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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 ACICLOVIR TEDEC 25 mg/ml 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 EL USUARIO

Aciclovir TEDEC 25 mg/ml solución para perfusión EFG

Lea todo el prospecto detenidamente antes de empezar a usar este 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 o farmacéutico.
  • Este medicamento se le ha recetado solamente a usted y no debe dárselo a otras personas, aunque tengan los mismo síntomas que usted, ya que puede perjudicarles.
  • Si experimenta efectos adversos consulte a su médico o farmacéutico, incluso si se trata de efectos adversos que no aparecen en este prospecto. Ver sección 4.

Contenido del prospecto:

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

1. Qué es Aciclovir Tedec y para qué se utiliza

Aciclovir pertenece al grupo farmacoterapéutico de los antivirales activos contra herpes virus.

Este medicamento está indicado en:

  • Tratamiento de infecciones por virus herpes simple.
  • Prevención de infecciones por virus herpes simple en pacientes inmunocomprometidos.
  • Tratamiento de pacientes inmunodeprimidos con herpes zóster, especialmente en infecciones cutáneas progresivas o diseminadas.
  • Tratamiento de infecciones por el virus herpes simple en neonatos.
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 usar Aciclovir Tedec

No use Aciclovir Tedec :

  • Si es alérgico a aciclovir, valaciclovir, ganciclovir o a cualquiera de los demás componentes de este medicamento (incluidos en la sección 6).

Advertencias y precauciones

Consulte a su médico o farmacéutico antes de empezar a usar aciclovir :

  • Si padece alguna enfermedad de riñón o tiene usted edad avanzada, es posible que su médico utilice una dosis más baja. Asimismo, debe beber suficiente cantidad de líquido durante el tratamiento para mantener una hidratación adecuada.
  • Si se utiliza en pacientes que hayan sido sometidos a trasplantes renales, su médico debe vigilar la función renal, ya que puede producirse un ligero aumento de la creatinina o de la urea sérica que podría confundirse con una reacción de rechazo.

Consulte a su médico, incluso si alguna de las circunstancias anteriormente mencionadas le hubiera ocurrido alguna vez.

Otros medicamentos y Aciclovir Tedec

Informe a su médico o farmacéutico si está utilizando, o ha utilizado recientemente o podría tener que utilizar cualquier otro medicamento.

Embarazo, lactancia y fertilidad

Si está embarazada o en periodo de lactancia, cree que podría estar embarazada o tiene intención de quedarse embarazada, consulte a su médico o farmacéutico antes de utilizar este medicamento.

No se ha demostrado la seguridad de este medicamento en mujeres embarazadas, solo se utilizará en aquellos casos en que la valoración del beneficio/riesgo por parte de su médico aconseje su uso.

Aciclovir se excreta por leche materna.

Conducción y uso de máquinas

No se dispone de datos que limiten esta actividad.

Aciclovir Tedeccontiene sodio y metabisulfito de sodio

Este medicamento contiene 39,3 mg de sodio (componente principal de la sal de mesa/para cocinar) en cada ampolla. Esto equivale al 1,965% de la ingesta diaria máxima de sodio recomendada para un adulto.

Este medicamento puede producir reacciones alérgicas graves y broncoespasmo (sensación repentina de ahogo) porque contiene metabisulfito de sodio.

3. Cómo usar Aciclovir Tedec

Siga exactamente las instrucciones de administración de este medicamento indicadas por su médico. En caso de duda consulte de nuevo a su médico o farmacéutico.

Recuerde usar su medicamento.

Este medicamento y su forma de administración le ha sido prescrito exclusivamente a usted. No debe darlo nunca a otras personas ni ser utilizado para otros tipos de trastornos.

Su médico le indicará la dosis y la duración de su tratamiento con aciclovir intravenoso. En infecciones agudas por virus herpes simple, 5 días de tratamiento suele ser lo adecuado, no obstante la duración del tratamiento dependerá de la gravedad de la infección, estado del enfermo y respuesta al tratamiento. El tratamiento de la encefalitis herpética y del herpes simple neonatal normalmente tiene 10 días de duración. La duración de la administración profiláctica de aciclovir intravenoso se determinará por la duración del período de riesgo.

La dosis recomendada es:

Adultos

Función renal normal

Pacientes con infecciones por virus herpes simple (excepto encefalitis herpética) o virus varicela zóster: dosis de 5 mg/kg, cada 8 horas.

Pacientes inmunocomprometidos con infecciones producidas por virus varicela zóster o con encefalitis herpética: dosis de 10 mg/kg, cada 8 horas.

Función renal alterada

La administración de aciclovir intravenoso en pacientes con la función renal alterada debe ser realizada con precaución.

Se recomiendan las siguientes modificaciones en caso de disfunción renal:

Aclaramiento de creatinina

(ml/min)

Dosis original

Dosis ajustada

25 – 50

5 mg/kg cada 8 horas

10 mg/kg cada 8 horas

5 mg/kg cada 12 horas

10 mg/kg cada 12 horas

10 – 25

5 mg/kg cada 8 horas

10 mg/kg cada 8 horas

5 mg/kg cada 24 horas

10 mg/kg cada 24 horas

0 – 10

5 mg/kg cada 8 horas

10 mg/kg cada 8 horas

2,5 mg/kg cada 24 horas

5 mg/kg cada 24 horas

después de la diálisis

Uso en niñosy adolescentes

La dosis de aciclovir intravenoso para niños entre 3 meses y 12 años se calcula en base a la superficie corporal.

Niños con infecciones producidas por virus herpes simple o varicela zóster: dosis de 250 mg/m2 de superficie corporal, cada 8 horas.

Niños inmunocomprometidos con varicela zóster o niños con encefalitis herpética: dosis de 500 mg/m2 de superficie corporal, cada 8 horas.

Los niños con función renal alterada requieren unas modificaciones apropiadas de acuerdo al grado de alteración.

La dosis de aciclovir en neonatos (herpes simple): 10 mg/kg cada 8 horas.

Uso en pacientes de edad avanzada

Se deberá reducir la dosis en aquellos pacientes que padezcan insuficiencia renal.

Si estima que la acción de aciclovir es demasiado fuerte o débil, comuníqueselo a su médico.

Si usa más Aciclovir Tedec del que debe

Si usted ha usado una dosis más alta de la debida, consulte inmediatamente a su médico o farmacéutico. En la administración de dosis únicas de hasta 80 mg/kg no se han observado efectos secundarios. Aciclovir intravenoso es dializable.

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

Si olvidó usarAciclovir Tedec

No administre una dosis doble para compensar las dosis olvidadas.

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.

Algunos pacientes tratados con aciclovir intravenoso han presentado los siguientes síntomas: aumento de los enzimas hepáticos, disminución de los índices hematológicos, erupciones y fiebre, náuseas y vómitos.

Trastornos del sistema nervioso: agitación, confusión, temblor, dificultad de movimientos, dificultad al hablar, confusión o imaginación de cosas (alucinaciones), convulsiones, somnolencia, encefalopatía (alteración del cerebro), coma. Estos efectos son generalmente reversibles y normalmente aparecieron en pacientes con alteraciones renales o con factores predisponentes.

En algunos pacientes se observó un aumento rápido y reversible de los niveles sanguíneos de urea o creatinina, circunstancia que se cree debida a los altos niveles plasmáticos del fármaco y al estado de hidratación de los pacientes. Por ello, es imprescindible que el nivel de hidratación sea el adecuado.

Comunicación de efectos adversos

Si experimenta cualquier tipo de efectos 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: https://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 Aciclovir Tedec

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

Antes de la dilución: No requiere condiciones especiales de conservación.

Después de la dilución: El período de validez de este medicamento después de su dilución es de 8 horas a 25ºC y 24 horas a 2-8ºC.

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.

6. Contenido del envase e información adicional

Composición de Aciclovir Tedec

El principio activo es aciclovir. Cada ampolla contiene 250 mg de aciclovir.

Los demás componentes (excipientes) son: metabisulfito de sodio (E-223), hidróxido de sodio, citrato de sodio (E-331), ácido clorhídrico, agua para preparaciones inyectables y nitrógeno.

Aspecto del producto y contenido del envase

Aciclovir Tedec 25 mg/ml es una solución para perfusión. Se presenta en ampollas de vidrio blanco. La solución es un líquido transparente incoloro o amarillo pálido. Cada envase contiene 5 ampollas. También se presenta en envase clínico de 50 ampollas.

Titular de la autorización de comercialización y responsable de la fabricación

Meiji Pharma Spain, S.A.

Avda. de Madrid, 94

28802 Alcalá de Henares, Madrid (España)

Fecha de la última revisión de este prospecto: mayo 2021

Otras fuentes de información

La información detallada de este medicamento está disponible en la página web de la Agencia Española de Medicamentos y Productos Sanitarios (AEMPS) https://www.aemps.gob.es

--------------------------------------------------------------------------------------------------------------------------------

Esta información está destinada únicamente a profesionales del sector sanitario

La solución se debe administrar únicamente por vía intravenosa y de manera continua pero muy lenta, de tal modo que se administre en un periodo no inferior a una hora.

Si procede, se recomienda hacer la dilución inmediatamente antes de ser utilizada. La solución no utilizada deberá desecharse. En caso de aparecer turbidez visible o cristalización antes o durante la infusión, la solución deberá ser rechazada.

Forma de administración

Perfusión intravenosa sin dilución:

La solución se administra mediante una bomba de perfusión de ritmo controlado, en un período no inferior a una hora.

Perfusión con dilución:

La solución puede ser diluida para su administración mediante perfusión. La dilución se hace total o parcialmente, según la dosis necesaria, adicionándola y mezclándola como mínimo con 50 ml de solución infusora, para obtener una solución de concentración máxima del 0,5% (250 mg/50 ml). El contenido de 2 ampollas (500 mg de aciclovir) puede adicionarse a 100 ml de solución infusora, y en el caso de que la dosis requerida sea superior a 500 mg se puede utilizar un segundo volumen de solución infusora.

Este medicamento es compatible con las siguientes soluciones:

  • Cloruro de sodio (0,45%, 0,9% p/v).
    • Cloruro de sodio (0,18% p/v) y glucosa (4% p/v).
    • Cloruro de sodio (0,45 % p/v) y glucosa (2,5% p/v)
    • Lactato de sodio (solución Hartmann)

Se debe agitar enérgicamente para asegurar una perfecta mezcla.

Tras la inyección accidental de aciclovir intravenoso, puede aparecer una grave inflamación en el tejido extravascular, a veces seguida de ulceraciones. La perfusión mediante bombas mecánicas posee mayores riesgos que la perfusión por gravedad. Puede producirse flebitis e inflamación en el lugar de la perfusión.

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Experience and qualifications:

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If you are unsure about a diagnosis, preparing for surgery, or want to discuss your test results – Dr Yakovenko will help you evaluate your options and move forward with confidence.

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Lina Travkina

Family medicine 13 years exp.

Dr. Lina Travkina is a licensed family and preventive medicine doctor based in Italy. She provides online consultations for adults and children, supporting patients across all stages of care – from acute symptom management to long-term health monitoring and prevention.

Areas of medical care include:

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Antonio Cayatte

General medicine 44 years exp.

Dr Antonio Cayatte is a physician in General and Acute Medicine with over 30 years of experience across clinical care, medical research, and education. He offers online consultations for adults with a wide range of symptoms, both acute and chronic. His clinical background includes: 

  • assessment of sudden or unclear symptoms
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Dr. Antonio Cayatte provides comprehensive care for a broad spectrum of common health concerns, including:

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Sviatoslav Chekhun

Oncology 13 years exp.

Dr. Sviatoslav Chekhun is a medical oncologist with international clinical and research experience, specializing in modern medical oncology and a personalized approach to cancer treatment.

Currently (since 2025), he works as a Medical Oncologist at Institut Català d’Oncologia (Girona, Spain). Previously, he completed his residency in Medical Oncology and was involved in clinical research at Hospital Universitari Germans Trias i Pujol.

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Earlier in his career, he worked as a medical oncologist at the Kyiv City Clinical Oncological Center and contributed to regulatory evaluation of medicinal products at the State Expert Center of the Ministry of Health of Ukraine.

When to consult Dr. Chekhun:

  •  for diagnosis or clarification of a cancer diagnosis
  •  to obtain a second opinion on an existing treatment plan 
  •  when you need a personalized treatment strategy 
  •  for interpretation of test results, CT, MRI, PET-CT, and biopsies 
  •  when choosing between treatment options (chemotherapy, targeted therapy, immunotherapy) 
  •  in case of doubts about treatment strategy or disease progression 

Consultation format

Dr. Chekhun provides online consultations, where you can receive:

  •  expert second opinion 
  •  detailed case review 
  •  recommendations based on current international treatment guidelines 
  •  personalized treatment and follow-up plan 

Important:
Prescription and monitoring of medications must be carried out by your treating physician in an in-person (offline) setting. An online consultation does not replace a face-to-face visit but helps you make more informed decisions about your treatment.

Dr. Sviatoslav Chekhun combines clinical practice, research, and international experience, enabling him to provide patients with modern, evidence-based approaches in oncology.

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Frequently Asked Questions

Is a prescription required for ACICLOVIR TEDEC 25 mg/ml SOLUTION FOR INFUSION?

ACICLOVIR TEDEC 25 mg/ml 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 ACICLOVIR TEDEC 25 mg/ml SOLUTION FOR INFUSION?

The active ingredient in ACICLOVIR TEDEC 25 mg/ml SOLUTION FOR INFUSION is aciclovir. This information helps identify medicines with the same composition but different brand names.

Who manufactures ACICLOVIR TEDEC 25 mg/ml SOLUTION FOR INFUSION?

ACICLOVIR TEDEC 25 mg/ml SOLUTION FOR INFUSION is manufactured by Meiji Pharma Spain S.A.. Pharmacy brands and packaging may differ depending on the distributor.

Which doctors can assess the use of ACICLOVIR TEDEC 25 mg/ml 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 ACICLOVIR TEDEC 25 mg/ml 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.

How to buy ACICLOVIR TEDEC 25 mg/ml SOLUTION FOR INFUSION in Spain?

Spain has a well-developed healthcare infrastructure across major cities such as Madrid, Barcelona, Valencia, and Seville. Pharmacies are widely available and operate under strict regulations, ensuring access to prescribed medications.

You can buy ACICLOVIR TEDEC 25 mg/ml SOLUTION FOR INFUSION in Madrid, Barcelona, Seville, or Valencia at any local pharmacy with a valid prescription.

To obtain a prescription, you can use Oladoctor:

What are the alternatives to ACICLOVIR TEDEC 25 mg/ml SOLUTION FOR INFUSION?

Other medicines with the same active substance (aciclovir) include ACICLOVIR ACCORD 25 mg/ml CONCENTRATE FOR INFUSION SOLUTION, ACICLOVIR ACCORD 250 mg POWDER FOR INJECTABLE SOLUTION AND FOR INFUSION, ACICLOVIR ALTAN 250 mg POWDER FOR 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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