GELOCATIL 1 g Tablets

Paracetamol

Paracetamol is effective in reducing pain and fever.

It is indicated for symptomatic relief of occasional mild or moderate pain, such as headache, toothache, muscle pain (muscle spasms) or back pain (lumbago) and in febrile states.

Gelocatil is indicated for adults.

Do not take Gelocatil:

• if you are allergic (hypersensitive) to paracetamol or to any of the other components of Gelocatil.

Be careful with Gelocatil:

• Do not take more of the medicine than recommended in the section 3. How to take Gelocatil 1 g Tablets.
• Avoid using this medicine with other medicines that contain paracetamol, for example, cold and flu medicines, as high doses may cause liver damage. Do not use more than one medicine that contains paracetamol without consulting your doctor.
• Chronic alcoholics should be careful not to take more than 2 grams of paracetamol in 24 hours.
• Patients with kidney, liver, heart, or lung diseases and patients with anemia should consult their doctor before taking this medicine.

• If you are being treated with any medicine for epilepsy, consult your doctor before taking this medicine, as when used together, it may reduce the effectiveness and increase the hepatotoxicity of paracetamol, especially in high-dose treatments.
• Patients who are asthmatic and sensitive to acetylsalicylic acid should consult their doctor before taking this medicine.
• Inform your doctor immediately if during treatment with Gelocatil:

If you have severe diseases, such as severe renal insufficiency or sepsis (when bacteria and their toxins circulate in the blood, causing damage to organs), or if you suffer from malnutrition, chronic alcoholism, or if you are also taking flucloxacillin (an antibiotic). A severe disease called metabolic acidosis (a blood and fluid anomaly) has been reported in patients in these situations when using paracetamol at regular doses for a prolonged period or when taking paracetamol with flucloxacillin. Symptoms of metabolic acidosis may include: severe difficulty breathing with deep and rapid breathing, drowsiness, feeling unwell (nausea), and vomiting.

Use of other medicines:

Inform your doctor or pharmacist if you are using or have recently used other medicines, including those purchased without a prescription.

In particular, if you are using some of the following medicines, as it may be necessary to modify the dose of some of them or interrupt treatment:

• Medicines to prevent blood clots: Oral anticoagulants (acenocoumarol, warfarin)
• Medicines to treat epilepsy: Antiepileptics (lamotrigine, phenytoin, or other hydantoins, phenobarbital, methylphenobarbital, primidone, carbamazepine)
• Medicines to treat tuberculosis: (isoniazid, rifampicin)
• Medicines to treat depression and seizures: Barbiturates (used as hypnotics, sedatives, and anticonvulsants)
• Medicines to lower blood cholesterol levels: (colestiramine)
• Medicines used to increase urine elimination (diuretics of the loop, such as those in the furosemide group)
• Medicines used to treat gout (probencid and sulfinpyrazone)
• Medicines used to prevent nausea and vomiting: Metoclopramide and domperidone
• Medicines used to treat high blood pressure (hypertension) and heart rhythm disorders (arrhythmias): Propranolol.
• Flucloxacillin (antibiotic), due to a serious risk of blood and fluid anomaly (called metabolic acidosis) that requires urgent treatment (see section 2).

Interference with laboratory tests:

If you are to have any laboratory tests (including blood and urine tests, etc.), inform your doctor that you are taking/using this medicine, as it may alter the results.

Taking Gelocatil with food and drinks:

The taking of this medicine with food does not affect its efficacy.

Use in children:

Do not use in children under 18 years.

Pregnancy:

Consult your doctor or pharmacist before using any medicine.

In case of need, Gelocatil 1g tablets may be used during pregnancy. 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 do not decrease or if you need to take the medicine more frequently.

Lactation:

Consult your doctor or pharmacist before using any medicine.

Paracetamol passes into breast milk, so women in the lactation period should consult their doctor or pharmacist before taking this medicine.

Driving and operating machines:

The influence of paracetamol on the ability to drive and operate machines is negligible or insignificant.

Gelocatil contains sodium

This medicine contains less than 23 mg of sodium (1 mmol) per tablet; it is essentially "sodium-free".

Follow these instructions unless your doctor has given you different instructions. Consult your doctor or pharmacist if you have any doubts.

The usual dose is:

Adults:

Take 1 tablet every 6 - 8 hours, as needed. Do not take more than 3 grams (3 tablets) in 24 hours.

Patients with liver disease: consult your doctor before taking this medication.

You should take the amount of medication prescribed by your doctor with a minimum interval of 8 hours between each dose.

You should not take more than 2 tablets of paracetamol in 24 hours, divided into 2 doses.

Patients with kidney disease: consult your doctor before taking this medication.

Take a maximum of 500 milligrams per dose.

Due to the dose, 1 gram of paracetamol, the medication is not indicated for this group of patients.

This medication is taken orally.

The tablets should be swallowed whole or broken in half with the help of a glass of liquid, preferably water.

The tablets are scored, which allows them to be broken in half.The score is only for breaking the tablet if it is difficult to swallow it whole.

Always use the smallest effective dose.

It is essential to avoid high daily doses of paracetamol for prolonged periods of time, as this increases the risk of adverse effects such as liver damage.

The administration of this medication is subject to the appearance of pain or fever. As these symptoms disappear, treatment should be discontinued.

If the pain persists for more than 5 days, the fever for more than 3 days, or if the pain or fever worsen or other symptoms appear, treatment should be interrupted and your doctor consulted.

Ifyou take more Gelocatil 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), abdominal pain and inflammation of the pancreas (pancreatitis).

If you have ingested an overdose, you should go to a medical center immediately, even if you do not notice the symptoms, as they often do not appear until 3 days after ingestion of the overdose, even in cases of severe poisoning.

The treatment of an overdose is more effective if it is initiated within 4 hours of medication ingestion.

Patients undergoing treatment with barbiturates or chronic alcoholics may be more susceptible to the toxicity of a paracetamol overdose.

Incase of overdose or accidental ingestion, go to a medical center immediately or call the Toxicological Information Service (phone 91 562 04 20), indicating the medication and the amount ingested.

Like all medications, Gelocatil may have adverse effects, although not everyone will experience them.

Rare adverse effects that may occur (between 1 and 10 of every 10,000 people) are: discomfort, low blood pressure (hypotension), and increased levels of transaminases in the blood.

Very rare adverse effects that may occur (in fewer than 1 of every 10,000 people) are: kidney diseases, cloudy urine, allergic dermatitis (skin rash), jaundice (yellow discoloration of the skin), blood disorders (agranulocytosis, leucopenia, neutropenia, hemolytic anemia) and hypoglycemia (low blood sugar). Rarely, severe skin reactions have been reported.

Paracetamol can damage the liver when taken in high doses or for prolonged periods.

Adverse effects of unknown frequency (cannot be estimated from available data): A serious disease that can make the blood more acidic (designated as metabolic acidosis) in patients with severe disease who use paracetamol (see section 2).

Reporting 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 System for Pharmacovigilance of Medicinal Products for Human Use:https://www.notificaram.es. By reporting adverse effects, you can contribute to providing more information about the safety of this medication.

Keep out of reach and sight of children.

This medication does not require special conditions for conservation.

Do not use this medication after the expiration date that appears on the packaging after CAD. The expiration date is the last day of the month indicated.

Medications should not be disposed of through drains or in the trash. Deposit the packaging and medications you no longer need at the SIGRE collection point of the pharmacy. If in doubt, ask your pharmacist how to dispose of the packaging and medications you no longer need. By doing so, you will help protect the environment.

Composition of Gelocatil:

Each tablet contains 1 gram of paracetamol as the active ingredient.

The other components (excipients) are magnesium stearate, povidone, anhydrous colloidal silica, potato starch, and pregelatinized cornstarch.

Appearance of the product and contents of the package:

Gelocatil is presented in oral tablets.

The tablets are oblong, scored on one face, and white in color.

The boxes contain 4 and 10 tablets.

Holder of the marketing authorization:

Ferrer Internacional, S.A.

Gran Vía Carlos III, 94

08028 – Barcelona

Responsible for manufacturing:

Ferrer Internacional, S.A.

Joan XXIII, 10

08950 – Esplugues de Llobregat (Barcelona)

or

Ferrer Internacional, S.A.

Joan Buscallá, 1-9

08173 - Sant Cugat del Vallés (Barcelona)

Date of the last review of this leaflet:February 2025

The detailed and updated information on this medication is available on the website of the Spanish Agency of Medicines and Medical Devices (AEMPS)http://www.aemps.gob.es/