Land: Storbritannia
Språk: engelsk
Kilde: MHRA (Medicines & Healthcare Products Regulatory Agency)
Carbocisteine
Esteve Pharmaceuticals Ltd
R05CB03
Carbocisteine
75mg/1ml
Oral solution
Oral
No Controlled Drug Status
Valid as a prescribable product
BNF: 03070000; GTIN: 5039021000152
WHAT IS IN THIS LEAFLET 1. What Carbocisteine oral solution in sachet is and what it is used for 2. What you need to know before you take Carbocisteine oral solution in sachet 3. How to take Carbocisteine oral solution in sachet 4. Possible side effects 5. How to store Carbocisteine oral solution in sachet 6. Contents of the pack and other information 1. WHAT CARBOCISTEINE ORAL SOLUTION IN SACHET IS AND WHAT IT IS USED FOR This medicine belongs to a group of medicines called “mucolytics”. It works by making mucus (phlegm) less sticky. This makes the mucus easier to cough up. This medicine is used for problems with the breathing passages (respiratory tract). This medicine is indicated in adults and children over 15 years. 2. WHAT YOU NEED TO KNOW BEFORE YOU TAKE CARBOCISTEINE ORAL SOLUTION IN SACHET DO NOT TAKE CARBOCISTEINE ORAL SOLUTION IN SACHET: - if you are allergic to carbocisteine or any of the other ingredients contained in Carbocisteine oral solution in sachet, - if you have an ulcer in your stomach or gut (small intestine). When in doubt, you should always consult a doctor or pharmacist. PLEASE TAKE SPECIAL CARE WITH CARBOCISTEINE ORAL SOLUTION IN SACHET: Consult your doctor immediately: • if you have thick, purulent sputum or fever, • if you suffer from chronic illness (long-term) of the bronchi or lungs, • if you are elderly, • if you have had an ulcer in your stomach or gut, • if you are taking other medicines known to cause bleeding in the gut. PRECAUTIONS FOR USE This medicine should always be accompanied by voluntary efforts to cough, which help expectoration. Do not take cough medicine (to stop coughing) or medicine that dries out bronchial secretions during the treatment period with carbocisteine. CONSULT A DOCTOR IF NO IMPROVEMENT IS SEEN. OTHER MEDICINES AND CARBOCISTEINE ORAL SOLUTION IN SACHET Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines, even if it is medication obtained without a prescription. This medicine contains ca Les hele dokumentet
OBJECT 1 CARBOCISTEINE 750MG/10ML SUGAR-FREE ORAL SOLUTION IN SACHET Summary of Product Characteristics Updated 19-Nov-2017 | Intrapharm Laboratories Limited 1. Name of the medicinal product Carbocisteine unither pharmaceuticals 750mg/10ml sugar-free oral solution in sachet Carbocisteine 750mg/10ml sugar-free oral solution in sachet 2. Qualitative and quantitative composition Each 10 ml of oral solution contains 750 mg of carbocisteine Excipients with known effect: sodium methyl para-hydroxybenzoate (E 219) 15mg per dose sorbitol liquid (non-crystallising) 1.3g per dose maltitol, liquid 1.3g per dose sodium 97.5mg per dose ethanol (trace) For the full list of excipients, see section 6.1. 3. Pharmaceutical form Oral solution in sachet. Limpid, viscous, light brown solution. 4. Clinical particulars 4.1 Therapeutic indications This medicine is indicated in adults and children over 15 years for the adjunctive therapy of respiratory tract disorders characterised by excessive, viscous mucus, including chronic obstructive airways disease. 4.2 Posology and method of administration FOR ADULTS AND CHILDREN OVER 15 YEARS ONLY Oral route. One 10 ml sachet contains 750 mg of carbocisteine. The standard dose is 750 mg, 3 times a day (i.e. 2250mg), or 1 sachet, 3 times a day. The dose should be reduced to 1500mg daily in divided doses when a satisfactory response is obtained i.e. dose reduction from 3 sachets per day to 2 sachets per day (taken separately). This medicine is appropriate for patients following a low sugar or low calorie diet. 4.3 Contraindications Hypersensitivity to the active substance(s) or to any of the excipients listed in section 6.1. Active peptic ulceration 4.4 Special warnings and precautions for use Special warning Productive coughs that represent a fundamental element in bronchial-pulmonary defences should be respected. The association of bronchial mucous modifiers with anti-cough medicines and/or substances that dry out secretions (atropinic) is not rational. This medicine contains sodium methyl para- Les hele dokumentet