Gentamicin B. Braun 3 mg/ ml Norge - norsk - Statens legemiddelverk

gentamicin b. braun 3 mg/ ml

2care4 aps - gentamicinsulfat - infusjonsvæske, oppløsning - 3 mg/ ml

Gentamicin B. Braun 3 mg/ ml Norge - norsk - Statens legemiddelverk

gentamicin b. braun 3 mg/ ml

2care4 aps - gentamicinsulfat - infusjonsvæske, oppløsning - 3 mg/ ml

TechneScan PYP 20 mg Norge - norsk - Statens legemiddelverk

technescan pyp 20 mg

curium netherlands b.v. - natriumpyrofosfat - preparasjonssett til radioaktive legemidler - 20 mg

Targocid 400 mg Norge - norsk - Statens legemiddelverk

targocid 400 mg

sanofi-aventis norge (3) - teikoplanin - pulver til injeksjonsvæske/infusjonsvæske oppløsning eller mikstur, oppløsning - 400 mg

Quofenix Den europeiske union - norsk - EMA (European Medicines Agency)

quofenix

a. menarini industrie farmaceutiche riunite s.r.l. - delafloxacin meglumine - fellesskapsmessige infeksjoner - antibakterielle midler for systemisk bruk, - quofenix is indicated for the treatment of the following infections in adults:acute bacterial skin and skin structure infections (absssi),community-acquired pneumonia (cap), when it is considered inappropriate to use other antibacterial agents that are commonly recommended for the initial treatment of these infections (see sections 4. 4 og 5. det bør vurderes å offisielle retningslinjer for riktig bruk av antibakterielle midler.

Tigecycline Accord Den europeiske union - norsk - EMA (European Medicines Agency)

tigecycline accord

accord healthcare s.l.u. - tigecycline - soft tissue infections; intraabdominal infections; bacterial infections; skin diseases, infectious - antibakterielle midler for systemisk bruk, - tygecycline accord er indisert hos voksne og hos barn fra en alder av åtte år for behandling av følgende infeksjoner (se kapittel 4. 4 og 5. 1):kompliserte hud-og bløtdelsinfeksjoner (cssti), med unntak av diabetiker foten infeksjoner (se kapittel 4. 4)komplisert intra-abdominal infeksjoner (ciai)tygecycline accord bør bare brukes i situasjoner hvor andre alternative antibiotika er ikke egnet (se kapittel 4. 4, 4. 8 og 5. det bør vurderes å offisielle retningslinjer for riktig bruk av antibakterielle midler.

Clindamycin Navamedic 300 mg Norge - norsk - Statens legemiddelverk

clindamycin navamedic 300 mg

navamedic asa - klindamycinfosfat - infusjonsvæske, oppløsning - 300 mg

Clindamycin Navamedic 600 mg Norge - norsk - Statens legemiddelverk

clindamycin navamedic 600 mg

navamedic asa - klindamycinfosfat - infusjonsvæske, oppløsning - 600 mg

Jayempi Den europeiske union - norsk - EMA (European Medicines Agency)

jayempi

nova laboratories ireland limited - azathioprine - graft-avvisning - immunsuppressive - jayempi is indicated in combination with other immunosuppressive agents for the prophylaxis of transplant rejection in patients receiving allogenic kidney, liver, heart, lung or pancreas transplants. azathioprine is indicated in immunosuppressive regimens as an adjunct to immunosuppressive agents that form the mainstay of treatment (basis immunosuppression). jayempi is used as an immunosuppressant antimetabolite either alone or, more commonly, in combination with other agents (usually corticosteroids) and/ or procedures which influence the immune response. jayempi is indicated in patients who are intolerant to glucocorticosteroids or if the therapeutic response is inadequate despite treatment with high doses of glucocorticosteroids, in the following diseases:severe active rheumatoid arthritis (chronic polyarthritis) that cannot be kept under control by less toxic agents (disease-modifying anti-rheumatic -medicinal products – dmards)auto-immune hepatitis systemic lupus erythematosusdermatomyositispolyarteritis nodosapemphigus vulgaris and bullous pemphigoidbehçet’s diseaserefractory auto-immune haemolytic anaemia, caused by warm igg antibodieschronic refractory idiopathic thrombocytopenic purpurajayempi is used for the treatment of moderately severe to severe forms of chronic inflammatory bowel disease (ibd) (crohn’s disease or ulcerative colitis) in patients in whom glucocorticosteroid therapy is necessary, but where glucocorticosteroids are not tolerated, or in whom the disease is untreatable with other common means of first choice. it is also indicated in adult patients in relapsing multiple sclerosis, if an immunomodulatory therapy is indicated but beta interferon therapy is not possible, or a stable course has been achieved with previous treatment with azathioprine. 3jayempi is indicated for the treatment of generalised myasthenia gravis. depending on the severity of the disease, jayempi should be given in combination with glucocorticosteroids because of slow onset of action at the beginning of treatment and the glucocorticosteroid dose should be gradually reduced after several months of treatment.

Oxbryta Den europeiske union - norsk - EMA (European Medicines Agency)

oxbryta

pfizer europe ma eeig  - voxelotor - anemia; anemia, hemolytic; anemia, sickle cell - other hematological agents - oxbryta is indicated for the treatment of haemolytic anaemia due to sickle cell disease (scd) in adults and paediatric patients 12 years of age and older as monotherapy or in combination with hydroxycarbamide.