Země: Nizozemsko
Jazyk: nizozemština
Zdroj: CBG-MEB (College ter Beoordeling van Geneesmiddelen)
CLARITROMYCINE 25 mg/ml
Sandoz B.V. Veluwezoom 22 1327 AH ALMERE
J01FA09
CLARITROMYCINE 25 mg/ml
Granulaat voor orale suspensie
COPOLYMEER VAN ETHYLACRYLAAT-METHACRYLZUUR (1:1) ; FRUIT-PUNCH SMAAKSTOFPOEDER ; GLYCEROLMONOSTEARAAT (E 471) ; HYPROMELLOSE (E 464) ; KALIUMSORBAAT (E 202) ; MACROGOL 6000 ; MALTODEXTRINE ; MALTOL (E 636) ; NATRIUMZETMEELOCTENYLSUCCINAAT (E 1450) ; POLOXAMEER 188 ; POLYSORBAAT 80 (E 433) ; POVIDON K 30 (E 1201) ; SACCHAROSE ; SILICIUMDIOXIDE (E 551) ; TITAANDIOXIDE (E 171) ; TRIETHYLCITRAAT (E 1505) ; XANTHAANGOM (E 415),
Oraal gebruik
Clarithromycin
Hulpstoffen: COPOLYMEER VAN ETHYLACRYLAAT-METHACRYLZUUR (1:1); FRUIT-PUNCH SMAAKSTOFPOEDER; GLYCEROLMONOSTEARAAT (E 471); HYPROMELLOSE (E 464); KALIUMSORBAAT (E 202); MACROGOL 6000; MALTODEXTRINE; MALTOL (E 636); NATRIUMZETMEELOCTENYLSUCCINAAT (E 1450); POLOXAMEER 188; POLYSORBAAT 80 (E 433); POVIDON K 30 (E 1201); SACCHAROSE; SILICIUMDIOXIDE (E 551); TITAANDIOXIDE (E 171); TRIETHYLCITRAAT (E 1505); XANTHAANGOM (E 415);
1900-01-01
Sandoz B.V. Page 1/11 Claritromycine Sandoz ® 125 mg/5 ml, Claritromycine Sandoz ® 250 mg/5 ml, granulaat voor orale suspensie RVG 30789-30791 1311-V11 1.3.1.3 Bijsluiter Maart 2021 PACKAGE LEAFLET: INFORMATION FOR THE PATIENT CLARITROMYCINE SANDOZ® 125 MG/5 ML, GRANULAAT VOOR ORALE SUSPENSIE CLARITROMYCINE SANDOZ® 250 MG/5 ML, GRANULAAT VOOR ORALE SUSPENSIE clarithromycin 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 [Nationally completed name] is and what it is used for 2. What you need to know before you take [Nationally completed name] 3. How to take [Nationally completed name] 4. Possible side effects 5. How to store [Nationally completed name] 6. Contents of the pack and other information 1. WHAT [NATIONALLY COMPLETED NAME] IS AND WHAT IT IS USED FOR Clarithromycin is an antibiotic which belongs to the group of macrolide antibiotics. It stops the growth of certain bacteria. [Nationally completed name] is used to treat: • Throat and sinus infections • Middle ear infections in children • Chest infections, such as bronchitis and pneumonia • Skin and soft-tissue infections • Gastric ulcers caused by the bacterium Helicobacter pylori. 2. WHAT YOU NEED TO KNOW BEFORE YOU TAKE [NATIONALLY COMPLETED NAME] DO NOT TAKE [ N ATIONALLY COMPLETED NAME] • if you are ALLERGIC to clarithromycin, other macrolide antibiotics or any of the other ingredients of this medicine (listed in section 6) • if you or someone in your family has a history of HEART RHYTHM DISORDERS (ventricular arrhyth Přečtěte si celý dokument
Sandoz B.V. Page 1/25 Claritromycine Sandoz 125 mg/5 ml, Claritromycine Sandoz 250 mg/5 ml, granulaat voor orale suspensie RVG 30789-30791 1311-V8 1.3.1.1 Samenvatting van de Productkenmerken Maart 2021 SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT Claritromycine Sandoz 125 mg/5 ml, granulaat voor orale suspensie Claritromycine Sandoz 250 mg/5 ml, granulaat voor orale suspensie 2 QUALITATIVE AND QUANTITATIVE COMPOSITION After reconstitution 1 ml oral suspension contains 25 mg of clarithromycin, 5 ml oral suspension contain 125 mg of clarithromycin. Excipient with known effect: Each 5 ml ready-for-use suspension contains 2.4 g of sucrose. After reconstitution 1 ml oral suspension contains 50 mg of clarithromycin, 5 ml oral suspension contain 250 mg of clarithromycin. Excipient with known effect: Each 5 ml ready-for-use suspension contains 2.4 g of sucrose. For the full list of excipients, see section 6.1. 3 PHARMACEUTICAL FORM Granules for oral suspension. White to beige granules. 4 CLINICAL PARTICULARS 4.1 THERAPEUTIC INDICATIONS [Nationally completed name] is indicated in adults, adolescents and children, 6 months to 12 years, for the treatment of the following acute and chronic infections, when caused by clarithromycin susceptible organisms. • Infections of the upper respiratory tract such as tonsillitis/pharyngitis, as an alternative when beta lactam antibiotics are not appropriate. • Acute otitis media in children. • Infections of the lower respiratory tract such as community acquired pneumonia. • Sinusitis and acute exacerbation of chronic bronchitis in adults and adolescents over 12 years of age • Skin infections and soft tissue infections of mild to moderate severity. Sandoz B.V. Page 2/25 Claritromycine Sandoz 125 mg/5 ml, Claritromycine Sandoz 250 mg/5 ml, granulaat voor orale suspensie RVG 30789-30791 1311-V8 1.3.1.1 Samenvatting van de Productkenmerken Maart 2021 In appropriate combination with antibacterial therapeutic regimens and an appropriate ulcer healing medicinal Přečtěte si celý dokument