APO-KETAMINE ketamine (as hydrochloride) 200 mg/2 mL solution for injection ampoule

Country: Awstralja

Lingwa: Ingliż

Sors: Department of Health (Therapeutic Goods Administration)

Ingredjent attiv:

ketamine hydrochloride, Quantity: 115.34 mg/mL (Equivalent: ketamine, Qty 100 mg/mL)

Disponibbli minn:

Arrotex Pharmaceuticals Pty Ltd

INN (Isem Internazzjonali):

Ketamine hydrochloride

Għamla farmaċewtika:

Injection, solution

Kompożizzjoni:

Excipient Ingredients: water for injections

Rotta amministrattiva:

Intramuscular, Intravenous

Unitajiet fil-pakkett:

5's

Tip ta 'preskrizzjoni:

(S8) Controlled Drug

Indikazzjonijiet terapewtiċi:

Ketamine is recommended:,1. As the sole anaesthetic agent for diagnostic and surgical procedures that do not require skeletal muscle relaxation. Ketamine is best suited for short procedures and it can be used with additional doses, for longer procedures;,2. For the induction of anaesthesia prior to the administration of other general anaesthetic agents;,3. To supplement low-potency agents, such as nitrous oxide.

Sommarju tal-prodott:

Visual Identification: Clear colourless to slightly yellow solution.; Container Type: Ampoule; Container Material: Glass Type I Clear; Container Life Time: 36 Months; Container Temperature: Store below 30 degrees Celsius; Container Closure: Neither child resistant closure nor restricted flow insert

L-istatus ta 'awtorizzazzjoni:

Licence status A

Data ta 'l-awtorizzazzjoni:

2014-11-12