BUSPIRONE-10 TABLET

Država: Kanada

Jezik: angleščina

Source: Health Canada

Aktivna sestavina:

BUSPIRONE HYDROCHLORIDE

Dostopno od:

PRO DOC LIMITEE

Koda artikla:

N05BE01

INN (mednarodno ime):

BUSPIRONE

Odmerek:

10MG

Farmacevtska oblika:

TABLET

Sestava:

BUSPIRONE HYDROCHLORIDE 10MG

Pot uporabe:

ORAL

Enote v paketu:

100

Tip zastaranja:

Prescription

Terapevtsko območje:

MISCELLANEOUS ANXIOLYTICS SEDATIVES AND HYPNOTICS

Povzetek izdelek:

Active ingredient group (AIG) number: 0116263001; AHFS:

Status dovoljenje:

APPROVED

Datum dovoljenje:

2022-01-05

Lastnosti izdelka

_BUSPIRONE _
_Page 1 of 38_
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
BUSPIRONE-5
PR
BUSPIRONE-10
Buspirone Hydrochloride Tablets
5 mg and 10 mg, Oral
USP
Anxiolytic
PRO DOC LTÉE
2925, boul. Industriel
Laval, Québec
H7L 3W9
Submission Control Number: 259313
Date of Initial Authorization:
January 15, 1997
Date of Revision:
December
31, 2021
Buspirone
Buspirone En PM.pdf
Pg. 1
_ _
_BUSPIRONE _
_Page 2 of 38_
RECENT MAJOR LABEL CHANGES
1 Indications, 1.2 Geriatrics
11/2021
2 Contraindications
04/2021
3 Serious warnings and precautions box
11/2021
4 Dosage and administration, 4.1 Dosing Considerations
11/2021
7 Warnings and precautions, General
11/2021
7 Warnings and Precautions, Serotonin Toxicity/Serotonin Syndrome
04/2021
7 Warnings and precautions, Dependence/Tolerance
11/2021
7 Warnings and precautions, Withdrawal
11/2021
7 Warnings and precautions, Falls and Fractures
11/2021
7 Warnings and precautions, 7.1.4 Geriatrics
11/2021
8 Adverse Reactions, 8.5 Post-Market Adverse Reactions
11/2021
9 Drug Interactions
04/2021
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
...................................................................................................