Suedia - suedeză - Läkemedelsverket (Medical Products Agency)

accord healthcare b.v. - abakavir - filmdragerad tablett - 300 mg - abakavir 300 mg aktiv substans

Suedia - suedeză - Läkemedelsverket (Medical Products Agency)

accord healthcare b.v. - midazolamhydroklorid - injektions- / infusionsvätska, lösning i förfylld spruta - 1 mg/ml - midazolamhydroklorid 1,11 mg aktiv substans

Suedia - suedeză - Läkemedelsverket (Medical Products Agency)

accord healthcare b.v. - ondansetronhydrokloriddihydrat - injektions- / infusionsvätska, lösning i förfylld spruta - 4 mg - ondansetronhydrokloriddihydrat 4,98 mg aktiv substans

Suedia - suedeză - Läkemedelsverket (Medical Products Agency)

accord healthcare b.v. - ondansetronhydrokloriddihydrat - injektions- / infusionsvätska, lösning i förfylld spruta - 8 mg - ondansetronhydrokloriddihydrat 9,96 mg aktiv substans

Uniunea Europeană - suedeză - EMA (European Medicines Agency)

accord healthcare s.l.u. - doxorubicin hydrochloride, liposomal - ovarian neoplasms; sarcoma, kaposi; multiple myeloma - doxorubicin - zolsketil pegylated liposomal is a medicine used to treat the following types of cancer in adults:• breast cancer that has spread to other parts of the body in patients at risk of heart problems. zolsketil pegylated liposomal is used on its own for this disease;• advanced ovarian cancer in women whose previous treatment including a platinum-based cancer medicine has stopped working;• multiple myeloma (a cancer of the white blood cells in the bone marrow), in patients with progressive disease who have received at least one other treatment in the past and have already had, or are unsuitable for, a bone marrow transplantation. zolsketil pegylated liposomal is used in combination with bortezomib (another cancer medicine);• kaposi’s sarcoma in patients with aids who have a very damaged immune system. kaposi’s sarcoma is a cancer that causes abnormal tissue to grow under the skin, on moist body surfaces or on internal organs. zolsketil pegylated liposomal contains the active substance doxorubicin and is a ‘hybrid medicine’. this means that it is similar to a ‘reference medicine’ containing the same active substance called adriamycin. however, in zolsketil pegylated liposomal the active substance is enclosed in tiny fatty spheres called liposomes, whereas this is not the case for adriamycin.

Uniunea Europeană - suedeză - EMA (European Medicines Agency)

accord healthcare s.l.u. - teriparatid - osteoporos - calciumhomeostas - sondelbay 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)

accord healthcare s.l.u. - plerixafor - multiple myeloma; hematopoietic stem cell transplantation - immunstimulatorer, - adult patientsplerixafor accord is indicated in combination with granulocyte-colony stimulating factor (g-csf) to enhance mobilisation of haematopoietic stem cells to the peripheral blood for collection and subsequent autologous transplantation in adult patients with lymphoma or multiple myeloma whose cells mobilise poorly (see section 4. paediatric patients (1 to less than 18 years)plerixafor accord is indicated in combination with g-csf to enhance mobilisation of haematopoietic stem cells to the peripheral blood for collection and subsequent autologous transplantation in children with lymphoma or solid malignant tumours, either:- pre-emptively, when circulating stem cell count on the predicted day of collection after adequate mobilization with g-csf (with or without chemotherapy) is expected to be insufficient with regards to desired hematopoietic stem cells yield, or- who previously failed to collect sufficient haematopoietic stem cells (see section 4.

Suedia - suedeză - Läkemedelsverket (Medical Products Agency)

accord healthcare b.v. - naloxonhydrokloriddihydrat - injektions- / infusionsvätska, lösning i förfylld spruta - 0,4 mg/ml - naloxonhydrokloriddihydrat 0,44 mg aktiv substans

Uniunea Europeană - suedeză - EMA (European Medicines Agency)

accord healthcare s.l.u. - dabigatran etexilate mesilate - venous thromboembolism; arthroplasty, replacement - antitrombotiska medel - prevention of venous thromboembolic events.

Suedia - suedeză - Läkemedelsverket (Medical Products Agency)

alk-abelló a/s - allergen, bigift - injektionsvätska, suspension - 100 000 sq-e/ml - allergen, bigift 100000 sq-u aktiv substans; aluminiumoxid, hydratiserad 4 mg adjuvans - insekter