


Ask a doctor about a prescription for IBUPROFEN STADAPHARM 400 MG ORAL SUSPENSION
Package Leaflet: Information for the User
Ibuprofeno Stadapharm 400 mg Oral Suspension
Read the entire package leaflet carefully before starting to take this medication, as it contains important information for you.
Follow the administration instructions for the medication contained in this package leaflet or as indicated by your doctor or pharmacist.
Contents of the Package Leaflet
Ibuprofen, the active ingredient of this medication, acts by reducing pain and fever.
This medication is used in adults and adolescents from 12 years old and weighing more than 40 kg for the symptomatic relief of occasional mild or moderate pain, such as headaches, dental, menstrual, muscle (cramps) or back (lumbago) pain, as well as in febrile conditions.
Do not take Ibuprofeno Stadapharm:
Warnings and Precautions
Consult your doctor or pharmacist before starting to take this medication.
Inform your doctor:
It is essential that you use the smallest dose that relieves/controls the pain and do not take this medication for longer than necessary to control your symptoms.
Infections
Ibuprofeno Stadapharm may mask the signs of an infection, such as fever and pain. Consequently, Ibuprofeno Stadapharm may delay the appropriate treatment of the infection, which may increase the risk of complications. This has been observed in bacterial pneumonia and bacterial skin infections related to chickenpox. If you take this medication while having an infection and the symptoms of the infection persist or worsen, consult a doctor without delay.
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 this medication if:
Similarly, this type of medication may 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 Ibuprofeno Stadapharm treatment and seek immediate medical attention if you notice any of the symptoms related to these severe skin reactions described in section 4.
Children and Adolescents
There is a risk of kidney damage in dehydrated children and adolescents.
Taking Ibuprofeno Stadapharm with Other Medications
Tell your doctor or pharmacist if you are taking, have recently taken, or may need to take any other medication, including those purchased without a prescription.
The following medications may interfere and should not be taken with ibuprofen without first consulting your doctor:
Other medications may also affect or be affected by ibuprofen treatment. Therefore, you should always consult your doctor or pharmacist before using ibuprofen with other medications.
Interference with Analytical Tests
If you are going to undergo any diagnostic tests (including blood tests, urine tests, skin tests using allergens, etc.), inform your doctor that you are taking this medication, as it may alter the results.
Taking Ibuprofeno Stadapharm with Food, Drinks, and Alcohol
You can take it alone or with food. In general, it is recommended to take it before meals to reduce the possibility of stomach upset.
If you drink alcohol while taking this medication, you may be more prone to side effects.
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 medication.
Pregnancy
Do not take ibuprofen if you are in the last 3 months of pregnancy, as it may harm the fetus or cause problems during delivery. It may cause kidney and heart problems in your fetus. It may affect your and your baby's tendency to bleed and delay or prolong delivery more than expected. You should not take ibuprofen during the first 6 months of pregnancy unless it is clearly necessary and as indicated by your doctor. If you need treatment during this period or while trying to become pregnant, you should take the minimum dose for the shortest possible time. From the 20th week of pregnancy, ibuprofen may cause kidney problems in your fetus if taken for more than a few days, which may 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 monitoring.
Fertility
For female patients of childbearing age, it should be noted that medications like ibuprofen have been associated with a decrease in fertility.
Breastfeeding
Although the medication levels in breast milk are negligible, it is recommended to consult your doctor in cases of long-term treatment or high doses during breastfeeding.
Driving and Using Machines
If you experience dizziness, vertigo, vision changes, or other symptoms while taking this medication, you should not drive or operate machinery. If you only take one dose of ibuprofen or for a short period, it is not necessary to take special precautions.
Ibuprofeno Stadapharm Contains Sodium and Maltitol Liquid (E-965)
Patients on low-sodium diets should note that this medication contains 57.94 mg (2.5 mmol) of sodium per sachet.
This medication contains maltitol liquid (E-965). If your doctor has told you that you have an intolerance to certain sugars, consult with them before taking this medication.
Follow exactly the administration instructions of the medication contained in this prospectus as indicated by your doctor or pharmacist. In case of doubt, ask your doctor or pharmacist.
It is important to always take the smallest dose that relieves the pain and you should not take the medication for longer than necessary to control your symptoms.
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 symptoms (such as fever and pain) persist or worsen (see section 2).
Dosage
Adults and adolescents (over 40 kg in weight) from 12 years:
The recommended dose is one sachet (400 mg of ibuprofen) every 4-8 hours, depending on the intensity of the symptoms and the response to treatment. Do not take more than 3 sachets (1,200 mg) within 24 hours.
Elderly patients:
The dosage should be established by the doctor, as it may be necessary to reduce the usual dose. Elderly people are more likely to experience adverse effects.
Patients with kidney, liver, or heart disease:
Reduce the dose and consult your doctor. Ibuprofen should not be used in patients with severe renal, hepatic, or cardiac insufficiency.
If symptoms worsen, if fever persists for more than 3 days or pain for more than 5 days (3 days in adolescents), you should consult your doctor.
The administration of this medication is subject to the appearance of pain or fever. As these disappear, the medication should be suspended.
Use in children and adolescents:
The use of this medication is not recommended in children or adolescents with a weight of less than 40 kg.
Method of administration
This medication is a suspension, administered orally.
It is necessary to homogenize the suspension before taking it, as indicated in the following figure:

1 – Press with your fingers the top and bottom of the sachet several times
2 – Press from top to bottom and vice versa for at least 30 seconds
It can be taken directly from the sachet or diluted in water.
In case of digestive discomfort, it is recommended to take the medication with meals.
If you take more Ibuprofeno Stadapharm than you should
If you have taken more oral suspension than you should or have accidentally ingested the contents of the package, consult your doctor or pharmacist or the Toxicology Information Service, phone: 91 5620420, indicating the medication and the amount ingested. It is recommended to bring the package and the prospectus of the medication to the healthcare professional.
If you have taken more Ibuprofeno Stadapharm than you should, or if a child has accidentally ingested the medication, consult with a doctor or go to the nearest hospital to find out about the risk and ask for advice on the measures to be taken.
Symptoms of overdose may include nausea, stomach pain, vomiting (which may contain bloody sputum), headache, ringing in the ears, confusion, and involuntary eye movement. At high doses, symptoms of drowsiness, chest pain, palpitations, loss of consciousness, convulsions (mainly in children), weakness, and dizziness, blood in the urine, low potassium levels in the blood, chills, and breathing difficulties have been reported
It is rare for more severe symptoms to appear, such as intestinal bleeding, low blood pressure, low body temperature, metabolic acidosis, convulsions, altered kidney function, coma, adult respiratory distress, and transient respiratory arrest in children (after ingesting large amounts).
If a severe poisoning has occurred, the doctor will take the necessary measures.
If you forget to take Ibuprofeno Stadapharm
Do not take a double dose to make up for forgotten doses.
If you forget to take your corresponding dose, take it as soon as you remember. However, if the time of the next dose is very close, skip the forgotten dose and take the next dose at its usual time.
If you have any other doubts about the use of this medication, ask your doctor or pharmacist.
Like all medications, this medication can cause adverse effects, although not all people experience them.
The incidence of adverse effects is lower in short treatments and if the daily dose is below the maximum recommended dose.
The frequencies shown below refer to the short-term use of maximum daily doses of up to 1,200 mg of oral ibuprofen:
Disorientation or confusion, depression, vertigo, tinnitus (ringing or sounds in the ear), reversible toxic amblyopia, liver damage, edema (swelling caused by fluid accumulation in tissues), optic neuritis.
Exacerbation of inflammation-related infections has been observed coinciding with the use of NSAIDs. If signs of infection or worsening of symptoms occur during the use of ibuprofen, it is recommended to consult a doctor as soon as possible.
Colitis and Crohn's disease (chronic disease in which the immune system attacks the intestine, causing inflammation that usually produces bloody diarrhea).
Generalized red scaly rash, with bumps under the skin and blisters, accompanied by fever at the start of treatment (acute generalized exanthematous pustulosis). Stop taking Ibuprofeno Stadapharm if you experience these symptoms and seek immediate medical attention. See also section 2.
The skin becomes sensitive to light.
Chest pain, which can be a sign of a potentially severe allergic reaction called Kounis syndrome.
A severe skin reaction known as DRESS syndrome can occur. The symptoms of DRESS syndrome include: skin rash, lymph node inflammation, and elevated eosinophils (a type of white blood cell).
If any of the following adverse effects occur, discontinue treatment and consult your doctor immediately:
Reporting of adverse effects
If you experience any type of adverse effect, consult your doctor or pharmacist, even if it is a possible adverse effect that does not appear in this prospectus. You can also report them directly through the Spanish Pharmacovigilance System for Human Use Medicines, www.notificaRAM.es.
Keep this medication out of sight and reach of children.
Store below 30°C.
Do not use this medication after the expiration date that appears on the package after CAD. The expiration date is the last day of the month indicated.
Medications should not be thrown down the drain or into the trash. Deposit the packages and medications you no longer need in the SIGRE Point of the pharmacy. In case of doubt, ask your pharmacist how to dispose of the packages and medications you no longer need. This way, you will help protect the environment.
Composition of Ibuprofeno Stadapharm
Appearance of the product and package contents
Ibuprofeno Stadapharm is a white oral suspension with a strawberry flavor contained in single-dose sachets of 10 ml formed by a polyester, aluminum, polyester, and polyethylene complex.
It is presented in packages of 12 units or 20 units.
Only some package sizes may be marketed.
Marketing authorization holder and manufacturer
Marketing authorization holder
Laboratorio STADA, S.L.
Frederic Mompou, 5
08960 Sant Just Desvern (Barcelona)
Spain
Manufacturer
ALCALA FARMA, S.L.
Avenida de Madrid, 82
28802 Alcalá de Henares (Madrid)
“or”
ZINEREO PHARMA, S.L.U.
A Relva, s/n, O Porriño,
36410 Pontevedra
“or”
FARMALIDER, S.A.
C/Aragoneses, 2
28108 Alcobendas (Madrid)
“or”
EDEFARM S.L.
Polígono Industrial Enchilagar del Rullo, 117
46191 Villamarchante (Valencia)
Date of the last revision of this prospectus: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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