Sverige - svenska - Läkemedelsverket (Medical Products Agency)

ebb medical ab - flutikasonpropionat; salmeterolxinafoat - inhalationsspray, suspension - 25 mikrogram/250 mikrogram/dos - salmeterolxinafoat 36,32 mikrog aktiv substans; flutikasonpropionat 250 mikrog aktiv substans

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

ebb medical ab - flutikasonpropionat; salmeterolxinafoat - inhalationsspray, suspension - 25 mikrogram/250 mikrogram/dos - salmeterolxinafoat 36,32 mikrog aktiv substans; flutikasonpropionat 250 mikrog aktiv substans

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

ebb medical ab - flutikasonpropionat; salmeterolxinafoat - inhalationsspray, suspension - 25 mikrogram/125 mikrogram/dos - flutikasonpropionat 125 mikrog aktiv substans; salmeterolxinafoat 36,32 mikrog aktiv substans

Europeiska unionen - svenska - EMA (European Medicines Agency)

insmed netherlands b.v. - amikacin sulfate - infektioner i luftvägarna - antibakteriella medel för systemiskt bruk, - arikayce liposomal is indicated for the treatment of non-tuberculous mycobacterial (ntm) lung infections caused by mycobacterium avium complex (mac) in adults with limited treatment options who do not have cystic fibrosis.

Europeiska unionen - svenska - EMA (European Medicines Agency)

astrazeneca ab - formoterol fumarate dihydrate, glycopyrronium bromide, budesonide - pulmonell sjukdom, kronisk obstruktiv - läkemedel mot obstruktiv lungsjukdom, - trixeo aerosphere is indicated as a maintenance treatment in adult patients with moderate to severe chronic obstructive pulmonary disease (copd) who are not adequately treated by a combination of an inhaled corticosteroid and a long acting beta2 agonist or combination of a long-acting beta2 agonist and a long acting muscarinic antagonist.

Europeiska unionen - svenska - EMA (European Medicines Agency)

vetcare oy - medetomidine hydrochloride, vatinoxan hydrochloride - psykoleptika, hypnotika och lugnande medel - hundar - to provide restraint, sedation and analgesia during conduct of non-invasive, non-painful or mildly painful procedures and examinations intended to last no more than 30 minutes.

Europeiska unionen - svenska - EMA (European Medicines Agency)

astrazeneca ab - budesonide, formoterol fumarate dihydrate, glycopyrronium bromide - pulmonell sjukdom, kronisk obstruktiv - läkemedel mot obstruktiv lungsjukdom, - riltrava aerosphere is indicated as a maintenance treatment in adult patients with moderate to severe chronic obstructive pulmonary disease (copd) who are not adequately treated by a combination of an inhaled corticosteroid and a long-acting beta2 agonist or combination of a long-acting beta2 agonist and a long-acting muscarinic antagonist (for effects on symptoms control and prevention of exacerbations see section 5.

Europeiska unionen - svenska - EMA (European Medicines Agency)

recordati ireland ltd. - lidokain, prilocaine - sexuell dysfunktion, fysiologisk - bedövningsmedel - behandling av primär prematur utlösning hos vuxna män.

Europeiska unionen - svenska - EMA (European Medicines Agency)

plethora pharma solutions limited - lidokain, prilocaine - för tidig utlösning - bedövningsmedel - senstend är indicerat för behandling av primär tidig utlösning hos män.

Europeiska unionen - svenska - EMA (European Medicines Agency)

ceva santé animale - tulatromycin - antibakteriella medel för systemisk användning - 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. förekomsten av sjukdomen i besättningen bör fastställas före 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. förekomsten av sjukdomen i besättningen bör fastställas före metafylaktisk behandling. the product should only be used if pigs are expected to develop the disease within 2–3 days. får: behandling av de tidiga stadierna av infektiös pododermatit (fotrot) i samband med virulent dichelobacter nodosus som kräver systemisk behandling.