Vancomycin Powder for Injection 250 mg

Hereโ€™s the detailed profile for Vancomycin Powder for Injection 250 mg ๐Ÿ‘‡


๐Ÿ’‰ Vancomycin Powder for Injection 250 mg


๐Ÿ“˜ Description:

  • Vancomycin is a glycopeptide antibiotic.
  • Given by intravenous infusion for systemic infections.
  • Mechanism: Inhibits bacterial cell wall synthesis by binding to D-Ala-D-Ala of peptidoglycan โ†’ bactericidal against susceptible Gram-positive organisms.
  • The 250 mg vial is reconstituted and diluted before administration.

๐Ÿ“„ Prescription / Indications:

Used in serious Gram-positive infections, especially when resistant to or unsuitable for ฮฒ-lactams:

  • Methicillin-resistant Staphylococcus aureus (MRSA) infections
  • Endocarditis (native/prosthetic valve)
  • Osteomyelitis, septic arthritis
  • Bacteremia & sepsis due to resistant Gram-positives
  • Lower respiratory tract infections (pneumonia)
  • Skin and soft tissue infections
  • Meningitis (with other agents)
  • Alternative in serious penicillin allergy cases

๐Ÿ‘‰ Not absorbed orally, so IV route is required for systemic infections.


๐ŸŒฟ Nature / Drug Class:

  • Glycopeptide antibiotic
  • Bactericidal (Gram-positive spectrum)

โœ… Advantages:

  • Highly effective against MRSA and resistant Gram-positives
  • Alternative for patients with severe ฮฒ-lactam allergy
  • Available in multiple vial strengths (250 mg, 500 mg, 1 g) for dosing flexibility

โš ๏ธ Precautions:

Contraindications:

  • Known hypersensitivity to vancomycin

Use with caution in:

  • Renal impairment โ†’ requires dose adjustment and monitoring
  • Concurrent nephrotoxic drugs (e.g., aminoglycosides, amphotericin B)
  • Ototoxicity risk with prolonged therapy or high serum levels

Adverse effects:

  • Infusion-related reactions: โ€œRed man syndromeโ€ (flushing, hypotension, rash if infused too fast)
  • Nephrotoxicity
  • Ototoxicity (rare but serious)
  • Phlebitis at infusion site

๐Ÿ’Š Dosage (Adults):

  • 15โ€“20 mg/kg IV every 8โ€“12 hours, adjusted by renal function and serum trough levels
  • Dose individualized using therapeutic drug monitoring (TDM)

๐Ÿ’‰ Administration:

  • Reconstitute 250 mg vial with sterile water โ†’ further dilute in 100โ€“250 mL of compatible IV fluid (e.g., 0.9% NaCl, 5% dextrose)
  • Infuse slowly over โ‰ฅ60 minutes (to avoid red man syndrome)

๐Ÿ“ฆ Common Packaging:

  • Vials: 250 mg, 500 mg, 1 g (powder for reconstitution)

โ„๏ธ Storage Conditions:

  • Store vials at room temperature (<25ยฐC), protected from light
  • After reconstitution: stable for 24 hours at room temp or 7 days refrigerated (2โ€“8ยฐC)

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