FLUCONAZOLE Dakota Pharm

Information principale

  • Nom commercial:
  • FLUCONAZOLE Dakota Pharm 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 50 ml
  • Type d'ordonnance:
  • liste I
  • Utiliser pour:
  • Humains
  • Type medicin:
  • médicament allopathique

Documents

Localisation

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

Information thérapeutique

  • Descriptif du produit:
  • 375 942-9 ou 4009 375 942 9 5 - 1 flacon(s) en verre de 50 ml - Déclaration d'arrêt de commercialisation:03/03/2009;375 943-5 ou 4009 375 943 5 6 - 5 flacon(s) en verre de 50 ml - Déclaration de commercialisation non communiquée:;375 944-1 ou 4009 375 944 1 7 - 10 flacon(s) en verre de 50 ml - Déclaration de commercialisation non communiquée:;375 945-8 ou 4009 375 945 8 5 - 1 flacon(s) en verre de 100 ml - Déclaration d'arrêt de commercialisation:25/03/2009;375 947-0 ou 4009 375 947 0 7 - 5 flacon(s) en verre de 100 ml - Déclaration de commercialisation non communiquée:;375 948-7 ou 4009 375 948 7 5 - 10 flacon(s) en verre de 100 ml - Déclaration de commercialisation non communiquée:;375 949-3 ou 4009 375 949 3 6 - 1 flacon(s) en verre de 200 ml - Déclaration d'arrêt de commercialisation:23/12/2008;375 950-1 ou 4009 375 950 1 8 - 5 flacon(s) en verre de 200 ml - Déclaration de commercialisation non communiquée:;375 951-8 ou 4009 375 951 8 6 - 10 flacon(s) en verre de 200 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:
  • 65979183
  • Date de l'autorisation:
  • 23-05-2006
  • Dernière mise à jour:
  • 10-08-2017

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

NOTICE

Misàjour:22/05/2008

Dénominationdumédicament

FLUCONAZOLEDAKOTAPHARM2mg/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-CEQUEFLUCONAZOLEDAKOTAPHARM2mg/ml,solutionpourperfusionETDANSQUELS

CASEST-ILUTILISE?

2.QUELLESSONTLESINFORMATIONSACONNAITREAVANTD'UTILISERFLUCONAZOLEDAKOTA

PHARM2mg/ml,solutionpourperfusion?

3.COMMENTUTILISERFLUCONAZOLEDAKOTAPHARM2mg/ml,solutionpourperfusion?

4.QUELSSONTLESEFFETSINDESIRABLESEVENTUELS?

5.COMMENTCONSERVERFLUCONAZOLEDAKOTAPHARM2mg/ml,solutionpourperfusion?

6.INFORMATIONSSUPPLEMENTAIRES

1.QU'EST-CEQUEFLUCONAZOLEDAKOTAPHARM2mg/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'UTILISERFLUCONAZOLEDAKOTA

PHARM2mg/ml,solutionpourperfusion?

Listedesinformationsnécessairesavantlaprisedumédicament

Sansobjet.

Contre-indications

N'utilisezjamaisFLUCONAZOLEDAKOTAPHARM2mg/ml,solutionpourperfusiondanslescas

suivants:

allergieconnueaufluconazoleetauxsubstancesapparentées(azolés)

pendantlagrossesseetl'allaitement,saufavismédical

enassociationavec:

lecisapride(médicamentutilisédanslerefluxgastro-œsophagien)

lepimozide(médicamentutilisédanscertainstroublesdel'humeur)

l'halofantrine(médicamentutilisédansletraitementdupaludisme).

Précautionsd'emploi;misesengardespéciales

FaitesattentionavecFLUCONAZOLEDAKOTAPHARM2mg/ml,solutionpourperfusion:

Précautionsd'emploi

Chezlafemmeenpérioded'activitégénitale,unecontraceptionestindispensable.

Misesengardespéciales

Encasdesurvenuedesymptômesévocateursd'atteintehépatiquegrave(fatigueimportante,anorexie,

nauséespersistantes,vomissements,jaunisse),vousdevezconsulterunmédecin.

Sivousavezpréalablementprésentéuneréactioncutanéeassociéeàlaprisedefluconazoleouunautre

dérivéazolé,encasdesurvenuedelésionsbulleuses,vousdevezconsulterunmédecinleplusrapidement

possible.

Cemédicamentcontient3,57mg(soit0,155mmol)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.COMMENTUTILISERFLUCONAZOLEDAKOTAPHARM2mg/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'effetdeFLUCONAZOLEDAKOTAPHARM2mg/ml,solutionpour

perfusionesttropfortoutropfaible,consultezvotremédecinouvotrepharmacien.

Moded'administration

Perfusionintraveineuse.

Duréedetraitement

Laduréedetraitementdépenddelaréponsecliniqueetdel'indication.

DANSTOUSLESCAS,RESPECTERSTRICTEMENTL'ORDONNANCEDEVOTREMEDECIN.

Symptômesetinstructionsencasdesurdosage

SivousavezprisplusdeFLUCONAZOLEDAKOTAPHARM2mg/ml,solutionpourperfusionquevous

n'auriezdû:consultezimmédiatementvotremédecinouvotrepharmacien.

Instructionsencasd'omissiond'uneoudeplusieursdoses

SivousoubliezdeprendreFLUCONAZOLEDAKOTAPHARM2mg/ml,solutionpourperfusion:ne

prenezpasdedosedoublepourcompenserladosequevousavezoubliédeprendre.

Risquedesyndromedesevrage

Sansobjet.

4.QUELSSONTLESEFFETSINDESIRABLESEVENTUELS?

Descriptiondeseffetsindésirables

Commetouslesmédicaments,FLUCONAZOLEDAKOTAPHARM2mg/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.COMMENTCONSERVERFLUCONAZOLEDAKOTAPHARM2mg/ml,solutionpourperfusion?

Tenirhorsdelaportéeetdelavuedesenfants.

Datedepéremption

NepasutiliserFLUCONAZOLEDAKOTAPHARM2mg/ml,solutionpourperfusionaprèsladatede

péremptionmentionnéesurlaboîte,leflacon.

Conditionsdeconservation

Avantouverture:Pasdeprécautionsparticulièresdeconservation.

Aprèsouverture:leproduitdoitêtreutiliséimmédiatement.Encasd'utilisationnonimmédiate,lesduréeset

conditionsdeconservationaprèsdilutionetavantutilisationrelèventdelaseuleresponsabilitédel'utilisateur.

Sinécessaire,misesengardecontrecertainssignesvisiblesdedétérioration

Lesmédicamentsnedoiventpasêtrejetésautoutàl'égoutouaveclesorduresménagères.Demandezà

votrepharmaciencequ'ilfautfairedesmédicamentsinutilisés.Cesmesurespermettrontdeprotéger

votrepharmaciencequ'ilfautfairedesmédicamentsinutilisés.Cesmesurespermettrontdeprotéger

l'environnement.

6.INFORMATIONSSUPPLEMENTAIRES

Listecomplètedessubstancesactivesetdesexcipients

QuecontientFLUCONAZOLEDAKOTAPHARM2mg/ml,solutionpourperfusion?

Lasubstanceactiveest:

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

Pour1mldesolutionpourperfusion.

Unflaconde50mlcontient100mgdefluconazole.

Unflaconde100mlcontient200mgdefluconazole.

Unflaconde200mlcontient400mgdefluconazole.

Lesautrescomposantssont:

Chloruredesodium,eaupourpréparationsinjectables.

Formepharmaceutiqueetcontenu

Qu'est-cequeFLUCONAZOLEDAKOTAPHARM2mg/ml,solutionpourperfusionetcontenude

l'emballageextérieur?

Cemédicamentseprésentesousformedesolutioninjectablepourperfusionintraveineuseenflaconde50ml,

100mlou200ml.

Nometadressedutitulairedel'autorisationdemisesurlemarchéetdutitulairedel'autorisationde

fabricationresponsabledelalibérationdeslots,sidifférent

Titulaire

SANOFIAVENTISFRANCE

1-13,boulevardRomainRolland

75014Paris

Exploitant

SANOFIAVENTISFRANCE

1-13,boulevardRomainRolland

75014PARIS

Fabricant

DAKOTAPHARM

1-13boulevardRomainRolland

75014PARIS

NomsdumédicamentdanslesEtatsmembresdel'EspaceEconomiqueEuropéen

Sansobjet.

Dated’approbationdelanotice

Ladernièredateàlaquellecettenoticeaétéapprouvéeestle{date}.

AMMsouscirconstancesexceptionnelles

Sansobjet.

InformationsInternet

DesinformationsdétailléessurcemédicamentsontdisponiblessurlesiteInternetdel’Afssaps(France).

Informationsréservéesauxprofessionnelsdesanté

Sansobjet.

Autres

Sansobjet.

4-12-2018

Surveillance du marché

Surveillance du marché

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.

France - Agence Nationale du Médicament Vétérinaire

8-11-2018

Manage Your Asthma: Know Your Triggers and Treatment Options

Manage Your Asthma: Know Your Triggers and Treatment Options

You can manage your asthma by taking medications approved by the FDA. Before going to the pharmacy, get a proper diagnosis from a doctor and together develop an asthma action plan.

FDA - U.S. Food and Drug Administration

3-11-2018

Janssen Issues Voluntary Nationwide Recall for one lot of ORTHO-NOVUM 1/35 and two lots of ORTHO-NOVUM 7/7/7 Due to Incorrect Veridate Dispenser Instructions

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FDA - U.S. Food and Drug Administration

22-10-2018

Promise Pharmacy Issues Voluntary Nationwide Recall of Prednisolone and Gatifloxacin Ophthalmic Solution 1%/0.5% Sterile Due to Small Particulate Floating in the Solution

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FDA - U.S. Food and Drug Administration

18-10-2018

October 18, 2018: Pharmacist Indicted for Taking Drugs, Carrying Firearm in Violation of Court Order

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FDA - U.S. Food and Drug Administration

28-9-2018

Debate on research dissemination at the Danish Medicines Agency

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On 1 October, the Danish Medicines Agency and the Danish Society for Pharmacoepidemiology have invited a number of researchers, doctors and communication officers from research institutions throughout Denmark to a debate on how the findings of new health research can be disseminated most responsibly. The debate meeting can be followed live on the Danish Medicines Agency’s Facebook profile.

Danish Medicines Agency

17-9-2018

September 11, 2018: Columbus Pharmacist Sentenced for Health Care Fraud Scheme

September 11, 2018: Columbus Pharmacist Sentenced for Health Care Fraud Scheme

September 11, 2018: Columbus Pharmacist Sentenced for Health Care Fraud Scheme

FDA - U.S. Food and Drug Administration

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

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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

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FDA - U.S. Food and Drug Administration

4-9-2018

Safer prescription of blood thinning agents

Safer prescription of blood thinning agents

A collaboration between pharmaceutical companies, pharmacies and authorities has eliminated a common cause of dosing errors involving blood thinning agents.

Danish Medicines Agency

28-8-2018

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

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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

23-8-2018

August 22, 2018: Louisiana Pharmacist Convicted of Trafficking and Selling Stolen Medication

August 22, 2018: Louisiana Pharmacist Convicted of Trafficking and Selling Stolen Medication

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FDA - U.S. Food and Drug Administration

20-8-2018

August 17, 2018: Unlicensed Pharmacy Technician Pleads Guilty to Working at New England Compounding Center

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FDA - U.S. Food and Drug Administration

2-8-2018

"Jian Pai Natural Skin Care Cream" contains antifungal drugs not listed on the label, which may pose serious health risks

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Health Canada testing of “Jian Pai Natural Skin Care Cream,” also called ‘’Yikangshuang,” found that it contains two antifungal drugs (fluconazole and miconazole) that are not listed on the product label, and may pose serious health risks.

Health Canada

2-8-2018

La crème naturelle pour la peau Jian Pai contient des antifongiques qui ne figurent pas sur l’étiquette et qui pourraient poser de graves risques pour la santé

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Canadiens en santé

28-7-2018

Ranier’s Rx Laboratory Issues Voluntary Recall of All Sterile Compounded Products Within Expiry Due to Lack of Sterility Concerns

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FDA - U.S. Food and Drug Administration

18-7-2018

FDA Investigating Multistate Outbreak of Salmonella Sandiego Infections Linked to Hy-Vee Spring Pasta Salad

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FDA - U.S. Food and Drug Administration

18-7-2018

Hy-Vee Voluntarily Recalls Spring Pasta Salad Due to Reported Illnesses

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FDA - U.S. Food and Drug Administration

13-7-2018

Scientific guideline:  Guideline on good pharmacogenomic practice - First version, adopted

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Europe - EFSA - European Food Safety Authority EFSA Journal

11-7-2018

July 10, 2018: Former Des Moines Pharmacy Technician Sentenced for Illegally Tampering with Fentanyl

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FDA - U.S. Food and Drug Administration

11-7-2018

July 10: 2018: Former Pharmacy Technician Indicted for Stealing Fentanyl, Morphine

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FDA - U.S. Food and Drug Administration

15-6-2018

Compounded Products Containing Triamcinolone-Moxifloxacin by Guardian Pharmacy Services (Dallas, Texas): Alert to Health Professionals - Adverse Events Reported After Receiving Eye Injections

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FDA - U.S. Food and Drug Administration

1-6-2018

Demulen 30 birth control pills: Packages containing broken or chipped pills

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Health Canada

1-6-2018

Emballages de contraceptifs oraux Demulen 30 qui comprennent des comprimés endommagés

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Canadiens en santé

11-5-2018

Reviews of Pediatric Studies Conducted under BPCA and PREA from 2012 – present

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FDA - U.S. Food and Drug Administration

10-5-2018

May 10, 2018: Former New Hampshire Pharmacist Sentenced to Two Years in Prison for Drug-Related Offenses

May 10, 2018: Former New Hampshire Pharmacist Sentenced to Two Years in Prison for Drug-Related Offenses

May 10, 2018: Former New Hampshire Pharmacist Sentenced to Two Years in Prison for Drug-Related Offenses

FDA - U.S. Food and Drug Administration

17-4-2018

March 27, 2018: Compounding Pharmacy Owner Sentenced to Five Years in Prison for $10.5 Million Health Care Fraud

March 27, 2018: Compounding Pharmacy Owner Sentenced to Five Years in Prison for $10.5 Million Health Care Fraud

March 27, 2018: Compounding Pharmacy Owner Sentenced to Five Years in Prison for $10.5 Million Health Care Fraud

FDA - U.S. Food and Drug Administration

16-4-2018

Women taking birth control pills reminded to return any packages for replacement if the pills are missing or look unusual

Women taking birth control pills reminded to return any packages for replacement if the pills are missing or look unusual

In light of continuing complaints of quality issues involving certain prescription birth control pills, Health Canada is reminding women to check their packages of birth control pills. If you notice anything unusual in the package, such as missing or damaged pills, you should return the package to the pharmacy for replacement as soon as possible. Skipping a dose because the pill is missing, or taking a damaged (for example, chipped or fragmented) pill, may increase the risk of pregnancy because less acti...

Health Canada

16-4-2018

Les femmes qui prennent des pilules anticonceptionnelles doivent retourner les emballages pour les faire remplacer s’il manque des comprimés ou s’ils ont un aspect inhabituel

Les femmes qui prennent des pilules anticonceptionnelles doivent retourner les emballages pour les faire remplacer s’il manque des comprimés ou s’ils ont un aspect inhabituel

À la lumière des plaintes constantes concernant la qualité de certaines pilules anticonceptionnelles, Santé Canada rappelle aux femmes de vérifier leurs emballages de pilules anticonceptionnelles. Si vous remarquez quelque chose d’inhabituel dans l’emballage, comme des comprimés manquants ou endommagés, vous devez retourner l’emballage à votre pharmacie pour le faire remplacer le plus tôt possible. Le fait de sauter une dose parce qu’il manque un comprimé ou de prendre un comprimé endommagé (par exemple,...

Canadiens en santé

28-3-2018

DKMA Update March 2018

DKMA Update March 2018

In this issue of DKMA Update you can read about evidence; changes to Tramadol’s summary of product characteristics; inspections of the sale of OTC medicines outside pharmacies and much more

Danish Medicines Agency

8-3-2018

Recommandation de suspension immédiate et rappel du Zinbryta®, médicament utilisé dans le traitement de la sclérose en plaques

Recommandation de suspension immédiate et rappel du Zinbryta®, médicament utilisé dans le traitement de la sclérose en plaques

Risque de troubles cérébraux inflammatoires graves L’Agence européenne de médicaments (EMA) recommande la suspension immédiate au sein de l'Union européenne (UE) et le rappel des lots dans les pharmacies et hôpitaux du Zinbryta® (daclizumab bêta), médicament utilisé dans le traitement de

Ministère de la Santé - Luxembourg

25-1-2018

How to Buy Medicines Safely From an Online Pharmacy

How to Buy Medicines Safely From an Online Pharmacy

How can you tell if an online pharmacy is operating legally? The FDA's BeSafeRx web page can help you identify and avoid rogue online pharmacies. The FDA has tips for buying medicines online safely.

FDA - U.S. Food and Drug Administration

22-12-2017

Retrait des produits infantiles PICOT et MILUMEL

Retrait des produits infantiles PICOT et MILUMEL

Les autorités Luxembourgeoises ont été informées du rappel des produits infantiles PICOT et MILUMEL suivants au niveau des pharmacies au Luxembourg en raison d’une suspicion de présence de Salmonelles: Produit de la gamme PICOT MAGICMIX PICOT PDR EPAISSIS 300G PICOT ACTION

Ministère de la Santé - Luxembourg

3-11-2017

New Director of Division for Pharmacovigilance & Medical Devices

New Director of Division for Pharmacovigilance & Medical Devices

Jens Piero Quartarolo has been appointed new Director of Division for Pharmacovigilance & Medical Devices and will form part of the Danish Medicines Agency's leadership team.

Danish Medicines Agency

12-9-2017

E2B acknowledgment format change

E2B acknowledgment format change

Companies that use the Danish Medicines Agency's Pharmacovigilance System should be aware that we have changed the MessageFormatRelease value from 2.0 to 1.0.

Danish Medicines Agency

11-9-2017

DKMA Update

DKMA Update

Our newsletter Danish Pharmacovigilance Update changes name to DKMA Update and will from now on contain information about medicinal products in general, patient safety and life science.

Danish Medicines Agency

1-8-2017

Withdrawal of one more batch of counterfeit packs of the schizophrenia medicine Xeplion 150 mg

Withdrawal of one more batch of counterfeit packs of the schizophrenia medicine Xeplion 150 mg

German and Danish parallel importers and the Danish Medicines Agency are now withdrawing the fourth batch of Xeplion 150 mg from wholesale distributors, hospitals and pharmacies, because the batch contains counterfeit packs.

Danish Medicines Agency

27-7-2017

Counterfeit packs of the schizophrenia medicine Xeplion 150 mg

Counterfeit packs of the schizophrenia medicine Xeplion 150 mg

One German and several Danish parallel importers and the Danish Medicines Agency have withdrawn several batches of Xeplion 150 mg from wholesale distributors, hospitals and pharmacies, because the batches contained counterfeit packs.

Danish Medicines Agency

8-6-2017

Danish Pharmacovigilance Update, May 2017

Danish Pharmacovigilance Update, May 2017

The May issue of Danish Pharmacovigilance Update.

Danish Medicines Agency

22-5-2017

Danish Pharmacovigilance Update, April 2017

Danish Pharmacovigilance Update, April 2017

The April issue of Danish Pharmacovigilance Update.

Danish Medicines Agency

18-4-2017

Danish Pharmacovigilance Update, March 2017

Danish Pharmacovigilance Update, March 2017

The March issue of Danish Pharmacovigilance Update.

Danish Medicines Agency

6-3-2017

Danish Pharmacovigilance Update, February 2017

Danish Pharmacovigilance Update, February 2017

The February issue of Danish Pharmacovigilance Update.

Danish Medicines Agency

3-2-2017

Danish Pharmacovigilance Update, January 2017

Danish Pharmacovigilance Update, January 2017

The January issue of Danish Pharmacovigilance Update.

Danish Medicines Agency

6-1-2017

Danish Pharmacovigilance Update, December 2016

Danish Pharmacovigilance Update, December 2016

The December issue of Danish Pharmacovigilance Update.

Danish Medicines Agency

20-12-2016

New chair of PhVWP-V

New chair of PhVWP-V

Lisbet Vesterager Borge, veterinarian, has been elected chair of the European Pharmacovigilance Working Party Veterinary (PhVWP-V).

Danish Medicines Agency

9-12-2016

Danish Pharmacovigilance Update, November 2016

Danish Pharmacovigilance Update, November 2016

The November issue of Danish Pharmacovigilance Update.

Danish Medicines Agency

15-11-2016

Danish Pharmacovigilance Update, October 2016

Danish Pharmacovigilance Update, October 2016

The October issue of Danish Pharmacovigilance Update.

Danish Medicines Agency

3-11-2016

Danish Pharmacovigilance Update, September 2016

Danish Pharmacovigilance Update, September 2016

The September issue of Danish Pharmacovigilance Update.

Danish Medicines Agency

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

30-8-2018

Consultation: Referral of proposed amendment to the current Poisons Standard to the meeting of the ACMS, March 2019

Consultation: Referral of proposed amendment to the current Poisons Standard to the meeting of the ACMS, March 2019

Advisory Committee on Medicines Scheduling to consider upscheduling of modified release paracetamol to 'Pharmacist Only'. Closing date 31 October 2018

Therapeutic Goods Administration - Australia

30-8-2018

Modified release paracetamol

Modified release paracetamol

Advisory Committee on Medicines Scheduling to consider upscheduling of modified release paracetamol to 'Pharmacist Only'

Therapeutic Goods Administration - Australia

28-8-2018

EU/3/18/2057 (Pharm Research Associates (UK) Limited)

EU/3/18/2057 (Pharm Research Associates (UK) Limited)

EU/3/18/2057 (Active substance: 1-(2-hydroxyethyl)-8-{[5-(4-methylpiperazin-1-yl)-2-(trifluoromethoxy) phenyl]amino}-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide fumarate salt) - Orphan designation - Commission Decision (2018)5729 of Tue, 28 Aug 2018 European Medicines Agency (EMA) procedure number: EMA/OD/051/18

Europe -DG Health and Food Safety

24-5-2018

Consultation:  miconazole and fluconazole: proposed advisory statements for medicines

Consultation: miconazole and fluconazole: proposed advisory statements for medicines

The TGA is seeking comments on the proposed RASML statements for OTC medicines containing miconazole or fluconazole. Closing date: 21 June 2018

Therapeutic Goods Administration - Australia

23-3-2018

EU/3/18/1991 (TurnKey PharmaConsulting Ireland Limited)

EU/3/18/1991 (TurnKey PharmaConsulting Ireland Limited)

EU/3/18/1991 (Active substance: Docosahexaenoic acid ethyl ester) - Orphan designation - Commission Decision (2018)1880 of Fri, 23 Mar 2018 European Medicines Agency (EMA) procedure number: EMA/OD/235/17

Europe -DG Health and Food Safety

23-3-2018

EU/3/18/2003 (Pharmadev Healthcare Ltd)

EU/3/18/2003 (Pharmadev Healthcare Ltd)

EU/3/18/2003 (Active substance: Ribavirin) - Orphan designation - Commission Decision (2018)1891 of Fri, 23 Mar 2018 European Medicines Agency (EMA) procedure number: EMA/OD/225/17

Europe -DG Health and Food Safety

23-3-2018

EU/3/18/2002 (Pharmadev Healthcare Ltd)

EU/3/18/2002 (Pharmadev Healthcare Ltd)

EU/3/18/2002 (Active substance: Ribavirin) - Orphan designation - Commission Decision (2018)1890 of Fri, 23 Mar 2018 European Medicines Agency (EMA) procedure number: EMA/OD/224/17

Europe -DG Health and Food Safety