GELOCATIL650 mgOral Solution
Paracetamol
Read the entire leaflet carefully because it contains important information for you.
This medication can be obtained without a prescription. Nevertheless, to obtain the best results, it should be used with care.
Contents of the leaflet:
Paracetamol is effective in reducing pain and fever.
It is indicated for the symptomatic relief of occasional mild or moderate pain, such as headache, dental, muscular (cramps) or back (lumbago) pain and in febrile states.
Gelocatil is indicated in adults and adolescents over 14 years of age.
Do not take Gelocatil if:
Be careful with Gelocatil:
Use of other medications:
Inform your doctor or pharmacist if you are using or have recently used other medications, including those purchased without a prescription.
In particular, if you are using any of the following medications, it may be necessary to modify the dose of some of them or interrupt treatment:
Interference with analytical tests:
If you are going to have any analytical test (including blood, urine, etc.), inform your doctor that you are taking/using this medication, as it may alter the results.
Taking Gelocatil with food and drinks
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.
Use in children:
Pregnancy
Consult your doctor or pharmacist before using any medication.
IMPORTANT FOR WOMEN
If you are pregnant or think you may be pregnant, consult your doctor before taking this medication. The use of medications during pregnancy can be dangerous for the embryo or fetus and should be monitored by your doctor.
In case of necessity, Gelocatil 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.
Breastfeeding
Consult your doctor or pharmacist before using any medication.
Paracetamol passes into breast milk, so breastfeeding women should consult their 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.
Gelocatil contains propylene glycol, sorbitol, methyl p-hydroxybenzoate (E-218), propyl p-hydroxybenzoate (E-216), and sodium:
This medication contains 1300 mg of propylene glycol in each sachet.
If you are pregnant or breastfeeding, do not take this medication unless recommended by your doctor. Your doctor may perform additional checks while you are taking this medication.
If you have liver or kidney failure, do not take this medication unless recommended by your doctor. Your doctor may perform additional checks while you are taking this medication.
If the child is under 5 years of age, consult your doctor or pharmacist, especially if they have been given other medications that contain propylene glycol or alcohol.
This medication contains 1300 mg of sorbitol in each sachet.
Sorbitol is a source of fructose. If your doctor has told you that you (or your child) have an intolerance to certain sugars, or have been diagnosed with hereditary fructose intolerance (HFI), a rare genetic disease, in which the patient cannot break down fructose, consult your doctor before taking this medication.
It may cause allergic reactions (possibly delayed) because it contains methyl p-hydroxybenzoate (E-218) and propyl p-hydroxybenzoate (E-216).
This medication contains less than 23 mg of sodium (1mmol) per sachet; it is essentially "sodium-free".
Follow these instructions unless your doctor has given you different instructions. Consult your doctor or pharmacist if you have doubts.
The normal dose is:
Adults and adolescents over 14 years of age (weight 64-65 kg): Take 1 sachet every 4-6 hours, as needed. Do not take more than 3 grams (4 sachets) in 24 hours.
Patient with liver disease: before taking this medication, they must consult their doctor.
They should take the prescribed amount of medication by their doctor with a minimum interval of 8 hours between each dose.
They should not take more than 3 sachets of paracetamol in 24 hours, divided into 3 doses.
Patient with kidney disease: before taking this medication, they must consult their doctor.
Take a maximum of 500 milligrams of paracetamol per dose.
Due to the dose, 650 milligrams of paracetamol, this medication is not indicated for this group of patients.
This medication is taken orally.
The contents of the sachet can be taken diluted in a liquid, preferably water, or directly. Once the sachet is opened, consume all its contents.
Always use the lowest effective dose.
High daily doses of paracetamol should be avoided during prolonged periods of time, as the risk of adverse effects such as liver damage increases.
The administration of this medication is subject to the appearance of pain or fever. As they disappear, treatment should be suspended.
If the pain persists for more than 5 days, the fever for more than 3 days, or the pain or fever worsen, or other symptoms appear, treatment should be interrupted and a doctor consulted.
If you takemore 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 pancreatitis (inflammation of the pancreas).
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 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.
Like all medications, Gelocatil can have adverse effects, although not all people experience them.
Paracetamol may damage the liver when taken in high doses or in prolonged treatments.
Reporting adverse effects
If you experience any type of adverse effect, consult your doctor or pharmacist, even if it is a possible adverse effect not mentioned in this leaflet. You can also report them directly through the Spanish Medication Surveillance System for Human Use: https://www.notificaram.es. By reporting adverse effects, you can contribute to providing more information on the safety of this medication.
Keep out of the reach and sight of children.
No special storage conditions are required.
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 thrown away through the sewers or in the trash. Deposit the packaging 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 packaging and medications you no longer need. This way, you will help protect the environment.
Composition of Gelocatil:
Each sachet contains 650 milligrams of paracetamol.
The other components are sodium saccharin, propylene glycol, macrogol, sorbitol (E-420), methyl p-hydroxybenzoate and propyl p-hydroxybenzoate (E-218 and E-216), povidone K12, neohesperidin DC, ammonium sulfito caramel (E-150-d), raspberry flavor, strawberry flavor, ascorbic acid or sodium hydroxide, and purified water.
Appearance of the product and packaging content:
Gelocatil is a clear oral solution with a slight amber tone, presented in single-dose sachets.
The boxes are of 4 and 12 sachets.
Marketing authorization holder:
Ferrer Internacional, S.A.
Gran Vía Carlos III, 94
08028 - Barcelona
Manufacturer:
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 revision of this leaflet:February 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/
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