Vanomycin tablet

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Vancomycin is a glycopeptide antibiotic used primarily for serious Gram-positive infections. Importantly, it is not available as an oral tablet for systemic use - it is given IV for systemic infections. Oral vancomycin capsules/solution exist only for gut-limited infections (C. difficile colitis) because oral vancomycin is not absorbed systemically.
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vancomycin oral tablet formulation uses dosage

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Here is a comprehensive overview of Vancomycin (commonly misspelled "Vanomycin"):

Vancomycin - Complete Drug Profile

What It Is

Vancomycin is a glycopeptide antibiotic produced by Streptomyces orientalis. It inhibits early stages of cell wall peptidoglycan synthesis, making it bactericidal against most Gram-positive organisms.

Spectrum of Activity (Gram-positive organisms only)

  • Staphylococcus aureus including MRSA and coagulase-negative staphylococci
  • Streptococcus species including S. pneumoniae
  • Enterococcus species
  • Bacillus, Corynebacterium jeikeium
  • Gram-positive anaerobes: Peptostreptococcus, Actinomyces, Clostridium, Propionibacterium
  • NOT active against Gram-negative organisms
(Harrison's Principles of Internal Medicine 22E)

Formulations - KEY POINT

FormulationRoutePurpose
IV solutionIntravenousSystemic infections (MRSA sepsis, endocarditis, pneumonia, osteomyelitis)
Oral capsules / solutionOral (PO)C. difficile infection & S. aureus enterocolitis ONLY
There is no vancomycin "tablet." The oral form comes as capsules (Vancocin) or the IV powder dissolved in water/juice. Oral vancomycin is poorly absorbed from the gut - this is actually why it works for C. difficile: it stays in the colon at very high concentrations without causing systemic toxicity.

Clinical Uses

IV Vancomycin (systemic):
  • MRSA infections: bacteremia, endocarditis, pneumonia, osteomyelitis, skin/soft tissue infections
  • Alternative for MSSA when patient cannot tolerate beta-lactams
  • Empiric coverage in suspected Gram-positive sepsis
  • CNS shunt infections
Oral Vancomycin (gut-limited):
  • First-line treatment for Clostridioides difficile infection (CDI)
    • Standard dose: 125 mg every 6 hours x 10 days (as effective as 500 mg QID)
    • Severe/fulminant CDI: 500 mg QID
  • Staphylococcus aureus enterocolitis
(Sleisenger & Fordtran's GI and Liver Disease; Jawetz Medical Microbiology 28E)
Note: IV vancomycin does NOT work for CDI - effective colonic concentrations are not achieved parenterally.

Pharmacokinetics

  • Oral: Poorly/not absorbed systemically - stays in gut lumen (ideal for CDI)
  • IV: Widely distributed in tissues; excreted renally - requires dose adjustment in renal impairment
  • PK/PD target: AUC/MIC ratio >400 is the best predictor of efficacy (concentration-dependent killing)
  • Trough target for MRSA: 15-20 mcg/mL

Adverse Effects

EffectDetails
NephrotoxicityMost important; risk increases with trough >20 mcg/mL; worsened by aminoglycosides
Red Man Syndrome (Vancomycin Infusion Reaction)Histamine-mediated erythematous rash on face/neck/trunk from rapid infusion; treat with diphenhydramine + slow infusion
OtotoxicityRare with modern purified formulations; was more common historically
ThrombophlebitisAt IV site
LeukopeniaUncommon
(Harrison's 22E; Jawetz Medical Microbiology 28E)

Resistance Concerns

  • VISA (Vancomycin-Intermediate S. aureus): MIC 4-8 mcg/mL
  • VRSA (Vancomycin-Resistant S. aureus): via acquisition of vanA genes from VRE
  • VRE (Vancomycin-Resistant Enterococci): major problem; VanA type also resistant to teicoplanin; VanB type remains susceptible to teicoplanin
  • For enterococcal sepsis/endocarditis, vancomycin must be combined with an aminoglycoside

Monitoring

  • Renal function (serum creatinine) regularly
  • Vancomycin serum levels (trough or AUC monitoring)
  • Auditory function if prolonged use

Important Practical Note

The IV powder for injection can be dissolved in water and given orally for CDI at a much lower cost than branded Vancocin capsules - this is a commonly used cost-saving strategy in clinical practice. (Sleisenger & Fordtran)
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