User Information: Package Insert
Read this entire package insert carefully before taking this medicine, as it contains important information for you.
Contents of the package and additional information
Neobrufen belongs to a group of medications called nonsteroidal anti-inflammatory drugs (NSAIDs).
This medication is used for the treatment of fever, the treatment of moderate pain including migraine, the treatment of arthritis (inflammation of the joints, including those of the hands and feet, leading to swelling and pain), juvenile rheumatoid arthritis, osteoarthritis (a chronic disorder that causes cartilage damage), ankylosing spondylitis (inflammation affecting the joints of the spine), non-rheumatic inflammation, and primary dysmenorrhea (painful menstruation).
Warnings and precautions
Consult your doctor or pharmacist before starting to take Neobrufen:
This risk is higher when using high doses and prolonged treatment, especially in patients with a history of peptic ulcer disease and in elderly patients. In these cases, your doctor may consider associating a stomach protector medication.
It is essential to use the smallest dose that relieves or controls pain and not to take this medication for longer than necessary to control your symptoms.
Signs of allergic reactions to ibuprofen, such as respiratory problems, facial and neck swelling (angioedema), and chest pain, have been reported. Stop using Neobrufen immediately and contact your doctor or emergency medical services if you observe any of these signs.
Precautions in elderly patients
Elderly patients have a higher frequency of adverse reactions to NSAIDs, especially gastrointestinal bleeding and perforation, which can be fatal.
Severe 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), generalized acute pustular psoriasis (PEGA), have been reported in association with ibuprofen treatment. Discontinue Neobrufen treatment and seek medical attention immediately if you notice any of the symptoms related to these severe skin reactions described in section 4.
NSAIDs, 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 or treatment duration.
Inform your doctor or pharmacist before taking Neobrufen if:
-You have heart problems, including heart failure, angina (chest pain), or have had a heart attack, coronary artery bypass surgery, peripheral artery disease (circulation problems in the legs or feet due to narrowing or blockage of the arteries), or any type of stroke (including a "mini-stroke" or transient ischemic attack "TIA").
-You have high blood pressure, diabetes, high cholesterol, a family history of heart disease or stroke, or are a smoker. This type of medication may also cause fluid retention, especially in patients with heart failure and/or high blood pressure.
Respiratory disorders
Ibuprofen should be used with caution in patients with or a history of asthma, chronic bronchitis, or allergic diseases, as it has been reported to cause bronchospasm, urticaria, or angioedema in these patients.
Precautions during pregnancy and in fertile women
Due to the association of NSAID administration with an increased risk of congenital anomalies/abortions, the administration of Neobrufen is not recommended during the first and second trimesters of pregnancy, except in cases where it is strictly necessary. In these cases, the dose and duration will be limited to the minimum possible. It is believed that the risk increases with the dose and duration of treatment.
The administration of Neobrufen is contraindicated in the third trimester of pregnancy.
For fertile women, it is essential to consider that NSAIDs have been associated with a decrease in fertility.
Infections
Neobrufen may mask the signs of an infection, such as fever and pain. Consequently, Neobrufen may delay the appropriate treatment of the infection, increasing the risk of complications. This has been observed in pneumonia caused by bacteria and skin infections related to chickenpox. If you take this medication while having an infection and the infection symptoms persist or worsen, consult your doctor without delay.
Other medications and Neobrufen
Inform your doctor or pharmacist if you are using, have used recently, or may need to use any other medication.
Neobrufen may affect or be affected by other medications. For example:
Other medications may also affect or be affected by Neobrufen treatment. Therefore, always consult your doctor or pharmacist before using Neobrufen with other medications.
Neobrufen may alter the following laboratory tests:
Inform your doctor if you are to undergo a clinical analysis and are taking or have recently taken ibuprofen.
Neobrufen with food and beverages
It is recommended to take Neobrufen dissolved in a glass of water. You can take it alone or with food. In general, it is recommended to take it during meals or immediately after eating to reduce the possibility of stomach discomfort. Do not take alcohol, as it may increase gastrointestinal adverse reactions.
Pregnancy, lactation, and fertility
Consult your doctor or pharmacist before using any medication.
The use of this medication is not recommended for women trying to become pregnant.
Do not take ibuprofen during pregnancy, especially during the third trimester (see section on precautions during pregnancy and in fertile women), as it may harm the fetus or cause complications during delivery. It may cause kidney and heart problems in your fetus. It may affect your predisposition and that of your baby to bleeding and delay or prolong delivery more than expected.
Do not take Neobrufen during the first 6 months of pregnancy unless absolutely necessary and advised by your doctor. If you need treatment during this period or while trying to become pregnant, you should use the lowest dose for the shortest time necessary. From week 20 of pregnancy onwards, Neobrufen may cause kidney problems in your fetus if taken for more than a few days, which may cause low amniotic fluid levels (oligohydramnios) or narrowing of the blood vessels (ductus arteriosus) in your baby's heart. If you need treatment for a period longer than a few days, your doctor may recommend additional monitoring.
Although only small amounts of the medication pass into breast milk, it is recommended not to take ibuprofen for prolonged periods during lactation.
If you experience dizziness, vertigo, visual disturbances, or other symptoms while taking this medication, do not drive or operate hazardous machinery. If you only take a single dose of Neobrufen or for a short period, no special precautions are necessary.
Ibuprofen may delay your reaction time, which should be taken into account before engaging in activities that require increased vigilance, such as driving and operating machinery.
This applies to a greater extent when combined with alcohol
This medication contains saccharose.If your doctor has indicated that you have an intolerance to certain sugars, consult with them before taking this medication.
Patients with diabetes mellitus should note that this medication contains 3.3 g of saccharose per packet.
This medication contains 197 mg of sodium(main component of table salt/for cooking) in each packet. This is equivalent to 9.9% of the recommended daily maximum sodium intake for an adult.
Consult your doctor or pharmacist if you need 2 or more packets daily for a prolonged period, especially if you have been recommended a low-sodium diet.
Follow exactly the administration instructions of this medication as indicated by your doctor. In case of doubt, consult your doctor or pharmacist again.
Your doctor will indicate the duration of treatment with Neobrufen. Do not discontinue treatment beforehand, as this will not yield the expected results. Similarly, do not use this medication for a longer period than indicated by your doctor.
The most effective dose should be used for the shortest duration necessary to alleviate symptoms.If you have an infection, consult a doctor without delay if symptoms (such as fever and pain) persist or worsen (see section 2).
Adverse effects can be minimized by taking the lowest effective dose for the shortest duration necessary to control symptoms.
Adults and adolescents over 14 years:
The recommended dose in adults and adolescents over 14 years is one packet (600 mg) every 6 to 8 hours, depending on the severity of the condition and response to treatment.
In some cases, higher doses may be required, but in any case, it is recommended not to exceed the maximum daily dose of 2400 mg in adults and 1600 mg in adolescents 14 to 18 years old.
Use in children and adolescents under 14 years:
This medication is not recommended for use in children or adolescents under 14 years old, as the ibuprofen dose contained is not suitable for the recommended dosage in these patients.
Older patients:
If you are over 60 years old, your doctor may prescribe a lower dose than usual. If so, the dose can only be increased once your doctor has confirmed that you tolerate the medication well.
Patients with kidney and/or liver diseases:
If you have a kidney and/or liver disease, your doctor may prescribe a lower dose than usual. If so, take the exact dose prescribed by your doctor.
If you estimate that the action of Neobrufen is too strong or too weak, inform your doctor or pharmacist.
Administration form
This medication is administered orally.
To achieve a faster onset of action, the dose can be taken on an empty stomach. It is recommended that patients with sensitive stomachs take ibuprofen with food.
Ensure that the ibuprofen granules are dissolved in sufficient water. You may feel a transient burning sensation in the mouth or throat when taking ibuprofen granules.
If you take more Neobrufen than you should:
If you have taken more Neobrufen than you should, or if a child has accidentally ingested the medication, consult your doctor or pharmacist immediately or call the Toxicological Information Service, phone: 91 562 04 20, indicating the medication and the amount ingested, or go to the nearest hospital to inform yourself about the risk and ask for advice on the measures to be taken.
It is recommended to bring the packaging and the medication leaflet to the healthcare professional.
Normally, symptoms of overdose occur 4 to 6 hours after taking ibuprofen.
Overdose symptoms may include nausea, stomach pain, vomiting (which may contain blood-tinged mucus), headache, ringing in the ears, confusion, involuntary eye movement, and muscle coordination problems. At high doses, symptoms of drowsiness, chest pain, palpitations, loss of consciousness, seizures (mainly in children), weakness, and dizziness have been reported. In rare cases, cases of metabolic acidosis, decreased body temperature, kidney function impairment, stomach and intestinal bleeding, coma, transient loss of breathing (apnea), central and respiratory nervous system depression have been reported. Cases of cardiovascular toxicity (low blood pressure, decreased heart rate, and increased heart rate) have also been reported.
If a severe intoxication has occurred, renal insufficiency and liver damage may occur. In these cases, the doctor will take the necessary measures.
In case of ingestion of significant amounts, activated charcoal should be administered.
If you forget to take Neobrufen
Do not take a double dose to compensate for the missed doses.
If you forget to take your dose, take it as soon as you remember. However, if the next scheduled dose is close, skip the missed dose and take the next dose at its usual time.
The side effects of medicines such as Neobrufen are more common in people over 65 years old.
The incidence of side effects is lower in short-term treatments and if the daily dose is below the maximum recommended dose.
Disorientation or confusion, depression, irritability, nervousness, psychotic reaction,vertigo, tinnitus (golpes or sounds in the ear), auditory disturbances, reversible toxic amblyopia,hepatic lesions, edema (swelling caused by fluid accumulation in tissues), optic neuritis, anaphylactic reaction (in case of severe generalized hypersensitivity reaction may appear facial swelling, tongue and larynx, dyspnea (shortness of breath), tachycardia, hypotension (anaphylaxis, angioedema or severe shock), aseptic meningitis (inflammation of the meninges, which are the membranes that protect the brain and spinal cord, not caused by bacteria). In most cases where aseptic meningitis has been reported with ibuprofen, the patient had some form of autoimmune disease (such as systemic lupus erythematosus and other collagen diseases) which was a risk factor. The symptoms of aseptic meningitis observed were neck stiffness, headache, nausea, vomiting, fever or disorientation. Other side effects are platelet decrease,decrease in white blood cells (may manifest as frequent infections with fever, chills or sore throat), decrease in red blood cells (may manifest as difficulty breathing and pale skin),neutropenia (decrease in neutrophils) and agranulocytosis (very large decrease in neutrophils), aplastic anemia (bone marrow insufficiency to produce different types of cells), hemolytic anemia (premature destruction of red blood cells). The first symptoms are: fever, sore throat, superficial ulcers in the mouth, pseudogripal symptoms, extreme fatigue, bleeding and bruises of unknown cause.
Exacerbation of inflammation related to infections coinciding with the use of NSAIDs has been observed. If signs of infection or these worsen during the use of ibuprofen, it is recommended to see a doctor as soon as possible.
Exacerbation of colitis and Crohn's disease (chronic disease in which the immune system attacks the intestine, causing inflammation that produces diarrhea with blood).
A severe skin reaction known as DRESS syndrome (by its English acronym) may occur. The symptoms of DRESS syndrome include: skin rash, lymph node inflammation and elevated eosinophils (a type of white blood cell).
Generalized red scaly rash, with bumps under the skin and blisters located mainly in skin folds, trunk and upper limbs, accompanied by fever at the beginning of treatment (generalized acute pustular exanthema). Stop taking Neobrufen if you experience these symptoms and seek medical attention immediately. See section 2.
If any of the following side effects appear, interrupt treatment and seek medical attention immediately:
Reporting of side effects
If you experience any type of side effect, consult your doctor, pharmacist or nurse, even if it is a possible side effect that does not appear in this leaflet. You can also report them directly through the Spanish System for the Vigilance of Medicines for Human Use:https://www.notificaram.es
By reporting side effects, you can contribute to providing more information on the safety of this medicine.
Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date that appears on the packaging after “CAD or EXP”. The expiration date is the last day of the month indicated.
Do not store at a temperature above 25°C.
Medications should not be disposed of through drains or in the trash. Dispose of packaging and medications you no longer need at the SIGRE collection point at the pharmacy. If in doubt, ask your pharmacist how to dispose of packaging and medications you no longer need. By doing so, you will help protect the environment.
Composition of Neobrufen 600 mg effervescent granule
Appearance of the product and content of the packaging
White effervescent granule. Each package contains 40 or 20 sachets.
Holder of the marketing authorization and responsible for manufacturing
Holder:
Viatris Healthcare Limited
Damastown Industrial Park
Mulhuddart, Dublin 15
Dublin
Responsible for manufacturing:AbbVie S.R.L., 04011 Campoverde di Aprilia, Latina. Italy.
You can request more information about this medication by contacting the local representative of the holder of the marketing authorization:
Viatris Pharmaceuticals, S.L.
C/ General Aranaz, 86
28027 Madrid
Spain
This leaflet has been reviewed in January 2024
The detailed information about this medication is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS)
https://www.aemps.gob.es/
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