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Vancomycin Therapy

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‫‪Vancomycin‬‬

‫اعداد الصيدالني‬
‫عقيل يونس‬
Introduction
• Antibacterial , tricyclic glycopeptide antibiotic.
• Used to treat gram-positive infection caused by :
1. Bactericidal :
• Methicillin-resistant S. aureus (MRSA), multidrug-resistant 
S. epidermidis (MRSE) & C. Difficile .
• Individuals with serious allergy to penicillins or to beta-
lactam antimicrobials .

2. Bacteriostatic :
• Enterococci
Mechanism of action
• Vancomycin acts by inhibiting cell wall biosynthesis of
bacteria.
• blocks glycopeptide polymerization by binding tightly to D-
alanyl-D-alanine portion of cell wall precursor
• Prevents cross -linking of the peptidoglycan layer .
Dosage Forms
• Capsule (Vancocin) :
125mg & 250mg

• Injection, lyophilized powder for reconstitution :


500mg, 750mg, 1g, 5g & 10g
Dosage Forms
• Kit, powder for oral solution (Firvanq) :
3.75g, 7.5g, 10.5g & 15g

• Injection, single-dose flexible bag :


500mg/100ml, 750mg/150ml, 1g/200ml,
1.25g/250ml, 1.5g/300ml, 1.75g/350ml &
2g/400ml
Pharmacokinetic data
• Bioavailability : (Oral) Negligible
(IV) Peak serum time immediately after completion
of infusion
• Protein bound : ~50%
• VD : 0.3-0.43 L/kg (IV)
• Metabolism : Excreted unchanged
• Half-life : (IV) 4-6 hr (normal renal function); 7.5 days (anephric
patients)
• Excretion : Urine
Indications
• Staphylococcal Enterocolitis
• Clostridium difficile-associated Diarrhea
• Infective Endocarditis
• Septicemia
• Skin and skin structure infections
• Bone Infections
• Lower Respiratory Tract Infections
• Preoperative Antimicrobial Prophylaxis (Off-label)
• Surgical Prophylaxis (Off-label)
Administration
• Solutions :
D5W/0.9% NaCl, D5W, D10W, LR & 0.9% NaCl,

• IV Preparation :
Add 10 mL of SWI to 500-mg vial and 20 mL of SWI to 1-g vial to yield
50 mg/mL solution; further dilution is required, depending on
method of administration .

• Intermittent infusion:
Dilute 500 mg with ≥100 mL of diluent and 1 g with ≥200 mL of
diluent (NS or D5W) Over 60 min .
Dose
• Adult :
• Loading dose : 20 to 35 mg/kg (based on actual body weight, rounded to
the nearest 250 mg increment; not to exceed 3000 mg)
• Initial maintenance dose and interval : Typically 15 to 20 mg/kg
every 8 to 12 hours
• Pediatric :
• Initial dose : Typically 15 mg/kg per dose IV every 6 to 8 hours
(every-6-hour interval for serious infections) &maximum daily
dose: 4 g/day .
• Renal impairment :
• Mild-to-severe: Initial dose should be no less than 15 mg/kg
• Functionally anephric patients: Initial dose of 15 mg/kg of body
weight to achieve prompt therapeutic serum concentration; start
at 1.9 mg/kg/24 hr after the initial dose of 15 mg/kg
Adverse Effects (IV)
• Hypersensitivity reactions (eg, anaphylaxis, “red man syndrome”) .
• Severe dermatologic reactions such as toxic epidermal necrolysis (TEN), Stevens-
Johnson syndrome (SJS) .
• Acute kidney injury and interstitial nephritis
• Tinnitus, hearing loss, vertigo
• Agranulocytosis, neutropenia, pancytopenia, leukopenia, thrombocytopenia,
eosinophilia .
• Pseudomembranous colitis
• Cardiac arrest, chest pain
• General discomfort, fever, chills & phlebitis .
• Muscle pain
• Dizziness
• Wheezing, dyspnea
• Hypotension, shock, vasculitis
Drug interactions
• Contraindicated :
BCG vaccine live
Typhoid vaccine live
• Serious – Use alternative :
Bacitracin
Cholera vaccine
• Monitor Closely :
Amikacin
Amphotericin B deoxycholate
Conjugated estrogens
Cyclosporine
Deferasirox
Digoxin
Methotrexate
Piperacillin
Warnings
• Contraindicated during pregnancy because lead to ototoxic &
nephrotoxic on infants .
• Contraindicated to Hypersensitivity Patients.
• Rapid IV administration may result in flushing, pruritus, hypotension,
erythema, and urticaria .
• Risk of AKI increases as systemic exposure increases; additional risk
factors for AKI include concomitant use of nephrotoxic drugs, patients
with pre-existing renal impairment, or with comorbidities that
predispose to renal impairment So should Use caution in patients
with renal impairment .
• Prolonged use may result in fungal or bacterial superinfection .

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