RATIO-FENOFIBRATE MC CAPSULE

Negara: Kanada

Bahasa: Inggris

Sumber: Health Canada

Beli Sekarang

Unduh Karakteristik produk (SPC)
22-09-2014

Bahan aktif:

FENOFIBRATE

Tersedia dari:

TEVA CANADA LIMITED

Kode ATC:

C10AB05

INN (Nama Internasional):

FENOFIBRATE

Dosis:

200MG

Bentuk farmasi:

CAPSULE

Komposisi:

FENOFIBRATE 200MG

Rute administrasi :

ORAL

Unit dalam paket:

30/100

Jenis Resep:

Prescription

Area terapi:

FRIBIC ACID DERIVATIVES

Ringkasan produk:

Active ingredient group (AIG) number: 0118895001; AHFS:

Status otorisasi:

CANCELLED POST MARKET

Tanggal Otorisasi:

2019-09-16

Karakteristik produk

                                PRODUCT MONOGRAPH
Pr
RATIO-FENOFIBRATE MC
Fenofibrate Capsules
67 mg and 200 mg
Lipid Metabolism Regulator
Teva Canada Limited
30 Novopharm Court
Toronto, Ontario
Canada M1B 2K9
Control No. 176744
Date of Revision:
September 9, 2014
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_Page 2 of 39_
PRODUCT MONOGRAPH
PR
RATIO-FENOFIBRATE MC
FENOFIBRATE CAPSULES
67 MG AND 200 MG
THERAPEUTIC
CLASSIFICATION
Lipid Metabolism Regulator
ACTIONS AND CLINICAL PHARMACOLOGY
Fenofibrate lowers elevated serum lipids by decreasing the low density
lipoprotein (LDL)
fraction rich in cholesterol and the very low density lipoprotein
(VLDL) fraction rich in
triglycerides. In addition, fenofibrate increases the high density
lipoprotein (HDL) cholesterol
fraction.
Fenofibrate appears to have a greater depressant effect on the VLDL
than on the low density
lipoproteins (LDL). Therapeutic doses of fenofibrate produce
elevations of HDL cholesterol, a
reduction in the content of the low density lipoproteins cholesterol,
and a substantial reduction in
the triglyceride content of VLDL.
The mechanism of action of fenofibrate has not been definitively
established. Work carried out
to date suggests that fenofibrate:
enhances the liver elimination of cholesterol as bile salts;
inhibits the biosynthesis of triglycerides and enhances the catabolism
of VLDL by
increasing the activity of lipoprotein lipase;
has an inhibitory effect on the biosynthesis of cholesterol by
modulating the activity of
HMG-CoA reductase.
Metabolism and Excretion
After oral administration with food, fenofibrate is rapidly hydrolysed
to fenofibric acid, the active
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_Page 3 of 39_
metabolite. In man it is mainly excreted through the kidney. Half-life
is about 20 hours. In
patients with severe renal failure, significant accumulation was
observed with a large increase in
half-life. Therefore, the dose of fenofibrate may need to be reduced,
depending on the rate of
creatinine clearance.
Distribution
Fenofibrate acid is extensively bound (>99%) to plasma albumin. This
binding is not saturable.
Absorption
Fenofibrat
                                
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