ENALAPRIL

Informació principal

  • Denominació comercial:
  • ENALAPRIL BELMAC 10 mg 500 comprimidos
  • formulario farmacéutico:
  • Comprimidos
  • Vía de administración:
  • Oral
  • Utilitza per:
  • Humans
  • Tipo de medicina:
  • medicament al·lopàtic

Documents

Localització

  • Disponible en:
  • ENALAPRIL BELMAC 10 mg 500 comprimidos
    Andorra
  • Idioma:
  • català

Altres dades

Estat

  • Font:
  • CedimCat - Centre d'Informació de Medicaments de Catalunya
  • Número d'autorització:
  • 619346
  • última actualització:
  • 07-06-2018

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

ENALAPRIL BELMAC 10 mg 500 comprimidos

enalapril

Indicacions

Medicament que dilata els vasos sanguinis i normalitza la pressi

sangu

nia (ANTIHIPERTENSIU).

Consideracions

Prengui els comprimits 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'aconsella que prengui aquest medicament sempre en les mateixes condicions per tal d'augmentar la seva

efic

cia.

Prengui aquest medicament sempre a la mateixa hora.

Segueixi estrictament la pauta indicada pel seu metge pel que fa a dosi i freq

眉猫

ncia d'administraci

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

Si fa molt temps que pren aquest medicament, NO deixi de prendre-ho de forma brusca sense consultar-

ho abans amb el seu metge.

Avisi el seu metge si pateix intoler

ncia a alguns sucres o diabetis.

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

, problemes de fetge o problemes de cor.

Aquest medicament modifica l'acci

d'altres f

rmacs, NO prengui altres medicaments sense consultar

abans al seu metge o farmac

utic.

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

seguir per augmentar l'efic

cia d'aquest medicament.

Procuri NO fumar, NO abusar de begudes alcoh

liques NI de begudes amb cafe

na (caf

, te,

refrescs de cola) NI prendre salses picants NI menjars irritants i seguir la dieta especial que el seu metge

li recomani, 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.

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

Aquest medicament pot modificar el resultat d'algunes an

lisis de sang.

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

Interrompi immediatament el tractament i AVISI al seu metge si durant el tractament apareix inflor i

envermelliment dels llavis, la llengua i la cara.

Avisi el seu metge si durant el tractament apareix tos seca, dolor abdominal, dificultat per respirar, una

coloraci

groguenca a la pell o als ulls, febre o mal de gola.

Aquest medicament pot produir mol

sties gastrointestinals (n

usees, v

mits, etc.), mal de cap, visi

borrosa i erupcions cut

nies.

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.

VIA ORAL.

23-7-2018

FDA continues taking key actions on bulk drug substances used for compounding to advance the regulatory framework governing compounded drugs and to protect patients

FDA continues taking key actions on bulk drug substances used for compounding to advance the regulatory framework governing compounded drugs and to protect patients

FDA continues making progress on bulk drug substances for compounding

FDA - U.S. Food and Drug Administration

28-6-2018

Statement from FDA Commissioner Scott Gottlieb, M.D., on agency’s continued efforts relating to compounded drugs for patients who cannot use an FDA-approved drug

Statement from FDA Commissioner Scott Gottlieb, M.D., on agency’s continued efforts relating to compounded drugs for patients who cannot use an FDA-approved drug

Statement from FDA Commissioner Scott Gottlieb, M.D., on agency’s continued efforts relating to compounded drugs for patients who cannot use an FDA-approved drug

FDA - U.S. Food and Drug Administration

16-5-2018

FDA Drug Safety Communication: FDA warns that gadolinium-based contrast agents (GBCAs) are retained in the body; requires new class warnings

FDA Drug Safety Communication: FDA warns that gadolinium-based contrast agents (GBCAs) are retained in the body; requires new class warnings

FDA is requiring a new class warning and other safety measures for all gadolinium-based contrast agents (GBCAs) for magnetic resonance imaging (MRI) concerning gadolinium remaining in patients’ bodies, including the brain, for months to years after receiving these drugs. Gadolinium retention has not been directly linked to adverse health effects in patients with normal kidney function, and we have concluded that the benefit of all approved GBCAs continues to outweigh any potential risks.

FDA - U.S. Food and Drug Administration

15-3-2019

#FDA CDRH is responsible for protecting and promoting the public health.  We assure that patients and providers have timely and continued access to safe, effective, and high-quality medical devices and safe radiation-emitting products.  #MedicalDevice

#FDA CDRH is responsible for protecting and promoting the public health. We assure that patients and providers have timely and continued access to safe, effective, and high-quality medical devices and safe radiation-emitting products. #MedicalDevice

#FDA CDRH is responsible for protecting and promoting the public health. We assure that patients and providers have timely and continued access to safe, effective, and high-quality medical devices and safe radiation-emitting products. #MedicalDevice

FDA - U.S. Food and Drug Administration

20-2-2019


Opinion/decision on a Paediatric investigation plan (PIP): Enalapril (maleate), decision type: , therapeutic area: , PIP number: P/0357/2018

Opinion/decision on a Paediatric investigation plan (PIP): Enalapril (maleate), decision type: , therapeutic area: , PIP number: P/0357/2018

Opinion/decision on a Paediatric investigation plan (PIP): Enalapril (maleate), decision type: , therapeutic area: , PIP number: P/0357/2018

Europe - EMA - European Medicines Agency

19-12-2018


Enalapril: List of nationally authorised medicinal products - PSUSA/00001211/201803

Enalapril: List of nationally authorised medicinal products - PSUSA/00001211/201803

Enalapril: List of nationally authorised medicinal products - PSUSA/00001211/201803

Europe - EMA - European Medicines Agency

26-11-2018

It would also help make sure that newer devices reflect more modern technologies and standards that can improve patient care and outcomes. It would help the overall product environment continue to evolve in the direction toward safer, more effective devic

It would also help make sure that newer devices reflect more modern technologies and standards that can improve patient care and outcomes. It would help the overall product environment continue to evolve in the direction toward safer, more effective devic

It would also help make sure that newer devices reflect more modern technologies and standards that can improve patient care and outcomes. It would help the overall product environment continue to evolve in the direction toward safer, more effective devices.

FDA - U.S. Food and Drug Administration

13-11-2018

#DYK November is #DiabetesAwarenessMonth. As the number of people diagnosed with diabetes continues to grow, @US_FDA  encourages patients and caregivers to beware of illegally markets  diabetes treatments. Check out our Consumer Update on this issue  http

#DYK November is #DiabetesAwarenessMonth. As the number of people diagnosed with diabetes continues to grow, @US_FDA encourages patients and caregivers to beware of illegally markets diabetes treatments. Check out our Consumer Update on this issue http

#DYK November is #DiabetesAwarenessMonth. As the number of people diagnosed with diabetes continues to grow, @US_FDA encourages patients and caregivers to beware of illegally markets diabetes treatments. Check out our Consumer Update on this issue https://go.usa.gov/xPfDx  pic.twitter.com/OGwOusdP1w

FDA - U.S. Food and Drug Administration

22-7-2018

Even when Essure is no longer sold, the #FDA will remain vigilant in protecting patients who’ve already had this device implanted. We’ll continue to monitor adverse events and publicly communicate any new safety findings on this - and any other device. ht

Even when Essure is no longer sold, the #FDA will remain vigilant in protecting patients who’ve already had this device implanted. We’ll continue to monitor adverse events and publicly communicate any new safety findings on this - and any other device. ht

Even when Essure is no longer sold, the #FDA will remain vigilant in protecting patients who’ve already had this device implanted. We’ll continue to monitor adverse events and publicly communicate any new safety findings on this - and any other device. https://www.bloomberg.com/news/articles/2018-07-20/bayer-to-stop-selling-contraceptive-implant-after-threats-by-fda …

FDA - U.S. Food and Drug Administration