Augmentin Tablets

Riik: Austraalia

keel: inglise

Allikas: Department of Health (Therapeutic Goods Administration)

Osta kohe

Avaliku hindamisaruande Avaliku hindamisaruande (PAR)
25-05-2019

Toimeaine:

amoxicillin trihydrate, Quantity: 286.9 mg (Equivalent: amoxicillin trihydrate, Qty 250 mg); potassium clavulanate, Quantity: 149.5 mg (Equivalent: clavulanic acid, Qty 125 mg)

Saadav alates:

Aspen Pharmacare Australia Pty Ltd

Ravimvorm:

Tablet, film coated

Koostis:

Excipient Ingredients: colloidal anhydrous silica; sodium starch glycollate; magnesium stearate; microcrystalline cellulose; dimeticone 200; titanium dioxide; propylene glycol; hypromellose; ethylcellulose

Manustamisviis:

Oral

Ühikuid pakis:

15, 90(E), 3 tablets, 30

Klass:

Medicine Registered

Retsepti tüüp:

(S4) Prescription Only Medicine, Not scheduled. Not considered by committee

Näidustused:

AUGMENTIN is indicated in the treatment of the following infections when caused by AUGMENTIN sensitive, beta-lactamase producing organisms: Skin and Skin Structure Infections, including cases caused by beta-lactamase producing S. aureus, E. coli and Klebsiella spp. (only some strains may be sensitive). Urinary Tract Infections, including cases caused by beta-lactamase producing E. coli, P. mirabilis & Klebsiella spp. Upper Respiratory Tract Infections, such as sinusitis, including cases caused by beta-lactamase producing H.influenzae and M.catarrhalis, and otitis media, especially cases caused by beta-lactamase producing H. influenzae, M. catarrhalis and S. aureus. Lower Respiratory Tract Infections, especially cases caused by beta-lactamase producing H.influenzae and M.catarrhalis. Appropriate culture and susceptibility studies should be performed to identify the causative organism(s) and determine its (their) susceptibility to AUGMENTIN. However, when there is reason to believe an infection may involve any

Toote kokkuvõte:

Visual Identification: white, oval biconvex tablet approx 16mm in length embossed with Augmentin on one side; Container Type: Blister Pack; Container Life Time: 18 Months; Container Temperature: Store below 25 degrees Celsius

Volitamisolek:

Registered

Loa andmise kuupäev:

1991-08-14

Vaadake dokumentide ajalugu