5 ml of Nurofen for children with strawberry flavor suspension contains 100 mg of ibuprofen, which belongs to a group of nonsteroidal anti-inflammatory drugs (NSAIDs). The medicine relieves symptoms such as fever, pain, and swelling by acting at the site of their occurrence.
The medicine is intended for use in infants and children in the following cases:
Nurofen for children with strawberry flavor should not be used in patients:
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Severe skin reactions have been reported with the use of Nurofen for children with strawberry flavor. If the following occur: any skin rash, changes in mucous membranes, blisters or other symptoms of an allergic reaction, you should stop taking Nurofen for children with strawberry flavor and seek medical attention immediately, as these may be the first symptoms of a very severe skin reaction. See section 4.
When using Nurofen for children with strawberry flavor, you should consult a doctor if the child has previously had:
In the case of chickenpox, it is recommended to avoid using the medicine.
Infections
Nurofen for children with strawberry flavor may mask the symptoms of an infection, such as fever and pain. Therefore, Nurofen for children with strawberry flavor may delay the use of appropriate infection treatment and, as a result, lead to an increased risk of complications.
This has been observed in the course of bacterial pneumonia and bacterial skin infections associated with chickenpox. If the patient is taking this medicine during an infection, and the symptoms of the infection persist or worsen, they should consult a doctor immediately.
In dehydrated children, there is a risk of kidney function disorder.
There is a risk of gastrointestinal bleeding, ulceration or perforation, which can be fatal and does not necessarily have to be preceded by warning signs or may occur in patients who have had such warning signs.
In the event of gastrointestinal bleeding or ulceration, the medicine should be discontinued immediately. Patients with a history of gastrointestinal diseases, especially the elderly (Nurofen for children with strawberry flavor may also be used by adults), should inform their doctor about any unusual gastrointestinal symptoms (especially bleeding), especially during the initial treatment period.
Prolonged use of different painkillers may lead to kidney damage with a risk of kidney failure (analgesic nephropathy).
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Taking medicines such as ibuprofen may be associated with a small increased risk of heart attack (myocardial infarction) or stroke. This risk increases with long-term use of high doses of the medicine. You should not use higher doses or longer treatment than recommended. If symptoms persist, worsen or do not improve after 3 days, or if new symptoms occur, you should consult a doctor.
In the case of heart problems, a history of stroke, or suspected risk of these disorders (e.g. high blood pressure, diabetes, high cholesterol, smoking), you should discuss the treatment with a doctor or pharmacist.
This medicine belongs to a group of medicines (nonsteroidal anti-inflammatory drugs) that may adversely affect female fertility. This effect is temporary and disappears after the end of treatment.
During pregnancy and breastfeeding, or if you suspect that you are pregnant, or if you plan to become pregnant, you should consult a doctor or pharmacist before using this medicine.
During the first 6 months of pregnancy, it is not recommended to use the medicine. During the last three months of pregnancy, you should not take the medicine, as it may increase the risk of complications in the mother and child during the perinatal period.
Ibuprofen may pass into breast milk in small amounts. There are no known cases of adverse reactions in breastfed infants, so there is no need to discontinue breastfeeding.
If the patient has previously been diagnosed with intolerance to some sugars, they should consult a doctor before taking the medicine.
You should tell your doctor or pharmacist about all medicines you are currently taking or have recently taken, as well as any medicines you plan to take, even those that are available without a prescription.
You should avoid taking Nurofen for children if you are using other nonsteroidal anti-inflammatory drugs (including cyclooxygenase-2 inhibitors, such as celecoxib or etoricoxib), acetylsalicylic acid, or other painkillers.
Nurofen for children should be used with caution with the following medicines:
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This medicine should always be used exactly as described in the patient leaflet or as directed by a doctor or pharmacist. In case of doubt, you should consult a doctor or pharmacist.
You should use the smallest effective dose for the shortest period necessary to relieve the symptoms. If the symptoms of an infection (such as fever and pain) persist or worsen, you should consult a doctor immediately (see section 2).
A measuring spoon with a capacity of 2.5 ml/5 ml is attached to the packaging to facilitate dosing.
You should shake the bottle before use.
or
A dosing device in the form of a syringe with a scale facilitating dosing is attached to the packaging.
For oral use.
The medicine is intended for short-term use only.
The recommended daily dose of the medicine is 20-30 mg per kilogram of body weight, divided into equal doses administered at intervals of 6 to 8 hours. You should not use a higher dose of the medicine than recommended.
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Age | Body weight (kg) | Recommended dosing |
Infants from 3 to 6 months, with a body weight over 5 kg |
| 50 mg (2.5 ml) up to 3 times in 24 hours |
Infants from 6 to 12 months | 7.7 - 9 | 50 mg (2.5 ml) up to 3-4 times in 24 hours |
Children from 1 to 3 years | 10-16 | 100 mg (5 ml) up to 3 times in 24 hours |
Children from 4 to 6 years |
| 150 mg (7.5 ml) up to 3 times in 24 hours |
Children from 7 to 9 years |
| 200 mg (10 ml) up to 3 times in 24 hours |
Children from 10 to 12 years |
| 300 mg (15 ml) up to 3 times in 24 hours |
Children under 6 months old can be given the medicine only after consulting a doctor.
You should not use this medicine in children with a body weight of less than 5 kg.
In the case of children aged 3-5 months, you should consult a doctor if the symptoms worsen or do not improve after 24 hours.
In the case of children over 6 months old, you should consult a doctor if the administration of the medicine is necessary for more than 3 days or if the symptoms worsen.
Post-vaccination fever (children aged 3-6 months): The recommended daily dose of the medicine is 1 x 50 mg; if necessary, a second dose of 1 x 50 mg can be taken after 6 hours. You should not exceed the dose of 2 x 50 mg in 24 hours. If the fever does not decrease, you should consult a doctor.
Cases of overdose are rare. However, if the patient has used a higher dose of Nurofen for children with strawberry flavor than recommended or if a child has accidentally taken the medicine, you should always consult a doctor or go to the nearest hospital to get an opinion on the possible health risk and advice on what actions to take in such a case.
Symptoms may include nausea, stomach pain, vomiting (which may contain blood), headaches, ringing in the ears, disorientation, and nystagmus. After taking a large dose, drowsiness, chest pain, palpitations, loss of consciousness, seizures (mainly in children), weakness, and dizziness, blood in the urine, feeling cold, and breathing problems may occur.
The following may also occur: abdominal pain or, less frequently, diarrhea, gastrointestinal bleeding, very rarely excitement or coma, metabolic acidosis, increased prothrombin time/INR, acute kidney failure or liver damage, and in patients with asthma - worsening of asthma symptoms.
There is no specific antidote. Treatment is symptomatic and supportive, consisting of cleansing the body. The doctor will monitor heart function and control vital signs, if they are stable. The doctor will consider administering activated charcoal orally within 1 hour of overdose.
In the case of frequent or prolonged seizures, the doctor will administer diazepam or lorazepam intravenously. In the case of patients with asthma, the doctor will administer bronchodilators.
You should not use a double dose to make up for a missed dose.
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Like all medicines, this medicine can cause side effects, although not everybody gets them.
During short-term use of ibuprofen in doses available without a prescription, the following side effects have been observed. When using ibuprofen for other indications and long-term, other side effects may occur.
If you experience any side effects, including any possible side effects not listed in the leaflet, you should consult a pharmacist or doctor.
Side effects are ranked according to frequency of occurrence using the following terms:
Very common (occurring more frequently than 1 in 10 patients)
Common (occurring more frequently than 1 in 100 patients)
Uncommon (occurring more frequently than 1 in 1,000 patients)
Rare (occurring more frequently than 1 in 10,000 patients)
Very rare (occurring less frequently than 1 in 10,000 patients)
hypersensitivity with hives and itching
headaches
stomach pain, nausea, and indigestion
skin rash
dizziness, insomnia, agitation, irritability, or feeling tired. In individual cases, depression, psychotic reactions, and tinnitus have been reported.
diarrhea, bloating, constipation, vomiting, and gastritis
edema
blood disorders
severe hypersensitivity reactions, including face, tongue, and throat edema, dyspnea, tachycardia, and hypotension (anaphylaxis, angioedema, or shock)
aseptic meningitis
heart failure and edema
hypertension
respiratory tract reactivity, including asthma, bronchospasm, or dyspnea
peptic ulcer, perforation, or gastrointestinal bleeding, black stools, and bloody vomiting, oral ulceration, exacerbation of ulcerative colitis and Crohn's disease
liver disorders
bullous reactions, including Stevens-Johnson syndrome, erythema multiforme, and toxic epidermal necrolysis
severe skin and soft tissue infections in the course of chickenpox. Worsening of infectious conditions (e.g. necrotizing fasciitis) has been reported during the use of some painkillers (NSAIDs).
acute kidney failure
decreased hemoglobin levels
severe skin reactions known as DRESS syndrome may occur. The symptoms of DRESS syndrome include: skin rash, fever, lymph node swelling, and increased eosinophil count (a type of white blood cell)
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a red scaly rash with thickening under the skin and blisters, usually located in skin folds, on the torso, and upper limbs, with fever occurring at the beginning of treatment (acute generalized exanthematous pustulosis). If such symptoms occur, you should stop taking Nurofen for children with strawberry flavor and seek medical attention immediately. See also section 2.
the skin becomes sensitive to light
you should tell your doctor or pharmacist.
If you experience any side effects, including any possible side effects not listed in the leaflet, you should 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:
Al. Jerozolimskie 181C, 02-222 Warsaw, tel.: 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.
By reporting side effects, you can help provide more information on the safety of the medicine.
There are no special recommendations for storage conditions.
The opened packaging should be used within 6 months.
The medicine should be stored out of sight and reach of children.
The medicine should not be used after the expiry date stated on the packaging. The expiry date refers to the last day of the given month.
Medicines should not be disposed of via wastewater or household waste containers. You should ask your pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
5 ml of Nurofen for children with strawberry flavor contains:
Active substance: ibuprofen 100 mg
Other ingredients are: polysorbate 80, glycerol, liquid maltitol, sodium saccharin, citric acid monohydrate, sodium citrate, xanthan gum, sodium chloride, strawberry flavor 500244E, bromhexine hydrochloride, purified water.
A bottle containing 100 ml or 150 ml of oral suspension 100 mg/5 ml.
A measuring spoon with a capacity of 2.5 ml/5 ml is attached to the packaging to facilitate dosing.
Reckitt Benckiser (Poland) S.A.
Reckitt Benckiser
ul. Okunin 1
05-100 Nowy Dwór Mazowiecki
RB NL Brands B.V.
WTC Schiphol Airport,
Schiphol Boulevard 207,
1118 BH Schiphol,
Netherlands
To obtain more detailed information, you should contact the representative of the marketing authorization holder:
Reckitt Benckiser (Poland) S.A.
ul. Okunin 1
05-100 Nowy Dwór Mazowiecki
Hotline number: 801 88 88 07
Date of last update of the leaflet: 03/2021
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