PRIVA-PRAVASTATIN TABLET

ประเทศ: แคนาดา

ภาษา: อังกฤษ

แหล่งที่มา: Health Canada

สารออกฤทธิ์:

PRAVASTATIN SODIUM

มีจำหน่ายจาก:

PHARMAPAR INC

รหัส ATC:

C10AA03

INN (ชื่อสากล):

PRAVASTATIN

ปริมาณ:

40MG

แบบฟอร์มเภสัชกรรม:

TABLET

องค์ประกอบ:

PRAVASTATIN SODIUM 40MG

เส้นทางการบริหาร:

ORAL

หน่วยในแพ็คเกจ:

100/500

ประเภทใบสั่งยา:

Prescription

พื้นที่บำบัด:

HMG-COA REDUCTASE INHIBITORS

สรุปสินค้า:

Active ingredient group (AIG) number: 0122563003; AHFS:

สถานะการอนุญาต:

CANCELLED POST MARKET

วันที่อนุญาต:

2022-07-29

สรุปลักษณะสินค้า

_Priva-PRAVASTATIN _
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PRODUCT MONOGRAPH
PR
PRIVA-PRAVASTATIN
Pravastatin Sodium Tablets, USP
10 mg, 20 mg and 40 mg
LIPID METABOLISM REGULATOR
PHARMAPAR INC.
DATE OF PREPARATION:
100-5950, Ch. de la Côte de Liesse
September 1, 2015
Mont-Royal
Qc, H4T 1E2
Control # 186294
_Priva-PRAVASTATIN _
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TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL
INFORMATION................................................................
3
SUMMARY PRODUCT INFORMATION
....................................................................................
3
INDICATIONS AND CLINICAL USE
..........................................................................................
3
CONTRAINDICATIONS
...............................................................................................................
5
WARNINGS AND PRECAUTIONS
..............................................................................................
5
ADVERSE REACTIONS
..............................................................................................................
10
DRUG INTERACTIONS
..............................................................................................................
13
DOSAGE AND ADMINISTRATION
..........................................................................................
15
OVERDOSAGE
............................................................................................................................
16
ACTION AND CLINICAL PHARMACOLOGY
........................................................................
16
STORAGE AND STABILITY
......................................................................................................
18
DOSAGE FORMS, COMPOSITION AND PACKAGING
......................................................... 18
PART II: SCIENTIFIC INFORMATION
.....................................................................................
19
PHARMACEUTICAL INFORMATION
......................................................................................
19
C