Suomi - suomi - Fimea (Suomen lääkevirasto)

aristo pharma gmbh - gabapentinum - kapseli, kova - 300 mg - gabapentiini

Suomi - suomi - Fimea (Suomen lääkevirasto)

aristo pharma gmbh - gabapentinum - kapseli, kova - 400 mg - gabapentiini

Euroopan unioni - suomi - EMA (European Medicines Agency)

sfl pharmaceuticals deutschland gmbh - nyxthracis - anthrax - immunoseerumit ja immunoglobuliinit, - obiltoxaximab sfl is indicated in combination with appropriate antibacterial drugs in all age groups for treatment of inhalational anthrax due to bacillus anthracis (see section 5. obiltoxaximab sfl is indicated in all age groups for post-exposure prophylaxis of inhalational anthrax when alternative therapies are not appropriate or are not available (see section 5.

Euroopan unioni - suomi - EMA (European Medicines Agency)

sanofi pasteur - neisseria meningitidis group c polysaccharide conjugated to tetanus toxoid, neisseria meningitidis group a polysaccharide conjugated to tetanus toxoid, neisseria meningitidis group y polysaccharide conjugated to tetanus toxoid, neisseria meningitidis group w-135 polysaccharide conjugated to tetanus toxoid - meningiitti, meningokokki - rokotteet - menquadfi is indicated for active immunisation of individuals from the age of 12 months and older against invasive meningococcal disease caused by neisseria meningitidis serogroups a, c, w, and y. the use of this vaccine should be in accordance with available official recommendations.

Euroopan unioni - suomi - EMA (European Medicines Agency)

bluebird bio (netherlands) b.v. - elivaldogene autotemcel - adrenoleukodystrophy - muut hermoston huumeet - treatment of early cerebral adrenoleukodystrophy in patients less than 18 years of age, with an abcd1 genetic mutation, and for whom a human leukocyte antigen (hla) matched sibling haematopoietic stem cell donor is not available.

Euroopan unioni - suomi - EMA (European Medicines Agency)

bial portela & companhia s.a. - opicapone - parkinsonin tauti - parkinson-lääkkeet - ontilyv is indicated as adjunctive therapy to preparations of levodopa/ dopa decarboxylase inhibitors (ddci) in adult patients with parkinson’s disease and end-of-dose motor fluctuations who cannot be stabilised on those combinations.

Euroopan unioni - suomi - EMA (European Medicines Agency)

mylan pharmaceuticals limited - darunaviiria - hiv-infektiot - antiviraalit systeemiseen käyttöön - darunavir, co-administered with low dose ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of patients with human immunodeficiency virus (hiv-1) infection (see section 4. darunavir mylan 75 mg, 150 mg, 300 mg and 600 mg tablets may be used to provide suitable dose regimens (see section 4. 2):hoitoon hiv-1-infektio antiretroviraalisen hoidon (art)-kokenut aikuisille potilaille, mukaan lukien ne, jotka ovat olleet erittäin esikäsitelty. hoitoon hiv-1-infektion hoitoon lapsipotilailla, alkaen 3-vuotiaiden ja vähintään 15 kg kehon paino. päättäessään aloittaa hoitoa darunaviirin ja pieniannoksisen ritonaviirin kanssa, erityistä huomiota olisi kiinnitettävä hoidon historia potilaan ja malleja liittyviä mutaatioita eri aineet. genotypic or phenotypic testing (when available) and treatment history should guide the use of darunavir (see sections 4. 2, 4. 4 ja 5. darunaviirin ja pieniannoksisen ritonaviirin kanssa on tarkoitettu yhdessä muiden antiretroviraalisten lääkkeiden hoitoon potilailla, joilla on ihmisen immuunikatovirus (hiv-1) hoitoon.  darunavir co-administered with cobicistat is indicated in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus (hiv-1) infection in adults and adolescents (aged 12 years and older, weighing at least 40 kg) (see section 4.  darunavir mylan 400 mg and 800 mg tablets may be used to provide suitable dose regimens for the treatment of hiv-1 infection in adult and paediatric patients from the age of 3 years and at least 40 kg body weight who are: antiretroviral therapy (art)-naïve (see section 4.  art-experienced with no darunavir resistance associated mutations (drv-rams) and who have plasma hiv-1 rna < 100,000 copies/ml and cd4+ cell count ≥ 100 cells x 10⁶/l. päättäessään aloittaa hoitoa darunaviirin kanssa niin taiteen saaneilla potilailla todettiin testaus olisi oppaan käytön darunaviiri (ks. kohdat 4. 2, 4. 3, 4. 4 ja 5.

Euroopan unioni - suomi - EMA (European Medicines Agency)

les laboratoires servier - trifluridine, tipiracil hydrochloride - paksusuolen vajaatoiminta - antineoplastiset aineet - colorectal cancerlonsurf is indicated in combination with bevacizumab for the treatment of adult patients with metastatic colorectal cancer (crc) who have received two prior anticancer treatment regimens including fluoropyrimidine-, oxaliplatin- and irinotecan-based chemotherapies, anti-vegf agents, and/or anti-egfr agents. lonsurf is indicated as monotherapy for the treatment of adult patients with metastatic colorectal cancer (crc) who have been previously treated with, or are not considered candidates for, available therapies including fluoropyrimidine-, oxaliplatin- and irinotecan-based chemotherapies, anti-vegf agents, and anti egfr agentsgastric cancerlonsurf is indicated as monotherapy for the treatment of adult patients with metastatic gastric cancer including adenocarcinoma of the gastroesophageal junction, who have been previously treated with at least two prior systemic treatment regimens for advanced disease.

Euroopan unioni - suomi - EMA (European Medicines Agency)

glaxosmithkline biologicals s.a. - a / indonesia / 05/2005 (h5n1), kuten käytetty kanta (pr8-ibcdc-rg2) - influenza, human; immunization; disease outbreaks - rokotteet - aktiivinen immunisointi influenssa-a-viruksen h5n1-alatyypin suhteen. tämä käyttöaihe perustuu immunogeenisuutta terveillä henkilöillä, ikä 18 vuotta alkaen annon jälkeen kaksi annosta rokotetta, joka valmistetaan h5n1-alatyypin kantoja. prepandrix tulee käyttää virallisen ohjeistuksen mukaisesti.