Package Leaflet: Information for the User
Bisoprolol Bluefish 1.25 mg Tablets EFG
bisoprolol fumarate
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the Package Leaflet
Bisoprolol Bluefish contains the active substance bisoprolol fumarate. Bisoprolol fumarate belongs to a group of medicines called beta-blockers. These medicines work by affecting the body's response to certain nerve impulses, especially in the heart. As a result, bisoprolol slows the heart rate and makes the heart more efficient at pumping blood throughout the body.
Heart failure occurs when the heart muscle is weak and unable to pump enough blood to meet the body's needs.
Bisoprolol is used to:
Do not take Bisoprolol Bluefish
if you have any of the following conditions:
Do not take Bisoprolol Bluefish if you have any of the following heart problems:
Warnings and precautions
Tell your doctor before starting to take bisoprolol if you have any of the following conditions; your doctor may want to take special precautions (such as providing additional treatment or performing more frequent tests):
During treatment
Also, tell your doctor if you are going to:
Children and adolescents
Bisoprolol is not recommended for use in children and adolescents.
Other medicines and Bisoprolol Bluefish
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines.
Do not take the following medicines with bisoprolol without special advice from your doctor:
However, do not stop taking these medicines without consulting your doctor first.
Consult your doctor before taking the following medicines with bisoprolol; your doctor may need to monitor your condition more frequently:
Pregnancy and breastfeeding
Pregnancy
Bisoprolol is not recommended during pregnancy. There is a risk that the use of bisoprolol during pregnancy may harm the baby. If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medicine. Your doctor will decide whether you can take bisoprolol during pregnancy.
Breastfeeding
It is not known whether bisoprolol passes into breast milk, and therefore, breastfeeding is not recommended during treatment with bisoprolol.
Driving and using machines
Your ability to drive or use machines may be affected, depending on how well you tolerate the medicine. Be especially careful at the start of treatment, when the dose is increased, or the medication is changed, and also in combination with alcohol.
Bisoprolol Bluefish contains sodium
This medicine contains less than 1 mmol of sodium (23 mg) per 1.25 mg tablet; this is essentially "sodium-free".
Follow the instructions for administration of this medicine exactly as told by your doctor. In case of doubt, consult your doctor or pharmacist again.
Treatment with bisoprolol requires regular monitoring by your doctor. This is particularly necessary at the start of treatment, during dose increase, and when stopping treatment.
Take the tablet with a little water in the morning, with or without food. Do not crush or chew the tablet.
Treatment with bisoprolol is usually long-term.
Adults and elderly patients
Hypertension or angina pectoris
The maximum recommended dose is 20 mg once daily.
Stable chronic heart failure
Treatment should be initiated by a doctor with experience in the treatment of chronic heart failure.
Treatment with bisoprolol should be started at a low dose and gradually increased. Your doctor will decide how to increase the dose, and this will usually be done as follows:
The maximum recommended daily dose of bisoprolol is 10 mg.
Depending on how well you tolerate the medicine, your doctor may also decide to prolong the time between dose increases. If your condition worsens or you no longer tolerate the medicine, it may be necessary to reduce the dose again or stop treatment. In some patients, a maintenance dose lower than 10 mg of bisoprolol may be sufficient.
Your doctor will tell you what to do.
Normally, if you need to stop treatment completely, your doctor will advise you to gradually reduce the dose, as otherwise, your condition may worsen.
Use in patients with kidney and/or liver impairment
In patients with kidney impairment and in patients with severe liver impairment, the dose of bisoprolol should not exceed 10 mg once daily.
Use in children and adolescents
The use of bisoprolol is not recommended in children and adolescents.
If you take more Bisoprolol Bluefish than you should
If you have taken more tablets of bisoprolol than you should, tell your doctor immediately. Your doctor will decide what measures are necessary.
Symptoms of an overdose may include a decrease in heart rate, severe difficulty breathing, dizziness, or tremors (due to low blood sugar).
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately, or call the Toxicology Information Service, phone: 91 562 04 20, indicating the medicine and the amount taken.
If you forget to take Bisoprolol Bluefish
If you forget to take a dose, take it as soon as you remember, unless it is time to take the next dose. Do not take a double dose to make up for the forgotten dose. Take your usual dose the next morning.
If you stop taking Bisoprolol Bluefish
Do not stop treatment suddenly or change the recommended dose unless your doctor tells you to. Otherwise, your condition may worsen significantly. If you are considering stopping treatment, your doctor will advise you how to gradually reduce the dose to avoid any adverse effects.
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.
To prevent serious side effects, talk to your doctor immediately if a side effect is severe, occurs suddenly, or worsens rapidly. The most serious side effectsare related to heart function:
If you feel dizzy or weak, or have difficulty breathing, contact your doctor as soon as possible.
Below are mentioned other side effects according to their frequency of possible occurrence:
Common (may affect up to 1 in 10 people)
*These symptoms occur at the start of treatment in patients with hypertension or angina pectoris. They are usually mild and disappear in 1-2 weeks.
Uncommon (may affect up to 1 in 100 people)
Rare (may affect up to 1 in 1,000 people)
Very rare (may affect up to 1 in 10,000 people)
Reporting of side effects
If you experience any side effects, talk to your doctor or pharmacist, even if it is possible that they are not listed in this leaflet. You can also report side effects directly to the Spanish Medicines 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 use this medicine after the expiry date stated on the packaging after EXP. The expiry date is the last day of the month indicated.
Store below 25°C.
Medicines should not be disposed of via wastewater or household waste. Return any unused medicine to a pharmacy for proper disposal. Ask your pharmacist how to dispose of medicines no longer needed. This will help protect the environment.
Composition of Bisoprolol Bluefish
The active substance is bisoprolol fumarate
Bisoprolol Bluefish 1.25 mg: each tablet contains 1.25 mg of bisoprolol fumarate.
The other ingredients are:
microcrystalline cellulose, anhydrous colloidal silica, sodium croscarmellose, sodium carboxymethyl starch (type A), and magnesium stearate.
Appearance of the product and pack contents
White to off-white, round, biconvex tablet, engraved with "1.25" and smooth on the other side.
It is packaged in blisters made of PVC/PVDC-Al or PVC/PCTFE-Al.
Pack size:
20 tablets.
Marketing authorization holder and manufacturer
Marketing authorization holder:
Bluefish Pharmaceuticals AB
P.O. Box 49013
100 28 Stockholm
Sweden
Manufacturer:
Chanelle Medical Unlimited Company
Loughrea,
County Galway
Ireland
You can obtain more information about this medicine by contacting the local representative of the marketing authorization holder:
Bluefish Pharma S.L.U
AP 36007
2832094 Madrid, Sucursal 36
This medicine is authorized in the EEA member states with the following names:
Portugal: Bisoprolol Bluefish 1.25 mg tablets
Spain: Bisoprolol Bluefish 1.25 mg tablets EFG
Date of last revision of this leaflet:October 2024
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/
The average price of BISOPROLOL BLUEFISH 1.25 mg TABLETS in October, 2025 is around 2.5 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.