
Ask a doctor about a prescription for APIRETAL 24 mg/mL ORAL SUSPENSION
Package Leaflet: Information for the Patient
Apiretal 24 mg/ml Oral Suspension
Paracetamol
Read this package leaflet carefully before starting to take this medicine, as it contains important information for you.
Contents of the Package Leaflet:
Apiretal belongs to a group of medicines called analgesics and antipyretics.
This medicine is indicated for the symptomatic treatment of febrile states and for the relief of mild or moderate pain.
Do not take Apiretal:
Warnings and Precautions
Consult your doctor or pharmacist before starting to take Apiretal.
During treatment with Apiretal, inform your doctor immediately if:
Children
In children under 2 years of age, consult your doctor to indicate the dose to be taken.
Taking Apiretal with other medicines
Inform your doctor or pharmacist if you are taking, have taken, or may need to take any other medicine recently.
In particular, if you are using medicines that contain any of the following active ingredients, as it may be necessary to modify the dose or interrupt treatment of either of them:
It should not be used with other analgesics (pain-relieving medicines) without consulting your doctor.
As a general rule for any medicine, it is recommended to inform your doctor or pharmacist systematically if you are being treated with another medicine. In the case of treatment with oral anticoagulants, it can be administered occasionally as the analgesic of choice.
Interference with analytical tests
If you are going to have any diagnostic tests (including blood tests, urine tests, etc.), inform your doctor that you are taking this medicine, as it may alter the results.
Taking Apiretal with food, drinks, and alcohol
The use of paracetamol in patients who regularly consume alcohol (three or more alcoholic beverages per day: beer, wine, liquor, etc.) may cause liver damage.
Taking this medicine with food does not affect its efficacy.
Pregnancy, breastfeeding, and fertility
Consult your doctor or pharmacist before using any medicine.
In case of necessity, Apiretal can be used during pregnancy. You should use the lowest possible dose that reduces pain or fever and use it for the shortest possible time. Contact your doctor or midwife if the pain or fever does not decrease or if you need to take the medicine more frequently.
Paracetamol passes into breast milk, so breastfeeding women should consult their doctor before taking this medicine.
Driving and using machines
No effects have been described that modify the ability to drive and use machines.
Apiretal contains saccharose, methyl parahydroxybenzoate (E-218), propyl parahydroxybenzoate (E-217), and azorubine (carmoisine) (E-122).
This medicine contains saccharose. If your doctor has told you that you have an intolerance to certain sugars, consult with them before taking this medicine.
Patients with diabetes mellitus should note that this medicine contains 0.4 g of saccharose per ml.
It can cause allergic reactions (possibly delayed) because it contains methyl parahydroxybenzoate (E-218) and propyl parahydroxybenzoate (E-217).
This medicine may cause allergic reactions because it contains azorubine (carmoisine) (E-122). It can cause asthma, especially in patients allergic to acetylsalicylic acid.
Follow the administration instructions of the medicine contained in this package leaflet or as indicated by your doctor, pharmacist, or nurse. In case of doubt, ask your doctor, pharmacist, or nurse.
It is necessary to respect the posologies defined according to weight. The child's age according to weight is given for information purposes.
The recommended daily dose of paracetamol is approximately 60 mg/kg/day, divided into 4 or 6 daily doses, i.e., 15 mg/kg every 6 hours or 10 mg/kg every 4 hours.
For administration of 15 mg/kg every 6 hours, the schedule is as follows, where the doses can be repeated with a minimum interval of 6 hours, without exceeding a total of 4 doses in 24 hours.
Child's weight (approximate age) | Maximum dosing (per dose) | Volume (ml) |
2.7 - 5 kg (0 to 3 months): | 40 - 75 mg | 1.7 - 3 ml |
5 - 8 kg (4 to 11 months): | 80 - 120 mg | 3 - 5.0 ml |
Up to 10.5 kg (12 to 23 months): | 120 - 160 mg | 5 - 6.5 ml |
Up to 13 kg (2 to 3 years): | 160 - 195 mg | 6.5 - 8 ml |
Up to 18.5 kg (4 to 5 years): | 195 - 280 mg | 8 - 11.5 ml |
Up to 24 kg (6 to 8 years): | 280 - 360 mg | 11.5 - 15 ml |
Up to 32 kg (9 to 10 years): | 360 - 480 mg | 15 - 20 ml |
If the desired effects are not achieved within 3-4 hours of administration, the dose can be advanced every 4 hours, in which case 10 mg/kg will be administered.
Adults and adolescents over 15 years:
The recommended dose is 20 ml to 40 ml per dose as needed every 4-6 hours. The doses should be spaced at least 4 hours apart. Do not exceed 120 ml(3 g of paracetamol) per day.
Always use the lowest effective dose to control symptoms. The doses should be repeated as long as symptoms persist.
Patients with liver disease:Consult your doctor before taking this medicine.
You should take the prescribed amount of medicine with a minimum interval of 8 hours between each dose.
Patients with kidney disease:Consult your doctor before taking this medicine.
Depending on your disease, your doctor will indicate whether you should take your medicine with a minimum interval of 6 or 8 hours.
Elderly patients:Consult your doctor before taking this medicine, as you may need a dose reduction.
Instructions for the correct administration of the preparation
The suspension is for oral administration.
Use the oral syringe included in the package to measure the dose, and take the suspension alone, or diluted in water or another liquid, or mixed with milk or pap.
It can be taken with or without food. For rapid relief of pain, take the medicine without food.
Administration of the medicine is subject to the appearance of pain or fever. As they disappear, the medication should be suspended.
If the symptoms worsen or if the fever persists for more than 3 days or the pain for more than 3 days in children or 5 days in adults (2 days for throat pain), you should consult your doctor.
If you take more Apiretal than you should
If you have taken more Apiretal than you should, go to a medical center immediately, even if you do not have symptoms, as they often do not appear until 3 days after ingestion, even in cases of severe poisoning.
The symptoms of overdose may be: dizziness, vomiting, loss of appetite, yellowing of the skin and eyes (jaundice), and abdominal pain.
Paracetamol overdose is considered to be a single dose of more than 6 gin adults and more than 100 mg/kg of body weightin children. Treatment of overdose is most effective if started within 4 hours of taking the medicine.
Patients being treated with barbiturates or chronic alcoholics may be more sensitive to the toxicity of a paracetamol overdose.
In case of overdose or accidental ingestion, go to a medical center immediately or, if not possible, call the Toxicology Information Service, phone 91 562 04 20, indicating the medicine and the amount taken. It is recommended to take the package and package leaflet of the medicine to the healthcare professional.
If you forget to take Apiretal
Do not take a double dose to make up for forgotten doses; simply take the forgotten dose when you remember, taking the following doses with the indicated separation between doses (at least 4 hours).
If you stop treatment with Apiretal
If you have any other doubts about the use of this medicine, ask your doctor, pharmacist, or nurse.
Like all medicines, Apiretal can cause side effects, although not everyone gets them.
Paracetamol's adverse reactions are, in general, rare (may affect up to 1 in 1,000 patients) or very rare (may affect up to 1 in 10,000 patients).
In rare cases, general discomfort or sudden discomfort due to a drop in blood pressure (hypotension) may occur. It is also rare to find elevated levels of certain liver proteins (liver transaminases).
Very rarely, it can damage the liver at high doses or prolonged treatments. Also, very rarely, the following may appear: kidney disease, cloudy urine, allergic dermatitis (skin rash), jaundice (yellowing of the skin), blood disorders (agranulocytosis, leukopenia, neutropenia, hemolytic anemia), and hypoglycemia (low blood sugar).
Very rare cases of serious skin reactions have been reported.
Frequency not known (cannot be estimated from available data): a serious disease that can make the blood more acidic (called metabolic acidosis) in patients with severe disease using paracetamol (see section 2).
If you experience side effects, consult your doctor, pharmacist, or nurse, even if they are not listed in this package leaflet.
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiration date indicated on the package after CAD. The expiration date is the last day of the month indicated.
No special storage conditions are required.
Medicines should not be disposed of through wastewater or household waste. Deposit the packages and medicines you no longer need at the SIGRE collection point in the pharmacy. If in doubt, ask your pharmacist how to dispose of packages and medicines you no longer need. This will help protect the environment.
Composition of Apiretal
Appearance of the product and package contents
Red/pink suspension with a sweet taste. It is presented in a glass bottle, amber in color, containing 120 ml of suspension, with a safety screw cap and an adapter for incorporating the oral syringe (5 ml), which is also included.
Marketing Authorization Holder
Laboratorios ERN, S.A.
C/Perú, 228
08020 Barcelona, Spain
Manufacturer
Laboratorios INIBSA, S.A.
Crta. Sabadell a Granollers, Km 14.5 (Lliçà de Vall)
08185 Barcelona
Spain
Date of the last revision of this package leaflet:February 2025.
Other sources of information
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/.
The best alternatives with the same active ingredient and therapeutic effect.
Discuss dosage, side effects, interactions, contraindications, and prescription renewal for APIRETAL 24 mg/mL ORAL SUSPENSION – subject to medical assessment and local rules.