Isoket Retard 20 tablets

Riik: Suurbritannia

keel: inglise

Allikas: MHRA (Medicines & Healthcare Products Regulatory Agency)

Osta kohe

Infovoldik Infovoldik (PIL)
30-11--0001
Toote omadused Toote omadused (SPC)
02-05-2019

Toimeaine:

Isosorbide dinitrate

Saadav alates:

Forum Health Products Ltd

ATC kood:

C01DA08

INN (Rahvusvaheline Nimetus):

Isosorbide dinitrate

Annus:

20mg

Ravimvorm:

Modified-release tablet

Manustamisviis:

Oral

Klass:

No Controlled Drug Status

Retsepti tüüp:

Valid as a prescribable product

Toote kokkuvõte:

BNF: 02060100; GTIN: 5015366084835 05012748616073

Infovoldik

                                PACKAGE LEAFLET: INFORMATION FOR THE USER
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 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 Isoket Retard is and what it is used for
2. What you need to know before you take Isoket Retard
3. How to take Isoket Retard
4. Possible side effects
5. How to store Isoket Retard
6. Contents of the pack and other information
1. WHAT ISOKET RETARD IS AND WHAT IT IS USED FOR
Isoket Retard belongs to a group of medicines
called organic nitrates. Organic nitrates work by
widening the blood vessels in your heart to allow
an increased amount of blood to flow to areas
which need it.
Isoket Retard is used to prevent and treat angina
pectoris. Angina usually feels like a tight pain in the
chest, neck or arm area. The pain comes from the
heart muscle and is a sign that part of it is not getting
enough oxygen for the amount of work it is doing.
2. WHAT YOU NEED TO KNOW BEFORE YOU TAKE
ISOKET RETARD
DO NOT TAKE ISOKET RETARD IF:
•
You are allergic to isosorbide dinitrate, other
nitrates or any of the other ingredients of this
medicine (listed in section 6)
4021405 10/386 1409
ISOKET
®
RETARD
20 MG
TABLETS
Isosorbide dinitrate
•
You suffer from anaemia (reduction in red blood
cells which can make the skin pale and cause
weakness or breathlessness)
•
You have had a heart attack (myocardial infarction)
•
You have had a brain haemorrhage (bleeding)
•
You have had a head injury (trauma)
•
You have a low blood volume (hypovolaemia)
•
You have very low blood pressure
•
Your blood has stopped circula
                                
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Toote omadused

                                SUMMARY OF PRODUCT CHARACTERISTICS
1
NAME OF THE MEDICINAL PRODUCT
ISOKET RETARD 20 TABLETS
2
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each tablet contains isosorbide dinitrate 20 mg in a prolonged release
formulation.
Excipients with known effect: 157.95 mg lactose monohydrate
For the full list of excipients, see section 6.1.
3
PHARMACEUTICAL FORM
Prolonged release tablets.
White with break score, marked IR 20 on the upper side and with
SCHWARZ
PHARMA on the reverse side.
4
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
For the prophylaxis and treatment of angina pectoris.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
_Adults:_ One tablet to be taken twice daily without chewing and with
a sufficient amount of
fluid. The second dose should be given 6 to 8 hours after the first
dose. For patients with
higher nitrate requirements the dose may be increased to one tablet
three times daily, but
ensuring a 12 hours treatment free interval every 24 hours.
_Elderly population:_ Clinical experience has not necessitated
alternative advice for use in
elderly patients.
_Paediatric population:_ The safety and efficacy of Isoket Retard has
yet to be established.
Method of administration
For oral administration
4.3
CONTRAINDICATIONS
Hypersensitivity to the active substance or to any of the excipients
listed in section 6.1.
This product should not be given to patients with a known sensitivity
to nitrates, very low
blood pressure, acute myocardial infarction with low filling pressure,
marked anaemia, head
trauma, cerebral haemorrhage, acute circulatory failure, severe
hypotension or hypovolaemia.
Phosphodiesterase inhibitors (e.g. Sildenafil) have been shown to
potentiate the hypotensive
effects of nitrates, and their co-administration with nitrates or
nitric oxide donors is therefore
contraindicated.
During nitrate therapy, the soluble guanylate cyclase stimulator
riociguat must not be used
(see section 4.5).
4.4
SPECIAL WARNINGS AND PRECAUTIONS FOR USE
These tablets should be used with caution in patients who are
sufferi
                                
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