


Ask a doctor about a prescription for DILUTOL 10 mg TABLETS
Leaflet:informationfor the user
Dilutol 10 mg tablets
Torasemide
Read the entire leaflet carefully before starting to take this medication
Contents of the leaflet
5. Storage of DILUTOL 10 mg tablets.
DILUTOL 10 mg contains torasemide, which belongs to the group of medications called antihypertensive diuretics.
DILUTOL 10 mg is indicated for the treatment and prevention of edema (fluid retention) due to congestive heart failure, liver, and kidney disease.
Do not take DILUTOL 10 mg
Warnings and precautions
Consult your doctor or pharmacist before starting to take Dilutol.
Children
Since the safety and efficacy of torasemide in children (under 18 years) have not been established, its use is not recommended in this population.
Use in elderly patients
No differences in efficacy or safety have been observed according to the patient's age.
Use of Dilutol 10 mg with other medications
Inform your doctor or pharmacist if you are using, have recently used, or may need to use another medication.
You should also inform your doctor if you are using any of the following medications that may interact with torasemide:
Taking Dilutol 10 mg with food and drinks
The tablets can be taken with or without food. They are swallowed without chewing, with a little liquid, preferably in the morning.
Pregnancy, breastfeeding, and fertility
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using any medication.
The use of torasemide is not recommended during pregnancy or in breastfeeding women, as it is unknown whether torasemide passes into breast milk.
Driving and using machines
This medication may affect your ability to drive or use machines, especially if taken simultaneously with alcohol.
Dilutol 10 mg contains lactose
If your doctor has told you that you have an intolerance to certain sugars, consult with them before taking this medication.
Follow the administration instructions for this medication exactly as indicated by your doctor or pharmacist. If in doubt, consult your doctor or pharmacist.
Remember to take your medication.
They can be administered at any time regarding meals, at your convenience. They are swallowed without chewing, with a little liquid, preferably with breakfast.
Your doctor will indicate the duration of your treatment with Dilutol. Do not stop treatment before, as it may worsen your condition.
The recommended dose in adults is:
In edema associated with congestive heart failure, kidney, or liver disease:The initial dose ranges from 5 mg to 20 mg per day, in a single dose, but your doctor may increase it up to approximately double if deemed necessary.
If you take more Dilutol 10 mg than you should
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately, or go to the nearest hospital, or call the Toxicology Information Service, phone (91) 562 04 20, indicating the medication and the amount ingested. It is recommended to bring the packaging and the leaflet of the medication to the healthcare professional.
In case of overdose, excessive urine production may occur, and drowsiness, confusion, weakness, and dizziness may appear.
If you forget to take Dilutol 10 mg
Do not take a double dose to make up for the forgotten dose.
Take your dose as soon as you remember, and the next day, take it at the corresponding time.
If you have any other questions about the use of this medication, ask your doctor or pharmacist.
Like all medications, this medication can cause side effects, although not everyone experiences them.
Side effects can occur with the following frequencies:
Very common: affects more than 1 in 10 patients treated.
Common: affects between 1 and 10 in 100 patients treated.
Uncommon: affects between 1 and 10 in 1,000 patients treated.
Rare: affects between 1 and 10 in 10,000 patients treated.
Very rare: affects less than 1 in 10,000 patients treated.
Frequency not known: cannot be estimated from the available data.
The following side effects have been reported:
Common:
Increased blood pH (metabolic alkalosis), electrolyte and fluid imbalance (e.g., decreased total blood volume, decreased sodium and/or potassium in blood), headache, dizziness, gastrointestinal disorders (e.g., loss of appetite, abdominal pain, nausea, vomiting, diarrhea, constipation), muscle spasms, fatigue, tiredness.
Uncommon:
Increased liver enzymes, urinary retention, increased gallbladder volume, increased uric acid, glucose, and lipids (such as triglycerides or cholesterol) in the blood.
Rare:
Increased urea and/or creatinine in the blood.
Very rare:
Allergic skin reactions (itching and skin rashes), sensitivity to sunlight.
Frequency not known:
Severe skin reactions (e.g., Stevens-Johnson syndrome, toxic epidermal necrolysis), decreased platelet and/or white blood cell count, anemia, cerebral ischemia (decreased blood flow to the brain), numbness in the body (paresthesia), confusion, visual disturbances, ringing in the ears (tinnitus), deafness, myocardial infarction (heart attack), decreased heart blood flow (myocardial ischemia), angina pectoris, loss of consciousness (syncope), hypotension, blood vessel obstruction (embolism), dry mouth, pancreatitis (inflammation of the pancreas).
Reporting side effects
If you experience any side effects, consult your doctor or pharmacist, even if they are not listed in this leaflet. You can also report them directly through the Spanish Medication Surveillance System for Human Use: 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.
Do not use this medication after the expiration date stated 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. Ask your pharmacist how to dispose of the packaging and medications you no longer need. This will help protect the environment.
Composition of Dilutol 10 mg tablets
The active ingredient is torasemide.
The other components are hydrated lactose, cornstarch, colloidal silicon dioxide, and magnesium stearate.
Appearance of the product and contents of the pack
Dilutol 10 mg are white or almost white round tablets. The tablets are presented in PVC-aluminum blisters, and each pack contains 30 tablets.
Marketing authorization holder and manufacturer
Holder:
Viatris Healthcare Limited
Damastown Industrial Park
Mulhuddart, Dublin 15
Dublin
Ireland
Manufacturer:
Madaus GmbH
51101 Cologne
Germany
You can request more information about this medication by contacting the local representative of the marketing authorization holder:
Viatris Pharmaceuticals, S.L.
C/ General Aranaz, 86
28027 - Madrid
Spain
Date of the last revision of this leaflet:July 2018
Detailed and updated information about this medication is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) (https://www.aemps.gob.es).
The average price of DILUTOL 10 mg TABLETS in October, 2025 is around 5.29 EUR. Prices may vary depending on the region, pharmacy, and whether a prescription is required. Always check with a local pharmacy or online source for the most accurate information.
The best alternatives with the same active ingredient and therapeutic effect.
Discuss dosage, side effects, interactions, contraindications, and prescription renewal for DILUTOL 10 mg TABLETS – subject to medical assessment and local rules.