Patient leaflet - Bisoprolol Viatris 5 mg film-coated tablets
1. What Bisoprolol fumarate is and what it is used for
This medicine contains the active substance bisoprolol fumarate, which belongs to a family of medicines called beta-blockers. Beta-blockers protect the heart against too much activity. Bisoprolol is used in combination with other medicines to treat stable heart failure.
Heart failure occurs when the heart muscle is too weak to pump blood around the circulation adequately. This results in breathlessness and swelling.
Bisoprolol slows down the heart rate and makes the heart more efficient at pumping blood around the body.
Bisoprolol fumarate 5 mg and 10 mg tablets are also used to treat high blood pressure (hypertension) and angina pectoris (chest pain caused by blockages in the arteries that supply the heart muscle).
2. What you need to know before you take Bisoprolol fumarate
Do not take Bisoprolol fumarate if you:
are allergic to bisoprolol or any of the other
ingredients of this medicine (listed in section 6)
- have severe asthma
have a slow or irregular heart rate. Ask your doctor
if you are not sure
- have very low blood pressure
have severe blood circulation problems (which
may cause your fingers and toes to tingle or turn pale or blue)
have heart failure that suddenly becomes worse
and/or that may require hospital treatment
have excess acid in the blood, a condition known
as metabolic acidosis
have untreated phaeochromocytoma, a rare
tumour of the adrenal gland
Warnings and precautions
Talk to your doctor or pharmacist before taking this medicine if you:
- have asthma or chronic lung disease
have diabetes. Bisoprolol can hide the symptoms
of low blood sugar
- are fasting from solid food
have any heart problems
- have any liver or kidney problems
have any problems with the circulation in your
limbs, are taking verapamil or diltiazem, medicines used to treat heart conditions. Concomitant use is not recommended, see also “Other medicines and Bisoprolol fumarate”
- have (or have had) psoriasis (a recurring skin rash)
have phaeochromocytoma (a rare tumour of the
adrenal gland). Your doctor will need to treat this before prescribing bisoprolol for you
have a thyroid problem. The tablets can hide
symptoms of an overactive thyroid.
During Treatment
Talk to your doctor or pharmacist if you:
are going to be given a general anaesthetic during
an operation – tell your doctor that you are taking bisoprolol
are treated for hypersensitivity (allergic) reactions.
Bisoprolol may make your allergy worse or more difficult to treat
have chronic lung disease or less severe asthma
please inform your doctor immediately if you start to experience new difficulties in breathing, cough, wheezing after exercise, etc. when using bisoprolol
worsening of symptoms of blockage of the main
blood vessels to the legs, especially at the start of treatment.
Children and adolescents
No information is available on the use of this medicine in children.
Other medicines and Bisoprolol fumarate
Tell your doctor or pharmacist if you are already taking or using any of the following as they may interact with your medicine:
medicines for controlling the blood pressure or
medicines for heart problems (such as amiodarone, amlodipine, clonidine, digitalis glycosides, diltiazem, disopyramide, felodipine, flecainide, lidocaine, methyldopa, moxonidine, nifedipine, phenytoin, propafenone, quinidine, rilmenidine, verapamil)
medicines for depression e.g. imipramine,
amitriptyline, moclobemide
medicines to treat mental illness e.g.
phenothiazines such as levomepromazine
medicines used for anaesthesia during an
operation (see also “Warnings and precautions”)
medicines used to treat epilepsy e.g. barbiturates
such as phenobarbital
certain pain killers (for instance acetyl salicylic acid,
diclofenac, indomethacin, ibuprofen, naproxen)
medicines for asthma or medicines used for a blocked
nose
medicines used for certain eye disorders such as
glaucoma (increased pressure in the eye) or used to widen the pupil of the eye
certain medicines to treat clinical shock (e. g.
adrenaline, dobutamine, noradrenaline)
- mefloquine, a medicine for malaria
all these drugs as well as bisoprolol may influence
the blood pressure and/or heart function.
Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines.
Pregnancy, breast‑feeding and fertility
Bisoprolol can be harmful to the pregnancy and/or to the child (increased possibility of premature birth, miscarriage, retarded growth, low blood glucose level and reduced heart rate of the child).
Therefore do not use this medicine during pregnancy.
It is unknown if bisoprolol is excreted in the breast milk. Breast-feeding during the use of this medicine is therefore not recommended.
No information is available on the effects of bisoprolol on fertility.
If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your
doctor or pharmacist for advice before taking this medicine.
Driving and using machines
The use of bisoprolol may sometimes result in dizziness or fatigue (see ‘Possible side-effects’). If you suffer from these side effects, do not operate vehicles and/or machines. These side-effects are likely to happen at the start of treatment, or with a change in the amount of bisoprolol you take.
Bisoprolol fumarate contains sodium
This medicine contains less than 1 mmol sodium (23 mg) per tablet, that is to say essentially ‘sodium-free’
5 mg, 7.5 mg and 10 mg tablets only:
Bisoprolol fumarate tablets contain sunset yellow
Sunset yellow (E110) may cause allergic reactions.
3. How to take Bisoprolol fumarate
Always take this medicine exactly as your doctor has told you. Check with your doctor or pharmacist if you are not sure.
Adults
Chest pain and high blood pressure (angina and hypertension)
Your doctor will start the treatment with the lowest possible dose (5 mg). Your doctor will monitor you closely at the start of treatment. Your doctor will increase your dose to obtain the best possible dosage for you.
The maximum recommended dose is 20 mg once per day.
Patients with kidney disease
Patients with severe kidney disease should not exceed 10 mg of bisoprolol once daily. Please consult your doctor before starting to use this medicine.
Patients with liver disease
Patients with severe liver disease should not exceed 10 mg of bisoprolol once daily. Please consult your doctor before starting to use this medicine.
Heart failure
Before you start using Bisoprolol fumarate tablets, you should already be taking other medicines for heart failure including an ACE-inhibitor, a diuretic and (as an added option) a cardiac glycoside.
Treatment with bisoprolol must be started at a low dose and increased gradually. Your doctor will decide how to increase the dose, and this will normally be done in the following way:
- 1.25 mg bisoprolol once daily for one week
- 2.5 mg bisoprolol once daily for one week
- 3.75 mg bisoprolol once daily for one week
- 5 mg bisoprolol once daily for four weeks
- 7.5 mg bisoprolol once daily for four weeks
10 mg bisoprolol once daily for maintenance
(on-going) therapy.
The maximum recommended daily dose is 10 mg bisoprolol.
Depending on how well you tolerate the medicine, your doctor may also decide to lengthen the time between dose increases. If your condition gets worse or you no longer tolerate the drug, it may be necessary to reduce the dose again or to interrupt treatment. In some patients a maintenance dose lower than 10 mg bisoprolol may be sufficient.
Your doctor will tell you what to do.
Use in children and adolescents
The use of Bisoprolol is not recommended as there is insufficient experience with the use of this medicine in children and adolescents.
Date / Remarks Date / Remarks Date / Remarks Date / Remarks Date / Remarks
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ART-1165-03
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PL 04569/1254-9
400547677, 400547678, 400547681,
400547684
Mylan Laboratories Ltd, FDF 4
(Jedcherla, Hyderabad ), IN
NA
653245
1
NA
NA
Myriad Pro
NA
9 pt
Update in Labeling
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NA
Adobe Indesign 2020
United Kingdom (GB)
LIT. (OUTSERT) BISOPROLOL FUMARATE TAB (COMMON) GB V3
75084669
75078176
Printed Literature
1
Flat - 312 x 448 mm
Folded Size - 32 x 32 mm
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NA
40gsm ITC Tribeni Paper
Supply Leaflet in folded form as proposed size
FORM-000647341_00-12-20 Elderly patients
In general an adjustment of the dose is not needed. It is recommended to start with the lowest possible dose.
If you notice that the Bisoprolol dose is too strong or does not work well enough, please consult your doctor or pharmacist.
Route and/or method of administration:
- The tablets should be taken in the morning
- Swallow the tablets with a glass of water.
- The tablets should not be chewed.
The 2.5 mg, 3.75 mg, 5 mg, 7.5 mg and 10 mg
tablets can be divided into equal doses. The 1.25 mg tablets should not be broken.
If you take more Bisoprolol fumarate than you should
If you take more Bisoprolol fumarate than you should contact your doctor or casualty department immediately. Take the container and any remaining tablets with you.
If you forget to take Bisoprolol fumarate Do not take a double dose to make up for the forgotten dose. Take the next dose on time. If you miss several doses, contact your doctor.
If you stop taking Bisoprolol fumarate
If you suddenly stop taking Bisoprolol fumarate you are likely to suffer from side effects. Your doctor will reduce your dose slowly over 2 weeks.
If you have any further questions on the use of this medicine, please ask your doctor or pharmacist.
4. Possible side effects
Like all medicines, this medicine can cause side effects, although not everybody gets them.
The following side effects are important and will require immediate action if you experience them. You should stop taking Bisoprolol fumarate and see your doctor immediately if the following symptoms occur:
Very common side effects (affecting more than 1 in 10 people):
- slow heart beat
Common side effects (affecting fewer than 1 in 10 people):
worsening of heart failure causing increased
breathlessness and / or retention of fluid if you have chronic heart failure.
Uncommon side effects (affecting fewer than 1 in 100 people):
worsening of heart failure if you have
hypertension or angina pectoris
- depression
breathing problems in patients with asthma or
chronic lung disease
Rare side effects (affecting fewer than 1 in 1,000 people):
inflammation of the liver (hepatitis) causing
abdominal pain, loss of appetite and sometimes jaundice with yellowing of the whites of the eyes and skin and dark urine
Allergic reactions such as itching, redness and
skin rash. Severe allergic reactions may involve face, neck, tongue, mouth or throat swelling, or difficulty breathing.
If you feel dizzy or weak, or have breathing difficulties please contact your doctor as soon as possible.
The following side-effects have also been reported:
Common side effects (affecting fewer than 1 in 10 people):
- cold hands and/or feet
- numbness of hands and/or feet
- low blood pressure
- feeling sick, vomiting, diarrhoea, constipation
- tiredness*
headache*.
Uncommon side effects (affecting fewer than 1 in 100 people):
- worsening of irregular heart beat
- sleep disorder
- dizziness when standing up
- muscle weakness, muscle cramps.
Rare side effects (affecting fewer than 1 in 1,000 people):
- changes in blood test results
reduced tear flow (can be a problem if you wear
contact lenses)
- hearing disorders
- blocked, runny nose
failure to get and maintain an erection (erectile
dysfunction)
- nightmares
- hallucination (imagining things)
- fainting.
Very rare side effects (affecting fewer than 1 in 10,000 people):
- inflammation of the eye (conjunctivitis)
aggravation of the skin condition psoriasis or the
appearance of a similar dry, scaly rash
- hair loss.
* if treated for high blood pressure or angina then these symptoms occur especially at the beginning of treatment, or if your dosage changes. They are generally mild and often disappear within 1 to 2 weeks.
Reporting of side effects
If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme at: www.mhra.gov.uk/yellowcard. By reporting side effects, you can help provide more information on the safety of this medicine.
5. How to store Bisoprolol fumarate
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiry date which is stated on the carton and the bottle or blister after EXP. The expiry date refers to the last day of that month.
Blister: Store below 30°C.
Bottle: This medicinal product does not require any special storage conditions.
Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.
6. Contents of the pack and other information
What Bisoprolol fumarate film‑coated tablets contain:
Each film-coated tablet contains either 1.25 mg, 2.5 mg, 3.75 mg, 5 mg, 7.5 mg or 10 mg of the active ingredient bisoprolol fumarate.
The other ingredients are:
Tablet: Cellulose microcrystalline, butylhydroxyanisole, colloidal anhydrous silica, magnesium stearate, sodium lauril sulfate, croscarmellose sodium, iron oxide yellow (E172) (2.5 mg, 3.75 mg, 5 mg and 7.5 mg tablets only), iron oxide red (E172) (10 mg tablets only).
Film coat: Titanium dioxide (E171), talc, hypromellose (E464), quinoline yellow (5 mg and 7.5 mg tablets only), iron oxide yellow (E172) (3.75 mg and 10 mg tablets only), indigo carmine (E132) (5 mg tablet only), sunset yellow (E110)
(5 mg, 7.5 mg and 10 mg tablets only) (see section 2 “Bisoprolol fumarate contains sunset yellow”).
What Bisoprolol fumarate looks like and contents of the pack
Film-coated tablet
1.25 mg tablet: White, oval, biconvex film-coated tablets; ‘BL’ & ‘1’ engraved on one face of the tablet; ‘M’ engraved on the other face of the tablet.
2.5 mg tablet: White to off-white, oval, biconvex film-coated tablets with side notches; ‘BL’ &’ 2’ engraved on either side of the scoreline on one face of the tablet; ‘M’ engraved on the other face of the tablet.
3.75 mg tablet: Cream, oval, biconvex film-coated tablets with side notches; ‘BL’ & ‘3’ engraved on either side of the scoreline on one face of the tablet; ‘M’ engraved on the other face of the tablet.
5 mg tablet: Pale yellow, oval, biconvex film-coated tablets with side notches; ‘BL’ & ‘4’ engraved on either side of the scoreline on one face of the tablet; ‘M’ engraved on the other face of the tablet.
7.5 mg tablet: Yellow, oval, biconvex film-coated tablets with side notches; ‘BL’ & ‘5’ engraved on either side of the scoreline on one face of the tablet; ‘M’ engraved on the other face of the tablet.
10 mg tablet: Pale orange to light orange, oval, biconvex film-coated tablets with side notches; ‘BL’ & ‘6’ engraved on either side of the scoreline on one face of the tablet; ‘M’ engraved on the other face of the tablet.
Bisoprolol fumarate tablets are packed in blister packs containing 10, 20, 28, 30, 50, 56, 84, 90, 98 and 100 film-coated tablets. Bisoprolol fumarate tablets are packed in bottles containing 10, 28, 30, 50, 56, 84, 98, 100, 500, 1000 film-coated tablets.
Not all pack sizes may be marketed.
Marketing Authorisation Holder:
Mylan,
Potters Bar,
Hertfordshire,
EN6 1TL,
United Kingdom.
Manufacturers:
Mylan UK Healthcare Limited
Building 20,
Station Close,
Potters Bar,
EN6 1TL,
United Kingdom.
McDermott Laboratories (trading as
Gerard Laboratories),
35/36 Baldoyle Industrial Estate,
Grange Road,
Dublin 13,
Ireland.
Generics [UK] Ltd,
Station Close,
Potters Bar,
Hertfordshire,
EN6 1TL,
United Kingdom.
Mylan Hungary Kft.,
Mylan útca 1.,
Komárom,
2900,
Hungary.
Mylan S.A.S (Meyzieu),
Zac des Gaulnes,
360 Avenue Henri Schneider,
69330 Meyzieu,
France.
This leaflet was last revised in 01/2022
75084669 ART-1165-03
Date / Remarks Date / Remarks Date / Remarks Date / Remarks Date / Remarks
Date / Remarks
Date / Remarks
Date / Remarks
22.02.2022 / KLD Shared
Date / Remarks
Date / Remarks
dd / mm / yy dd / mm / yy 2 of 2
Die Line
NA
100%
02/03/22 17:44 ART-1165-03
ART-1165-03
2367206
NA
PL 04569/1254-9
400547677, 400547678, 400547681,
400547684
Mylan Laboratories Ltd, FDF 4
(Jedcherla, Hyderabad ), IN
NA
653245
1
NA
NA
Myriad Pro
NA
9 pt
Update in Labeling
NA
NA
Adobe Indesign 2020
United Kingdom (GB)
LIT. (OUTSERT) BISOPROLOL FUMARATE TAB (COMMON) GB V3
75084669
75078176
Printed Literature
1
Flat - 312 x 448 mm
Folded Size - 32 x 32 mm
NA
NA
NA
40gsm ITC Tribeni Paper
Supply Leaflet in folded form as proposed size
FORM-000647341_00-12-20