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Europska unija — odluke Europske komisije

Ukinuta odobrenja, povlačenje serija lijekova, pisma zdravstvenim radnicima i novi lijekovi EU — svakodnevno, automatski. Zadnje ažuriranje: 13. 11. 2026. 08:55

Sve Ukinuta odobrenja8 Povlačenje serija2 Novi lijekovi (EU) Sigurnost (DHPC)1 Europska unija39

Izvori: promjene pratimo na temelju informacija Agencije za lijekove i medicinske proizvode (HALMED) — rješenja o ukidanju odobrenja, obavijesti o povlačenju serija i pisma zdravstvenim radnicima. Odluke o centralizirano odobrenim lijekovima dolaze iz registra Unije Europske komisije (oznaka EU). Nestašice i liste lijekova HZZO-a ovdje (još) nisu uključene.

5. 10. 2026.ponedjeljak, 5. listopada 2026.

otvori dan ◀ ▶ 10 događaja
Odluka Europske komisije EU Yuvanci
br. EU/1/24/1859 · odobreno 27. 9. 2024. · Yuvanci is indicated as substitution therapy for the long-term treatment of pulmonary arterial hypertension (P… · Janssen-Cilag International NV · Macitentan / Tadalafil · ATC C02KX54
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Odluka Europske komisije EU Vevzuo
br. EU/1/25/1945 · odobreno 25. 6. 2025. · Prevention of skeletal related events (pathological fracture, radiation to bone, spinal cord compression or su… · Biosimilar Collaborations Ireland Limited · denosumab · ATC M05BX04
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Odluka Europske komisije EU Tenofovir disoproxil Viatris
br. EU/1/16/1129 · odobreno 8. 12. 2016. · HIV-1 infection Tenofovir disoproxil 245 mg film-coated tablets are indicated in combination with other antir… · Viatris Limited · Tenofovir disoproxil · ATC J05AF07
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Odluka Europske komisije EU Mirvaso
br. EU/1/13/904 · odobreno 21. 2. 2014. · Mirvaso is indicated for the symptomatic treatment of facial erythema of rosacea in adult patients. · Galderma S.A.,the Netherlands Branch · brimonidine · ATC D11AX21
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Odluka Europske komisije EU Memantine Accord
br. EU/1/13/880 · odobreno 4. 12. 2013. · Treatment of patients with moderate to severe Alzheimer's disease. · Accord Healthcare S.L.U. · memantine · ATC N06DX01
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Odluka Europske komisije EU Kovaltry
br. EU/1/15/1076 · odobreno 18. 2. 2016. · Treatment and prophylaxis of bleeding in patients with haemophilia A (congenital factor VIII deficiency). Kova… · Bayer AG · octocog alfa · ATC B02BD02
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Odluka Europske komisije EU Kostaive
br. EU/1/24/1873 · odobreno 12. 2. 2025. · Kostaive is indicated for active immunisation to prevent COVID-19 caused by SARS-CoV-2 in individuals 18 years… · Arcturus Therapeutics Europe B.V. · zapomeran · ATC J07BX03
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Odluka Europske komisije EU ELAHERE
br. EU/1/24/1866 · odobreno 14. 11. 2024. · ELAHERE as monotherapy is indicated for the treatment of adult patients with folate receptor-alpha (FRα) posit… · AbbVie Deutschland GmbH & Co. KG · mirvetuximab soravtansine · ATC L01FX26
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Odluka Europske komisije EU Dazparda
br. EU/1/26/2029 · odobreno 27. 4. 2026. · Dazparda is indicated for treatment of diabetes mellitus in adults, adolescents and children aged 1 year and a… · Sandoz GmbH · insulin aspart · ATC A10AB05
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Odluka Europske komisije EU Daxas
br. EU/1/10/636 · odobreno 5. 7. 2010. · Daxas is indicated for maintenance treatment of severe chronic obstructive pulmonary disease (COPD) (FEV1 post… · AstraZeneca AB · roflumilast · ATC R03DX07
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29. 9. 2026.utorak, 29. rujna 2026.

otvori dan ◀ ▶ 1 događaj
Odluka Europske komisije EU Nexviadyme
br. EU/1/21/1579 · odobreno 24. 6. 2022. · Nexviadyme (avalglucosidase alfa) is indicated for long-term enzyme replacement therapy for the treatment of p… · Sanofi B.V. · avalglucosidase alfa · ATC A16AB22
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28. 9. 2026.ponedjeljak, 28. rujna 2026.

otvori dan ◀ ▶ 4 događaja · 1 važnih
Povučeno u EU EU ZINPLAVA
br. EU/1/16/1156 · odobreno 18. 1. 2017. · ZINPLAVA is indicated for the prevention of recurrence of Clostridioides difficile infection (CDI) in adult an… · Merck Sharp & Dohme B.V. · bezlotoxumab · ATC J06BC03
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Odluka Europske komisije EU ZINPLAVA
br. EU/1/16/1156 · odobreno 18. 1. 2017. · ZINPLAVA is indicated for the prevention of recurrence of Clostridioides difficile infection (CDI) in adult an… · Merck Sharp & Dohme B.V. · bezlotoxumab · ATC J06BC03
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Odluka Europske komisije EU Cegfila
br. EU/1/19/1409 · odobreno 19. 12. 2019. · Reduction in the duration of neutropenia and the incidence of febrile neutropenia in adult patients treated wi… · Mundipharma Corporation (Ireland) Limited · pegfilgrastim · ATC L03AA13
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Odluka Europske komisije EU Baiama
br. EU/1/24/1887 · odobreno 13. 1. 2025. · Baiama is indicated for adults for the treatment of • neovascular (wet) age-related macular degeneration (AMD… · Formycon AG · Aflibercept · ATC S01LA05
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26. 9. 2026.subota, 26. rujna 2026.

otvori dan ◀ ▶ 7 događaja
Novo odobrenje EU EU Zokovea
br. EU/1/26/2062 · Zokovea is indicated for the post exposure prophylaxis of COVID 19 in adults and adolescents aged 12 years and… · Shionogi B.V. · ensitrelvir · ATC J05AE16
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Novo odobrenje EU EU Ubeslo
br. EU/1/26/2055 · Ubeslo is indicated in adults with primary hypercholesterolaemia (heterozygous familial and non familial) or m… · A. Menarini International Licensing S.A. · Obicetrapib · ATC C10AX
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Novo odobrenje EU EU Tafamidis Accord
br. EU/1/26/2065 · Tafamidis Accord is indicated for the treatment of hereditary transthyretin amyloidosis in adult patients with… · Accord Healthcare S.L.U. · tafamidis · ATC N07XX08
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Novo odobrenje EU EU Ruxolitinib Viatris
br. EU/1/26/2064 · Myelofibrosis (MF) Ruxolitinib Viatris is indicated for the treatment of disease-related splenomegaly or … · Viatris Limited · ruxolitinib · ATC L01EJ01
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Novo odobrenje EU EU Riociguat Accord
br. EU/1/26/2059 · Chronic thromboembolic pulmonary hypertension (CTEPH) Riociguat Accord is indicated for the treatment of ad… · Accord Healthcare S.L.U. · riociguat · ATC C02KX05
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Novo odobrenje EU EU Nylaspeg
br. EU/1/26/2051 · Reduction in the duration of neutropenia and the incidence of febrile neutropenia in adult patients treated wi… · QILU PHARMA SPAIN S.L. · pegfilgrastim · ATC L03AA13
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Novo odobrenje EU EU Evlarco
br. EU/1/26/2056 · Evlarco is indicated in adults with primary hypercholesterolaemia (heterozygous familial and non familial) or … · A. Menarini International Licensing S.A. · obicetrapib / ezetimibe
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25. 9. 2026.petak, 25. rujna 2026.

otvori dan ◀ ▶ 14 događaja · 1 važnih
Ukinuto u EU EU Aumseqa
br. EU/1/25/2006 · odobreno 12. 2. 2026. · Aumseqa as monotherapy is indicated for: • the first line treatment of adult patients with advanced non small… · SFL Pharmaceuticals Deutschland GmbH · aumolertinib · ATC L01EB11
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Novo odobrenje EU EU Cavoley
br. EU/1/26/2066 · Reduction in the duration of neutropenia and the incidence of febrile neutropenia in adult patients treated wi… · CuraTeQ Biologics s.r.o · Pegfilgrastim · ATC L03AA13
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Odluka Europske komisije EU Vizamyl
br. EU/1/14/941 · odobreno 22. 8. 2014. · This medicinal product is for diagnostic use only. VIZAMYL is a radiopharmaceutical indicated for Positron Em… · GE Healthcare AS · flutemetamol (18F) · ATC V09AX04
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Odluka Europske komisije EU Vaxelis
br. EU/1/15/1079 · odobreno 15. 2. 2016. · Vaxelis (DTaP-HB-IPV-Hib) is indicated for primary and booster vaccination in infants and toddlers from the ag… · MCM Vaccine B.V. · Diphtheria, tetanus, pertussis (acellular, component), hepatitis B (rDNA), poliomyelitis (inactivated) and haemophilus type b conjugate vaccine (adsorbed) · ATC J07CA09
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Odluka Europske komisije EU Sialanar
br. EU/1/16/1135 · odobreno 15. 9. 2016. · Symptomatic treatment of severe sialorrhoea (chronic pathological drooling) in children and adolescents aged 3… · Proveca Pharma Limited · glycopyrronium bromide · ATC A03AB02
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Odluka Europske komisije EU RIULVY
br. EU/1/25/1947 · odobreno 28. 7. 2025. · RIULVY is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing … · Neuraxpharm Pharmaceuticals, S.L. · Tegomil fumarate · ATC L04AX10
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Odluka Europske komisije EU Champix
br. EU/1/06/360 · odobreno 26. 9. 2006. · indicated for smoking cessation in adults · Pfizer Europe MA EEIG · varenicline tartrate · ATC N07BA03
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Odluka Europske komisije EU Briumvi
br. EU/1/23/1730 · odobreno 31. 5. 2023. · Briumvi is indicated for the treatment of adult patients with relapsing forms of multiple sclerosis (RMS) with… · Neuraxpharm Pharmaceuticals, S.L. · ublituximab · ATC L04AG14
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Odluka Europske komisije EU Usymro
br. EU/1/25/1957 · odobreno 14. 8. 2025. · Adult Crohn’s Disease Usymro is indicated for the treatment of adult patients with moderately to severely ac… · Gedeon Richter Plc. · ustekinumab · ATC L04AC05
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Odluka Europske komisije EU Ozurdex
br. EU/1/10/638 · odobreno 27. 7. 2010. · OZURDEX is indicated for the treatment of adult patients with: • Visual impairment due to diabetic macular oe… · AbbVie Deutschland GmbH & Co. KG · dexamethasone · ATC S01BA01
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Odluka Europske komisije EU Lacosamide Adroiq
br. EU/1/23/1732 · odobreno 31. 5. 2023. · Lacosamide Adroiq is indicated as monotherapy in the treatment of partial-onset seizures with or without secon… · Extrovis EU Kft. · lacosamide · ATC N03AX18
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Odluka Europske komisije EU Imlygic
br. EU/1/15/1064 · odobreno 16. 12. 2015. · Imlygic is indicated for the treatment of adults with unresectable melanoma that is regionally or distantly me… · Amgen Europe B.V. · talimogene laherparepvec · ATC L01XL02
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Odluka Europske komisije EU Humira
br. EU/1/03/256 · odobreno 8. 9. 2003. · Juvenile idiopathic arthritis Polyarticular juvenile idiopathic arthritis Humira in combination with met… · AbbVie Deutschland GmbH & Co. KG · Adalimumab · ATC L04AB04
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Odluka Europske komisije EU Aumseqa
br. EU/1/25/2006 · odobreno 12. 2. 2026. · Aumseqa as monotherapy is indicated for: • the first line treatment of adult patients with advanced non small… · SFL Pharmaceuticals Deutschland GmbH · aumolertinib · ATC L01EB11
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