


Ask a doctor about a prescription for NUROFEN 400 mg FILM-COATED TABLETS
Package Leaflet: Information for the User
NUROFEN 400 mg Coated Tablets
Ibuprofen
Read all of this leaflet carefully before you start taking this medicine, because it contains important information for you.
Follow exactly the administration instructions 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 it worsens or does 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 Nurofen
Warnings and precautions
Consult your doctor or pharmacist before starting to take Nurofen:
In dehydrated adolescents, there is a risk of renal function deterioration.
Ibuprofen has been reported to cause signs of allergic reaction to this medicine, such as respiratory problems, swelling of the face and neck area (angioedema), and chest pain. Stop using ibuprofen immediately and contact your doctor or the emergency medical service immediately if you observe any of these signs.
Cardiovascular precautions
Anti-inflammatory/analgesic medications like ibuprofen may be associated with a small increased risk of suffering a 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 Nurofen if:
Similarly, this type of medication can cause fluid retention, especially in patients with heart failure and/or high blood pressure (hypertension).
Skin reactions
Severe skin reactions, such as exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS syndrome), and acute generalized exanthematous pustulosis (AGEP), have been reported in association with ibuprofen treatment. Discontinue Nurofen treatment and seek immediate medical attention if you notice any symptoms related to these severe skin reactions described in section 4.
Infections
Nurofen may mask the signs of an infection, such as fever and pain. Consequently, Nurofen may delay 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.
Use of Nurofen with other medicines
Tell your doctor or pharmacist that you are using, have recently used, or may need to use any other medicine.
Nurofen may affect or be affected by other medicines. For example:
Other medications may also affect or be affected by Nurofen treatment. Therefore, you should always consult your doctor or pharmacist before using Nurofen with other medications.
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 Nurofen with food, drink, and alcohol
You can take it alone or with food. In general, it is recommended to take it during meals or with milk to reduce the possibility of stomach discomfort.
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
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.
Pregnancy
Do not take ibuprofen if you are in the last 3 months of pregnancy, as it may cause kidney and heart problems in the fetus. It may affect your tendency and that of your baby to bleed and delay or prolong labor more than expected. Avoid taking ibuprofen during the first 6 months of pregnancy unless your doctor indicates it. In these cases, the dose and duration will be limited to the minimum possible.
From the 20th week of pregnancy, ibuprofen may cause kidney problems in the fetus if taken for more than a few days, which can lead to 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 medications of the Nurofen type 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 notice dizziness, vertigo, vision changes, or other symptoms while taking this medicine, do not drive or use hazardous machinery.
This medicine contains sucrose. If your doctor has told you that you have an intolerance to certain sugars, consult with them before taking this medicine.
This medicine contains 27.42 mg of sodium (main component of table salt/cooking salt) per tablet. This is equivalent to 1.37% of the maximum recommended daily sodium intake for an adult.
Follow exactly the administration instructions 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 time necessary 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 400 mg dose of ibuprofen. Other presentations are 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 notice digestive discomfort.
Taking this medicine is subject to the appearance of pain or fever. As these 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 Nurofen than you should
If you have taken more medicine than you should, or if a child has accidentally ingested the medicine, consult a doctor immediately 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.
Symptoms of overdose may include nausea, stomach pain, vomiting (which may contain blood), headache, rapid involuntary eye movements, ringing in the ears, and confusion. At high doses, intestinal bleeding, hypotension, metabolic acidosis, symptoms of drowsiness, chest pain, palpitations, loss of consciousness, convulsions (mainly in children), coma, weakness, and dizziness, blood in urine, low potassium levels in blood, chills, and breathing problems have been reported.
In case of ingestion of significant amounts, activated charcoal should be administered. Gastric lavage will be considered if significant amounts have been ingested and within 60 minutes after ingestion.
Like all medications, Nurofen 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.
STOP taking this medication and seek medical help immediately if you experience:
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). Prolongation of bleeding time, edema (fluid retention), high blood pressure, and heart failure have also been observed in association with treatments with medications like Nurofen.
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 is not listed in this leaflet. You can also report them directly through the Spanish Pharmacovigilance System for Human Use Medications: https://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 shown on the packaging after CAD. The expiration date is the last day of the month indicated.
Medications should not be thrown away in drains or trash. Deposit the packaging and medications you no longer need at the pharmacy's SIGRE point. 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.
Nurofen Composition
Each coated tablet contains 400 mg of ibuprofen as the active ingredient.
The other components are:
Core: sodium croscarmellose, sodium lauryl sulfate, sodium citrate (E-331), stearic acid, anhydrous colloidal silica.
Coating: sodium carmellose, talc, dried acacia, sucrose, titanium dioxide (E-171), macrogol 6000, industrial methylated alcohol, and purified water.
Printing ink containing red iron oxide (E-172), Shellac glaze in SD-45, n-butyl alcohol, isopropyl alcohol, propylene glycol (E-1520), ammonium hydroxide, and simethicone.
Product Appearance and Package Contents
Nurofen is a biconvex, white or off-white coated tablet.
It is presented in a package containing 12 coated tablets packaged in PVC/PVdC/Al or PVC/Al blisters.
Marketing Authorization Holder and Manufacturer
Holder:
Reckitt Benckiser Healthcare, S.A.
C/ Mataró, 28 - 08403 Granollers – Barcelona
Spain
Manufacturer:
RB NL Brands B.V.
Schiphol Blvd 207, 1118 BH Schiphol, Netherlands
Date of Last Revision of this Leaflet:October 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/
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