E.E.S. 200mg/5ml 200ml Granules

Manufacturer ARBOR Active Ingredient Erythromycin Suspension(er ith roe MYE sin) Pronunciation er ith roe MYE sin
It is used to treat or prevent bacterial infections.It may be given to you for other reasons. Talk with the doctor.
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Drug Class
Antibiotic
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Pharmacologic Class
Macrolide antibiotic
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Pregnancy Category
Category B
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FDA Approved
Mar 1952
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DEA Schedule
Not Controlled

Overview

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What is this medicine?

Erythromycin is an antibiotic that stops the growth of bacteria. It's used to treat various bacterial infections, including those of the respiratory tract, skin, and some sexually transmitted infections. It works by preventing bacteria from making the proteins they need to grow and multiply.
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How to Use This Medicine

Taking Your Medication Correctly

To get the most benefit from your medication, follow your doctor's instructions carefully. Read all the information provided with your medication and follow the instructions closely. You can take this medication with or without food, unless your doctor advises you to take it differently. Before using, shake the medication well to ensure the ingredients are mixed properly.

When taking a liquid dose, measure it carefully using the measuring device that comes with the medication. If a measuring device is not provided, ask your pharmacist for one to ensure accurate dosing. Continue taking your medication as directed by your doctor or healthcare provider, even if you start feeling better.

Storing and Disposing of Your Medication

Different brands of this medication may have specific storage requirements. Some may need to be refrigerated, while others should be stored at room temperature. If you're unsure about how to store your medication, consult with your pharmacist. It's also important to know how long you can store your medication before it needs to be discarded.

Keep all medications in a safe and secure location, out of the reach of children and pets.

What to Do If You Miss a Dose

If you miss a dose, take it as soon as you remember. However, if it's close to the time for your next scheduled dose, skip the missed dose and resume your regular dosing schedule. Do not take two doses at the same time or take extra doses to make up for a missed one.
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Lifestyle & Tips

  • Take the medication exactly as prescribed by your doctor, even if you start feeling better. Do not skip doses or stop taking it early, as this can lead to antibiotic resistance.
  • Shake the oral suspension well before each use.
  • Measure the liquid medicine with a special dose-measuring spoon or cup, not a regular table spoon.
  • Erythromycin ethylsuccinate (E.E.S.) can be taken with or without food. If it causes stomach upset, try taking it with food.
  • Avoid grapefruit juice, as it can increase the levels of erythromycin in your body.
  • Inform your doctor about all other medications you are taking, including over-the-counter drugs, herbal supplements, and vitamins, as erythromycin can interact with many other drugs.

Dosing & Administration

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Adult Dosing

Standard Dose: 400 mg (equivalent to 200 mg/5ml x 10ml) every 6 hours or 800 mg (equivalent to 200 mg/5ml x 20ml) every 12 hours
Dose Range: 1600 - 4000 mg

Condition-Specific Dosing:

Streptococcal infections: 400 mg every 6 hours for 10 days
Mycoplasma pneumoniae: 400 mg every 6 hours for 5-10 days
Legionnaires' disease: 400-800 mg every 6 hours
Pertussis: 400 mg every 6 hours for 14 days
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Pediatric Dosing

Neonatal: Not established for routine use; specific dosing for ophthalmia neonatorum or pertussis prophylaxis may apply (e.g., 10-12.5 mg/kg/dose every 6 hours)
Infant: 30-50 mg/kg/day in divided doses every 6 hours
Child: 30-50 mg/kg/day in divided doses every 6 hours (max 4 g/day)
Adolescent: 30-50 mg/kg/day in divided doses every 6 hours (max 4 g/day) or adult dose if weight > 40 kg
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Dose Adjustments

Renal Impairment:

Mild: No adjustment needed
Moderate: No adjustment needed
Severe: No adjustment needed for typical doses; for doses > 4 g/day, consider dose reduction or extended interval
Dialysis: Not significantly removed by hemodialysis or peritoneal dialysis; no supplemental dose needed

Hepatic Impairment:

Mild: No adjustment
Moderate: Use with caution; monitor LFTs
Severe: Use with caution; dose reduction may be necessary; monitor LFTs and clinical signs of toxicity

Pharmacology

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Mechanism of Action

Erythromycin binds to the 50S ribosomal subunit of susceptible microorganisms, thereby inhibiting bacterial protein synthesis without affecting nucleic acid synthesis. It is generally considered bacteriostatic, but may be bactericidal at high concentrations or against highly susceptible organisms.
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Pharmacokinetics

Absorption:

Bioavailability: Approximately 18-45% (Erythromycin Ethylsuccinate, varies by formulation and individual)
Tmax: 2-4 hours
FoodEffect: Erythromycin ethylsuccinate absorption is generally not significantly affected by food and may be taken with or without meals. Taking with food may reduce gastrointestinal upset.

Distribution:

Vd: 0.7-1.1 L/kg
ProteinBinding: 70-90%
CnssPenetration: Limited (poor penetration into CSF, even with inflamed meninges)

Elimination:

HalfLife: 1.5-3 hours (prolonged in hepatic impairment)
Clearance: Not available (highly variable)
ExcretionRoute: Mainly biliary/fecal (10-15% renal)
Unchanged: Approximately 2-5% (renal)
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Pharmacodynamics

OnsetOfAction: Rapid
PeakEffect: Within 2-4 hours (plasma concentration)
DurationOfAction: Dependent on dosing interval (typically 6-12 hours based on half-life and MIC)

Safety & Warnings

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Side Effects

Urgent Side Effects: Seek Medical Help Right Away

Although rare, some people may experience severe and potentially life-threatening side effects while taking this medication. If you notice any of the following symptoms, contact your doctor or seek immediate medical attention:

Signs of an allergic reaction, such as:
+ Rash or hives
+ Itching or red, swollen, blistered, or peeling skin (with or without fever)
+ Wheezing or tightness in the chest or throat
+ Difficulty breathing, swallowing, or talking
+ Unusual hoarseness or swelling of the mouth, face, lips, tongue, or throat
Signs of liver problems, including:
+ Dark urine
+ Fatigue
+ Decreased appetite
+ Upset stomach or stomach pain
+ Light-colored stools
+ Vomiting
+ Yellow skin or eyes
Signs of a severe skin reaction (Stevens-Johnson syndrome/toxic epidermal necrolysis), such as:
+ Red, swollen, blistered, or peeling skin (with or without fever)
+ Red or irritated eyes
+ Sores in the mouth, throat, nose, or eyes
Difficulty urinating or changes in urine output
Severe dizziness or fainting
Rapid heartbeat
Abnormal heartbeat (long QT on ECG), which can be life-threatening. This risk may be increased when taking other medications with this drug. Seek medical help immediately if you experience an irregular heartbeat.
Diarrhea, particularly if it is severe, bloody, or watery. Although diarrhea is common with antibiotics, a rare but potentially life-threatening condition called C. diff-associated diarrhea (CDAD) may occur. If you experience stomach pain, cramps, or severe diarrhea, contact your doctor promptly.
Hearing loss, which may be temporary but can be more likely to occur if you have kidney problems or take high doses of this medication. If you experience hearing problems, contact your doctor right away.

Other Possible Side Effects

Most people taking this medication do not experience significant side effects, but some may occur. If you notice any of the following symptoms or if they persist or bother you, contact your doctor:

Diarrhea
Stomach pain
Upset stomach
Vomiting
Decreased appetite

This is not an exhaustive list of possible side effects. If you have questions or concerns about side effects, consult your doctor. You can also report side effects to the FDA at 1-800-332-1088 or online at https://www.fda.gov/medwatch.
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Seek Immediate Medical Attention If You Experience:

  • Severe or watery diarrhea, especially if it contains blood or mucus (may be a sign of C. difficile infection)
  • Yellowing of the skin or eyes (jaundice), dark urine, pale stools (signs of liver problems)
  • Severe stomach pain or cramping
  • Unusual tiredness, muscle pain or weakness, dark urine (signs of muscle breakdown, especially if taking statins)
  • Fast, pounding, or irregular heartbeat, dizziness, fainting (signs of heart rhythm problems)
  • Significant hearing loss or ringing in the ears (tinnitus)
  • Rash, itching, swelling (especially of the face, tongue, or throat), severe dizziness, trouble breathing (signs of an allergic reaction)
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Before Using This Medicine

Before Taking This Medication: Important Information to Share with Your Doctor

It is essential to inform your doctor about the following:

Any allergies you have, including allergies to this medication, its components, or other substances. Be sure to describe the allergic reaction and its symptoms.
Certain health conditions, such as:
+ Abnormal heartbeat patterns, including a prolonged QTc interval on an electrocardiogram (ECG)
+ Slow heartbeat
+ Low potassium or magnesium levels

Additionally, tell your doctor about all the medications you are currently taking, including:

Prescription and over-the-counter (OTC) medications
Natural products
* Vitamins

Some medications, particularly those used to treat mood disorders, abnormal heart rhythms, or migraine headaches, may interact with this medication and should not be taken concurrently. This is not an exhaustive list, and it is crucial to discuss all your medications and health conditions with your doctor.

To ensure your safety, consult with your doctor and pharmacist about all your medications and health problems before taking this medication. Do not start, stop, or change the dose of any medication without first consulting your doctor to confirm that it is safe to do so.
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Precautions & Cautions

Important Information for Patients Taking This Medication

It is crucial that you inform all your healthcare providers, including doctors, nurses, pharmacists, and dentists, that you are taking this medication.

If you are taking this medication long-term, your doctor may recommend regular blood tests to monitor your condition. Be sure to discuss this with your doctor.

This medication may interfere with certain laboratory tests. Therefore, it is essential to notify all your healthcare providers and laboratory personnel that you are taking this medication.

Do not take this medication for longer than prescribed, as this may increase the risk of a second infection.

If you are following a low-sodium or sodium-free diet, consult your doctor before taking this medication, as some products may contain sodium.

If you have myasthenia gravis, discuss your condition with your doctor. If your symptoms worsen, contact your doctor immediately. Additionally, be aware that myasthenia gravis symptoms, such as new or worsening muscle weakness, difficulty chewing or swallowing, breathing problems, droopy eyelids, or changes in vision (including blurred vision or double vision), can occur in people without a history of the condition. If you experience any of these symptoms, seek medical attention right away.

If you are 65 years or older, use this medication with caution, as you may be more susceptible to side effects.

If you are pregnant, planning to become pregnant, or breastfeeding, consult your doctor to discuss the potential benefits and risks to you and your baby.

Special Considerations for Newborns

In newborns taking this medication, a severe stomach problem can occur. If your child vomits or becomes irritable during feeding, contact your doctor immediately.
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Overdose Information

Overdose Symptoms:

  • Severe nausea
  • Vomiting
  • Abdominal pain
  • Diarrhea
  • Hearing loss (reversible)
  • Pancreatitis (rare)
  • Cholestatic hepatitis (rare)

What to Do:

Seek immediate medical attention or call a Poison Control Center (1-800-222-1222). Treatment is generally supportive, including gastric lavage and symptomatic management.

Drug Interactions

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Contraindicated Interactions

  • Colchicine (in patients with renal or hepatic impairment)
  • Lurasidone
  • Pimozide
  • Ergotamine, Dihydroergotamine
  • Lovastatin, Simvastatin (due to increased risk of rhabdomyolysis)
  • Eliglustat (in patients who are CYP2D6 poor metabolizers or taking strong/moderate CYP2D6 inhibitors)
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Major Interactions

  • Amiodarone, Disopyramide, Dofetilide, Dronedarone, Ibutilide, Quinidine, Sotalol (increased risk of QT prolongation/Torsades de Pointes)
  • Warfarin (increased anticoagulant effect)
  • Carbamazepine, Phenytoin, Valproic acid (increased levels of anticonvulsants)
  • Theophylline (increased theophylline levels)
  • Cyclosporine, Tacrolimus (increased immunosuppressant levels)
  • Cisapride (increased risk of QT prolongation)
  • Statins (e.g., Atorvastatin, Rosuvastatin - increased risk of myopathy/rhabdomyolysis)
  • Oral contraceptives (potential decreased efficacy)
  • Sildenafil, Tadalafil, Vardenafil (increased PDE5 inhibitor levels)
  • Alprazolam, Midazolam, Triazolam (increased benzodiazepine levels)
  • Digoxin (increased digoxin levels in some patients)
  • Quetiapine (increased quetiapine levels)
  • Ranolazine (increased ranolazine levels)
  • Verapamil, Diltiazem (increased risk of hypotension, bradycardia, lactic acidosis)
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Moderate Interactions

  • Corticosteroids (e.g., Methylprednisolone - increased corticosteroid levels)
  • Cimetidine (may increase erythromycin levels)
  • Fluconazole, Itraconazole, Ketoconazole (may increase erythromycin levels)
  • Rifampin (may decrease erythromycin levels)
  • Clindamycin, Lincomycin (antagonistic effect)
  • Chloramphenicol (antagonistic effect)
  • Zidovudine (decreased zidovudine levels)
  • Omeprazole (increased omeprazole levels)
  • Tolterodine (increased tolterodine levels in CYP2D6 poor metabolizers)
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Minor Interactions

  • Antacids (may decrease absorption if taken concurrently, separate by 2 hours)
  • Food (Erythromycin base absorption is decreased by food, but ethylsuccinate is not significantly affected)

Monitoring

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Baseline Monitoring

Liver Function Tests (LFTs)

Rationale: To establish baseline and identify pre-existing hepatic impairment, especially in patients with risk factors or prior history of liver disease.

Timing: Prior to initiation, if clinically indicated.

Electrocardiogram (ECG)

Rationale: To assess baseline QTc interval, especially in patients with pre-existing cardiac conditions, electrolyte imbalances, or concomitant use of other QT-prolonging drugs.

Timing: Prior to initiation, if clinically indicated.

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Routine Monitoring

Clinical response to therapy

Frequency: Daily during acute treatment

Target: Resolution of infection symptoms

Action Threshold: Lack of improvement or worsening symptoms may indicate treatment failure, resistance, or incorrect diagnosis.

Liver Function Tests (LFTs)

Frequency: Periodically, especially with prolonged therapy (>14 days) or in patients with hepatic impairment

Target: Within normal limits or stable

Action Threshold: Significant elevation (e.g., >3x ULN) may warrant dose reduction or discontinuation.

Renal Function (BUN, Creatinine)

Frequency: Periodically, if prolonged therapy or pre-existing renal impairment

Target: Within normal limits or stable

Action Threshold: Significant changes may indicate renal dysfunction, though erythromycin is primarily hepatically eliminated.

Electrolytes (Potassium, Magnesium)

Frequency: Periodically, if risk factors for QT prolongation or concomitant diuretic use

Target: Within normal limits

Action Threshold: Hypokalemia or hypomagnesemia should be corrected to reduce risk of arrhythmias.

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Symptom Monitoring

  • Diarrhea (especially severe or persistent, may indicate C. difficile-associated diarrhea)
  • Nausea, vomiting, abdominal pain (common GI side effects)
  • Yellowing of skin or eyes, dark urine, pale stools (signs of hepatotoxicity)
  • Unusual fatigue, muscle weakness, dark urine (signs of rhabdomyolysis, especially with statin co-administration)
  • Palpitations, dizziness, syncope (signs of QT prolongation/arrhythmias)
  • Hearing loss or tinnitus (rare, usually reversible ototoxicity)

Special Patient Groups

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Pregnancy

Erythromycin is generally considered safe for use during pregnancy (Pregnancy Category B). It is often used as an alternative for penicillin-allergic pregnant women.

Trimester-Specific Risks:

First Trimester: No evidence of increased risk of major birth defects.
Second Trimester: No evidence of increased risk of adverse outcomes.
Third Trimester: No evidence of increased risk of adverse outcomes.
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Lactation

Erythromycin is excreted into breast milk in small amounts. It is generally considered compatible with breastfeeding (Lactation Risk L2 - safer drug). Monitor breastfed infant for gastrointestinal disturbances (e.g., diarrhea, candidiasis) or rash.

Infant Risk: Low risk of adverse effects. Potential for altered gut flora, but generally well-tolerated.
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Pediatric Use

Widely used in pediatric patients. Dosing is weight-based. Caution in neonates due to potential for infantile hypertrophic pyloric stenosis (IHPS), especially with erythromycin base or estolate forms; ethylsuccinate has a lower but still present risk. Monitor for feeding intolerance and vomiting.

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Geriatric Use

No specific dose adjustment is typically required based on age alone. However, geriatric patients may be more susceptible to QT prolongation, hearing loss, and drug interactions due to polypharmacy, renal/hepatic impairment, and underlying comorbidities. Monitor closely for adverse effects and drug interactions.

Clinical Information

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Clinical Pearls

  • Erythromycin ethylsuccinate (E.E.S.) is generally better tolerated gastrointestinally than erythromycin base and can be taken with or without food.
  • It is a potent CYP3A4 inhibitor, leading to numerous significant drug interactions. Always review concomitant medications.
  • Risk of QT prolongation and Torsades de Pointes, especially with pre-existing cardiac conditions, electrolyte imbalances, or co-administration of other QT-prolonging drugs.
  • Can cause reversible hearing loss, particularly with high doses or in patients with renal impairment.
  • Cholestatic hepatitis is a rare but serious adverse effect, more common with the estolate salt but can occur with others.
  • Erythromycin is an effective prokinetic agent and is sometimes used off-label for gastroparesis, though this is not its primary indication.
  • Infantile hypertrophic pyloric stenosis (IHPS) is a rare but serious concern in neonates and young infants treated with erythromycin, particularly the base or estolate forms. Parents should be advised to monitor for persistent vomiting.
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Alternative Therapies

  • Penicillins (e.g., Amoxicillin, Penicillin V - if not allergic)
  • Cephalosporins (e.g., Cephalexin)
  • Tetracyclines (e.g., Doxycycline)
  • Fluoroquinolones (e.g., Levofloxacin, Moxifloxacin)
  • Clindamycin
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Cost & Coverage

Average Cost: Varies widely, typically $20-$100+ per 200ml bottle of 200mg/5ml suspension
Generic Available: Yes
Insurance Coverage: Tier 1 or 2 (Generic)
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General Drug Facts

If your symptoms or health issues persist or worsen, it is essential to contact your doctor for further guidance. To ensure your safety, never share your medication with others or take someone else's medication. Some medications may come with an additional patient information leaflet, so it's a good idea to check with your pharmacist. If you have any questions or concerns about this medication, don't hesitate to discuss them with your doctor, nurse, pharmacist, or other healthcare provider. In the event of a suspected overdose, immediately call your local poison control center or seek medical attention. When seeking help, be prepared to provide information about what was taken, the amount, and the time it happened.