Latvija - latviešu - Zāļu valsts aģentūra

orifarm healthcare a/s, denmark - skābes acetylsalicylicum, magnija oxidum - apvalkotā tablete - 75 mg/10,5 mg

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

regeneron ireland designated activity company (dac) - cemiplimab - karcinoma, švamšā šūna - antineoplastiski līdzekļi - cutaneous squamous cell carcinomalibtayo as monotherapy is indicated for the treatment of adult patients with metastatic or locally advanced cutaneous squamous cell carcinoma (mcscc or lacscc) who are not candidates for curative surgery or curative radiation. basal cell carcinomalibtayo as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic basal cell carcinoma (labcc or mbcc) who have progressed on or are intolerant to a hedgehog pathway inhibitor (hhi). non-small cell lung cancerlibtayo as monotherapy is indicated for the first-line treatment of adult patients with non-small cell lung cancer (nsclc) expressing pd-l1 (in ≥ 50% tumour cells), with no egfr, alk or ros1 aberrations, who have:locally advanced nsclc who are not candidates for definitive chemoradiation, ormetastatic nsclc. libtayo in combination with platinum‐based chemotherapy is indicated for the first‐line treatment of adult patients with nsclc expressing pd-l1 (in ≥ 1% of tumour cells), with no egfr, alk or ros1 aberrations, who have:locally advanced nsclc who are not candidates for definitive chemoradiation, ormetastatic nsclc. cervical cancerlibtayo as monotherapy is indicated for the treatment of adult patients with recurrent or metastatic cervical cancer and disease progression on or after platinum-based chemotherapy.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

merck sharp & dohme b.v. - doravirine, lamivudīnu, tenofovir disoproxil fumarate - hiv infekcijas - antivirals for treatment of hiv infections, combinations - delstrigo ir indicēts, lai ārstētu pieaugušos ar hiv inficēti 1 bez pagātnes vai tagadnes pierādījumus par pretestību nnrti klases, lamivudīnu, vai tenofovir. delstrigo is also indicated for the treatment of adolescents aged 12 years and older weighing at least 35 kg who are infected with hiv-1 without past or present evidence of resistance to the nnrti class, lamivudine, or tenofovir and who have experienced toxicities which preclude the use of other regimens that do not contain tenofovir disoproxil.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

merck sharp & dohme b.v. - doravirine - hiv infekcijas - pretvīrusu līdzekļi sistēmiskai lietošanai - pifeltro is indicated, in combination with other antiretroviral medicinal products, for the treatment of adults, and adolescents aged 12 years and older weighing at least 35 kg infected with hiv 1 without past or present evidence of resistance to the nnrti class.

Latvija - latviešu - Zāļu valsts aģentūra

correvio, france - tirofibāns - koncentrāts infūziju šķīduma pagatavošanai - 250 μg/ml

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

roche registration gmbh - vismodegib - karcinoma, bazālā šūna - antineoplastiski līdzekļi - erivedge ir norādīts ārstēšanai pieaugušiem pacientiem ar:- simptomātiska metastātisku bazālo šūnu karcinomu - lokāli papildu bazālo šūnu karcinomu nepiemērotu operācijas vai radioterapijas.

Latvija - latviešu - Zāļu valsts aģentūra

sanoswiss uab, lithuania - anastrozols - apvalkotā tablete - 1 mg

Latvija - latviešu - Zāļu valsts aģentūra

accord healthcare b.v., netherlands - anastrozols - apvalkotā tablete - 1 mg

Latvija - latviešu - Zāļu valsts aģentūra

teva pharma b.v., netherlands - anastrozols - apvalkotā tablete - 1 mg

Latvija - latviešu - Zāļu valsts aģentūra

astrazeneca uk limited, united kingdom - anastrozols - apvalkotās tabletes - 1 mg