Prospecto:information for the patient
Paracetamol Viatris 1 g tablets EFG
Read this prospectus carefully before starting to take this medication, as it contains important information for you.
1.What isParacetamol Viatrisand for what it is used
2.What you need to know before starting to takeParacetamol Viatris
3.How to takeParacetamol Viatris
4.Possible adverse effects
5.Storage ofParacetamol Viatris
6.Contents of the package and additional information
Paracetamol Viatris belongs to a group of medicines called analgesics and antipyretics.
This medicine is used for the symptomatic treatment of mild to moderate pain and febrile states in adults and adolescents aged 15 years and older with a body weight of 50 kg or more.
Do not take Paracetamol Viatris:
Warnings and precautions
Consult your doctor or pharmacist before starting to take Paracetamol Viatris:
Inform your doctor immediately if you experience:
Severe diseases, such as severe kidney failure or sepsis (when bacteria and their toxins circulate in the blood, causing damage to organs), or if you have chronic malnutrition, 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.
Children and adolescents
Consult your doctor or pharmacist for children under 15 years, as there are other presentations with doses adapted to this group of patients.
Other medications and Paracetamol Viatris
Inform your doctor or pharmacist if you are using, have used recently, or may need to use any other medication, including those purchased without a prescription.
Particularly, if you are using some of the following medications, as it may be necessary to modify the dose of some of them or interrupt treatment:
Interference with analytical tests
Inform your doctor if you are undergoing any analytical tests (including blood and urine tests, etc.) as this medication may alter the results.
Taking Paracetamol Viatris with food and drinks
The use of paracetamol in patients who regularly consume alcohol (3 or more alcoholic beverages: beer, wine, liquor, etc. per day) may cause liver damage.
The taking of this medication with food does not affect its efficacy.
Pregnancy and breastfeeding
Pregnancy
Consult your doctor or pharmacist if you are pregnant or breastfeeding, think you may be pregnant, or intend to become pregnant before using this medication.
Paracetamol can be used during pregnancy if necessary. 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 women breastfeeding should consult their doctor or pharmacist before taking this medication.
Driving and operating machinery
The influence of paracetamol on the ability to drive and operate machinery is negligible or insignificant.
Remember to take your medication. This medication should be taken orally. According to your preferences, the tablets can be taken directly or divided in half with water, milk, or fruit juice.
The tablet can be divided into equal doses.
Doserecommendedis:
Adults and adolescents over 15 years and weight over 50 kg:1 tablet every 4-6 hours,up to a maximum of 4 tablets per day.
Renal problems:
In case of moderate renal problems, the usual dose is half a tablet (500 mg of paracetamol) every 6 hours.
In case of severe kidney problems, the usual dose is half a tablet (500 mg of paracetamol) every 8 hours.
Liver problems:
In case of liver problems, consult your doctor. Your doctor may decide to reduce your dose.
In case of chronic alcoholism, the dose should not exceed 2 g per day.
Older patients:should consult their doctor.
Use in children and adolescents
In children under 15 years and weight less than 50 kg, consult your doctor or pharmacist as there may be other presentations available with doses adapted to these patients.
If it is estimated that the action of this medication is too strong or too weak, inform your doctor or pharmacist.
When requiring doses lower than 1 g of paracetamol per intake, other paracetamol presentations should be used that adapt to the required dosing.
If you take moreParacetamol Viatristhan you should
If you have taken moreparacetamolthan you should:
You should consult your doctor or pharmacist immediately.
The symptoms of overdose may be: dizziness, vomiting, loss of appetite, yellowish discoloration of the skin and eyes (jaundice), abdominal pain, and pancreatitis inflammation.
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, even in cases of severe intoxication.
The treatment of an overdose is more effective if it is initiated within 4 hours of taking the medication.
Patients undergoing barbiturate treatment 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 Toxicological Information Service (phone 91 562 04 20), indicating the medication and the amount ingested.
If you forgot to takeParacetamol Viatris
Do not take a double dose to compensate for the missed doses, simply take the missed dose when you remember, taking the next doses with the indicated interval (at least 4 hours).
Like all medications,this medicationmay have adverse effects, although not all people will experience them.
Rare Adverse Effectsthat 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 Effectsthat 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 Effectsof Unknown Frequency(cannot be estimated from available data): A serious disease that can make the blood more acidic (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.
Keepthis medicationout of the sight and reach of children.
This medication does not require special storage conditions.
Do not usethis medicationafter the expiration date that appears on the packaging after CAD or EXP. The expiration date is the last day of the month indicated.
Do not dispose of medications through drains or trash. Dispose of packaging and unused medications at the SIGRE collection pointat the pharmacy. If in doubt, ask your pharmacist how to dispose of unused packaging and medications. By doing so, you will help protect the environment.
Composition of Paracetamol Viatris
The active ingredient is paracetamol. Each tablet contains 1 g of paracetamol.
The other components are: maize pregelatinised starch , stearic acid (E-570) , pellucid povidone (E-1201) , crospovidone (E-1202) , microcrystalline cellulose and vegetable origin magnesium stearate (E-470b) .
Appearance of the product and content of the packaging
Paracetamol Viatris tablets are oblong, biconvex, scored and white, packaged in blisters in containers of 20 and 40 tablets.
Only some sizes of containers may be commercially marketed.
Holder of the marketing authorization and responsible for manufacturing
Holder of the marketing authorization
Viatris Pharmaceuticals, S.L.U
C/ General Aranaz, 86
28027 - Madrid
Spain
Responsible for manufacturing
Toll Manufacturing Services, S.L.
C/ Aragoneses, 2.
28108 - Alcobendas (Madrid)
Spain
Or
Rovi Pharma Industrial Services, S.A.
Vía Complutense, 140
28805 - Alcalá de Henares (Madrid)
Spain
Or
Pharmaloop, S.L.
C/ Bolivia, 15, Polig. Industrial Azque
28806 - Alcalá de Henares (Madrid)
Spain
Or
Farmalider, S.A.
C/ Aragoneses, 2
28108 - Alcobendas (Madrid)
Spain
Last review date of this leaflet: February 2025
The detailed information of this medicine is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS) https://www.aemps.gob.es/
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