Страна: Канада
мова: англійська
Джерело: Health Canada
BUPROPION HYDROCHLORIDE
PHARMASCIENCE INC
N06AX12
BUPROPION
100MG
TABLET (EXTENDED-RELEASE)
BUPROPION HYDROCHLORIDE 100MG
ORAL
60
Prescription
MISCELLANEOUS ANTIDEPRESSANTS
Active ingredient group (AIG) number: 0131140002; AHFS:
APPROVED
2009-04-28
PRODUCT MONOGRAPH PR PMS-BUPROPION SR Bupropion Hydrochloride Sustained Release Tablets, House Standard 100 mg and 150 mg Antidepressant PHARMASCIENCE INC. Date of Revision: 6111 Royalmount Ave, Suite 100 April 25, 2017 Montréal, Québec H4P 2T4 www.pharmascience.com Control number: 204578 _Product Monograph pms-BUPROPION SR _ _Page 2 of 39 _ TABLE OF CONTENTS PART I: HEALTH PROFESSIONAL INFORMATION ..................................................... 3 SUMMARY PRODUCT INFORMATION ........................................................................... 3 INDICATIONS AND CLINICAL USE ................................................................................. 3 CONTRAINDICATIONS ...................................................................................................... 4 WARNINGS AND PRECAUTIONS ..................................................................................... 4 ADVERSE REACTIONS ..................................................................................................... 11 DRUG INTERACTIONS ..................................................................................................... 16 DOSAGE AND ADMINISTRATION ................................................................................. 19 OVERDOSAGE ................................................................................................................... 21 ACTION AND CLINICAL PHARMACOLOGY ............................................................... 22 STORAGE AND STABILITY ............................................................................................. 26 DOSAGE FORMS, COMPOSITION AND PACKAGING ................................................ 26 PART II: SCIENTIFIC INFORMATION ........................................................................... 27 PHARMACEUTICAL INFORMATION ............................................................................. 27 CLINICAL TRIALS .................................................................................................... Прочитайте повний документ