Valsts: Kanāda
Valoda: angļu
Klimata pārmaiņas: Health Canada
CLONAZEPAM
BAUSCH HEALTH, CANADA INC.
N03AE01
CLONAZEPAM
1MG
TABLET
CLONAZEPAM 1MG
ORAL
100/500
Targeted (CDSA IV)
BENZODIAZEPINES
Active ingredient group (AIG) number: 0111558004; AHFS:
APPROVED
2021-03-10
PRODUCT MONOGRAPH CLONAPAM ® Clonazepam Tablets, USP 0.5 mg. 1 mg, and 2 mg ANTICONVULSANT BAUSCH HEALTH, CANADA INC. DATE OF REVISION: 2150 St-Elzear Blvd. West September 1, 2021 Laval, Quebec H7L 4A8 Control #: 253836 _T/C_ _CLONAPAM_ _®_ _ Product Monograph Page 2 of 34_ _ _ 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.....................................................................................................12 DRUG INTERACTIONS .....................................................................................................14 DOSAGE AND ADMINISTRATION ..................................................................................16 OVERDOSAGE ..................................................................................................................17 ACTION AND CLINICAL PHARMACOLOGY..................................................................19 STORAGE AND STABILITY .............................................................................................20 SPECIAL HANDLING INSTRUCTIONS ............................................................................20 DOSAGE FORMS, COMPOSITION AND PACKAGING ...................................................21 PART II: SCIENTIFIC INFORMATION............................................................................... 22 PHARMACEUTICAL INFORMATION ..............................................................................22 CLINICAL TRIALS ................................................... Izlasiet visu dokumentu