Package Leaflet: Information for the User
Ibudol 400 mg Soft Capsules
Ibuprofen
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Follow the instructions for administration of the medicine contained in this leaflet or as indicated by your doctor or pharmacist.
Contents of the Package Leaflet
Ibuprofen, the active ingredient of this medicine, acts by reducing pain and fever.
It is indicated in adults and adolescents over 12 years for the symptomatic relief of occasional mild or moderate pain, such as headache, dental, menstrual, muscular (cramps) or back (lumbago) pain, as well as in febrile conditions.
You should consult a doctor if your symptoms worsen or do not improve, if the fever persists for more than 3 days or the pain for more than 3 days in adolescents or 5 days in adults.
Do not take Ibudol:
Warnings and precautions
With ibuprofen, signs of allergic reaction to this medicine have been reported, such as respiratory problems, swelling of the face and neck (angioedema), and chest pain. Stop using Ibudol immediately and contact your doctor or emergency medical services immediately if you notice any of these signs.
Consult your doctor or pharmacist before starting to take this medicine:
In dehydrated adolescents, there is a risk of renal function deterioration.
Cardiovascular precautions
Anti-inflammatory/analgesic medications like ibuprofen may be associated with a small increased risk of heart attack or stroke, especially when used in high doses. Do not exceed the recommended dose or treatment duration.
You should discuss your treatment with your doctor or pharmacist before taking this medicine if:
Similarly, these types of medications can cause fluid retention, especially in patients with heart failure and/or high blood pressure (hypertension).
Skin reactions
Be careful with Ibudol:
Severe skin reactions, such as exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), and acute generalized exanthematous pustulosis (AGEP), have been reported in association with ibuprofen treatment. Stop taking Ibudol and seek medical attention immediately if you notice any of these symptoms related to severe skin reactions described in section 4.
Infections
This medicine may hide the signs of an infection, such as fever and pain. Consequently, this medicine may delay the appropriate treatment of the infection, which can increase the risk of complications. This has been observed in bacterial pneumonia and bacterial skin infections related to chickenpox. If you take this medicine while having an infection and the symptoms of the infection persist or worsen, consult a doctor without delay.
Other medicines and Ibudol
Tell your doctor or pharmacist that you are using, have recently used, or may need to use any other medicine.
This medicine may affect or be affected by other medicines.
For example:
Other medicines may also affect or be affected by treatment with ibuprofen. Therefore, you should always consult your doctor or pharmacist before using Ibudol with other medicines.
Interaction with analytical tests:
If you are going to undergo any diagnostic test (including blood tests, urine tests, skin tests using allergens, etc.), inform your doctor that you are taking or have recently taken this medicine, as it may alter the results.
Taking Ibudol with food, drink, and alcohol
You can take it alone or with food. It is generally recommended to take it during meals or with milk to reduce the possibility of stomach upset.
Do not take ibuprofen with alcohol to avoid damaging the stomach.
Taking ibuprofen by patients who habitually consume alcohol (3 or more alcoholic beverages - beer, wine, liquor... per day) may cause stomach bleeding.
Pregnancy, breastfeeding, and fertility
Pregnancy
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medicine.
Do not take Ibudol if you are in the last 3 months of pregnancy, as it may harm the fetus or cause problems during delivery. It may cause kidney and heart problems in your fetus. It may affect your and your baby's tendency to bleed and delay or prolong labor more than expected. You should not take Ibudol during the first 6 months of pregnancy unless it is clearly necessary and as indicated by your doctor. If you need treatment during this period or while trying to become pregnant, you should take the minimum dose for the shortest possible time. From the 20th week of pregnancy, Ibudol may cause kidney problems in your fetus if taken for more than a few days, which may cause low levels of amniotic fluid surrounding the baby (oligohydramnios) or narrowing of a blood vessel (ductus arteriosus) in the baby's heart. If you need treatment for more than a few days, your doctor may recommend additional checks.
Breastfeeding
This medicine passes into breast milk, but it can be taken during breastfeeding if used at the recommended dose for the shortest possible time.
Fertility
For female patients of childbearing age, it should be noted that ibuprofen medications have been associated with a decrease in fertility. Avoid taking this medicine if you are trying to become pregnant.
Driving and using machines
If you feel dizzy, vertigo, vision changes, or other symptoms while taking this medicine, do not drive or use hazardous machinery.
Ibudol contains sorbitol liquid (E-420) and Ponceau 4R (E-124)
This medicine contains 110.4 mg of sorbitol liquid (E-420) in each capsule.
Sorbitol is a source of fructose. If your doctor has indicated that you (or your child) have an intolerance to certain sugars, or have been diagnosed with hereditary fructose intolerance (HFI), a rare genetic disease, consult your doctor before taking this medicine.
This medicine may cause allergic reactions because it contains Ponceau 4R (E-124). It can cause asthma, especially in patients allergic to acetylsalicylic acid.
This medicine contains less than 39 mg (1 mmol) of potassium per capsule, so it is considered "essentially potassium-free".
Follow the instructions for administration of the medicine contained in this leaflet or as indicated by your doctor. In case of doubt, ask your doctor or pharmacist.
The recommended dose is:
Do not take more than 3 tablets (1200 mg) in 24 hours.
The lowest effective dose should be used for the shortest necessary time to relieve symptoms. If you have an infection, consult your doctor without delay if the symptoms (such as fever and pain) persist or worsen (see section 2).
Use in children and adolescents under 12 years
Children under 12 years should not take this medicine due to the 400mg dose of ibuprofen. There are other presentations more suitable for this population.
How to take:
This medicine is taken orally.
Swallow the medicine with a little water.
Take the medicine with meals or with milk, especially if you experience digestive discomfort.
Taking this medicine is subject to the appearance of pain or fever. As they disappear, the medication should be discontinued.
In adolescents from 12 to 18 years, if the use of this medicine is required for more than 3 days or if the symptoms worsen, a doctor should be consulted.
In adults, if the symptoms worsen, if the fever persists for more than 3 days or the pain for more than 5 days, a doctor should be consulted.
If you take more Ibudol than you should
If you take or administer accidentally more medicine than you should, or if a child has ingested the medicine accidentally, consult immediately with a doctor or call the toxicology information service, phone 915620420, indicating the medicine and the amount used, or go to the nearest hospital to find out about the risk and ask for advice on the measures to be taken. It is recommended to take the package and the leaflet of the medicine to the healthcare professional.
The symptoms of an overdose may include stomach pain, nausea, vomiting (which may contain bloody sputum), headache, involuntary eye movements, ringing in the ears. At high doses, intestinal bleeding, hypotension, metabolic acidosis, coma, somnolence, chest pain, palpitations, loss of consciousness, convulsions (mainly in children), weakness, and dizziness, blood in urine, low potassium levels in the blood, chills, and breathing problems have been reported.
In case of ingestion of large amounts, activated charcoal should be administered. Gastric lavage will be considered if large amounts have been ingested and within 60 minutes after ingestion.
Like all medications, this medication can have adverse effects, although not all people suffer from them.
Adverse effects are more common in people over 65 years of age. The incidence of adverse effects is lower in short treatments and if the daily dose is below the maximum recommended dose.
Chest pain, which can be a sign of a potentially serious allergic reaction called Kounis syndrome.
Discontinue treatment with Ibudol and seek immediate medical attention if you notice any of the following symptoms:
Inform your doctor if you experience the following adverse effects:
Frequent:(may affect up to 1 in 10 people)
Uncommon:(may affect up to 1 in 100 people)
Rare:(may affect up to 1 in 1,000 people)
Very Rare:(in less than 1 in 10,000 patients)
Frequency Not Known:(cannot be estimated from available data)
Medications of this type may be associated with a slight increase in the risk of heart attack or stroke (myocardial infarction or stroke). Prolonged bleeding time, edema (fluid retention), high blood pressure, and heart failure have also been observed in association with treatments with ibuprofen medications.
Based on experience with NSAIDs, cases of interstitial nephritis (kidney disorder), nephrotic syndrome (disorder characterized by protein in the urine and body swelling), and renal failure (sudden loss of kidney function) cannot be excluded.
Reporting of Adverse Effects
If you experience any type of adverse effect, consult your doctor, pharmacist, or nurse, even if it is an adverse effect that does not appear in this prospectus. You can also report them directly through the Spanish Pharmacovigilance System for Human Use Medications http://www.notificaram.es. By reporting adverse effects, you can contribute to providing more information on the safety of this medication.
Keep this medication out of 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.
Do not use this medication if you observe deterioration of the capsules.
Medications should not be thrown away through drains or into the trash. Deposit the packaging and medications you no longer need at the SIGRE point in the pharmacy. In case of doubt, ask your pharmacist how to dispose of the packaging and medications you no longer need. This way, you will help protect the environment.
Composition of Ibudol
Each soft capsule contains 400 mg of ibuprofen as the active ingredient.
The other components are:
Appearance of Ibudol and Package Contents:
Oval-shaped capsules (approximately 15 mm long and 10 mm wide) with a transparent and red gelatin coating. The capsule has a white logo printed on one of its faces.
It is presented in packages containing 10 or 20 soft capsules packaged in PVC/PVdC/Al (transparent or opaque) or PVC/PE/PVdC/Al (transparent or opaque) blisters.
Marketing Authorization Holder and Manufacturer
Kern Pharma, S.L.
Venus, 72 - Pol. Ind. Colón II
08228 Terrassa - Barcelona
Spain
Date of the Last Revision of this Prospectus:July 2024
Detailed and updated information on this medication is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/