Magyarország - magyar - OGYÉI (Országos Gyógyszerészeti és Élelmezés-egészségügyi Intézetről)

remedia homöopathie gmbh -

Magyarország - magyar - OGYÉI (Országos Gyógyszerészeti és Élelmezés-egészségügyi Intézetről)

boiron laboratoires -

Magyarország - magyar - OGYÉI (Országos Gyógyszerészeti és Élelmezés-egészségügyi Intézetről)

boiron laboratoires -

Európai Unió - magyar - EMA (European Medicines Agency)

ge healthcare b.v. - ioflupán (123i) - tomography, emission-computed, single-photon; lewy body disease; parkinson disease; alzheimer disease - diagnosztikai radiofarmakonok - ez a gyógyszer csak diagnosztikai célra használható. a datscan jelzi kimutatására veszteség a funkcionális dopaminerg neuronok terminálok a striatum:a felnőtt betegek klinikailag bizonytalan parkinson-szindrómák, például a korai tünetek annak érdekében, hogy segítse különbséget esszenciális tremor a parkinson-szindrómák kapcsolatos idiopátiás parkinson-kór, sclerosis rendszer sorvadás, progresszív supranuclear bénulás. a datscan nem tudja megkülönböztetni a parkinson-kór, sclerosis rendszer sorvadás, progresszív supranuclear bénulás. felnőtt betegeknél, segít megkülönböztetni valószínű demencia a lewy-testek alzheimer-kór. a datscan nem tud különbséget demencia a lewy-testek, a parkinson-kór, demencia.

Európai Unió - magyar - EMA (European Medicines Agency)

cis bio international - ioflupán (123i) - radionuclide imaging; dementia; movement disorders - diagnosztikai radiofarmakonok - ez a gyógyszer csak diagnosztikai célra használható. striascan jelzi kimutatására veszteség a funkcionális dopaminerg neuronok terminálok a striatum:a felnőtt betegek klinikailag bizonytalan parkinson-szindrómák, például a korai tünetek annak érdekében, hogy segítse különbséget esszenciális tremor a parkinson-szindrómák kapcsolatos idiopátiás parkinson-kór, sclerosis rendszer sorvadás, valamint progresszív supranuclear bénulás. striascan nem tudja megkülönböztetni a parkinson-kór, sclerosis rendszer sorvadás, valamint progresszív supranuclear bénulás. felnőtt betegeknél, segít megkülönböztetni valószínű demencia a lewy-testek alzheimer-kór. striascan nem tud különbséget demencia a lewy-testek, valamint a parkinson-kór, demencia.

Európai Unió - magyar - EMA (European Medicines Agency)

pinax pharma gmbh - az ioflupán (123i) - radionuclide imaging; dementia; movement disorders - diagnosztikai radiofarmakonok - ez a gyógyszer csak diagnosztikai célra használható. celsunax is indicated for detecting loss of functional dopaminergic neuron terminals in the striatum:in adult patients with clinically uncertain parkinsonian syndromes, for example those with early symptoms, in order to help differentiate essential tremor from parkinsonian syndromes related to idiopathic parkinson’s disease, multiple system atrophy and progressive supranuclear palsy.  celsunax is unable to discriminate between parkinson's disease, multiple system atrophy and progressive supranuclear palsy. felnőtt betegeknél, segít megkülönböztetni valószínű demencia a lewy-testek alzheimer-kór.  celsunax is unable to discriminate between dementia with lewy bodies and parkinson’s disease dementia.

Európai Unió - magyar - EMA (European Medicines Agency)

abbvie deutschland gmbh co. kg - adalimumab - spondylitis, ankylosing; arthritis, juvenile rheumatoid; uveitis; colitis, ulcerative; psoriasis; arthritis, psoriatic; crohn disease; arthritis, rheumatoid - immunszuppresszánsok - kérjük, olvassa el a termékinformációs dokumentumot.

Európai Unió - magyar - EMA (European Medicines Agency)

sun pharmaceutical industries europe b.v. - kapecitabin - stomach neoplasms; breast neoplasms; colonic neoplasms; colorectal neoplasms - kapecitabin - a kapecitabin a iii. stádiumú (dukes-fázisú) vastagbélrák műtétet követő betegek adjuváns kezelésére javallt. capecitabine jelzi a metasztatikus colorectalis rák. capecitabine javallt első vonalbeli kezelés előrehaladott gyomorrák kombinálva egy platina-alapú kezelés. kapecitabinnal kombinációban docetaxel javallt, a betegek kezelése, lokálisan előrehaladott vagy metasztatikus emlőrákban szenvedő meghibásodása után a citotoxikus kemoterápia. az előző terápianak tartalmaznia kellett egy antraciklin. capecitabine is monoterápiában a kezelés a betegek, lokálisan előrehaladott vagy metasztatikus emlőrákban szenvedő meghibásodása után a taxánok egy antraciklin tartalmú kemoterápiás kezelés vagy, akinek további antraciklin terápia nem javasolt.

Európai Unió - magyar - EMA (European Medicines Agency)

merck sharp & dohme b.v. - pembrolizumab - melanoma; hodgkin disease; carcinoma, renal cell; carcinoma, non-small-cell lung; carcinoma, transitional cell; squamous cell carcinoma of head and neck; urologic neoplasms; endometrial neoplasms - daganatellenes szerek - melanomakeytruda as monotherapy is indicated for the treatment of adults and adolescents aged 12 years and older with advanced (unresectable or metastatic) melanoma. keytruda as monotherapy is indicated for the adjuvant treatment of adults and adolescents aged 12 years and older with stage iib, iic, or with stage iii melanoma and lymph node involvement who have undergone complete resection. non small cell lung carcinoma (nsclc)keytruda as monotherapy is indicated for the adjuvant treatment of adults with non-small cell lung carcinoma who are at high risk of recurrence following complete resection and platinum based chemotherapy (for selection criteria, see section 5. keytruda as monotherapy is indicated for the first line treatment of metastatic non small cell lung carcinoma in adults whose tumours express pd l1 with a ≥ 50% tumour proportion score (tps) with no egfr or alk positive tumour mutations. keytruda, in combination with pemetrexed and platinum chemotherapy, is indicated for the first-line treatment of metastatic non squamous non small cell lung carcinoma in adults whose tumours have no egfr or alk positive mutations. keytruda, in combination with carboplatin and either paclitaxel or nab paclitaxel, is indicated for the first line treatment of metastatic squamous non small cell lung carcinoma in adults. keytruda  as monotherapy is indicated for the treatment of locally advanced or metastatic non small cell lung carcinoma in adults whose tumours express pd l1 with a ≥ 1% tps and who have received at least one prior chemotherapy regimen. betegek egfr vagy lÚgos pozitív tumor mutációk is kapott célzott terápia átvétele előtt keytruda. classical hodgkin lymphoma (chl)keytruda as monotherapy is indicated for the treatment of adult and paediatric patients aged 3 years and older with relapsed or refractory classical hodgkin lymphoma who have failed autologous stem cell transplant (asct) or following at least two prior therapies when asct is not a treatment option. urothelial carcinomakeytruda as monotherapy is indicated for the treatment of locally advanced or metastatic urothelial carcinoma in adults who have received prior platinum containing chemotherapy. keytruda as monotherapy is indicated for the treatment of locally advanced or metastatic urothelial carcinoma in adults who are not eligible for cisplatin containing chemotherapy and whose tumours express pd l1 with a combined positive score (cps) ≥ 10. head and neck squamous cell carcinoma (hnscc)keytruda, as monotherapy or in combination with platinum and 5 fluorouracil (5 fu) chemotherapy, is indicated for the first line treatment of metastatic or unresectable recurrent head and neck squamous cell carcinoma in adults whose tumours express pd l1 with a cps ≥ 1. keytruda as monotherapy is indicated for the treatment of recurrent or metastatic head and neck squamous cell carcinoma in adults whose tumours express pd l1 with a ≥ 50% tps and progressing on or after platinum containing chemotherapy. renal cell carcinoma (rcc)keytruda, in combination with axitinib, is indicated for the first line treatment of advanced renal cell carcinoma in adults. keytruda  as monotherapy is indicated for the adjuvant treatment of adults with renal cell carcinoma at increased risk of recurrence following nephrectomy, or following nephrectomy and resection of metastatic lesions (for selection criteria, please see section 5. microsatellite instability high (msi-h) or mismatch repair deficient (dmmr) cancerscolorectal cancer (crc)keytruda as monotherapy is indicated for theadults with msi-h or dmmr colorectal cancer in the following settings:first line treatment of metastatic microsatellite instability high (msi h) or mismatch repair deficient (dmmr) colorectal cancer in adults;treatment of unresectable or metastatic colorectal cancer after previous fluoropyrimidine based combination therapy.  non-colorectal cancerskeytruda as monotherapy is indicated for the treatment of the following msi h or dmmr tumours in adults with:advanced or recurrent endometrial carcinoma, who have disease progression on or following prior treatment with a platinum containing therapy in any setting and who are not candidates for curative surgery or radiation;unresectable or metastatic gastric, small intestine, or biliary cancer, who have disease progression on or following at least one prior therapy. oesophageal carcinomakeytruda, in combination with platinum and fluoropyrimidine based chemotherapy, is indicated for the first-line treatment of locally advanced unresectable or metastatic carcinoma of the oesophagus or her-2 negative gastroesophageal junction adenocarcinoma, in adults whose tumours express pd l1 with a cps ≥ 10. triple negative breast cancer (tnbc)keytruda, in combination with chemotherapy as neoadjuvant treatment, and then continued as monotherapy as adjuvant treatment after surgery, is indicated for the treatment of adults with locally advanced, or early stage triple negative breast cancer at high risk of recurrence. keytruda, in combination with chemotherapy, is indicated for the treatment of locally recurrent unresectable or metastatic triple negative breast cancer in adults whose tumours express pd l1 with a cps ≥ 10 and who have not received prior chemotherapy for metastatic disease. endometrial carcinoma (ec)keytruda, in combination with lenvatinib, is indicated for the treatment of advanced or recurrent endometrial carcinoma in adults who have disease progression on or following prior treatment with a platinum containing therapy in any setting and who are not candidates for curative surgery or radiation. cervical cancerkeytruda, in combination with chemotherapy with or without bevacizumab, is indicated for the treatment of persistent, recurrent, or metastatic cervical cancer in adults whose tumours express pd l1 with a cps ≥ 1. gastric or gastro-oesophageal junction (gej) adenocarcinomakeytruda, in combination with trastuzumab, fluoropyrimidine and platinum-containing chemotherapy, is indicated for the first-line treatment of locally advanced unresectable or metastatic her2-positive gastric or gastro-oesophageal junction adenocarcinoma in adults whose tumours express pd-l1 with a cps ≥ 1.

Magyarország - magyar - OGYÉI (Országos Gyógyszerészeti és Élelmezés-egészségügyi Intézetről)

icn polfa rzeszow s.a. - midazolam -