Leaflet: Information for the user
Paracetamol Ordesa 1 g coated tablets EFG
paracetamol
Read the entire leaflet carefully before starting to take this medication, as it contains important information for you.
Keep this leaflet, as you may need to read it again. If you have any questions, consult your doctor or pharmacist.
This medication has been prescribed to you only, and you should not give it to others, even if they have the same symptoms as you, as it may harm them.
If you experience side effects, consult your doctor, pharmacist, or nurse, even if they are side effects not listed in this leaflet. See section 4.
Contents of the leaflet
Paracetamol belongs to the group of medications called analgesics and antipyretics.
It is indicated for the treatment of symptoms of pain and fever.
Do not take Paracetamol Ordesa:
Warnings and precautions:- Do not take more than the recommended dose in section 3. How to take Paracetamol Ordesa.
During treatment with Paracetamol Ordesa, inform your doctor immediately if:
Other medications and Paracetamol OrdesaInform your doctor or pharmacist if you are taking
Paracetamol may interact with the following medications:
Do not use with other analgesics (pain-relieving medications) without consulting your doctor.
As a general rule for any medication, it is recommended to systematically inform your doctor or pharmacist if you are being treated with another medication. In the case of treatment with oral anticoagulants, it can be administered occasionally as the analgesic of choice.
Interference with laboratory tests:
If you are going to have any laboratory tests (including blood tests, urine tests, skin tests that use allergens, etc.), inform your doctor that you are taking this medication, as it may alter the results of these tests.
Taking Paracetamol Ordesa with food, drinks, and alcohol:
The use of paracetamol in patients who habitually consume alcohol (3 or more alcoholic beverages: beer, wine, liquor... per day) may cause liver damage.
Taking this medication with food does not affect its efficacy.
Pregnancy and breastfeeding
Consult your doctor or pharmacist before using any medication.
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor before taking this medication.
If necessary, Paracetamol Ordesa 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 if the pain or fever does not decrease or if you need to take the medication more frequently.
Taking medications during pregnancy can be hazardous to the embryo or fetus and should be monitored by your doctor.
Small amounts of paracetamol may appear in breast milk; therefore, it is recommended that you consult your doctor or pharmacist before taking this medication.
Driving and using machines:
The influence of paracetamol on the ability to drive and use machines is nil or insignificant.
This medication contains less than 1 mmol of sodium (23 mg) per coated tablet; it is essentially "sodium-free".
Follow these instructions unless your doctor has given you different instructions. Remember to take your medication. Paracetamol should be taken orally.
The normal dose is:
Adults and children over 15 years: the usual dose is 1 tablet (1 g of paracetamol) 3 times a day. The doses should be spaced at least 4 hours apart. Do not take more than 4 tablets (4 g) in 24 hours.
Patient with liver disease: before taking this medication, they must consult their doctor. They should take the amount of medication prescribed by their doctor with a minimum interval of 8 hours between each dose.
Do not take more than 2 grams of paracetamol in 24 hours, divided into 2 doses.
Patient with kidney disease: before taking this medication, they must consult their doctor. Take a maximum of 500 milligrams per dose.
Due to the dose, 1 g of paracetamol, it is not indicated for this group of patients.
Elderly patients: should consult their doctor.
Use in children: Do not use in children under 15 years of age.
If you think the action of Paracetamol is too strong or too weak, inform your doctor or pharmacist. When lower doses of paracetamol are required (less than 1000 milligrams per dose), other presentations of paracetamol that are suitable for the required dosage should be used.
If you take more Paracetamol Ordesa than you should:
You should consult your doctor or pharmacist immediately.
The symptoms of overdose may be: dizziness, vomiting, loss of appetite, yellowing of the skin and eyes (jaundice), and abdominal pain.
If you have ingested an overdose, you should go to a medical center immediately, even if you do not notice symptoms, as they often do not appear until 3 days after ingestion, even in cases of severe poisoning. Treatment of overdose is more effective if started within 4 hours of ingestion of the medication.
Patient being treated with barbiturates or chronic alcoholics may be more susceptible to the toxicity of a paracetamol overdose.
In case of overdose or accidental ingestion, go to a medical center immediately or call the Toxicology Information Service (telephone 91 562 04 20), indicating the medication and the amount ingested.
If you forget to take Paracetamol Ordesa
Do not take a double dose to make up for forgotten doses; simply take the forgotten dose when you remember, taking the next doses with the indicated interval between doses (at least 4 hours).
Like all medications, this medication can cause side effects, although not everyone gets them.
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).
Rare side effects that may occur (between 1 and 10 in every 10,000 people) are: discomfort, low blood pressure (hypotension), and increased levels of transaminases in the blood.
Very rare side effects that may occur (in less than 1 in every 10,000 people) are: kidney disease, cloudy urine, allergic dermatitis (skin rash), jaundice (yellowing of the skin), blood disorders (agranulocytosis, leucopenia, neutropenia, hemolytic anemia), and hypoglycemia (low blood sugar). Very rare cases of severe skin reactions have been reported.
Paracetamol can damage the liver when taken in high doses or for prolonged periods.
Reporting side effects
If you experience any side effects, consult your doctor or pharmacist, even if they are possible side effects not listed in this leaflet. You can also report them directly through the Spanish Pharmacovigilance System for Human Use Medications: https://www.notificaram.es. By reporting side effects, you can contribute to providing more information on the safety of this medication.
Keep this medication out of the sight and reach of children.
This medication does not require special storage conditions.
Do not use this medication after the expiration date shown on the packaging after CAD. The expiration date is the last day of the month indicated.
Medications should not be disposed of through wastewater or household waste. Deposit the packaging and medications you no longer need at the SIGRE collection point in your pharmacy. Ask your pharmacist how to dispose of the packaging and medications you no longer need. This will help protect the environment.
Composition of Paracetamol Ordesa:
Each tablet contains 1 g of paracetamol as the active ingredient.
The other components (excipients) are sodium starch glycolate (Type A), pregelatinized corn starch, povidone K30 (E-1201), stearic acid (E-570), and crospovidone (E-1202).
Appearance of the product and package contents:
Paracetamol Ordesa is presented in oral tablets.
The tablets are oblong, biconvex, white, with a score line on one face and marked with PC on the other face.
In packages of 20 and 40 tablets and a clinical package of 500 tablets, packaged in PVC/PVdC/Aluminum blisters.
Marketing authorization holder and manufacturer:
Marketing authorization holder
Laboratorios Ordesa S.L.
Torre Ponent, Passeig de la Zona Franca number 107, 14th floor,
08038 Barcelona
Spain
Manufacturer
SAG Manufacturing S.L.U
Crta. N-I, Km 36,
San Agustín de Guadalix,
28750 Madrid
Spain
or
Galenicum Health, S.L.U.
Sant Gabriel, 50
Esplugues de Llobregat
08950 Barcelona
Spain
Date of the last revision of this leaflet: May 2025
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/