AMITRIPTYLINE TABLET

Valsts: Kanāda

Valoda: angļu

Klimata pārmaiņas: Health Canada

Aktīvā sastāvdaļa:

AMITRIPTYLINE HYDROCHLORIDE

Pieejams no:

SIVEM PHARMACEUTICALS ULC

ATĶ kods:

N06AA09

SNN (starptautisko nepatentēto nosaukumu):

AMITRIPTYLINE

Deva:

50MG

Zāļu forma:

TABLET

Kompozīcija:

AMITRIPTYLINE HYDROCHLORIDE 50MG

Ievadīšanas:

ORAL

Vienības iepakojumā:

100/1000

Receptes veids:

Prescription

Ārstniecības joma:

TRICYCLICS AND OTHER NOREPINEPHRINE-REUPTAKE INHIBITORS

Produktu pārskats:

Active ingredient group (AIG) number: 0101524003; AHFS:

Autorizācija statuss:

CANCELLED POST MARKET

Autorizācija datums:

2018-11-01

Produkta apraksts

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PRODUCT MONOGRAPH
Pr
AMITRIPTYLINE
(Amitriptyline Hydrochloride, USP)
10mg, 25mg, and 50mg tablets
Antidepressant
Sivem Parmaceuticals ULC
4705 Dobrin Street
Saint-Laurent, Quebec
Canada H4R 2P7
www.sivem.ca
Date of Preparation:
February 03, 2016
Control Number: 191591
_Pr_
_AMITRIPTYLINE _
_ 2 of 10 _
ACTION
Amitriptyline hydrochloride is a tricyclic antidepressant with
sedative properties. Its
mechanism of action in man is not known. Amitriptyline inhibits the
membrane pump
mechanism responsible for the re-uptake of transmitter amines, such as
norepinephrine and
serotonin, thereby increasing their concentration at the synaptic
clefts of the brain.
Amitriptyline has pronounced anticholinergic properties and produces
EKG changes and
quinidine-like effects on the heart (See ADVERSE REACTIONS). It also
lowers the
convulsive threshold and causes alterations in EEG and sleep patterns.
Orally administered amitriptyline is readily absorbed and rapidly
metabolized. Steady-state
plasma concentrations vary widely and this variation may be
genetically determined.
Amitriptyline is primarily excreted in the urine, mostly in the form
of metabolites, with some
excretion also occurring in the feces.
INDICATIONS
AMITRIPTYLINE (amitriptyline hydrochloride USP) is indicated for the
relief of symptoms of
depressive illness.
CONTRAINDICATIONS
Known hypersensitivity. Amitriptyline should not be given
concomitantly with or within at
least 14 days following the discontinuance of a MAO inhibitor. Then
initiate dosage of
amitriptyline cautiously with gradual increase in dosage until optimum
response is achieved.
Amitriptyline is not recommended during the acute recovery phase
following myocardial
infarction, and in the presence of acute congestive heart failure.
WARNINGS
Arrhythmias, sinus tachycardia, and prolongation of the conduction
time have been reported,
particularly with high doses of amitriptyline. A few instances of
unexpected death have been
reported in patients with cardiovascular disorders. M