Riik: Kanada
keel: inglise
Allikas: Health Canada
SILDENAFIL (SILDENAFIL CITRATE)
PHARMARIS CANADA INC
G04BE03
SILDENAFIL
100MG
TABLET
SILDENAFIL (SILDENAFIL CITRATE) 100MG
ORAL
4/8
Prescription
PHOSPHODIESTERASE TYPE 5 INHIBITORS
Active ingredient group (AIG) number: 0136261003; AHFS:
APPROVED
2017-09-22
PRODUCT MONOGRAPH PR PRZ-SILDENAFIL Sildenafil (as Sildenafil citrate) Tablets 100 mg cGMP-Specific Phosphodiesterase Type 5 Inhibitor Treatment of Erectile Dysfunction Pharmaris Canada Inc. Date of Revision: 8310-130 th Street, Suite 102, November 26, 2019 Surrey, British Columbia V3W 8J9 Control # 233376 TABLE OF CONTENTS PART I: HEALTH PROFESSIONAL INFORMATION ............................................................................ 3 SUMMARY PRODUCT INFORMATION ............................................................................................. 3 INDICATIONS AND CLINICAL USE ................................................................................................... 3 CONTRAINDICATIONS ........................................................................................................................ 3 WARNINGS AND PRECAUTIONS ...................................................................................................... 4 ADVERSE REACTIONS ........................................................................................................................ 7 DRUG INTERACTIONS ....................................................................................................................... 12 DOSAGE AND ADMINISTRATION ................................................................................................... 15 OVERDOSAGE ..................................................................................................................................... 16 ACTION AND CLINICAL PHARMACOLOGY ................................................................................. 17 STORAGE AND STABILITY .............................................................................................................. 19 SPECIAL HANDLING INSTRUCTIONS ............................................................................................ 20 DOSAGE FORMS, COMPOSITION AND PACKAGING .................................................................. 20 PART II: SCIENTIFIC INFORMAT Lugege kogu dokumenti