Cinet 30 mg filmom obložene

Glavna informacija

  • Trgovački naziv:
  • Cinet 30 mg filmom obložene tablete
  • Doziranje:
  • 30 mg
  • Farmaceutski oblik:
  • filmom obložena tableta
  • Sastav:
  • Urbroj: jedna tableta sadrži 30 mg cinakalceta (u obliku cinakalcetklorida)
  • Tip recepta:
  • na recept, u ljekarni ograničeni recept
  • Koristi za:
  • Ljudi
  • Vrsta lijekova:
  • alopatski lijek
  • Proizveden od:
  • Remedica Ltd., Limassol, Cipar

Dokument

Lokalizacija

  • Na raspolaganju u:
  • Cinet 30 mg filmom obložene tablete
    Hrvatska
  • Jezik:
  • hrvatski

Terapeutski informacija

  • Proizvod sažetak:
  • Pakiranje: 28 tableta u blisteru, u kutiji [HR-H-250873303-01] Urbroj: 381-12-01/30-17-12

Druge informacije

Status

  • Izvor:
  • HALMED Agencija za lijekove i medicinske proizvode - Agency for medicinal products and medical devices of Croatia
  • Broj odobrenja:
  • HR-H-250873303
  • Datum autorizacije:
  • 13-07-2017
  • Zadnje ažuriranje:
  • 04-06-2018

Uputu o lijeku

Uputa o lijeku: Informacije za korisnika

Cinet 30 mg filmom obložene tablete

Cinet 60 mg filmom obložene tablete

Cinet 90 mg filmom obložene tablete

cinakalcet

Pažljivo pročitajte cijelu uputu prije nego počnete uzimati ovaj lijek jer sadrži Vama važne

podatke.

Sačuvajte ovu uputu. Možda ćete je trebati ponovno pročitati.

Ako imate dodatnih pitanja, obratite se Vašem liječniku, ljekarniku ili medicinskoj sestri.

Ovaj je lijek propisan samo Vama. Nemojte ga davati drugima. Može im štetiti, čak i ako su

njihovi znakovi bolesti jednaki Vašima.

Ako primijetite bilo koju nuspojavu, potrebno je obavijestiti Vašeg liječnika, ljekarnika ili

medicinsku sestru. To uključuje i svaku moguću nuspojavu koja nije navedena u ovoj uputi.

Pogledajte dio 4.

Što se nalazi u ovoj uputi:

1.

Što je Cinet i za što se koristi?

2.

Što morate znati prije nego počnete uzimati Cinet?

3.

Kako uzimati Cinet?

4.

Moguće nuspojave

5.

Kako čuvati Cinet?

6.

Sadržaj pakiranja i druge informacije

1.

Što je Cinet i za što se koristi?

Cinet kontrolira vrijednosti paratireoidnog hormona (PTH), kalcija i fosfora u Vašem organizmu.

Koristi se u liječenju poremećaja povezanih s paratireoidnim žlijezdama. Paratireoide su četiri male

žlijezde na vratu, pokraj štitnjače, koje proizvode paratireoidni hormon (PTH).

Cinet se koristi:

za liječenje sekundarnog hiperparatireoidizma u bolesnika s ozbiljnom bubrežnom bolesti koji

trebaju dijalizu da bi se krv očistila od štetnih produkata

da bi se smanjila visoka razina kalcija u krvi (hiperkalcemija) u bolesnika s rakom

paratireoidnih žlijezda

da bi se smanjila visoka razina kalcija u krvi (hiperkalcemija) u bolesnika s primarnim

hiperparatireoidizmom kod kojih odstranjenje žlijezde nije moguće.

U primarnom i sekundarnom hiperparatireoidizmu paratireoidne žlijezde proizvode previše PTH-a.

„Primarni“ znači da hiperparatireoidizam nije posljedica nekog drugog poremećaja, a „sekundarni“ da

je hiperparatireoidizam uzrokovan drugim poremećajem, npr. bolesti bubrega. Oba, i primarni i

sekundarni hiperparatireoidizam mogu uzrokovati gubitak kalcija iz kosti, što može biti uzrok bolova

u kostima i prijeloma, poremećaja krvi i oštećenja srčanih krvnih žila, nastanka bubrežnih kamenaca,

psihičkih poremećaja i kome.

2.

Što morate znati prije nego počnete uzimati Cinet

Nemojte uzimati Cinet:

ako ste alergični na cinakalcet ili neki drugi sastojak ovog lijeka (naveden u dijelu 6).

H A L M E D

13 - 07 - 2017

O D O B R E N O

Upozorenja i mjere opreza

Obratite se Vašem liječniku, ljekarniku ili medicinskoj sestri prije nego uzmete Cinet.

Prije nego što počnete uzimati Cinet, obavijestite svojeg liječnika o tome imate li ili ste bilo kada

imali:

napadaje (konvulzije). Rizik pojave napadaja veći je ako ste ih već doživjeli;

problema s jetrom;

zatajenje srca.

U bolesnika liječenih cinakalcetom zabilježeni su događaji opasni po život i smrtni ishodi povezani s

niskim razinama kalcija (hipokalcemijom).

Niske razine kalcija mogu utjecati na srčani ritam. Obavijestite svog liječnika ako, dok uzimate Cinet,

osjetite neobično ubrzano ili jako lupanje srca, ako imate tegobe sa srčanim ritmom ili ako uzimate

lijekove za koje se zna da uzrokuju tegobe sa srčanim ritmom.

Za dodatne informacije, pročitajte dio 4.

Tijekom liječenja Cinetom obavijestite svojeg liječnika:

ako ste počeli ili prestali pušiti, jer to može utjecati na djelovanje Cineta.

Djeca i adolescenti

Djeca mlađa od 18 godina ne smiju uzimati Cinet.

Drugi lijekovi i Cinet

Obavijestite Vašeg liječnika ili ljekarnika ako uzimate, nedavno ste uzeli ili biste mogli uzeti bilo koje

druge lijekove.

Obavijestite svojeg liječnika ako uzimate sljedeće lijekove, jer oni mogu utjecati na djelovanje

Cineta:

lijekovi za liječenje kože i gljivičnih infekcija (ketokonazol, itrakonazol i vorikonazol);

lijekovi za liječenje bakterijskih infekcija (telitromicin, rifampicin i ciprofloksacin);

lijek koji se koristi za liječenje HIV infekcija i AIDS (ritonavir);

lijek kojim se liječi depresija (fluvoksamin).

Cinet može utjecati na djelovanje sljedećih lijekova:

lijekova za liječenje depresije (amitriptilin, desipramin, nortriptilin i klomipramin);

lijekova kojima se liječi poremećaj srčanog ritma (flekainid i propafenon);

lijek koji se koristi za liječenje visokoga krvnog tlaka (metoprolol).

Cinet s hranom i pićem

Cinet treba uzeti s hranom ili neposredno nakon obroka.

Trudnoća, dojenje i plodnost

Ako ste trudni ili dojite, mislite da biste mogli biti trudni ili planirate trudnoću, obratite se Vašem

liječniku ili ljekarniku za savjet prije nego uzmete ovaj lijek.

Cinet nije ispitivan u trudnica. U slučaju trudnoće, Vaš liječnik može promijeniti terapiju jer Cinet

može biti štetan za Vaše nerođeno dijete.

Nije poznato izlučuje li se Cinet u majčino mlijeko. Vaš liječnik će raspraviti s Vama trebate li prestati

dojiti ili prekinuti liječenje Cinetom.

H A L M E D

13 - 07 - 2017

O D O B R E N O

Upravljanje vozilima i strojevima

Nisu provedena ispitivanja utjecaja na sposobnost upravljanja vozilima i rada sa strojevima. Omaglica

i napadaji prijavljeni su od bolesnika liječenih cinakalcetom. Ako ste imali navedeno, Vaša sposobnost

upravljanja vozilom i sposobnost rada na strojevima može biti smanjena.

Cinet sadrži laktozu

Ako Vam je liječnik rekao da ne podnosite neke šećere, savjetujte se s liječnikom prije uzimanja ovog

lijeka.

3.

Kako uzimati Cinet?

Uvijek uzmite ovaj lijek točno onako kako Vam je rekao Vaš liječnik ili ljekarnik. Provjerite s Vašim

liječnikom ili ljekarnikom ako niste sigurni. Vaš liječnik će Vam reći koliko Cineta morate uzeti.

Cinet se mora uzeti kroz usta, s jelom ili neposredno nakon obroka. Tablete se moraju uzeti cijele i ne

smiju se prepoloviti.

Vaš liječnik redovito će Vam vaditi krv tijekom liječenja kako bi pratio Vaš napredak i po potrebi

prilagodio dozu lijeka.

Ako se liječite zbog sekundarnog hiperparatireoidizma

Uobičajena početna doza Cineta je 30 mg (jedna tableta) jednom na dan.

Ako se liječite zbog karcinoma paratireoidnih žlijezda i primarnog hiperparatireoidizma

Uobičajena početna doza Cineta je 30 mg (jedna tableta) dva puta na dan.

Ako uzmete više Cineta nego što ste trebali

Ako uzmete više Cineta nego što ste trebali, morate odmah kontaktirati liječnika. Mogući znakovi

predoziranja su utrnulost ili trnci oko usta, bolovi u mišićima ili grčevi i napadaji.

Ako ste zaboravili uzeti Cinet

Nemojte uzeti dvostruku dozu kako biste nadoknadili zaboravljenu dozu.

Ako ste zaboravili uzeti dozu Cineta, sljedeću dozu uzmite u uobičajeno vrijeme.

U slučaju bilo kakvih nejasnoća ili pitanja u vezi s primjenom ovog lijeka, obratite se svom liječniku,

ljekarniku ili medicinskoj sestri.

4.

Moguće nuspojave

Kao i svi lijekovi, ovaj lijek može uzrokovati nuspojave iako se one neće pojaviti kod svakoga.

Ako osjetite utrnulost ili trnce oko usta, bolove u mišićima ili grčeve i napadaje, odmah o tome

obavijestite liječnika. Te nuspojave mogu biti znakovi da je Vaša vrijednost kalcija preniska

(hipokalcemija).

Vrlo česte: mogu se javiti u više od 1 na 10 osoba

mučnina i povraćanje (ove su nuspojave obično blage i ne traju dugo).

Česte: mogu se javiti u manje od 1 na 10 osoba

omaglica

utrnulost ili osjećaj trnaca (parestezija)

gubitak (anoreksija) ili smanjenje apetita

bol u mišićima (mijalgija)

H A L M E D

13 - 07 - 2017

O D O B R E N O

slabost (astenija)

osip

smanjene razine testosterona

visoke razine kalija u krvi (hiperkalemija)

alergijske reakcije (preosjetljivost)

glavobolja

napadaji (konvulzije)

niski krvni tlak (hipotenzija)

infekcije gornjeg dišnog sustava

otežano disanje (dispneja)

kašalj

loša probava (dispepsija)

proljev

bol u trbuhu, bol u gornjem dijelu trbuha

zatvor

mišićni grčevi

bol u leđima

niske razine kalcija u krvi (hipokalcemija).

Nepoznato: učestalost se ne može procijeniti iz dostupnih podataka

koprivnjača (urtikarija)

oticanje lica, usnica, usta, jezika ili grla, što može uzrokovati teškoće s gutanjem ili disanjem

(angioedem)

neobično ubrzano ili jako lupanje srca, koje može biti povezano s niskim razinama kalcija u

krvi (produljenje QT intervala i ventrikularna aritmija uzrokovana hipokalcemijom).

Nakon uzimanja cinakalceta kod vrlo malog broja bolesnika sa zatajenjem srca došlo je do pogoršanja

stanja i pada krvnog tlaka (hipotenzije).

Dodatne nuspojave kod djece i adolescenata

Primjena cinakalceta u djece i adolescenata nije određena. Smrtni ishod bio je zabilježen u jednog

adolescenta u kliničkom ispitivanju, koji je imao vrlo nisku razinu kalcija u krvi (hipokalcemiju).

Prijavljivanje nuspojava

Ako primijetite bilo koju nuspojavu, potrebno je obavijestiti Vašeg liječnika, ljekarnika ili medicinsku

sestru. To uključuje i svaku moguću nuspojavu koja nije navedena u ovoj uputi. Nuspojave možete

prijaviti izravno putem nacionalnog sustava za prijavu nuspojava navedenog u Dodatku V*.

Prijavljivanjem nuspojava možete pridonijeti u procjeni sigurnosti ovog lijeka.

5.

Kako čuvati Cinet?

Ovaj lijek čuvajte izvan pogleda i dohvata djece.

Ovaj lijek se ne smije upotrijebiti nakon isteka roka valjanosti navedenog na kutiji. Rok valjanosti

odnosi se na zadnji dan navedenog mjeseca.

Ovaj lijek ne zahtijeva posebne uvjete čuvanja.

Nikada nemojte nikakve lijekove bacati u otpadne vode ili kućni otpad. Pitajte Vašeg ljekarnika kako

baciti lijekove koje više ne koristite. Ove će mjere pomoći u očuvanju okoliša.

H A L M E D

13 - 07 - 2017

O D O B R E N O

6.

Sadržaj pakiranja i druge informacije

Što Cinet sadrži?

Djelatna tvar je cinakalcet

Cinet 30 mg filmom obložene tablete: jedna tableta sadrži 30 mg cinakalceta (u obliku

cinakalcetklorida).

Cinet 60 mg filmom obložene tablete: jedna tableta sadrži 60 mg cinakalceta (u obliku

cinakalcetklorida).

Cinet 90 mg filmom obložene tablete: jedna tableta sadrži 90 mg cinakalceta (u obliku

cinakalcetklorida).

Ostali sastojci su:

Jezgra tablete: škrob, prethodno geliran (kukuruzni), povidon K-30 (E1201), krospovidon vrst A

(E1202), silicijev dioksid, koloidni, bezvodni, magnezijev stearat (E572).

Film ovojnica: hipromeloza 15 (E464), laktoza hidrat, triacetin (E1518), titanijev dioksid (E171), žuti

željezov oksid (E172), indigo karmin (E132).

Kako Cinet izgleda i sadržaj pakiranja?

Cinet 30 mg filmom obložene tablete su svijetlozelene, ovalne, filmom obložene tablete s oznakom

„30“ na jednoj strani. Dimenzije tablete su 8,1 mm x 5,2 mm ± 5%.

Cinet 60 mg filmom obložene tablete su svijetlozelene, ovalne, filmom obložene tablete s oznakom

„60“ na jednoj strani. Dimenzije tablete su 10,0 mm x 6,3 mm ± 5%.

Cinet 90 mg filmom obložene tablete su svijetlozelene, ovalne, filmom obložene tablete s oznakom

„90“ na jednoj strani. Dimenzije tablete su 11,6 mm x 7,3 mm ± 5%.

28 (2 x14) filmom obloženih tableta u blisteru, u kutiji.

Nositelj odobrenja za stavljanje lijeka u promet i proizvoĎač

Nositelj odobrenja:

Alpha-Medical d.o.o.

Dragutina Golika 36

10 000 Zagreb

Proizvođač:

Remedica Ltd

Aharnon Str., Limassol Industrial Estate,

3056 Limassol

Cipar

Način i mjesto izdavanja lijeka

Lijek se izdaje na recept, u ljekarni.

Ova je uputa zadnji put revidirana u srpnju 2017.

H A L M E D

13 - 07 - 2017

O D O B R E N O

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Camber Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Montelukast Tablets USP, 10mg 30Ct. due to Product/Label Mix-Up

Camber Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Montelukast Tablets USP, 10mg 30Ct. due to Product/Label Mix-Up

Camber Pharmaceuticals, Inc. is voluntarily recalling one single lot of Montelukast Sodium Tablets, USP 10mg, to the consumer level. This recall of one batch of Montelukast Sodium Tablets, USP 10mg, lot# MON17384 Exp. 12/31/2019, was prompted because a complaint of a sealed bottle labeled as Montelukast 10mg 30 ct found to contain 90 tablets of Losartan Potassium Tablets, USP 50mg

FDA - U.S. Food and Drug Administration

31-8-2018

Peer review of the pesticide risk assessment of the active substance cypermethrin

Peer review of the pesticide risk assessment of the active substance cypermethrin

Published on: Thu, 30 Aug 2018 00:00:00 +0200 The conclusions of EFSA following the peer review of the initial risk assessments carried out by the competent authorities of the rapporteur Member State Belgium and co‐rapporteur Member State Germany for the pesticide active substance cypermethrin are reported. The context of the peer review was that required by Commission Implementing Regulation (EU) No 844/2012. The conclusions were reached on the basis of the evaluation of the representative uses of cype...

Europe - EFSA - European Food Safety Authority Publications

10-8-2018

Westminster Pharmaceuticals, LLC. Issues Voluntary Nationwide Recall of Levothyroxine and Liothyronine (Thyroid Tablets, USP) Due to Risk of Adulteration

Westminster Pharmaceuticals, LLC. Issues Voluntary Nationwide Recall of Levothyroxine and Liothyronine (Thyroid Tablets, USP) Due to Risk of Adulteration

Westminster Pharmaceuticals, LLC is voluntarily recalling all lots, within expiry, of Levothyroxine and Liothyronine (Thyroid Tablets, USP) 15 mg, 30 mg, 60 mg, 90 mg, & 120 mg to the wholesale level. These products are being recalled as a precaution because they were manufactured using active pharmaceutical ingredients that were sourced prior to the FDA’s Import Alert of Sichuan Friendly Pharmaceutical Co., Ltd., which as a result of a 2017 inspection were found to have deficiencies with Current Good Ma...

FDA - U.S. Food and Drug Administration

6-8-2018

G & C Raw, LLC Recalls Pat's Cat Turkey, and Ground Lamb Pet Food, because of Possible Listeria Monocytogenes Health Risk

G & C Raw, LLC Recalls Pat's Cat Turkey, and Ground Lamb Pet Food, because of Possible Listeria Monocytogenes Health Risk

G & C Raw, of Versailles, OH is recalling 30 1-lb containers of Pat's Cat Turkey Cat Food and 40 2-lb containers of Ground Lamb Dog Food because it has the potential to be contaminated with Listeria monocytogenes. Listeria monocytogenes can cause serious and sometimes fatal infections in animals eating the products.

FDA - U.S. Food and Drug Administration

31-7-2018

July 30, 2018: Two People Guilty of Distributing Tramadol Pills

July 30, 2018: Two People Guilty of Distributing Tramadol Pills

July 30, 2018: Two People Guilty of Distributing Tramadol Pills

FDA - U.S. Food and Drug Administration

17-7-2018

Blokhuis kondigt grootschalige extra vaccinatie aan: Ruim half miljoen kinderen krijgen oproep

Blokhuis kondigt grootschalige extra vaccinatie aan: Ruim half miljoen kinderen krijgen oproep

Volgend jaar worden zo’n 650.000 kinderen extra opgeroepen om zich te laten inenten tegen de zeer ernstige infectieziekte meningokokken. Het gaat om kinderen die zijn geboren na 1 januari 2001 en voor mei 2004. Dat laat staatssecretaris Paul Blokhuis (VWS) weten in een brief aan de Tweede Kamer. Reden voor deze maatregel is dat in de afgelopen jaren een stijging te zien is van het aantal mensen dat de infectie meningokokken type W oploopt. Met deze extra vaccinatieronde moet die groei worden ingedamd. He...

Netherlands - Ministerie van Volksgezondheid, Welzijn en Sport

30-10-2018

EU/3/14/1250 (Akcea Therapeutics UK Ltd)

EU/3/14/1250 (Akcea Therapeutics UK Ltd)

EU/3/14/1250 (Active substance: Phosphorothioate oligonucleotide targeted to transthyretin) - Transfer of orphan designation - Commission Decision (2018)7282 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/098/13/T/01

Europe -DG Health and Food Safety

30-10-2018

EU/3/18/2080 (Freeline Therapeutics Ltd)

EU/3/18/2080 (Freeline Therapeutics Ltd)

EU/3/18/2080 (Active substance: Recombinant adeno-associated viral vector serotype S3 containing codon-optimised expression cassette encoding human coagulation factor IX variant) - Orphan designation - Commission Decision (2018)7281 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/127/18

Europe -DG Health and Food Safety

30-10-2018

EU/3/18/2079 (Spark Therapeutics Ireland Ltd)

EU/3/18/2079 (Spark Therapeutics Ireland Ltd)

EU/3/18/2079 (Active substance: Recombinant adeno-associated viral vector containing a bioengineered capsid and a codon-optimised expression cassette to drive the expression of the SQ form of a B-domain deleted human coagulation factor VIII) - Orphan designation - Commission Decision (2018)7280 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/104/18

Europe -DG Health and Food Safety

30-10-2018

EU/3/18/2078 (Sellas Life Sciences Limited)

EU/3/18/2078 (Sellas Life Sciences Limited)

EU/3/18/2078 (Active substance: Peptides YMFPNAPYL, SGQAYMFPNAPYLPSCLES, RSDELVRHHNMHQRNMTKL and PGCNKRYFKLSHLQMHSRKHTG) - Orphan designation - Commission Decision (2018)7279 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/091/18

Europe -DG Health and Food Safety

30-10-2018

EU/3/18/2077 (Worphmed Srl)

EU/3/18/2077 (Worphmed Srl)

EU/3/18/2077 (Active substance: Melatonin) - Orphan designation - Commission Decision (2018)7278 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/077/18

Europe -DG Health and Food Safety

30-10-2018

EU/3/18/2076 (Orphan Europe S.A.R.L.)

EU/3/18/2076 (Orphan Europe S.A.R.L.)

EU/3/18/2076 (Active substance: Glycine, L-alanine, L-arginine, L-aspartic acid, L-cysteine, L-cystine, L-glutamic acid, L-histidine, L-lysine monohydrate, L-methionine, L-phenylalanine, L-proline, L-serine, L-threonine, L-tryptophan, L-tyrosine, taurine) - Orphan designation - Commission Decision (2018)7277 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/100/18

Europe -DG Health and Food Safety

30-10-2018

EU/3/18/2075 (Consorcio Centro de InvestigaciOn BiomEdica en Red M.P.)

EU/3/18/2075 (Consorcio Centro de InvestigaciOn BiomEdica en Red M.P.)

EU/3/18/2075 (Active substance: Gefitinib) - Orphan designation - Commission Decision (2018)7276 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/090/18

Europe -DG Health and Food Safety

30-10-2018

EU/3/18/2074 (PhaRA bvba)

EU/3/18/2074 (PhaRA bvba)

EU/3/18/2074 (Active substance: Avapritinib) - Orphan designation - Commission Decision (2018)7275 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/079/18

Europe -DG Health and Food Safety

30-10-2018

EU/3/18/2073 (Fondazione Telethon)

EU/3/18/2073 (Fondazione Telethon)

EU/3/18/2073 (Active substance: Autologous CD34+ haematopoietic stem and progenitor cells genetically modified with the lentiviral vector IDUA LV, encoding for the alpha-L-iduronidase cDNA) - Orphan designation - Commission Decision (2018)7274 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/113/18

Europe -DG Health and Food Safety

30-10-2018

EU/3/18/2071 (Loxo Oncology Limited)

EU/3/18/2071 (Loxo Oncology Limited)

EU/3/18/2071 (Active substance: 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile) - Orphan designation - Commission Decision (2018)7272 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/125/18

Europe -DG Health and Food Safety

30-10-2018

EU/3/18/2072 (FGK Representative Service GmbH)

EU/3/18/2072 (FGK Representative Service GmbH)

EU/3/18/2072 (Active substance: 6'-(R)-methyl-5-O-(5-amino-5,6-dideoxy-alpha-L-talofuranosyl)-paromamine sulfate) - Orphan designation - Commission Decision (2018)7273 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/102/18

Europe -DG Health and Food Safety

30-9-2018

Roteas (Daiichi Sankyo Europe GmbH)

Roteas (Daiichi Sankyo Europe GmbH)

Roteas (Active substance: edoxaban) - PSUSA - Modification - Commission Decision (2018)5089 of Sun, 30 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/PSUSA/10387/201710

Europe -DG Health and Food Safety

17-9-2018

Reminder: the FDA is accepting applications through Sept. 30, 2018, for the #FDAInnovationChallenge for devices to help combat #opioid addiction.   Submissions will be evaluated based on the feasibility, potential public health impact and novelty of the c

Reminder: the FDA is accepting applications through Sept. 30, 2018, for the #FDAInnovationChallenge for devices to help combat #opioid addiction. Submissions will be evaluated based on the feasibility, potential public health impact and novelty of the c

Reminder: the FDA is accepting applications through Sept. 30, 2018, for the #FDAInnovationChallenge for devices to help combat #opioid addiction. Submissions will be evaluated based on the feasibility, potential public health impact and novelty of the concept.

FDA - U.S. Food and Drug Administration

30-8-2018

Steglatro (Merck Sharp and Dohme B.V.)

Steglatro (Merck Sharp and Dohme B.V.)

Steglatro (Active substance: ertugliflozin) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)5789 of Thu, 30 Aug 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4315/T/2

Europe -DG Health and Food Safety

30-8-2018

Fluenz Tetra (AstraZeneca AB)

Fluenz Tetra (AstraZeneca AB)

Fluenz Tetra (Active substance: influenza vaccine (live attenuated, nasal)) - Centralised - Variation - Commission Decision (2018)5815 of Thu, 30 Aug 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2617/II/82

Europe -DG Health and Food Safety

3-8-2018

Scandonest and associated names

Scandonest and associated names

Scandonest and associated names (Active substance: mepivacaine) - Community Referrals - Art 30 - Commission Decision (2018)5380 of Fri, 03 Aug 2018 European Medicines Agency (EMA) procedure number: EMEA/H/A-30/1455

Europe -DG Health and Food Safety

1-8-2018

Bridion (Merck Sharp and Dohme B.V.)

Bridion (Merck Sharp and Dohme B.V.)

Bridion (Active substance: sugammadex) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)5213 of Wed, 01 Aug 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/885/T/30

Europe -DG Health and Food Safety

30-7-2018

Nityr (Cycle Pharmaceuticals Ltd)

Nityr (Cycle Pharmaceuticals Ltd)

Nityr (Active substance: nitisinone) - Centralised - Authorisation - Commission Decision (2018)5446 of Mon, 30 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4582

Europe -DG Health and Food Safety

30-7-2018

Esmya (Gedeon Richter Plc.)

Esmya (Gedeon Richter Plc.)

Esmya (Active substance: ulipristal) - Referral - Commission Decision (2018)5101 of Mon, 30 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2041/A-20

Europe -DG Health and Food Safety

30-7-2018

Aimovig (Novartis Europharm Limited)

Aimovig (Novartis Europharm Limited)

Aimovig (Active substance: erenumab) - Centralised - Authorisation - Commission Decision (2018)5102 of Mon, 30 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4447

Europe -DG Health and Food Safety

30-7-2018

Besponsa (Pfizer Europe MA EEIG)

Besponsa (Pfizer Europe MA EEIG)

Besponsa (Active substance: inotuzumab ozogamicin) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)5104 of Mon, 30 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4119/T/7

Europe -DG Health and Food Safety

30-7-2018

Segluromet (Merck Sharp and Dohme B.V.)

Segluromet (Merck Sharp and Dohme B.V.)

Segluromet (Active substance: ertugliflozin / metformin hydrochloride) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)5103 of Mon, 30 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4314/T/2

Europe -DG Health and Food Safety

30-7-2018

Invokana (Janssen-Cilag International NV)

Invokana (Janssen-Cilag International NV)

Invokana (Active substance: canagliflozin) - Centralised - Renewal - Commission Decision (2018)5105 of Mon, 30 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2649/R/37

Europe -DG Health and Food Safety

30-7-2018

NovoEight (Novo Nordisk A/S)

NovoEight (Novo Nordisk A/S)

NovoEight (Active substance: turoctocog alfa) - Centralised - 2-Monthly update - Commission Decision (2018)5093 of Mon, 30 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2719/II/23

Europe -DG Health and Food Safety

30-7-2018

Hyrimoz (Sandoz GmbH)

Hyrimoz (Sandoz GmbH)

Hyrimoz (Active substance: adalimumab) - Centralised - Authorisation - Commission Decision (2018)5097 of Mon, 30 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4320

Europe -DG Health and Food Safety

30-7-2018

Halimatoz (Sandoz GmbH)

Halimatoz (Sandoz GmbH)

Halimatoz (Active substance: adalimumab) - Centralised - Authorisation - Commission Decision (2018)5098 of Mon, 30 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4866

Europe -DG Health and Food Safety

30-7-2018

Rasagiline ratiopharm (Teva B.V.)

Rasagiline ratiopharm (Teva B.V.)

Rasagiline ratiopharm (Active substance: rasagiline) - Centralised - Yearly update - Commission Decision (2018)5108 of Mon, 30 Jul 2018

Europe -DG Health and Food Safety

30-7-2018

Hefiya (Sandoz GmbH)

Hefiya (Sandoz GmbH)

Hefiya (Active substance: adalimumab) - Centralised - Authorisation - Commission Decision (2018)5099 of Mon, 30 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4865

Europe -DG Health and Food Safety

30-7-2018

Alsitek (AB Science)

Alsitek (AB Science)

Alsitek (Active substance: masitinib) - Refusal of authorisation - Commission Decision (2018)5109 of Mon, 30 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4398

Europe -DG Health and Food Safety

30-7-2018

UBAC (Laboratorios Hipra, S.A.)

UBAC (Laboratorios Hipra, S.A.)

UBAC (Active substance: Streptococcus uberis vaccine (inactivated)) - Centralised - Authorisation - Commission Decision (2018)5152 of Mon, 30 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/V/C/4595

Europe -DG Health and Food Safety

30-7-2018

Apoquel (Zoetis Belgium S.A.)

Apoquel (Zoetis Belgium S.A.)

Apoquel (Active substance: Oclacitinib maleate) - Centralised - Renewal - Commission Decision (2018)5153 of Mon, 30 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/V/C/2688/R/13

Europe -DG Health and Food Safety

30-7-2018

Ofev (Boehringer Ingelheim International GmbH)

Ofev (Boehringer Ingelheim International GmbH)

Ofev (Active substance: Nintedanib) - PSUSA - Modification - Commission Decision (2018)5115 of Mon, 30 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/PSUSA/10319/201710

Europe -DG Health and Food Safety

30-7-2018

Ceplene (Noventia Pharma Srl)

Ceplene (Noventia Pharma Srl)

Ceplene (Active substance: Histamine dihydrochloride) - Centralised - Renewal - Commission Decision (2018)5116 of Mon, 30 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/796/R/36

Europe -DG Health and Food Safety

30-7-2018

Zalmoxis (MolMed S.p.A.)

Zalmoxis (MolMed S.p.A.)

Zalmoxis (Active substance: Allogeneic T cells genetically modified with a retroviral vector encoding for a truncated form of the human low affinity nerve growth factor receptor (?LNGFR) and the herpes simplex I virus thymidine kinase (HSV-TK Mut2)) - Centralised - Renewal - Commission Decision (2018)5118 of Mon, 30 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2801/R/10

Europe -DG Health and Food Safety

30-7-2018

Trazimera (Pfizer Europe MA EEIG)

Trazimera (Pfizer Europe MA EEIG)

Trazimera (Active substance: trastuzumab) - Centralised - Authorisation - Commission Decision (2018)5095 of Mon, 30 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4463

Europe -DG Health and Food Safety

30-7-2018

RXULTI (Otsuka Pharmaceutical Europe Ltd)

RXULTI (Otsuka Pharmaceutical Europe Ltd)

RXULTI (Active substance: brexpiprazole) - Centralised - Authorisation - Commission Decision (2018)5088 of Mon, 30 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/3841

Europe -DG Health and Food Safety

24-7-2018

ACV meeting statement, Meeting 8, 30 May 2018

ACV meeting statement, Meeting 8, 30 May 2018

Advisory Committee on Vaccines meeting statement

Therapeutic Goods Administration - Australia

11-7-2018

Vantavo (Merck Sharp and Dohme B.V.)

Vantavo (Merck Sharp and Dohme B.V.)

Vantavo (Active substance: alendronic acid / colecalciferol) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)4511 of Wed, 11 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/1180/T/30

Europe -DG Health and Food Safety

11-7-2018

Tovanor Breezhaler (Novartis Europharm Limited)

Tovanor Breezhaler (Novartis Europharm Limited)

Tovanor Breezhaler (Active substance: glycopyrronium bromide) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)4526 of Wed, 11 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2690/T/30

Europe -DG Health and Food Safety