


Ask a doctor about a prescription for NUROFEN RAPID 400 mg SOFT CAPSULES
Package Leaflet: Information for the User
NUROFEN RAPID 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 mild or moderate occasional 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 Nurofen Rapid:
Warnings and precautions
Consult your doctor or pharmacist before starting to take Nurofen Rapid:
In dehydrated adolescents, there is a risk of renal function deterioration.
With ibuprofen, signs of allergic reaction to this medicine have been reported, 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), and acute generalized exanthematous pustulosis (AGEP), have been reported in association with ibuprofen treatment. Discontinue Nurofen treatment and seek medical attention immediately if you notice any symptoms related to these severe skin reactions described in section 4.
Infections
Nurofen Rapid may mask the signs of an infection, such as fever and pain. Consequently, Nurofen Rapid 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 Rapid 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 medicines may also affect or be affected by Nurofen treatment. Therefore, you should always consult your doctor or pharmacist before using Nurofen with other medicines.
Interaction with laboratory tests:
If you are going to undergo any diagnostic test (including blood tests, urine tests, skin tests that use allergens, etc.), inform your doctor that you are taking or have recently taken this medicine, as it may alter the test results.
Taking Nurofen Rapid 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 like Nurofen Rapid 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.
This medicine contains cochineal red A (Ponceau 4R), (E-124), potassium, sorbitol (E-420), and soybean oil
This medicine may cause allergic reactions because it contains cochineal red A (Ponceau 4R) (E-124). It can cause asthma, especially in patients allergic to acetylsalicylic acid.
Patient with renal insufficiency or with low-potassium diets should note that this medicine contains 31.23 mg (0.8 mmol) of potassium per capsule.
This medicine contains 69.13 mg of sorbitol (E-420) in each capsule.
Sorbitol is a source of fructose. If your doctor has told you that you (or your child) have an intolerance to certain sugars, or have been diagnosed with hereditary fructose intolerance (HFI), a rare genetic disease, in which the patient cannot break down fructose, consult your doctor before taking this medicine.
For information on soybean oil, see the "Do not take Nurofen Rapid" section.
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 duration 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 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 notice digestive discomfort.
Taking this medicine is subject to the appearance of pain or fever. As they disappear, the medication should be suspended.
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 Rapid than you should
If you take or administer accidentally more medicine than you should, or if a child has taken 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.
Symptoms of 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, symptoms of drowsiness, chest pain, palpitations, loss of consciousness, convulsions (mainly in children), 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 medicines, this medicine 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 medicine and seek medical help immediately if you experience:
Tell 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)
Medicines 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 medicines like Nurofen Rapid.
Based on experience with NSAIDs, cases of interstitial nephritis (kidney disorder), nephrotic syndrome (disorder characterized by protein in the urine and body swelling), and kidney 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 leaflet. You can also report them directly through the Spanish Pharmacovigilance System for Human Use Medicines http://www.notificaram.es. By reporting adverse effects, you can contribute to providing more information on the safety of this medicine.
Keep this medicine out of sight and reach of children.
Store in the original packaging to protect it from moisture.
Store below 30 °C.
Do not use this medicine 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 medicine if you notice deterioration of the capsules.
Medicines should not be thrown away through wastewater or household waste. Deposit the packaging and medicines 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 medicines you no longer need. This way, you will help protect the environment.
Nurofen Rapid Composition
Each soft capsule contains 400 mg of ibuprofen as the active ingredient.
The other components are:
Core: polyethylene glycol (macrogol) 600, potassium hydroxide, purified water.
Capsule: gelatin, liquid sorbitol (E-420), cochinilla red A (Ponceau 4R) (E-124), lecithin (E-322) (derived from soy), isopropanol, nitrogen, medium-chain triglycerides, and printing ink containing hypromellose (E-464), titanium dioxide (E-171), propylene glycol (E-1520), isopropyl alcohol, and purified water.
Product Appearance and Package Contents:
Nurofen Rapid are oval, transparent, red soft capsules with a white identification logo.
They come in packages containing 10 or 20 soft capsules packaged in PVC/PE/PVdC/Al or PVC/PVdC/Al blisters. Only some package sizes may be marketed.
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 the Last Revision of this Leaflet:October 2024
Detailed and updated information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS)http://www.aemps.gob.es/
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