FLUSENIDE 20 MG TABLETS

Spain

It is used to treat high blood pressure (hypertension), prevent and treat lack of blood supply due to cerebral infarction, and prevent neuron damage caused by the contraction of blood vessels following a hemorrhage.

Brand name FLUSENIDE 20 MG TABLETS
Dosage form tablets
Active substance / Dosage
Prescription type Prescription Only Medicine
Registration number 56464

Frequently asked questions

How should I take Flusemide?

You must follow your doctor's instructions exactly. Tablets should be swallowed without chewing with sufficient liquid, avoiding grapefruit juice. They can be taken with or between meals, but it is recommended not to take them with very fatty foods.

When should I not take this medication?

You must not take it if you are allergic to nicardipine or its components, if you have had recent cerebral hemorrhages, if you have increased intracranial pressure (intracranial hypertension), if you are pregnant, if you are breastfeeding, if you have advanced narrowing of the heart valves (aortic stenosis), or if you are under 18 years of age.

What side effects can Flusemide cause?

It may cause effects such as palpitations, low blood pressure, swelling in the arms and legs, dizziness, headache, drowsiness, insomnia, nausea, digestive problems (constipation or diarrhea), weakness, a feeling of flushing, or frequent urge to urinate. In rare or unknown frequency cases, there may be fluid accumulation in the lungs or allergic reactions.

Can I take other medications while using Flusemide?

You must inform your doctor if you are taking other drugs, as some may interact. For example, cimetidine, carbamazepine, digoxin, rifampicin, or medications for the immune system (such as cyclosporine, tacrolimus, or sirolimus) may alter its effect. It can also be combined with diuretics or beta-blockers, but with caution due to the risk of blood pressure drops when standing up.

What should I do if I forget a dose or take too much?

If you forget a dose, do not take a double dose to make up for it. In case of taking too much or an accidental overdose, consult your doctor, pharmacist, or call the Toxicological Information Service.

Should I take any special care with food or drink?

You may take it with or between meals, but it is recommended to avoid foods high in fat. Additionally, you must not take the medication with grapefruit juice.

Instructions for use

Patient Information Leaflet

Introduction

Patient Information Leaflet

Flusemide 20 mg tablets

Nicardipine hydrochloride

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

  • Keep this leaflet as you may need to read it again.
  • If you have any questions, ask your doctor or pharmacist.
  • This medicine has been prescribed for you only and must not be given to other people, even if they have the same symptoms as you, because it could harm them.
  • If you experience any adverse effects, consult your doctor or pharmacist, even if they are effects not listed in this leaflet. See section 4.

Leaflet Contents

  1. What Flusemide is and what it is used for
  2. What you need to know before taking Flusemide
  3. How to take Flusemide
  4. Possible adverse effects
  5. How to store Flusemide
  6. Contents of the pack and other information

1. What Flusemide is and what it is used for

Nicardipine hydrochloride, the active substance in Flusemide, is a drug belonging to the group of calcium antagonists that acts on blood vessels by relaxing smooth muscle. It also increases blood flow at the cerebral level.

This medicine is indicated for:

  • Treatment of essential, mild to moderate arterial hypertension (high blood pressure).
  • Prevention and treatment of cerebral ischemia (reduced blood supply) due to cerebral infarction.
  • Prevention of neuronal damage caused by constriction of cerebral blood vessels following hemorrhage.

2. What you need to know before taking Flusemide

Do not take Flusemide:

  • if you are allergic to nicardipine or to any of the other components of this medicine (listed in section 6).
  • if you have recently had cerebral hemorrhage.
  • if you have intracranial hypertension (increased pressure inside the skull).
  • if you are pregnant or breastfeeding.
  • if you have advanced aortic stenosis (abnormal narrowing of the opening of one of the heart valves).
  • if you are under 18 years of age.

Warnings and precautions

Consult your doctor or pharmacist before starting to take Flusemide.

If you experience pain within 30 minutes after starting treatment or after increasing the dose, stop taking this medicine.

Immediate relief of chest pain during an acute or sudden angina attack should be treated with a different type of medication.

This medicine should be used with caution (e.g., close monitoring at the start of treatment) in:

  • patients with heart problems,
  • patients with liver and/or kidney problems,
  • elderly patients,
  • patients who have had a stroke (cerebral infarction or hemorrhage).

If you are scheduled to undergo any diagnostic tests (including blood or urine tests, etc.), inform your doctor that you are taking/using this medicine, as it may alter test results.

Children and adolescents

This medicine is contraindicated in individuals under 18 years of age.

Taking Flusemide with other medicines

Inform your doctor or pharmacist if you are taking, have recently taken, or might need to take any other medicines.

Some medicines may interact with this medicine, requiring a dose adjustment or discontinuation of one of the treatments.

Cimetidine (used for gastric ulcers) increases plasma levels of nicardipine.

Caution should be exercised when carbamazepine (used for epilepsy) and nicardipine are administered together.

This medicine may be used in combination with other drugs for the treatment of high blood pressure (beta-blockers, diuretics), but the possibility of an additive effect leading to postural hypotension (a drop in blood pressure when sitting up after lying down or standing up after sitting) should be considered.

Elevated levels of cyclosporine (used as an immunosuppressant) have been reported when used concomitantly with nicardipine.

Concomitant administration of nicardipine and digoxin (used to treat certain heart conditions) may increase the effects of digoxin.

Rifampicin (used to treat certain infectious diseases) may substantially reduce plasma levels of nicardipine; therefore, the combined use of rifampicin and nicardipine should be done with caution.

In particular, inform your doctor if you are taking other medicines to control the body's immune system, such as cyclosporine, tacrolimus, or sirolimus.

Taking Flusemide with food, drinks, and alcohol

Nicardipine may be taken independently of meals, except as indicated in section 3.

Use in pregnant or breastfeeding women

This medicine must not be used during pregnancy.

Cases of acute pulmonary edema (abnormal accumulation of fluid in the lungs) have been reported when nicardipine is used during pregnancy.

This medicine must not be used during breastfeeding.

Driving and using machines

This medicine should be used with caution in patients whose activities require alertness and who have experienced dizziness during treatment with this drug. For this reason, especially at the beginning of treatment, caution is advised when driving vehicles or operating machinery, or such activities should be avoided until the response to the medicine is satisfactory.

Flusemide contains lactose

This medicine contains lactose. If your doctor has informed you that you have an intolerance to certain sugars, consult with him/her before taking this medicine.

3. How to take Flusemide

Follow exactly the instructions for use of this medicine as given by your doctor or pharmacist. If in doubt, consult your doctor or pharmacist again.

The dose must be adjusted individually according to the therapeutic response achieved in each patient.

Treatment of essential arterial hypertension

The recommended dose for the treatment of essential hypertension is 1 tablet of 20 mg three times daily, which may be increased to a dose of 30 mg three times daily. Before increasing the dose, three days should elapse at the initial dose to achieve stable plasma concentrations.

A dose of 30 mg cannot be administered with this medicine.

Prevention and treatment of ischemia due to cerebral infarction

The recommended dose for the prevention and treatment of ischemia following cerebral infarction is 20 to 30 mg three times daily.

A dose of 30 mg cannot be administered with this medicine.

Prevention of neuronal damage due to constriction of cerebral blood vessels following hemorrhage

The prevention of neurological deterioration caused by cerebral vasospasm after subarachnoid hemorrhage is 120 mg daily (2 tablets of 20 mg three times daily), which may subsequently be reduced to 1 tablet of 20 mg three times daily.

The tablet score is intended solely for ease of breaking the tablet and facilitating swallowing, but not for dividing it into equal doses.

The tablets of this medicine must be swallowed whole, without chewing, with sufficient liquid, but not with grapefruit juice. They may be taken during or between meals, but administration with fatty foods is not recommended.

If you take more Flusemide than you should

In case of overdose or accidental ingestion, consult your doctor or pharmacist or call the Toxicology Information Service at telephone number 91 562 04 20, indicating the medicine and the amount ingested.

If you forget to take Flusemide

Do not take a double dose to make up for missed doses.

If you stop taking Flusemide

When treatment with nicardipine is discontinued prematurely, your original symptoms may return. Therefore, take this medicine for as long as your doctor prescribes, even if your symptoms have disappeared. Always consult your doctor if you decide to stop treatment.

If you have any further questions about the use of this medicine, ask your doctor or pharmacist.

4. Possible adverse effects

Like all medicines, this medicine can cause adverse effects, although not everyone will experience them.

Uncommon adverse effects (may affect up to 1 in 100 patients):

Palpitations, hypotension, fluid accumulation in arms and legs (peripheral edema), dizziness, headache (cephalalgia), somnolence, insomnia, nausea, gastric discomfort, constipation, diarrhea, increased salivation, feeling of weakness (asthenia), suffocation, frequent urination.

Rare adverse effects (may affect up to 1 in 1,000 patients):

Increased liver enzymes.

Adverse effects of unknown frequency (cannot be estimated from available data):

Abnormal fluid accumulation in the lungs (acute pulmonary edema), abnormally low platelet count (thrombocytopenia); flushing and anaphylactic reaction.

Reporting of adverse effects

If you experience any type of adverse effect, consult your doctor or pharmacist, even if it is a possible adverse effect not listed in this leaflet. You may also report them directly via the Spanish Pharmacovigilance System for Human Medicines: https://www.notificaram.es. By reporting adverse effects, you can help provide more information on the safety of this medicine.

5. Storage of Flusemide

Keep this medicine out of sight and reach of children.

Do not use this medicine after the expiry date stated on the carton after EXP.

The expiry date refers to the last day of the month indicated.

Medicines must not be disposed of via wastewater or household waste. Dispose of unused medicines and their containers at the SIGRE Point located at your pharmacy. If you have any doubts, ask your pharmacist how to properly dispose of medicines and containers you no longer need. This will help protect the environment.

6. Contents of the pack and other information

Composition of Flusemide

  • The active substance is nicardipine hydrochloride.
  • The other components are lactose, corn starch, microcrystalline cellulose, colloidal silicon dioxide, povidone, and magnesium stearate.

Appearance of the product and contents of the pack

Light yellow, round, scored tablets.

Available in packs of 30 or 60 tablets.

Only certain pack sizes may be marketed.

Marketing Authorization Holder and Manufacturer

Laboratorios Q Pharma S.L.

C/ Portugal 27, Entlo C

Alicante 03003 Spain

Date of the most recent review of this leaflet: April 2020

Detailed and up-to-date information on this medicinal product is available on the website of the Spanish Agency of Medicines and Health Products (AEMPS) http://www.aemps.gob.es/

The original data is available in the language of the country of manufacture.

Data source: Online Medicines Information Centre (CIMA) — AEMPS

Data last verified: September 21, 2026