(Intravenous Solution for injection)
The trading (patented) name of a preparation - HAEMODESUM-PHARMATECH
The international name -
THE COMPOSITION AND THE FORM OF RELEASE
1 litre of a solution contains
Polyvinylpyrrolidone ..... 60 g
Sodium Cloride ............. 5.50 g
Potassium Cloride ............... 0.42 g
Calcium Cloride ............ 0.56 g
Magnesium Cloride ............ 0.005 g
Sodium Hydrocarbonate ... 0.23 g
Other components: water for an injection.
200, 250, 400, 500 ml of soltuion in plastic PVC containers.
It's effect is caused by the ability low-molecular polyvinylpyrrolidone to connect toxins, which circulates in blood, and quickly removes them from the organism. The preparation increases diuresis.
INDICATIONS FOR ADMINISTRATION
Administered during detoxication at toxic forms of gastroenteric diseases (salmonellosis, dysentery, etc.), including children. Intoxications of a various origin (cancer, beam, postoperative, alcoholic, an intoxication resulting from renal insufficiency), burns in the stage of intoxication, peritonitis, septic conditions, toxicosis during preganancy and other pathological processes, accompanied by intoxication.
Haemodesum is administered intravenously with controlled rate 40-80 drop/min. For adults single dose up to 300-500 ml. For children up to 5-10 ml / kg. Repeated injections are made by 12 hour intervals and more at the end of the previous injection. The number of application and the overall amount of infused Haemodesum is dependant on the pathologic(al) process.
Its administration mostly patients with heavy health conditions should be under doctor's control.
PREGNANCY AND THE LACTATION
Contra-indications are not revealed.
Before the administration of the solution warm up to +35 - +37 oC.
STORAGE CONDITIONS AND SHELF LIFE
The preparation should be stored in usual conditions at temperature +0-+ 20 oC. Freezing does not render any influence on the quality of a preparation. Expiry date - 3 years.