Latvija - latviešu - Zāļu valsts aģentūra

baltijas terapeitiskais serviss, sia, latvia - albumīns, cilvēka - Šķīdums infūzijām - 50 g/l

Latvija - latviešu - Pārtikas un veterinārais dienests, Zemkopības ministrija

intervet international b.v., nīderlande - human chorionic gonadotrophin, gonadotropinum sericum equinum - pulveris un šķīdinātājs šķīduma injekcijām pagatavošanai - cūkas

Latvija - latviešu - Pārtikas un veterinārais dienests, Zemkopības ministrija

intervet international b.v., nīderlande - human chorionic gonadotrophin, gonadotropinum sericum equinum - pulveris un šķīdinātājs šķīduma injekcijām pagatavošanai - cūkas

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

novartis europharm limited - eltrombopags - purpura, trombocitopēnija, idiopātija - other systemic hemostatics, antihemorrhagics - revolade is indicated for the treatment of adult patients with primary immune thrombocytopenia (itp) who are refractory to other treatments (e. corticosteroids, immunoglobulins) (see sections 4. 2 un 5. revolade is indicated for the treatment of paediatric patients aged 1 year and above with primary immune thrombocytopenia (itp) lasting 6 months or longer from diagnosis and who are refractory to other treatments (e. corticosteroids, immunoglobulins) (see sections 4. 2 un 5. revolade is indicated in adult patients with chronic hepatitis c virus (hcv) infection for the treatment of thrombocytopenia, where the degree of thrombocytopenia is the main factor preventing the initiation or limiting the ability to maintain optimal interferon-based therapy (see sections 4. 4 and 5. revolade is indicated in adult patients with acquired severe aplastic anaemia (saa) who were either refractory to prior immunosuppressive therapy or heavily pretreated and are unsuitable for haematopoietic stem cell transplantation (see section 5.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

horizon therapeutics ireland dac - inebilizumab - neuromyelitis optica - imūnsupresanti - uplizna is indicated as monotherapy for the treatment of adult patients with neuromyelitis optica spectrum disorders (nmosd) who are anti-aquaporin 4 immunoglobulin g (aqp4-igg) seropositive (see section 5.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

gedeon richter plc. - follitropin alfa - anovulācija - dzimumhormoni un dzimumsistēmas modulatori dzimumorgānu sistēma, - 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. klīniskajos pētījumos pacientiem, tika noteikti ar endogēns seruma lh līmenis < 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.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

holostem s.r.l - ex vivo paplašinātas autologas cilvēka radzenes epitēlija šūnas, kas satur cilmes šūnas - stem cell transplantation; corneal diseases - oftalmoloģiskie līdzekļi - Ārstēšana pieaugušiem pacientiem ar vidēji smagu limbal cilmes šūnu trūkums (radzenes virspusēji neovascularisation, ar vismaz diviem radzenes kvadrantos centrālā radzenes iesaistot klātbūtni nosaka un stipri samazinājusies redzes asums), vienpusējas vai divpusējas, jo fiziska vai ķīmiska acs apdegumi. biopsijai ir nepieciešams vismaz 1-2 mm2 nekaitēta limbus.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

molmed spa - allogeneic t cells genetically modified with a retroviral vector encoding for a truncated form of the human low affinity nerve growth factor receptor (Δlngfr) and the herpes simplex i virus thymidine kinase (hsv-tk mut2) - hematopoietic stem cell transplantation; graft vs host disease - antineoplastiski līdzekļi - zalmoxis tiek norādīts kā palīglīdzekļa ārstēšanas haploidentical asinsrades cilmes šūnu transplantācija (hsct) pieaugušo pacientu ar augsta riska hematoloģisko malignancies.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

dompe farmaceutici s.p.a. - recombinant human nerve growth factor - keratitis - oftalmoloģiskie līdzekļi - pieaugušajiem vidēji smags (ilgstošs epitēlija defekts) vai smaga (radzenes čūla) neirotropātais keratīts.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

hipra human health s.l. - sars-cov-2 virus recombinant spike (s) protein receptor binding domain (rbd) fusion heterodimer – b.1.351-b.1.1.7 strains - covid-19 virus infection - vakcīnas - bimervax is indicated as a booster for active immunisation to prevent covid-19 in individuals 16 years of age and older who have previously received a mrna covid-19 vaccine.