Symtuza Европска Унија - Мелтешки - EMA (European Medicines Agency)

symtuza

janssen-cilag international nv - darunavir, kobikistat, emtricitabine, tenofovir alafenamide - infezzjonijiet ta 'hiv - antivirals for systemic use, antivirals for treatment of hiv infections, combinations - symtuza huwa indikat għat-trattament tal-virus ta ' immunodefiċjenza umani tat-tip 1 (hiv‑1) infezzjoni fl-adulti u l-adolexxenti (età 12-il sena u aktar antiki mal-korp tal-mill-inqas 40 kg piż). genotypic testing should guide the use of symtuza.

Namuscla Европска Унија - Мелтешки - EMA (European Medicines Agency)

namuscla

lupin europe gmbh - mexiletine hydrochloride - myotonic disturbi - terapija kardijaka - namuscla huwa indikat għall-kura sintomatika ta myotonia f'pazjenti adulti b'nuqqas distrofiċi myotonic disturbi.

Xromi Европска Унија - Мелтешки - EMA (European Medicines Agency)

xromi

nova laboratories ireland limited - hydroxycarbamide - anemija, sickle cell - aġenti antineoplastiċi - il-prevenzjoni ta vaso-okklusivi komplikazzjonijiet tal-marda taċ-ċelluli sickle fil-pazjenti ta ' aktar minn 2 snin ta'età.

Zynrelef Европска Унија - Мелтешки - EMA (European Medicines Agency)

zynrelef

heron therapeutics, b.v. - bupivacaine, meloxicam - uġigħ, wara l-operazzjoni - anestetiċi - zynrelef is indicated for treatment of somatic postoperative pain from small- to medium-sized surgical wounds in adults (see section 5.

OvuGel Европска Унија - Мелтешки - EMA (European Medicines Agency)

ovugel

vetoquinol - triptorelin acetate - ormoni u analogi pitwitarji u ipotalamiċi - pigs (sows for reproduction) - for the synchronisation of ovulation in weaned sows to enable a single fixed-time artificial insemination.

Evrysdi Европска Унија - Мелтешки - EMA (European Medicines Agency)

evrysdi

roche registration gmbh  - risdiplam - atrofija muskolari, spinali - mediċini oħra għal disturbi fis-sistema muskoloskeletali - evrysdi is indicated for the treatment of 5q spinal muscular atrophy (sma) in patients with a clinical diagnosis of sma type 1, type 2 or type 3 or with one to four smn2 copies.

Imatinib Koanaa Европска Унија - Мелтешки - EMA (European Medicines Agency)

imatinib koanaa

koanaa healthcare gmbh - imatinib mesilate - leukemia, myelogenous, chronic, bcr-abl positive; precursor cell lymphoblastic leukemia-lymphoma; myelodysplastic-myeloproliferative diseases; hypereosinophilic syndrome; dermatofibrosarcoma; gastrointestinal stromal tumors - aġenti antineoplastiċi - imatinib koanaa is indicated for the treatment ofadult and paediatric patients with newly diagnosed philadelphia chromosome (bcr-abl) positive (ph+) chronic myeloid leukaemia (cml) for whom bone marrow transplantation is not considered as the first line of treatment. adult and paediatric patients with ph+ cml in chronic phase after failure of interferon-alpha therapy, or in accelerated phase or blast crisis. adult and paediatric patients with newly diagnosed philadelphia chromosome positive acute lymphoblastic leukaemia (ph+ all) integrated with chemotherapy. adult patients with relapsed or refractory ph+ all as monotherapy. adult patients with myelodysplastic/myeloproliferative diseases (mds/mpd) associated with platelet-derived growth factor receptor (pdgfr) gene re-arrangements. adult patients with advanced hypereosinophilic syndrome (hes) and/or chronic eosinophilic leukaemia (cel) with fip1l1-pdgfrα rearrangement. the effect of imatinib on the outcome of bone marrow transplantation has not been determined. imatinib koanaa is indicated forthe treatment of adult patients with kit (cd 117) positive unresectable and/or metastatic malignant gastrointestinal stromal tumours (gist). the adjuvant treatment of adult patients who are at significant risk of relapse following resection of kit (cd117)-positive gist. pazjenti li għandhom livell baxx jew l-riskju baxx ħafna ta ' rikorrenza m'għandhomx jirċievu kura awżiljarja. the treatment of adult patients with unresectable dermatofibrosarcoma protuberans (dfsp) and adult patients with recurrent and/or metastatic dfsp who are not eligible for surgery. in adult and paediatric patients, the effectiveness of imatinib is based on overall haematological and cytogenetic response rates and progression-free survival in cml, on haematological and cytogenetic response rates in ph+ all, mds/mpd, on haematological response rates in hes/cel and on objective response rates in adult patients with unresectable and/or metastatic gist and dfsp and on recurrence-free survival in adjuvant gist. the experience with imatinib in patients with mds/mpd associated with pdgfr gene re-arrangements is very limited (see section 5. Ħlief fil għadhom kif ġew dijanjostikati cml ta ' fażi kronika, m'hemmx provi kliniċi li juru benefiċċju kliniku jew żieda fis-sopravivenza għal dawn il-mard.

Bonqat Европска Унија - Мелтешки - EMA (European Medicines Agency)

bonqat

orion corporation - pregabalin - antiepileptics - qtates - alleviation of acute anxiety and fear associated with transportation and veterinary visits.

Zenalpha Европска Унија - Мелтешки - EMA (European Medicines Agency)

zenalpha

vetcare oy - medetomidine hydrochloride, vatinoxan hydrochloride - psikoterapewtiċi, ipnotiċi u sedattivi - klieb - 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.

Contacera Европска Унија - Мелтешки - EMA (European Medicines Agency)

contacera

zoetis belgium sa - meloxicam - anti-inflammatory and anti-rheumatic products, non-steroids - horses; pigs; cattle - cattlefor-użu fil-infezzjoni respiratorja akuta b'terapija antibijotika xierqa biex jitnaqqsu s-sinjali kliniċi. għal użu fid-dijarea flimkien ma 'terapija mill-ġdid ta' idratazzjoni mill-ħalq biex jitnaqqsu s-sinjali kliniċi f'għoġġiela ta 'aktar minn ġimgħa ta' età u baqar żgħar li ma jreddgħux. għal terapija aġġuntiva fit-trattament ta 'mastite akuta, flimkien ma' terapija antibijotika. għall-eżenzjoni ta 'uġigħ ta' wara l-operazzjoni wara t-tqaxxir fl-għoġġiela. pigsfor l-tnaqqis tas-sintomi ta'zappip u ta'infjammazzjoni fid-disturbi lokomotorji mhux infettivi u għal terapija addizzjonali fit-trattament ta 'settiċemija puwerperali u toxaemia (mastite-metrite-agalaktja) ma' terapija antibijotika adattata. horsesfor-użu sabiex tittaffa l-infjammazzjoni u serħan mill-uġigħ akut kif ukoll kroniku disturbi muskolu-skeletrali. għall-eżenzjoni ta 'uġigħ assoċjat ma' kolika ekwina.