DOPAGEN Tablets 125 Milligram

국가: 아일랜드

언어: 영어

출처: HPRA (Health Products Regulatory Authority)

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제품 특성 요약 제품 특성 요약 (SPC)
06-05-2024

유효 성분:

METHYLDOPA

제공처:

Mercury Pharmaceuticals (Ireland) Ltd

복용량:

125 Milligram

약제 형태:

Tablets

승인 날짜:

1981-11-04

제품 특성 요약

                                PART II
SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
Dopagen Tablets 125 mg.
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each tablet contains Methyldopa equivalent to 125 mg
anhydrous methyldopa.
For excipients, see 6.1.
3 PHARMACEUTICAL FORM
Yellow, film-coated tablets embossed ‘a’ on
one face and ‘M/125’ on the other.
4 CLINICAL PARTICULARS 
4.1 THERAPEUTIC INDICATIONS
In the treatment of hypertension.
4.2 POSOLOGY AND METHOD OF ADMINSTRATION
Dopagen tablets are for oral administration only.
_Adults:_
The usual dose is 250 - 500mg daily with
subsequent slow increments until optimal control is achieved. Maintenance 
dosage is usually 0.5 to 2.0 grams daily in divided
doses. The maximum recommended daily dosage is 3 grams.
_Children: _
The usual initial dosage is 10mg/kg body weight daily in 2 to 4
divided doses with gradual increments until optimal 
control is achieved. The usual maintenance dose is 10 to
65mg/kg daily, but a maximum dose of 3g or 65mg/kg, 
whichever is less, should not be exceeded.
_Elderly: _
In older patients, syncope may be related to an increased
sensitivity and to atherosclerosis and may be avoided by using 
lower doses.
4.3 CONTRAINDICATIONS
1)
Hypersensitivity to methyldopa or to any of the components in
these tablets.
2)
Active liver disease.
3)
Depression.
4)
Concurrent use of monoamine oxidase inhibitors (MAOIs).
5)
Methyldopa is not recommended
for the treatment of phaeochromocytoma.
IRISH MEDICINES BOARD
________________________________________________________________________________________________________________________
_Date Printed 24/02/2006_
_CRN 2020443_
_page number: 1_
4.4 SPECIAL WARNINGS AND PRECAUTIONS FOR USE
Methyldopa may give rise to haemolytic anaemia,
the occurrence of which necessitates stopping the drug and the 
initiation of appropriate therapy. Leucopenia and
thrombocytopenia may
                                
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