Available at Pharmaegy Pharmacy. Use as directed by your doctor.
Megamox ES 600 mg/5 ml 42.9 mg/5
Composition:
Amoxicillin 600 mg/5 ml (as trihydrate)
Clavulanic acid 42.9 mg/5 ml (as potassium salt)
Description:
Megamox ES is a combination antibiotic containing amoxicillin, a penicillin-class antibacterial, and clavulanic acid, a beta-lactamase inhibitor. This formulation is designed to treat infections caused by susceptible bacteria and reduce the development of drug-resistant strains. It is supplied as a powder for oral suspension and must be reconstituted before use.
Indications:
Megamox ES is indicated for the treatment of pediatric patients with recurrent or persistent acute otitis media caused by:
-Streptococcus pneumoniae (penicillin MICs ≤ 2 mcg/ml)
-Haemophilus influenzae (including beta-lactamase-producing strains)
-Moraxella catarrhalis (including beta-lactamase-producing strains)
Dosage and Administration:
Pediatric patients (3 months and older):
90 mg/kg/day of amoxicillin component divided every 12 hours for 10 days.
(This provides 6.4 mg/kg/day of clavulanic acid.)
8kg- 3.0 ml twice daily
12kg- 4.5 ml twice daily
16kg- 6.0 ml twice daily
20kg- 7.5 ml twice daily
24kg- 9.0 ml twice daily
28kg-10.5 ml twice daily
32kg-12.0 ml twice daily
36kg-13.5 ml twice daily
Pediatric patients > 40 kg and Adults:
Experience is not available. Adults should not substitute Megamox ES for tablet formulations.
Patients with hepatic impairment:
Use with caution and monitor hepatic function regularly.
Preparation of Suspension:
Tap bottle to loosen powder.
Add approximately 2/3 of the total water for reconstitution, shake vigorously.
Add the remaining water up to the marked line, shake vigorously again.
Each 5 ml after reconstitution contains: 600 mg amoxicillin + 42.9 mg clavulanic acid.
Important: Shake well before each use.
Administration:
Take at the start of a meal to minimize gastrointestinal discomfort and enhance clavulanic acid absorption.
Contraindications:
-History of serious hypersensitivity reactions (e.g., anaphylaxis, Stevens-Johnson syndrome) to amoxicillin, clavulanate, penicillins, or cephalosporins.
-History of cholestatic jaundice or hepatic dysfunction associated with amoxicillin/clavulanic acid use.
Warnings and Precautions:
-Monitor for signs of hypersensitivity reactions. Discontinue if allergic reactions occur.
-Use with caution in patients with hepatic impairment.
Side Effects:
Side effects associated with Megamox ES may include:
-Serious hypersensitivity reactions, including:
Anaphylaxis, Stevens-Johnson syndrome
-Jaundice (especially cholestatic jaundice)
-Hepatic dysfunction
-If signs of an allergic reaction (rash, itching, facial swelling, or difficulty breathing) or symptoms of liver dysfunction (yellowing of the skin or eyes, dark urine) occur, the use of the medication should be discontinued immediately, and medical attention should be sought.
Storage Conditions:
Store reconstituted suspension in a refrigerator (2–8°C).
Discard after 10 days.
Packaging:
A carton contains one bottle of powder for reconstitution to 100 ml suspension and a package insert.
Megamox ES 642.9 mg / 5 ml suspension 100 ml
Description
Megamox ES 600 mg/5 ml 42.9 mg/5
Composition:
Amoxicillin 600 mg/5 ml (as trihydrate)
Clavulanic acid 42.9 mg/5 ml (as potassium salt)
Description:
Megamox ES is a combination antibiotic containing amoxicillin, a penicillin-class antibacterial, and clavulanic acid, a beta-lactamase inhibitor. This formulation is designed to treat infections caused by susceptible bacteria and reduce the development of drug-resistant strains. It is supplied as a powder for oral suspension and must be reconstituted before use.
Indications:
Megamox ES is indicated for the treatment of pediatric patients with recurrent or persistent acute otitis media caused by:
-Streptococcus pneumoniae (penicillin MICs ≤ 2 mcg/ml)
-Haemophilus influenzae (including beta-lactamase-producing strains)
-Moraxella catarrhalis (including beta-lactamase-producing strains)
Dosage and Administration:
Pediatric patients (3 months and older):
90 mg/kg/day of amoxicillin component divided every 12 hours for 10 days.
(This provides 6.4 mg/kg/day of clavulanic acid.)
8kg- 3.0 ml twice daily
12kg- 4.5 ml twice daily
16kg- 6.0 ml twice daily
20kg- 7.5 ml twice daily
24kg- 9.0 ml twice daily
28kg-10.5 ml twice daily
32kg-12.0 ml twice daily
36kg-13.5 ml twice daily
Pediatric patients > 40 kg and Adults:
Experience is not available. Adults should not substitute Megamox ES for tablet formulations.
Patients with hepatic impairment:
Use with caution and monitor hepatic function regularly.
Preparation of Suspension:
Tap bottle to loosen powder.
Add approximately 2/3 of the total water for reconstitution, shake vigorously.
Add the remaining water up to the marked line, shake vigorously again.
Each 5 ml after reconstitution contains: 600 mg amoxicillin + 42.9 mg clavulanic acid.
Important: Shake well before each use.
Administration:
Take at the start of a meal to minimize gastrointestinal discomfort and enhance clavulanic acid absorption.
Contraindications:
-History of serious hypersensitivity reactions (e.g., anaphylaxis, Stevens-Johnson syndrome) to amoxicillin, clavulanate, penicillins, or cephalosporins.
-History of cholestatic jaundice or hepatic dysfunction associated with amoxicillin/clavulanic acid use.
Warnings and Precautions:
-Monitor for signs of hypersensitivity reactions. Discontinue if allergic reactions occur.
-Use with caution in patients with hepatic impairment.
Side Effects:
Side effects associated with Megamox ES may include:
-Serious hypersensitivity reactions, including:
Anaphylaxis, Stevens-Johnson syndrome
-Jaundice (especially cholestatic jaundice)
-Hepatic dysfunction
-If signs of an allergic reaction (rash, itching, facial swelling, or difficulty breathing) or symptoms of liver dysfunction (yellowing of the skin or eyes, dark urine) occur, the use of the medication should be discontinued immediately, and medical attention should be sought.
Storage Conditions:
Store reconstituted suspension in a refrigerator (2–8°C).
Discard after 10 days.
Packaging:
A carton contains one bottle of powder for reconstitution to 100 ml suspension and a package insert.
Highlights
Effective for pain relief and fever reduction..
Suitable for adults and children as directed..
Fast-acting formula with proven safety profile.
Available in various dosage forms and pack sizes.
Directions for use
Use as directed by your doctor.
Storage
Store in a cool, dry place away from sunlight.
Administration Instructions
Follow the prescribed method of administration as advised by your healthcare provider.