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MUCIBRÓN 3 mg/ml ORAL SOLUTION

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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 MUCIBRÓN 3 mg/ml ORAL SOLUTION

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

Mucibrón 3 mg/ml

solución oral

Ambroxol hidrocloruro

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

Siga exactamente las instrucciones de administración del medicamento contenida en este prospecto o las indicadas por su farmacéutico.

  • Conserve este prospecto, ya que puede tener que volver a leerlo.
  • Si necesita consejo o más información, consulte a su farmacéutico.
  • Si experimenta efectos adversos, consulte a su médico o farmacéutico, incluso si se trata de efectos adversos que no aparecen en este prospecto.

Si los síntomas empeoran o persisten después de 5 días de tratamiento, o se produce: fiebre erupciones de la piel, dolor de cabeza persistente o dolor de garganta, debe consultar a un médico.

Contenido del prospecto

  1. Qué es Mucibrón y para qué se utiliza
  2. Qué necesita saber antes de empezar a tomar Mucibrón
  3. Cómo tomar Mucibrón
  4. Posibles efectos adversos

5 Conservación de Mucibrón

  1. Contenido del envase e información adicional

:

1. Qué es mucibrón y para qué se utiliza

Mucibrón pertenece al grupo de medicamentos denominados mucolíticos.

El ambroxol, principio activo de este medicamento, actúa disminuyendo la viscosidad del moco, fluidificándolo y facilitando su eliminación.

Reduce la viscosidad de los mocos y flemas, facilitando su expulsión, en catarros y gripes para adultos y niños a partir de 2 años.

Debe consultar a un médico si empeora o si no mejora después de 5 días de tratamiento.

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 mucibrón

No tome mucibrón

Si es alérgico al ambroxol 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 tomar mucibrón

Se han recibido notificaciones de reacciones cutáneas graves asociadas a la administración de ambroxol. Si le aparece una erupción en la piel (incluidas lesiones de las mucosas de, por ejemplo, la boca, la garganta, la nariz, los ojos y los genitales), deje de usar mucibrón y consulte a su médico inmediatamente.Si tiene problemas con el funcionamiento de los bronquios debe evitar tomar mucolíticos.

Si tiene problemas con el funcionamiento del hígado o riñón, o antecedentes de úlcera de estómago o duodeno, consulte a su médico antes de utilizar este medicamento porque puede que tenga que reducirle la cantidad de medicamento por toma.

Pacientes con intolerancia conocida a la histamina deben evitar el tratamiento con este medicamento durante períodos largos de tratamiento. Los síntomas de intolerancia son: dolor de cabeza, rinitis y picor.

Interacción de mucibrón con otros medicamentos:

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

La toma conjunta de este medicamento con medicamentos para disminuir la tos (antitusivos) puede provocar la acumulación de secreciones pulmonares debido a la disminución del reflejo de la tos.

La administración de este medicamento junto con antibióticos (amoxicilina, cefuroxima, eritromicina, doxiciclina) eleva la concentración de antibiótico en tejido pulmonar.

Interacción de mucibrón con alimentos y bebidas

No se debe tomar con las comidas y se tomará con un vaso de agua. Tomar más líquidos puede aumentar la actividad de este medicamento.

Embarazo, lactancia y fertilidad

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

Ambroxol solo se usará durante el embarazo, especialmente durante el primer trimestre, solo si su médico se lo indica.

Las madres en período de lactancia solamente lo tomaran si su médico se lo indica

Conducción y uso de máquinas

No se han observado efectos sobre la capacidad de conducir y utilizar maquinaria.

Mucibrón contiene sorbitol

Este medicamento contiene 350 mg de sorbitol (E-420) en cada mililitro de solución oral.

El sorbitol es una fuente de fructosa. Si su médico le ha indicado que usted (o su hijo) padecen una intolerancia a ciertos azúcares, o se les ha diagnosticado intolerancia hereditaria a la fructosa (IHF), una enfermedad genética rara, en la que el paciente no puede descomponer la fructosa, consulte usted (o su hijo) con su médico antes de tomar este medicamento.

El sorbitol puede provocar malestar gastrointestinal y un ligero efecto laxante.

Mucibrón contiene parahidroxibenzoato de metilo y parahidroxibenzoato de propilo

Puede producir reacciones alérgicas (posiblemente retardadas) porque contiene parahidroxibenzoato de metilo (E-218) y parahidroxibenzoato de propilo (E-216).

Mucibrón contiene alcohol bencílico

Este medicamento contiene 0,00012 mg de alcohol bencílico por mililitro de solución oral.

El alcohol bencílico puede provocar reacciones alérgicas.

Consulte con su médico o farmaceútico si está embarazada o en periodo de lactancia. Esto es debido a que se pueden acumular grandes cantidades de alcohol bencílico en su organismo y provocar efectos adversos (acidosis metabólica).

Consulte a su médico o farmacéutico si tiene enfermedades de hígado o riñón. Esto es debido a que se pueden acumular en el organismo grandes cantidades de alcohol bencílico y provocar efectos adversos (acidosis metabólica).

El alcohol bencílico se ha relacionado con el riesgo de efectos adversos graves que incluyen problemas respiratorios (“síndrome de jadeo”) en niños.

No administre este medicamento a su recién nacido (hasta de 4 semanas de edad) a menos que se lo haya recomendado su médico.

Este medicamento no se debe utilizar durante más de una semana en niños menores de 3 años de edad a menos que se lo indique su médico o farmacéutico.

Mucibrón contiene sodio

Este medicamento contiene menos de 23 mg de sodio (1 mmol) por mililitro de solución oral; esto es, esencialmente, “exento de sodio”.

3. Cómo tomar mucibrón

Siga exactamente las instrucciones de administración del medicamento contenidas en este prospecto o las indicadas por su médico o farmacéutico. En caso de dudas, pregunte a su farmacéutico.

La dosis recomendada es:

Adultos y adolescentes a partir de 12 años:

La dosis normal es de 10 ml (30mg), 3 veces al día (cada 8 horas).

Uso en niños

Niños menores de 2 años

Está contraindicado.

Niños de2 a5 años

La dosis normal es de 2,5 ml hasta 3 veces al día.

Niños de6 a12 años

La dosis normal es de 5 ml hasta 3 veces al día.

Pacientes con enfermedades de los riñones y/o del hígado:Si padece una enfermedad de los riñones y/o del hígado, es posible que su médico le recete una dosis más baja de lo habitual.

Como tomar:

Este medicamento se toma por vía oral.

Medir la cantidad de medicamento a tomar con el dosificador que se incluye en la caja. Beber directamente del dosificador y tomar un vaso de líquido (preferentemente agua). Después de cada toma lavar el dosificador

No se debe tomar con las comidas.

Si los síntomas empeoran o persisten después de 5 días de tratamiento, o se produce: fiebre, erupciones en la piel, dolor de cabeza persistente o dolor de garganta, debe consultar a un médico

Si toma más mucibrón del que debiera

Si toma más medicamento del que debe podrá notar agitación a corto plazo y diarrea.

La sobredosis accidental o intencionada puede producir un aumento de la producción de saliva, náuseas, vómitos y bajada de la presión arterial.

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.

Si olvido tomar mucibrón:

No tome una dosis doble para compensar la dosis olvidada.

Si los síntomas continúan, vuelva a tomar el medicamento de la misma forma que se indica en el apartado 3. Cómo tomar mucibrón.

Si tiene cualquier otra duda sobre el uso de este medicamento, pregunte a su 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, mucibrón puede producir efectos adversos, aunque no todas las personas los sufran.

Poco frecuentes pueden afectar hasta 1 de cada 100 pacientes: nauseas, vómitos, dolor de estómago, fiebre.

Raros (pueden afectar hasta a 1 de cada 1.000 personas): reacciones de hipersensibilidad, exantema, urticaria.

Frecuencia no conocida (no puede estimarse a partir de los datos disponibles): reacciones anafilácticas, tales como shock anafiláctico, angioedema (hinchazón de rápida progresión de la piel, de los tejidos subcutáneos, de las mucosas o de los tejidos submucosos) y prurito. Reacciones adversas cutáneas graves (tales como eritema multiforme, síndrome de Stevens-Johnson/necrolisis epidérmica tóxica y pustulosis exantematosa generalizada aguda).

Al primer síntoma de alergia deje de tomar el medicamento y consulte a su médico o farmacéutico.

Si experimenta efectos adversos, consulte a su médico o farmacéutico, incluso si se trata de efectos adversos que no aparecen en este prospecto.

Comunicación de efectos adversos

Si experimenta cualquier tipo de efecto adverso, consulte a su médico, farmacéutico o enfermero, 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 mucibrón

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

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.

Este medicamento no requiere condiciones especiales de conservación.

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 la farmacia. En caso de duda 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 de mucibrón

El principio activo es ambroxol hidrocloruro. Cada ml de solución contienen 3 mg de ambroxol hidrocloruro.

Los demás componentes (excipientes) son: Ácido tartárico, ácido cítrico monohidrato, edetato de disodio, hidroxietilcelulosa, parahidroxibenzoato de metilo (E-218), parahidroxibenzoato de propilo (E- 216), citrato de sodio, sorbitol (E-420), esencia de fresa (contiene glucosa en maltodextrina procedente de maíz y alcohol bencílico) y agua purificada.

Aspecto del producto y contenido del envase

Mucibrón 3 mg/ml solución oral se presenta en forma de solución. Su aspecto es ligeramente viscoso, transparente o débilmente opaco, prácticamente incoloro o ligeramente coloreado y con olor a fresa. Cada envase contiene 200 ml en un frasco de polietileno tereftalato de color topacio. Se incluye un dosificador con medidas para: 2,5, 5, 7,5, 10 y 15 ml.

Titular de la autorización de comercialización y responsable de la fabricación

LABORATORIOS NORMON, S.A.

Ronda de Valdecarrizo, 6 – 28760 Tres Cantos – Madrid (ESPAÑA)

Fecha de la última revisión de este prospecto: Octubre 2021

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

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Discuss questions about MUCIBRÓN 3 mg/ml ORAL SOLUTION, including use, safety considerations and prescription review, subject to medical assessment and local regulations.

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Hocine Lokchiri

General medicine 21 years exp.

Dr. Hocine Lokchiri is a French consultant with over 20 years of experience in General and Emergency Medicine. He works with adults and children, helping patients with urgent symptoms, infections, sudden health changes and everyday medical concerns that require timely evaluation. His background includes clinical practice in France, Switzerland and the United Arab Emirates, which allows him to navigate different healthcare systems and manage a wide range of conditions with confidence. Patients value his calm, structured approach, clear explanations and evidence-based decision-making.

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Tomasz Grzelewski

Dermatology 21 years exp.

Dr Tomasz Grzelewski is an MD, PhD specialist in allergy, paediatrics, general practice and sports medicine, with a clinical focus on dermatology, endocrinology, allergology and sports-related health. He has more than 20 years of clinical experience and completed his medical training at the Medical University of Łódź, where he defended his PhD thesis with distinction. His doctoral research was recognised by the Polish Society of Allergology for its innovative contribution to the field. Throughout his career, he has gained extensive expertise in diagnosing and managing a wide range of allergic and paediatric conditions, including modern allergen desensitisation techniques.

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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.

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Alina Tsurkan

Family medicine 13 years exp.

Dr. Alina Tsurkan is a licensed family medicine physician based in Portugal, offering online consultations for adults and children. She provides professional primary care, with a focus on prevention, accurate diagnosis, and long-term management of acute and chronic conditions.

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Yevgen Yakovenko

General surgery 12 years exp.

Dr. Yevgen Yakovenko is a licensed surgeon and general practitioner in Spain and Germany. He specialises in general, paediatric, and oncological surgery, internal medicine, and pain management. He offers online consultations for adults and children, combining surgical precision with therapeutic support. Dr Yakovenko works with patients across different countries and provides care in Ukrainian, Russian, English, and Spanish.

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Frequently Asked Questions

Is a prescription required for MUCIBRÓN 3 mg/ml ORAL SOLUTION?
MUCIBRÓN 3 mg/ml ORAL SOLUTION does not require 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 MUCIBRÓN 3 mg/ml ORAL SOLUTION?
The active ingredient in MUCIBRÓN 3 mg/ml ORAL SOLUTION is ambroxol. This information helps identify medicines with the same composition but different brand names.
Who manufactures MUCIBRÓN 3 mg/ml ORAL SOLUTION?
MUCIBRÓN 3 mg/ml ORAL SOLUTION is manufactured by Laboratorios Normon S.A.. Pharmacy brands and packaging may differ depending on the distributor.
Which doctors can assess the use of MUCIBRÓN 3 mg/ml ORAL SOLUTION 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 MUCIBRÓN 3 mg/ml ORAL SOLUTION 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 MUCIBRÓN 3 mg/ml ORAL SOLUTION?
Other medicines with the same active substance (ambroxol) include AMBROXOL ALDO-UNION 15 mg/2 ml ORAL SOLUTION OR CONCENTRATE FOR NEBULIZER INHALATION, AMBROXOL CINFA 3 mg/ml SYRUP, AMBROXOL CINFA 6 mg/ml SYRUP. 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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