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CONDROITIN SULFATE ABAMED 400 mg ORAL SOLUTION GRANULES

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This page is for general information. Consult a doctor for personal advice. Call emergency services if symptoms are severe.
About the medicine

How to use CONDROITIN SULFATE ABAMED 400 mg ORAL SOLUTION GRANULES

Translated with AI

This page provides general information and does not replace a doctor’s consultation. Always consult a doctor before taking any medication. Seek urgent medical care if symptoms are severe.

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Introducción

Prospecto: Información para el usuario

Condroitina sulfato Abamed 400 mg granulado para solución oral

Sulfato sódico de condroitina

Lea todo el prospecto detenidamente antes de empezar a tomar el medicamento, porque contiene información importante para usted.

  • Conserve este prospecto, ya que puede tener que volver a leerlo.
  • Si tiene alguna duda, consulte a su médico, farmacéutico o enfermero.
  • Este medicamento se le ha recetado solamente a usted, y no debe dárselo a otras personas, aunque tengan los mismos síntomas que usted, ya que puede perjudicarles.
  • Si experimenta efectos adversos, consulte a su médico, farmacéutico o enfermero, incluso si se trata de efectos adversos que no aparecen en este prospecto. Ver sección 4.

Contenido del prospecto:

  1. Qué es Condroitina sulfato Abamed y para qué se utiliza
  2. Qué necesita saber antes de empezar a tomar Condroitina sulfato Abamed
  3. Cómo tomar Condroitina sulfato Abamed
  4. Posibles efectos adversos
  5. Conservación de Condroitina sulfato Abamed
  6. Contenido del envase e información adicional

1. Qué es Condroitina sulfato Abamed y para qué se utiliza

Este medicamento está indicado en el tratamiento sintomático de la artrosis. Pertenece al grupo de los antiinflamatorios y antirreumáticos no esteroideos.

Doctor consultation

Not sure if this medicine is right for you?

Discuss your symptoms and treatment with a doctor online.

2. Qué necesita saber antes de empezar a tomar Condroitina sulfato Abamed

No tomeCondroitina sulfato Abamed

  • Si es alérgico (hipersensible) a sulfato sódico de condroitina o a cualquiera de los demás componentes de este medicamento.

Advertencias y precauciones

Consulte a su médico o farmacéutico antes de empezar a tomar este medicamento.

  • Tenga precaución si padece alguna enfermedad grave del riñón, del hígado o del corazón.

Uso deCondroitina sulfato Abamedcon otros medicamentos

Informe a su médico o farmacéutico si está tomando, ha tomado recientemente o podría tener que tomar cualquier otro medicamento.

La administración de sulfato sódico de condroitina a dosis muy superiores a las recomendadas, junto con algún medicamento antiagregante plaquetario para prevenir la trombosis, tales como ácido acetilsalicílico, dipiridamol, clopidrogel, ditazol, trifusal y ticlopidina, puede aumentar levemente el efecto de los medicamentos anteriormente citados.

Embarazo, lactancia y fertilidad

No se recomienda tomar este medicamento ni durante el embarazo ni durante la lactancia.

Conducción y uso de máquinas

No es de esperar que sulfato sódico de condroitina afecte a la capacidad de conducir vehículos y utilizar máquinas.

Condroitina sulfato Abamed contiene amarillo anaranjado S (E-110), sodio y sorbitol (E-420):

Este medicamento puede producir reacciones alérgicas porque contiene amarillo anaranjado S (E-110). Puede provocar asma, especialmente en pacientes alérgicos al ácido acetilsalicílico.

Este medicamento contiene sorbitol (E-420). Si su médico le ha indicado que padece una intolerancia a ciertos azúcares, consulte con él antes de tomar este medicamento.

Los pacientes con dietas pobres en sodio deben tener en cuenta que este medicamento contiene 37,97 mg (1,65 mmol) de sodio por sobre.

3. Cómo tomar Condroitina sulfato Abamed

Siga exactamente las instrucciones de administración de este medicamento indicadas por su médico. Su médico le indicará la duración de su tratamiento con sulfato sódico de condroitina.

En caso de duda, consulte de nuevo a su médico o farmacéutico. Recuerde tomar su medicamento.

La dosis recomendada es de 2 sobres (dosis diaria total de sulfato sódico de condroitina: 800 mg)) al día, preferiblemente en una sola toma (2 sobres a la vez) durante al menos 3 meses. No obstante, en pacientes con sintomatología inflamatoria importante, y siempre que el médico lo considere oportuno, podrá iniciarse el tratamiento con una dosis de 1.200 mg (3 sobres al día, en una sola toma o en 2 tomas) durante las primeras 4 ó 6 semanas para seguir con 800 mg (2 sobres al día preferiblemente en una sola toma) hasta completar el periodo de administración de al menos 3 meses.

El tratamiento se administrará como mínimo durante 3 meses, tras los cuales se realizará un período de descanso de 2 meses, para posteriormente volver a reiniciar el tratamiento siguiendo el mismo ciclo.

Verter el contenido de los sobres en un vaso y disolverlo en un poco de agua antes de su administración. La toma puede realizarse antes, durante o después de las comidas.

Si toma másCondroitina sulfato Abamed del que debe

En caso de sobredosis o ingesta accidental, consulte inmediatamente a su médico, farmacéutico o llame al Servicio de Información Toxicológica, al teléfono 91 562 04 20, indicando el medicamento y la cantidad ingerida.

Si olvidó tomarCondroitina sulfato Abamed

No tome una dosis doble para compensar las dosis olvidadas.

Si interrumpe el tratamiento conCondroitina sulfato Abamed

No suspenda el tratamiento antes, ya que su eficacia podría verse reducida.

Si tiene cualquier otra duda sobre el uso de este medicamento, pregunte a su médico, farmacéutico o enfermero.

Medicine questions

Started taking the medicine and have questions?

Discuss your symptoms and treatment with a doctor online.

4. Posibles efectos adversos

Al igual que todos los medicamentos, este medicamento puede producir efectos adversos, aunque no todas las personas los sufran.

En raras ocasiones (pueden afectar hasta 1 de cada 10.000 personas) se ha descrito la aparición de náuseas y/o alteraciones gastrointestinales, que generalmente no requieren la suspensión del tratamiento.

En muy raras ocasiones (pueden afectar hasta 1 de cada 10.000 personas), en pacientes con insuficiencia renal y/o cardiaca, se ha descrito algún caso de edema y/o retención de agua.

En muy raras ocasiones (pueden afectar hasta 1 de cada 10.000 personas) se ha comunicado alguna reacción de tipo alérgico.

Comunicación de efectos adversos

Si experimenta cualquier tipo de efecto adverso, consulte a su médico o farmacéutico, incluso si se trata de posibles efectos adversos que no aparecen en este prospecto. También puede comunicarlos directamente a través del Sistema Español de Farmacovigilancia de Medicamentos de Uso Humano: www.notificaRAM.es. Mediante la comunicación de efectos adversos usted puede contribuir a proporcionar más información sobre la seguridad de este medicamento.

5. Conservación de Condroitina sulfato Abamed

Mantener este medicamento fuera de la vista y del alcance de los niños.

No requiere condiciones especiales de conservación.

No utilice este medicamento después de la fecha de caducidad que aparece en el envase después de “CAD.:”. La fecha de caducidad es el último día del mes que se indica.

Los medicamentos no se deben tirar por los desagües ni a la basura. Deposite los envases y los medicamentos que no necesita en el Punto SIGRE de su farmacia habitual. Pregunte a su farmacéutico cómo deshacerse de los envases y de los medicamentos que no necesita. De esta forma, ayudará a proteger el medio ambiente.

6. Contenido del envase e información adicional

Composición deCondroitina sulfato Abamed

  • El principio activo es sulfato sódico de condroitina. Cada sobre contiene 400 mg de sulfato sódico de condroitina.
  • Los demás componentes (excipientes) son: ácido cítrico anhidro, aroma de naranja, sacarina sódica, amarillo anaranjado S (E110), sílice coloidal anhidra y sorbitol.

Aspecto del producto y contenido del envase

Este medicamento se presenta en forma de granulado anaranjado para solución oral. Cada envase contiene 60 sobres (contiene 2 cajas de 30 sobres).

Titular de la autorización de comercialización y responsable de la fabricación.

Titular

Qualix Pharma, S.L.

C/ Botánica 137-139

08908 L’Hospitalet de Llobregat

(Barcelona)

España

Fabricante

Kern Pharma S.L.

Polígono Ind. Colón II

Venus, 72

08228 Terrassa

(Barcelona)

Fecha de la última revisión de este prospecto:Noviembre 2015.

La información detallada y actualizada de este medicamento está disponible en la página Web de la Agencia Española del Medicamento y Productos Sanitarios (AEMPS) www.aemps.gob.es/

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Frequently Asked Questions

Is a prescription required for CONDROITIN SULFATE ABAMED 400 mg ORAL SOLUTION GRANULES?
CONDROITIN SULFATE ABAMED 400 mg ORAL SOLUTION GRANULES requires a prescription in Spain. You can check with a doctor online whether this medicine may be appropriate for your situation.
What is the active substance in CONDROITIN SULFATE ABAMED 400 mg ORAL SOLUTION GRANULES?
The active ingredient in CONDROITIN SULFATE ABAMED 400 mg ORAL SOLUTION GRANULES is chondroitin sulfate. This information helps identify medicines with the same composition but different brand names.
Who manufactures CONDROITIN SULFATE ABAMED 400 mg ORAL SOLUTION GRANULES?
CONDROITIN SULFATE ABAMED 400 mg ORAL SOLUTION GRANULES is manufactured by Qualix Pharma S.L.. Pharmacy brands and packaging may differ depending on the distributor.
Which doctors can assess the use of CONDROITIN SULFATE ABAMED 400 mg ORAL SOLUTION GRANULES online?
Doctors such as Family doctors, Psychiatrists, Dermatologists, Cardiologists, Endocrinologists, Gastroenterologists, Pulmonologists, Nephrologists, Rheumatologists, Hematologists, Infectious disease physicians, Allergists, Geriatricians, Paediatricians, Oncologists may assess whether CONDROITIN SULFATE ABAMED 400 mg ORAL SOLUTION GRANULES is appropriate, depending on your situation and local regulations. You can book an online consultation to discuss your symptoms and possible next steps.
What are the alternatives to CONDROITIN SULFATE ABAMED 400 mg ORAL SOLUTION GRANULES?
Other medicines with the same active substance (chondroitin sulfate) include CONDRODIN 400 HARD CAPSULES, CONDROITIN SULFATE ABAMED 400 mg HARD CAPSULES, CONDROITIN SULFATE KERN PHARMA 400 mg HARD CAPSULES. These may have different brand names or formulations but contain the same therapeutic ingredient. Always consult a doctor before switching or starting a new medicine.
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