CARBETOCIN INJECTION SOLUTION

Maa: Kanada

Kieli: englanti

Lähde: Health Canada

Osta se nyt

Lataa Valmisteyhteenveto (SPC)
18-09-2023

Aktiivinen ainesosa:

CARBETOCIN

Saatavilla:

JUNO PHARMACEUTICALS CORP.

ATC-koodi:

H01BB03

INN (Kansainvälinen yleisnimi):

CARBETOCIN

Annos:

100MCG

Lääkemuoto:

SOLUTION

Koostumus:

CARBETOCIN 100MCG

Antoreitti:

INTRAVENOUS

Kpl paketissa:

15G/50G

Prescription tyyppi:

Prescription

Terapeuttinen alue:

OXYTOCICS

Tuoteyhteenveto:

Active ingredient group (AIG) number: 0132909001; AHFS:

Valtuutuksen tilan:

APPROVED

Valtuutus päivämäärä:

2019-06-07

Valmisteyhteenveto

                                PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
CARBETOCIN INJECTION
1 mL solution in pre-filled syringes – 100 mcg / mL
For Intravenous (IV) Use Only
Uterotonic Agent
Juno Pharmaceuticals Corp.
402-2233 Argentia Road
Mississauga, ON
L5N 2X7
Date of Initial Authorization:
June 7, 2019
Date of Revision:
September 18, 2023
Submission Control No: 274705
Carbetocin Injection
Page 1 of 24
Carbetocin Injection
Page 2 of 24
RECENT MAJOR LABEL CHANGES
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
.....................................................................................
4
1.
INDICATIONS
...............................................................................................................................
4
1.1
PEDIATRICS
...................................................................................................................................
4
1.2
GERIATRICS
...................................................................................................................................
4
2.
CONTRAINDICATIONS
..................................................................................................................
4
4.
DOSAGE AND ADMINISTRATION
..................................................................................................
4
4.4
ADMINISTRATION
.........................................................................................................................
5
5.
OVERDOSAGE
..............................................................................................................................
5
6.
DOSAGE FORMS, STRENGTHS, COMPOSITION AND PACKAGING
................................................... 5
7.
WARNINGS AND PRECAUTIONS
...................................................................................................
6
7.1
SPECIAL POPULATIONS
.................................................................................................................
7
7.1.1 PREGNANT WOMEN:
.........................................
                                
                                Lue koko asiakirja
                                
                            

Asiakirjat muilla kielillä

Valmisteyhteenveto Valmisteyhteenveto ranska 11-09-2020

Etsi tähän tuotteeseen liittyviä ilmoituksia