| SKU | ISG002622 |
| Brand | Curam |
| Categories | Medication & Treatments |
| Color | black |
| Concentrations | 457 Mg |
| Shop by Concerns | Skin Infection |
| Gender | Unisex |
| Shop By Goals | Ear and Sinus Infection Relief |
| Imported Or Local | Local |
| Ingredient | Amoxicillin Clavulanic acid |
| UPC | 6223002641963 |
| Size | 70 Ml |
| Specialty | Broad Spectrum Clinically Tested Systemic Antibiotic |
| Sub Categories | Systemic Antibiotic |
| Warning | Allergy to probiotics or capsule components Prescription only Use with caution in kidney impairment Use with caution in liver impairment Risk of Antibiotic-Associated Diarrhea |
Curam 457 Mg 70 ml
Description:
Curam 457 mg/5 ml powder for oral suspension 70 ml is a prescription systemic antibiotic medicine containing the combination of amoxicillin and clavulanic acid (amoxicillin/clavulanate). It belongs to the beta-lactam penicillin class and is used to treat a wide range of bacterial infections in adults and children, particularly those caused by beta-lactamase–producing organisms that are resistant to amoxicillin alone. After reconstitution, it is taken orally as a flavored suspension, making it especially suitable for pediatric use and for patients who have difficulty swallowing tablets.
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 and local guidelines.
Active Ingredients / Key Components:
- Amoxicillin (as amoxicillin trihydrate) – 457 mg per 5 ml (exact breakdown of amoxicillin vs clavulanic acid in this strength is not provided in the available data; refer to the official product leaflet for precise amounts).
- Clavulanic acid (as potassium clavulanate) – present in fixed combination with amoxicillin (exact mg per 5 ml not available in the provided information; consult the package insert for detailed concentration).
- Excipients: The full list of inactive ingredients (flavoring agents, sweeteners, suspending agents, preservatives, etc.) is not available in the provided information. Please refer to the official leaflet for a complete ingredient list.
Dosage & Administration / How to Use:
- Curam 457 mg/5 ml is for oral use only and must be reconstituted with water by the pharmacist according to the manufacturer’s instructions before use.
- Shake the bottle well before each dose to ensure a uniform suspension.
- Dosage is individualized based on the patient’s weight, age, severity of infection, and kidney function. Always follow your doctor’s prescription exactly.
- Typical pediatric dosing: calculated in mg/kg/day of the amoxicillin component, divided into 2–3 doses per day. The 457 mg/5 ml strength is usually used for higher-dose regimens in more severe infections (exact dosing schedule must be determined by a physician).
- Adults and adolescents who cannot swallow tablets may also use the suspension; the dose should be equivalent to the recommended tablet dose, as prescribed by the doctor.
- It is generally recommended to take the suspension at the start of a meal to improve absorption and reduce the risk of gastrointestinal side effects.
- Use the provided measuring spoon or oral syringe to ensure accurate dosing. Do not use household teaspoons.
- Complete the full course of therapy even if symptoms improve early, unless your doctor instructs you to stop, to reduce the risk of resistance and relapse.
- If a dose is missed, take it as soon as you remember unless it is almost time for the next dose. Do not double the dose to make up for a missed one.
Clinical Benefits:
- Broad-spectrum antibacterial activity against many common respiratory, ear, sinus, skin, and urinary pathogens.
- Effective against beta-lactamase–producing bacteria due to the presence of clavulanic acid, which protects amoxicillin from enzymatic degradation.
- Helps rapidly reduce infection-related symptoms such as fever, pain, cough, earache, sinus pressure, and urinary discomfort when used appropriately.
- Oral suspension form is convenient for children and patients who have difficulty swallowing tablets, improving adherence to therapy.
- Well-established safety and efficacy profile when used under medical supervision and according to guidelines.
Warnings & Contraindications:
- Contraindicated in patients with a known hypersensitivity (allergy) to amoxicillin, clavulanic acid, other penicillins, or any component of the formulation.
- Use with extreme caution in patients with a history of severe immediate hypersensitivity reactions (e.g., anaphylaxis) to beta-lactam antibiotics such as cephalosporins or carbapenems.
- Patients with a history of cholestatic jaundice or hepatic dysfunction associated with amoxicillin/clavulanate should not receive this product again.
- Use with caution in patients with liver impairment or kidney impairment; dose adjustment or special monitoring may be required.
- Prolonged use may result in overgrowth of non-susceptible organisms, including fungi; if superinfection occurs, appropriate measures should be taken.
- Antibiotic-associated colitis (including Clostridioides difficile–associated diarrhea) can occur; if severe or persistent diarrhea develops, contact a doctor immediately and do not use anti-diarrheal medicines without medical advice.
- Consult your doctor before use if pregnant or breastfeeding. Amoxicillin/clavulanate is generally used in pregnancy only when clearly needed and prescribed by a physician.
- Inform your doctor about all other medicines you are taking, especially anticoagulants (e.g., warfarin), allopurinol, methotrexate, or other antibiotics, as interactions may occur.
- May interfere with some laboratory tests (e.g., urine glucose tests using non-enzymatic methods); inform the laboratory staff that you are taking this medication.
- Not intended to diagnose, treat, cure, or prevent any disease without a doctor’s prescription and supervision.
- Keep out of reach of children.
Side Effects:
- Common side effects: nausea, vomiting, diarrhea, abdominal pain, soft stools, and mild skin rash.
- Less common side effects: headache, dizziness, oral or vaginal candidiasis (thrush), changes in taste.
- Allergic reactions: rash, itching, hives, swelling of the face, lips, tongue, or throat, and difficulty breathing. These may indicate a serious allergic reaction; seek emergency medical attention immediately.
- Serious but rare side effects: severe skin reactions (e.g., Stevens–Johnson syndrome), severe persistent diarrhea or bloody stools (possible antibiotic-associated colitis), liver problems (jaundice, dark urine, severe fatigue), or unusual bruising/bleeding. Stop the medicine and contact a doctor immediately if these occur.
- If any side effects worsen or you notice any other unusual symptoms, contact your healthcare provider promptly.
Storage Instructions:
Before reconstitution: Store the unopened bottle in a cool, dry place below the temperature specified in the package insert, away from direct sunlight and moisture. Keep container tightly closed and out of reach of children.
After reconstitution: Store the prepared oral suspension in a refrigerator if recommended by the manufacturer (usually 2–8 °c). Do not freeze. Use within the period indicated in the leaflet (commonly 7–10 days) and discard any remaining suspension after this time. Always keep the bottle tightly closed when not in use.
Specifications:
- Product type: Prescription systemic antibiotic oral suspension.
- Strength: 457 mg amoxicillin/clavulanic acid per 5 ml (exact component breakdown not available in provided data; refer to official leaflet).
- Form: Powder for oral suspension to be reconstituted with water.
- Pack size: 70 ml (final volume 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.


