Bisoprolol fumarate Pinewood 10 mg film-coated tablets

Krajina: Írsko

Jazyk: angličtina

Zdroj: HPRA (Health Products Regulatory Authority)

Aktívna zložka:

BISOPROLOL FUMARATE

Dostupné z:

Pinewood Laboratories Ltd

ATC kód:

C07AB07

INN (Medzinárodný Name):

BISOPROLOL FUMARATE

Forma lieku:

Film-coated tablet

Terapeutické oblasti:

bisoprolol

Dátum Autorizácia:

2024-02-16

Príbalový leták

PACKAGE LEAFLET
PACKAGE LEAFLET: INFORMATION FOR THE USER
BISOPROLOL FUMARATE PINEWOOD 1.25 MG FILM-COATED TABLETS BISOPROLOL FUMARATE PINEWOOD 2.5 MG FILM-COATED TABLETS BISOPROLOL FUMARATE PINEWOOD 3.75 MG FILM-COATED TABLETS BISOPROLOL FUMARATE PINEWOOD 5 MG FILM-COATED TABLETS BISOPROLOL FUMARATE PINEWOOD 7.5 MG FILM-COATED TABLETS BISOPROLOL FUMARATE PINEWOOD 10 MG FILM-COATED TABLETS
bisoprolol fumarate
The name of this medicine is Bisoprolol fumarate Pinewood 1.25 mg
film-coated tablets, Bisoprolol
fumarate Pinewood 2.5 mg film-coated tablets, Bisoprolol fumarate
Pinewood 3.75 mg film-coated
tablets, Bisoprolol fumarate Pinewood 5 mg film-coated tablets,
Bisoprolol fumarate Pinewood 7.5
mg film-coated tablets, Bisoprolol fumarate Pinewood 10 mg film-coated
tablets which will be called
Bisoprolol fumarate Pinewood throughout this leaflet.
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.

If you have any further questions, ask your doctor or your pharmacist.

This medicine has been prescribed for you only. Do not pass it on to
others. It may harm them,
even if their signs of illness are the same as yours.

If you get any side effects, talk to your doctor or pharmacist. This
includes any possible side
effects not listed in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET:
1.
What Bisoprolol fumarate Pinewood is and what it is used for
2.
What you need to know before you take Bisoprolol fumarate Pinewood
3.
How to take Bisoprolol fumarate Pinewood
4.
Possible side effects
5.
How to store Bisoprolol fumarate Pinewood
6.
Contents of the pack and other information
1.
WHAT BISOPROLOL FUMARATE PINEWOOD IS AND WHAT IT IS USED FOR
The active substance in Bisoprolol fumarate Pinewood is bisoprolol
fumarate. Bisoprolol fumarate
belongs to a group of medicines called beta-blockers. These medicines
work by affecting the body`s
response to some nerve impulses, especially in the hear

Súhrn charakteristických

Health Products Regulatory Authority
16 February 2024
CRN00CX88
Page 1 of 8
SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
Bisoprolol fumarate Pinewood 10 mg film-coated tablets
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each film coated tablet contains 10 mg of bisoprolol fumarate.
For the full list of excipients, see section 6.1.
3 PHARMACEUTICAL FORM
Film-coated tablet
Pale-orange, round shaped with diameter of approx. 8.00 mm biconvex
film coated tablets debossed with 'C' and score line on
one side and '37' on other side.
The tablet can be divided into equal doses.
4 CLINICAL PARTICULARS
4.1 THERAPEUTIC INDICATIONS
Treatment of stable chronic heart failure with reduced systolic left
ventricular function in addition to ACE inhibitors, and
diuretics, and optionally cardiac glycosides (for additional
information see section 5.1).
4.2 POSOLOGY AND METHOD OF ADMINISTRATION
_Adults:_
Standard treatment of CHF consists of an ACE inhibitor (or an
angiotensin receptor blocker in case of intolerance to ACE
inhibitors), a beta-blocker, diuretics, and when appropriate cardiac
glycosides. Patients should be stable (without acute failure)
when bisoprolol treatment is initiated.
It is recommended that the treating physician should be experienced in
the management of chronic heart failure.
Transient worsening of heart failure, hypotension, or bradycardia may
occur during the titration period and thereafter.
_Titration phase_
_ _
The treatment of stable chronic heart failure with bisoprolol requires
a titration phase
The treatment with bisoprolol is to be started with a gradual
uptitration according to the following steps:

1.25 mg once daily for 1 week, if well tolerated increase to

2.5 mg once daily for a further week, if well tolerated increase to

3.75 mg once daily for a further week, if well tolerated increase to

5 mg once daily for the 4 following weeks, if well tolerated increase
to

7.5 mg once daily for the 4 following weeks, if well tolerated
increase to

10 mg once daily for