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Update sections 2, 4.1, 4.4, 4.5, 5.1, 6.4 and 10 as noted below in bold following renewal of licence.
2. Qualitative and Quantitative Composition Erythromycin (as erythromycin ethylsuccinate) 250 mg per 5 ml Excipients - contains sorbital (E420) 1176 mg/5ml, Sodium methylhydroxybenzoate (E219) 5mg/5ml and Sodium propylhydroxybenzoate (E217) 1mg/5ml. This medicinal product contains 4.21 mg of sodium per ml of suspension (equates to 21.05mg/5ml dose). For a full list of excipients, see section 6.1. 4.1 Therapeutic Indications Erythromycin is indicated for the treatment of infections caused by erythromycin sensitive organisms. Consideration should be given to official guidance on the appropriate use of antibacterial agents. 4.4 Special warnings and precautions for use Erythromycin is excreted principally by the liver, so caution should be exercised in administering the antibiotic to patients with impaired hepatic function or concomitantly receiving potentially hepatotoxic agents. Hepatic dysfunction including increased liver enzymes and hepatocellular and/or cholestatic hepatitis, with or without jaundice, has been infrequently reported with erythromycin. The use of erythromycin in patients concurrently taking drugs metabolised by the cytochrome P450 system may be associated with elevations in serum levels of these drugs (see sections 4.5). Serum concentrations should be closely monitored in patients receiving erythromycin. Prolonged or repeated use of erythromycin may result in overgrowth of non-susceptible bacteria. If super-infection occurs, erythromycin should be discontinued and appropriate therapy instituted. There have been reports of infantile hypertrophic pyloric stenosis (IHPS) occurring in infants following erythromycin therapy. In one cohort of 157 newborns who were given erythromycin for pertussis prophylaxis, seven neonates (5%) developed symptoms of non-bilious, vomiting or irritability with feeding and were subsequently diagnosed as having IHPS requiring surgical pyloromyotomy. Since erythromycin may be used in the treatment of conditions in infants which are associated with significant mortality or morbidity (such as pertussis or chlamydia), the benefit of erythromycin therapy needs to be carefully considered against the potential risk of developing IHPS. Parents should be informed to contact their physician if vomiting or irritability occur. There have been reports suggesting erythromycin does not reach the foetus in adequate concentrations to prevent congenital syphilis. Infants born to women treated during pregnancy with oral erythromycin for early syphilis should be treated with an appropriate penicillin regimen. As with other broad spectrum antibiotics, pseudomembranous colitis has been reported rarely with erythromycin (see section 4.8). Rhabdomyolysis with or without renal impairment has been reported in seriously ill patients receiving erythromycin concomitantly with lovastatin (see section 4.5). There have been reports that erythromycin may aggravate the weakness of patients with myasthenia gravis. Colchicine toxicity has been reported in patients receiving erythromycin concomitantly with colchicines (see section 4.5). Laboratory Tests: Erythromycin interferes with the fluorometric determination of urinary catecholamines. Contains sorbital (E420). Patients with rare hereditary problems of fructose intolerance should not take this medicine. Contains parahydroxybenzoates which may cause allergic reactions (possibly delayed). This medicinal product contains 4.21 mg of sodium per ml of suspension (equates to 21.05 mg/5ml dose). This needs to be taken into consideration when prescribing for patients on a sodium-restricted diet. 4.5 Interactions with other medicinal products and other forms of interaction Erythromycin significantly alters the metabolism of terfenadine and astemizole when taken concomitantly. Rare cases of serious cardiovascular adverse events, including cardiac arrest, Torsade de Pointes, and other ventricular arrhythmias, and also, in the case of terfenadine, death, have been observed. Elevated cisapride levels have been reported in patients receiving erythromycin concomitantly. This may result in QT prolongation and cardiac arrhythmias including ventricular tachycardia, ventricular fibrillation and Torsade de Pointes. Similar effects have been observed with concomitant administration of pimozide and other macrolide antibiotics, e.g. clarithromycin. Post-marketing reports indicate that c-administration of erythromycin with ergotamine or dihydroergotamine has been associated with acute ergot toxicity characterised by vasospasm and ischemia of the extremities and other tissues including the central nervous system (see section 4.3). The concomitant use of the above drugs with erythromycin is contraindicated (see 4.3 Contraindications). Concurrent use of erythromycin and high doses of theophylline may be associated with an increase in serum theophylline levels and potential theophylline toxicity. In case of theophylline toxicity and/or elevated serum theophylline levels, the dose of theophylline should be reduced while the patient is receiving erythromycin therapy. When oral erythromycin is given concurrently with theophylline, there is also a significant decrease in erythromycin serum concentrations. The decrease could result in subtherapeutic concentrations of erythromycin. The use of erythromycin in patients who are receiving digoxin may result in potentiation of the effects of digoxin due to reduction in the rate of excretion. Monitoring of serum digoxin levels should be considered. Rhabdomyolysis with or without renal impairment has been reported in seriously ill patients receiving erythromycin concomitantly with lovastatin. Erythromycin is an inhibitor of CYP 3A4. The use of erythromycin in patients concurrently taking drugs metabolised by the cytochrome P450 system may be associated with elevations in serum levels of these other drugs. There have been reports of interactions of erythromycin with astemizole, carbamazepine, cyclosporin, hexabarbital, phenytoin, alfentanil, disopyramide, bromocryptine, valproate, tacrolimus, quinidine, cilostazol, methylprednisolone, rifabutin, sildenafil, vinblastine, terfenadine. Serum concentrations of drugs metabolised by the cytochrome P450 system should be monitored closely in patients concurrently receiving erythromycin. Triazolobenzodiazepines (such as triazolam and alprazolam) and related benzodiazepines: Erythromycin has been reported to decrease the clearance of trizolam, midazolum and zopiclone and thus may increase pharmacologic effect of these benzodiazepines. HMG-CoA Reductase Inhibitors: Erythromycin has been reported to increase concentrations of HMG-CoA reductase inhibitors (e.g. lovastatin and simvastatin). Rare reports of rhabdomyolysis have been reported in patients taking these drugs concomitantly (see section 4.4). There have been reported of increased anticoagulant effects when erythromycin and oral anticoagulants were used concomitantly. There have been post-marketing reports of colchicines toxicity with concomitant use of erythromycin and colchicines (see section 4.4). 5.1 Pharmacodynamic properties ATC Code: J0IFA Pharmacotherapeutic group: Macrolides Erythromycin ethylsuccinate is less susceptible than erythromycin to the adverse effect of gastric acid. It is absorbed from the small intestine. It is widely distributed throughout body tissues. Little metabolism occurs and only about 5% is excreted in the urine. It is excreted principally by the liver. 6.4 Special Precautions for Storage Do not store above 25°C. Keep the bottle tightly closed. 10. Date of (Partial) Revision of the Text September 2010
Erythromycin (as erythromycin ethylsuccinate) 250 mg per 5 ml
Excipients - contains sorbital (E420) 1176 mg/5ml, Sodium methylhydroxybenzoate (E219) 5mg/5ml and Sodium propylhydroxybenzoate (E217) 1mg/5ml. This medicinal product contains 4.21 mg of sodium per ml of suspension (equates to 21.05mg/5ml dose).
For a full list of excipients, see section 6.1.
4.1 Therapeutic Indications
Erythromycin is indicated for the treatment of infections caused by erythromycin sensitive organisms. Consideration should be given to official guidance on the appropriate use of antibacterial agents.
4.4 Special warnings and precautions for use
Erythromycin is excreted principally by the liver, so caution should be exercised in administering the antibiotic to patients with impaired hepatic function or concomitantly receiving potentially hepatotoxic agents. Hepatic dysfunction including increased liver enzymes and hepatocellular and/or cholestatic hepatitis, with or without jaundice, has been infrequently reported with erythromycin.
The use of erythromycin in patients concurrently taking drugs metabolised by the cytochrome P450 system may be associated with elevations in serum levels of these drugs (see sections 4.5). Serum concentrations should be closely monitored in patients receiving erythromycin.
Prolonged or repeated use of erythromycin may result in overgrowth of non-susceptible bacteria. If super-infection occurs, erythromycin should be discontinued and appropriate therapy instituted.
There have been reports of infantile hypertrophic pyloric stenosis (IHPS) occurring in infants following erythromycin therapy. In one cohort of 157 newborns who were given erythromycin for pertussis prophylaxis, seven neonates (5%) developed symptoms of non-bilious, vomiting or irritability with feeding and were subsequently diagnosed as having IHPS requiring surgical pyloromyotomy. Since erythromycin may be used in the treatment of conditions in infants which are associated with significant mortality or morbidity (such as pertussis or chlamydia), the benefit of erythromycin therapy needs to be carefully considered against the potential risk of developing IHPS. Parents should be informed to contact their physician if vomiting or irritability occur.
There have been reports suggesting erythromycin does not reach the foetus in adequate concentrations to prevent congenital syphilis. Infants born to women treated during pregnancy with oral erythromycin for early syphilis should be treated with an appropriate penicillin regimen.
As with other broad spectrum antibiotics, pseudomembranous colitis has been reported rarely with erythromycin (see section 4.8).
Rhabdomyolysis with or without renal impairment has been reported in seriously ill patients receiving erythromycin concomitantly with lovastatin (see section 4.5).
There have been reports that erythromycin may aggravate the weakness of patients with myasthenia gravis.
Colchicine toxicity has been reported in patients receiving erythromycin concomitantly with colchicines (see section 4.5).
Laboratory Tests:
Erythromycin interferes with the fluorometric determination of urinary catecholamines.
Contains sorbital (E420). Patients with rare hereditary problems of fructose intolerance should not take this medicine. Contains parahydroxybenzoates which may cause allergic reactions (possibly delayed).
This medicinal product contains 4.21 mg of sodium per ml of suspension (equates to 21.05 mg/5ml dose). This needs to be taken into consideration when prescribing for patients on a sodium-restricted diet.
4.5 Interactions with other medicinal products and other forms of interaction
Erythromycin significantly alters the metabolism of terfenadine and astemizole when taken concomitantly. Rare cases of serious cardiovascular adverse events, including cardiac arrest, Torsade de Pointes, and other ventricular arrhythmias, and also, in the case of terfenadine, death, have been observed. Elevated cisapride levels have been reported in patients receiving erythromycin concomitantly. This may result in QT prolongation and cardiac arrhythmias including ventricular tachycardia, ventricular fibrillation and Torsade de Pointes. Similar effects have been observed with concomitant administration of pimozide and other macrolide antibiotics, e.g. clarithromycin.
Post-marketing reports indicate that c-administration of erythromycin with ergotamine or dihydroergotamine has been associated with acute ergot toxicity characterised by vasospasm and ischemia of the extremities and other tissues including the central nervous system (see section 4.3).
The concomitant use of the above drugs with erythromycin is contraindicated (see 4.3 Contraindications).
Concurrent use of erythromycin and high doses of theophylline may be associated with an increase in serum theophylline levels and potential theophylline toxicity. In case of theophylline toxicity and/or elevated serum theophylline levels, the dose of theophylline should be reduced while the patient is receiving erythromycin therapy.
When oral erythromycin is given concurrently with theophylline, there is also a significant decrease in erythromycin serum concentrations. The decrease could result in subtherapeutic concentrations of erythromycin.
The use of erythromycin in patients who are receiving digoxin may result in potentiation of the effects of digoxin due to reduction in the rate of excretion. Monitoring of serum digoxin levels should be considered.
Rhabdomyolysis with or without renal impairment has been reported in seriously ill patients receiving erythromycin concomitantly with lovastatin.
Erythromycin is an inhibitor of CYP 3A4. The use of erythromycin in patients concurrently taking drugs metabolised by the cytochrome P450 system may be associated with elevations in serum levels of these other drugs. There have been reports of interactions of erythromycin with astemizole, carbamazepine, cyclosporin, hexabarbital, phenytoin, alfentanil, disopyramide, bromocryptine, valproate, tacrolimus, quinidine, cilostazol, methylprednisolone, rifabutin, sildenafil, vinblastine, terfenadine.
Serum concentrations of drugs metabolised by the cytochrome P450 system should be monitored closely in patients concurrently receiving erythromycin.
Triazolobenzodiazepines (such as triazolam and alprazolam) and related benzodiazepines: Erythromycin has been reported to decrease the clearance of trizolam, midazolum and zopiclone and thus may increase pharmacologic effect of these benzodiazepines.
HMG-CoA Reductase Inhibitors: Erythromycin has been reported to increase concentrations of HMG-CoA reductase inhibitors (e.g. lovastatin and simvastatin). Rare reports of rhabdomyolysis have been reported in patients taking these drugs concomitantly (see section 4.4).
There have been reported of increased anticoagulant effects when erythromycin and oral anticoagulants were used concomitantly.
There have been post-marketing reports of colchicines toxicity with concomitant use of erythromycin and colchicines (see section 4.4).
5.1 Pharmacodynamic properties
ATC Code: J0IFA
Pharmacotherapeutic group: Macrolides
Erythromycin ethylsuccinate is less susceptible than erythromycin to the adverse effect of gastric acid. It is absorbed from the small intestine. It is widely distributed throughout body tissues. Little metabolism occurs and only about 5% is excreted in the urine. It is excreted principally by the liver.
6.4 Special Precautions for Storage
Do not store above 25°C. Keep the bottle tightly closed.
September 2010