Unjoni Ewropea - Malti - EMA (European Medicines Agency)

orion corporation - dexmedetomidine hydrochloride - sistema nervuża, ipnotiċi u sedattivi oħrajn - klieb - tnaqqis ta 'ansjetà akuta u biża' assoċjati mal-ħsejjes fil-klieb.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

intervet international bv - tildipirosin - antiinfectives għall-użu sistemiku - pigs; cattle - 40 mg/ml soluzzjoni għall-injezzjoni għall-pigstreatment u metaphylaxis tal-marda respiratorja fil-majjali (srd) assoċjata ma ' actinobacillus pleuropneumoniae, pasteurella multocida, bordetella bronchiseptica u haemophilus parasuis sensittivi għal tildipirożin. il-preżenza tal-marda fil-merħla għandha tiġi kkonfermata qabel ma tiġi implimentata l-metaphylaxis. 180 mg/ml soluzzjoni għall-injezzjoni għall-cattlefor-trattament u l-prevenzjoni tal-marda respiratorja fil-bovini (brd) assoċjata ma ' mannheimia haemolytica, pasteurella multocida u histophilus somni sensittivi għall-tildipirożin. il-preżenza tal-marda fil-merħla għandha tiġi kkonfermata qabel it-trattament preventiv.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

biogen netherlands b.v. - dimetil fumarate - sklerosi multipla - immunosoppressanti - tecfidera is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

bausch health ireland limited - methylnaltrexone bromide - opioid-related disorders; constipation - periferali tal-opioid ta ' l-antagonisti tar-riċettur - trattament ta 'stitikezza li tittieħed mill-opjojdi f'pazjenti b'mard avvanzat li qed jirċievu kura palljattiva meta r-rispons għat-terapija laxattiva normali ma kienx biżżejjed.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

rad neurim pharmaceuticals eec sarl - melatonin - sleep initiation and maintenance disorders; autistic disorder - psikolettiċi - slenyto huwa indikat għat-trattament ta 'nuqqas ta' rqad fit-tfal u l-adolexxenti ta ' minn 2-18-il bl-awtiżmu-ispettru disturb (petite) u / jew smith-magenis-sindromu, fejn l-irqad-iġjene miżuri ġew insuffiċjenti.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

mylan ireland limited - dimetil fumarate - l-isklerożi multipla, sklerożi multipla li tirkadi u tbatti - immunosoppressanti - dimethyl fumarate mylan is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

zaklady farmafarmaceutyczne polpharma s.aceutyczne polpharma s.a. - dimetil fumarate - l-isklerożi multipla, sklerożi multipla li tirkadi u tbatti - immunosoppressanti - dimethyl fumarate polpharma is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

laboratorios lesvi s.l. - dimetil fumarate - l-isklerożi multipla, sklerożi multipla li tirkadi u tbatti - immunosoppressanti - dimethyl fumarate neuraxpharma is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

teva gmbh - dimetil fumarate - multiple sclerosis, relapsing-remitting; multiple sclerosis - immunosoppressanti - dimethyl fumarate teva is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

accord healthcare s.l.u. - dimetil fumarate - multiple sclerosis, relapsing-remitting; multiple sclerosis - immunosoppressanti - dimethyl fumarate accord is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).