Organic Nature Propolis 30% Liquid

Land: Australien

Sprog: engelsk

Kilde: Department of Health (Therapeutic Goods Administration)

Aktiv bestanddel:

Propolis dry extract

Tilgængelig fra:

H C L Manufacturers Pty Ltd

INN (International Name):

Propolis dry extract

Klasse:

Medicine Listed (Export Only)

Autorisation status:

Listed (Export Only)

Indlægsseddel

MAREVAN
®
M
A
R
E
V
A
N
CONSUMER MEDICINE INFORMATION (CMI) SUMMARY
The full CMI on the next page has more details. If you are worried
about using this medicine, speak to your doctor or pharmacist.
1.
WHY AM I USING MAREVAN?
MAREVAN contains the active ingredient warfarin. MAREVAN is used to
prevent blood from excessive clotting or forming harmful
clots. For more information, see Section 1. Why am I using MAREVAN? in
the full CMI.
2.
WHAT SHOULD I KNOW BEFORE I USE MAREVAN?
Do not use if you have ever had an allergic reaction to MAREVAN or any
of the ingredients listed at the end of the CMI.
TALK TO YOUR DOCTOR IF YOU HAVE ANY OTHER MEDICAL CONDITIONS, TAKE ANY
OTHER MEDICINES, OR ARE PREGNANT OR PLAN TO BECOME
PREGNANT OR ARE BREASTFEEDING. For more information, see Section 2.
What should I know before I use MAREVAN? in the full CMI.
3.
WHAT IF I AM TAKING OTHER MEDICINES?
Some medicines may interfere with MAREVAN and affect how it works.
A list of these medicines is in Section 3. What if I am taking other
medicines? in the full CMI.
4.
HOW DO I USE MAREVAN?
•
Follow your doctor’s directions exactly about how much MAREVAN to
take. Different people require different amounts of this
medicine, and the dosage is adjusted to suit you. Your doctor will
determine how much to take through blood tests.
•
MAREVAN should be taken at about the same time each day.
More instructions can be found in Section 4. How do I use MAREVAN? in
the full CMI.
5.
WHAT SHOULD I KNOW WHILE USING MAREVAN?
THINGS YOU
SHOULD DO
•
Remind any doctor, dentist or pharmacist you visit that you are using
MAREVAN.
•
If you are going to have surgery, tell the surgeon or anaesthetist
that you are taking this medicine.
•
If you become pregnant while taking this medicine, tell your doctor
immediately.
•
If you are about to have any blood tests, tell your doctor that you
are taking this medicine.
THINGS YOU
SHOULD NOT DO
•
Do not stop taking your medicine or lower the dosage without checking
with your doctor.
•
There are two brands of w

Produktets egenskaber

AUSTRALIAN PRODUCT INFORMATION
MAREVAN
®
_warfarin sodium _
1
NAME OF THE MEDICINE
Warfarin sodium
2
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each MAREVAN tablet contains 1 mg, 3 mg or 5 mg of warfarin sodium as
the active ingredient.
Excipients of known effect: sugars as lactose and sulfites.
For the full list of excipients, see Section 6.1 LIST OF EXCIPIENTS.
3
PHARMACEUTICAL FORM
MAREVAN 1 mg tablets are a flat fawn coloured tablet with bevelled
edge, scored and embossed with “M”
above and “1” below.
MAREVAN 3 mg tablets are flat blue coloured tablet with bevelled edge,
scored and embossed with “M”
above and “3” below.
MAREVAN 5 mg tablets are flat pink coloured tablet with bevelled edge,
scored and embossed with “M”
above and “5” below.
4
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
MAREVAN is indicated for the prophylaxis and/or treatment of venous
thrombosis and its extension and
pulmonary embolism.
MAREVAN is indicated for the prophylaxis and/or treatment of the
thromboembolic complications associated
with atrial fibrillation.
MAREVAN is not indicated in patients with lone atrial fibrillation who
are less than 60 years of age with no
risk factors (e.g. previous thromboembolism (TIA, ischaemic stroke),
diabetes mellitus, hypertension) and an
otherwise normal heart.
MAREVAN is indicated for use as an adjunct in the treatment of
coronary occlusion.
4.2
DOSE AND METHOD OF ADMINISTRATION
It cannot be emphasised too strongly that treatment of each patient is
a highly individualised matter.
MAREVAN, a narrow therapeutic range (index) drug, may be affected by
factors such as other drugs, dietary
Vitamin K and genetic variations in CYP2CP and VKORC1 enzymes. Dosage
should be controlled by
periodic determinations of International Normalised Ratio (INR) or
other suitable coagulation tests and the
condition being treated (see Section 4.2 DOSE AND METHOD OF
ADMINISTRATION – Administration).
The following ranges of INR may be considered for the following listed
conditions or procedures; ho