Европска Унија - Чешки - EMA (European Medicines Agency)

dipharma arzneimittel gmbh - sapropterin-dihydrochloridu - fenylketonurie - jiné zažívací trakt a produkty metabolismu, - sapropterin dipharma is indicated for the treatment of hyperphenylalaninaemia (hpa) in adults and paediatric patients of all ages with phenylketonuria (pku) who have been shown to be responsive to such treatment. sapropterin dipharma is also indicated for the treatment of hyperphenylalaninaemia (hpa) in adults and paediatric patients of all ages with tetrahydrobiopterin (bh4) deficiency who have been shown to be responsive to such treatment.

Чешка - Чешки - Adama

adama - suspenzní koncentrát - metamitron + quinmerac - herbicidy

Чешка - Чешки - Adama

adama - suspenzní koncentrát - metazachlor + quinmerac - herbicidy

Чешка - Чешки - Adama

adama - suspenzní koncentrát - metazachlor - herbicidy

Чешка - Чешки - Adama

adama - suspenzní koncentrát - chlorotoluron + diflufenican + pendimethalin - herbicidy

Европска Унија - Чешки - EMA (European Medicines Agency)

sun pharmaceutical industries (europe) b.v. - ertapenem sodný - bakteriální infekce - ertapenem - treatmentertapenem sun is indicated in paediatric patients (3 months to 17 years of age) and in adults for the treatment of the following infections when caused by bacteria known or very likely to be susceptible to ertapenem and when parenteral therapy is required (see sections 4. 4 a 5. 1):- intra-abdominal infections- community acquired pneumonia- acute gynaecological infections- diabetic foot infections of the skin and soft tissue (see section 4. 4)preventionertapenem sun is indicated in adults for the prophylaxis of surgical site infection following elective colorectal surgery (see section 4. pozornost by měla být věnována oficiálním doporučením pro správné používání antibakteriálních látek.

Европска Унија - Чешки - EMA (European Medicines Agency)

mylan pharmaceuticals limited - teriflunomid - roztroušená skleróza, relaps-remitentní - imunosupresiva - teriflunomide mylan is indicated for the treatment of adult patients and paediatric patients aged 10 years and older (body weight > 40 kg) with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 of the smpc for important information on the population for which efficacy has been established).

Европска Унија - Чешки - EMA (European Medicines Agency)

accord healthcare s.l.u. - teriflunomid - roztroušená skleróza, relaps-remitentní - imunosupresiva, selektivní imunosupresiva - teriflunomide accord is indicated for the treatment of adult patients and paediatric patients aged 10 years and older with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 for important information on the population for which efficacy has been established).

Чешка - Чешки - SUKL (Státní ústav pro kontrolu léčiv)

exeltis czech s.r.o., praha array - 11275 drospirenon; 578 ethinylestradiol - potahovaná tableta - 0,02mg/3mg - drospirenon a ethinylestradiol

Чешка - Чешки - SUKL (Státní ústav pro kontrolu léčiv)

exeltis czech s.r.o., praha array - 11275 drospirenon; 578 ethinylestradiol - potahovaná tableta - 0,03mg/3mg - drospirenon a ethinylestradiol