PHOLCOLIN Unknown 5 MG/5ml
देश: आयरलैंड
भाषा: अंग्रेज़ी
स्रोत: HPRA (Health Products Regulatory Authority)
उत्पाद विशेषताएं
(SPC)
26-05-2024
इस उत्पाद के लिए कुछ दस्तावेज़ वर्तमान में उपलब्ध नहीं हैं, आप हमारी ग्राहक सेवा को अनुरोध भेज सकते हैं और जैसे ही हम उन्हें प्राप्त करने में सक्षम होंगे, हम आपको सूचित करेंगे।
अनुरोध भेजा।
अनुरोध भेजा।
सक्रिय संघटक:
PHOLCODINE
थमां उपलब्ध:
Mercury Pharmaceuticals (Ireland) Ltd
डोज़:
5 MG/5ml
फार्मास्यूटिकल फॉर्म:
Unknown
प्राधिकरण की तारीख:
1978-04-01
उत्पाद विशेषताएं
PART II
SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
Pholcolin 5 mg/5 ml Oral Solution
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each 5ml of solution contains Pholcodine 5 mg.
For excipients, see 6.1.
3 PHARMACEUTICAL FORM
Oral solution
Amber coloured, sweet tasting oral solution.
4 CLINICAL PARTICULARS
4.1 THERAPEUTIC INDICATIONS
In the management of non-productive cough.
4.2 POSOLOGY AND METHOD OF ADMINISTRATION
Pholcolin is for oral administration.
Adults:
10mg up to three times daily.
Children:
1 - 2 years:
2.5 mg up to three times daily.
Over 2 years:
5.0 mg up to three times daily.
4.3 CONTRAINDICATIONS
Use in patients with hypersensitivity or idiosyncratic response to pholcodine.
4.4 SPECIAL WARNINGS AND PRECAUTIONS FOR USE
This product should only be used for suppression of non-productive cough.
Pholcolin is not for use in infants less than 1 year without consulting a doctor.
If symptoms persist of worsen, the doctor should be consulted.
The product should not be taken for persistent or chronic cough such as occurs with smoking, asthma or emphysema or
if the cough is accompanied by excessive mucus (phlegm), unless directed by a doctor.
This medicinal product contains Nipasept sodium, a preservative which contains hydroxybenzoates that may
sometimes cause allergic reactions (possibly delayed).
IRISH MEDICINES BOARD
________________________________________________________________________________________________________________________
_Date Printed 18/01/2007_
_CRN 2032334_
_page number: 1_
This medicinal product contains less than 1 mmol sodium per dose, i.e. essentially ‘sodium free’.
4.5 INTERACTION WITH OTHER MEDICINAL PRODUCTS AND OTHER FORMS OF INTERACTION
Concomitant administration of alcohol or other CNS depressants may lead to greater drowsiness and sedation.
4.
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