NeisVac-C 10 mikrogram/dosis injektionsvæske, suspension, fyldt injektionssprøjte Đan Mạch - Tiếng Đan Mạch - Lægemiddelstyrelsen (Danish Medicines Agency)

neisvac-c 10 mikrogram/dosis injektionsvæske, suspension, fyldt injektionssprøjte

pfizer aps - clostridium tetani, toxoid, neisseria meningitidis polysaccharid serogruppe c, stamme c11, de-o-acetyleret - injektionsvæske, suspension, fyldt injektionssprøjte - 10 mikrogram/dosis

Verorab 3,25 IE pulver og solvens til injektionsvæske, suspension, fyldt injektionssprøjte Đan Mạch - Tiếng Đan Mạch - Lægemiddelstyrelsen (Danish Medicines Agency)

verorab 3,25 ie pulver og solvens til injektionsvæske, suspension, fyldt injektionssprøjte

sanofi pasteur - rabiesvirus stamme, wistar pm/wi 38-1503-3m (inaktiveret) - pulver og solvens til injektionsvæske, suspension, fyldt injektionssprøjte - 3,25 ie

Vaxneuvance Liên Minh Châu Âu - Tiếng Đan Mạch - EMA (European Medicines Agency)

vaxneuvance

merck sharp & dohme b.v.  - pneumococcal polysaccharide conjugate vaccine (adsorbed) - pneumokokinfektioner - pneumococcus, purified polysaccharides antigen conjugated - vaxneuvance is indicated for active immunisation for the prevention of invasive disease, pneumonia and acute otitis media caused by streptococcus pneumoniae in infants, children and adolescents from 6 weeks to less than 18 years of age. vaxneuvance is indicated for active immunisation for the prevention of invasive disease and pneumonia caused by streptococcus pneumoniae in individuals 18 years of age and older. se afsnit 4. 4 og 5. 1 for information om beskyttelse mod specifikke pneumokokserotyper. the use of vaxneuvance should be in accordance with official recommendations.

Docetaxel Mylan Liên Minh Châu Âu - Tiếng Đan Mạch - EMA (European Medicines Agency)

docetaxel mylan

mylan s.a.s. - docetaxel - head and neck neoplasms; carcinoma, non-small-cell lung; adenocarcinoma; prostatic neoplasms; breast neoplasms - antineoplastiske midler - behandling af brystkræft, særlige former for lungekræft (ikke-småcellet lungekræft), prostatakræft, mavekræft eller hoved og hals kræft.

Boostrix injektionsvæske, suspension Đan Mạch - Tiếng Đan Mạch - Lægemiddelstyrelsen (Danish Medicines Agency)

boostrix injektionsvæske, suspension

glaxosmithkline pharma a/s - bordetella pertussis, filamentøs hæmagglutinin (fha), bordetella pertussis, pertactin (prn/69 kilodalton ydermembranprotein), bordetella pertussis, toxoid, clostridium tetani, toxoid, corynebacterium diphtheria, toxoid - injektionsvæske, suspension

Tulaven Liên Minh Châu Âu - Tiếng Đan Mạch - EMA (European Medicines Agency)

tulaven

ceva santé animale - tulathromycin - antibakterielle midler til systemisk brug - cattle; pigs; sheep - cattle: treatment and metaphylaxis of bovine respiratory disease (brd) associated with mannheimia haemolytica, pasteurella multocida, histophilus somni and mycoplasma bovis susceptible to tulathromycin. tilstedeværelsen af ​​sygdommen i besætningen bør etableres inden metafylaktisk behandling. treatment of infectious bovine keratoconjunctivitis (ibk) associated with moraxella bovis susceptible to tulathromycin. pigs: treatment and metaphylaxis of swine respiratory disease (srd) associated with actinobacillus pleuropneumoniae, pasteurella multocida, mycoplasma hyopneumoniae, haemophilus parasuis and bordetella bronchiseptica susceptible to tulathromycin. tilstedeværelsen af ​​sygdommen i besætningen bør etableres inden metafylaktisk behandling. the product should only be used if pigs are expected to develop the disease within 2–3 days. får: behandling af de tidlige stadier af infektiøs pododermatitis (fodrot) forbundet med virulent dichelobacter nodosus, der kræver systemisk behandling.