ORGARAN SOLUTION

Ülke: Kanada

Dil: İngilizce

Kaynak: Health Canada

şimdi satın al

Indir Ürün özellikleri (SPC)
09-02-2018

Aktif bileşen:

DANAPAROID SODIUM

Mevcut itibaren:

ASPEN PHARMACARE CANADA INC.

ATC kodu:

B01AB09

INN (International Adı):

DANAPAROID

Doz:

750UNIT

Farmasötik formu:

SOLUTION

Kompozisyon:

DANAPAROID SODIUM 750UNIT

Uygulama yolu:

INTRAVENOUS

Paketteki üniteler:

10X0.6ML AMPS

Reçete türü:

Prescription

Terapötik alanı:

HEPARINS

Ürün özeti:

Active ingredient group (AIG) number: 0126753002; AHFS:

Yetkilendirme durumu:

APPROVED

Yetkilendirme tarihi:

2018-02-09

Ürün özellikleri

                                1
PRODUCT
MONOGRAPH
-
HIT
PR
ORGARAN
®
Danaparoid Sodium Injection
750 anti-Xa units/ampoule
(1250 anti-Xa units/mL)
Anticoagulant/Antithrombotic Agent
(Heparinoid)
Aspen Pharmacare Canada Inc.
111 Queen Street East, Suite 450,
Toronto, Ontario, M5C 1S2
Control No.
212405
Date of approval: February 9, 2018
2
TABLE
OF
CONTENTS
ACTIONS AND CLINICAL PHARMACOLOGY
.....................................................................
3
INDICATIONS AND CLINICAL USE
........................................................................................
4
CONTRAINDICATIONS
...............................................................................................................
5
WARNINGS
.....................................................................................................................................
5
PRECAUTIONS
..............................................................................................................................
9
DRUG INTERACTIONS
.............................................................................................................
15
ADVERSE REACTIONS
.............................................................................................................
16
SYMPTOMS AND TREATMENT OF OVERDOSAGE
......................................................... 20
DOSAGE AND ADMINISTRATION
.........................................................................................
20
PHARMACEUTICAL INFORMATION
...................................................................................
27
AVAILABILITY OF DOSAGE FORM
......................................................................................
28
PHARMACOLOGY
.....................................................................................................................
29
TOXICOLOGY
.............................................................................................................................
31
CLINICAL TRIALS
..........................................................................
                                
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