RIVA-SILDENAFIL TABLET

Riik: Kanada

keel: inglise

Allikas: Health Canada

Osta kohe

Toote omadused Toote omadused (SPC)
28-12-2012

Toimeaine:

SILDENAFIL (SILDENAFIL CITRATE)

Saadav alates:

LABORATOIRE RIVA INC.

ATC kood:

G04BE03

INN (Rahvusvaheline Nimetus):

SILDENAFIL

Annus:

25MG

Ravimvorm:

TABLET

Koostis:

SILDENAFIL (SILDENAFIL CITRATE) 25MG

Manustamisviis:

ORAL

Ühikuid pakis:

4/8/30

Retsepti tüüp:

Prescription

Terapeutiline ala:

PHOSPHODIESTERASE TYPE 5 INHIBITORS

Toote kokkuvõte:

Active ingredient group (AIG) number: 0136261001; AHFS:

Volitamisolek:

CANCELLED PRE MARKET

Loa andmise kuupäev:

2016-02-04

Toote omadused

                                PRODUCT MONOGRAPH
PR RIVA-SILDENAFIL
Sildenafil tablets (as sildenafil citrate)
25 mg, 50 mg and 100 mg
cGMP-Specific Phosphodiesterase Type 5 Inhibitor
Treatment of Erectile Dysfunction
LABORATOIRE RIVA INC.
DATE OF PREPARATION:
660 Boul. Industriel
December 18, 2012
Blainville Québec
J7C 3V4
SUBMISSION CONTROL NO: 160584
_Riva-SILDENAFIL V Product Monograph Page 2 of 46_
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
.........................................................................................................
10
DOSAGE AND ADMINISTRATION
.....................................................................................
14
OVERDOSAGE
.......................................................................................................................
15
ACTION AND CLINICAL PHARMACOLOGY
................................................................... 16
STORAGE AND
STABILITY.................................................................................................
19
SPECIAL HANDLING INSTRUCTIONS
..............................................................................
19
DOSAGE FORMS, COMPOSITION AND PACKAGING
.................................................... 19
PART II: SCIENTIFIC INFORMATION
.....................................................................................
21
PHARMACEUTICAL INFOR
                                
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