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Home > Drugs > Glycopeptide antibiotics > Vancomycin > Vancomycin Dosage
Glycopeptide antibiotics
https://themeditary.com/dosage-information/vancomycin-dosage-7184.html

Vancomycin Dosage

Drug Detail:Vancomycin (Vancomycin (oral) [ van-koe-mye-sin ])

Drug Class: Glycopeptide antibiotics

Contents
Uses Warnings Before Taking Dosage Side effects Interactions FAQ

Usual Adult Dose for Bacterial Infection

500 mg IV every 6 hours OR 1 g IV every 12 hours

Comments:

  • This drug should be administered at a rate up to 10 mg/min or over 1 hour, whichever is longer.
  • Doses should be determined by patient-specific factors (e.g., obesity, age).

Use: Empirical treatment of serious/severe staphylococcal infections caused by susceptible strains of methicillin-resistant staphylococci in patients who are allergic to penicillin, failed to respond/cannot receive other drugs (e.g., penicillins, cephalosporins), and/or to treat organisms that are resistant to other drugs

Infectious Diseases Society of America (IDSA) Recommendations:
15 mg/kg IV every 12 hours

Comments:
  • Treatment plus an aminoglycoside should be used for ampicillin-resistant, vancomycin-sensitive Enterococcus faecalis/Enterococcus faecium.

Uses:
  • Preferred treatment for IV catheter-related bloodstream infections caused by methicillin-resistant Staphylococcus aureus (MRSA)/coagulase-negative staphylococci, ampicillin-resistant, vancomycin-sensitive E faecalis/E faecium, Corynebacterium jeikeium (Group JK)
  • Alternative treatment for IV catheter-related bloodstream infections caused by methicillin-susceptible Staphylococcus aureus (MSSA)/coagulase-negative staphylococci, ampicillin-susceptible E faecalis/E faecium

American Society of Health-System Pharmacists (ASHP), IDSA, Surgical Infection Society (SIS), and Society for Infectious Diseases Pharmacists (SIDP) Recommendations:
Serious MRSA Infections:
Intermittent infusion: 15 to 20 mg/kg IV per day, given in divided doses every 6 to 8 hours

Critically Ill Patients:
Intermittent infusion:
  • Initial dose: 20 to 35 mg/kg IV ONCE
  • Maximum dose: 3000 mg/dose

Continuous infusion:
  • Loading dose: 15 to 20 mg/kg IV ONCE
  • Maintenance dose: 30 to 40 mg/kg via IV infusion
  • Maximum dose: 60 mg/kg/day

Comments:
  • Doses should be determined by patient-specific factors (e.g., obesity, age, serum creatinine).
  • The target steady-state continuous infusion concentration is 20 to 25 mg/L in patients who are critically ill.

Use: Treatment of patients with known/suspected serious MRSA infections

Usual Adult Dose for Endocarditis

500 mg IV every 6 hours OR 1 g IV every 12 hours

Comments:

  • This drug should be administered at a rate up to 10 mg/min or over 1 hour, whichever is longer.
  • Doses should be determined by patient-specific factors (e.g., obesity, age).
  • Successful treatment of diphtheroid endocarditis has been reported.

Uses:
  • Empirical treatment of staphylococcal endocarditis caused by susceptible strains of methicillin-resistant staphylococci in patients who are allergic to penicillin, failed to respond/cannot receive other drugs (e.g., penicillins, cephalosporins), and/or to treat organisms that are resistant to other drugs
  • Empirical treatment (with an aminoglycoside) of endocarditis caused by enterococci, Streptococcus bovis, or Streptococcus viridans
  • Empirical treatment (with an aminoglycoside and/or rifampin) of early-onset prosthetic valve endocarditis caused by Staphylococcus epidermidis or diphtheroids

American Heart Association (AHA) and IDSA Recommendations:
15 to 20 mg/kg per day IV every 8 to 12 hours
  • Maximum dose: 2 g/dose

Duration of treatment:
  • Native Valve Endocarditis: At least 4 weeks
  • Prosthetic Valve Endocarditis: At least 6 weeks

Comments:
  • Patients may not require the addition of gentamicin or rifampin.
  • Patients with native valve endocarditis caused by oxacillin-resistant staphylococci may require at least 6 weeks of treatment.

Uses:
  • Treatment of endocarditis caused by highly penicillin-susceptible and relatively resistant to penicillin viridians group streptococci (VGS) and Streptococcus gallolyticus (bovis) in patients who cannot tolerate penicillin or ceftriaxone
  • Treatment of endocarditis involving a prosthetic value/other prosthetic material caused by VGS and S gallolyticus (bovis)
  • Alternative treatment of endocarditis caused by oxacillin-resistant staphylococci in patients with immediate-type hypersensitivity to beta-lactam antibiotics
  • Treatment of penicillin-resistant endocarditis caused by enterococci in patients unable to tolerate beta-lactam antibiotics

Usual Adult Dose for Pseudomembranous Colitis

Clostridioides (Clostridium) difficile-associated diarrhea: 125 mg orally 4 times a day

  • Duration of therapy: 10 days

Enterocolitis: 500 mg to 2 g orally per day, given in divided doses 3 to 4 times a day
  • Maximum dose: 2 g/day
  • Duration of therapy: 7 to 10 days

Comment: Formulations administered parenterally will not treat colitis.

Uses:
  • Treatment of C difficile-associated diarrhea
  • Treatment of enterocolitis caused by S aureus (including MRSA)

Society of Healthcare Epidemiology of America (SHEA) and IDSA Recommendations:
Initial treatment of severe C difficile infection (CDI): 125 mg orally 4 times a day
  • Duration of therapy: 10 to 14 days

Severe, complicated CDI: 500 mg orally 4 times a day AND 500 mg (in 100 mL normal saline) rectally every 6 hours with/without IV metronidazole

Comments:
  • Rectal formulations should be administered as a retention enema.
  • The first recurrence of CDI may be treated with the initial treatment regimen; a second recurrence of CDI may be treated with a tapered/pulsed regimen of this drug.

Uses:
  • Initial treatment of patients with severe CDI
  • Initial treatment of patients with complicated, severe CDI

Usual Adult Dose for Enterocolitis

Clostridioides (Clostridium) difficile-associated diarrhea: 125 mg orally 4 times a day

  • Duration of therapy: 10 days

Enterocolitis: 500 mg to 2 g orally per day, given in divided doses 3 to 4 times a day
  • Maximum dose: 2 g/day
  • Duration of therapy: 7 to 10 days

Comment: Formulations administered parenterally will not treat colitis.

Uses:
  • Treatment of C difficile-associated diarrhea
  • Treatment of enterocolitis caused by S aureus (including MRSA)

Society of Healthcare Epidemiology of America (SHEA) and IDSA Recommendations:
Initial treatment of severe C difficile infection (CDI): 125 mg orally 4 times a day
  • Duration of therapy: 10 to 14 days

Severe, complicated CDI: 500 mg orally 4 times a day AND 500 mg (in 100 mL normal saline) rectally every 6 hours with/without IV metronidazole

Comments:
  • Rectal formulations should be administered as a retention enema.
  • The first recurrence of CDI may be treated with the initial treatment regimen; a second recurrence of CDI may be treated with a tapered/pulsed regimen of this drug.

Uses:
  • Initial treatment of patients with severe CDI
  • Initial treatment of patients with complicated, severe CDI

Usual Adult Dose for Pneumonia

500 mg IV every 6 hours OR 1 g IV every 12 hours

Comments:

  • This drug should be administered at a rate up to 10 mg/min or over 1 hour, whichever is longer.
  • Doses should be determined by patient-specific factors (e.g., obesity, age).

Use: Empirical treatment of lower respiratory tract infections caused by susceptible strains of methicillin-resistant staphylococci in patients who are allergic to penicillin, failed to respond/cannot receive other drugs (e.g., penicillins, cephalosporins), and/or to treat organisms that are resistant to other drugs

IDSA Recommendations:
15 mg/kg IV every 8 to 12 hours
  • Some experts recommend a loading dose of 25 to 30 mg/kg IV ONCE (severe illness)

Uses:
  • Empiric treatment of clinically suspected ventilator-associated pneumonia where MRSA coverage is appropriate
  • Add-on empiric treatment of hospital-acquired pneumonia in patients not at high risk of mortality but with MRSA risk factors
  • Add-on empiric treatment of hospital-acquired pneumonia in patients at high risk of mortality or with receipt of IV antibiotics within the previous 90 days

Usual Adult Dose for Nosocomial Pneumonia

500 mg IV every 6 hours OR 1 g IV every 12 hours

Comments:

  • This drug should be administered at a rate up to 10 mg/min or over 1 hour, whichever is longer.
  • Doses should be determined by patient-specific factors (e.g., obesity, age).

Use: Empirical treatment of lower respiratory tract infections caused by susceptible strains of methicillin-resistant staphylococci in patients who are allergic to penicillin, failed to respond/cannot receive other drugs (e.g., penicillins, cephalosporins), and/or to treat organisms that are resistant to other drugs

IDSA Recommendations:
15 mg/kg IV every 8 to 12 hours
  • Some experts recommend a loading dose of 25 to 30 mg/kg IV ONCE (severe illness)

Uses:
  • Empiric treatment of clinically suspected ventilator-associated pneumonia where MRSA coverage is appropriate
  • Add-on empiric treatment of hospital-acquired pneumonia in patients not at high risk of mortality but with MRSA risk factors
  • Add-on empiric treatment of hospital-acquired pneumonia in patients at high risk of mortality or with receipt of IV antibiotics within the previous 90 days

Usual Adult Dose for Osteomyelitis

500 mg IV every 6 hours OR 1 g IV every 12 hours

Comments:

  • This drug should be administered at a rate up to 10 mg/min or over 1 hour, whichever is longer.
  • Doses should be determined by patient-specific factors (e.g., obesity, age).

Use: Empirical treatment of bone infections caused by susceptible strains of methicillin-resistant staphylococci in patients who are allergic to penicillin, failed to respond/cannot receive other drugs (e.g., penicillins, cephalosporins), and/or to treat organisms that are resistant to other drugs

IDSA Recommendations:
15 to 20 mg/kg IV every 12 hours
  • Duration of therapy: 4 to 6 weeks

Uses:
  • First choice treatment for native vertebral osteomyelitis caused by oxacillin-resistant staphylococci, penicillin-resistant Enterococcus species
  • Alternative treatment for native vertebral osteomyelitis caused by oxacillin-susceptible staphylococci
  • Alternative treatment for native vertebral osteomyelitis caused by penicillin-susceptible Enterococcus species, Enterobacteriaceae, beta-hemolytic streptococci, or Propionibacterium acnes in patients allergic to penicillin

Usual Adult Dose for Sepsis

500 mg IV every 6 hours OR 1 g IV every 12 hours

Comments:

  • This drug should be administered at a rate up to 10 mg/min or over 1 hour, whichever is longer.
  • Doses should be determined by patient-specific factors (e.g., obesity, age).

Use: Empirical treatment of septicemia caused by susceptible strains of methicillin-resistant staphylococci in patients who are allergic to penicillin, failed to respond/cannot receive other drugs (e.g., penicillins, cephalosporins), and/or to treat organisms that are resistant to other drugs

Usual Adult Dose for Skin or Soft Tissue Infection

500 mg IV every 6 hours OR 1 g IV every 12 hours

Comments:

  • This drug should be administered at a rate up to 10 mg/min or over 1 hour, whichever is longer.
  • Doses should be determined by patient-specific factors (e.g., obesity, age).

Use: Empirical treatment of skin and skin structure infections caused by susceptible strains of methicillin-resistant staphylococci in patients who are allergic to penicillin, failed to respond/cannot receive other drugs (e.g., penicillins, cephalosporins), and/or to treat organisms that are resistant to other drugs

IDSA Recommendations:
15 mg/kg IV every 6 to 12 hours

Comment: Multidrug resistant organisms may require daily doses up to 60 mg/kg.

Uses:
  • First-line treatment of treatment of skin and soft tissue infections (SSTIs) caused by MRSA in patients who require parenteral treatment
  • Alternative treatment of SSTIs in patients with penicillin allergies
  • Treatment of incisional surgical site infections of the lower trunk or extremity away from the axilla/perineum
  • First-line treatment of necrotizing infections of the skin, fascia, and muscle caused by mixed infections

Usual Adult Dose for Bacteremia

IDSA Recommendations:
15 to 20 mg/kg IV every 8 to 12 hours

  • Duration of treatment: Up to 6 weeks, depending on the severity of infection

Use: Treatment of bacteremia

Usual Adult Dose for Meningitis

IDSA, American Academy of Neurology (AAN), American Association of Neurological Surgeons (AANS), and Neurocritical Care Society (NCS) Recommendations:
30 to 60 mg/kg IV per day, given in divided doses every 8 to 12 hours

  • Some experts recommend: 15 mg/kg IV once, followed by 60 mg/kg per day continuous infusion
  • Maximum dose: 2 g/dose
  • Duration of treatment: At least 2 weeks

Comment: Surgical evaluation is recommended for patients with septic thromboses, empyema, and/or abscesses.

Uses:
  • Treatment of patients with healthcare-associated ventriculitis and meningitis caused by methicillin-resistant staphylococci
  • In combination with a third-generation cephalosporin, treatment of patients with healthcare-associated ventriculitis and meningitis caused by Streptococcus pneumoniae
  • Alternative treatment of patients with healthcare-associated ventriculitis and meningitis caused by methicillin-sensitive staphylococci or P acnes
  • Treatment of patients with brain abscess, subdural empyema, and/or spinal epidural abscess
  • Treatment of patients with septic thrombosis of cavernous/dural venous sinus

Usual Adult Dose for CNS Infection

IDSA, American Academy of Neurology (AAN), American Association of Neurological Surgeons (AANS), and Neurocritical Care Society (NCS) Recommendations:
30 to 60 mg/kg IV per day, given in divided doses every 8 to 12 hours

  • Some experts recommend: 15 mg/kg IV once, followed by 60 mg/kg per day continuous infusion
  • Maximum dose: 2 g/dose
  • Duration of treatment: At least 2 weeks

Comment: Surgical evaluation is recommended for patients with septic thromboses, empyema, and/or abscesses.

Uses:
  • Treatment of patients with healthcare-associated ventriculitis and meningitis caused by methicillin-resistant staphylococci
  • In combination with a third-generation cephalosporin, treatment of patients with healthcare-associated ventriculitis and meningitis caused by Streptococcus pneumoniae
  • Alternative treatment of patients with healthcare-associated ventriculitis and meningitis caused by methicillin-sensitive staphylococci or P acnes
  • Treatment of patients with brain abscess, subdural empyema, and/or spinal epidural abscess
  • Treatment of patients with septic thrombosis of cavernous/dural venous sinus

Usual Adult Dose for Febrile Neutropenia

National Comprehensive Cancer Network (NCCN) Recommendations:
15 mg/kg IV every 12 hours

Comments:

  • This drug should not be used as routine therapy for febrile neutropenia.
  • Empiric therapy should be reassessed within 2 to 3 days of initiation. If gram-positive organisms are not found, discontinuation of treatment should be considered.
  • Patients with resolved fever and neutrophil counts of at least 500 cells/mcL may discontinue therapy.

Use: Empiric prophylaxis in patients at high-risk for febrile neutropenia caused by serious gram-positive infections

Usual Adult Dose for Intraabdominal Infection

SIS and IDSA Recommendations:
15 to 20 mg/kg IV every 8 to 12 hours

Comment: Initial doses should be determined by total body weight.

Uses:

  • Empiric treatment of complicated intra-abdominal infections
  • Treatment of peritonitis caused by enterococci species or MRSA

International Society for Peritoneal Dialysis (ISPD) Recommendations:
Intermittent: 15 to 30 mg/kg intraperitoneally every 5 to 7 days

Duration of therapy:
  • Enterococcal peritonitis: 3 weeks
  • Culture-negative peritonitis: 2 weeks

Use: Treatment of bacterial peritonitis

Usual Adult Dose for Peritonitis

SIS and IDSA Recommendations:
15 to 20 mg/kg IV every 8 to 12 hours

Comment: Initial doses should be determined by total body weight.

Uses:

  • Empiric treatment of complicated intra-abdominal infections
  • Treatment of peritonitis caused by enterococci species or MRSA

International Society for Peritoneal Dialysis (ISPD) Recommendations:
Intermittent: 15 to 30 mg/kg intraperitoneally every 5 to 7 days

Duration of therapy:
  • Enterococcal peritonitis: 3 weeks
  • Culture-negative peritonitis: 2 weeks

Use: Treatment of bacterial peritonitis

Usual Adult Dose for Prevention of Perinatal Group B Streptococcal Disease

US Centers for Disease Control and Prevention (US CDC) Recommendations:
1 g IV every 12 hours until delivery

Use: Prevention of early-onset Group B streptococcal disease in patients with penicillin hypersensitivity and susceptibility is unknown/not possible or the isolates are resistant to erythromycin or clindamycin

Usual Adult Dose for Shunt Infection

IDSA, AAN, AANS, and NCS Recommendations:
Patients with slit ventricles: 5 mg via intraventricular route (plus gentamicin)
Patients with normal-sized ventricles: 10 mg via intraventricular route (plus gentamicin)
Patients with enlarged ventricles: 15 to 20 mg via intraventricular route (plus gentamicin)

Frequency of dosing:

  • External drain output less than 50 mL/day: Every 3 days
  • External drain output 50 to 100 mL/day: Every 2 days
  • External drain output 100 to 150 mL/day: Once a day
  • External drain output 150 to 200 mL/day: Increase the dose by 5 mg (plus gentamicin) and give once a day
  • External drain output 200 to 250 mL/day: Increase the dose by 10 mg (plus gentamicin) and give once a day

Use: Treatment of healthcare-associated ventriculitis and meningitis in patients who respond poorly to systemic antibiotics

Usual Adult Dose for Surgical Prophylaxis

ASHP, IDSA, SHEA, and SIS Recommendations:
15 mg/kg IV once, within 120 minutes before surgery

Uses:
Alternative agent for surgical prophylaxis in patients who have a beta-lactam allergy and are undergoing:

  • Cardiac procedures (e.g., coronary artery bypass, cardiac device insertion, ventricular assist devices)
  • Neurosurgery (e.g., elective craniotomy and cerebrospinal fluid-shunting procedures, implantation of intrathecal pumps)
  • Thoracic procedures (e.g., lobectomy, pneumonectomy, lung resection, thoracotomy, or video-assisted thorascopic surgery)
  • Some orthopedic procedures (e.g., spinal procedures without instrumentation, hip fracture repair)
  • Some urologic procedures (e.g., clean surgery without entry into urinary tract)
  • Heart, lung, and heart-lung transplantation procedures (e.g., heart transplantation, lung and heart-lung transplantation)
  • Clean-contaminated or clean plastic surgery procedures with risk factors

Alternative agent (in combination with an aminoglycoside, aztreonam, or fluoroquinolone) for surgical prophylaxis in patients who have a beta-lactam allergy and are undergoing:
  • Gastroduodenal procedures (e.g., procedures involving entry in to the lumen of the gastrointestinal tract or procedures not entering the GI tract in high-risk patients)
  • Some urologic procedures (e.g., clean surgery involving implanted prosthesis)

Usual Adult Dose for Head Injury

Armed Forces Infectious Disease Society (AFIDS), SIS, and IDSA Recommendations:
1 g IV every 12 hours plus ciprofloxacin

  • Duration of therapy: 5 days OR until cerebrospinal fluid leak is closed, whichever is longer

Use: Antimicrobial prophylaxis for patients with penicillin allergies who have a penetrating brain or spinal cord injury

Usual Pediatric Dose for Bacteremia

Neonates (Up to 1 month):
Initial dose: 15 mg/kg IV ONCE
Maintenance dose:

  • First week of life: 10 mg/kg IV every 12 hours
  • After first week of life: 10 mg/kg IV every 8 hours

Pediatric patients (1 month and older): 10 mg/kg IV every 6 hours

Comments:
  • This drug should be infused over 1 hour.
  • Premature infants may require longer dosing intervals.
  • Doses should be determined by patient-specific factors (e.g., obesity, age).

Uses:
  • Empirical treatment of serious/severe staphylococcal infections caused by susceptible strains of methicillin-resistant staphylococci in patients who are allergic to penicillin, failed to respond/cannot receive other drugs (e.g., penicillins, cephalosporins), and/or to treat organisms that are resistant to other drugs
  • Empirical treatment of septicemia caused by susceptible strains of methicillin-resistant staphylococci in patients who are allergic to penicillin, failed to respond/cannot receive other drugs (e.g., penicillins, cephalosporins), and/or to treat organisms that are resistant to other drugs
  • Empirical treatment of bone infections caused by susceptible strains of methicillin-resistant staphylococci in patients who are allergic to penicillin, failed to respond/cannot receive other drugs (e.g., penicillins, cephalosporins), and/or to treat organisms that are resistant to other drugs

American Academy of Pediatrics (AAP) Recommendations:
Empiric treatment:
Life-threatening infections: 15 mg/kg IV every 6 hours PLUS nafcillin OR oxacillin
Non-life-threatening infections without signs of sepsis: 15 mg/kg IV every 6 to 8 hours

Bacterial Infection:
Neonates (Up to 28 postnatal days):
Loading dose: 20 mg/kg IV ONCE
Gestational age 28 weeks or less:
  • Serum creatinine less than 0.5 mg/dL: 15 mg/kg IV every 12 hours
  • Serum creatinine 0.5 to 0.7 mg/dL: 20 mg/kg IV every 24 hours
  • Serum creatinine 0.8 to 1 mg/dL: 15 mg/kg IV every 24 hours
  • Serum creatinine 1.1 to 1.4 mg/dL: 10 mg/kg IV every 24 hours
  • Serum creatinine greater than 1.4 mg/dL: 15 mg/kg IV every 48 hours

Gestational age greater than 28 weeks:
  • Serum creatinine less than 0.7 mg/dL: 15 mg/kg IV every 12 hours
  • Serum creatinine 0.7 to 0.9 mg/dL: 20 mg/kg IV every 24 hours
  • Serum creatinine 1 to 1.2 mg/dL: 15 mg/kg IV every 24 hours
  • Serum creatinine 1.3 to 1.6 mg/dL: 10 mg/kg IV every 24 hours
  • Serum creatinine greater than 1.6 mg/dL: 15 mg/kg IV every 48 hours

Pediatric patients 28 days and older: 45 to 60 mg/kg IV per day, given in 3 to 4 divided doses

Invasive MRSA infections:
  • Infants and children: 60 to 70 mg/kg/day, given in divided doses via IV 4 times a day

Nonmeningeal pneumococcal infections:
  • Infants and Children: 40 to 45 mg/kg IV per day, given in divided doses every 6 to 8 hours

Comment: Serum concentrations should be used to guide ongoing treatment.

Uses:
  • Drug of choice for the treatment of life-threatening infections (e.g., septicemia, central nervous system [CNS] infections)
  • Drug of choice for the treatment of non-life-threatening infection without signs/symptoms of sepsis (e.g., skin infection, cellulitis, osteomyelitis, pyarthrosis) when rates of MRSA colonization and infection in the community are substantial.
  • Alternative treatment of MSSA in patients with serious penicillin and cephalosporin allergy
  • Drug of choice (with gentamicin) for the treatment of healthcare-associated, multi-drug resistant MRSA infections and oxacillin minimum inhibitory concentrations (MICs) of 4 mcg/mL or greater
  • Drug of choice (with gentamicin) for the treatment of community-associated, not multi-drug resistant MRSA infections and oxacillin MICs of 4 mcg/mL or greater
  • Alternative drug for the treatment of community-associated, not multi-drug resistant MRSA infections and oxacillin MICs of 4 mcg/mL or greater
  • Alternative drug (with linezolid with/without gentamicin) for the treatment of vancomycin-intermediately susceptible Staphylococcus aureus (VISA) infections with MICs of 4 to 16 mcg/mL
  • Alternative drug (with sulfamethoxazole-trimethoprim) for the treatment of VISA infections with MICs of 4 to 16 mcg/mL
  • Treatment of invasive pneumococcal infections

IDSA Recommendations:
Bacteremia:
15 mg/kg IV every 6 hours
  • Duration of therapy: 2 to 6 weeks, depending on the severity of infection

Bacterial Infection:
7 days or less and less than 1200 g: 15 mg/kg IV every 24 hours
7 days or less than 1200 to 2000 g: 10 to 15 mg/kg IV every 12 to 18 hours
7 days or less than greater than 2000 g: 10 to 15 mg/kg IV every 8 to 12 hours

8 to 30 days and less than 1200 g: 15 mg/kg IV every 24 hours
8 to 30 days and 1200 to 2000 g: 10 to 15 mg/kg IV every 8 to 12 hours
8 to 30 days and greater than 2000 g: 15 to 20 mg/kg IV every 8 hours

1 month to 18 years: 10 to 13.33 mg/kg IV every 6 to 8 hours
  • Maximum dose: 40 mg/kg/day

Uses:
  • Preferred treatment for IV catheter-related bloodstream infections caused by MRSA/coagulase-negative staphylococci, ampicillin-resistant, vancomycin-sensitive E faecalis/E faecium, C jeikeium (Group JK)
  • Alternative treatment for IV catheter-related bloodstream infections caused by MSSA/coagulase-negative staphylococci, ampicillin susceptible E faecalis/E faecium
  • Treatment of bacteremia

ASHP, IDSA, SIS, and SIDP Recommendations:
Serious MRSA Infections:
Neonates and children up to 3 months:
  • Initial dose: 10 to 20 mg/kg (total body weight) IV every 8 to 48 hours

3 months and older:
  • Initial dose: 60 to 80 mg/kg IV per day, given in divided doses every 6 to 8 hours
  • Maximum dose: 3600 mg/day

Comments:
  • Doses should be determined by patient-specific factors (e.g., obesity, age, serum creatinine).
  • Most patients over 3 months of age do not require doses exceeding 3000 mg/day.

Usual Pediatric Dose for Osteomyelitis

Neonates (Up to 1 month):
Initial dose: 15 mg/kg IV ONCE
Maintenance dose:

  • First week of life: 10 mg/kg IV every 12 hours
  • After first week of life: 10 mg/kg IV every 8 hours

Pediatric patients (1 month and older): 10 mg/kg IV every 6 hours

Comments:
  • This drug should be infused over 1 hour.
  • Premature infants may require longer dosing intervals.
  • Doses should be determined by patient-specific factors (e.g., obesity, age).

Uses:
  • Empirical treatment of serious/severe staphylococcal infections caused by susceptible strains of methicillin-resistant staphylococci in patients who are allergic to penicillin, failed to respond/cannot receive other drugs (e.g., penicillins, cephalosporins), and/or to treat organisms that are resistant to other drugs
  • Empirical treatment of septicemia caused by susceptible strains of methicillin-resistant staphylococci in patients who are allergic to penicillin, failed to respond/cannot receive other drugs (e.g., penicillins, cephalosporins), and/or to treat organisms that are resistant to other drugs
  • Empirical treatment of bone infections caused by susceptible strains of methicillin-resistant staphylococci in patients who are allergic to penicillin, failed to respond/cannot receive other drugs (e.g., penicillins, cephalosporins), and/or to treat organisms that are resistant to other drugs

American Academy of Pediatrics (AAP) Recommendations:
Empiric treatment:
Life-threatening infections: 15 mg/kg IV every 6 hours PLUS nafcillin OR oxacillin
Non-life-threatening infections without signs of sepsis: 15 mg/kg IV every 6 to 8 hours

Bacterial Infection:
Neonates (Up to 28 postnatal days):
Loading dose: 20 mg/kg IV ONCE
Gestational age 28 weeks or less:
  • Serum creatinine less than 0.5 mg/dL: 15 mg/kg IV every 12 hours
  • Serum creatinine 0.5 to 0.7 mg/dL: 20 mg/kg IV every 24 hours
  • Serum creatinine 0.8 to 1 mg/dL: 15 mg/kg IV every 24 hours
  • Serum creatinine 1.1 to 1.4 mg/dL: 10 mg/kg IV every 24 hours
  • Serum creatinine greater than 1.4 mg/dL: 15 mg/kg IV every 48 hours

Gestational age greater than 28 weeks:
  • Serum creatinine less than 0.7 mg/dL: 15 mg/kg IV every 12 hours
  • Serum creatinine 0.7 to 0.9 mg/dL: 20 mg/kg IV every 24 hours
  • Serum creatinine 1 to 1.2 mg/dL: 15 mg/kg IV every 24 hours
  • Serum creatinine 1.3 to 1.6 mg/dL: 10 mg/kg IV every 24 hours
  • Serum creatinine greater than 1.6 mg/dL: 15 mg/kg IV every 48 hours

Pediatric patients 28 days and older: 45 to 60 mg/kg IV per day, given in 3 to 4 divided doses

Invasive MRSA infections:
  • Infants and children: 60 to 70 mg/kg/day, given in divided doses via IV 4 times a day

Nonmeningeal pneumococcal infections:
  • Infants and Children: 40 to 45 mg/kg IV per day, given in divided doses every 6 to 8 hours

Comment: Serum concentrations should be used to guide ongoing treatment.

Uses:
  • Drug of choice for the treatment of life-threatening infections (e.g., septicemia, central nervous system [CNS] infections)
  • Drug of choice for the treatment of non-life-threatening infection without signs/symptoms of sepsis (e.g., skin infection, cellulitis, osteomyelitis, pyarthrosis) when rates of MRSA colonization and infection in the community are substantial.
  • Alternative treatment of MSSA in patients with serious penicillin and cephalosporin allergy
  • Drug of choice (with gentamicin) for the treatment of healthcare-associated, multi-drug resistant MRSA infections and oxacillin minimum inhibitory concentrations (MICs) of 4 mcg/mL or greater
  • Drug of choice (with gentamicin) for the treatment of community-associated, not multi-drug resistant MRSA infections and oxacillin MICs of 4 mcg/mL or greater
  • Alternative drug for the treatment of community-associated, not multi-drug resistant MRSA infections and oxacillin MICs of 4 mcg/mL or greater
  • Alternative drug (with linezolid with/without gentamicin) for the treatment of vancomycin-intermediately susceptible Staphylococcus aureus (VISA) infections with MICs of 4 to 16 mcg/mL
  • Alternative drug (with sulfamethoxazole-trimethoprim) for the treatment of VISA infections with MICs of 4 to 16 mcg/mL
  • Treatment of invasive pneumococcal infections

IDSA Recommendations:
Bacteremia:
15 mg/kg IV every 6 hours
  • Duration of therapy: 2 to 6 weeks, depending on the severity of infection

Bacterial Infection:
7 days or less and less than 1200 g: 15 mg/kg IV every 24 hours
7 days or less than 1200 to 2000 g: 10 to 15 mg/kg IV every 12 to 18 hours
7 days or less than greater than 2000 g: 10 to 15 mg/kg IV every 8 to 12 hours

8 to 30 days and less than 1200 g: 15 mg/kg IV every 24 hours
8 to 30 days and 1200 to 2000 g: 10 to 15 mg/kg IV every 8 to 12 hours
8 to 30 days and greater than 2000 g: 15 to 20 mg/kg IV every 8 hours

1 month to 18 years: 10 to 13.33 mg/kg IV every 6 to 8 hours
  • Maximum dose: 40 mg/kg/day

Uses:
  • Preferred treatment for IV catheter-related bloodstream infections caused by MRSA/coagulase-negative staphylococci, ampicillin-resistant, vancomycin-sensitive E faecalis/E faecium, C jeikeium (Group JK)
  • Alternative treatment for IV catheter-related bloodstream infections caused by MSSA/coagulase-negative staphylococci, ampicillin susceptible E faecalis/E faecium
  • Treatment of bacteremia

ASHP, IDSA, SIS, and SIDP Recommendations:
Serious MRSA Infections:
Neonates and children up to 3 months:
  • Initial dose: 10 to 20 mg/kg (total body weight) IV every 8 to 48 hours

3 months and older:
  • Initial dose: 60 to 80 mg/kg IV per day, given in divided doses every 6 to 8 hours
  • Maximum dose: 3600 mg/day

Comments:
  • Doses should be determined by patient-specific factors (e.g., obesity, age, serum creatinine).
  • Most patients over 3 months of age do not require doses exceeding 3000 mg/day.

Usual Pediatric Dose for Bacterial Infection

Neonates (Up to 1 month):
Initial dose: 15 mg/kg IV ONCE
Maintenance dose:

  • First week of life: 10 mg/kg IV every 12 hours
  • After first week of life: 10 mg/kg IV every 8 hours

Pediatric patients (1 month and older): 10 mg/kg IV every 6 hours

Comments:
  • This drug should be infused over 1 hour.
  • Premature infants may require longer dosing intervals.
  • Doses should be determined by patient-specific factors (e.g., obesity, age).

Uses:
  • Empirical treatment of serious/severe staphylococcal infections caused by susceptible strains of methicillin-resistant staphylococci in patients who are allergic to penicillin, failed to respond/cannot receive other drugs (e.g., penicillins, cephalosporins), and/or to treat organisms that are resistant to other drugs
  • Empirical treatment of septicemia caused by susceptible strains of methicillin-resistant staphylococci in patients who are allergic to penicillin, failed to respond/cannot receive other drugs (e.g., penicillins, cephalosporins), and/or to treat organisms that are resistant to other drugs
  • Empirical treatment of bone infections caused by susceptible strains of methicillin-resistant staphylococci in patients who are allergic to penicillin, failed to respond/cannot receive other drugs (e.g., penicillins, cephalosporins), and/or to treat organisms that are resistant to other drugs

American Academy of Pediatrics (AAP) Recommendations:
Empiric treatment:
Life-threatening infections: 15 mg/kg IV every 6 hours PLUS nafcillin OR oxacillin
Non-life-threatening infections without signs of sepsis: 15 mg/kg IV every 6 to 8 hours

Bacterial Infection:
Neonates (Up to 28 postnatal days):
Loading dose: 20 mg/kg IV ONCE
Gestational age 28 weeks or less:
  • Serum creatinine less than 0.5 mg/dL: 15 mg/kg IV every 12 hours
  • Serum creatinine 0.5 to 0.7 mg/dL: 20 mg/kg IV every 24 hours
  • Serum creatinine 0.8 to 1 mg/dL: 15 mg/kg IV every 24 hours
  • Serum creatinine 1.1 to 1.4 mg/dL: 10 mg/kg IV every 24 hours
  • Serum creatinine greater than 1.4 mg/dL: 15 mg/kg IV every 48 hours

Gestational age greater than 28 weeks:
  • Serum creatinine less than 0.7 mg/dL: 15 mg/kg IV every 12 hours
  • Serum creatinine 0.7 to 0.9 mg/dL: 20 mg/kg IV every 24 hours
  • Serum creatinine 1 to 1.2 mg/dL: 15 mg/kg IV every 24 hours
  • Serum creatinine 1.3 to 1.6 mg/dL: 10 mg/kg IV every 24 hours
  • Serum creatinine greater than 1.6 mg/dL: 15 mg/kg IV every 48 hours

Pediatric patients 28 days and older: 45 to 60 mg/kg IV per day, given in 3 to 4 divided doses

Invasive MRSA infections:
  • Infants and children: 60 to 70 mg/kg/day, given in divided doses via IV 4 times a day

Nonmeningeal pneumococcal infections:
  • Infants and Children: 40 to 45 mg/kg IV per day, given in divided doses every 6 to 8 hours

Comment: Serum concentrations should be used to guide ongoing treatment.

Uses:
  • Drug of choice for the treatment of life-threatening infections (e.g., septicemia, central nervous system [CNS] infections)
  • Drug of choice for the treatment of non-life-threatening infection without signs/symptoms of sepsis (e.g., skin infection, cellulitis, osteomyelitis, pyarthrosis) when rates of MRSA colonization and infection in the community are substantial.
  • Alternative treatment of MSSA in patients with serious penicillin and cephalosporin allergy
  • Drug of choice (with gentamicin) for the treatment of healthcare-associated, multi-drug resistant MRSA infections and oxacillin minimum inhibitory concentrations (MICs) of 4 mcg/mL or greater
  • Drug of choice (with gentamicin) for the treatment of community-associated, not multi-drug resistant MRSA infections and oxacillin MICs of 4 mcg/mL or greater
  • Alternative drug for the treatment of community-associated, not multi-drug resistant MRSA infections and oxacillin MICs of 4 mcg/mL or greater
  • Alternative drug (with linezolid with/without gentamicin) for the treatment of vancomycin-intermediately susceptible Staphylococcus aureus (VISA) infections with MICs of 4 to 16 mcg/mL
  • Alternative drug (with sulfamethoxazole-trimethoprim) for the treatment of VISA infections with MICs of 4 to 16 mcg/mL
  • Treatment of invasive pneumococcal infections

IDSA Recommendations:
Bacteremia:
15 mg/kg IV every 6 hours
  • Duration of therapy: 2 to 6 weeks, depending on the severity of infection

Bacterial Infection:
7 days or less and less than 1200 g: 15 mg/kg IV every 24 hours
7 days or less than 1200 to 2000 g: 10 to 15 mg/kg IV every 12 to 18 hours
7 days or less than greater than 2000 g: 10 to 15 mg/kg IV every 8 to 12 hours

8 to 30 days and less than 1200 g: 15 mg/kg IV every 24 hours
8 to 30 days and 1200 to 2000 g: 10 to 15 mg/kg IV every 8 to 12 hours
8 to 30 days and greater than 2000 g: 15 to 20 mg/kg IV every 8 hours

1 month to 18 years: 10 to 13.33 mg/kg IV every 6 to 8 hours
  • Maximum dose: 40 mg/kg/day

Uses:
  • Preferred treatment for IV catheter-related bloodstream infections caused by MRSA/coagulase-negative staphylococci, ampicillin-resistant, vancomycin-sensitive E faecalis/E faecium, C jeikeium (Group JK)
  • Alternative treatment for IV catheter-related bloodstream infections caused by MSSA/coagulase-negative staphylococci, ampicillin susceptible E faecalis/E faecium
  • Treatment of bacteremia

ASHP, IDSA, SIS, and SIDP Recommendations:
Serious MRSA Infections:
Neonates and children up to 3 months:
  • Initial dose: 10 to 20 mg/kg (total body weight) IV every 8 to 48 hours

3 months and older:
  • Initial dose: 60 to 80 mg/kg IV per day, given in divided doses every 6 to 8 hours
  • Maximum dose: 3600 mg/day

Comments:
  • Doses should be determined by patient-specific factors (e.g., obesity, age, serum creatinine).
  • Most patients over 3 months of age do not require doses exceeding 3000 mg/day.

Usual Pediatric Dose for Sepsis

Neonates (Up to 1 month):
Initial dose: 15 mg/kg IV ONCE
Maintenance dose:

  • First week of life: 10 mg/kg IV every 12 hours
  • After first week of life: 10 mg/kg IV every 8 hours

Pediatric patients (1 month and older): 10 mg/kg IV every 6 hours

Comments:
  • This drug should be infused over 1 hour.
  • Premature infants may require longer dosing intervals.
  • Doses should be determined by patient-specific factors (e.g., obesity, age).

Uses:
  • Empirical treatment of serious/severe staphylococcal infections caused by susceptible strains of methicillin-resistant staphylococci in patients who are allergic to penicillin, failed to respond/cannot receive other drugs (e.g., penicillins, cephalosporins), and/or to treat organisms that are resistant to other drugs
  • Empirical treatment of septicemia caused by susceptible strains of methicillin-resistant staphylococci in patients who are allergic to penicillin, failed to respond/cannot receive other drugs (e.g., penicillins, cephalosporins), and/or to treat organisms that are resistant to other drugs
  • Empirical treatment of bone infections caused by susceptible strains of methicillin-resistant staphylococci in patients who are allergic to penicillin, failed to respond/cannot receive other drugs (e.g., penicillins, cephalosporins), and/or to treat organisms that are resistant to other drugs

American Academy of Pediatrics (AAP) Recommendations:
Empiric treatment:
Life-threatening infections: 15 mg/kg IV every 6 hours PLUS nafcillin OR oxacillin
Non-life-threatening infections without signs of sepsis: 15 mg/kg IV every 6 to 8 hours

Bacterial Infection:
Neonates (Up to 28 postnatal days):
Loading dose: 20 mg/kg IV ONCE
Gestational age 28 weeks or less:
  • Serum creatinine less than 0.5 mg/dL: 15 mg/kg IV every 12 hours
  • Serum creatinine 0.5 to 0.7 mg/dL: 20 mg/kg IV every 24 hours
  • Serum creatinine 0.8 to 1 mg/dL: 15 mg/kg IV every 24 hours
  • Serum creatinine 1.1 to 1.4 mg/dL: 10 mg/kg IV every 24 hours
  • Serum creatinine greater than 1.4 mg/dL: 15 mg/kg IV every 48 hours

Gestational age greater than 28 weeks:
  • Serum creatinine less than 0.7 mg/dL: 15 mg/kg IV every 12 hours
  • Serum creatinine 0.7 to 0.9 mg/dL: 20 mg/kg IV every 24 hours
  • Serum creatinine 1 to 1.2 mg/dL: 15 mg/kg IV every 24 hours
  • Serum creatinine 1.3 to 1.6 mg/dL: 10 mg/kg IV every 24 hours
  • Serum creatinine greater than 1.6 mg/dL: 15 mg/kg IV every 48 hours

Pediatric patients 28 days and older: 45 to 60 mg/kg IV per day, given in 3 to 4 divided doses

Invasive MRSA infections:
  • Infants and children: 60 to 70 mg/kg/day, given in divided doses via IV 4 times a day

Nonmeningeal pneumococcal infections:
  • Infants and Children: 40 to 45 mg/kg IV per day, given in divided doses every 6 to 8 hours

Comment: Serum concentrations should be used to guide ongoing treatment.

Uses:
  • Drug of choice for the treatment of life-threatening infections (e.g., septicemia, central nervous system [CNS] infections)
  • Drug of choice for the treatment of non-life-threatening infection without signs/symptoms of sepsis (e.g., skin infection, cellulitis, osteomyelitis, pyarthrosis) when rates of MRSA colonization and infection in the community are substantial.
  • Alternative treatment of MSSA in patients with serious penicillin and cephalosporin allergy
  • Drug of choice (with gentamicin) for the treatment of healthcare-associated, multi-drug resistant MRSA infections and oxacillin minimum inhibitory concentrations (MICs) of 4 mcg/mL or greater
  • Drug of choice (with gentamicin) for the treatment of community-associated, not multi-drug resistant MRSA infections and oxacillin MICs of 4 mcg/mL or greater
  • Alternative drug for the treatment of community-associated, not multi-drug resistant MRSA infections and oxacillin MICs of 4 mcg/mL or greater
  • Alternative drug (with linezolid with/without gentamicin) for the treatment of vancomycin-intermediately susceptible Staphylococcus aureus (VISA) infections with MICs of 4 to 16 mcg/mL
  • Alternative drug (with sulfamethoxazole-trimethoprim) for the treatment of VISA infections with MICs of 4 to 16 mcg/mL
  • Treatment of invasive pneumococcal infections

IDSA Recommendations:
Bacteremia:
15 mg/kg IV every 6 hours
  • Duration of therapy: 2 to 6 weeks, depending on the severity of infection

Bacterial Infection:
7 days or less and less than 1200 g: 15 mg/kg IV every 24 hours
7 days or less than 1200 to 2000 g: 10 to 15 mg/kg IV every 12 to 18 hours
7 days or less than greater than 2000 g: 10 to 15 mg/kg IV every 8 to 12 hours

8 to 30 days and less than 1200 g: 15 mg/kg IV every 24 hours
8 to 30 days and 1200 to 2000 g: 10 to 15 mg/kg IV every 8 to 12 hours
8 to 30 days and greater than 2000 g: 15 to 20 mg/kg IV every 8 hours

1 month to 18 years: 10 to 13.33 mg/kg IV every 6 to 8 hours
  • Maximum dose: 40 mg/kg/day

Uses:
  • Preferred treatment for IV catheter-related bloodstream infections caused by MRSA/coagulase-negative staphylococci, ampicillin-resistant, vancomycin-sensitive E faecalis/E faecium, C jeikeium (Group JK)
  • Alternative treatment for IV catheter-related bloodstream infections caused by MSSA/coagulase-negative staphylococci, ampicillin susceptible E faecalis/E faecium
  • Treatment of bacteremia

ASHP, IDSA, SIS, and SIDP Recommendations:
Serious MRSA Infections:
Neonates and children up to 3 months:
  • Initial dose: 10 to 20 mg/kg (total body weight) IV every 8 to 48 hours

3 months and older:
  • Initial dose: 60 to 80 mg/kg IV per day, given in divided doses every 6 to 8 hours
  • Maximum dose: 3600 mg/day

Comments:
  • Doses should be determined by patient-specific factors (e.g., obesity, age, serum creatinine).
  • Most patients over 3 months of age do not require doses exceeding 3000 mg/day.

Usual Pediatric Dose for Endocarditis

Neonates (Up to 1 month):
Initial dose: 15 mg/kg IV ONCE
Maintenance dose:

  • First week of life: 10 mg/kg IV every 12 hours
  • After first week of life: 10 mg/kg IV every 8 hours

Pediatric patients (1 month and older): 10 mg/kg IV every 6 hours

Comments:
  • This drug should be infused over 1 hour.
  • Premature infants may require longer dosing intervals.
  • Doses should be determined by patient-specific factors (e.g., obesity, age).
  • Successful treatment of diphtheroid endocarditis has been reported.

Use:
  • Empirical treatment of staphylococcal endocarditis caused by susceptible strains of methicillin-resistant staphylococci in patients who are allergic to penicillin, failed to respond/cannot receive other drugs (e.g., penicillins, cephalosporins), and/or to treat organisms that are resistant to other drugs
  • Empirical treatment (with an aminoglycoside) of endocarditis caused by enterococci, S bovis, or S viridans
  • Empirical treatment (with an aminoglycoside and/or rifampin) of early-onset prosthetic valve endocarditis caused by S epidermidis or diphtheroids

AAP Recommendations:
Empiric treatment: 45 to 60 mg/kg/day, given in divided doses via IV every 6 to 8 hours
Invasive MRSA infections: 60 to 70 mg/kg/day, given in divided doses via IV 4 times a day

Uses:
  • Drug of choice for the treatment of life-threatening infections (e.g., endocarditis)
  • Drug of choice for the treatment of non-life-threatening infection without signs/symptoms of sepsis when rates of MRSA colonization and infection in the community are substantial.
  • Alternative treatment of MSSA in patients with serious penicillin and cephalosporin allergy
  • Drug of choice (with gentamicin) for the treatment of healthcare-associated, multi-drug resistant MRSA infections and oxacillin MICs of 4 mcg/mL or greater
  • Drug of choice (with gentamicin) for the treatment of community-associated, not multi-drug resistant MRSA infections and oxacillin MICs of 4 mcg/mL or greater
  • Alternative drug for the treatment of community-associated, not multi-drug resistant MRSA infections and oxacillin MICs of 4 mcg/mL or greater
  • Alternative drug (with linezolid with/without gentamicin) for the treatment of VISA infections with MICs of 4 to 16 mcg/mL
  • Alternative drug (with sulfamethoxazole-trimethoprim) for the treatment of VISA infections with MICs of 4 to 16 mcg/mL

AHA Recommendations:
40 to 60 mg/kg IV per day, given in divided doses every 6 to 12 hours
  • Maximum dose: 2 g/day

Duration of therapy:
  • Empirical treatment: 4 to 6 weeks
  • Staphylococci infection: 6 weeks

Comment: Gentamycin should be added to patients with enterococci infections.

Uses:
  • Treatment of native valve and prosthetic valve infective endocarditis
  • Empirical alternative treatment (with gentamicin) of community-acquired native valve or late prosthetic valve (over 1 year after surgery) endocarditis
  • Empirical treatment of nosocomial endocarditis associated with vascular cannulae or early prosthetic valve endocarditis (1 year or less after surgery)
  • Alternative treatment for streptococcal infections highly susceptible to penicillin G (e.g., Groups A, B, C, G nonenterococcal, Group D streptococci) and streptococci relatively resistant to penicillin (e.g., enterococci, less-susceptible S viridians)
  • Alternative treatment for endocarditis caused by S aureus or coagulase-negative staphylococci susceptible or resistant to penicillin G and/or oxacillin in patients highly allergic to beta-lactam antibiotics

Usual Pediatric Dose for Pseudomembranous Colitis

Oral solution:
Less than 18 years: 40 mg/kg orally in 3 to 4 divided doses

  • Maximum dose: 2 g/day
  • Duration of therapy: 7 to 10 days

Comments:
  • Safety and efficacy of capsule formulations have not been established in patients younger than 18 years of age.
  • Parenteral formulations will not treat colitis.

Uses:
  • Treatment of C difficile-associated diarrhea
  • Treatment of enterocolitis caused by S aureus (including MRSA)

AAP Recommendations:
Children:
FIRST OCCURRENCE:
Mild-moderate infection:
Failure to respond within 5 to 7 days, pregnant/breastfeeding, OR metronidazole-intolerant patients: 10 mg/kg orally every 6 hours
  • Maximum dose: 125 mg/dose
  • Duration of therapy: 10 days

Patients for whom oral therapy cannot reach colon: 500 mg (in 100 mL normal saline) rectally (as an enema) every 8 hours until symptoms improve PLUS oral metronidazole OR oral vancomycin

Severe infection: 10 mg/kg orally every 6 hours
  • Maximum dose: 125 mg/dose
  • Duration of therapy: 10 days

Severe and complicated infection:
No abdominal distention: 10 mg/kg orally every 6 hours PLUS metronidazole
  • Maximum dose: 125 mg/dose
  • Duration of therapy: 10 days

Complicated with ileus or toxic colitis and/or significant abdominal distention: 10 mg/kg orally every 6 hours PLUS 500 mg (in 100 mL normal saline) rectally (as an enema) every 8 hours until symptoms improve PLUS metronidazole
  • Maximum oral dose: 500 mg/dose
  • Duration of therapy: 10 days

FIRST RECURRENCE:
Mild-moderate infection:
Failure to respond within 5 to 7 days, pregnant/breastfeeding, OR metronidazole-intolerant patients: 10 mg/kg orally every 6 hours
  • Maximum dose: 125 mg/dose
  • Duration of therapy: 10 days

Patients for whom oral therapy cannot reach colon: 500 mg (in 100 mL normal saline) rectally (as an enema) every 8 hours until symptoms improve PLUS oral metronidazole OR oral vancomycin

Severe infection: 10 mg/kg orally every 6 hours
  • Maximum dose: 125 mg/dose

SECOND RECURRENCE:
Tapered regimen:
  • Week 1: 10 mg/kg orally 4 times a day for 7 days
  • Week 2: 10 mg/kg orally 3 times a day for 7 days
  • Week 3: 10 mg/kg orally 2 times a day for 7 days
  • Week 4: 10 mg/kg orally once a day for 7 days
  • Week 5: 10 mg/kg orally every other day for 7 days
  • Week 6: 10 mg/kg orally every 72 hours for 7 days
  • Maximum dose: 125 mg/dose

Alternative tapered regimen: 10 mg/kg orally 4 times a day for 14 days, then 10 mg/kg orally 2 times a day for 7 to 14 days, then 10 mg/kg orally every 2 to 3 days for 2 to 8 weeks
  • Maximum dose: 125 mg/dose

Pulse regimen: 10 mg/kg orally 4 times a day, then rifaximin OR nitazoxanide
  • Maximum dose: 125 mg/dose
  • Duration of therapy: 14 days

Comments:
  • Severe infection should be considered in the presence of leukocytosis, leukopenia, and/or worsening renal function.
  • Severe and complicated infection is defined as intensive care unit admission, hypotension/shock, pseudomembranous colitis by endoscopy, ileus, or toxic megacolon.

Use: Treatment of C difficile infection

Usual Pediatric Dose for Enterocolitis

Oral solution:
Less than 18 years: 40 mg/kg orally in 3 to 4 divided doses

  • Maximum dose: 2 g/day
  • Duration of therapy: 7 to 10 days

Comments:
  • Safety and efficacy of capsule formulations have not been established in patients younger than 18 years of age.
  • Parenteral formulations will not treat colitis.

Uses:
  • Treatment of C difficile-associated diarrhea
  • Treatment of enterocolitis caused by S aureus (including MRSA)

AAP Recommendations:
Children:
FIRST OCCURRENCE:
Mild-moderate infection:
Failure to respond within 5 to 7 days, pregnant/breastfeeding, OR metronidazole-intolerant patients: 10 mg/kg orally every 6 hours
  • Maximum dose: 125 mg/dose
  • Duration of therapy: 10 days

Patients for whom oral therapy cannot reach colon: 500 mg (in 100 mL normal saline) rectally (as an enema) every 8 hours until symptoms improve PLUS oral metronidazole OR oral vancomycin

Severe infection: 10 mg/kg orally every 6 hours
  • Maximum dose: 125 mg/dose
  • Duration of therapy: 10 days

Severe and complicated infection:
No abdominal distention: 10 mg/kg orally every 6 hours PLUS metronidazole
  • Maximum dose: 125 mg/dose
  • Duration of therapy: 10 days

Complicated with ileus or toxic colitis and/or significant abdominal distention: 10 mg/kg orally every 6 hours PLUS 500 mg (in 100 mL normal saline) rectally (as an enema) every 8 hours until symptoms improve PLUS metronidazole
  • Maximum oral dose: 500 mg/dose
  • Duration of therapy: 10 days

FIRST RECURRENCE:
Mild-moderate infection:
Failure to respond within 5 to 7 days, pregnant/breastfeeding, OR metronidazole-intolerant patients: 10 mg/kg orally every 6 hours
  • Maximum dose: 125 mg/dose
  • Duration of therapy: 10 days

Patients for whom oral therapy cannot reach colon: 500 mg (in 100 mL normal saline) rectally (as an enema) every 8 hours until symptoms improve PLUS oral metronidazole OR oral vancomycin

Severe infection: 10 mg/kg orally every 6 hours
  • Maximum dose: 125 mg/dose

SECOND RECURRENCE:
Tapered regimen:
  • Week 1: 10 mg/kg orally 4 times a day for 7 days
  • Week 2: 10 mg/kg orally 3 times a day for 7 days
  • Week 3: 10 mg/kg orally 2 times a day for 7 days
  • Week 4: 10 mg/kg orally once a day for 7 days
  • Week 5: 10 mg/kg orally every other day for 7 days
  • Week 6: 10 mg/kg orally every 72 hours for 7 days
  • Maximum dose: 125 mg/dose

Alternative tapered regimen: 10 mg/kg orally 4 times a day for 14 days, then 10 mg/kg orally 2 times a day for 7 to 14 days, then 10 mg/kg orally every 2 to 3 days for 2 to 8 weeks
  • Maximum dose: 125 mg/dose

Pulse regimen: 10 mg/kg orally 4 times a day, then rifaximin OR nitazoxanide
  • Maximum dose: 125 mg/dose
  • Duration of therapy: 14 days

Comments:
  • Severe infection should be considered in the presence of leukocytosis, leukopenia, and/or worsening renal function.
  • Severe and complicated infection is defined as intensive care unit admission, hypotension/shock, pseudomembranous colitis by endoscopy, ileus, or toxic megacolon.

Use: Treatment of C difficile infection

Usual Pediatric Dose for Skin or Soft Tissue Infection

Neonates (Up to 1 month):
Initial dose: 15 mg/kg IV ONCE
Maintenance dose:

  • First week of life: 10 mg/kg IV every 12 hours
  • After first week of life: 10 mg/kg IV every 8 hours

Pediatric patients (1 month and older): 10 mg/kg IV every 6 hours

Comments:
  • This drug should be administered over 1 hour.
  • Premature infants may require a longer dosing interval.
  • Doses should be determined by patient-specific factors (e.g., obesity, age).

Use:
  • Empirical treatment of skin and skin structure infections caused by susceptible strains of methicillin-resistant staphylococci in patients who are allergic to penicillin, failed to respond/cannot receive other drugs (e.g., penicillins, cephalosporins), and/or to treat organisms that are resistant to other drugs

AAP Recommendations:
Empiric treatment: 45 to 60 mg/kg/day, given in divided doses via IV every 6 to 8 hours
Invasive MRSA infections: 60 to 70 mg/kg/day, given in divided doses via IV 4 times a day

Uses:
  • Drug of choice for the treatment of life-threatening infections (e.g., septicemia)
  • Drug of choice for the treatment of non-life-threatening infection without signs/symptoms of sepsis (e.g., skin infection, cellulitis) when rates of MRSA colonization and infection in the community are substantial.
  • Alternative treatment of MSSA in patients with serious penicillin and cephalosporin allergy
  • Drug of choice (with gentamicin) for the treatment of healthcare-associated, multi-drug resistant MRSA infections and oxacillin MICs of 4 mcg/mL or greater
  • Drug of choice (with gentamicin) for the treatment of community-associated, not multi-drug resistant MRSA infections and oxacillin MICs of 4 mcg/mL or greater
  • Alternative drug for the treatment of community-associated, not multi-drug resistant MRSA infections and oxacillin MICs of 4 mcg/mL or greater
  • Alternative drug (with linezolid with/without gentamicin) for the treatment of VISA infections with MICs of 4 to 16 mcg/mL
  • Alternative drug (with sulfamethoxazole-trimethoprim) for the treatment of VISA infections with MICs of 4 to 16 mcg/mL

IDSA Recommendations:
10 to 15 mg/kg IV 3 to 4 times a day

Comments:
  • Patients with necrotizing infections may require up to a 13 mg/kg dose given IV every 8 hours plus piperacillin.
  • Patients with necrotizing infections caused by resistant S aureus may require 15 mg/kg given IV every 6 hours.

Use:
  • First-line treatment of treatment of SSTIs caused by MRSA in patients who require parenteral treatment
  • Alternative treatment of SSTIs in patients with penicillin allergies
  • First-line treatment of necrotizing infections of the skin, fascia, and muscle caused by mixed infections

Usual Pediatric Dose for Pneumonia

Neonates (Up to 1 month):
Initial dose: 15 mg/kg IV ONCE
Maintenance dose:

  • First week of life: 10 mg/kg IV every 12 hours
  • After first week of life: 10 mg/kg IV every 8 hours

Pediatric patients (1 month and older): 10 mg/kg IV every 6 hours

Comments:
  • This drug should be administered over 1 hour.
  • Premature infants may require a longer dosing interval.
  • Doses should be determined by patient-specific factors (e.g., obesity, age).

Use: Empirical treatment of lower respiratory tract infections caused by susceptible strains of methicillin-resistant staphylococci in patients who are allergic to penicillin, failed to respond/cannot receive other drugs (e.g., penicillins, cephalosporins), and/or to treat organisms that are resistant to other drugs

Pediatric Infectious Diseases Society (PIDS) and IDSA Recommendations:
10 to 20 mg/kg every 6 to 8 hours

Uses:
  • Alternative treatment of community acquired pneumonia caused by S pneumoniae with penicillin MICs of less than or equal to 2 mcg/mL, S pneumoniae resistant to penicillin (MICs at least 4 mcg/mL), Group A Streptococcus, or MSSA
  • Preferred treatment of community acquired pneumonia caused by MRSA (with/without susceptibility to clindamycin)

Usual Pediatric Dose for Intraabdominal Infection

AAP Recommendations:
Empiric treatment: 45 to 60 mg/kg/day, given in divided doses via IV every 6 to 8 hours
Invasive MRSA infections: 60 to 70 mg/kg/day, given in divided doses via IV 4 times a day

Uses:

  • Drug of choice for the treatment of life-threatening infections (e.g., septicemia)
  • Drug of choice for the treatment of non-life-threatening infection without signs/symptoms of sepsis (e.g., pyarthrosis) when rates of MRSA colonization and infection in the community are substantial.
  • Alternative treatment of MSSA in patients with serious penicillin and cephalosporin allergy
  • Drug of choice (with gentamicin) for the treatment of healthcare-associated, multi-drug resistant MRSA infections and oxacillin MICs of 4 mcg/mL or greater
  • Drug of choice (with gentamicin) for the treatment of community-associated, not multi-drug resistant MRSA infections and oxacillin MICs of 4 mcg/mL or greater
  • Alternative drug for the treatment of community-associated, not multi-drug resistant MRSA infections and oxacillin MICs of 4 mcg/mL or greater
  • Alternative drug (with linezolid with/without gentamicin) for the treatment of VISA infections with MICs of 4 to 16 mcg/mL
  • Alternative drug (with sulfamethoxazole-trimethoprim) for the treatment of VISA infections with MICs of 4 to 16 mcg/mL

SIS and IDSA Recommendations:
40 mg/kg IV per day, divided and given every 6 to 8 hours

Comment: This drug should be given as a 1-hour infusion.

Uses:
  • Treatment of complicated intra-abdominal infections
  • Treatment of peritonitis caused by Enterococci species or MRSA

ISPD Recommendations:
Prophylaxis: 25 mg/L intraperitoneally once

Treatment: 30 mg/kg intraperitoneally once, then 15 mg/kg intraperitoneally every 3 to 5 days

Uses:
  • Prophylaxis against peritonitis in patients with known MRSA colonization at risk of touch contamination during instillation of peritoneal dialysis fluid after system disconnection OR disconnection during peritoneal dialysis
  • Treatment of bacterial peritonitis

Usual Pediatric Dose for Peritonitis

AAP Recommendations:
Empiric treatment: 45 to 60 mg/kg/day, given in divided doses via IV every 6 to 8 hours
Invasive MRSA infections: 60 to 70 mg/kg/day, given in divided doses via IV 4 times a day

Uses:

  • Drug of choice for the treatment of life-threatening infections (e.g., septicemia)
  • Drug of choice for the treatment of non-life-threatening infection without signs/symptoms of sepsis (e.g., pyarthrosis) when rates of MRSA colonization and infection in the community are substantial.
  • Alternative treatment of MSSA in patients with serious penicillin and cephalosporin allergy
  • Drug of choice (with gentamicin) for the treatment of healthcare-associated, multi-drug resistant MRSA infections and oxacillin MICs of 4 mcg/mL or greater
  • Drug of choice (with gentamicin) for the treatment of community-associated, not multi-drug resistant MRSA infections and oxacillin MICs of 4 mcg/mL or greater
  • Alternative drug for the treatment of community-associated, not multi-drug resistant MRSA infections and oxacillin MICs of 4 mcg/mL or greater
  • Alternative drug (with linezolid with/without gentamicin) for the treatment of VISA infections with MICs of 4 to 16 mcg/mL
  • Alternative drug (with sulfamethoxazole-trimethoprim) for the treatment of VISA infections with MICs of 4 to 16 mcg/mL

SIS and IDSA Recommendations:
40 mg/kg IV per day, divided and given every 6 to 8 hours

Comment: This drug should be given as a 1-hour infusion.

Uses:
  • Treatment of complicated intra-abdominal infections
  • Treatment of peritonitis caused by Enterococci species or MRSA

ISPD Recommendations:
Prophylaxis: 25 mg/L intraperitoneally once

Treatment: 30 mg/kg intraperitoneally once, then 15 mg/kg intraperitoneally every 3 to 5 days

Uses:
  • Prophylaxis against peritonitis in patients with known MRSA colonization at risk of touch contamination during instillation of peritoneal dialysis fluid after system disconnection OR disconnection during peritoneal dialysis
  • Treatment of bacterial peritonitis

Usual Pediatric Dose for Surgical Prophylaxis

AAP Recommendations:
Neonates (72 hours) or older: 15 mg/kg IV ONCE

Uses:
Alternative agent for surgical prophylaxis in patients undergoing:

  • Cardiac surgical procedures (e.g., prosthetic valve/pacemaker, ventricular assist devices) where Staphylococcus epidermidis (including methicillin-resistant Staphylococcus epidermidis [MRSE]), Staphylococcus aureus (including MRSA), Corynebacterium species, and/or enteric gram-negative bacilli are likely
  • Neurosurgery (e.g., craniotomy, intrathecal baclofen shunt/ventricular shunt placement) where S epidermidis (including MRSE) or S aureus (including MRSA) are likely
  • Orthopedic (e.g., internal fixation of fractures, implantation of materials including prosthetic joint and spinal procedures with/without instrumentation) where S epidermidis (including MRSE) or S aureus (including MRSA) are likely
  • Thoracic (noncardiac) where S epidermidis S aureus (including MRSA), streptococci, or gram-negative enteric bacilli are likely

ASHP, IDSA, SHEA, and SIS Recommendations:
15 mg/kg IV once, within 120 minutes before surgery

Uses:
Alternative agent for surgical prophylaxis in patients who have a beta-lactam allergy and are undergoing:
  • Cardiac procedures (e.g., coronary artery bypass, cardiac device insertion, ventricular assist devices)
  • Neurosurgery (e.g., elective craniotomy and cerebrospinal fluid-shunting procedures, implantation of intrathecal pumps)
  • Thoracic procedures (e.g., lobectomy, pneumonectomy, lung resection, thoracotomy, or video-assisted thorascopic surgery)
  • Some orthopedic procedures (e.g., spinal procedures without instrumentation, hip fracture repair)
  • Some urologic procedures (e.g., clean surgery without entry into urinary tract)
  • Heart, lung, and heart-lung transplantation procedures (e.g., heart transplantation, lung and heart-lung transplantation)
  • Clean-contaminated or clean plastic surgery procedures with risk factors

Alternative agent (in combination with an aminoglycoside, aztreonam, or fluoroquinolone) for surgical prophylaxis in patients who have a beta-lactam allergy and are undergoing:
  • Gastroduodenal procedures (e.g., procedures involving entry in to the lumen of the gastrointestinal tract or procedures not entering the GI tract in high-risk patients)
  • Some urologic procedures (e.g., clean surgery involving implanted prosthesis)

Usual Pediatric Dose for Meningitis

AAP Recommendations:
Empiric treatment: 45 to 60 mg/kg/day, given in divided doses via IV every 6 to 8 hours

Infants and Children:
Meningitis: 60 to 70 mg/kg/day, given in divided doses via IV 4 times a day

Uses:

  • Drug of choice for the treatment of life-threatening infections (e.g., septicemia, CNS infections)
  • Drug of choice for the treatment of non-life-threatening infection without signs/symptoms of sepsis when rates of MRSA colonization and infection in the community are substantial.
  • Alternative treatment of MSSA in patients with serious penicillin and cephalosporin allergy
  • Drug of choice (with gentamicin) for the treatment of healthcare-associated, multi-drug resistant MRSA infections and oxacillin MICs of 4 mcg/mL or greater
  • Drug of choice (with gentamicin) for the treatment of community-associated, not multi-drug resistant MRSA infections and oxacillin MICs of 4 mcg/mL or greater
  • Alternative drug for the treatment of community-associated, not multi-drug resistant MRSA infections and oxacillin MICs of 4 mcg/mL or greater
  • Alternative drug (with linezolid with/without gentamicin) for the treatment of VISA infections with MICs of 4 to 16 mcg/mL
  • Alternative drug (with sulfamethoxazole-trimethoprim) for the treatment of VISA infections with MICs of 4 to 16 mcg/mL
  • Treatment of invasive pneumococcal meningitis

IDSA, AAN, AANS, and NCS Recommendations:
60 mg/kg IV per day, given in divided doses every 6 hours
  • Duration of therapy: 2 weeks

Use: Treatment of patients with healthcare-associated ventriculitis and meningitis

Usual Pediatric Dose for CNS Infection

AAP Recommendations:
Empiric treatment: 45 to 60 mg/kg/day, given in divided doses via IV every 6 to 8 hours

Infants and Children:
Meningitis: 60 to 70 mg/kg/day, given in divided doses via IV 4 times a day

Uses:

  • Drug of choice for the treatment of life-threatening infections (e.g., septicemia, CNS infections)
  • Drug of choice for the treatment of non-life-threatening infection without signs/symptoms of sepsis when rates of MRSA colonization and infection in the community are substantial.
  • Alternative treatment of MSSA in patients with serious penicillin and cephalosporin allergy
  • Drug of choice (with gentamicin) for the treatment of healthcare-associated, multi-drug resistant MRSA infections and oxacillin MICs of 4 mcg/mL or greater
  • Drug of choice (with gentamicin) for the treatment of community-associated, not multi-drug resistant MRSA infections and oxacillin MICs of 4 mcg/mL or greater
  • Alternative drug for the treatment of community-associated, not multi-drug resistant MRSA infections and oxacillin MICs of 4 mcg/mL or greater
  • Alternative drug (with linezolid with/without gentamicin) for the treatment of VISA infections with MICs of 4 to 16 mcg/mL
  • Alternative drug (with sulfamethoxazole-trimethoprim) for the treatment of VISA infections with MICs of 4 to 16 mcg/mL
  • Treatment of invasive pneumococcal meningitis

IDSA, AAN, AANS, and NCS Recommendations:
60 mg/kg IV per day, given in divided doses every 6 hours
  • Duration of therapy: 2 weeks

Use: Treatment of patients with healthcare-associated ventriculitis and meningitis

Usual Pediatric Dose for Shunt Infection

IDSA, AAN, AANS, and NCS Recommendations:
Patients with slit ventricles: 5 mg via intraventricular route (plus gentamicin)

Patients with normal-sized ventricles: 10 mg via intraventricular route (plus gentamicin)

Patients with enlarged ventricles: 15 to 20 mg via intraventricular route (plus gentamicin)

Frequency of dosing:

  • External drain output less than 50 mL/day: Every 3 days
  • External drain output 50 to 100 mL/day: Every 2 days
  • External drain output 100 to 150 mL/day: Once a day
  • External drain output 150 to 200 mL/day: Increase the dose by 5 mg (plus gentamicin) and give once a day
  • External drain output 200 to 250 mL/day: Increase the dose by 10 mg (plus gentamicin) and give once a day

Comment: Some experts recommend decreasing the dose by 60% when treating infants to account for lower cerebrospinal fluid volume (compared to adults).

Use: Treatment of healthcare-associated ventriculitis and meningitis in patients who respond poorly to systemic antibiotics

Usual Pediatric Dose for Head Injury

AFIDS, SIS, and IDSA Recommendations:
60 mg/kg, divided and given every 6 to 8 hours

  • Duration of therapy: 5 days OR until cerebrospinal fluid leak is closed, whichever is longer

Use: Antimicrobial prophylaxis for patients with penicillin allergies who have a penetrating brain or spinal cord injury

Renal Dose Adjustments

Mild to moderate renal dysfunction:

  • Initial dose: 15 mg/kg IV ONCE
  • Maintenance dose: The manufacturer product information should be consulted regarding dose adjustments in patients with this level of renal dysfunction.

Severe renal dysfunction and functionally anephric patients:
  • Initial dose: 15 mg/kg IV ONCE
  • Maintenance dose: 1.9 mg/kg IV every 24 hours OR 250 to 1000 mg IV once every several days

Patients with anuria:
  • Initial dose: 15 mg/kg IV ONCE
  • Maintenance dose: 1000 mg IV once every 7 to 10 days

Liver Dose Adjustments

Data not available

Dose Adjustments

Elderly patients: Dosing may be determined based on renal function.

Therapeutic drug monitoring/range: 10 to 20 mcg/mL (trough)

AAP, ASHP, IDSA, PIDS, and SIDP Recommendations:
Patients with suspected/definitive serious MRSA infections: 24-hour AUC level of 400 to 600 mg*hr/L (assuming a drug MIC of 1 mg/L)

Trough levels (1 to 2 hours after dosing):

  • Pediatric patients: Less than 15 mcg/mL
  • Neonates with a MIC 1 mg/L: 10 to 12 mg/L

Obesity:
Children:
  • Loading dose: 20 mg/kg (total body weight) IV ONCE

Adults:
  • Loading dose: 20 to 25 mg/kg (actual body weight) IV ONCE
  • Maintenance dose: Up to 4500 mg IV/day
  • Maximum dose: 3000 mg/dose (loading dose)

Comment: Children may require higher doses; patients may require more frequent therapeutic monitoring.

Precautions

US BOXED WARNINGS:
POTENTIAL RISK OF EXPOSURE TO EXCIPIENTS DURING EARLY PREGNANCY:

  • Some injection formulations contain the excipients polyethylene glycol (PEG 400) and N-acetyl D-alanine (NADA), which resulted in fetal malformations in animal reproduction studies at dose exposures approximately 8 and 32 times (respectively) higher than the exposures at the human equivalent dose.
Recommendation:
  • If use of this drug is needed during the first or second trimester of pregnancy, formulations not containing PEG 400 and NADA should be used.

CONTRAINDICATIONS:
  • Hypersensitivity to the active component or any of the ingredients
  • Use of formulations containing dextrose in patients with a known allergy to corn/corn products

Safety and efficacy of oral capsule formulations have not been established in patients younger than 18 years.

Consult WARNINGS section for additional precautions.

Dialysis

IDSA Recommendations:
Hemodialysis:

  • Empirical dosing for bacterial infections: 20 mg/kg loading dose IV (infused during the last hour of the dialysis session), then 500 mg IV during the last 30 minutes of each subsequent dialysis session

ISPD Recommendations:
Peritoneal Dialysis:
Pediatric patients:
  • High-risk gastrointestinal procedures: 10 mg/kg IV ONCE (Maximum dose: 1 g)

AAP, ASHP, IDSA, PIDS, and SIDP Recommendations:
Adults:
Continuous Renal Replacement Therapy (CRRT):
  • Loading dose: 20 to 25 mg/kg (actual body weight) IV, given at a CRRT rate of 20 to 25 mL/kg/hr
  • Maintenance dose: 7.5 to 10 mg/kg IV every 12 hours

Hybrid Dialysis:
  • Loading dose: 20 to 25 mg/kg (actual body weight) IV ONCE
  • Maintenance dose: 15 mg/kg IV after hemodialysis ends OR during the final 60 to 90 minutes of dialysis

Intermittent Hemodialysis: Patients should have predialysis serum concentration monitoring performed at least once a week

Other Comments

Administration advice:

  • This drug should be infused over at least 1 hour.
  • Lyophilized powder for injection may be mixed and given orally or via nasogastric tube.

Storage requirements:
  • Injection solutions: The manufacturer produce information should be consulted.
  • Lyophilized powder for injection: Vials may be stored in a refrigerator for up to 48 hours once reconstituted.
  • Oral solution: Store in refrigerated conditions (2 to 8C); protect from light and do not freeze.
  • Reconstituted solutions should be discarded after 14 days, if the solution appears hazy, or contains particles.

Reconstitution/preparation techniques:
  • Lyophilized powder for injection: Flavoring syrups may be added to the formulation to improve taste.

IV compatibility: The manufacturer product information should be consulted.

General:
  • Oral formulations are not systemically absorbed, and should be reserved for the treatment of staphylococcal enterocolitis and C difficile-associated diarrhea.
  • Parenteral formulations should not be used intravenously to treat staphylococcal enterocolitis and C difficile-associated diarrhea.
  • Limitations of use: Safety and efficacy of intrathecal (intralumbar/intraventricular) and peritoneal administration have not been established.
  • Some experts state that infusion solutions should not be given via IM injection, as necrosis may occur.

Monitoring:
  • GENERAL: Trough blood levels
  • GENITOURINARY: Periodic urinalysis
  • HEMATOLOGIC: Periodic leukocyte counts, especially in patients receiving concomitant neutropenia-inducing drugs and/or those undergoing prolonged treatment
  • HEPATIC: Periodic liver function tests
  • LOCAL: Localized infusion reactions
  • OTHER: Hearing tests, especially in patients given high doses and/or those over 60 to 65 years of age
  • RENAL: Renal function, especially in patients with renal dysfunction, those given high doses and/or in patients with high troughs

Patient advice:
  • Patients should be advised to avoid missing doses and to complete the entire course of therapy.
  • Patients should be instructed to report signs/symptoms of C difficile (e.g., watery/bloody stools, stomach cramps, fever), for up to 2 months after stopping treatment.

Frequently asked questions

  • Can you drink alcohol while taking vancomycin?
  • What is the difference between Firvanq and the CutisPharma FIRST-Vancomycin Compounding Kit?
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