What is the recommended dosing for clindamycin (clindamycin) in the treatment of Staphylococcus aureus infections?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: December 24, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Clindamycin Dosing for Staphylococcus aureus Infections

For adults with Staphylococcus aureus infections, administer clindamycin 600 mg IV or PO every 8 hours for complicated infections, or 300-450 mg PO every 6-8 hours for uncomplicated skin infections; for children, use 10-13 mg/kg/dose IV every 6-8 hours (maximum 40 mg/kg/day) or 30-40 mg/kg/day PO divided into 3-4 doses. 1

Adult Dosing by Infection Severity

Complicated Infections (Hospitalized Patients)

  • Administer 600 mg IV or PO every 8 hours for complicated skin and soft tissue infections, MRSA pneumonia, osteomyelitis, and septic arthritis 2, 1
  • For severe or life-threatening infections, escalate to 900 mg IV every 6-8 hours 1
  • This higher dosing (600 mg every 8 hours) supersedes FDA labeling and is based on superior clinical outcomes in IDSA guidelines 3, 1

Uncomplicated Outpatient Infections

  • Administer 300-450 mg PO every 6-8 hours (three to four times daily) for uncomplicated purulent cellulitis and simple skin infections 2, 3, 1
  • This regimen provides adequate coverage when combined with appropriate incision and drainage 2

Pediatric Dosing

Intravenous Administration

  • Administer 10-13 mg/kg/dose IV every 6-8 hours, not to exceed 40 mg/kg/day total for complicated skin and soft tissue infections, pneumonia, osteomyelitis, and septic arthritis 2, 3, 1
  • This dosing applies to stable children without ongoing bacteremia or endovascular infection 2, 3

Oral Administration

  • Administer 30-40 mg/kg/day divided into 3-4 doses for MRSA and methicillin-susceptible S. aureus (MSSA) infections 2, 3, 1
  • Transition to oral therapy once clinical improvement is evident and the strain is confirmed susceptible 2

Duration of Therapy

  • 5-10 days for uncomplicated skin and soft tissue infections, with 5 days sufficient if rapid improvement occurs 2, 3
  • 7-14 days for complicated skin and soft tissue infections, with longer duration reserved for slow clinical response 3, 1
  • Minimum 8 weeks for osteomyelitis 3, 1
  • 2-6 weeks for bacteremia and endocarditis, depending on source and presence of metastatic foci 3

Critical Resistance Considerations

Only use clindamycin when local MRSA clindamycin resistance rates are <10% 2, 3, 1. This is a crucial threshold because:

  • Inducible macrolide-lincosamide-streptogramin B (MLS_B) resistance in erythromycin-resistant MRSA strains can lead to treatment failure 1, 4
  • Resistance patterns vary dramatically by region; some areas report constitutive clindamycin resistance rates exceeding 25% 5
  • Against S. aureus isolates with inducible resistance, clindamycin fails to prevent regrowth of resistant phenotypes 4

Important Clinical Caveats

When Clindamycin Should NOT Be Used

  • Do not use for suspected infective endocarditis or endovascular source of infection due to high relapse rates and resistance development 3, 6
  • Avoid in areas with >10% clindamycin resistance rates as this significantly increases treatment failure risk 1
  • Not recommended for S. epidermidis infections (especially septicemia and endocarditis) due to high resistance rates 6

Source Control is Mandatory

  • Incision and drainage is the cornerstone of abscess treatment and may be sufficient alone for simple abscesses 3
  • Antibiotics provide limited benefit without adequate drainage, with 85-90% cure rates achieved with drainage alone 3
  • If no clinical improvement occurs within 48-72 hours, consider inadequate drainage or deeper infection requiring imaging 3

Advantages of Clindamycin

  • Provides dual coverage against both MRSA and β-hemolytic streptococci, making it ideal as monotherapy when both pathogens are suspected 2, 3
  • Excellent penetration and accumulation within leukocytes, potentially valuable for large abscesses 6
  • Particularly useful for mixed staphylococcal and anaerobic infections in skin, subcutaneous tissue, diabetic foot, and bone/joint infections 6

Common Pitfalls to Avoid

  • Never underdose serious infections by using 300 mg doses for complicated infections; always use 600 mg every 8 hours for MRSA and serious infections 3, 1
  • Do not prematurely discontinue treatment; ensure minimum treatment durations are met based on infection type 1
  • Monitor for Clostridium difficile diarrhea, especially in ambulatory long-term treatment of diabetic osteitis and chronic osteomyelitis 6
  • Be aware that clindamycin had lower recurrence rates (2.0%) compared to trimethoprim-sulfamethoxazole (7.1%) at 6-8 weeks in clinical trials 7

References

Guideline

Clindamycin Dosing for Staphylococcus aureus Infections

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Clindamycin Dosing Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Clindamycin resistance among Staphylococcus aureus strains in Israel: implications for empirical treatment of skin and soft tissue infections.

International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases, 2016

Research

Clindamycin as an anti-staphylococcal agent--indications and limitations.

Scandinavian journal of infectious diseases. Supplementum, 1984

Research

A Randomized Trial of Clindamycin Versus Trimethoprim-sulfamethoxazole for Uncomplicated Wound Infection.

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2016

Related Questions

What is the recommended dosage of clindamycin for treating wounds infected with Gram-positive (GP) Staphylococcus and Streptococcus?
What is the recommended dosage of Clindamycin (Clinda) for treating a purulent finger infection, 300mg or 450mg?
Will adding clindamycin (antibiotic) reduce Staphylococcus-induced toxins?
What is an alternate antibiotic for a finger infection in a patient with a penicillin allergy?
What is the follow-up care for a patient with an MRSA (Methicillin-resistant Staphylococcus aureus) abscess after treatment with Bactrim (trimethoprim/sulfamethoxazole) and clindamycin?
Which beta (beta blockers) has the least effect on blood pressure?
What is the recommended dosage and treatment plan for Cotrimixazole (trimethoprim/sulfamethoxazole)?
Is a GI (Gastrointestinal) cocktail contraindicated in an individual with epigastric abdominal pain secondary to an increase in NSAIDs (Non-Steroidal Anti-Inflammatory Drugs) or aspirin?
Can a patient feel pain in a propranolol (propranolol) overdose without significant central nervous system depression?
Is Empagliflozin (Empa) indicated for a patient with well-controlled Hemoglobin A1C (HbA1C) on Mounjaro (Tirzepatide) and complex atherosclerotic disease, hypertension, hypercholesterolemia, structural microvascular dysfunction, and atherosclerotic cardiovascular disease?
What is the best course of treatment for a 29-year-old female patient with borderline personality disorder (BPD), presenting with ongoing suicidal ideation, depressive symptoms, and a history of self-harm, who has previously been treated with Sertraline (selective serotonin reuptake inhibitor (SSRI)) and Wellbutrin (bupropion)?

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.