ইউরোপীয় ইউনিয়ন - বুলগেরিয় - EMA (European Medicines Agency)

biogen netherlands b.v. - пегинтерферон бета-1а - Множествена склероза - Иммуностимуляторы, - Лечение на пристъпно ремитентна множествена склероза при възрастни пациенти.

ইউরোপীয় ইউনিয়ন - বুলগেরিয় - EMA (European Medicines Agency)

biogen netherlands b.v. - натализумаб - Множествена склероза - Селективни имуносупресори - tysabri is indicated as single disease modifying therapy in adults with highly active relapsing remitting multiple sclerosis for the following patient groups: , patients with highly active disease activity despite a full and adequate course of treatment with at least one disease modifying therapy (dmt) (for exceptions and information about washout periods see sections 4. 4 и 5. 1), , or, patients with rapidly evolving severe relapsing remitting multiple sclerosis defined by 2 or more disabling relapses in one year, and with 1 or more gadolinium enhancing lesions on brain mri or a significant increase in t2 lesion load as compared to a previous recent mri.

ইউরোপীয় ইউনিয়ন - বুলগেরিয় - EMA (European Medicines Agency)

biogen idec ltd - даклизумаб - Множествена склероза - Имуносупресори - zinbryta е показан при възрастни пациенти за лечение на пристъпно форми на множествена склероза (rms).

ইউরোপীয় ইউনিয়ন - বুলগেরিয় - EMA (European Medicines Agency)

biogen netherlands b.v. - nusinersen sodium - Мускулна атрофия, спинална - Други лекарства в нервната система - spinraza е показан за лечение на 5q спинална мускулна атрофия.

ইউরোপীয় ইউনিয়ন - বুলগেরিয় - EMA (European Medicines Agency)

seagen b.v. - tucatinib - breast neoplasms; neoplasm metastasis - Антинеопластични средства - tukysa is indicated in combination with trastuzumab and capecitabine for the treatment of adult patients with her2‑positive locally advanced or metastatic breast cancer who have received at least 2 prior anti‑her2 treatment regimens.

ইউরোপীয় ইউনিয়ন - বুলগেরিয় - EMA (European Medicines Agency)

samsung bioepis nl b.v. - ранимизумаб - wet macular degeneration; macular edema; diabetic retinopathy; myopia, degenerative - Офталмологични - byooviz is indicated in adults for:the treatment of neovascular (wet) age-related macular degeneration (amd)the treatment of visual impairment due to diabetic macular oedema (dme)the treatment of proliferative diabetic retinopathy (pdr)the treatment of visual impairment due to macular oedema secondary to retinal vein occlusion (branch rvo or central rvo)the treatment of visual impairment due to choroidal neovascularisation (cnv).

ইউরোপীয় ইউনিয়ন - বুলগেরিয় - EMA (European Medicines Agency)

biogen netherlands b.v. - diroximel fumarate (biib098) - Множествена Склероза, Рецидивно-Ремиттирующее - Имуносупресори - vumerity is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis (see section 5. 1 for important information on the populations for which efficacy has been established).

ইউরোপীয় ইউনিয়ন - বুলগেরিয় - EMA (European Medicines Agency)

gedeon richter plc. - фолитропин алфа - Ановулация - Полови хормони и слиза на половата система, - 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. В клинични проучвания при тези пациенти са били идентифицирани ендогенен нивото на серумните нива на lh < 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.

ইউরোপীয় ইউনিয়ন - বুলগেরিয় - EMA (European Medicines Agency)

regeneron ireland designated activity company (dac) - cemiplimab - Карцином, сквамозна клетка - Антинеопластични средства - 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.

বুলগেরিয়া - বুলগেরিয় - Изпълнителна агенция по лекарствата

generics /uk/ limited - 30 mg modified - release tablets