MYLAN-ROSUVASTATIN TABLET

Država: Kanada

Jezik: angleščina

Source: Health Canada

Kupite ga zdaj

Lastnosti izdelka Lastnosti izdelka (SPC)
30-05-2017

Aktivna sestavina:

ROSUVASTATIN (ROSUVASTATIN CALCIUM)

Dostopno od:

MYLAN PHARMACEUTICALS ULC

Koda artikla:

C10AA07

INN (mednarodno ime):

ROSUVASTATIN

Odmerek:

40MG

Farmacevtska oblika:

TABLET

Sestava:

ROSUVASTATIN (ROSUVASTATIN CALCIUM) 40MG

Pot uporabe:

ORAL

Enote v paketu:

30/100

Tip zastaranja:

Prescription

Terapevtsko območje:

HMG-COA REDUCTASE INHIBITORS

Povzetek izdelek:

Active ingredient group (AIG) number: 0148963003; AHFS:

Status dovoljenje:

CANCELLED POST MARKET

Datum dovoljenje:

2018-05-10

Lastnosti izdelka

                                _Page 1 of 46 _
PRODUCT MONOGRAPH
PR
MYLAN-ROSUVASTATIN
Rosuvastatin Calcium Tablets
5 mg, 10 mg, 20 mg and 40 mg
LIPID METABOLISM REGULATOR
Mylan Pharmaceuticals ULC
85 Advance Road
Etobicoke, ON
M8Z 2S6
Submission Control No.: 205317
Date of Revision: May 11, 2017
_Page 2 of 46_
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
......................................... 3
SUMMARY PRODUCT INFORMATION
........................................................ 3
INDICATIONS AND CLINICAL USE
.............................................................. 3
CONTRAINDICATIONS
....................................................................................
4
WARNINGS AND PRECAUTIONS
.................................................................. 5
ADVERSE REACTIONS
..................................................................................
10
DRUG INTERACTIONS
...................................................................................
16
DOSAGE AND ADMINISTRATION
.............................................................. 22
OVERDOSAGE
..................................................................................................
24
ACTION AND CLINICAL PHARMACOLOGY
........................................... 24
STORAGE AND STABILITY
..........................................................................
27
DOSAGE FORMS, COMPOSITION AND PACKAGING ........................... 27
PART II: SCIENTIFIC INFORMATION
............................................................... 28
PHARMACEUTICAL INFORMATION
........................................................ 28
CLINICAL TRIALS
..........................................................................................
29
DETAILED PHARMACOLOGY
.....................................................................
33
TOXICOLOGY
..................................................................................................
34
REFERENCES
...................................................................................................
40
P
                                
                                Preberite celoten dokument
                                
                            

Dokumenti v drugih jezikih

Lastnosti izdelka Lastnosti izdelka francoščina 11-05-2017

Opozorila o iskanju, povezana s tem izdelkom