- Staphylococcal infections resistant to cloxacillin
- May be used as initial therapy in severely ill patients
- IV intermittent infusion: over 1 hour
0 - 14 days:
- < 28 weeks GA: 20 - 22 mg/kg/dose Q24h
- 29-34 weeks GA: 20 - 22 mg/kg/dose Q18h
- > 35 weeks GA: 20 - 22 mg/kg/dose Q12h
> 14 days:
- < 28 weeks corrected GA: 20 - 22 mg/kg/dose Q18h
- 29 - 34 weeks corrected GA: 20 - 22 mg/kg/dose Q12h
- > 35 weeks corrected GA: 20 - 22 mg/kg/dose Q8-12h
Infant (corrected GA > 42 weeks and PNA > 4 weeks):
- 15 mg/kg/dose Q6h
Dosage adjustment required in renal impairment. Refer to available references or clinical pharmacist for dosage adjustment
- Dermatologic: red man syndrome (associated with rapid infusion rate)
- Hematologic: eosinophilia, neutropenia
- Local: phlebitis
- Otic: ototoxicity associated with high drug levels
- Renal: nephrotoxicity (enhanced by aminoglycoside therapy)
- Baseline serum creatinine and Pre level. Repeat both once weekly. Pre (Trough) levels > 15 mg/L should be monitored a minimum of twice weekly
- WBC
- Infusion site
- Therapeutic drug levels:
- Serum Levels: Pre level only, 0 - 30 minutes before dose
- Initial level:
- Prior to 2nd or 3rd dose if:
- dosing intervals of Q12H or less frequent
- renal impairment
- Prior to 5th dose
- Prior to 2nd or 3rd dose if:
** When checking trough level, administer next dose as scheduled. Do not wait for level to be reported unless otherwise advised
- Pre (Trough) levels:
- 6 - 10 mg/L
- Infections (e.g. bacteremia) with coagulase negative staphylococci (i.e. S. epidermidis) including line infections
- 10 - 15 mg/L
- CNS infections, shunt infections or other deep-seated infections. Skin and soft tissue infections caused by methicillin resistant Staphylococcus aureus (MRSA)
- 15 - 20 mg/L
- These levels can be considered in individual patients with invasive or persistent methicillin resistant Staphylococcus aureus (MRSA) infections such as infective endocarditis, osteomyelitis, meningitis, pneumonia or severe soft tissue infections.
- 6 - 10 mg/L
- Post (Peak) levels: Not routine
IV intermittent infusion:
- Vancomycin 1000 mg vial
- Add 20 mL SWFI. Take 5 mL (250 mg) and add to 45 mL D5W
- Final concentration: 5 mg/mL
- Vancomycin 500 mg vial
- Add 10 mL SWFI. Take 5 mL (250 mg) and add to 45 mL D5W
- Final concentration: 5 mg/mL
- Solutions Compatible: dextrose, saline, dextrose-saline combinations
- Y-site Compatible: calcium, fentanyl, heparin (in low concentrations of 0.5 to 1 unit/mL used to maintain IV line potency), midazolam, morphine, pancuronium, SMOF, TPN
Incompatible: dexamethasone, heparin (concentrations greater than 1 unit/mL), phenobarbital
- Liu C, Bayer A, Cosgrove SE, Daum RS, Fridkin SK, Gorwitz RJ, Chambers HF. Clinical Practice Guidelines by the Infectious Diseases Society of America for the Treatment of Methicillin-Resistant Staphylococcus Aureus Infections in Adults and Children: Executive Summary. Clin Infect Dis. Feb 1 2011: 52 (3): 285-292
- Taketomo CK, Hodding JH, Kraus DM. Pediatric & Neonatal Dosage Handbook 22nd Edition. Hudson: Lexi-Comp Inc.; 2015.
- Trissel LA. Handbook on Injectable Drugs 19th Edition. Bethesda, Maryland; American Society of Health-System Pharmacists. 2017
- Rajon K, Vaillancourt R, Varughese N, Villarreal G. Vancomycin use, dosing and serum trough concentrations in the pediatric population: a retrospective institutional review. Pharmacy Practice 2017 Apr-Jun;15(2):887