Nexviadyme Den Europæiske Union - dansk - EMA (European Medicines Agency)

nexviadyme

sanofi b.v. - avalglucosidase alfa - glycogen opbevaring sygdom type ii - andre alimentary tract and metabolism produkter, - nexviadyme (avalglucosidase alfa) is indicated for long-term enzyme replacement therapy for the treatment of patients with pompe disease (acid α-glucosidase deficiency).

Ertapenem SUN Den Europæiske Union - dansk - EMA (European Medicines Agency)

ertapenem sun

sun pharmaceutical industries (europe) b.v. - ertapenemnatrium - bakterieinfektioner - 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 og 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. det bør overvejes at officielle vejledning om hensigtsmæssig brug af antibakterielle midler..

Teriflunomide Mylan Den Europæiske Union - dansk - EMA (European Medicines Agency)

teriflunomide mylan

mylan pharmaceuticals limited - teriflunomide - multipel sklerose, recidiverende-remitterende - immunosuppressiva - 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).

Nipruss 60 mg pulver til infusionsvæske, opløsning Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

nipruss 60 mg pulver til infusionsvæske, opløsning

orifarm a/s - natriumnitroprussiddihydrat - pulver til infusionsvæske, opløsning - 60 mg

Ruby-Fill 3,7 GBq radionuklidgenerator Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

ruby-fill 3,7 gbq radionuklidgenerator

jubilant pharmaceuticals nv - rubidium (82-rb) chlorid, strontium (82sr) chlorid - radionuklidgenerator - 3,7 gbq

Solifenacin/Tamsulosin "Stada" 6+0,4 mg tabletter med modificeret udløsning Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

solifenacin/tamsulosin "stada" 6+0,4 mg tabletter med modificeret udløsning

stada arzneimittel ag - solifenacinsuccinat, tamsulosinhydrochlorid - tabletter med modificeret udløsning - 6+0,4 mg