Almasry Pharmacy

E-Moxclav /5 312 Mg 60 ml

Short Description:
E-Moxclav 312 mg/5 ml dry mix for oral suspension 60 ml is a broad-spectrum antibiotic containing amoxicillin and clavulanic acid from EIPICO. It is used under medical supervision to treat respiratory, ear, sinus, skin, and urinary tract infections caused by susceptible bacteria, especially beta-lactamase–producing strains.

EGP 62EGP 66

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Specifications
SKUISG009956
BrandE-MoxclavLink Icon
Categories
Medication & Treatments
Concentrations
312 Mg
Shop by ConcernsSkin InfectionLink Icon, Bacterial InfectionsLink Icon, Lower Respiratory InfectionsLink Icon, Otitis MediaLink Icon, SinusitisLink Icon, Urinary Tract InfectionsLink Icon
Gender
Neutral
Shop By GoalsBacterial Infection TreatmentLink Icon, Respiratory Infection ControlLink Icon, Urinary Tract Infection ManagementLink Icon
Imported Or LocalLocal
Ingredient
Amoxicillin
Clavulanic acid
UPC
6221032150325
Size
60 Ml
Specialty
Beta-Lactamase Inhibitor
Broad Spectrum
Prescription only
Sub Categories
Anti Inflammatory And Anti Antibiotic
Warning
Allergy to vitamin B12
May Cause Diarrhea Or Allergic Reactions
Not Effective for Viral Infections
Use with caution in liver and kidney impairment
About the product

E-Moxclav /5 312 Mg 60 ml

Description:

E-Moxclav 312 mg/5 ml dry mix for oral suspension 60 ml is a prescription antibiotic medicine containing amoxicillin and clavulanic acid, manufactured by EIPICO. After reconstitution with water, it forms an oral suspension used to treat a wide range of bacterial infections in adults and children. The combination of amoxicillin (a penicillin-type antibiotic) with clavulanic acid (a beta-lactamase inhibitor) helps overcome resistance in beta-lactamase–producing bacteria, providing effective treatment for respiratory, ear, sinus, skin, and urinary tract infections. It should be used only under medical supervision and exactly as prescribed.


Indications:

  • Lower respiratory tract infections, including bronchitis and pneumonia, caused by beta-lactamase–producing isolates of Haemophilus influenzae and Moraxella catarrhalis.
  • Acute bacterial otitis media (middle ear infection) caused by beta-lactamase–producing H. influenzae and M. catarrhalis.
  • Acute bacterial sinusitis caused by beta-lactamase–producing H. influenzae and M. catarrhalis.
  • Skin and skin structure infections caused by beta-lactamase–producing Staphylococcus aureus, Escherichia coli, and Klebsiella species.
  • Urinary tract infections (UTIs) caused by beta-lactamase–producing E. coli, Klebsiella species, and Enterobacter species.
  • Other susceptible infections as determined by culture and sensitivity testing, according to physician judgment.

Active Ingredients / Key Components:

  • Amoxicillin (as amoxicillin trihydrate) – part of a total 312 mg of amoxicillin + clavulanic acid per 5 ml oral suspension (exact individual mg amounts are not specified in the available information (For full ingredient information, please check the product leaflet or the manufacturer’s official website.)).
  • Clavulanic acid (as potassium clavulanate) – part of a total 312 mg of amoxicillin + clavulanic acid per 5 ml oral suspension (exact individual mg amounts are not specified in the available information (For full ingredient information, please check the product leaflet or the manufacturer’s official website.)).
  • Excipients: The full list of inactive ingredients (suspending agents, sweeteners, flavoring agents, preservatives) is not available in the provided information. Refer to the package insert for complete composition.

Dosage & Administration / How to Use:

  • Reconstitution: Add the recommended amount of boiled and cooled water to the dry powder in the bottle up to the marked line, then shake well to obtain a uniform suspension. Shake vigorously before each dose. Exact water volume and reconstitution steps should be followed as per the package insert.
  • Route of administration: Oral use only.
  • Adult and pediatric dosage: The dose, frequency, and duration depend on body weight, age, severity of infection, and kidney function. Typical dosing is calculated in mg/kg/day of the amoxicillin component, divided into 2–3 doses daily. Use strictly according to your doctor’s prescription.
  • With or without food: It is generally recommended to take amoxicillin/clavulanic acid at the start of a meal to improve absorption and reduce gastrointestinal side effects.
  • Duration of treatment: Usually 5–14 days depending on infection type and severity. Do not stop treatment early even if symptoms improve, unless directed by your doctor.
  • Measuring the dose: Use the provided measuring spoon or oral syringe to ensure accurate dosing. Do not use household teaspoons.
  • Missed dose: If a dose is missed, take it as soon as you remember. If it is almost time for the next dose, skip the missed dose and continue your regular schedule. Do not double the dose.

Clinical Benefits:

  • Provides broad-spectrum antibacterial activity against many common respiratory, ear, sinus, skin, and urinary pathogens.
  • Clavulanic acid inhibits beta-lactamase enzymes, helping to overcome bacterial resistance and restore the activity of amoxicillin.
  • Helps relieve symptoms of infection such as fever, pain, cough, sore throat, earache, and urinary discomfort when used appropriately.
  • Oral suspension form is suitable for children and adults who have difficulty swallowing tablets, allowing weight-adjusted dosing.

Warnings & Contraindications:

  • Contraindicated in patients with a known hypersensitivity or allergy to amoxicillin, clavulanic acid, other penicillins, or any component of the formulation.
  • Use with extreme caution in patients with a history of severe allergic reactions to beta-lactam antibiotics (penicillins, cephalosporins, carbapenems), including anaphylaxis, angioedema, or severe skin reactions.
  • Contraindicated in patients with a history of cholestatic jaundice or hepatic dysfunction associated with previous amoxicillin/clavulanic acid use.
  • Use cautiously in patients with liver impairment or kidney impairment; dose adjustment may be required. Regular monitoring may be necessary.
  • Prolonged use may result in overgrowth of non-susceptible organisms, including fungi; if superinfection occurs, appropriate measures should be taken.
  • May reduce the effectiveness of oral contraceptives; additional contraceptive measures may be advisable during treatment.
  • Consult your doctor before use if pregnant or breastfeeding. Use only if clearly needed and prescribed by a healthcare professional.
  • Consult your doctor before use if you have kidney disease, liver disease, mononucleosis, history of gastrointestinal disease (especially colitis), or are taking other medications.
  • Not intended for viral infections such as common cold or influenza. Misuse or overuse of antibiotics can contribute to antibiotic resistance.
  • Keep out of reach of children.

Side Effects:
  • Common side effects: Nausea, vomiting, diarrhea, abdominal pain, soft stools, and mild skin rash. Taking the medicine at the start of a meal may help reduce gastrointestinal discomfort.
  • Less common side effects: Headache, dizziness, oral or vaginal candidiasis (thrush), changes in taste.
  • Serious side effects (seek immediate medical attention): Severe allergic reactions (rash, itching, swelling of face/lips/tongue/throat, difficulty breathing), severe persistent diarrhea or bloody stools (possible Clostridioides difficile–associated diarrhea), yellowing of skin or eyes, dark urine, unusual fatigue (possible liver problems), easy bruising or bleeding, severe skin reactions (Stevens–Johnson syndrome, toxic epidermal necrolysis).
  • If any side effect is severe, persistent, or concerning, stop the medicine and contact your doctor or pharmacist promptly.

Storage Instructions:

Store the dry powder in a cool, dry place below the temperature specified on the package, away from direct sunlight and moisture. Keep the bottle tightly closed before reconstitution. After reconstitution with water, store the oral suspension in a refrigerator if recommended by the manufacturer and use within the period stated in the leaflet (commonly 7–10 days). Do not freeze. Discard any unused suspension after the recommended period. Keep out of reach of children.


Specifications:
  • Product type: Antibiotic medicine (amoxicillin + clavulanic acid).
  • Form: Dry mix for oral suspension (reconstituted to liquid).
  • Strength: 312 mg/5 ml (combined amoxicillin + clavulanic acid; exact split not specified in available data).
  • Pack size: 60 ml bottle after reconstitution.
  • Route of administration: Oral.
  • Intended users: Adults and children as prescribed by a healthcare professional.

Disclaimer:
All pharmacy products are intended for general use only and do not replace professional medical advice, diagnosis, or treatment. Always consult a healthcare provider before use. Results may vary, and no specific outcomes are guaranteed. Products are not intended to diagnose, treat, cure, or prevent any disease unless stated. Follow label instructions carefully, as misuse may cause adverse effects. Compliance with local laws is the customer’s responsibility.

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