Brusartan 100mg

Nchi: Armenia

Lugha: Kiingereza

Chanzo: Դեղերի և բժշկական տեխնոլոգիաների փորձագիտական կենտրոնի գործունեության Հայաստանի Հանրապետությունում

Shusha Tabia za bidhaa (SPC)
06-06-2014

Viambatanisho vya kazi:

losartan (losartan potassium)

Inapatikana kutoka:

Brupharmexport sprl

INN (Jina la Kimataifa):

losartan (losartan potassium)

Kipimo:

100mg

Dawa fomu:

tablets film-coated

Dawa ya aina:

Prescription

Tabia za bidhaa

                                1
SUMMARY OF PRODUCT CHARACTERISTICS
1. NAME OF THE MEDICINAL PRODUCT
BRUSARTAN 50MG
BRUSARTAN 100MG
2. QUALITATIVE AND QUANTITATIVE COMPOSITION
Each BRUSARTAN 50 mg film-coated tablet contains 50 mg losartan
potassium.
Each BRUSARTAN 100 mg film-coated tablet contains 100 mg losartan
potassium.
For full list of excipients, see section 6.1.
3. PHARMACEUTICAL FORM
Film-coated tablet (tablet).
BRUSARTAN 50 mg: film-coated, white to off-white, oval shaped scored
tablets.
Tablets can be divided into equal halves.
BRUSARTAN 100 mg: film-coated, white to off-white, oval shaped scored
tablets.
Tablets can be divided into equal halves.
4. CLINICAL PARTICULARS
4.1 THERAPEUTIC INDICATIONS
Treatment of essential hypertension in adults and in children and
adolescents 6 – 18 years of age.
Treatment of renal disease in adult patients with hypertension and
type 2 diabetes mellitus with proteinuria
≥0.5 g/day as part of an anti-hypertensive treatment.
Treatment of chronic heart failure (in patients ≥60 years), when
treatment with Angiotensin-Converting
Enzyme
(ACE)
inhibitors
is
not
considered
suitable
due
to
incompatibility,
especially
cough,
or
contraindication. In patients with heart failure who have been
stabilized with an ACE inhibitor, a switch to
losartan is not recommended. The patients should have a left
ventricular ejection fraction ≤40% and should
be stabilized under the treatment of the chronic heart failure.
Reduction in the risk of stroke in hypertensive patients with left
ventricular hypertrophy documented by
ECG (see 5.1: LIFE study, Race).
4.2 POSOLOGY AND METHOD OF ADMINISTRATION
BRUSARTAN tablets should be swallowed with a glass of water.
BRUSARTAN may be administered with or without food.
2
HYPERTENSION
The usual starting and maintenance dose is 50 mg once daily for most
patients. The maximal anti-
hypertensive effect is attained 3 - 6 weeks after initiation of
therapy. Some patients may receive an additional
benefit by increasing the dose to 100 mg once daily (in the morning).
Losartan
may
be
adminis
                                
                                Soma hati kamili
                                
                            

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