ID | 425 |
No | 425 |
Brand Name | AUGMENTIN |
Ingredients | AMOXICILLIN TRIHYDRATE 229.580 MG
EQ.TO AMOXICILLIN 200 MG/ 5 ML
POTASSIUM CLAVULANATE 33.950 MG
EQ.TO CLAVULANIC ACID 28.5 MG / 5 ML |
Dosage Form | POWDER FOR SUSPENSION |
Primary Packaging | Bottle |
Storage | STORE BELOW 25'C |
Shelf Life | 24 MONTHS |
Pack Size | 70 ML/BOTTLE |
Dispensing Category | Prescription only |
ATC Classification | J01CB04 |
Pharmaceutical Class | ANTIBACTERIAL COMBINATIONS |
Indications | AUGMENTIN SUSPENSION IS INDICATED FOR SHORT TERM TREATMENT OF BACTERIAL INFECTIONS AT THE FOLLOWING SITES WHEN AMOXICILLIN RESISTANT BATA - LACTAMASE PRO DUCING STRAINS ARE SUSPECTED AS THE CAUSE. |
Contraindications | AUGMENTIN IS CONTRAINDICATED IN PATIENTS WITH A HISTORY OF HYPERSENSITIVITY TO BATA-LACTAMS, E.G. PENICILLINS AND CEPHALOSPORINS. PREVIOUS HISTORY ASSOCIATED JAUNDICE/HEPATIC DYSFUNCTION |
Side Effects | MUCOCUTANEOUS CANDIDIASIS, DIZZINESS, HEADACHE, DIARHHEA, NAUSEA, VOMITING, SKIN RASH, PRURITUS, URTICARIA |
Unit Price | - |
EDL |
Yes |
Description | WHITE TO OFF-WHITE FREE FLOWING POWDER , A WHITE TO OFF WHITE SUSPENSION IS FORMED WHICH SLOWLY DEPOSITS A WHITE SEDIMENT ON STANDING |
Note | |
License Owner | DKSH LAOS COMPANY LIMITED |
Manufacturer | GLAXO WELLCOME PRODUCTION |
Country | FRANCE |
Import Registration No | PL 10592/0072 |
Import Registration Date | 1995-10-23 |
Activity | CERTIFICATE RELEASED |
Applied Date | 2022-10-14 |
FDD Registration No | 11 I 3948/13 |
FDD Registration Date | 2023-03-31 |
Expiry Date | 2026-03-30 |