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AMINOPLASMAL PO 12.5% SOLUTION FOR INFUSION

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About the medicine

How to use AMINOPLASMAL PO 12.5% SOLUTION FOR INFUSION

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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 elusuario

Aminoplasmal PO 12,5% solución para perfusión

Lea todo el prospecto detenidamente antes de empezar a usar el medicamento.

  • Conserve este prospecto, ya que puede tener que volver a leerlo.
  • Si tiene alguna duda, consulte a su médico o farmacéutico.
  • Este medicamento se le ha recetado a usted personalmente y no debe dárselo a otras personas aunque tengan los mismos síntomas, ya que puede perjudicarles.
    • Si considera que alguno de los efectos adversos que sufre es grave o si aprecia cualquier efecto adverso no mencionado en este prospecto, informe a su médico o farmacéutico.

Contenido del prospecto:

  1. Qué es Aminoplasmal PO 12,5% y para qué se utiliza
  2. Antes de usar Aminoplasmal PO 12,5%
  3. Cómo usar Aminoplasmal PO 12,5%
  4. Posibles efectos adversos
    1. Conservación de Aminoplasmal PO 12,5%
    2. Información adicional

1. Qué es Aminoplasmal PO 12,5% y para qué se utiliza

Aminoplasmal PO 12,5% es un suplemento nutricional de administración intravenosa, que contiene sustancias esenciales para las funciones del organismo.

Se utiliza para cubrir las necesidades de proteínas y líquido que necesita el organismo, después de intervenciones quirúrgicas y traumatismos.

La administración de esta solución deberá siempre combinarse con un aporte adecuado de calorías (soluciones de glucosa o emulsiones grasas).

Doctor consultation

Not sure if this medicine is right for you?

Discuss your symptoms and treatment with a doctor online.

2. Antes de usar Aminoplasmal PO 12,5%

No use Aminoplasmal PO 12,5%

  • Si es alérgico (hipersensible) a cualquiera de los componentes de Aminoplasmal PO 12,5%.
  • Si es alérgico a cualquier aminoácido

Tenga especial cuidado con Aminoplasmal PO 12,5%

Si usted tiene:

  • alguna anomalía congénita (problema que existe al nacer) del metabolismo (degradación) de los aminoácidos
  • enfermedad grave del hígado
  • alteración de la función del riñón con valores anormales en los niveles del nitrógeno residual
  • hipercaliemia (exceso de potasio en sangre)
  • hiperhidratación (exceso de agua en el organismo)
  • insuficiencia cardiaca manifiesta
  • sustancia ácidas acumuladas en su sangre (acidosis metabólica)

Aminoplasmal PO 12,5% No deberá usarse en prematuros y recién nacidos

Se debe controlar de forma regular que los niveles de fluidos y electrolitos, equilibrio ácido, sean correctos.

Duración máxima de la administración: hasta 7 días, después de una operación (estado post-operatorio) o después de un accidente (estado post-traumático).

Su médico debe controlar de forma regular que los niveles de fluidos y electrolitos, el azúcar en sangre, proteínas séricas, equilibrio ácido base y la función del hígado y del riñón, sean correctos.

Uso de otros medicamentos

Informe a su médico o farmacéutico si está utilizando o ha utilizado recientemente otros medicamentos, incluso los adquiridos sin receta.

Las soluciones de aminoácidos cono Aminoplasmal PO 12,5% no deben usarse como soluciones portadoras de otros medicamentos. Si se mezclan con otros medicamentos, pueden darse reacciones que podrían estropear la solución.

Embarazo y lactancia

No debe administrarse Aminoplasmal PO 12,5% durante los tres primeros meses del embarazo.

Durante el resto del embarazo su médico decidirá, después de valorar los posibles beneficios y los riesgos de la administración de Aminoplasmal PO 12,5%, si puede tomar este medicamento.

Consulte a su médico o farmacéutico antes de utilizar cualquier medicamento.

Conducción y uso de máquinas

No procede

3. Cómo usar Aminoplasmal PO 12,5% solución para perfusión

Su médico deberá determinar la cantidad que usted necesita diariamente. La dosis normal es de 8 – 16 ml por kg de su peso corporal y por día (de 1 a 2 g de aminoácidos por kg de peso corporal y día).

Para que el aprovechamiento de los aminoácidos sea óptimo se recomienda que se administre de forma simultánea a Aminoplasmal PO 12,5%, de 100 a 200 kcal por gramo de nitrógeno.

Siga exactamente las instrucciones de administración de Aminoplasmal PO 12,5% indicadas por su médico. Consulte a su médico o farmacéutico si tiene dudas.

Si usa más Aminoplasmal PO 12,5% del que debiera

Es poco probable que esto suceda ya que su doctor determinará sus dosis diarias. Sin embargo, si usted recibiera una sobredosis o se les administrara la solución de una forma demasiado rápida, usted puede perder parte de los aminoácidos por la orina, y puede sentir náuseas, escalofríos o vómitos. Estos síntomas desaparecerán tan pronto como se interrumpa la perfusión o se reduzca la velocidad de la misma.

Si ha utilizado mas Aminoplasmal PO 12,5% de lo que debe, consulte inmediatamente a su médico, farmacéutico o llame al servicio de Información Toxicológica. Teléfono 91-562 04 20. indicando el medicamento y la cantidad utilizada.

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

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, Aminoplasmal PO 12,5% solución puede causar efectos adversos, aunque no todas las personas los sufran.

La frecuencia de los efectos adversos se clasifica en las siguientes categorías:

Muy frecuentes

Al menos 1 de cada 10 pacientes

Frecuentes

Al menos 1 de cada 100 pacientes

Poco frecuentes

Al menos 1 de cada 1.000 pacientes

Raras

Al menos 1 de cada 10.000 pacientes

Muy raras

En menos de 1 de cada 10.000 pacientes, incluyendo notificaciones aisladas

Se han comunicado los siguientes efectos adversos cuando se administra Aminoplasmal PO 12,5% solución:

Trastornos gastrointestinales

Poco frecuentes: náuseas y vómitos

Trastornos generales y alteraciones en el lugar de administración:

Poco frecuentes: dolor de cabeza, escalofríos y fiebre.

A su vez si la administración de la solución se realiza demasiado rápida pueden aparecer aparte de las reacciones adversas descritas, pérdidas de aminoácidos por la orina con el consecuente desequilibrio en los niveles de los mismos.

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 Aminoplasmal 12,5% solución para perfusión

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

No requiere condiciones especiales de conservación. Conservar el envase en el embalaje exterior para protegerlo de la luz. No congelar.

No utilice Aminoplasmal PO 12,5% después de la fecha de caducidad que aparece en el envase. 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. 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. Información Adicional

Composición de Aminoplasmal PO 12,5%:

Por 1 ml

Por 500 ml

Isoleucina

6,000 mg

3,000 g

Leucina

10,500 mg

5,250 g

Lisina Acetato

(equivalente a lisina 9,24 mg)

13,038 mg

6,519 g

Metionina

2,500 mg

1,250 g

Fenilalanina

5,250 mg

2,625 g

Treonina

6,000 mg

3,000 g

Triptófano

2,500 mg

1,250 g

Valina

8,000 mg

4,000 g

Arginina

10,750 mg

5,375 g

Histidina

6,750 mg

3,375 g

Aminoacético ácido

8,750 mg

4,375 g

Alanina

15,500 mg

7,750 g

Prolina

8,750 mg

4,375 g

Ácido Aspártico

1,125 mg

0,562 g

Asparragina monohidrato

(equivalente a Asparragina 1,122 mg/ml)

1,275 mg

0,637 g

Acetilcisteína

(equivalente a Cisteína 0,73 mg/ml)

1,000 mg

0,500 g

Ácido Glutámico

11,250 mg

5,625 g

Ornitina clorhidrato

(equivalente a ornitina 2,25 mg/ml)

2,875 mg

1,437 g

Serina

4,000 mg

2,000 g

Acetiltirosina

(equivalente a Tirosina 2,50 mg/ml)

3,075 mg

1,537 g

Electrolitos

mmol/l

mEq/l

Cloruros

17

17

Acetatos

63,2

63,2

Aminoácidos Totales

123 g/l

Nitrógeno total

19 g/l

Equivalencia a proteína

121 g/l

Osmolaridad teórica

1026 mOsm/l

pH

5,0 – 7,5

AAE/AAT

0,4

Valor Energético

? 500 kcal/l

Los demás componentes son: ácido cítrico y agua para preparaciones inyectables.

Aspecto de producto y contenido del envase

Aminoplasmal PO 12,5% es una solución para perfusión clara, incolora o con ligero color pajizo que se presenta en frascos de vidrio, cerrados con tapones de goma.

Este medicamento se presenta en frascos de 500 ml.

Titular de la autorización de comercialización y responsable de la fabricación

Titular de la autorización de comercialización:

  • Braun Medical, S.A.

Ctra. de Terrassa, 121

08191-Rubí (Barcelona)

España

Responsable de la fabricación:

  • Braun Melsungen AG

Carl-Braun Straße, 1

34212 Melsungen

Alemania

Este prospecto ha sido aprobado en Junio 2015.

La información detallada de este medicamento está disponible en la página Web de la Agencia Española de Medicamentos y Productos Sanitarios.

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Esta información está destinada únicamente a médicos o profesionales del sector sanitario:

Envases para un solo uso. Desechar el contenido remanente no utilizado tras finalizar la perfusión.

Sólo debe usarse la solución si el cierre del envase no está dañado y la solución es clara.

Usar el set de administración estéril para la administración.

Si en la nutrición parenteral completa es necesario añadir a este medicamento otros nutrientes como carbohidratos, lípidos, vitaminas y oligoelementos, la adición se debe realizar bajo estrictas condiciones de asepsia. Mezclar bien tras la inclusión de cualquier aditivo. Prestar especial atención a la compatibilidad.

La eliminación del medicamento no utilizado y de todos los materiales que hayan estado en contacto con él, se realizará de acuerdo con la normativa local.

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Frequently Asked Questions

Is a prescription required for AMINOPLASMAL PO 12.5% SOLUTION FOR INFUSION?
AMINOPLASMAL PO 12.5% SOLUTION FOR INFUSION 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 AMINOPLASMAL PO 12.5% SOLUTION FOR INFUSION?
The active ingredient in AMINOPLASMAL PO 12.5% SOLUTION FOR INFUSION is amino acids. This information helps identify medicines with the same composition but different brand names.
Who manufactures AMINOPLASMAL PO 12.5% SOLUTION FOR INFUSION?
AMINOPLASMAL PO 12.5% SOLUTION FOR INFUSION is manufactured by B Braun Medical S.A.. Pharmacy brands and packaging may differ depending on the distributor.
Which doctors can assess the use of AMINOPLASMAL PO 12.5% SOLUTION FOR INFUSION 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 AMINOPLASMAL PO 12.5% SOLUTION FOR INFUSION 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 AMINOPLASMAL PO 12.5% SOLUTION FOR INFUSION?
Other medicines with the same active substance (amino acids) include AMINOPLASMAL B.BRAUN 10% E SOLUTION FOR INFUSION, AMINOPLASMAL B.BRAUN 10% SOLUTION FOR INFUSION, AMINOPLASMAL B.BRAUN 15% SOLUTION FOR INFUSION. 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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