País: Irlanda
Língua: inglês
Origem: HPRA (Health Products Regulatory Authority)
Dexketoprofen
Menarini International Operations Luxembourg S.A.
M01AE; M01AE17
Dexketoprofen
12.5 milligram(s)
Granules for oral solution
Product subject to prescription which may be renewed (B)
Propionic acid derivatives; dexketoprofen
Not marketed
2011-09-02
1 PACKAGE LEAFLET: INFORMATION FOR THE USER KERAL 12.5 MG GRANULES FOR ORAL SOLUTION _ _ Dexketoprofen READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START TAKING THIS MEDICINE BECAUSE IT CONTAINS IMPORTANT INFORMATION FOR YOU. Keep this leaflet. You may need to read it again. If you have any further questions, ask your doctor or pharmacist. This medicine has been prescribed for you only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours. If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4. WHAT IS IN THIS LEAFLET : 1. What Keral is and what it is used for 2. What you need to know before you take Keral 3. How to take Keral 4. Possible side effects 5. How to store Keral 6. Contents of the pack and other information 1. WHAT KERAL IS AND WHAT IT IS USED FOR Keral is a pain killer from the group of medicines called non-steroidal anti-inflammatory drugs (NSAIDs). It is used for short term symptomatic treatment of mild to moderate acute pain, such as acute muscular pain or joint pain, painful periods (dysmenorrhoea), toothache. 2. WHAT YOU NEED TO KNOW BEFORE YOU TAKE KERAL DO NOT TAKE KERAL: If you are allergic to dexketoprofen or any of the other ingredients of this medicine (listed in section 6); If you are allergic to the acetylsalicylic acid or to other non-steroidal anti-inflammatory medicines; If you have asthma or have suffered attacks of asthma, acute allergic rhinitis (a short period of inflamed lining of the nose), nasal polyps (lumps within the nose due to allergy), urticaria (skin rash), angioedema (swollen face, eyes, lips, or tongue, or respiratory distress) or wheezing in the chest after taking acetylsalicylic acid or other non-steroidal anti-inflammatory medicines; If you have suffered from photoallergic or phototoxic reactions (a particular form of reddening and/or blistering of the skin exposed to sunlight) while taking ketoprof Leia o documento completo
SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT Keral 12.5 mg granules for oral solution. 2 QUALITATIVE AND QUANTITATIVE COMPOSITION Each sachet of granules for oral solution contains dexketoprofen 12.5 mg, as dexketoprofen trometamol. Excipients with known effect: Sucrose with colloidal silica: 1.20 - 1.22 g For the full list of excipients, see section 6.1. 3 PHARMACEUTICAL FORM Granules for oral solution, lemon yellow coloured granules. 4 CLINICAL PARTICULARS 4.1 THERAPEUTIC INDICATIONS Short term symptomatic treatment of acute pain of mild to moderate intensity, such as acute musculo-skeletal pain, dysmenorrhoea and dental pain. 4.2 POSOLOGY AND METHOD OF ADMINISTRATION Posology _Adults_ According to the nature and severity of pain, the recommended dosage is 12.5 mg every 4-6 hours or 25 mg every 8 hours. The total daily dose should not exceed 75 mg. Undesirable effects may be minimised by using the lowest effective dose for the shortest duration necessary to control symptoms (see section 4.4.). Keral is only intended for short term use and the treatment must be limited to the symptomatic period. _Elderly_ In elderly patients it is recommended to start the therapy at the lower end of the dosage range (50 mg total daily dose). The dosage may be increased to that recommended for the adult only after good general tolerance has been ascertained. Due to the possible adverse effect profile (see section 4.4), elderly individuals should receive particularly close monitoring. _Hepatic impairment_ Patients with mild to moderate hepatic dysfunction should start therapy at reduced doses (50 mg total daily dose) and be closely monitored. Keral should not be used in patients with severe hepatic dysfunction. _Renal impairment_ The initial dosage should be reduced to 50 mg total daily dose in patients with mildly impaired renal function (creatinine clearance 60 – 89 ml / min) (see section 4.4). Keral should not be used in patients with moderate to severe renal dysfunction (creatinine clearance 59 ml / min Leia o documento completo