Suedia - suedeză - Läkemedelsverket (Medical Products Agency)

orifarm ab - famciklovir - filmdragerad tablett - 500 mg - famciklovir 500 mg aktiv substans

Suedia - suedeză - Läkemedelsverket (Medical Products Agency)

medartuum ab - famciklovir - filmdragerad tablett - 500 mg - famciklovir 500 mg aktiv substans

Uniunea Europeană - suedeză - EMA (European Medicines Agency)

eurogenerics holdings b.v. - teriparatid - osteoporos - calciumhomeostas - qutavina is indicated in adults. behandling av osteoporos hos postmenopausala kvinnor och hos män med ökad risk för fraktur. in postmenopausal women, a significant reduction in the incidence of vertebral and non-vertebral fractures but not hip fractures have been demonstrated. behandling av osteoporos i samband med ihållande systemisk glukokortikoid behandlingen för kvinnor och män med ökad risk för fraktur.

Uniunea Europeană - suedeză - EMA (European Medicines Agency)

sun pharmaceutical industries europe b.v. - teriparatid - osteoporosis; osteoporosis, postmenopausal - calciumhomeostas - 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.

Suedia - suedeză - Läkemedelsverket (Medical Products Agency)

life medical aps - tiaminhydroklorid - injektionsvätska, lösning - 125 mg/ml - tiaminhydroklorid 125 mg aktiv substans

Suedia - suedeză - Läkemedelsverket (Medical Products Agency)

life medical aps - tiaminhydroklorid - injektionsvätska, lösning - 50 mg/ml - tiaminhydroklorid 50 mg aktiv substans

Suedia - suedeză - Läkemedelsverket (Medical Products Agency)

life medical aps - tiaminhydroklorid - injektionsvätska, lösning - 50 mg/ml - tiaminhydroklorid 50 mg aktiv substans

Suedia - suedeză - Läkemedelsverket (Medical Products Agency)

bayer ab - moxifloxacinhydroklorid - filmdragerad tablett - 400 mg - laktosmonohydrat hjälpämne; moxifloxacinhydroklorid 436,8 mg aktiv substans - moxifloxacin

Suedia - suedeză - Läkemedelsverket (Medical Products Agency)

pharmachim ab - moxifloxacinhydroklorid - filmdragerad tablett - 400 mg - moxifloxacinhydroklorid 436,8 mg aktiv substans; laktosmonohydrat hjälpämne - moxifloxacin

Suedia - suedeză - Läkemedelsverket (Medical Products Agency)

pharmachim ab - moxifloxacinhydroklorid - filmdragerad tablett - 400 mg - moxifloxacinhydroklorid 436,8 mg aktiv substans; laktosmonohydrat hjälpämne - moxifloxacin