PARLODEL TAB 2.5MG TABLET

국가: 캐나다

언어: 영어

출처: Health Canada

유효 성분:

BROMOCRIPTINE (BROMOCRIPTINE MESYLATE)

제공처:

NOVARTIS PHARMACEUTICALS CANADA INC

ATC 코드:

G02CB01

INN (국제 이름):

BROMOCRIPTINE

복용량:

2.5MG

약제 형태:

TABLET

구성:

BROMOCRIPTINE (BROMOCRIPTINE MESYLATE) 2.5MG

관리 경로:

ORAL

패키지 단위:

100

처방전 유형:

Prescription

치료 영역:

ERGOT-DERIVATIVE DOPAMINE RECEPTOR AGONISTS

제품 요약:

Active ingredient group (AIG) number: 0111278001; AHFS:

승인 상태:

CANCELLED POST MARKET

승인 날짜:

2007-07-18

제품 특성 요약

P
RODUCT
M
ONOGRAPH
PR
PARLODEL*
(bromocriptine mesylate)
Tablets 2.5 mg
_ _
Prolactin Inhibitor
Growth Hormone Suppressant in Acromegaly
Adjunctive Medication in Parkinson's Disease
Novartis Pharmaceuticals Canada Inc.
DATE OF PREPARATION:
Dorval, Quebec
Sept. 14, 1976
H9S 1A9
DATE OF REVISION:
Control#: 106906
June 6, 2007
*PARLODEL is a registered trademark.
- 2 -
PRODUCT MONOGRAPH
NAME OF DRUG
Pr
PARLODEL*
(bromocriptine mesylate)
Tablets 2.5 mg
THERAPEUTIC CLASSIFICATION
Prolactin Inhibitor
Growth Hormone Suppressant in Acromegaly
Adjunctive Medication in Parkinson's Disease
CLINICAL PHARMACOLOGY
PARLODEL* (bromocriptine mesylate) is a dopaminomimetic ergot
derivative with D
2
-type
dopamine receptor agonist activity, which also has D
1
dopamine receptor antagonist properties.
PARLODEL* inhibits the release and synthesis of prolactin by acting
directly on the prolactin
secreting cells of the anterior pituitary. In patients with
acromegaly, in addition to lowering
prolactin and elevated levels of growth hormone, PARLODEL* has a
beneficial effect on clinical
symptoms and on glucose tolerance.
- 3 -
The dopaminomimetic activity of PARLODEL* in the nigro-striatal
pathway is considered
responsible for the clinical benefits seen in patients with
Parkinson's disease.
The metabolism of dopamine, from exogenous and endogenous origin, is
known to involve the
formation of peroxides and free radicals. It has been postulated that
these agents may in fact
contribute to the progression of Parkinson's disease by accelerating
the rate at which neuronal cells
are lost. Bromocriptine's metabolic pathway does not involve the
formation of such peroxides and
free radicals. It has been suggested that because bromocriptine
attenuates the timing and rate of
levodopa dosage increase, early use of the drug may reduce risk of
formation of potentially toxic
peroxides and free radicals.
In man, bromocriptine is rapidly absorbed after oral administration
with an absorption half-life of
approximately 0.3 hours. An oral dose of 5 mg of brom