Ceraxon solution for i/m and i/v injection

Страна: Армения

Язык: английский

Источник: Դեղերի և բժշկական տեխնոլոգիաների փորձագիտական կենտրոնի գործունեության Հայաստանի Հանրապետությունում

Активный ингредиент:

citicoline (citicoline sodium)

Доступна с:

Ferrer International

код АТС:

N06BX06

ИНН (Международная Имя):

citicoline (citicoline sodium)

дозировка:

1000mg/4ml

Фармацевтическая форма:

solution for i/m and i/v injection

Штук в упаковке:

(5) ampoules 4ml

Тип рецепта:

Prescription

Статус Авторизация:

Registered

Дата Авторизация:

2018-12-27

Характеристики продукта

SUMMARY PRODUCT CHARACTERISTICS
1.
NAME OF THE MEDICINAL PRODUCT
CERAXON 1000 mg solution for injection
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
CERAXON 1000 mg solution for injection is supplied in 4 ml glass
ampoules. The active ingredient is
Cticoline sodium 1045mg (equal to the 1000mg Citicoline)
For a full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Solution for injection.
CERAXON 1000 mg solution for injection: Clear and colourless water
solution.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS

Ischemic stroke, acute phase and its neurological sequelae (as a part
of complex therapy)

Rehabilitation period of ischemic and hemorrhagic stroke

Traumatic Brain injury and its neurological sequelae, acute phase (as
a part of complex
therapy) and rehabilitation period

Cognitive and behavioural impairment secondary to chronic vascular and
degenerative cerebral
disorders.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
ADULTS:
The recommended dose is from 500 to 2,000 mg/day, depending on the
severity of the symptoms to be
treated.
It can be administered by intramuscular, slow intravenous route (from
3 to 5 minutes depending on the
administered dose) or in intravenous drop perfusion (dripping speed:
40-60 drops per minute).
THE DOSAGE RECOMMENDATIONS
_The acute phase of Ischemic stroke and Traumatic Brain injury_
:
1000mg every 12 hours from the first day after diagnosis.
,
treatment duration of at least 6 weeks.
It is
possible a transition to the oral forms of Ceraxon 3-5 days after
starting of treatment, if the swallowing
function is not impaired.
_Rehabilitation period of ischemic and hemorrhagic stroke,
rehabilitation period of Traumatic Brain injury, _
_Cognitive and behavioural impairment secondary to chronic vascular
and degenerative cerebral disorders: _
_ _
500-2000mg daily. The dosage and duration of treatment depend on the
severity of symptoms. The oral
forms of Ceraxon can be used also
See the instructions for preparation in section 6.6.
ELDERLY:
CERAXON does not need any s