Leaflet attached to the packaging: information for the user
Nurofen for Children Junior Strawberry
40 mg/ml, oral suspension
Ibuprofen
For children weighing from 20 kg (6 years) to 40 kg (12 years)
You should carefully read the contents of the leaflet before using the medicine, as it contains important information for the patient.
- This medicine should always be used exactly as described in the patient leaflet or as directed by a doctor or pharmacist.
- You should keep this leaflet, so you can read it again if you need to.
- If you need advice or more information, you should ask your pharmacist.
- If the patient experiences any side effects, including any possible side effects not listed in the leaflet, they should tell their doctor or pharmacist. See section 4.
- If after 3 days there is no improvement or the patient feels worse, they should contact their doctor.
Table of contents of the leaflet:
- 1. What is Nurofen for Children Junior Strawberry and what is it used for
- 2. Important information before using Nurofen for Children Junior Strawberry
- 3. How to use Nurofen for Children Junior Strawberry
- 4. Possible side effects
- 5. How to store Nurofen for Children Junior Strawberry
- 6. Contents of the packaging and other information
1. What is Nurofen for Children Junior Strawberry and what is it used for
Ibuprofen belongs to a group of medicines called Non-Steroidal Anti-Inflammatory Drugs (NSAIDs). The action of these medicines is to change the body's response to pain and elevated body temperature. Nurofen for Children Junior Strawberry is intended for short-term, symptomatic treatment of:
- fever,
- pain of mild to moderate severity.
If after 3 days there is no improvement or the patient feels worse, they should contact their doctor.
2. Important information before using Nurofen for Children Junior Strawberry
When not to use Nurofen for Children Junior Strawberry
- If the child is allergic to ibuprofen or other similar painkillers (NSAIDs) or any of the other ingredients of this medicine (listed in section 6).
- If the child has ever had breathing difficulties, asthma, hay fever, or swelling of the face and/or hands or hives after taking acetylsalicylic acid or other similar painkillers (NSAIDs).
- If the child has ever had bleeding or perforation of the gastrointestinal tract associated with previous use of NSAIDs.
- If the child currently has or has had stomach and/or duodenal ulcers (ulcer disease) or bleeding (two or more confirmed cases of ulcers or bleeding).
- If the child has severe liver and kidney failure.
- If the child has severe heart failure
- If the child has had bleeding in the brain (cerebral hemorrhage) or other active bleeding.
- If the child has blood clotting disorders, as ibuprofen may prolong bleeding time.
- If the child has blood production disorders of unknown origin.
- In children with severe dehydration (caused by vomiting, diarrhea, or insufficient fluid intake).
Do not take the medicine in the last 3 months of pregnancy.
Warnings and precautions
Before starting treatment with Nurofen for Children Junior Strawberry, you should discuss it with your doctor or pharmacist
- If the child has an infection - see below, section "Infections".
- If the child has certain inherited blood production disorders (e.g., acute intermittent porphyria).
- If the child has blood clotting disorders.
- If the child has certain skin diseases (systemic lupus erythematosus (SLE) or mixed connective tissue disease).
- If the child has intestinal diseases (ulcerative colitis or Crohn's disease), as their symptoms may worsen.
- If the child has or has had high blood pressure and/or heart failure.
- If the child has kidney function disorders.
- If the child has liver diseases. In the case of long-term use of Nurofen for Children Junior Strawberry, regular monitoring of liver function, kidney function, and blood morphology parameters is required.
- Caution is recommended when using other medicines that may increase the risk of gastrointestinal ulcers or bleeding, such as oral corticosteroids (e.g., prednisolone), blood thinners (e.g., warfarin), selective serotonin reuptake inhibitors (antidepressants), and antiplatelet agents (e.g., acetylsalicylic acid).
- If the child is taking other NSAIDs (including COX-2 inhibitors such as celecoxib or etoricoxib), as concurrent use of these medicines should be avoided.
- The occurrence of side effects can be reduced by using the smallest effective dose for the shortest possible time.
- Generally, continuous use of (various) painkillers can lead to persistent serious kidney diseases. This risk may increase during physical exertion associated with salt loss and dehydration. Therefore, it should be avoided.
- As a result of long-term use of any type of painkillers, headaches may occur, which should not be treated with increased doses of this medicine. In such a case, the medicine should be discontinued and a doctor consulted. The diagnosis of headache caused by drug abuse should be suspected in patients who have frequent or daily headaches despite (or due to) regular use of pain-relieving medicines.
- If the child has or has had asthma or allergic diseases that can cause shortness of breath.
- If the child has hay fever, nasal polyps, chronic obstructive pulmonary disease, there is an increased risk of allergic reactions. Allergic reactions can occur as asthma attacks (so-called analgesic-induced asthma), Quincke's edema, or hives.
- Nurofen for Children Junior Strawberry should be avoided in case of chickenpox (varicella).
- If the child has recently undergone major surgery (medical supervision is required).
- If the child is dehydrated, due to the increased risk of kidney failure in dehydrated children.
Infections
Nurofen for Children Junior Strawberry may mask the symptoms of infection, such as fever and pain. Therefore, Nurofen for Children Junior Strawberry may delay the use of appropriate infection treatment and consequently lead to increased risk of complications. This has been observed in bacterial pneumonia and bacterial skin infections associated with chickenpox. If the patient is taking this medicine during an ongoing infection, and the symptoms of the infection persist or worsen, they should immediately consult a doctor.
Skin reactions
Severe skin reactions have been reported with ibuprofen, 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). If the patient experiences any of the symptoms associated with these severe skin reactions described in section 4, they should immediately discontinue Nurofen for Children Junior Strawberry and seek medical attention.
Gastrointestinal bleeding, ulcers, or perforation, which can be fatal, have been reported during treatment with all NSAIDs, with or without warning signs, or in patients with serious gastrointestinal disorders. If gastrointestinal bleeding or ulcers occur, treatment should be discontinued immediately. The risk of gastrointestinal bleeding, ulcers, or perforation increases with the dose of NSAIDs in patients with a history of ulcers, especially with bleeding or perforation (see section 2 "When not to use Nurofen for Children Junior Strawberry") and in the elderly. These patients should start treatment with the smallest effective dose. For these patients and patients requiring concurrent administration of acetylsalicylic acid in low doses or medications that increase the risk of gastrointestinal reactions, concomitant treatment with protective agents (e.g., misoprostol or proton pump inhibitors) should be considered.
Taking painkillers and anti-inflammatory medicines, such as 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 and duration of treatment.
Before using Nurofen for Children Junior Strawberry, the patient should discuss treatment with their doctor or pharmacist if:
- The patient has heart diseases, such as heart failure, angina pectoris (chest pain), has had a heart attack, coronary artery bypass grafting, has peripheral artery disease (poor blood circulation in the legs due to narrowing or blockage of arteries), or has had any stroke (including mini-stroke or transient ischemic attack - TIA).
- The patient has high blood pressure, diabetes, high cholesterol levels, has a family history of heart disease or stroke, or smokes.
- Ibuprofen has been reported to cause symptoms of allergic reactions to this medicine, including breathing difficulties, face and throat swelling (angioedema), chest pain. If the patient notices any of these symptoms, they should immediately discontinue Nurofen for Children Junior Strawberry and contact their doctor or emergency services.
If any of the above cases apply to the child, they should consult their doctor before using Nurofen for Children Junior Strawberry.
Elderly patients
Elderly patients are at increased risk of side effects when using NSAIDs, particularly those affecting the stomach and intestines.
Patients with a history of gastrointestinal disorders, especially in the elderly, should report any unusual abdominal symptoms (mainly gastrointestinal bleeding), especially during the initial treatment phase.
Nurofen for Children Junior Strawberry and other medicines
Tell your doctor or pharmacist about all medicines the child is currently taking or has recently taken, as well as any medicines the child may be taking.
Nurofen for Children Junior Strawberry may affect the action of other medicines or other medicines may affect the action of Nurofen for Children Junior Strawberry. For example:
- blood-thinning medicines (e.g., acetylsalicylic acid, warfarin, ticlopidine)
- blood pressure-lowering medicines (e.g., ACE inhibitors such as captopril, beta-blockers such as atenolol, angiotensin II receptor antagonists such as losartan).
Some other medicines may also be affected or have an effect on treatment with Nurofen for Children Junior Strawberry. Therefore, before using Nurofen for Children Junior Strawberry with other medicines, you should always consult your doctor or pharmacist.
In particular, you should inform your doctor if the patient is taking:
- Other NSAIDs, including COX-2 inhibitors, as the risk of side effects may increase
- Digoxin (a medicine used for heart failure), as the effect of digoxin may be enhanced
- Corticosteroids (medicines containing cortisone or similar substances), as the risk of stomach ulcers and bleeding may increase
- Antiplatelet agents, as the risk of bleeding may increase
- Acetylsalicylic acid (in low doses), as the blood-thinning effect may be reduced
- Blood thinners (e.g., warfarin), as ibuprofen may enhance the effect of these medicines
- Phenytoin (a medicine used to treat epilepsy), as the effect of phenytoin may be enhanced
- Selective serotonin reuptake inhibitors (medicines used to treat depression), as they may increase the risk of gastrointestinal bleeding
- Lithium (a medicine used to treat manic-depressive disorders and depression), as the effect of lithium may be enhanced
- Probenecid and sulfinpyrazone (a medicine used to treat gout), as the excretion of ibuprofen may be delayed
- Blood pressure-lowering medicines and diuretics, as ibuprofen may weaken the effect of these medicines and may increase the risk of kidney function deterioration
- Diuretics that spare potassium, such as amiloride, potassium canrenoate, spironolactone, triamterene, as hyperkalemia may occur
- Methotrexate (a medicine used to treat cancer and rheumatism), as the effect of methotrexate may be enhanced
- Tacrolimus and cyclosporin (immunosuppressive medicines), as kidney damage may occur
- Zidovudine (in the treatment of HIV/AIDS), as the use of Nurofen may increase the risk of intracranial bleeding or bleeding leading to swelling in HIV-positive patients with hemophilia
- Sulfonylurea derivatives (oral antidiabetic medicines), as they may affect blood sugar levels
- Quinolone antibiotics, as the risk of seizures may increase
- Voriconazole and fluconazole (CYP2C9 inhibitors, used in fungal infections), as the effect of ibuprofen may be enhanced; the dose of ibuprofen should be reduced, especially when using high doses of ibuprofen with voriconazole or fluconazole
- Baclofen, as baclofen toxicity may develop after using ibuprofen
- Ritonavir, as ritonavir may increase the plasma concentration of NSAIDs
- Aminoglycosides, as NSAIDs may increase the excretion of aminoglycosides
Nurofen for Children Junior Strawberry and alcohol
Do not consume alcohol while using Nurofen for Children Junior Strawberry. Some side effects, such as those related to the gastrointestinal tract or central nervous system, may be more likely when taking alcohol and Nurofen for Children Junior Strawberry.
Pregnancy, breastfeeding, and fertility
If the patient is pregnant or breastfeeding, thinks they may be pregnant, or plans to have a child, they should consult their doctor or pharmacist before using this medicine.
Pregnancy
Do not use this medicine during the last 3 months of pregnancy. Use may cause kidney and heart problems in the unborn child. It may also affect the mother's and child's bleeding tendency and prolong or delay labor. Avoid using this medicine during the first 6 months of pregnancy, unless the doctor recommends otherwise. Taking ibuprofen for more than a few days after the start of the 20th week of pregnancy may cause kidney problems in the unborn child and lead to a low level of amniotic fluid surrounding the child (oligohydramnios) or narrowing of the arterial duct (ductal constriction) in the child's heart. If necessary, the doctor may recommend additional monitoring.
Breastfeeding
Only small amounts of ibuprofen and its breakdown products pass into breast milk. Nurofen for Children Junior Strawberry can be used during breastfeeding, if administered in the recommended doses and for the shortest possible time.
Fertility
Nurofen for Children Junior Strawberry belongs to a group of medicines (NSAIDs) that may affect fertility in women. This effect is temporary after stopping the medicine.
Driving and using machines
During short-term use, the medicine does not affect or has a negligible effect on the ability to drive and use machines.
- Nurofen for Children Junior Strawberry contains liquid maltitol. If the patient has previously been diagnosed with intolerance to some sugars, they should consult their doctor before taking the medicine.
- The medicine may have a mild laxative effect.
- The caloric value for maltitol is: 2.3 kcal/g
- Nurofen for Children Junior Strawberry contains less than 1 mmol of sodium (23 mg) per dose, so the medicine is considered "sodium-free".
- Nurofen for Children Junior Strawberry contains 16.45 mg of propylene glycol in each 5 ml of suspension.
3. How to use Nurofen for Children Junior Strawberry
Nurofen for Children Junior Strawberry should always be used exactly as described in the patient leaflet or as directed by a doctor or pharmacist. In case of doubt, consult a doctor or pharmacist.
Use the smallest effective dose for the shortest possible time.
If the symptoms of infection (such as fever and pain) persist or worsen, consult a doctor immediately (see section 2).
Recommended dose for pain and fever:
Child's weight (age) | Dose and administration | Frequency within 24 hours* |
20 to 29 kg (6 to 9 years) | 1 x 200 mg/5 ml (single use of the correct end of the measuring spoon) | 3 times |
30 to 40 kg (10 to 12 years) | 1 x 300 mg/7.5 ml (double use of the measuring spoon (5 ml and 2.5 ml)) | 3 times |
*Doses should be given every 6 to 8 hours.
Do not recommend for children under 6 years of age or weighing less than 20 kg.
In patients with sensitive stomachs, it is recommended to take Nurofen for Children Junior Strawberry with food.
WARNING: do not exceed the recommended dose.
For oral use
Method of administration using a measuring spoon
- 1. Shake the bottle well.
- 2. Use the end of the measuring spoon suitable for the required dose.
- 3. Pour the medicine into the measuring spoon.
- 4. Place the measuring spoon in the child's mouth and administer the dose.
- 5. After use, close the bottle. Wash the measuring spoon with warm water and let it dry. Store it in a place inaccessible to children.
Duration of treatment
This medicine is intended for short-term use only.If the child's symptoms persist for more than 3 days or the patient feels worse, they should consult a doctor.
If a higher than recommended dose of Nurofen for Children Junior Strawberry is taken:
If the patient has taken a higher dose of Nurofen for Children Junior Strawberry than recommended or if the child has accidentally taken the medicine, they should always consult a doctor or go to the nearest hospital to get an opinion on possible health risks and advice on what to do in such a case.
Symptoms of overdose may include nausea, stomach pain, vomiting (which may contain blood), gastrointestinal bleeding, headache, ringing in the ears, disorientation, and nystagmus or, less commonly, diarrhea. After taking a large dose, balance disorders, vision disorders, low blood pressure, excitement, disorientation, coma, hyperkalemia, metabolic acidosis, increased prothrombin time/INR, acute kidney failure, liver damage, respiratory depression, cyanosis, and worsening of asthma in asthmatic patients may occur.
If a dose of Nurofen for Children Junior Strawberry is missed:
Do not take a double dose to make up for a missed dose. If the patient forgets to take or administer a dose, they should take or administer it as soon as they remember, and then take or administer the next dose of the medicine at the recommended interval.
In case of any further doubts about using this medicine, consult a doctor or pharmacist.
4. Possible side effects
Like all medicines, Nurofen for Children Junior Strawberry can cause side effects, although not everybody gets them. The occurrence of side effects can be reduced by using the smallest effective dose for the shortest possible time. The child may experience one of the known side effects of NSAIDs. If side effects occur or in case of doubt, discontinue the medicine and consult a doctor as soon as possible. Elderly patients using this medicine belong to a group with an increased risk of side effects.
DISCONTINUE USE of the medicine and seek medical attention immediately if the child experiences:
- symptoms of gastrointestinal bleeding, such as severe abdominal pain, black tarry stools, vomiting blood or coffee grounds, or dark-colored vomit.
- symptoms of rare but serious allergic reactions, such as worsening of asthma, unexplained wheezing or shortness of breath, swelling of the face, tongue, or throat, difficulty breathing, rapid heartbeat, or low blood pressure leading to shock. Symptoms may occur even after the first use of the medicine. If any of these symptoms occur, seek medical attention immediately.
- red, non-raised, target-like, or circular patches on the torso, often with blisters in the center, peeling skin, mouth ulcers, genital ulcers, and eye ulcers. These severe skin reactions may be preceded by fever and flu-like symptoms (exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis). [Very rare - may occur in 1 in 10,000 people].
- widespread rash, high fever, swollen lymph nodes, and an increased number of eosinophils (a type of white blood cell) (DRESS syndrome) [Frequency not known - cannot be estimated from available data].
- red, peeling, widespread rash with bumps under the skin and blisters, mainly in skin folds, on the torso, and upper limbs, with accompanying fever. Symptoms usually appear at the beginning of treatment (acute generalized exanthematous pustulosis) [Frequency not known - cannot be estimated from available data].
If any of the side effects worsen or any side effects not listed in the leaflet occur, tell your doctor.
Frequent(may occur in 1 in 10 people)
- Gastrointestinal disorders, such as heartburn, abdominal pain, nausea, indigestion, diarrhea, vomiting, bloating (gas), constipation, and minor gastrointestinal bleeding, which in rare cases may cause anemia.
Uncommon(may occur in 1 in 100 people)
- Gastrointestinal ulcers, which may bleed or perforate, mouth ulcers, worsening of existing intestinal diseases (ulcerative colitis or Crohn's disease), stomach inflammation
- Central nervous system disorders, such as headaches, dizziness, insomnia, restlessness, or fatigue
- Vision disorders
- Various skin rashes
- Allergic reactions with hives and itching.
Rare(may occur in 1 in 1,000 people)
- Ringing in the ears (tinnitus)
- Increased blood urea levels, side pain and/or abdominal pain, blood in the urine, and fever, which may be symptoms of kidney damage (renal papillary necrosis)
- Increased blood uric acid levels
- Decreased hemoglobin levels.
Very rare(may occur in 1 in 10,000 people)
- Esophageal inflammation, pancreatitis, formation of intestinal strictures
- Heart failure, heart attack, and facial or hand swelling
- Decreased urine output and swelling (especially in patients with high blood pressure or impaired kidney function), kidney syndrome (nephrotic syndrome), and interstitial kidney disease, which may lead to acute kidney failure. If any of the above symptoms occur or if the patient feels unwell, they should discontinue Nurofen for Children Junior Strawberry and consult a doctor immediately, as these may be the first symptoms of kidney damage or failure
- Psychotic reactions and depression
- High blood pressure, blood vessel inflammation
- Rapid heartbeat
- Liver function disorders, liver damage (the first symptoms may be skin discoloration), especially during long-term treatment, liver failure, acute liver inflammation
- Blood production disorders - the first symptoms are: fever, sore throat, superficial mouth ulcers, flu-like symptoms, severe fatigue, nosebleeds, and unexplained bruising. In such cases, treatment should be discontinued immediately and a doctor consulted. Do not self-medicate with painkillers or antipyretics
- Severe skin and soft tissue infections during chickenpox
- Aseptic meningitis symptoms, such as stiff neck, headache, nausea, vomiting, fever, and impaired consciousness, have been observed with ibuprofen. Patients with autoimmune disorders (lupus, mixed connective tissue disease) are at higher risk of such symptoms. If such symptoms occur, seek medical attention immediately
- Hair loss (alopecia).
Frequency not known(cannot be estimated from available data)
- Chest pain, which may be a symptom of a potentially serious allergic reaction called Kounis syndrome.
- Respiratory tract reactions, including asthma, bronchospasm, shortness of breath.
- Skin becomes sensitive to light.
Medicines like this one may be associated with a small increased risk of heart attack (myocardial infarction) or stroke.
Reporting side effects
If side effects occur, including any side effects not listed in the leaflet, tell your doctor or pharmacist or nurse. Side effects can be reported directly to the Department of Drug Safety Monitoring of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products:
Jerozolimskie Avenue 181C, 02-222 Warsaw, phone: 22 49-21-301, fax: 22 49-21-309, website:
https://smz.ezdrowie.gov.pl
Side effects can also be reported to the marketing authorization holder.
Reporting side effects will help gather more information on the safety of this medicine.
5. How to store Nurofen for Children Junior Strawberry
Store in a place inaccessible to children.
Do not use Nurofen for Children Junior Strawberry after the expiration date stated on the carton and bottle. The expiration date refers to the last day of the month.
Do not store above 25°C.
After opening the bottle, the medicine should be used within 6 months.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
6. Contents of the packaging and other information
What Nurofen for Children Junior Strawberry contains
The active substance of the medicine is ibuprofen. Each 1 ml of oral suspension contains 40 mg of ibuprofen.
The other ingredients are: citric acid monohydrate, sodium citrate, sodium chloride, sodium saccharin, polysorbate 80, bromhexine hydrochloride, liquid maltitol, glycerol, xanthan gum, strawberry flavor 500244E (propylene glycol, ascorbic acid (E 300), natural and identical to natural flavoring substances), and purified water.
What Nurofen for Children Junior Strawberry looks like and contents of the pack
Nurofen for Children Junior Strawberry is a white suspension with a syrupy consistency and a characteristic strawberry smell.
Each bottle contains 100 ml, 150 ml, or 200 ml.
The packaging includes a double-ended measuring spoon (with a 2.5 ml measure with an inner mark of 1.25 ml on one end and a 5 ml measure on the other end) for accurate dosing.
Not all pack sizes may be marketed.
Marketing authorization holder and importer
Marketing authorization holder:
Reckitt Benckiser (Poland) S.A.
Okunin 1
05-100 Nowy Dwór Mazowiecki
Importer:
RB NL Brands B.V.
WTC Schiphol Airport,
Schiphol Boulevard 207,
1118 BH Schiphol,
Netherlands
To obtain more detailed information, contact the local representative of the marketing authorization holder:
Reckitt Benckiser (Poland) S.A.
Okunin 1
05-100 Nowy Dwór Mazowiecki
Phone: (22) 211 26 92
This medicinal product is authorized in the Member States of the European Economic Area under the following names:
Belgium | Nurofen voor Kinderen Suikervrij Rood 4% suspensie voor oraal gebruik |
Bulgaria | Нурофен за Юноши Ягода 200 mg/5 ml перорално суспензия |
Croatia | Nurofen Forte za djecu 200 mg/5 ml oralna suspenzija s okusom jagode |
Cyprus | Nurofen για Παιδιά 4% Φράουλα |
Czech Republic | Nurofen pro děti 4% jahoda |
Germany | Nurodon Schmerz-und Fiebersaft Erdbeer 40mg/ml Suspension zum Einnehmen |
Greece | Nurofen for Children 4% strawberry |
Hungary | Nurofen eperízû 40 mg/ml belsõleges szuszpenzió gyermekeknek |
Ireland | Nurofen for Children Six Plus Strawberry 200mg/5ml Oral Suspension |
Luxembourg | Nurofen pour Enfants 4% suspension buvable |
Netherlands | Nurofen voor Kinderen Aardbei suspensie, suspensie 200 mg/5ml |
Poland | Nurofen dla dzieci Junior truskawkowy |
Portugal | Nurofen Morango 40 mg/ml suspensão oral |
Romania | Nurofen Junior, cu aromă de căpşuni 200mg/5ml suspensie orală |
Slovakia | Nurofen pre deti 4% jahoda |
Date of last revision of the leaflet: 04/2025