国: オランダ
言語: オランダ語
ソース: CBG-MEB (College ter Beoordeling van Geneesmiddelen)
AZITROMYCINE 2-WATER 41,9 mg/ml SAMENSTELLING overeenkomend met ; AZITROMYCINE 0-WATER 40 mg/ml
Sandoz B.V. Veluwezoom 22 1327 AH ALMERE
J01FA10
AZITROMYCINE 2-WATER 41,9 mg/ml SAMENSTELLING overeenkomend met ; AZITROMYCINE 0-WATER 40 mg/ml
Poeder voor orale suspensie
ASPARTAAM (E 951) ; BANANENSMAAKSTOF ; GLYCEROLTRIACETAAT (E 1518) ; HYPROLOSE (E 463) ; KERSENSMAAKSTOF ; MALTODEXTRINE ; MAÏSZETMEEL, GEMODIFICEERD (MODIFICATIE ONBEKEND ; PROPYLEENGLYCOL (E 1520) ; SACCHAROSE ; SILICIUMDIOXIDE (E 551) ; TITAANDIOXIDE (E 171) ; TRINATRIUMFOSFAAT 0-WATER (E 339) ; VANILLESMAAKSTOF ; XANTHAANGOM (E 415), ASPARTAAM (E 951) ; BANANENSMAAKSTOF ; GLYCEROLTRIACETAAT (E 1518) ; HYPROLOSE (E 463) ; KERSENSMAAKSTOF ; MALTODEXTRINE ; MAÏSZETMEEL, GEMODIFICEERD (MODIFICATIE ONBEKEND, (E 1450) ; PROPYLEENGLYCOL (E 1520) ; SACCHAROSE ; SILICIUMDIOXIDE (E 551) ; TITAANDIOXIDE (E 171) ; TRINATRIUMFOSFAAT 0-WATER (E 339) ; VANILLESMAAKSTOF ; XANTHAANGOM (E 415), ASPARTAAM (E 951) ; HYPROLOSE (E 463) ; NATUURLIJKE EN KUNSTMATIGE SMAAKSTOFFEN ; SACCHAROSE ; SILICIUMDIOXIDE (E 551) ; TITAANDIOXIDE (E 171) ; TRINATRIUMFOSFAAT 0-WATER (E 339) ; XANTHAANGOM (E 415),
Oraal gebruik
Azithromycin
Hulpstoffen: ASPARTAAM (E 951); HYPROLOSE (E 463); NATUURLIJKE EN KUNSTMATIGE SMAAKSTOFFEN; SACCHAROSE; SILICIUMDIOXIDE (E 551); TITAANDIOXIDE (E 171); TRINATRIUMFOSFAAT 0-WATER (E 339); XANTHAANGOM (E 415);
1900-01-01
Sandoz B.V. Page 1/12 Azitromycine 200 mg/5 ml, poeder voor orale suspensie; RVG 34292 1313-V22 1.3.1.3 Package Leaflet Oktober 2022 BIJSLUITER: INFORMATIE VOOR DE PATIËNT AZITROMYCINE 200 MG/5 ML, POEDER VOOR ORALE SUSPENSIE azithromycin 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 Azithromycin is an antibiotic. It belongs to a group of antibiotics called macrolides. It is used to treat infections caused by bacteria. This medicine is usually prescribed to treat: - chest infections such as chronic bronchitis, pneumonia - infections of the tonsils, throat (pharyngitis) and sinuses - ear infections (acute otitis media) - skin and soft tissue infections, with exception of infected burn wounds - urethra and cervix infections caused by chlamydia. 2 WHAT YOU NEED TO KNOW BEFORE YOU TAKE [NATIONALLY COMPLETED NAME] DO NOT TAKE [NATIONALLY COMPLETED NAME] IF YOU ARE ALLERGIC (HYPERSENSITIVE) TO: • azithromycin Sandoz B.V. Page 2/12 Azitromycine 200 mg/5 ml, poeder voor orale suspensie; RVG 34292 1313-V22 1.3.1.3 Package Leaflet Oktober 2022 • erythromycin • other macrolide or ketolide antibiotic • any of the other ingredients of this medicine (listed in 完全なドキュメントを読む
Sandoz B.V. Page 1/23 Azitromycine 200 mg/5 ml, poeder voor orale suspensie; RVG 34292 1311-V22 1.3.1.1 Summary of Product Characteristics Oktober 2022 1. NAAM VAN HET GENEESMIDDEL Azitromycine 200 mg/5 ml, poeder voor orale suspensie 2. QUALITATIVE AND QUANTITATIVE COMPOSITION _ _ Each 5 ml reconstituted suspension contains 104.80 mg of azithromycin dihydrate equivalent to 100 mg of azithromycin. Each 1 ml reconstituted suspension contains 20.96 mg of azithromycin dihydrate equivalent to 20 mg of azithromycin. Excipients with known effect Each 5 ml reconstituted suspension contains 3.82 g of sucrose, 0.030 g of aspartame (E 951), up to 410 nanograms of benzyl alcohol, and up to 85 nanograms of sulphites. Each 5 ml reconstituted suspension contains 209.6 mg of azithromycin dihydrate equivalent to 200 mg of azithromycin. Each 1 ml reconstituted suspension contains 41.92 mg of azithromycin dihydrate equivalent to 40 mg of azithromycin. Excipients with known effect Each 5 ml reconstituted suspension contains 3.71 g of sucrose, 0.030 g of aspartame (E 951), up to 410 nanograms of benzyl alcohol and up to 85 nanograms of sulphites. For the full list of excipients, see section 6.1. 3. PHARMACEUTICAL FORM Powder for oral suspension. White to off-white crystalline powder. 4. CLINICAL PARTICULARS 4.1 THERAPEUTIC INDICATIONS Azithromycin powder for oral suspension is indicated for the treatment of the following infections, when caused by micro-organisms sensitive to azithromycin (see section 4.4 and 5.1): − acute bacterial sinusitis (adequately diagnosed) Sandoz B.V. Page 2/23 Azitromycine 200 mg/5 ml, poeder voor orale suspensie; RVG 34292 1311-V22 1.3.1.1 Summary of Product Characteristics Oktober 2022 − acute bacterial otitis media (adequately diagnosed) − pharyngitis, tonsillitis − acute exacerbation of chronic bronchitis (adequately diagnosed) − mild to moderately severe community acquired pneumonia − skin and soft tissue infections − uncomplicated _Chlamydia trachomatis_ urethritis and cervicitis Consid 完全なドキュメントを読む