Available Formulations

Erythromycin is available in multiple formulations to accommodate different clinical needs, patient populations, and routes of administration. Each formulation has unique pharmacokinetic properties affecting absorption, bioavailability, and dosing schedules.

Oral Formulations

Oral Erythromycin Formulations
Erythromycin Base
250mg, 333mg, 500mg tablets (enteric-coated)
Erythromycin Stearate
250mg, 500mg film-coated tablets
Erythromycin Ethylsuccinate
400mg tablets; 200mg/5mL, 400mg/5mL suspension
Erythromycin Estolate
250mg capsules; 125mg/5mL, 250mg/5mL suspension (discontinued in many countries)

Parenteral Formulation

  • Erythromycin Lactobionate: 500mg, 1g powder for IV infusion (reconstitute with sterile water)

Topical Formulations

  • Erythromycin 2% gel: 30g, 60g tubes for acne vulgaris
  • Erythromycin 2% solution: 60mL bottles with applicator pads
  • Erythromycin 2% ointment: 25g tubes for skin infections
  • Combination products: Erythromycin 3% + benzoyl peroxide 5% gel

Ophthalmic Formulation

  • Erythromycin 0.5% ophthalmic ointment: 3.5g tubes for conjunctivitis and neonatal prophylaxis

Adult Dosing Guidelines

Standard Oral Dosing

Indication Base/Stearate Dose Ethylsuccinate Dose Duration
Mild-moderate infections 250–500mg q6h 400–800mg q6h 7–14 days
Severe infections 500mg–1g q6h 800mg–1.6g q6h 10–14 days
Streptococcal pharyngitis 250–500mg q6h 400–800mg q6h 10 days
Pertussis 500mg q6h 800mg q6h 14 days
Chlamydial infections 500mg q6h 800mg q6h 7 days (14 days if pregnant)
Legionella pneumonia 500mg–1g q6h 800mg–1.6g q6h 14–21 days
Primary syphilis 500mg q6h 800mg q6h 14 days
Gastroparesis (off-label) 250mg TID (before meals) N/A Variable

Note: Ethylsuccinate produces lower serum levels; doses are approximately 1.6× those of base/stearate.

Intravenous Dosing

  • Standard dose: 15–20mg/kg/day divided q6h (maximum 4g/day)
  • Severe infections: Up to 4g/day in divided doses
  • Gastroparesis: 200–250mg IV q6–8h (infused over 45–60 minutes)

IV Administration:

  • Reconstitute with sterile water (1g in 20mL)
  • Further dilute in 100–250mL normal saline or D5W
  • Infuse over 20–60 minutes (rapid infusion increases risk of arrhythmias)
  • Maximum concentration: 5mg/mL for peripheral administration

Topical Dosing

  • Acne vulgaris: Apply 2% gel/solution twice daily to affected areas
  • Skin infections: Apply 2% ointment 2–3 times daily
  • Duration: 6–12 weeks for acne; 7–10 days for infections

Ophthalmic Dosing

  • Conjunctivitis: Apply 0.5–1cm ribbon to affected eye(s) 2–8 times daily
  • Prophylaxis (neonates): Single 0.5–1cm ribbon to each eye within 1 hour of birth

Pediatric Dosing

Age-Based Oral Dosing

Age/Weight Base/Stearate Ethylsuccinate Maximum Daily Dose
Neonates (<1 month) 10mg/kg q8–12h Not recommended 50mg/kg/day
Infants (1–12 months) 7.5–12.5mg/kg q6h 12.5–20mg/kg q6h 2g/day
Children (1–12 years) 7.5–12.5mg/kg q6h 12.5–25mg/kg q6h 2g/day
>45kg Use adult dosing 4g/day

Specific Pediatric Indications

  • Pertussis: 40–50mg/kg/day (base) divided q6h × 14 days
  • Pertussis prophylaxis: 40–50mg/kg/day divided q6h × 10 days
  • Chlamydial conjunctivitis/pneumonia: 50mg/kg/day (base) divided q6h × 14 days
  • Streptococcal pharyngitis: 40mg/kg/day divided q6–8h × 10 days

Administration Guidelines

Food Interactions by Formulation

Administration with Food
Base (enteric-coated)
Take 1 hour before or 2 hours after meals
Stearate
Take on empty stomach; food reduces absorption by 30–50%
Ethylsuccinate
May take with or without food; better tolerated with food
Estolate
May take with food to reduce GI upset

Important Administration Notes

  • Do not crush or chew enteric-coated tablets
  • Shake suspensions well before measuring dose
  • Use calibrated measuring device for liquid formulations
  • Store reconstituted suspension at room temperature; discard after 10 days
  • Separate from antacids by at least 2 hours
  • Complete full course even if symptoms improve

Dose Adjustments

Renal Impairment

No adjustment needed for mild-moderate impairment (CrCl >10 mL/min). In severe impairment or dialysis:

  • Consider 50–75% of normal dose
  • Maximum 1.5g/day in severe renal failure
  • Not removed by hemodialysis or peritoneal dialysis

Hepatic Impairment

  • Use with caution; erythromycin is hepatically metabolized
  • Avoid estolate formulation (increased hepatotoxicity risk)
  • Monitor liver function tests
  • Consider dose reduction in severe cirrhosis

Elderly Patients

  • No routine dose adjustment needed
  • Increased risk of ototoxicity with high doses
  • Monitor for QT prolongation
  • Consider drug interactions with concurrent medications

Special Populations

Pregnancy

  • FDA Category B (except estolate: contraindicated)
  • Preferred macrolide in pregnancy
  • Treatment of choice for chlamydial infections in pregnancy
  • Use standard adult doses

Lactation

  • Excreted in breast milk (small amounts)
  • Generally considered compatible with breastfeeding
  • Monitor infant for diarrhea, thrush
  • Alternative feeding method if infant develops adverse effects

Obesity

  • Use actual body weight for dosing
  • Maximum doses still apply
  • Consider IV route for severe infections (better tissue penetration)

Therapeutic Monitoring

Clinical Response

  • Improvement typically seen within 48–72 hours
  • Complete course even if symptoms resolve
  • Consider alternative therapy if no improvement by day 3

Laboratory Monitoring

  • Baseline liver function tests for prolonged therapy
  • Monitor INR if on warfarin (significant interaction)
  • Consider ECG if risk factors for QT prolongation
  • Culture and sensitivity for treatment failures

Missed Doses

Patient counseling for missed doses:

  • Take missed dose as soon as remembered
  • Skip if almost time for next dose
  • Do not double doses
  • Maintain regular dosing schedule
  • Set reminders for multiple daily doses

Storage Requirements

Storage Conditions
Tablets/Capsules
Room temperature (20–25°C); protect from moisture
Oral Suspension
Room temperature; discard 10 days after reconstitution
IV Powder
Room temperature; use within 8 hours of reconstitution
Topical Products
Room temperature; avoid freezing
Ophthalmic Ointment
Room temperature; discard 6 weeks after opening