THIOTEPA FOR INJECTION USP POWDER FOR SOLUTION

Страна: Канада

мова: англійська

Джерело: Health Canada

Активний інгредієнт:

THIOTEPA

Доступна з:

STERIMAX INC

Код атс:

L01AC01

ІПН (Міжнародна Ім'я):

THIOTEPA

Дозування:

100MG

Фармацевтична форма:

POWDER FOR SOLUTION

Склад:

THIOTEPA 100MG

Адміністрація маршрут:

INTRAVENOUS

Одиниць в упаковці:

15G/50G

Тип рецепту:

Prescription

Огляд продуктів:

Active ingredient group (AIG) number: 0107649002; AHFS:

Статус Авторизація:

APPROVED

Дата Авторизація:

2022-05-18

Характеристики продукта

_Thiotepa for Injection USP _
_Page 1 of 46 _
“Thiotepa for Injection USP is indicated:
_- in combination with other chemotherapeutic products as part of a
high-dose chemotherapy _
_(HDCT) consolidation regimen followed by autologous stem cell
transplantation (ASCT) for _
_adult patients with central nervous system (CNS) lymphoma_
_ _
and has been issued marketing authorization with conditions. Patients
should be advised of
the nature of the authorization. For further information for Thiotepa
for Injection USP please
refer to Health Canada’s Notice of Compliance with conditions - drug
products web site:
https://www.canada.ca/en/health-canada/services/drugs-health-products/drug-
products/notice-compliance/conditions.html. Note that trials to verify
the clinical benefit of
the medicinal ingredient in Thiotepa for Injection USP are being
carried out by the
manufacturer of the Canadian Reference Product.”
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
THIOTEPA FOR INJECTION USP
Lyophilised powder for solution upon reconstitution and dilution,
15 mg / vial and 100 mg / vial, intravenous
USP
Antineoplastic Agent
ATC code: L01AC01
SteriMax Inc.
2770 Portland Drive
Oakville, ON, Canada
L6H 6R4
Submission Control Number: 272936
Date of Initial Authorization:
May 18, 2022
Date of Revision:
October 4, 2023
_Thiotepa for Injection USP _
_Page 2 of 46 _
RECENT MAJOR LABEL CHANGES
Not Applicable
TABLE OF CONTENTS
SECTIONS OR SUBSECTIONS THAT ARE NOT APPLICABLE AT THE TIME OF
AUTHORIZATION ARE NOT LISTED.
RECENT MAJOR LABEL CHANGES
............................................................................................
2
TABLE OF CONTENTS
..............................................................................................................
2
PART I: HEALTH PROFESSIONAL INFORMATION
......................................................................
5
1
INDICATIONS
...............................................................................................................
5
1.1
Pediatrics
..