TEVA-FOSINOPRIL TABLET

Valsts: Kanāda

Valoda: angļu

Klimata pārmaiņas: Health Canada

Aktīvā sastāvdaļa:

FOSINOPRIL SODIUM

Pieejams no:

TEVA CANADA LIMITED

ATĶ kods:

C09AA09

SNN (starptautisko nepatentēto nosaukumu):

FOSINOPRIL

Deva:

20MG

Zāļu forma:

TABLET

Kompozīcija:

FOSINOPRIL SODIUM 20MG

Ievadīšanas:

ORAL

Vienības iepakojumā:

100

Receptes veids:

Prescription

Ārstniecības joma:

ANGIOTENSIN-CONVERTING ENZYME INHIBITORS

Produktu pārskats:

Active ingredient group (AIG) number: 0122777002; AHFS:

Autorizācija statuss:

APPROVED

Autorizācija datums:

2003-11-06

Produkta apraksts

PRODUCT MONOGRAPH
PR
TEVA-FOSINOPRIL
(Fosinopril sodium)
10 mg and 20 mg Tablets
Angiotensin Converting Enzyme Inhibitor
Teva Canada Limited
Date of Revision: MAR 07, 2024
30 Novopharm Court
Toronto, Ontario
M1B 2K9
www.tevacanada.com
Control #: 280055
2
PRODUCT MONOGRAPH
PR
TEVA-FOSINOPRIL
(fosinopril sodium)
10 mg and 20 mg Tablets
THERAPEUTIC CLASSIFICATION
Angiotensin Converting Enzyme Inhibitor
ACTION AND CLINICAL PHARMACOLOGY
TEVA-FOSINOPRIL (fosinopril sodium) is an angiotensin converting
enzyme (ACE) inhibitor
which is used in the treatment of mild to moderate essential
hypertension and in the management
of symptomatic congestive heart failure.
Following oral administration, TEVA-FOSINOPRIL, an ester prodrug, is
rapidly hydrolyzed to
fosinoprilat, its principal active metabolite.
ACE is a peptidyl dipeptidase that catalyzes the conversion of
angiotensin I to the
vasoconstrictor substance, angiotensin II. Angiotensin II also
stimulates aldosterone secretion by
the adrenal cortex. Inhibition of ACE activity leads to decreased
levels of angiotensin II thereby
resulting in decreased vasoconstriction and decreased aldosterone
secretion. The latter decrease
may result in a small increase in serum potassium. Decreased levels of
angiotensin II and the
accompanying lack of negative feedback on renal renin secretion
results in increases in plasma
renin activity.
ACE is identical to kininase II. Thus, fosinopril may interfere with
the degradation of
bradykinin, a potent peptide vasodilator. However, it is not known
whether this contributes to the
therapeutic effects of TEVA-FOSINOPRIL.
While the mechanism through which TEVA-FOSINOPRIL lowers blood
pressure appears to
result primarily from suppression of the renin-angiotensin-aldosterone
system, TEVA-
FOSINOPRIL has an antihypertensive effect even in patients with
low-renin hypertension.
The antihypertensive effect of angiotensin converting enzyme
inhibitors is generally lower in
black patients than in non-blacks.
3
PHARMACOKINETICS AND METABOLISM
Following oral admi