PRIVA-SILDENAFIL TABLET

Šalis: Kanada

kalba: anglų

Šaltinis: Health Canada

Veiklioji medžiaga:

SILDENAFIL (SILDENAFIL CITRATE)

Prieinama:

NORA PHARMA INC

ATC kodas:

G04BE03

INN (Tarptautinis Pavadinimas):

SILDENAFIL

Dozė:

100MG

Vaisto forma:

TABLET

Sudėtis:

SILDENAFIL (SILDENAFIL CITRATE) 100MG

Vartojimo būdas:

ORAL

Vienetai pakuotėje:

4/8

Recepto tipas:

Prescription

Gydymo sritis:

PHOSPHODIESTERASE TYPE 5 INHIBITORS

Produkto santrauka:

Active ingredient group (AIG) number: 0136261003; AHFS:

Autorizacija statusas:

CANCELLED POST MARKET

Leidimo data:

2023-07-01

Prekės savybės

PRODUCT MONOGRAPH
PR
PRIVA-SILDENAFIL
Sildenafil Citrate Tablets
25 mg, 50 mg, and 100 mg
,
cGMP-Specific Phosphodiesterase Type 5 Inhibitor
Treatment of Erectile Dysfunction
NORA PHARMA INC.
1565, Lionel-Boulet Boul.
Varennes, Quebec
J3X 1P7
Control #: 264224
Date
of
Preparation:
June 10, 2022
_Priva-SILDENAFIL_
Page 2 of 55
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....................................................................................................
11
DOSAGE AND
ADMINISTRATION................................................................................
14
OVERDOSAGE..................................................................................................................
15
ACTION AND CLINICAL
PHARMACOLOGY..............................................................
16
STORAGE AND
STABILITY...........................................................................................
19
DOSAGE FORMS, COMPOSITION AND
PACKAGING...............................................
19
PART II: SCIENTIFIC
INFORMATION.........................................................................
20
PHARMACEUTICAL
INFORMATION...........................................................................
20
CLINICAL
TRIALS...........................................................................................................
21
DETAILED
PHARMACOLOGY.................................