ERYTHROMYCIN LACTOBIONATE
Erythromycin DBL
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Reviewed by Dr
Carl Kuschel and Dorothy Cooper
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| September 1998
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Dose and Administration
- IV infusion by syringe pump over 60 minutes.
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Dose |
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Preterm neonates:
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10 mg/kg/dose 6 hourly
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Term neonates: ≤7 days:
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10-20 mg/kg/dose 12 hourly
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Term neonates: >7 days:
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10-20 mg/kg/dose 8 hourly
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Infants:
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10-20 mg/kg/dose 6-8 hourly
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Indications
- Suspected/proven infection with Mycoplasma pneumoniae, Ureaplasma urealyticum, and
Chlamydia trachomatis.
- As a substitute for penicillin in situations of significant hypersensitivity to penicillin.
- Treatment for and prophylaxis against Bordetella pertussis.
Contraindications and Precautions
- Known hypersensitivity to erythromycin or other macrolides.
- Infants with biliary tract obstruction.
- Caution in preterm infants, especially extreme immaturity.
- Caution in infants with jaundice, liver dysfunction, and biliary tract disease.
Interactions
- Increase serum digoxin levels.
- Midazolam: increases effect.
- Theophylline decreases
erythromycin blood levels and increases theophylline toxicity. Effect on half
life of caffeine has not been clarified.
- Never give erythromycin to a baby receiving cisapride because there is a risk of arrhythmia.
Clinical Pharmacology
Bacteriostatic antibiotic which
suppresses bacterial protein synthesis. The antibacterial spectrum is similar to
penicillin but extended to include Mycoplasma pneumoniae, Ureaplasma urealyticum
and Chlamydia trachomatis.
Vd 45% of body weight in adults.
Antibacterial levels are achievable in all tissues except brain and CSF. Highly
bound (64-98%) to human plasma protein. Hepatic excretion into bile as active
compound. Only 5-15% of administered dose excreted in the active form in the
urine. Plasma half life equals 2-4 hours.
Possible Adverse Effects
- Venous irritation, soft tissue injury at IV injection site.
- Pain, soft tissue injury at IM injection site. Not suitable for IM administration.
- Gastrointestinal disturbances (nausea, vomiting, diarrhoea).
- Jaundice, intrahepatic cholestasis.
- Reversible hearing loss (very high doses).
- Hypersensitivity reactions (urticaria, mild skin eruptions, anaphylaxis) rare.
- Sudden severe bradycardia after IV
administration. Prolongation of QT interval and ventricular arrhythmias with
rapid IV administration.
Special Considerations
- May antagonise action of penicillins, cephalosporins.
- Concurrent use with theophylline, phenytoin, carbamapezine, or
digoxin may be associated with elevation in serum
levels of these drugs. The dose of these drugs should be reduced in infants and
serum concentrations monitored closely.
- Reduce dose of erythromycin if severe jaundice and/or hepatic dysfunction.