Canada - fransk - Health Canada

apotex inc - tériparatide - solution - 250mcg - tériparatide 250mcg - parathyroid agents

Den europeiske union - maltesisk - EMA (European Medicines Agency)

sun pharmaceutical industries europe b.v. - teriparatide - osteoporosis; osteoporosis, postmenopausal - homeostasi tal-kalċju - 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.

Den europeiske union - engelsk - EMA (European Medicines Agency)

sun pharmaceutical industries europe b.v. - teriparatide - osteoporosis; osteoporosis, postmenopausal - calcium homeostasis - teriparatide sun is indicated in adults.treatment of osteoporosis in postmenopausal women and in men at increased risk of fracture (see section 5.1). 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 5.1).

Nederland - nederlandsk - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

aristo pharma gmbh wallenroder strasse 8-10 13435 berlijn (duitsland) - teriparatideacetaat hydraat samenstelling overeenkomend met ; ; teriparatide 250 µg/ml - oplossing voor injectie - azijnzuur (e 260), geconcentreerd ; mannitol (d-) (e 421) ; metacresol ; natriumacetaat 0-water (e 262) ; natriumhydroxide (e 524) ; water voor injectie ; zoutzuur (e 507)

Nederland - nederlandsk - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

teriparatideacetaat hydraat samenstelling overeenkomend met ; ; teriparatide 250 µg/ml - oplossing voor injectie - azijnzuur (e 260), geconcentreerd ; mannitol (d-) (e 421) ; metacresol ; natriumacetaat 0-water (e 262) ; natriumhydroxide (e 524) ; water voor injectie ; zoutzuur (e 507)

Australia - engelsk - Department of Health (Therapeutic Goods Administration)

generic health pty ltd - teriparatide, quantity: 0.25 mg/ml - injection, solution - excipient ingredients: glacial acetic acid; water for injections; sodium acetate; cresol; mannitol; hydrochloric acid; sodium hydroxide - teriparatide lupin is indicated for the treatment of osteoporosis in postmenopausal women and the treatment of primary osteoporosis in men when other agents are considered unsuitable and when there is a high risk of fractures. ,teriparatide lupin is indicated for the treatment of osteoporosis associated with sustained systemic glucocorticoid therapy in women and men at high risk for fracture.

Den europeiske union - latvisk - EMA (European Medicines Agency)

sun pharmaceutical industries europe b.v. - teriparatide - osteoporosis; osteoporosis, postmenopausal - kalcija homeostāze - 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.

Den europeiske union - gresk - EMA (European Medicines Agency)

sun pharmaceutical industries europe b.v. - teriparatide - osteoporosis; osteoporosis, postmenopausal - Ομοιοστασία ασβεστίου - 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.

Frankrike - fransk - ANSM (Agence Nationale de Sécurité du Médicament et des Produits de Santé)

biogaran - tériparatide 20 microgrammes - solution - 20 microgrammes - pour une dose 80 microlitres > tériparatide 20 microgrammes - homéostasie du calcium - classe pharmacothérapeutique : homéostasie du calcium, hormones parathyroïdiennes et analogues, code atc : h05aa02 .teriparatide biogaran contient une substance active, le tériparatide qui est utilisé pour renforcer les os et réduire le risque de fractures en stimulant la formation osseuse.teriparatide biogaran est destiné au traitement de l'ostéoporose chez les adultes. l'ostéoporose est une maladie qui rend vos os fins et fragiles. cette maladie touche particulièrement les femmes après la ménopause mais peut également toucher les hommes. l’ostéoporose est également fréquente chez les patients recevant des corticoïdes.

Israel - engelsk - Ministry of Health

kamada ltd, israel - teriparatide - solution for injection - teriparatide 0.250 mg / 1 ml - teriparatide - treatment of postmenopausal women with osteoporosis at high risk for fractureteriparatide kamada is indicated for the treatment of postmenopausal women with osteoporosis at high risk for fracture, defined as a history of osteoporotic fracture, multiple risk factors for fracture, or patients who have failed or are intolerant to other available osteoporosis therapy. in postmenopausal women with osteoporosis, teriparatide kamada increases bmd reduces the risk of vertebral and nonvertebral fractures.increase of bone mass in men with primary or hypogonadal osteoporosis at high risk for fractureteriparatide kamada is indicated to increase bone mass in men with primary or hypogonadal osteoporosis at high risk for fracture, defined as a history of osteoporotic fracture, multiple risk factors for fracture, or patients who have failed or are intolerant to other available osteoporosis therapy.treatment of men and women with glucocorticoid-induced osteoporosis at high risk for fractureteriparatide kamada is indicated for the treatment of men and women with osteoporosis associated with sustained systemic glucocorticoid therapy (daily dosage equivalent to 5 mg or greater of prednisone) at high risk for fracture, defined as a history of osteoporotic fracture, multiple risk factors for fracture, or patients who have failed or are intolerant to other available osteoporosis therapy.