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Erythrocin Lactobionate Side Effects Center
Medical Editor: John P. Cunha, DO, FACOEP
Erythromycin Lactobionate I.V. is an antibiotic used to treat various types of infections. This medication is available in generic form. Common side effects include nausea, vomiting, diarrhea/loose stools, stomach pain, or pain/redness at the injection site.
For the treatment of severe infections in adults and pediatric patients, the recommended intravenous dose of erythromycin lactobionate is 15 to 20 mg/kg/day. Higher doses, up to 4 g/day, may be given for severe infections. Erythromycin lactobionate may interact with theophylline, carbamazepine, digoxin, oral anticoagulants, antihistamines, cyclosporine, hexobarbital, phenytoin, alfentanil, disopyramide, lovastatin, bromocriptine, valproate, terfenadine, and astemizole. Tell your doctor all medications and supplements you use. During pregnancy, erythromycin lactobionate should be used only if prescribed. Erythromycin lactobionate passes into breast milk. Nursing women should exercise caution. Consult your doctor before breastfeeding.
Our Erythromycin Lactobionate I.V. Side Effects Drug Center provides a comprehensive view of available drug information on the potential side effects when taking this medication.
This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
What is Prescribing information?
The FDA package insert formatted in easy-to-find categories for health professionals and clinicians.
Erythrocin Lactobionate FDA Prescribing Information: Side Effects
Erythromycin diffuses readily into most body fluids. In the absence of meningeal inflammation, low concentrations are normally achieved in the spinal fluid but the passage of the drug across the blood-brain barrier increases in meningitis. Erythromycin crosses the placental barrier and is excreted in breast milk. Erythromycin is not removed by peritoneal dialysis or hemodialysis.
In the presence of normal hepatic function, erythromycin is concentrated in the liver and is excreted in the bile; the effect of hepatic dysfunction on biliary excretion of erythromycin is not known. From 12 to 15 percent of intravenously administered erythromycin is excreted in active form in the urine.
Intravenous infusion of 500 mg of erythromycin lactobionate at a constant rate over 1 hour in fasting adults produced a mean serum erythromycin level of approximately 7 mcg/mL at 20 minutes, 10 mcg/mL at 1 hour, 2.6 mcg/mL at 2.5 hours, and 1 mcg/mL at 6 hours.
Mechanism of Action
Erythromycin acts by inhibition of protein synthesis by binding 50 S ribosomal subunits of susceptible organisms. It does not affect nucleic acid synthesis.
Interactions with Other Antibiotics
Antagonism has been demonstrated in vitro between erythromycin and clindamycin, lincomycin and chloramphenicol.
Many strains of Haemophilus influenzae are resistant to erythromycin, but are susceptible to erythromycin and sulfonamides used concomitantly.
Development of Resistance
Resistance to erythromycin in S. aureus may emerge during therapy.
Erythromycin has been shown to be active against most strains of the following organisms both in vitro and in clinical infections (see INDICATIONS AND USAGE):
Gram-positive bacteria Aerobic
Staphylococcus aureus (methicillin-susceptible strains only)
At least 90 percent of the following microorganisms exhibit an in vitro minimum inhibitory concentration (MIC) less than or equal to the susceptible breakpoint for erythromycin. However, the efficacy of erythromycin in treating clinical infections due to these microorganisms has not been established in adequate and well-controlled trials.
When available, the clinical microbiology laboratory should provide cumulative results of the in vitro susceptibility test results for antimicrobial drugs used in resident hospitals to the physician as periodic reports that describe the susceptibility profile of nosocomial and community-acquired pathogens. These reports should aid the physician in selecting the most effective antimicrobial.
Quantitative methods are used to determine antimicrobial minimum inhibitory concentrations (MICs). These MICs provide estimates of the susceptibility of bacteria to antimicrobial compounds. The MICs should be determined using a standardized procedure. Standardized procedures are based on a dilution method (broth or agar)1 or equivalent with standardized inoculum concentrations and standardized concentrations of erythromycin powder. The MIC values should be interpreted according to the criteria provided in Table 1.
Quantitative methods that require measurement of zone diameters also provide reproducible estimates of the susceptibility of bacteria to antimicrobial compounds. One such standardized procedure2 requires the use of standardized inoculum concentrations. This procedure uses paper disks impregnated with 15 mcg of erythromycin to test the susceptibility of microorganisms to erythromycin. The disk diffusion interpretive criteria are provided in Table 1.
Table 1: Susceptibility
Interpretive Criteria for Erythromycin
|Pathogen||Susceptibility Interpretive Criteria|
|Minimum Inhibitory Concentration (mcg/mL)||Disk Diffusion (zone diameter in mm)|
|Staphylococcus spp.||≤ 0.5||1 to 4||≥ 8||≥ 23||14 to 22||≤ 13|
|Enterococcus spp.||≤ 0.5||1 to 4||≥ 8||≥ 23||14 to 22||≤ 13|
|Streptococcus pneumoniaea,b||≤ 0.25||0.5||≥ 1||≥ 21||16 to 20||≤ 15|
|Streptococcus spp. (p-hemolytic group)a,b||≤ 0.25||0.5||≥ 1||≥ 21||16 to 20||≤ 15|
|Streptococcus spp. (Viridans group)a,b||≤ 0.25||0.5||≥ 1||≥ 21||16 to 20||≤ 15|
|a The MIC interpretive criteria for Streptococcus pneumoniae,
Streptococcus spp. (β-hemolytic group), and Streptococcus spp. (Viridans
group) are applicable only to tests performed by broth microdilution
using cation-adjusted Mueller-Hinton broth supplemented with 2 to 5% lysed
horse blood inoculated with a direct colony suspension and incubated in ambient
air at 35 ± 2°C for 20 to 24 hours.
b The zone diameter interpretive criteria for Streptococcus pneumoniae, Streptococcus spp. (β-hemolytic group), and Streptococcus spp. (Viridans group) are applicable only to tests performed using Mueller-Hinton agar supplemented with 5% defibrinated sheep blood inoculated with a direct colony suspension and incubated in 5% CO2 at 35 ± 2°C for 20 to 24 hours.
A report of Susceptible indicates that the antimicrobial is likely to inhibit growth of the pathogen if the antimicrobial compound in the blood reaches the concentrations usually achievable. A report of Intermediate indicates that the result should be considered equivocal, and, if the microorganism is not fully susceptible to alternative, clinically feasible drugs, the test should be repeated. This category implies possible clinical applicability in body sites where the drug is physiologically concentrated or in situations where a high dosage of drug can be used. This category also provides a buffer zone, which prevents small, uncontrolled technical factors from causing major discrepancies in interpretation. A report of Resistant indicates that the antimicrobial is not likely to inhibit growth of the pathogen if the antimicrobial compound in the blood reaches the concentrations usually achievable and other therapy should be selected.
Standardized susceptibility test procedures require the use of quality control microorganisms to control the technical aspects of the test procedures3. Standard Erythromycin powder should provide the following range of values noted in Table 2.
Table 2: Acceptable Quality Control Ranges for
|QC Strain||Minimum Inhibitory Concentration (mcg/mL)||Disk Diffusion (zone diameter in mm)|
|Enterococcus faecalis ATCC 29212||1 to 4||NAa|
|Staphylococcus aureus ATCC 29213||0.25 to 1||NA|
|Staphylococcus aureus ATCC 25923||NA||22 to 30|
|Streptococcus pneumoniae ATCC 49619b||0.03 to 0.12c||25 to 30d|
|a not applicable
b This organism may be used for validation of susceptibility test results when testing Streptococcus spp. other than S. pneumoniae.
c This quality control range for S. pneumoniae is applicable only to tests performed by broth microdilution using cation-adjusted Mueller-Hinton broth supplemented with 2 to 5% lysed horse blood inoculated with a direct colony suspension and incubated in ambient air at 35 ± 2°C for 20 to 24 hours.
d This quality control zone diameter range is applicable only to tests performed using Mueller-Hinton agar supplemented with 5% defibrinated sheep blood inoculated with a direct colony suspension and incubated in 5% CO2 at 35 ± 2°C for 20 to 24 hours.
1. Clinical and Laboratory Standards Institute. Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria That Grow Aerobically; Approved Standard-9th Edition. Clinical and Laboratory Standards Institute document M07-A9. Clinical and Laboratory Standards Institute, 950 West Valley Road, Suite 2500, Wayne, Pennsylvania 19087-1898 USA, 2012.
2. Clinical and Laboratory Standards Institute. Performance Standards for Antimicrobial Disk Susceptibility Tests; Approved Standard-11th Edition. Clinical and Laboratory Standards Institute document M02-A11. Clinical and Laboratory Standards Institute, 950 West Valley Road, Suite 2500, Wayne, Pennsylvania 19087-1898 USA, 2012.
3. Clinical and Laboratory Standards Institute. Performance Standards for Antimicrobial Susceptibility Testing; 22nd Informational Supplement. CLSI document M100-S22. Clinical and Laboratory Standards Institute, 950 West Valley Road, Suite 2500, Wayne, Pennsylvania 19087-1898 USA, 2012.
Read the entire FDA prescribing information for Erythrocin Lactobionate (Erythromycin Lactobionate) »
Additional Erythrocin Lactobionate Information
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