Cefazolin (Ancef) Flashcards

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Questions and Answers

What is the drug class of Cefazolin?

  • First generation cephalosporin (correct)
  • Macrolide
  • Second generation cephalosporin
  • Penicillin

What is the pregnancy category of Cefazolin?

B

What are therapeutic uses of Cefazolin?

To treat bone and joint infections, genital infections, and endocarditis; also used for respiratory, urinary, and skin infections.

What is the mode of action of Cefazolin?

<p>Inhibition of cell wall synthesis, causing cell death; bactericidal effect.</p> Signup and view all the answers

Which of the following are potential side effects of Cefazolin? (Select all that apply)

<p>Abdominal cramps (A), Nausea (C), Rash (D)</p> Signup and view all the answers

What are some adverse reactions associated with Cefazolin?

<p>Superinfections, urticarial, seizures (high doses), and anaphylaxis.</p> Signup and view all the answers

What are the contraindications for using Cefazolin?

<p>Hypersensitivity to cephalosporins; caution with hypersensitivity to penicillins, renal disease, and during lactation.</p> Signup and view all the answers

What are some drug interactions with Cefazolin?

<p>Increase effect with probenecid; increase toxicity with loop diuretics, aminoglycosides, colistin, vancomycin; decrease effect with tetracyclines and erythromycin.</p> Signup and view all the answers

What lab interactions may occur with Cefazolin?

<p>May increase BUN, serum creatinine, AST, ALT, ALP, LDH, bilirubin.</p> Signup and view all the answers

What are the pharmacokinetics of Cefazolin?

<p>Absorption: IM, IV; Distribution: PB: 85%; Metabolism: 1.5-2.5 hrs; Excretion: 70% excreted unchanged in urine.</p> Signup and view all the answers

What are the pharmacodynamics characteristics for IM and IV administration of Cefazolin?

<p>IM: Onset: rapid; Peak: 0.5-2hr; IV: Onset: immediate; Peak: 5-15min.</p> Signup and view all the answers

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Study Notes

Drug Class

  • Classified as a first generation cephalosporin antibiotic.

Pregnancy Category

  • Assigned category B, indicating no known risks to human fetus based on available studies.

Therapeutic Uses

  • Treats bone and joint infections, genital infections, and endocarditis.
  • Effective against respiratory, urinary, and skin infections when combined with cefaclor.

Mode of Action

  • Functions by inhibiting cell wall synthesis, which leads to bacterial cell death.
  • Demonstrates a bactericidal effect.

Side Effects

  • Common side effects include abdominal cramps and fever.
  • Other effects with cefazolin and cefaclor may include anorexia, nausea, vomiting, diarrhea, and rash.

Adverse Reactions

  • Potential for superinfections and urticarial reactions with cefazolin and cefaclor.
  • Life-threatening adverse effects of cefazolin can include seizures (especially at high doses) and anaphylaxis.

Contraindications

  • Should not be used in patients with hypersensitivity to cephalosporins.
  • Caution is advised for those with a history of hypersensitivity to penicillins, renal disease, or during lactation.

Drug Interactions

  • Probenecid can enhance the effects of cefazolin and cefaclor.
  • May increase toxicity when used with loop diuretics, aminoglycosides, colistin, or vancomycin.
  • Effectiveness can be decreased when used with tetracyclines or erythromycin.

Lab Interactions

  • May result in increased levels of BUN, serum creatinine, AST, ALT, ALP, LDH, and bilirubin.

Pharmacokinetics

  • Administered via intramuscular (IM) or intravenous (IV) routes.
  • Plasma binding at approximately 85%.
  • Exhibits a metabolism time of 1.5 to 2.5 hours.
  • Around 70% is excreted unchanged in urine.

Pharmacodynamics

  • For IM administration: rapid onset, peak effects within 0.5 to 2 hours, duration unclear.
  • For IV administration: immediate onset, peak effects within 5 to 15 minutes, duration unclear.

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