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Latest Drugs
Cardiology Drug Data - A-Z (Espanol)
Drug Class Description
Betabloqueantes con otros antihipertensivosDrug Description
COMPRIMIDOSPresentation
Oral. Adultos: Dosis inicial: medio comprimido al día en una única toma. Al cabo de 7-14 días, puede aumentarse la dosis, en caso necesario a 1 comprimido al día o a medio comprimido 2 veces al día. Dosis de mantenimiento: 1 comprimido una vez al día.Indications
Tratamiento de la hipertensión arterial.Adult Dosage
Sustancia prohibida en el deporte de competición, susceptible de producir un resultado positivo en un control de dopaje.Contra Indications
Hipersensibilidad al medicamento. Trastornos de la conducción cardiaca. Insuficiencia cardiaca descompensada. Bradicardia sinusal, infarto agudo de miocardio. Insuficiencia hepática y/o renal grave. Embarazo y lactancia.Special Precautions
Precaución en pacientes con insuficiencia renal y/o hepática, accidentes vasculares cerebrales, trastornos electrolíticos, asma, diabetes, hiperuricemia e historial de gota. Evitar la suspensión brusca de tratamientos prolongados.Interactions
Puede modificar la acción de los hipoglucemiantes.Adverse Reactions
Ocasionalmente, frialdad de extremidades, fatiga muscular, náuseas, mareos hipoetnsión, cefalea, molestias gastrointestinales. Con tratamientos prolongados, riesgo hipokalemia. Excepcionalmente, reacciones alérgicas, discrasias sanguíneas, edema, depresión.Manufacturer
FIDES ECOPHARMAAdvert for Healthcare Professionals Only
Related News
New review of Cryoballoon Ablation treatment for Atrial Fibrillation Cardiology Page
A new research review comparing the efficacy and safety of cryoballoon ablation for Atrial Fibrillation finds that a single cryoballoon ablation procedure for paroxysmal AF results in high acute and medium-term efficacy rates, with lower success rates when used as stand-alone therapy for persistent AF. The rate of complications is relatively low and includes a 6.38% incidence of PNP, most of which is transient. The review also looks at results of the STOP-AF trial, which found that 70 percent of patients with Atrial Fibrillation who were treated with Medtronic's Arctic Fox cryoballoon ablation freezing technique are free of any heart rhythm irregularities one year out from having the procedure. (Heart Rhythm, Volume 8, Issue 9 , Pages 1444-1451, September 2011)
New Drug Eluting Stents safer for PCI patients Cardiology Page
Results from the SCAAR Study, presented at the European Society of Cardiology Congress 2011, showed that Percutaneous Coronary Intervention with "new generation" Drug Eluting Stents (DES), was associated with a 38% lower risk of clinically meaningful restenosis and a 50% lower risk of stent thrombosis compared to old generation DES. The SCAAR study evaluated the long-term outcome in all patients who underwent stent implantation with bare metal stents, "older generation" drug eluting stents, and "new generation" drug eluting stents in Sweden. Further studies are needed to discriminate which component of the new generation DES is involved in decreasing the incidence of stent thrombosis and restenosis.
EMA confirms risk benefit of Multaq Cardiology Page
EMA has confirmed a positive benefit-risk balance for Multaq (dronedarone) from Sanofi- Aventis for the treatment of a newly defined population of paroxysmal and persistent Atrial Fibrillation patients, following its review under the Article 20 procedure. A new indication for Multaq is: indicated for the maintenance of sinus rhythm after successful cardioversion in adult clinically stable patients with paroxysmal or persistent atrial fibrillation.
