
Ask a doctor about a prescription for TORASEMIDE TEVA-RATIO 10 mg TABLETS
Package Leaflet: Information for the User
Torasemide Teva-ratio 5 mg Tablets EFG
Torasemide Teva-ratio 10 mg Tablets EFG
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.Keep this leaflet. You may need to read it again.
Contents of the pack
Torasemide is a medicine that belongs to the group of medicines called antihypertensive diuretics.
Torasemide is indicated for:
Do not take Torasemide Teva-ratio
Warnings and precautions
Consult your doctor or pharmacist before starting to take torasemide.
Children and adolescents
Since the safety and efficacy of torasemide in children (< 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.
Other medicines and Torasemide Teva-ratio
Tell your doctor or pharmacist if you are taking, have recently taken, or might take other medicines.
You should also inform your doctor if you are taking any of the following medicines that may interact with torasemide:
Taking Torasemide Teva-ratio with food, drinks, and alcohol
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 are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.
The use of torasemide is not recommended during pregnancy or in breastfeeding women, as it is not known whether torasemide passes into breast milk.
Driving and using machines
This medicine may affect your ability to drive or use machines, especially if taken simultaneously with alcohol.
Torasemide Teva-ratio contains lactose and sodium
This medicine contains lactose. If your doctor has told you that you have an intolerance to some sugars, consult them before taking this medicine.
This medicine contains less than 1 mmol of sodium (23 mg) per tablet; this is, essentially, "sodium-free".
Follow exactly the administration instructions of this medicine contained in this leaflet or as indicated by your doctor or pharmacist. If in doubt, consult your doctor or pharmacist.
Your doctor will indicate the duration of your treatment with torasemide. Do not stop treatment before, as it could worsen your disease.
Remember to take your medicine. It can be administered at any time regarding meals, at your convenience. It is swallowed without chewing, with a little liquid, preferably with breakfast. The tablet can be divided into equal doses.
The recommended dose in adults is:
In edema associated with congestive heart failure, renal or hepatic disease.
The initial dose ranges from 5 mg to 20 mg per day, in a single dose, but your doctor may increase it to approximately double if deemed necessary.
In hypertension.
The initial dose is 2.5 to 5 mg per day, in a single dose, but your doctor may increase it to 10 mg per day or prescribe another additional antihypertensive.
If you take more Torasemide Teva-ratio than you should
If you have taken more torasemide than you should, consult your doctor or pharmacist immediately. In case of overdose, an increased amount of urine may be produced, and drowsiness, confusion, weakness, and dizziness may appear. In case of overdose or accidental ingestion, also consult the Toxicological Information Service, telephone 91 562 04 20.
If you forget to take Torasemide Teva-ratio
Do not take a double dose to make up for forgotten doses. Take your dose as soon as you remember and, the next day, take it at the corresponding time.
If you have any further questions on the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Side effects may appear 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.
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, 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 spots), 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 in blood, anemia, cerebral ischemia (decreased blood flow to the brain), numbness in the body (paresthesia), confusional state, visual disturbance, ringing in the ears (tinnitus), deafness, infarction (acute myocardial infarction), lack of heart blood flow (myocardial ischemia), angina pectoris, loss of consciousness (syncope), hypotension, obstruction of blood vessels (embolism), dry mouth, pancreatitis (inflammation of the pancreas).
Reporting of side effects:
If you experience any side effects, talk to your doctor or pharmacist, even if they are not listed in this leaflet. You can also report side effects directly through the Spanish Medicines and Health Products Agency's website: https://www.notificaram.es. By reporting side effects, you can help provide more information on the safety of this medicine.
Keep this medicine out of the sight and reach of children.
Do not store above 30°C.
Do not use this medicine after the expiry date which is stated on the carton and blister after EXP. The expiry date is the last day of the month shown.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help protect the environment.
Composition of Torasemide Teva-ratio
Appearance of the product and pack contents
Torasemide Teva-ratio 5 mg: biconvex, round, white or almost white tablets, scored on one side and marked with 915 on the other. They are available in packs of 30 tablets.
Torasemide Teva-ratio 10 mg: biconvex, round, white or almost white tablets, scored on one side and marked with 916 on the other. They are available in packs of 30 tablets.
Marketing authorisation holder and manufacturer
Marketing authorisation holder
Teva Pharma, S.L.U.
C/ Anabel Segura, 11 Edificio Albatros B, 1ª Planta
28108 Alcobendas, Madrid
Spain
Manufacturer
Teva Operations Poland sp. z.o.o.
Ul. Mogilska 80, 31-546 Kraków
Poland
or
Merckle GmbH
Ludwig-Merckle-Strasse, 3
Blaubeuren CP: D-89143
Germany
or
Pliva Hrvatska d.o.o.
Prilaz Baruna Filipovica 25, Zagreb
Croatia
Date of last revision of this leaflet:June 2025
Detailed information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/
You can access detailed and updated information about this medicine by scanning the QR code included in the packaging with your mobile phone (smartphone). You can also access this information at the following internet address: https://cima.aemps.es/cima/dochtml/p/72174/P_72174.html
QR code + URL
The average price of TORASEMIDE TEVA-RATIO 10 mg TABLETS in November, 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.
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Discuss dosage, side effects, interactions, contraindications, and prescription renewal for TORASEMIDE TEVA-RATIO 10 mg TABLETS – subject to medical assessment and local rules.