Antidol 1 g solucion oral

Package Leaflet: Information for the User

Antidol 1 g Oral Solution

Paracetamol

Read this leaflet carefully before you start taking this medicine because it contains important information for you.

Follow exactly the administration instructions for the medicine contained in this leaflet or those indicated by your doctor, pharmacist, or nurse.

• Keep this leaflet, as you may need to read it again.
• If you need advice or more information, consult your pharmacist.
• If you experience any side effects, consult your doctor, pharmacist, or nurse, even if they are not listed in this leaflet. See section 4.
• You should consult a doctor if the symptoms worsen or if the fever persists for more than 3 days or the pain for more than 5 days.

1. What is Antidol and what it is used for

2. What you need to know before starting to take Antidol

3. How to take Antidol

4. Possible side effects

5. Storage of Antidol

6. Contents of the pack and additional information

This medication contains paracetamol. Paracetamol is effective in reducing pain and fever.

It is used for the relief of occasional mild or moderate pain, such as headache, toothache, muscle pain (muscle spasms) or back pain (lower back pain) and in febrile states, in adults and adolescents over 15 years old and weighing more than 50 kg.

Do not takeAntidol

• If you are allergic to paracetamol or any of the other components of this medication (listed in section 6).

Warnings and precautions

Consult your doctor, pharmacist, or nurse before starting to takeAntidol.

• Do not take more medication than recommended in section 3. How to takeAntidol.
• Avoid using this medication with other medications that contain paracetamol, such as cold and flu medications, as high doses can cause liver damage. Do not use more than one medication that contains paracetamol without consulting your doctor.
• Chronic alcoholics should be careful not to take more than 2 g/24 hours of paracetamol.
• Patients with kidney, liver, heart, or lung diseases, or patients with anemia (decreased hemoglobin levels in the blood, due or not due to a decrease in red blood cells), or patients with chronic malnutrition or dehydration, should consult their doctor before taking this medication.
• When taking medication for epilepsy, consult your doctor before taking this medication, as it can reduce the effectiveness and increase the hepatotoxicity of paracetamol, especially with high doses of paracetamol.
• Patients with asthma sensitive to acetylsalicylic acid should consult their doctor before taking this medication.
• 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 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 respiratory distress with deep and rapid breathing, drowsiness, feeling unwell (nausea), and vomiting.

Children and adolescents

Due to the dose, the use of this medication is not indicated in children or adolescents under 15 years or weighing less than 50 kg.

Other medications andAntidol

Inform your doctor or pharmacist if you are using, have used recently, or may need to use any other medication.

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:

• Medications to prevent blood clots: Oral anticoagulants (acenocoumarol, warfarin).
• Medications to treat epilepsy: Antiepileptics (lamotrigine, phenytoin, or other hydantoins, phenobarbital, metharbital, primidone, carbamazepine).
• Medications to treat tuberculosis: (isoniazid, rifampicin).
• Medications to treat depression and seizures: Barbiturates (used as hypnotics, sedatives, and anticonvulsants).
• Medications to lower blood cholesterol levels: (colestiramine).
• Medications used to increase urine elimination (diuretics such as furosemide).
• Medications used to treat gout (probencid and sulfinpyrazone).
• Medications used to prevent nausea and vomiting: Metoclopramide and domperidone.
• Medications used to treat high blood pressure and heart rhythm disorders (arrhythmias): Propranolol.

Also inform your doctor or pharmacist if you are taking:

• Flucloxacillin (antibiotic), due to a severe risk of blood and fluid imbalance (denominated metabolic acidosis with high anion gap) that must be treated urgently (see section 2).

Do not use with other analgesics (pain-relieving medications) without consulting your doctor.

As a general rule for any medication, it is recommended to inform your doctor or pharmacist if you are taking another medication. In the case of oral anticoagulants, it may be necessary to administer this medication occasionally as the preferred analgesic.

Interference with analytical tests

If you are to undergo any analytical test (including blood and urine tests, etc.), inform your doctor that you are taking this medication, as it may alter the results.

Paracetamol may alter the values of uric acid and glucose determinations.

Use ofAntidolwith food, drinks, and alcohol

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

Pregnancy, breastfeeding, and fertility

If you are pregnant or breastfeeding, think you may be pregnant, or intend to become pregnant, consult your doctor or pharmacist before using this medication.

The consumption of medications during pregnancy can be hazardous to the embryo or fetus, and should be monitored by your doctor.

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.

Antidolcontains propylene glycol (E-1520), sodium, and azorubine (E-122).

This medication contains 88.7 mg of propylene glycol in each sachet.

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

This medication may cause allergic reactions because it contains azorubine. It may cause asthma, especially in patients allergic to acetylsalicylic acid.

Follow exactly the medication administration instructions contained in this leaflet or those indicated by your doctor. If in doubt, ask your doctor or pharmacist.

The recommended dose is:

Adults and adolescents over 15 years and weighing more than 50 kg:

Take 1 g of paracetamol (1 sachet) every 6-8 hours, 3 times a day. Do not take more than 3 g of paracetamol (3 sachets) in 24 hours.

Always take the lowest effective dose.

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

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

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

For sore throat, the medication should not be taken for more than 2 consecutive days without consulting a doctor.

Patients with kidney disease:

This medication does not follow the recommended dosage for these patients.

Patients with liver disease:

You should consult your doctor before starting to take 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 g of paracetamol (2 sachets) in 24 hours, divided into several doses.

Administration form

This medication is taken orally.

The contents of the sachet can be taken directly, or diluted in a liquid, preferably water. Once the sachet is opened, consume all its contents.

If you take moreAntidolthan you should

You should consult your doctor or pharmacist immediately. In case of overdose or accidental ingestion, go immediately to a medical center or call the Toxicological Information Service, phone 91 562 04 20, indicating the medication and the amount ingested.

The symptoms of overdose may be: dizziness, vomiting, loss of appetite, yellowish discoloration of the skin and eyes (jaundice), and abdominal pain.

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

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

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

If you forgot to takeAntidol

Do not take a double dose to compensate for the missed doses.

Like all medications, this medication may produce adverse effects, although not all people will experience them.

Rare adverse effects that may affect up to 1 in 1,000 people are: discomfort, low blood pressure (hypotension), and increased levels of transaminases in the blood.

Very rare adverse effects that may affect up to 1 in 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) and severe skin reactions.

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).

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

Reporting Adverse Effects

If you experience any type of adverse effect, consult your doctor or pharmacist, even if it is an 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:www.notificaRAM.es.

By reporting adverse effects, you can contribute to providing more information about the safety of this medication.

Keep this medication out of the sight and reach of children.

No special storage conditions are required.

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.

Do not dispose of medications through drains or in the trash. Dispose of packaging and unused medications at the SIGRE collection point at the pharmacy. If in doubt, ask your pharmacist how to dispose of packaging and unused medications. By doing so, you will help protect the environment.

Composition ofAntidol

The active ingredient is paracetamol. Each sachet contains 1 g of paracetamol.

The other components are: macrogol 400, glycerol (E-422), sodium saccharin, strawberry aroma, raspberry aroma (contains propylene glycol (E-1520)), flavor enhancer (azorubine (E-122)) and purified water.

Appearance ofAntidoland contents of the packaging

Clear, red-colored oral solution, free of suspended particles and with a characteristic strawberry/raspberry odor.

Each package contains 10 sachets with 10 ml of solution each, packaged in single-dose sachets made of PET/ALU/PET/PE complex.

Holder of the marketing authorization

Cinfa Laboratories, S.A.

Olaz-Chipi Highway, 10. Areta Industrial Estate

31620 Huarte (Navarra) – Spain

Responsible for manufacturing

Farmalider, S.A.

Aragoneses Street, 2

28108 Alcobendas, Madrid - Spain

or

Edefarm, S.L

Enchilagar del Rullo Industrial Estate, 117

46191, Villamarchante, Valencia - Spain

or

Cinfa Laboratories, S.A.

Olaz-Chipi Highway, 10. Areta Industrial Estate

31620 Huarte (Navarra) – Spain

Last review date of this leaflet:February 2025

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