IXIA PLUS 20/12,5

Informació principal

  • Denominació comercial:
  • IXIA PLUS 20/12,5 mg 28 comprimidos recubiertos
  • formulario farmacéutico:
  • Comprimidos
  • Vía de administración:
  • Oral
  • Utilitza per:
  • Humans
  • Tipo de medicina:
  • medicament al·lopàtic

Documents

Localització

  • Disponible en:
  • IXIA PLUS 20/12,5 mg 28 comprimidos recubiertos
    Andorra
  • Idioma:
  • català

Altres dades

Estat

  • Font:
  • CedimCat - Centre d'Informació de Medicaments de Catalunya
  • Número d'autorització:
  • 654283
  • última actualització:
  • 08-06-2018

Prospecte: composició, indicacions, interacció, posologia, embaràs, lactància, reaccions adverses

IXIA PLUS 20/12,5 mg 28 comprimidos

recubiertos

olmesart

n+hidroclorotiazida

Indicacions

Medicament que augmenta la quantitat d'orina (DI

TIC) i ajuda a regular la pressi

sangu

(ANTIHIPERTENSIU).

Consideracions

NO prengui aquest medicament si

s al

rgic a SULFAMIDES.

Prengui els comprimits sencers, sense partir ni mastegar, empassant-los amb ajuda d'un got d'aigua.

Pot prendre aquest medicament amb o sense aliments; si t

sties d'est

mac, prengui'l amb

algun aliment.

s aconsellable que prengui aquest medicament al mat

o al migdia, per tal d'evitar haver d'aixecar-se

a la nit a orinar.

Tot i trobar-se millor, NO deixi de prendre aquest medicament durant el temps indicat pel seu metge.

Avisi el seu metge si pateix o ha patit problemes de cor, problemes de rony

o problemes de fetge.

Si vost

猫 茅

s diab

tic/a, tingui en compte que aquest medicament pot alterar els nivells de glucosa en

sang i orina.

Aquest medicament modifica l'acci

d'altres f

rmacs, NO prengui altres medicaments sense consultar

abans al seu metge o farmac

utic.

Durant el tractament, eviti aixecar-se de forma brusca per tal d'evitar possibles mareigs.

s possible que el seu metge li recomani una dieta especial, que conv

seguir per augmentar l'efic

cia d'aquest medicament.

NO utilitzi substituts de la sal de taula ni suplements de potassi sense coneixement del seu metge.

NO fumi NI begui mentre duri el tractament, d'aquesta manera augmentar

l'efic

cia d'aquest

medicament.

Mentre prengui aquest medicament procuri NO prendre grans quantitats de begudes amb cafe

na (caf

, te, refrescs de cola).

Informi immediatament el seu metge si est

embarassada o creu que pot estar-ho, aix

com si qued

s embarassada durant el tractament.

Avisi al seu metge si t

algun fill a qui estigui alletant.

Efectes adversos

Aquest medicament pot produir mareigs i sensaci

de cansament.

Si not

s qualsevol altre s

mptoma que creu que pot ser causat per aquest medicament, digui-li-ho al

seu metge.

Posologia

Prengui 1 comprimit a l'esmorzar.

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12-4-2019

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12-4-2019

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12-4-2019

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12-4-2019

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Europe -DG Health and Food Safety

12-4-2019

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EU/3/17/1848 (IntraBio Ireland Ltd)

EU/3/17/1848 (Active substance: Acetylleucine) - Transfer of orphan designation - Commission Decision (2019)2935 of Fri, 12 Apr 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000005357

Europe -DG Health and Food Safety

12-4-2019

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EU/3/18/1977 (GW Pharma (International) B.V)

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Europe -DG Health and Food Safety

12-4-2019

EU/3/17/1959 (GW Pharma (International) B.V)

EU/3/17/1959 (GW Pharma (International) B.V)

EU/3/17/1959 (Active substance: Cannabidiol) - Transfer of orphan designation - Commission Decision (2019)2925 of Fri, 12 Apr 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000004767

Europe -DG Health and Food Safety

12-4-2019

EU/3/17/1921 (GW Pharma (International) B.V)

EU/3/17/1921 (GW Pharma (International) B.V)

EU/3/17/1921 (Active substance: Cannabidivarin) - Transfer of orphan designation - Commission Decision (2019)2928 of Fri, 12 Apr 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000004766

Europe -DG Health and Food Safety

12-4-2019

EU/3/17/1920 (GW Pharma (International) B.V)

EU/3/17/1920 (GW Pharma (International) B.V)

EU/3/17/1920 (Active substance: Cannabidiol) - Transfer of orphan designation - Commission Decision (2019)2927 of Fri, 12 Apr 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000004765

Europe -DG Health and Food Safety

12-4-2019

EU/3/17/1855 (GW Pharma (International) B.V)

EU/3/17/1855 (GW Pharma (International) B.V)

EU/3/17/1855 (Active substance: Cannabidiol) - Transfer of orphan designation - Commission Decision (2019)2926 of Fri, 12 Apr 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000004607

Europe -DG Health and Food Safety

12-4-2019

EU/3/16/1621 (GW Pharma (International) B.V)

EU/3/16/1621 (GW Pharma (International) B.V)

EU/3/16/1621 (Active substance: Delta-9-tetrahydrocannabinol and cannabidiol from extracts of the Cannabis sativa L. plant) - Transfer of orphan designation - Commission Decision (2019)2924 of Fri, 12 Apr 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000004763

Europe -DG Health and Food Safety

12-4-2019

EU/3/14/1339 (GW Pharma (International) B.V)

EU/3/14/1339 (GW Pharma (International) B.V)

EU/3/14/1339 (Active substance: Cannabidiol) - Transfer of orphan designation - Commission Decision (2019)2923 of Fri, 12 Apr 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000004708

Europe -DG Health and Food Safety

12-4-2019

EU/3/18/2126 (JVM Europe B.V.)

EU/3/18/2126 (JVM Europe B.V.)

EU/3/18/2126 (Active substance: Human glucagon-like peptide-2 analogue linked to a human immunoglobulin Fc fragment) - Transfer of orphan designation - Commission Decision (2019)2922 of Fri, 12 Apr 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000005194

Europe -DG Health and Food Safety

12-4-2019

EU/3/18/2035 (JVM Europe B.V.)

EU/3/18/2035 (JVM Europe B.V.)

EU/3/18/2035 (Active substance: Efpegsomatropin) - Transfer of orphan designation - Commission Decision (2019)2921 of Fri, 12 Apr 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000005050

Europe -DG Health and Food Safety

12-4-2019

EU/3/18/2022 (JVM Europe B.V.)

EU/3/18/2022 (JVM Europe B.V.)

EU/3/18/2022 (Active substance: Glucagon analogue linked to a human immunoglobulin Fc fragment) - Transfer of orphan designation - Commission Decision 2920 of Fri, 12 Apr 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000005277

Europe -DG Health and Food Safety

12-4-2019

EU/3/17/1926 (Envigo CRS S.A.)

EU/3/17/1926 (Envigo CRS S.A.)

EU/3/17/1926 (Active substance: Ofranergene obadenovec) - Transfer of orphan designation - Commission Decision (2019)2915 of Fri, 12 Apr 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000005420

Europe -DG Health and Food Safety

12-4-2019

EU/3/17/1879 (Envigo CRS S.A.)

EU/3/17/1879 (Envigo CRS S.A.)

EU/3/17/1879 (Active substance: Asp-Arg-Val-Tyr-Ile-His-Pro) - Transfer of orphan designation - Commission Decision (2019)2914 of Fri, 12 Apr 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000005415

Europe -DG Health and Food Safety

12-4-2019

EU/3/14/1241 (Envigo CRS S.A.)

EU/3/14/1241 (Envigo CRS S.A.)

EU/3/14/1241 (Active substance: Asp-Arg-Val-Tyr-Ile-His-Pro) - Transfer of orphan designation - Commission Decision (2019)2913 of Fri, 12 Apr 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000005424

Europe -DG Health and Food Safety

12-4-2019

EU/3/12/1002 (Envigo CRS S.A.)

EU/3/12/1002 (Envigo CRS S.A.)

EU/3/12/1002 (Active substance: Adenovirus-associated vector containing human Fas-c gene) - Transfer of orphan designation - Commission Decision (2019)2911 of Fri, 12 Apr 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000005423

Europe -DG Health and Food Safety

12-4-2019

EU/3/12/1093 (Regulis Consulting Europe Limited)

EU/3/12/1093 (Regulis Consulting Europe Limited)

EU/3/12/1093 (Active substance: 1,2:5,6-Dianhydrogalactitol) - Transfer of orphan designation - Commission Decision (2019)2919 of Fri, 12 Apr 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000005923

Europe -DG Health and Food Safety

12-4-2019

EU/3/15/1539 (Audentes Therapeutics Netherlands B.V.)

EU/3/15/1539 (Audentes Therapeutics Netherlands B.V.)

EU/3/15/1539 (Active substance: Adeno-associated viral vector serotype 8 containing the human MTM1 gene) - Transfer of orphan designation - Commission Decision (2019)2918 of Fri, 12 Apr 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000004956

Europe -DG Health and Food Safety

12-4-2019

EU/3/15/1588 (Regulis Consulting Europe Limited)

EU/3/15/1588 (Regulis Consulting Europe Limited)

EU/3/15/1588 (Active substance: (R)-1-[1-(4-acetoxy-3,3-dimethyl-2-oxo-butyl)-2-oxo-5-(pyridin-2-yl)-2,3-dihydro-1H-benzo[e][1,4]diazepin-3-yl]-3-(3-methylamino-phenyl)-urea) - Transfer of orphan designation - Commission Decision (2019)2917 of Fri, 12 Apr 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000005712

Europe -DG Health and Food Safety

12-4-2019

EU/3/07/452 (Regulis Consulting Europe Limited)

EU/3/07/452 (Regulis Consulting Europe Limited)

EU/3/07/452 (Active substance: R-1-[2,3-dihydro-2-oxo-1-pivaloylmethyl-5-(2-pyridyl)-1 H -1,4-benzodiazepin-3-yl]-3-(3-methylaminophenyl)urea) - Transfer of orphan designation - Commission Decision (2019)2916 of Fri, 12 Apr 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000005708

Europe -DG Health and Food Safety

12-4-2019


Referral: Lemtrada,  alemtuzumab, Article 20 procedures, Procedure started

Referral: Lemtrada,  alemtuzumab, Article 20 procedures, Procedure started

Referral: Lemtrada,  alemtuzumab, Article 20 procedures, Procedure started

Europe - EMA - European Medicines Agency

9-4-2019


Orphan designation: 9-cis, 12-cis-11,11-D2-linoleic acid ethyl ester, Treatment of infantile neuroaxonal dystrophy, 26/02/2019, Positive

Orphan designation: 9-cis, 12-cis-11,11-D2-linoleic acid ethyl ester, Treatment of infantile neuroaxonal dystrophy, 26/02/2019, Positive

Orphan designation: 9-cis, 12-cis-11,11-D2-linoleic acid ethyl ester, Treatment of infantile neuroaxonal dystrophy, 26/02/2019, Positive

Europe - EMA - European Medicines Agency

8-4-2019


Orphan designation: N-[(1R)-1-phenylethyl]-6-{1H-pyrazolo[3,4-d]pyrimidin-4-yl}quinazolin-2-amine, Treatment of fragile X syndrome, 20/04/2017, Positive

Orphan designation: N-[(1R)-1-phenylethyl]-6-{1H-pyrazolo[3,4-d]pyrimidin-4-yl}quinazolin-2-amine, Treatment of fragile X syndrome, 20/04/2017, Positive

Orphan designation: N-[(1R)-1-phenylethyl]-6-{1H-pyrazolo[3,4-d]pyrimidin-4-yl}quinazolin-2-amine, Treatment of fragile X syndrome, 20/04/2017, Positive

Europe - EMA - European Medicines Agency

3-4-2019

Submissions received: Fees and charges proposal 2019-20

Submissions received: Fees and charges proposal 2019-20

We thank those individuals and organisations who lodged submissions for their valuable contribution

Therapeutic Goods Administration - Australia

28-3-2019


20 years of sampling and testing of centrally authorised products: 1998 – 2017

20 years of sampling and testing of centrally authorised products: 1998 – 2017

20 years of sampling and testing of centrally authorised products: 1998 – 2017

Europe - EMA - European Medicines Agency

28-3-2019


20 years of sampling and testing programme for medicines authorised for the EU

20 years of sampling and testing programme for medicines authorised for the EU

20 years of sampling and testing programme for medicines authorised for the EU

Europe - EMA - European Medicines Agency

20-3-2019

EU/3/13/1154 (Diamond ROC EOOD)

EU/3/13/1154 (Diamond ROC EOOD)

EU/3/13/1154 (Active substance: Fosbretabulin tromethamine) - Transfer of orphan designation - Commission Decision (2019)2145 of Wed, 20 Mar 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000003817

Europe -DG Health and Food Safety

18-3-2019


Orphan designation: Human haptoglobin, Treatment of sickle cell disease, 09/12/2011, Positive

Orphan designation: Human haptoglobin, Treatment of sickle cell disease, 09/12/2011, Positive

Orphan designation: Human haptoglobin, Treatment of sickle cell disease, 09/12/2011, Positive

Europe - EMA - European Medicines Agency

18-3-2019


Orphan designation: Lomitapide, Treatment of familial chylomicronaemia, 17/12/2010, Positive

Orphan designation: Lomitapide, Treatment of familial chylomicronaemia, 17/12/2010, Positive

Orphan designation: Lomitapide, Treatment of familial chylomicronaemia, 17/12/2010, Positive

Europe - EMA - European Medicines Agency

15-3-2019


Orphan designation: Dantrolene sodium, Treatment of Wolfram syndrome, 12/12/2016, Positive

Orphan designation: Dantrolene sodium, Treatment of Wolfram syndrome, 12/12/2016, Positive

Orphan designation: Dantrolene sodium, Treatment of Wolfram syndrome, 12/12/2016, Positive

Europe - EMA - European Medicines Agency