TEVA-HYDROMORPHONE TABLET

Страна: Канада

Язык: английский

Источник: Health Canada

Активный ингредиент:

HYDROMORPHONE HYDROCHLORIDE

Доступна с:

TEVA CANADA LIMITED

код АТС:

N02AA03

ИНН (Международная Имя):

HYDROMORPHONE

дозировка:

8MG

Фармацевтическая форма:

TABLET

состав:

HYDROMORPHONE HYDROCHLORIDE 8MG

Администрация маршрут:

ORAL

Штук в упаковке:

100

Тип рецепта:

Narcotic (CDSA I)

Терапевтические области:

OPIATE AGONISTS

Обзор продуктов:

Active ingredient group (AIG) number: 0108698005; AHFS:

Статус Авторизация:

CANCELLED POST MARKET

Дата Авторизация:

2021-07-30

Характеристики продукта

Teva-HYDROmorphone
Page 1 of 37
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
N
TEVA-HYDROMORPHONE
(HYDROMORPHONE HYDROCHLORIDE TABLETS, USP)
Tablets: 1 mg, 2 mg, 4 mg and 8 mg, Oral
Opioid Analgesic
Teva Canada Limited
30 Novopharm Court
Toronto, Ontario
M1B 2K9
www.tevacanada.com
Submission Control No.: 244765
Date of Revision: Nov 13, 2020
Teva-HYDROmorphone
Page 2 of 37
RECENT MAJOR LABEL CHANGES
7 WARNINGS AND PRECAUTIONS Neurologic, Serotonin toxicity / Serotonin
syndrome
NOV, 2020
7 WARNINGS AND PRECAUTIONS, Respiratory, Sleep Apnea
NOV, 2020
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
................................................................ 4
1
INDICATIONS
....................................................................................................................
4
1.1 Pediatrics
.....................................................................................................................
4
1.2 Geriatrics
......................................................................................................................
4
2
CONTRAINDICATIONS
.....................................................................................................
4
3
SERIOUS WARNINGS AND PRECAUTIONS BOX
.......................................................... 5
4
DOSAGE AND ADMINISTRATION
...................................................................................
6
4.1 Dosing Considerations
.................................................................................................
6
4.2 Recommended Dose and Dosage Adjustment
............................................................. 6
4.3 Administration
.....................