FLUCONAZOLE Mylan Pharma

Information principale

  • Nom commercial:
  • FLUCONAZOLE Mylan Pharma 2 mg/ml, solution pour perfusion
  • Dosage:
  • 2 mg
  • forme pharmaceutique:
  • solution
  • Composition:
  • composition pour 1 ml de solution pour perfusion > fluconazole : 2 mg
  • Mode d'administration:
  • intraveineuse
  • Unités en paquet:
  • 1 flacon(s) en verre de 25 ml
  • Type d'ordonnance:
  • liste I
  • Utiliser pour:
  • Humains
  • Type medicin:
  • médicament allopathique

Documents

Localisation

  • Disponible en:
  • FLUCONAZOLE Mylan Pharma 2 mg/ml, solution pour perfusion
    France
  • Langue:
  • français

Information thérapeutique

  • Descriptif du produit:
  • 378 215-0 ou 4009 378 215 0 6 - 1 flacon(s) en verre de 200 ml - Déclaration d'arrêt de commercialisation:26/06/2008;378 207-8 ou 4009 378 207 8 3 - 1 flacon(s) en verre de 50 ml - Déclaration d'arrêt de commercialisation:01/10/2008;378 211-5 ou 4009 378 211 5 5 - 1 flacon(s) en verre de 100 ml - Déclaration d'arrêt de commercialisation:17/07/2008;378 203-2 ou 4009 378 203 2 5 - 1 flacon(s) en verre de 25 ml - Déclaration de commercialisation non communiquée:;378 212-1 ou 4009 378 212 1 6 - 5 flacon(s) en verre de 100 ml - Déclaration de commercialisation non communiquée:;378 213-8 ou 4009 378 213 8 4 - 10 flacon(s) en verre de 100 ml - Déclaration de commercialisation non communiquée:;378 214-4 ou 4009 378 214 4 5 - 20 flacon(s) en verre de 100 ml - Déclaration de commercialisation non communiquée:;378 216-7 ou 4009 378 216 7 4 - 5 flacon(s) en verre de 200 ml - Déclaration de commercialisation non communiquée:;378 217-3 ou 4009 378 217 3 5 - 10 flacon(s) en verre de 200 ml - Déclaration de commercialisation non communiquée:;378 219-6 ou 4009 378 219 6 4 - 20 flacon(s) en verre de 200 ml - Déclaration de commercialisation non communiquée:;378 204-9 ou 4009 378 204 9 3 - 5 flacon(s) en verre de 25 ml - Déclaration de commercialisation non communiquée:;378 205-5 ou 4009 378 205 5 4 - 10 flacon(s) en verre de 25 ml - Déclaration de commercialisation non communiquée:;378 206-1 ou 4009 378 206 1 5 - 20 flacon(s) en verre de 25 ml - Déclaration de commercialisation non communiquée:;378 208-4 ou 4009 378 208 4 4 - 5 flacon(s) en verre de 50 ml - Déclaration de commercialisation non communiquée:;378 209-0 ou 4009 378 209 0 5 - 10 flacon(s) en verre de 50 ml - Déclaration de commercialisation non communiquée:;378 210-9 ou 4009 378 210 9 4 - 20 flacon(s) en verre de 50 ml - Déclaration de commercialisation non communiquée:;

Autres informations

Statut

  • Source:
  • ANSM - Agence Nationale de Sécurité du Médicament et des Produits de Santé
  • Statut de autorisation:
  • Archivée
  • Numéro d'autorisation:
  • 61821976
  • Date de l'autorisation:
  • 09-01-2007
  • Dernière mise à jour:
  • 23-06-2018

Notice: composition, indications thérapeutiques, interactions, posologie, effets indésirable, grossesse, allaitement

NOTICE

Misàjour:09/01/2009

Dénominationdumédicament

FLUCONAZOLEMYLANPHARMA2mg/ml,solutionpourperfusion

Encadré

Veuillezlireattentivementl'intégralitédecettenoticeavantd'utilisercemédicament.

Gardezcettenotice,vouspourriezavoirbesoindelarelire.

Sivousaveztouteautrequestion,sivousavezundoute,demandezplusd'informationsàvotremédecin

ouàvotrepharmacien.

Cemédicamentvousaétépersonnellementprescrit.Neledonnezjamaisàquelqu'und'autre,mêmeen

casdesymptômesidentiques,celapourraitluiêtrenocif.

Sil'undeseffetsindésirablesdevientgraveousivousremarquezuneffetindésirablenonmentionné

danscettenotice,parlez-enàvotremédecinouàvotrepharmacien.

Sommairenotice

Danscettenotice:

1.QU'EST-CEQUEFLUCONAZOLEMYLANPHARMA2mg/ml,solutionpourperfusionETDANSQUELS

CASEST-ILUTILISE?

2.QUELLESSONTLESINFORMATIONSACONNAITREAVANTD'UTILISERFLUCONAZOLEMYLAN

PHARMA2mg/ml,solutionpourperfusion?

3.COMMENTUTILISERFLUCONAZOLEMYLANPHARMA2mg/ml,solutionpourperfusion?

4.QUELSSONTLESEFFETSINDESIRABLESEVENTUELS?

5.COMMENTCONSERVERFLUCONAZOLEMYLANPHARMA2mg/ml,solutionpourperfusion?

6.INFORMATIONSSUPPLEMENTAIRES

1.QU'EST-CEQUEFLUCONAZOLEMYLANPHARMA2mg/ml,solutionpourperfusionETDANSQUELS

CASEST-ILUTILISE?

Classepharmacothérapeutique

Ils'agitd'unANTIMYCOSIQUEAUSAGESYSTEMIQUE.

(J:Anti-infectieux)

Illuttecontreledéveloppementdeschampignonsmicroscopiques.

Indicationsthérapeutiques

Cemédicamentestindiquédansletraitement:

Chezl'adulte:

descryptococcosesneuro-méningées

descandidosessystémiques,œsophagienneseturinaires.

Chezlenourrissonetl'enfant:

Chezlenourrissonetl'enfant:

descandidosesoropharyngéeschezl'immunodéprimé

descandidosessystémiques,œsophagienneseturinaires

descryptococcosesneuro-méningées.

CemédicamentestégalementutilisédanslapréventiondesinfectionsàCandidasensibleschezl'adulte

leucémiqueetprésentantunediminutiondunombredecertainsglobulesblancsconsécutiveautraitement

reçu.

2.QUELLESSONTLESINFORMATIONSACONNAITREAVANTD'UTILISERFLUCONAZOLEMYLAN

PHARMA2mg/ml,solutionpourperfusion?

Listedesinformationsnécessairesavantlaprisedumédicament

Sansobjet.

Contre-indications

NeprenezjamaisFLUCONAZOLEMYLANPHARMA2mg/ml,solutionpourperfusiondanslescas

suivants:

allergieconnueaufluconazoleetauxsubstancesapparentées(azolés)

pendantlagrossesseetl'allaitement,saufavismédical

enassociationavec:

lecisapride(médicamentutilisédanslerefluxgastro-œsophagien)

lepimozide(médicamentutilisédanscertainstroublesdel'humeur)

l'halofantrine(médicamentutilisédansletraitementdupaludisme).

Précautionsd'emploi;misesengardespéciales

FaitesattentionavecFLUCONAZOLEMYLANPHARMA2mg/ml,solutionpourperfusion:

Précautionsd'emploi

Chezlafemmeenpérioded'activitégénitale,unecontraceptionestindispensable.

Misesengardespéciales

Encasdesurvenuedesymptômesévocateursd'atteintehépatiquegrave(fatigueimportante,anorexie,

nauséespersistantes,vomissements,jaunisse),vousdevezconsulterunmédecin.

Sivousavezpréalablementprésentéuneréactioncutanéeassociéeàlaprisedefluconazoleouunautre

dérivéazolé,encasdesurvenuedelésionsbulleuses,vousdevezconsulterunmédecinleplusrapidement

possible.

Cemédicamentcontient3,54mg(soit0,154mmol)desodium/mldesolutioninjectable,entenircomptechez

lespersonnessuivantunrégimepauvreensel,strict.

Interactionsavecd'autresmédicaments

Priseouutilisationd'autresmédicaments:

Cemédicamentnedoitpasêtreutiliséenassociationaveclecisapride(médicamentutilisédanslereflux

gastro-œsophagien),lepimozide(médicamentutilisédanscertainstroublesdel'humeur)etl'halofantrine

(médicamentutilisédansletraitementdupaludisme).

Sivousprenezouavezprisrécemmentunautremédicament,ycomprisunmédicamentobtenusans

ordonnance,parlez-enàvotremédecinouàvotrepharmacien.

Interactionsaveclesalimentsetlesboissons

Sansobjet.

Sansobjet.

Interactionsaveclesproduitsdephytothérapieouthérapiesalternatives

Sansobjet.

Utilisationpendantlagrossesseetl'allaitement

Grossesseetallaitement

Cemédicamentnedoitpasêtreutilisépendantlagrossesseetenpérioded'allaitement,saufavismédical.

Demandezconseilàvotremédecinouàvotrepharmacienavantdeprendretoutmédicament.

Sportifs

Sansobjet.

Effetssurl'aptitudeàconduiredesvéhiculesouàutiliserdesmachines

Sansobjet.

Listedesexcipientsàeffetnotoire

Listedesexcipientsàeffetnotoire:sodium.

3.COMMENTUTILISERFLUCONAZOLEMYLANPHARMA2mg/ml,solutionpourperfusion?

Instructionspourunbonusage

Sansobjet.

Posologie,Modeet/ouvoie(s)d'administration,Fréquenced'administrationetDuréedutraitement

Posologie

Adulte:

Cryptococcoses:400mg/jourpendant6à8semainespuis200mg/jour(àviechezlespatientsatteints

deSIDA).

Candidosesœsophagiennes:100mg/jour.

Candidosesurinaires:100à200mg/jour.

Candidosessystémiques:800mgle1 er jourpuis400mg/jour.

Préventiondescandidoses:laposologierecommandéeestde400mg/jenuneprisequotidienne.

L'administrationdefluconazoledoitdébuterdèsl'initiationdelachimiothérapieouduconditionnementdela

greffe.Elledoitsepoursuivrejusqu'à7joursaprèslaremontéedestauxdespolynucléairesneutrophiles

audessusde1000/mm 3

oupendantuneduréepluslongue(jusqu'à75jours).

Enfantetnourrisson:

Candidosesoropharyngéeschezl'immunodéprimé:3mg/kg/jtoutesles24heures.

Candidosessystémiques,œsophagienneseturinaires:6-12mg/kg/jtoutesles24heures.

Cryptococcosesneuro-méningées:6-12mg/kg/jtoutesles24heures(àviechezlespatientsatteintsde

SIDA).

Aucuneposologien'estproposéechezleprématuré,lenouveau-néàtermeetjusqu'à28joursdevie.

Sivousavezl'impressionquel'effetdeFLUCONAZOLEMYLANPHARMA2mg/ml,solutionpour

perfusionesttropfortoutropfaible,consultezvotremédecinouvotrepharmacien.

Moded'administration

Perfusionintraveineuse.

Duréedetraitement

Laduréedetraitementdépenddelaréponsecliniqueetdel'indication.

DANSTOUSLESCAS,RESPECTERSTRICTEMENTL'ORDONNANCEDEVOTREMEDECIN.

Symptômesetinstructionsencasdesurdosage

SivousavezprisplusdeFLUCONAZOLEMYLANPHARMA2mg/ml,solutionpourperfusionquevous

n'auriezdû:consultezimmédiatementvotremédecinouvotrepharmacien.

Instructionsencasd'omissiond'uneoudeplusieursdoses

SivousoubliezdeprendreFLUCONAZOLEMYLANPHARMA2mg/ml,solutionpourperfusion:ne

prenezpasdedosedoublepourcompenserladosequevousavezoubliédeprendre.

Risquedesyndromedesevrage

Sansobjet.

4.QUELSSONTLESEFFETSINDESIRABLESEVENTUELS?

Descriptiondeseffetsindésirables

Commetouslesmédicaments,FLUCONAZOLEMYLANPHARMA2mg/ml,solutionpourperfusionest

susceptibled'avoirdeseffetsindésirables,bienquetoutlemonden'ysoitpassujet:

Leseffetsgastro-intestinauxetcutanéssontleseffetsindésirableslespluscourammentrencontrés.

Effetsgastro-intestinaux:nausées,flatulence,douleursabdominales,diarrhées.

Effetsallergiquesetcutanés:rashs,réactionscutanéessévères,réactionsallergiques.

Descasdechutedecheveuxgénéralementréversiblesontétérapportés.

Effetsgénéraux:mauxdetête.

Effetshépatiques:augmentationdestransaminaseshépatiques(enzymesdufoie)généralement

réversiblesàl'arrêtdutraitement,desatteinteshépatiquessévères.

Effetshématologiques:leucopénies(quantitéinsuffisantedeglobulesblancsdanslesang),

thrombopénies(tauxanormalementbasdeplaquettes,élémentsdusangimportantsdanslacoagulation).

Sivousremarquezdeseffetsindésirablesnonmentionnésdanscettenotice,ousicertainseffetsindésirables

deviennentgraves,veuillezeninformervotremédecinouvotrepharmacien.

5.COMMENTCONSERVERFLUCONAZOLEMYLANPHARMA2mg/ml,solutionpourperfusion?

Tenirhorsdelaportéeetdelavuedesenfants.

Datedepéremption

NepasutiliserFLUCONAZOLEMYLANPHARMA2mg/ml,solutionpourperfusionaprèsladatede

péremptionmentionnéesurlaboîte,leflacon.

Conditionsdeconservation

Avantouverture:Pasdeprécautionsparticulièresdeconservation.

Aprèsouverture:leproduitdoitêtreutiliséimmédiatement.Encasd'utilisationnonimmédiate,lesduréeset

conditionsdeconservationaprèsdilutionetavantutilisationrelèventdelaseuleresponsabilitédel'utilisateur.

Cemédicamentestcompatibleaveclesliquidesdeperfusionsuivants:

lesolutéglucoséà20%

lasolutiondeRinger

lasolutiondeRinger

lasolutiondeHartmann

lechloruredepotassiumensolutéglucosé

lebicarbonatedesodium.

Sinécessaire,misesengardecontrecertainssignesvisiblesdedétérioration

Lesmédicamentsnedoiventpasêtrejetésautoutàl'égoutouaveclesorduresménagères.Demandezà

votrepharmaciencequ'ilfautfairedesmédicamentsinutilisés.Cesmesurespermettrontdeprotéger

l'environnement.

6.INFORMATIONSSUPPLEMENTAIRES

Listecomplètedessubstancesactivesetdesexcipients

QuecontientFLUCONAZOLEMYLANPHARMA2mg/ml,solutionpourperfusion?

Lasubstanceactiveest:

Fluconazole........................................................................................................................................2

Pour1mldesolutionpourperfusion.

Unflaconde25mlcontient50mgdefluconazole

Unflaconde50mlcontient100mgdefluconazole.

Unflaconde100mlcontient200mgdefluconazole.

Unflaconde200mlcontient400mgdefluconazole

Lesautrescomposantssont:

Chloruredesodium,hydroxydedesodium,acidechlorhydrique,eaupourpréparationsinjectables.

Formepharmaceutiqueetcontenu

Qu'est-cequeFLUCONAZOLEMYLANPHARMA2mg/ml,solutionpourperfusionetcontenude

l'emballageextérieur?

Cemédicamentseprésentesousformedesolutioninjectablepourperfusionintraveineuseenflaconde25ml,

50ml,100mlou200ml.

Nometadressedutitulairedel'autorisationdemisesurlemarchéetdutitulairedel'autorisationde

fabricationresponsabledelalibérationdeslots,sidifférent

Titulaire

MYLANSAS

117AlléedesParcs

69800SAINT-PRIEST

FRANCE

Exploitant

MYLANSAS

117AlléedesParcs

69800SAINT-PRIEST

FRANCE

Fabricant

PHARMATHENS.A

Dervenakion6

PALLINI15351-ATTIKIS

GRECE

NomsdumédicamentdanslesEtatsmembresdel'EspaceEconomiqueEuropéen

Sansobjet.

Dated’approbationdelanotice

Ladernièredateàlaquellecettenoticeaétéapprouvéeestle{date}.

AMMsouscirconstancesexceptionnelles

Sansobjet.

InformationsInternet

DesinformationsdétailléessurcemédicamentsontdisponiblessurlesiteInternetdel’Afssaps(France).

Informationsréservéesauxprofessionnelsdesanté

Sansobjet.

Autres

Sansobjet.

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Surveillance du marché

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Une fois l’autorisation de mise sur le marché (AMM) délivrée, et au-delà de la pharmacovigilance, une surveillance du marché des médicaments vétérinaires est assurée sous différents aspects.

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28-11-2018

Information Update - Mylan-Valsartan medications voluntarily recalled as a precaution due to an impurity

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Health Canada

28-11-2018

Mise à jour -Rappel volontaire de médicaments Mylan-Valsartan par mesure de précaution en raison de la présence d’une impureté

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27-11-2018

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21-11-2018

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Several store-brand pain or sinus relief tablets recalled because consumers may be unable to access important safety information

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ACM PHARMA - BELLEGARDE

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11-9-2018

Risk assessment of substances used in food supplements: the example of the botanical Gymnema sylvestre

Risk assessment of substances used in food supplements: the example of the botanical Gymnema sylvestre

Published on: Tue, 28 Aug 2018 00:00:00 +0200 Botanicals and preparations derived from these are among the substances frequently added to foods and food supplements, yet the safety of many botanicals has not been systematically assessed. In the context of the EU‐FORA fellowship programme, the fellow performed an assessment on the safety of the botanical Gymnema sylvestre, in accordance with EFSA's guidance on the assessment of safety of botanicals. Although preparations of G. sylvestre are marketed as f...

Europe - EFSA - European Food Safety Authority Publications

11-9-2018

Pharm D Solutions, LLC Issues Voluntary Nationwide Recall of all Sterile Compounded Drugs Due to A Potential Lack of Sterility Assurance

Pharm D Solutions, LLC Issues Voluntary Nationwide Recall of all Sterile Compounded Drugs Due to A Potential Lack of Sterility Assurance

Pharm D Solutions, LLC is voluntarily recalling all sterile compounded drug products within expiry to the clinic, physician or consumer level. These drug products are being voluntarily recalled due to concerns that practices at the pharmacy have the potential to pose a risk of contamination to products that are intended to be sterile. These concerns arose following a routine inspection of the pharmacy by FDA.

FDA - U.S. Food and Drug Administration

7-9-2018

SCA Pharmaceuticals LLC. Issues Voluntary Nationwide Recall of Furosemide 100 mg in 0.9% Sodium Chloride due to Presence of Precipitate

SCA Pharmaceuticals LLC. Issues Voluntary Nationwide Recall of Furosemide 100 mg in 0.9% Sodium Chloride due to Presence of Precipitate

, SCA Pharmaceuticals LLC (“SCA Pharma”) is voluntarily recalling 7 lots of the injectable product Furosemide 100 mg in 0.9% Sodium Chloride 100 mg bag to the consumer level. This product is being recalled for visible particulate matter believed to be furosemide precipitate.

FDA - U.S. Food and Drug Administration

28-8-2018

New recommendations for use of Xofigo for treatment of prostate cancer which has spread to the bones

New recommendations for use of Xofigo for treatment of prostate cancer which has spread to the bones

The EU's Pharmacovigilance Risk Assessment Committee (PRAC) has adopted new recommendations for use of Xofigo for treatment of prostate cancer which has spread to the bones (bone metastases). Xofigo should only be used in symptomatic patients who have had two previous treatments for prostate cancer and who cannot be treated with other medicines.

Danish Medicines Agency

26-11-2018

Wakix (Bioprojet Pharma)

Wakix (Bioprojet Pharma)

Wakix (Active substance: Pitolisant hydrochloride) - Centralised - Yearly update - Commission Decision (2018)7974 of Mon, 26 Nov 2018

Europe -DG Health and Food Safety

26-11-2018

Alunbrig (Takeda Pharma A/S)

Alunbrig (Takeda Pharma A/S)

Alunbrig (Active substance: brigatinib) - Centralised - Authorisation - Commission Decision (2018)7976 of Mon, 26 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4248/

Europe -DG Health and Food Safety

22-11-2018

Fulphila (Mylan S.A.S.)

Fulphila (Mylan S.A.S.)

Fulphila (Active substance: pegfilgrastim) - Centralised - Authorisation - Commission Decision (2018)7880 of Thu, 22 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4915

Europe -DG Health and Food Safety

21-11-2018

EU/3/18/2081 (Pharma Gateway AB)

EU/3/18/2081 (Pharma Gateway AB)

EU/3/18/2081 (Active substance: 3-(3-(3,5-dimethyl-1H-pyrazol-4-yl)propoxy)-4-fluorobenzoic acid) - Orphan designation - Commission Decision (2018)7790 of Wed, 21 Nov 2018 European Medicines Agency (EMA) procedure number: EMA/OD/096/18

Europe -DG Health and Food Safety

21-11-2018

EU/3/15/1567 (TMC Pharma (EU) Limited)

EU/3/15/1567 (TMC Pharma (EU) Limited)

EU/3/15/1567 (Active substance: Recombinant human interleukin-3 truncated diphtheria toxin fusion protein) - Transfer of orphan designation - Commission Decision (2018)7816 of Wed, 21 Nov 2018 European Medicines Agency (EMA) procedure number: EMA/OD/064/15/T/02

Europe -DG Health and Food Safety

21-11-2018

EU/3/18/2101 (TMC Pharma Services Ltd)

EU/3/18/2101 (TMC Pharma Services Ltd)

EU/3/18/2101 (Active substance: Setmelanotide) - Orphan designation - Commission Decision (2018)7811 of Wed, 21 Nov 2018 European Medicines Agency (EMA) procedure number: EMA/OD/143/18

Europe -DG Health and Food Safety

21-11-2018

EU/3/18/2091 (Pharma Gateway AB)

EU/3/18/2091 (Pharma Gateway AB)

EU/3/18/2091 (Active substance: Glucagon) - Orphan designation - Commission Decision (2018)7801 of Wed, 21 Nov 2018 European Medicines Agency (EMA) procedure number: EMA/OD/108/18

Europe -DG Health and Food Safety

21-11-2018

EU/3/18/2083 (MaaT PHARMA)

EU/3/18/2083 (MaaT PHARMA)

EU/3/18/2083 (Active substance: Allogeneic faecal microbiota, pooled) - Orphan designation - Commission Decision (2018)7792 of Wed, 21 Nov 2018 European Medicines Agency (EMA) procedure number: EMA/OD/123/18

Europe -DG Health and Food Safety

21-11-2018

EU/3/18/2082 (Takeda Pharma A/S)

EU/3/18/2082 (Takeda Pharma A/S)

EU/3/18/2082 (Active substance: 5-{(1R,2R)-2-[(cyclopropylmethyl)amino]cyclopropyl}-N-(tetrahydro-2H-pyran-4-yl)thiophene-3-carboxamide monohydrochloride) - Orphan designation - Commission Decision (2018)7791 of Wed, 21 Nov 2018 European Medicines Agency (EMA) procedure number: EMA/OD/040/18

Europe -DG Health and Food Safety

12-11-2018

Neupro (UCB Pharma S.A.)

Neupro (UCB Pharma S.A.)

Neupro (Active substance: Rotigotine) - Centralised - Yearly update - Commission Decision (2018)7551 of Mon, 12 Nov 2018

Europe -DG Health and Food Safety

1-11-2018

Protopic (Leo Pharma A/S)

Protopic (Leo Pharma A/S)

Protopic (Active substance: Tacrolimus) - Centralised - Yearly update - Commission Decision (2018)7343 of Thu, 01 Nov 2018

Europe -DG Health and Food Safety

29-10-2018

Sustiva (Bristol-Myers Squibb Pharma EEIG)

Sustiva (Bristol-Myers Squibb Pharma EEIG)

Sustiva (Active substance: efavirenz) - Centralised - 2-Monthly update - Commission Decision (2018)7252 of Mon, 29 Oct 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/249/II/145/G

Europe -DG Health and Food Safety

25-10-2018

Xtandi (Astellas Pharma Europe B.V.)

Xtandi (Astellas Pharma Europe B.V.)

Xtandi (Active substance: enzalutamide) - Centralised - 2-Monthly update - Commission Decision (2018)7132 of Thu, 25 Oct 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2639/II/39G

Europe -DG Health and Food Safety

22-10-2018

Velphoro (Vifor Fresenius Medical Care Renal Pharma France)

Velphoro (Vifor Fresenius Medical Care Renal Pharma France)

Velphoro (Active substance: mixture of polynuclear iron(iii)-oxyhydroxide, sucrose and starches) - Centralised - Yearly update - Commission Decision (2018)6972 of Mon, 22 Oct 2018

Europe -DG Health and Food Safety

16-10-2018

Dexxience (Portola Pharma UK Limited)

Dexxience (Portola Pharma UK Limited)

Dexxience (Active substance: betrixaban) - Refusal of authorisation - Commission Decision (2018)6226 of Tue, 16 Oct 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4309

Europe -DG Health and Food Safety

2-10-2018

Lamivudine Teva Pharma B.V. (Teva B.V.)

Lamivudine Teva Pharma B.V. (Teva B.V.)

Lamivudine Teva Pharma B.V. (Active substance: Lamivudine) - Centralised - Yearly update - Commission Decision (2018)6476 of Tue, 02 Oct 2018

Europe -DG Health and Food Safety

2-10-2018

Zoledronic acid Mylan (Mylan S.A.S.)

Zoledronic acid Mylan (Mylan S.A.S.)

Zoledronic acid Mylan (Active substance: zoledronic acid) - Centralised - Yearly update - Commission Decision (2018)6486 of Tue, 02 Oct 2018

Europe -DG Health and Food Safety

1-10-2018

EU/3/16/1762 (Pharma Gateway AB)

EU/3/16/1762 (Pharma Gateway AB)

EU/3/16/1762 (Active substance: Synthetic 15-amino-acid macrocyclic peptide acylated with a polyethyleneglycol palmitoylated linker) - Transfer of orphan designation - Commission Decision (2018)6399 of Mon, 01 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/107/16/T/01

Europe -DG Health and Food Safety

1-10-2018

Gefitinib Mylan (Mylan S.A.S.)

Gefitinib Mylan (Mylan S.A.S.)

Gefitinib Mylan (Active substance: gefitinib) - Centralised - Authorisation - Commission Decision (2018)6406 of Mon, 01 Oct 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4826

Europe -DG Health and Food Safety

24-9-2018

NeuroBloc (Sloan Pharma S.a.r.l.)

NeuroBloc (Sloan Pharma S.a.r.l.)

NeuroBloc (Active substance: Botulinum Toxin Type B) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)6221 of Mon, 24 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/000301/T/0101

Europe -DG Health and Food Safety

24-9-2018

Rasilez (Noden Pharma DAC)

Rasilez (Noden Pharma DAC)

Rasilez (Active substance: aliskiren) - Centralised - Yearly update - Commission Decision (2018)6229 of Mon, 24 Sep 2018

Europe -DG Health and Food Safety

24-9-2018

Kigabeq (ORPHELIA Pharma SAS)

Kigabeq (ORPHELIA Pharma SAS)

Kigabeq (Active substance: vigabatrin) - Centralised - Authorisation - Commission Decision (2018)6224 of Mon, 24 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4534

Europe -DG Health and Food Safety

24-9-2018

INCRELEX (Ipsen Pharma)

INCRELEX (Ipsen Pharma)

INCRELEX (Active substance: Mecasermin) - Centralised - Yearly update - Commission Decision (2018)6240 of Mon, 24 Sep 2018

Europe -DG Health and Food Safety

19-9-2018

Hulio (Mylan S.A.S.)

Hulio (Mylan S.A.S.)

Hulio (Active substance: adalimumab) - Centralised - Authorisation - Commission Decision (2018)6107 of Wed, 19 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/004429/0000

Europe -DG Health and Food Safety

19-9-2018

Pregabalin Mylan Pharma (Mylan S.A.S.)

Pregabalin Mylan Pharma (Mylan S.A.S.)

Pregabalin Mylan Pharma (Active substance: pregabalin) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018) 6097 of Wed, 19 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/3962/T/08

Europe -DG Health and Food Safety

19-9-2018

Memantine Mylan (Mylan S.A.S.)

Memantine Mylan (Mylan S.A.S.)

Memantine Mylan (Active substance: Memantine) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)5972 of Wed, 19 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2660/T/12

Europe -DG Health and Food Safety

19-9-2018

Pregabalin Mylan (Mylan S.A.S.)

Pregabalin Mylan (Mylan S.A.S.)

Pregabalin Mylan (Active substance: pregabalin) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018) 5971 of Wed, 19 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4078/T/10

Europe -DG Health and Food Safety

19-9-2018

Agenda:  Agenda – 12th Pharmacovigilance stakeholder forum

Agenda: Agenda – 12th Pharmacovigilance stakeholder forum

Europe - EMA - European Medicines Agency

19-9-2018

 12th Pharmacovigilance stakeholder forum, European Medicines Agency, London, UK, From: 24-Sep-2018, To: 24-Sep-2018

12th Pharmacovigilance stakeholder forum, European Medicines Agency, London, UK, From: 24-Sep-2018, To: 24-Sep-2018

This forum brings together regulators with patients, healthcare professionals and industry, to take stock of what we have achieved and what needs to be the focus over the coming years.

Europe - EMA - European Medicines Agency

17-9-2018

 European Medicines Agency (EMA) Human Scientific Committees' Working Parties with Patients’ and Consumers’ Organisations (PCWP) and with Healthcare Professionals’ Organisations (HCPWP), European Medicines Agency, London, UK, From: 25-Sep-2018, To: 25-Sep

European Medicines Agency (EMA) Human Scientific Committees' Working Parties with Patients’ and Consumers’ Organisations (PCWP) and with Healthcare Professionals’ Organisations (HCPWP), European Medicines Agency, London, UK, From: 25-Sep-2018, To: 25-Sep

This joint Patients' and Consumers' Working Party (PCWP) and Healthcare Professionals' Working Party (HCPWP) meeting will include results of the 2017 EMA perception survey. EMA regulatory science to 2025 will be discussed together with updates on Good Pharmacovigilance Practices (GVP). The Topic Group on Digital media and health will feedback to the working parties’ members. Participants will also receive an update on ongoing work on electronic product information and on availability of authorised med...

Europe - EMA - European Medicines Agency

12-9-2018

 Risk management plan information day, European Medicines Agency, London, UK, From: 25-Oct-2018, To: 25-Oct-2018

Risk management plan information day, European Medicines Agency, London, UK, From: 25-Oct-2018, To: 25-Oct-2018

This information day will update participants on the Agency’s medicine risk management activities and provide advice to marketing authorisation holders and applicants on drafting a risk management plan (RMP) in view of the full implementation of the second revision of the RMP template after the transitional period has elapsed. It will also provide an opportunity for an exchange of experiences with this template between regulators and industry. A dedicated session will discuss the streamlining of safety s...

Europe - EMA - European Medicines Agency

12-9-2018

ADCETRIS (Takeda Pharma A/S)

ADCETRIS (Takeda Pharma A/S)

ADCETRIS (Active substance: Brentuximab vedotin) - Centralised - Annual renewal - Commission Decision (2018)5973 of Wed, 12 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2455/R/58

Europe -DG Health and Food Safety

29-8-2018

Fulvestrant Mylan (Mylan S.A.S.)

Fulvestrant Mylan (Mylan S.A.S.)

Fulvestrant Mylan (Active substance: fulvestrant) - Centralised - 2-Monthly update - Commission Decision (2018)5774 of Wed, 29 Aug 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/004649/IB/0001

Europe -DG Health and Food Safety

29-8-2018

Cometriq (Ipsen Pharma)

Cometriq (Ipsen Pharma)

Cometriq (Active substance: cabozantinib) - PSUSA - Modification - Commission Decision (2018)5761 of Wed, 29 Aug 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/PSUSA/10180/201711

Europe -DG Health and Food Safety

29-8-2018

Rasilez HCT (Noden Pharma DAC)

Rasilez HCT (Noden Pharma DAC)

Rasilez HCT (Active substance: aliskiren hemifumarate / hydrochlorothiazide) - Centralised - Renewal - Commission Decision (2018)5769 of Wed, 29 Aug 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/964/R/87

Europe -DG Health and Food Safety

28-8-2018

EU/3/18/2056 (Nogra Pharma Limited)

EU/3/18/2056 (Nogra Pharma Limited)

EU/3/18/2056 (Active substance: (S)-(-)-3-(4-aminophenyl)-2-methoxypropanoic acid) - Orphan designation - Commission Decision (2018)5728 of Tue, 28 Aug 2018 European Medicines Agency (EMA) procedure number: EMA/OD/075/18

Europe -DG Health and Food Safety

28-8-2018

EU/3/18/2061 (Pharma Gateway AB)

EU/3/18/2061 (Pharma Gateway AB)

EU/3/18/2061 (Active substance: Autologous glioma tumour cells treated with antisense molecule directed against the insulin-like growth factor type 1 receptor) - Orphan designation - Commission Decision (2018)5739 of Tue, 28 Aug 2018 European Medicines Agency (EMA) procedure number: EMA/OD/049/18

Europe -DG Health and Food Safety

27-8-2018

Yescarta (Kite Pharma EU B.V.)

Yescarta (Kite Pharma EU B.V.)

Yescarta (Active substance: axicabtagene ciloleucel) - Centralised - Authorisation - Commission Decision (2018)5718 of Mon, 27 Aug 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4480

Europe -DG Health and Food Safety

27-8-2018

Entyvio (Takeda Pharma A/S)

Entyvio (Takeda Pharma A/S)

Entyvio (Active substance: vedolizumab) - PSUSA - Modification - Commission Decision (2018)5712 of Mon, 27 Aug 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/PSUSA/10186/201711

Europe -DG Health and Food Safety

27-8-2018

Arixtra (Aspen Pharma Trading Limited)

Arixtra (Aspen Pharma Trading Limited)

Arixtra (Active substance: Fondaparinux sodium) - PSUSA - Modification - Commission Decision (2018)5708 of Mon, 27 Aug 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/403/PSUSA/1467-201712

Europe -DG Health and Food Safety