Unjoni Ewropea - Malti - EMA (European Medicines Agency)

astrazeneca ab - formoterol fumarate dihydrate, glycopyrronium bromide, budesonide - mard tal-pulmun, obstructive kronika - mediċini għall-imblokkar tal-passaġġ tan-nifs mard, - 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.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

astrazeneca ab - glycopyrronium, formoterol fumarate dihydrate - mard tal-pulmun, obstructive kronika - formoterol u glycopyrronium bromide - bevespi aerosphere huwa indikat bħala l-manutenzjoni bronkodilatur-kura biex ittaffi s-sintomi fil-pazjenti adulti bil-marda pulmonari ostruttiva kronika (copd).

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

glaxosmithkline trading services limited - fluticasone furoate, bromur tal-umeclidinium, trifenatate tal-vilanterol - mard tal-pulmun, obstructive kronika - mediċini għall-imblokkar tal-passaġġ tan-nifs mard, - temybric ellipta huwa indikat bħala kura ta 'manteniment f'pazjenti adulti b'indeboliment moderat jew sever tal-marda pulmonari ostruttiva kronika (copd) li ma jkunux qed jiġu kkurati b'taħlita ta' kortikosterojdi meħuda man-nifs u li jaħdem fit-tul β2-agonist jew kombinazzjoni ta taġixxi fit-tul β2-agonist u li jaħdem fit-tul muskariniċi antagonist (għall-effetti fuq il-kontroll tas-sintomi u l-prevenzjoni tal-aggravar tal-attakki ara sezzjoni 5.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

astrazeneca ab - budesonide, formoterol fumarate dihydrate, glycopyrronium bromide - mard tal-pulmun, obstructive kronika - mediċini għall-imblokkar tal-passaġġ tan-nifs mard, - 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.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

teva pharma b.v.  - clopidogrel (as hydrobromide) - peripheral vascular diseases; acute coronary syndrome; myocardial infarction; stroke - aġenti antitrombotiċi - il-prevenzjoni ta aterotrombotiċi eventsclopidogrel huwa indikat f': pazjenti adulti li jbatu minn infart mijokardijaku (minn ftit jiem sa inqas minn 35 jum), puplesija iskemika (minn 7 ijiem sa inqas minn 6 xhur) jew mard arterjali periferali;f'pazjenti adulti li jsofru mis-sindromu koronarju akut: mhux elevazzjoni tas-segment st sindromu koronarju akut (anġina instabbli jew mhux-mewġa-q infart mijokardijaku), li jinkludu pazjenti fi proċess li titpoġġa stent wara intervent koronarju perkutanju, flimkien ma ' acetylsalicylic acid (asa);elevazzjoni tas-segment st infart mijokardijaku akut, flimkien ma ' asa f'medikament pazjenti kkurati b'eliġibbli għat-terapija trombolitika. il-prevenzjoni ta aterotrombotiċi u avvenimenti tromboemboliċi fil-fibrillazzjoni ta 'l-fibrillationin pazjenti adulti li jbatu minn fibrillazzjoni atrijali li jkollhom mill-inqas fattur ta' riskju wieħed għall-episodji vaskulari, mhumiex adattati għall-kura bil-vitamina k antagonisti (vka) u li għandhom baxx-riskju ta'fsada, clopidogrel huwa indikat, flimkien ma ' asa għall-prevenzjoni tal-aterotrombotiċi u avvenimenti tromboemboliċi, inkluż puplesija.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

sanofi pasteur europe - filamentous haemagglutinin, haemophilus influenzae type b polysaccharide (polyribosylribitol phosphate), hepatitis b surface antigen, pertussis toxoid, poliovirus (inactivated) type 1 (mahoney strain) produced on vero cells, poliovirus (inactivated) type 2 (mef-1 strain) produced on vero cells, poliovirus (inactivated) type 3 (saukett strain) produced on vero cells, tetanus protein, tetanus toxoid adsorbed on aluminium hydroxide, hydrated, diphtheria toxoid - hepatitis b; tetanus; immunization; meningitis, haemophilus; whooping cough; poliomyelitis; diphtheria - vaċċini - hexyon (dtap-ipv-hb-hib) huwa indikat għat-tilqim primarja u booster tat-trabi u toddlers minn sitt ġimgħat ta ' età kontra diphtheria, tetanus, pertussis, epatite b, poliomyelitis u invażivi mard ikkawżat minn influwenza Ħemofillika tip b (hib). l-użu ta ' dan il-vaċċin għandha tkun skond ir-rakkomandazzjonijiet uffiċjali.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

merck sharp & dohme b.v.  - pneumococcal polysaccharide conjugate vaccine (adsorbed) - infezzjonijiet pnewmokokkali - 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. ara t-taqsimiet 4. 4 u 5. 1 għal informazzjoni dwar il-protezzjoni kontra serotipi pnewmokokkiċi speċifiċi. the use of vaxneuvance should be in accordance with official recommendations.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

laboratorios hipra, s.a. - erysipelothrix rhusiopathiae, strain r32e11 (mhux attivat) - immunologicals for suidae, inactivated bacterial vaccines (including mycoplasma, toxoid and chlamydia) escherichia + clostridium - majjali - għall-immunizzazzjoni attiva ta 'l-irġiel u tan-nisa, l-majjali biex tnaqqas is-sinjali kliniċi (leżjonijiet tal-ġilda u deni) ta' erysipelas majjali kkawżata minn erysipelothrix rhusiopathiae, serotip 1 u serotip 2.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

laboratorios hipra, s.a. - parvovirus tal-ħnieżer, strain nadl-2 u erysipelothrix rhusiopathiae, strain r32e11 (inattivat) - immunologicals for suidae, inactivated viral and inactivated bacterial vaccines - majjali - għall-immunizzazzjoni attiva ta 'majjali femminili għall-protezzjoni tal-proġenija kontra infezzjoni transplacental ikkawżata minn parvovirus tal-ħnieżer. għall-immunizzazzjoni attiva ta 'l-irġiel u tan-nisa, l-majjali biex tnaqqas is-sinjali kliniċi (leżjonijiet tal-ġilda u deni) ta' erysipelas majjali kkawżata minn erysipelothrix rhusiopathiae, serotip 1 u serotip 2.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

zoetis belgium s.a. - leptospira interrogans serogrupp ma ' serotip bratislava, razza mslb 1088, l. interrogans serogrupp icterohaemorrhagiae serotip icterohaemorrhagiae, razza mslb 1089, l. interrogans serogrupp canicola serotip canicola, razza mslb 1090, l. kirschneri serogrupp grippotyphosa serotip grippotyphosa, razza mslb 1091 (kollha mhux attivat) - vaċċini batterjali inattivati (inkluż mycoplasma, toxoid u chlamydia), immunoloġiċi għall-canidae - klieb - tilqim attiv ta 'klieb ta' sitt ġimgħat għall-prevenzjoni tal-sinjali kliniċi, l-infezzjoni u l-eskrezzjoni fl-awrina kkawżati minn leptospira serovars bratislava, canicola, grippotyphosa u icterohaemorrhagiae. il-bidu tal-immunità: intwera l-immunità minn 4 ġimgħat wara t-tlestija tal-kors primarju. tul ta 'żmien tal-immunità: mill-inqas sena wara l-kors primarju tat-tilqim.