Unione Europea - italiano - EMA (European Medicines Agency)

sun pharmaceutical industries (europe) b.v. - ertapenem sodico - infezioni batteriche - 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 e 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. dovrebbero essere prese in considerazione le linee guida ufficiali sull'uso appropriato degli agenti antibatterici..

Unione Europea - italiano - EMA (European Medicines Agency)

novartis europharm limited  - gozetotide - imaging dei radionuclidi - radiofarmaci diagnostici - questo medicinale è solo per uso diagnostico. locametz, after radiolabelling with gallium 68, is indicated for the detection of prostate specific membrane antigen (psma) positive lesions with positron emission tomography (pet) in adults with prostate cancer (pca) in the following clinical settings:primary staging of patients with high risk pca prior to primary curative therapy,suspected pca recurrence in patients with increasing levels of serum prostate specific antigen (psa) after primary curative therapy,identification of patients with psma positive progressive metastatic castration resistant prostate cancer (mcrpc) for whom psma targeted therapy is indicated (see section 4.

Unione Europea - italiano - EMA (European Medicines Agency)

novartis europharm limited  - lutetium (177lu) vipivotide tetraxetan - prostatica neoplasie, castrazione-resistente - radiofarmaci terapeutici - pluvicto in combination with androgen deprivation therapy (adt) with or without androgen receptor (ar) pathway inhibition is indicated for the treatment of adult patients with progressive prostate-specific membrane antigen (psma)-positive metastatic castration-resistant prostate cancer (mcrpc) who have been treated with ar pathway inhibition and taxane based chemotherapy.

Unione Europea - italiano - EMA (European Medicines Agency)

sun pharmaceutical industries europe b.v. - teriparatide - osteoporosis; osteoporosis, postmenopausal - omeostasi del calcio - teriparatide sun is indicated in adults. treatment of osteoporosis in postmenopausal women and in men at increased risk of fracture (see section 5. in postmenopausal women, a significant reduction in the incidence of vertebral and non-vertebral fractures but not hip fractures has been demonstrated. treatment of osteoporosis associated with sustained systemic glucocorticoid therapy in women and men at increased risk for fracture (see section 5.

Unione Europea - italiano - EMA (European Medicines Agency)

neuraxpharm pharmaceuticals s.l. - ublituximab - multiple sclerosis, relapsing-remitting; multiple sclerosis - immunosoppressori - briumvi is indicated for the treatment of adult patients with relapsing forms of multiple sclerosis (rms) with active disease defined by clinical or imaging features.

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

fidia farmaceutici spa - epoetina alfa - preparazione iniettabile - "1000 ui//0.5ml soluz inettabile in siringa preriempita -uso sottocutaneo o endovenoso" siringa preriempita (vetro) 0,5 ml (2000

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

fidia farmaceutici spa - epoetina alfa - preparazione iniettabile - "10000 ui/1,0ml soluzione iniettabile in siringa preriempita-uso sottocutaneo o endovenoso-siringa preriempita (vetro)" 1,0ml(10

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

fidia farmaceutici spa - epoetina alfa - preparazione iniettabile - "10000 ui/1,0ml soluzione iniettabile in siringa preriempita-uso sottocutaneo o endovenoso-siringa preriempita (vetro)" 1,0ml(10

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

fidia farmaceutici spa - epoetina alfa - preparazione iniettabile - "2000 ui/1,0ml soluz inettabile in siringa preriempita -uso sottocutaneo o endovenoso" siringa preriempita (vetro) 1,0 ml (2000

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

fidia farmaceutici spa - epoetina alfa - preparazione iniettabile - "2000 ui/1,0ml soluz inettabile in siringa preriempita -uso sottocutaneo o endovenoso" siringa preriempita (vetro) 1,0 ml (2000