VITAROS CREAM

Država: Kanada

Jezik: angleščina

Source: Health Canada

Kupite ga zdaj

Prenos Lastnosti izdelka (SPC)
09-01-2015

Aktivna sestavina:

ALPROSTADIL

Dostopno od:

BGP PHARMA ULC

Koda artikla:

G04BE01

INN (mednarodno ime):

ALPROSTADIL

Odmerek:

220MCG

Farmacevtska oblika:

CREAM

Sestava:

ALPROSTADIL 220MCG

Pot uporabe:

TOPICAL

Enote v paketu:

100MG

Tip zastaranja:

Prescription

Terapevtsko območje:

MISCELLANEOUS VASODILATATING AGENTS

Povzetek izdelek:

Active ingredient group (AIG) number: 0115288013; AHFS:

Status dovoljenje:

APPROVED

Datum dovoljenje:

2015-01-22

Lastnosti izdelka

                                _ _
_VITAROS_
_™ _
_Product Monograph _
_Page 1 of 38_
PRODUCT MONOGRAPH
Pr
VITAROS™
alprostadil
Cream 220 mcg/ 100 mg, 330 mcg/ 100 mg
Alprostadil for Treatment of Male Erectile Dysfunction
BGP Pharma Inc.
8401 Trans-Canada Highway
St-Laurent, Qc H4S 1Z1
Control Number : 180901
Date of Preparation:
January 8, 2015
_ _
_VITAROS_
_™_
_ Product Monograph _
_Page 2 of 38_
TABLE OF CONTENTS PAGE
PART I: HEALTH PROFESSIONAL INFORMATION
.........................................................3
SUMMARY PRODUCT INFORMATION
........................................................................3
INDICATIONS AND CLINICAL USE
..............................................................................3
CONTRAINDICATIONS
...................................................................................................3
WARNINGS AND PRECAUTIONS
..................................................................................4
ADVERSE REACTIONS
....................................................................................................6
DRUG INTERACTIONS
..................................................................................................12
DOSAGE AND ADMINISTRATION
..............................................................................12
OVERDOSAGE
................................................................................................................13
OVERDOSAGE
................................................................................................................13
ACTION AND CLINICAL PHARMACOLOGY
............................................................13
STORAGE AND STABILITY
..........................................................................................16
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................16
PART II: SCIENTIFIC INFORMATION
...............................................................................17
PHARMACEUTICAL INFORMATION
.......................................................................
                                
                                Preberite celoten dokument
                                
                            

Opozorila o iskanju, povezana s tem izdelkom

Ogled zgodovine dokumentov