via loss of porins D. Enzymatic inactivation via acetylation

A, B, C โ€” Target mutations, increased efflux pumps, and loss of porins

25
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What is the primary elimination route for macrolide antibiotics? A. Hepatic elimination B. Unchanged renal excretion C. Active tubular secretion in nephrons D. Pulmonary exhalation

A. Hepatic elimination

26
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Macrolide antibiotics are most frequently used to treat infections caused by: A. Enteric Gram-negative bacilli B. Urinary tract pathogens C. Respiratory tract pathogens D. Anaerobic intra-abdominal pathogens

C. Respiratory tract pathogens

27
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Which macrolide is most strongly associated with gastrointestinal side effects and QTc prolongation compared to others in its class? A. Azithromycin B. Clarithromycin C. Telithromycin D. Erythromycin

D. Erythromycin

28
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Salt formation (soluble or insoluble) of Erythromycin occurs at which structural location? A. The C11 hydroxyl group B. The tertiary amine on the C5 sugar C. The C9 keto group D. The macrolactone ring ester

B. The tertiary amine on the C5 sugar

29
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Telithromycin, a ketolide derivative, structurally differs from classic macrolides by specifically lacking which group? A. The macrolactone ring B. The keto substitution at C3 C. The bottom sugar D. The alkyl-aryl extension chain

C. The bottom sugar

30
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Which adverse effects are classically associated with Tetracycline therapy? (Select ALL that apply) A. Tooth discoloration B. Red man syndrome C. Photosensitivity D. Peripheral neuropathy

A, C โ€” Tooth discoloration and photosensitivity

31
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To prevent impaired absorption caused by chelation, ingested metals/cations must be separated from which antibiotic class? A. Aminoglycosides B. Oxazolidinones C. Glycopeptides D. Tetracyclines

D. Tetracyclines

32
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Tetracyclines are described as amphoteric because they contain: A. Both acidic and basic functional groups B. Two strong basic groups C. Neutral aromatic ring structures only D. Highly lipophilic aliphatic chains

A. Both acidic and basic functional groups

33
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What structural feature allows Tigecycline to overcome efflux pump-mediated resistance? A. A C8 methoxy group B. A fluorine substitution C. A tert-butyl (t-butyl) group D. A lactone ring expansion

C. A tert-butyl (t-butyl) group

34
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Which lincosamide antibiotic carries a significantly higher rate of causing GI issues and Clostridioides difficile colitis? A. Lincomycin B. Vancomycin C. Telithromycin D. Clindamycin

D. Clindamycin

35
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Linezolid and Tedizolid belong to which antimicrobial class? A. Oxazolidinones B. Streptogramins C. Lincosamides D. Glycylcyclines

A. Oxazolidinones

36
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When comparing Tedizolid to Linezolid, Tedizolid is: A. Less potent than Linezolid B. More potent than Linezolid C. Equivalent in potency but less bioavailable D. Exclusively administered via inhalation

B. More potent than Linezolid

37
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What is the approximate oral bioavailability of oxazolidinones? A. 25% B. 50% C. 100% D. 75%

C. 100%

38
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Which of the following adverse effects are associated with Oxazolidinone use? (Select ALL that apply) A. Optic neuropathy B. Peripheral neuropathy C. Hematologic toxicity (e.g., myelosuppression) D. Nephrotoxicity

A, B, C โ€” Optic neuropathy, peripheral neuropathy, and hematologic toxicity

39
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Co-administration of Oxazolidinones with SSRIs, SNRIs, or MAOIs increases the risk of which life-threatening drug-drug interaction? A. QT prolongation and Torsades de Pointes B. Severe rhabdomyolysis C. Serotonin Syndrome D. Acute Stevens-Johnson Syndrome

C. Serotonin Syndrome

40
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Aminoglycosides are routinely administered intravenously (IV) because they: A. Undergo rapid first-pass hepatic degradation B. Cause immediate severe gastric ulceration C. Are inactivated by stomach acid D. Exhibit poor oral absorption

D. Exhibit poor oral absorption

41
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What is the primary clinical indication for using oral aminoglycosides? A. Systemic bacteremia B. Local GI infections C. Pyelonephritis D. Bacterial meningitis

B. Local GI infections

42
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Which of the following represent specific enzymatic resistance mechanisms against aminoglycosides? (Select ALL that apply) A. Acetylation B. Adenylation C. Phosphorylation D. Oxidation

A, B, C โ€” Acetylation, adenylation, and phosphorylation

43
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Cephalosporins are intrinsically inactive against which of the following organisms? (Select ALL that apply) A. Escherichia coli B. Enterococcus species C. Listeria monocytogenes D. Klebsiella pneumoniae

B, C โ€” Enterococcus species and Listeria monocytogenes

44
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Monobactams (Aztreonam) are specifically indicated for patients with: A. Severe renal failure B. True penicillin allergy C. Resistant C. difficile infection D. G6PD deficiency

B. True penicillin allergy

45
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Carbapenems exhibit a severe drug-drug interaction leading to loss of seizure control when co-administered with: A. Warfarin B. Methotrexate C. Valproic acid D. Phenytoin

C. Valproic acid

46
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Which adverse effect profile is specifically associated with cephalosporins featuring an NMTT side chain? A. Ototoxicity and vestibular toxicity B. Tendon rupture and tendinitis C. Bleeding and prothrombin deficiency D. Pulmonary fibrosis

C. Bleeding and prothrombin deficiency

47
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Which glycopeptide antibiotic is administered orally solely for the treatment of Clostridioides difficile? A. Telavancin B. Vancomycin C. Dalbavancin D. Oritavancin

B. Vancomycin

48
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When should a serum trough level for a glycopeptide (e.g., Vancomycin) be drawn? A. 30 minutes before the 4th dose B. Immediately after finishing the 1st dose C. 2 hours after the 2nd dose D. 12 hours after the final dose

A. 30 minutes before the 4th dose

49
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When should a serum peak level for a glycopeptide be recorded? A. 30 minutes before the next infusion B. Immediately upon starting the infusion C. 1 hour after finishing the infusion D. 6 hours post-infusion

C. 1 hour after finishing the infusion

50
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Red man syndrome is an infusion-related reaction primarily caused by which antibiotic? A. Daptomycin B. Linezolid C. Aztreonam D. Vancomycin

D. Vancomycin

51
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Which long-acting lipoglycopeptides provide up to 2 weeks of MRSA coverage with a single-infusion regimen? (Select ALL that apply) A. Dalbavancin B. Oritavancin C. Vancomycin D. Telavancin

A, B โ€” Dalbavancin and Oritavancin

52
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Lipopeptides (such as Daptomycin) are clinically ineffective for treating which type of infection? A. Complicated skin infections B. Pneumonia C. Right-sided endocarditis D. Bacteremia

B. Pneumonia