Clindamycin
General
- Type: Other antibiotic
- Dosage Forms: IM, IV, PO (75mg; 150mg; 300mg; 75mg/5mL)
- Common Trade Names: Cleocin
Adult Dosing
General
- PO:
- 150-450mg PO q6h
- First Dose: 150-450mg PO x 1
- Max: 450mg/dose PO (increased risk of C. diff at higher doses)
- IM:
- 1200-2700mg/day IM divided q6-12h
- First Dose: 600mg IM x 1
- Max: 600mg/dose IM
- IV
- 1200-2700mg/day IV divided q6-12h
- First Dose: 600-900mg IV x 1
- 4800mg/day IV
Cellulitis Possibly due to MRSA (Unlabled Use)[1]
- 60-120 kg: 300 mg Q8H. >120kg: 450 mg Q8H. [2]
Strep. Pharyngitis
- 300mg PO q8 x 10 days[3]
Bacterial Vaginosis
- Clindamycin 300mg PO BID x 7 days
PID
- PO (Mild-mod)
- 450mg PO q6h x 14 days
- Use with ceftriaxone or cefoxitin/probenecid if no proceeding IV treatment
- IV (Severe)
- 900mg IV q8
- Use with gentamicin and switch to PO after 24h of clinical improvement
Babesiosis
- Clindamycin 600mg PO q8hrs x 7-10 days (or 300-600mg IV q6hrs)
- Give with Quinine 650mg TID
Indications by Disease
| Disease | Dose | Context |
|---|---|---|
| Acute necrotizing ulcerative gingivitis | 300mg PO three times daily | Uncomplicated |
| Acute tetanus | 600mg IV (7.5mg/kg) q6hrs | Active tetanus alt |
| Anthrax | 900mg IV q8hrs | Inhalation/cutaneous with systemic illness; combined with Ciprofloxacin or Doxycycline |
| Babesiosis | 600mg PO q8hrs x 7-10 days (or 300-600mg IV q6hrs) | Severe parasitemia over 4 percent with Quinine |
| Bacterial vaginosis | 300 mg PO BID for 7 days | Alternative |
| Bacterial vaginosis | cream 2%, one full applicator (5 g) intravaginally Nightly for 7 days | First Line, Topical |
| Cellulitis | 600mg IV q8hrs | Inpatient |
| Cellulitis | 450mg PO TID | Outpatient |
| Dental abscess | 450 mg PO q8 hours x 7-14 days | Outpatient |
| Diabetic foot infection | 450mg PO q8hrs daily x 14 days | Mild DFI |
| Diabetic foot infection | 450mg PO q8hrs | Moderate DFI |
| Endocarditis | 600mg (20mg/kg) PO or IV | Dental Procedure Prophylaxis |
| Erysipelas | 450mg (5mg/kg) PO q8hrs x 10 days | PCN Allergic |
| Felon | 450mg PO q8hrs x 7 days | Outpatient |
| Impetigo | 450mg PO q8hrs (or 10mg/kg PO q6hrs) x 10 days | Oral therapy |
| Ludwig's angina | 600 mg IV q6 hrs | Immunocompetent, Penicillin allergy |
| Mammalian bites | 450mg (5mg/kg) PO q8hrs x 7 days | Human bites alt |
| Mammalian bites | 600mg IV q8hrs | Severe mammalian bite infection alt |
| Mammalian bites | 450mg (5mg/kg) PO q8hrs x 7 days | Cat and dog bites alt |
| Mastitis | 450mg PO q8hrs | Also provides MRSA coverage |
| Mastoiditis | 600mg IV q8 hours | Empiric |
| Neutropenic fever | 450mg PO q8hrs | Outpatient alt with Ciprofloxacin |
| Open fracture | 900 mg IV (immediately and q8 hours x 3 total doses) | Grade I & II, Cephalosporin allergy |
| Pelvic inflammatory disease | 900mg IV q8hr | Inpatient alternative; combined with Gentamicin |
| Periorbital cellulitis | 300mg Q8H | Outpatient |
| Peritonsillar abscess | 300mg PO Q6hrs x7-10d | Outpatient |
| Peritonsillar abscess | 600-900mg IV TID | Inpatient |
| Pneumocystis jirovecii pneumonia | 900mg IV q8hrs | Severe disease with Primaquine |
| Pneumocystis jirovecii pneumonia | 450mg PO q8hrs | Mild disease with Primaquine |
| Pneumonia (main) | 600mg IV | ICU, Low Risk (PCN allergy) |
| Postpartum endometritis | 900mg IV q8hrs | Preferred first line; <48hrs postpartum |
| Septic bursitis | 600 mg IV three times daily | Inpatient |
| Septic bursitis | 300 mg PO three times daily x 14 days | Outpatient |
| Streptococcal pharyngitis | 7 mg/kg/dose TID (maximum = 300 mg/dose) x 10 days | Penicillin Allergy (anaphylaxis) |
| Suppurative parotitis | 450mg PO three times daily | Outpatient |
| Toxoplasmosis | 600mg PO or IV q6hrs | Immunosuppressed alt |
Pediatric Dosing
General Infection (Severe)
- <1 week old
- <2kg
- 10mg/kg/day IM/IV divided q12
- First Dose: 5mg/kg IM/IV x 1
- >2kg
- 15mg/kg/day IM/IV divided q8h
- First Dose: 5mg/kg IM/IV x 1
- <2kg
- 1 week - 1 month
- <1.2kg
- 10mg/kg/day IM/IV divided q12h
- First Dose: 5mg/kg IM/IV x 1
- 1.2-2kg
- 15mg/kg/day IM/IV divided q8h
- First Dose: 5mg/kg IM/IV x 1
- >2kg
- 20mg/kg/day IM/IV divided q6-8h
- Alt: 30mg/kg/day IM/IV divided q6h
- First Dose: 5-7.5mg/kg IM/IV x 1
- <1.2kg
- >1 Month - Children
- 25-40mg/kg/day IM/IV divided q6-8h
- First Dose: 6.25-13.3mg/kg IM/IV x 1
- Max: 4.8 g/day IM/IV
- Adolescents
- 25-40mg/kg/day IM/IV divided q6-8h
- First Dose: 6.25-13.3mg/kg IM/IV x 1
- Max: 4.8 g/day IM/IV
General Infection (Mild-Moderate)
- Infants & Children
- PO:
- 10-25mg/kg/day PO divided q6-8h
- First Dose: 2.5-8.3mg/kg PO x 1
- Max: 1.8 g/day PO
- IM/IV:
- 15-25mg/kg/day IM/IV divided q6-8
- First Dose: 3.75-8.3mg/kg IM/IV x 1
- 4.8 g/day IM/IV
- PO:
- Adolescents
- PO:
- 150-300mg PO q6h
- First Dose: 150-300mg PO x 1
- Max: 1.8 g/day PO
- IM/IV:
- 25-40mg/kg/day IM/IV divided q6-8h
- First Dose: 6.25-13.3mg/kg IM/IV x 1
- Max: 4.8 g/day IM/IV
- PO:
Cellulitis Possibly due to MRSA (Unlabeled Use)[4]
- 10-13mg/kg/dose q6-8hrs PO x 5-10 days
- First Dose: 2.5-4.3mg/kg PO x 1
- Max: 40mg/kg/day
Otitis Media, Acute
- 2mo-5yo
- 30-40mg/kg/day PO divided q8h x 10 days
- 6-12yo
- 30-40mg/kg/day PO divided q8h x 5-10 days
Sinusitis
- 30-40mg/kg/day PO divided q8h x 10-14 days
- Use with cefixime or cefpodoxime
Streptococcal Pharyngitis
- 7mg/kg/dose PO q8h x 10 days[5]
- Max: 300mg/dose
Community-Acquired Pneumonia (>3mo)
- IV (Mod-Severe): 40mg/kg/day IV divided q6-8h x 10-14 days
- PO (Mild): 30-40mg/kg/day PO divided q6-8h x 7-10 days
Babesiosis
- 20-40mg/kg/day PO/IV divided q6-8h x 7-10 days
- Max: 600mg/dose
- Info: Use with quinine
Indications by Disease
| Disease | Dose | Context |
|---|---|---|
| Acute otitis media | 10mg/kg PO three times daily | Penicillin Allergy |
| Acute tetanus | 10-13mg/kg IV q8hrs (max 900mg/dose) | Pediatric Active tetanus alt |
| Anthrax | 7.5mg/kg q6hrs | Pediatric; combined with Ciprofloxacin or Doxycycline |
| Babesiosis | 20-40mg/kg/day PO divided TID x 7-10 days (max 600mg/dose) | Pediatric, with Quinine |
| Cellulitis | 30-40mg/kg/day PO divided TID (max 1.8g/day) | Pediatric Outpatient |
| Cellulitis | 10-13mg/kg IV q8hrs (max 900mg/dose) | Pediatric Inpatient |
| Dental abscess | 30mg/kg/day PO divided TID x 7-10 days (max 1.8g/day) | Pediatric Outpatient |
| Endocarditis | 20mg/kg PO or IV (max 600mg) | Pediatric Dental Prophylaxis, PCN Allergy |
| Erysipelas | 30mg/kg/day PO divided TID x 10 days (max 1.8g/day) | Pediatric PCN Allergy |
| Impetigo | 30mg/kg/day PO divided TID (max 1.8g/day) | Pediatric Oral, MRSA |
| Infectious tenosynovitis | 10mg/kg IV four times daily | Pediatrics |
| Ludwig's angina | 10-13mg/kg IV q8hrs (max 900mg/dose) | Pediatric PCN Allergy |
| Mammalian bites | 30mg/kg/day PO divided TID (max 1.8g/day) | Pediatric PCN allergy |
| Mammalian bites | 30mg/kg/day PO divided TID (max 1.8g/day) | Pediatric Human bites alt |
| Mastoiditis | 10-13mg/kg IV q8hrs (max 900mg/dose) | Pediatric |
| Open fracture | 10mg/kg IV (max 900mg) immediately then q8hrs x 3 doses | Pediatric Grade I & II, allergy |
| Osteomyelitis | 10mg/kg IV PO four times daily | Sickle Cell Disease |
| Periorbital cellulitis | 30 to 40 mg/kg per day in three to four equally divided doses, maximum 1.8 grams per day | Outpatient |
| Peritonsillar abscess | 30-40mg/kg/day PO divided TID (max 1.8g/day) | Pediatric Outpatient |
| Peritonsillar abscess | 10-13mg/kg IV q8hrs (max 900mg/dose) | Pediatric Inpatient |
| Pharyngitis | 7mg/kg/dose PO q8h x 10 days'"`UNIQ--ref-0000003E-QINU`"'; Max: 300mg/dose | Streptococcal Pharyngitis |
| Septic bursitis | 10mg/kg IV three times daily | Inpatient |
| Sinusitis | 30-40mg/kg/day PO divided q8h x 10-14 days; Use with cefixime or cefpodoxime | Sinusitis |
| Streptococcal pharyngitis | 7mg/kg/dose PO TID x 10 days (max 300mg/dose) | Pediatric PCN Allergy (severe) |
| Suppurative parotitis | 10mg/kg PO four times daily | Outpatient |
| Toxoplasmosis | 20-30mg/kg/day PO/IV divided q6hrs (max 2.4g/day) | Pediatric Sulfa Allergy alt |
Special Populations
- Pregnancy Rating: B
- Lactation risk categories: L4; enters breast milk/not recommended
- Renal Dosing (Adult & Pediatric)
- No adjustment
- No supplement for hemodialysis or peritoneal dialysis
- Hepatic Dosing (Adult & Pediatric)
- No adjustment
- Geriatric: See adult dosing
Contraindications
Black Box
- High risk for C. difficile associated diarrhea
- Reserve for serious infections where there is not alternative
- Discontinue immediately if significant diarrhea, abdominal cramps, or passage of blood or mucus with use
General
- Allergy to class/drug
- Ulcerative colitis
Adverse Reactions
Serious
- C. difficile associated diarrhea
- Thrombocytopenia
- Anaphylaxis
- Stevens-Johnson Syndrome
- Granulocytopenia
- Esophagitis
Common
- Diarrhea
- Nausea and Vomiting
- Abdominal Pain
- Rash
- Puritis
- Jaundice
- Urticaria
- Hypotension
- Thrombophlebitis (IV use)
Pharmacology
- Half-life: 2.4-3h
- Metabolism: Liver; CYP450
- Excretion: Urine, feces
- Mechanism of Action: Bacteriostatic or bactericidal, depending on bug/concentration
Administration
- PO:
- Give with full glass of water (minimize esophageal ulceration)
- Give spread around the day to promote constant serum levels
- IM:
- Give to deep I.M. sites
- Rotate sites
- Do not exceed 600mg per injection
- IV:
- Do NOT give as bolus
- Give by intermittent infusion over >10-60 minutes
- Max rate: 30mg/minute (do not exceed 1200mg/hour)
- Final concentration should not exceed 18mg/mL
Mechanism of Action
- Disrupts protein synthesis by binding the 50s ribosome subunit
Antibiotic Sensitivities[6]
Key
- S susceptible/sensitive (usually)
- I intermediate (variably susceptible/resistant)
- R resistant (or not effective clinically)
- S+ synergistic with cell wall antibiotics
- U sensitive for UTI only (non systemic infection)
- X1 no data
- X2 active in vitro, but not used clinically
- X3 active in vitro, but not clinically effective for Group A strep pharyngitis or infections due to E. faecalis
- X4 active in vitro, but not clinically effective for strep pneumonia
See Also
References
- ↑ Liu C, Bayer A, Cosgrove SE, et al, “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, 2011, 52(3):285-92. PubMed 21217178
- ↑ Reduction of Inappropriate Antibiotic Use and Improved Outcomes by Implementation of an Algorithm-Based Clinical Guideline for Nonpurulent Skin and Soft Tissue Infections. Ann Emerg Med. 2020 Feb 13. pii: S0196-0644(19)31453-2. doi: 10.1016/j.annemergmed.2019.12.012. [Epub ahead of print]
- ↑ CDC Website, accessed 2026-28-01. https://www.cdc.gov/group-a-strep/hcp/clinical-guidance/strep-throat.html
- ↑ Liu C, Bayer A, Cosgrove SE, et al, “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, 2011, 52(3):285-92. PubMed 21217178
- ↑ CDC Website, accessed 2026-28-01. https://www.cdc.gov/group-a-strep/hcp/clinical-guidance/strep-throat.html
- ↑ Sanford Guide to Antimicrobial Therapy 2014
