Zalmoxis Unia Europejska - polski - EMA (European Medicines Agency)

zalmoxis

molmed spa - allogenicznych komórek t genetycznie zmodyfikowanych z antyretrowirusowych wektor kodowania dla okrojonej formie ludzkiej niskie powinowactwo receptora czynnika wzrostu nerwu (Δlngfr) i herpes simplex wirus kinazy tymidyny (hsv-tk mut2) - hematopoietic stem cell transplantation; graft vs host disease - Środki przeciwnowotworowe - zalmoxis jest wskazany jako leczenie wspomagające w haploidentycznym transplantacji komórek macierzystych krwi (hsct) dorosłych pacjentów z hematologicznymi nowotworami złośliwymi wysokiego ryzyka.

Tecvayli Unia Europejska - polski - EMA (European Medicines Agency)

tecvayli

janssen-cilag international n.v. - teclistamab - szpiczak mnogi - Środki przeciwnowotworowe - tecvayli is indicated as monotherapy for the treatment of adult patients with relapsed and refractory multiple myeloma, who have received at least three prior therapies, including an immunomodulatory agent, a proteasome inhibitor, and an anti-cd38 antibody and have demonstrated disease progression on the last therapy.

Talvey Unia Europejska - polski - EMA (European Medicines Agency)

talvey

janssen-cilag international n.v. - talquetamab - szpiczak mnogi - Środki przeciwnowotworowe - talvey is indicated as monotherapy for the treatment of adult patients with relapsed and refractory multiple myeloma, who have received at least 3 prior therapies, including an immunomodulatory agent, a proteasome inhibitor, and an anti cd38 antibody and have demonstrated disease progression on the last therapy.

Nordimet Unia Europejska - polski - EMA (European Medicines Agency)

nordimet

nordic group b.v. - metotreksat - arthritis, psoriatic; psoriasis; arthritis, juvenile rheumatoid; arthritis, rheumatoid - Środki przeciwnowotworowe - nordimet is indicated for the treatment of:active rheumatoid arthritis in adult patients,polyarthritic forms of severe, active juvenile idiopathic arthritis (jia), when the response to nonsteroidal anti-inflammatory drugs (nsaids) has been inadequate,moderate to severe plaque psoriasis in adults who are candidates for systemic therapy, and severe psoriatic arthritis in adult patients, induction of remission in moderate steroid-dependent crohn's disease in adult patients, in combination with corticosteroids and for maintenance of remission, as monotherapy, in patients who have responded to methotrexate.

Wakix Unia Europejska - polski - EMA (European Medicines Agency)

wakix

bioprojet pharma - pitolisant - narkolepsja - inne leki na układ nerwowy - wakix is indicated in adults, adolescents and children from the age of 6 years for the treatment of narcolepsy with or without cataplexy (see also section 5.

Bemfola Unia Europejska - polski - EMA (European Medicines Agency)

bemfola

gedeon richter plc. - folitropina alfa - anovulation - hormony płciowe i modulatory układu rozrodczego, - in adult women:anovulation (including polycystic ovarian disease, pcod) in women who have been unresponsive to treatment with clomiphene citrate;stimulation of multifollicular development in patients undergoing superovulation for assisted reproductive technologies (art) such as in vitro fertilisation (ivf), gamete intra-fallopian transfer (gift) and zygote intra-fallopian transfer (zift);follitropin alfa in association with a luteinising hormone (lh) preparation is recommended for the stimulation of follicular development in women with severe lh and fsh deficiency. w badaniach klinicznych u tych pacjentów oceniali poziom endogennego lh w surowicy < 1. 2 iu / l. in adult men:follitropin alfa is indicated for the stimulation of spermatogenesis in men who have congenital or acquired hypogonadotrophic hypogonadism with concomitant human chorionic gonadotrophin (hcg) therapy.

Xtandi Unia Europejska - polski - EMA (European Medicines Agency)

xtandi

astellas pharma europe b.v. - enzalutamid - nowotwory stercza - terapia endokrynologiczna - xtandi is indicated for:the treatment of adult men with metastatic hormone-sensitive prostate cancer (mhspc) in combination with androgen deprivation therapy (see section 5. the treatment of adult men with high-risk non-metastatic castration-resistant prostate cancer (crpc) (see section 5. the treatment of adult men with metastatic crpc who are asymptomatic or mildly symptomatic after failure of androgen deprivation therapy in whom chemotherapy is not yet clinically indicated (see section 5. the treatment of adult men with metastatic crpc whose disease has progressed on or after docetaxel therapy.

Ertapenem SUN Unia Europejska - polski - EMA (European Medicines Agency)

ertapenem sun

sun pharmaceutical industries (europe) b.v. - ertapenem sodu - infekcje bakteryjne - 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 i 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. należy uwzględnić oficjalne zalecenia dotyczące właściwego stosowania antybiotyków agentów.