1. What is Ibuprofen Aldo-Union and what is it used for
2. What you need to know before starting to take Ibuprofen Aldo-Union
3. How to take Ibuprofen Aldo-Union
4. Possible side effects
5. Storage of Ibuprofen Aldo-Union
6. Contents of the pack and additional information
Ibuprofeno Aldo-Unión contains ibuprofen and belongs to a group of medicines called nonsteroidal anti-inflammatory drugs (NSAIDs).
This medicine is indicated for the treatment of:
Do not take Ibuprofeno Aldo-Unión:
Warnings and Precautions:
Consult your doctor, pharmacist, or nurse before starting to take Ibuprofeno Aldo-Unión.
Be cautious if:
Ibuprofeno Aldo-Unión may mask the signs of an infection, such as fever and pain. Therefore, it is possible that Ibuprofeno Aldo-Unión may delay the appropriate treatment of the infection, which may increase the risk of complications. This has been observed in pneumonia caused by bacteria and skin infections related to chickenpox. If you take this medication while having an infection and the infection symptoms persist or worsen, consult a doctor without delay.
Cardiovascular Precautions:
Nonsteroidal anti-inflammatory drugs like ibuprofen may be associated with a small increase in the risk of heart attack or stroke, especially when used in high doses. Do not exceed the recommended dose or treatment duration.
Inform your doctor or pharmacist before taking Ibuprofeno Aldo-Unión if:
Additionally, this type of medication may cause fluid retention, especially in patients with heart failure and/or high blood pressure (hypertension).
Skin Reactions:
Severe skin reactions associated with treatment with Ibuprofeno Aldo-Unión have been reported. Stop taking Ibuprofeno Aldo-Unión and see your doctor immediately if you experience any skin rash, mucous membrane lesions, blisters, or other signs of allergy, as these may be the first signs of a severe skin reaction. See section 4.
Precautions during Pregnancy and in Women of Childbearing Age:
Due to the association of ibuprofen administration with an increased risk of congenital anomalies/abortions, it is not recommended to administer this medication during the first and second trimesters of pregnancy, except in cases where it is strictly necessary. In these cases, the dose and duration will be limited to the minimum possible.
In the third trimester, the administration of ibuprofen is contraindicated.
For women of childbearing age, it should be noted that ibuprofen-type medications have been associated with a decrease in the ability to conceive.
Use of Ibuprofeno Aldo-Unión with Other Medications:
Inform your doctor or pharmacist if you are using, have used recently, or may need to use any other medication.
Ibuprofeno Aldo-Unión may affect or be affected by other medications. For example:
Other medications may also affect or be affected by treatment with Ibuprofeno Aldo-Unión. Therefore, always consult your doctor or pharmacist before using Ibuprofeno Aldo-Unión with other medications.
The use of ibuprofen may alter the following laboratory tests:
- Bleeding time (may be prolonged for 1 day after stopping treatment)
- Blood glucose concentration (may decrease)
- Creatinine clearance (may decrease)
- Hematocrit or hemoglobin (may decrease)
- Serum concentrations of urea nitrogen and creatinine and potassium (may increase)
- With liver function tests: increase in transaminase values
Inform your doctor if you are about to undergo a clinical analysis and are taking or have recently taken ibuprofen.
Taking Ibuprofeno Aldo-Unión with Food, Drinks, and Alcohol:
It is recommended to take Ibuprofeno Aldo-Unión with milk or with food, or immediately after eating, to reduce the possibility of stomach discomfort.
Do not take it with alcohol.
The use of ibuprofen in patients who regularly consume alcohol (three or more alcoholic beverages - beer, wine, liquor - per day) may cause stomach hemorrhage.
Pregnancy, Breastfeeding, and Fertility:
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medication.
Do not take ibuprofen during pregnancy, especially during the third trimester (see section on precautions during pregnancy and in women of childbearing age).
Although only small amounts of the medication pass into breast milk, it is recommended not to take ibuprofen for extended periods during breastfeeding. You do not need to stop breastfeeding during a short treatment with the recommended dose for pain and fever.
Driving and Operating Machines:
If you experience dizziness, vertigo, visual disturbances, or other symptoms while taking this medication, you should not drive or operate machinery. If you only take a single dose of ibuprofen or for a short period, you do not need to take special precautions.
Ibuprofeno Aldo-Unión contains sodium benzoate (E-211), glycerol (E-422), and maltitol (E-965).
This medication, containing glycerol as an excipient, may be harmful at high doses. It may cause headaches, stomach discomfort, and diarrhea.
This medication contains 10 mg of sodium benzoate (as sodium benzoate) in each unit of volume (5ml).
Sodium benzoate may increase the risk of jaundice (yellowing of the skin and eyes) in newborns (up to 4 weeks old).
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This medication contains maltitol (E-965), so if your doctor has told you that you have an intolerance to certain sugars, consult with them before taking this medication.
Follow exactly the administration instructions of this medication indicated by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.
The most effective dose should be used for the shortest duration necessary to relieve symptoms. If you have an infection, consult a doctor promptly if symptoms (such as fever and pain) persist or worsen (see section 2).
Remember to take your medication.
Your doctor will indicate the duration of treatment with Ibuprofeno Aldo-Unión.Do not discontinue treatment beforehand, as this will not yield the expected results. Similarly, do not use this medication for a longer period than indicated by your doctor.
Ibuprofeno Aldo-Unión is an oral suspension for administration.
Instructions for use:
To ensure accurate dosing, the container includes a 5 ml oral syringe. First, shake the suspension, then insert the dosing syringe into the perforated cap, invert the bottle, pull the plunger until the liquid reaches the prescribed amount by your doctor, return the bottle to its initial position, and remove the dosing syringe.
The syringe should be cleaned and dried after each use.
If you have a sensitive stomach, take the medication with meals.
Use in children and adolescents
The dose of ibuprofen administered depends on the age and weight of the child. For children aged 6 months to 12 years, the recommended daily dose is 20 to 30 mg/kg of body weight, divided into three or four doses (see table). The interval between doses will depend on the evolution of symptoms, but will never be less than 4 hours.
Age | Body weight | Dosage |
Infants of 6 to 12 months | Approx. 7.7 – 9 kg | 2.5 ml 3 to 4 times a day (corresponds to 150-200 mg of ibuprofen/day) |
Infants of 1 to 2 years Children of 2 to 3 years | Approx. 10 to 15 kg | 5 ml 3 times a day (corresponds to 300 mg of ibuprofen/day) |
Children of 4 to 6 years | Approx. 16 to 20 kg | 7.5 ml 3 times a day (equivalent to 450 mg of ibuprofen/day) |
Children of 7 to 9 years | Approx. 21 to 29 kg | 10 ml 3 times a day (equivalent to 600 mg of ibuprofen/day) |
Children of 10 to 12 years | Approx. 30 to 40 kg | 15 ml 3 times a day (equivalent to 900 mg of ibuprofen/day) |
For the treatment of juvenile rheumatoid arthritis, higher doses may be necessary, although it is recommended not to exceed 40 mg/kg/day of ibuprofen.
It is not recommended to use ibuprofen in infants under six months.
Adults and adolescents 12 years and older: The recommended dose is 20 ml 3 to 4 times a day (equivalent to 1200-1600 mg of ibuprofen/day), as long as symptoms persist.
Older patients: In general, no special dose adjustments are required.
Patients with renal or hepatic insufficiency: Your doctor will adjust the dose.
If you estimate that the action of this medication is too strong or too weak, inform your doctor or pharmacist.
If you have taken more Ibuprofeno than you should, or if a child has accidentally ingested the medication, consult a doctor immediately or go to the nearest hospital to inform yourself about the risk and ask for advice on the measures to be taken. You can also call the Toxicological Information Service, phone: 91 562 04 20, indicating the medication and the amount ingested. It is recommended to bring the container and the medication package to the healthcare professional.
The symptoms of overdose may include nausea, stomach pain, vomiting (which may contain blood), gastrointestinal bleeding (see section 4 below), diarrhea, headache, ringing in the ears, confusion, and involuntary eye movement. Agitation, drowsiness, disorientation, or coma may also occur. Occasionally, patients develop seizures. At high doses, symptoms of drowsiness, chest pain, palpitations, loss of consciousness, seizures (mainly in children), weakness, and dizziness have been reported. Additionally, blood in the urine, low potassium levels in the blood, chills, and breathing difficulties may occur. Furthermore, the prothrombin time/INR may be prolonged, probably due to interference with the actions of circulating clotting factors. Acute renal failure and liver damage may occur. It is possible that asthma symptoms will worsen in asthmatics. Additionally, low blood pressure and reduced breathing may occur.
If a severe overdose has occurred, the doctor will take the necessary measures.
In case of ingestion of significant amounts, activated charcoal should be administered. Gastric lavage may be considered if significant amounts have been ingested and within 60 minutes of ingestion.
If you forgot to take Ibuprofeno Aldo-Unión:
Do not take a double dose to compensate for the missed doses.
If you forget to take your scheduled dose, take it as soon as you remember. However, if the next scheduled dose is soon, skip the missed dose and take the next dose at its regular time.
Like all medications, this medication may cause side effects, although not everyone will experience them.
The side effects of medications such as ibuprofen are more common in people over 65 years old.
The incidence of side effects is lower in short-term treatments and if the daily dose is below the maximum recommended dose.
The following side effects have been observed:
Gastrointestinal:
The most frequent side effects that occur with medications such as Ibuprofen are gastrointestinal: peptic ulcers, digestive bleeding, perforations (in some cases fatal), especially in elderly patients. Nausea, vomiting, diarrhea, flatulence, constipation, stomach burning, abdominal pain, blood in stool, mouth ulcers, worsening of ulcerative colitis and Crohn's disease ((a chronic disease in which the immune system attacks the intestine causing inflammation that usually produces bloody diarrhea) have also been observed.
Less frequently, gastritis has been observed.
Rarely: esophageal inflammation, esophageal stricture (esophageal stenosis), exacerbation of intestinal diverticulum disease, non-specific hemorrhagic colitis (gastroenteritis that presents with bloody diarrhea).
Very rarely: pancreatitis.
Cardiovascular:
Chest pain, which can be a sign of a potentially severe allergic reaction called Kounis syndrome.
Medications such as Ibuprofen may be associated with a moderate increase in the risk of suffering a heart attack ("myocardial infarction") or stroke ("cerebral infarction").
Edema (fluid retention), hypertension, and heart failure have also been observed in association with treatments with Ibuprofen Aldo-Union type medications.
Dermatological:
Frequent: skin rash.
Infrequent: skin redness, itching or swelling of the skin, purpura (purple spots on the skin).
Very rarely: hair loss, erythema multiforme (skin lesion), light-sensitive skin reactions, inflammation of skin blood vessels.
Exceptionally, severe skin infections and soft tissue complications during chickenpox may occur.
Stop treatment with ibuprofen and seek immediate medical attention if you notice any of the following symptoms:
Immune system:
Infrequent: transient edema in skin areas, mucous membranes, or sometimes in internal organs (angioedema),
nasal mucosa inflammation, bronchospasm (bronchi constriction that prevents air from reaching the lungs).
Rare: severe allergic reactions (anaphylactic shock). In case of severe generalized hypersensitivity reactions, facial swelling, tongue, and larynx swelling, bronchospasm, asthma, tachycardia, hypotension, and shock may occur.
Very rarely: joint pain and fever (lupus erythematosus).
Central nervous system:
Frequent: fatigue or drowsiness, headache, dizziness, or feeling unsteady.
Rare: paresthesia (numbness, tingling, prickling, etc. more frequent in hands, feet, arms, or legs). Very rarely: aseptic meningitis (inflammation of the meninges, which are the membranes that protect the brain and spinal cord, not caused by bacteria). In most cases where aseptic meningitis has been reported with ibuprofen, the patient had some form of autoimmune disease (such as systemic lupus erythematosus or other collagen diseases), which was a risk factor. The symptoms of aseptic meningitis observed were neck stiffness, headache, nausea, vomiting, fever, or disorientation.
Psychiatric:
Infrequent: insomnia, anxiety, restlessness. Rare: disorientation or confusion, nervousness, irritability, depression, psychotic reaction.
Auditory:
Frequent: vertigo. Infrequent: ringing or buzzing in the ears. Rare: hearing difficulty.
Ocular:
Infrequent: vision disturbances. Rare: abnormal or blurred vision.
Blood:
Rare: decreased platelets, decreased white blood cells (may manifest as frequent infections with fever, chills, or sore throat), decreased red blood cells (may manifest as difficulty breathing and pale skin), decreased granulocytes (a type of white blood cell that may predispose to infections), pancytopenia (deficiency of red, white, and platelet cells in the blood), agranulocytosis (very large decrease in granulocytes), aplastic anemia (insufficiency of the bone marrow to produce different types of cells) or hemolytic anemia (premature destruction of red blood cells).
Initial symptoms are: fever, sore throat, superficial mouth ulcers, flu-like symptoms, extreme fatigue, nasal bleeding, and skin bleeding. Very rarely: prolonged bleeding time.
Renal:
Based on experience with NSAIDs in general, cases of interstitial nephritis (kidney disorder), nephrotic syndrome (characterized by protein in the urine and body swelling), and renal insufficiency (sudden loss of kidney function) cannot be ruled out.
Heptatic:
Medications such as Ibuprofen Aldo-Union may be associated, in rare cases, to liver damage. Other rare side effects are: hepatitis (inflammation of the liver), liver function abnormalities, and jaundice (yellowing of the skin and eyes).
Unknown frequency: liver insufficiency (severe deterioration of the liver).
General:
Worsening of inflammation during infectious processes.
Until now, no severe allergic reactions have been reported with ibuprofen, although they cannot be ruled out. The manifestations of this type of reaction could be fever, skin rash, abdominal pain, intense and persistent headache, nausea, vomiting, facial swelling, tongue, and throat swelling, difficulty breathing, asthma, palpitations, hypotension, or shock.
If any of the side effects mentioned below appear, stop treatment and seek immediate medical attention:
Reporting of side effects
If you experience any type of side effect, consult your doctor, pharmacist, or nurse, even if it is a possible side effect that does not appear in this prospectus.You can also report them directly through theSistema Español de Farmacovigilancia de Medicamentos de Uso Humano: https://www.notificaram.es.By reporting side effects, you can contribute to providing more information on the safety of this medication.
Keep this medication out of the sight and reach of children.
No special storage conditions are required.
Do not use this medication after the expiration date that appears on the packaging after CAD:. The expiration date is the last day of the month indicated.
Medications should not be disposed of through drains or in the trash. Dispose of the packaging and medications you no longer need at your local SIGRE collection point.At your pharmacy, ask your pharmacist how to dispose of unused packaging and medications. By doing so, you will help protect the environment.
Composition of Ibuprofeno Aldo-Unión
Appearance of the product and contents of the packaging
The medicine, after being shaken, will give rise to a white suspension with an orange odor. It is presented in a 200 ml bottle and includes a 5 ml dosing syringe.
Holder of the marketing authorization and responsible for manufacturing:
Laboratorio Aldo-Unión, S.L.
Calle Baronesa de Maldá, 73
08950 Esplugues de Llobregat
BARCELONA – SPAIN
Date of the last review of this leaflet: November 2024
The detailed and updated information on this medicine is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS)http://www.aemps.gob.es/
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