Sianta 75 mg hard capsules

দেশ: মাল্টা

ভাষা: ইংরেজি

সূত্র: Medicines Authority

থেকে পাওয়া:

Egis Pharmaceuticals PLC Kereszturi Ut 30-38 1106 Budapest, Hungary

এটিসি কোড:

B01AE07

INN (আন্তর্জাতিক নাম):

DABIGATRAN ETEXILATE 75 mg

ফার্মাসিউটিকাল ফর্ম:

HARD CAPSULE

রচনা:

DABIGATRAN ETEXILATE 75 mg

প্রেসক্রিপশন টাইপ:

POM

থেরাপিউটিক এলাকা:

ANTITHROMBOTIC AGENTS

পণ্য সারাংশ:

Licence number in the source country: N/A

অনুমোদন অবস্থা:

Authorised

অনুমোদন তারিখ:

2024-01-31

তথ্য লিফলেট

1
PACKAGE LEAFLET: INFORMATION FOR THE
PATIENT
SIANTA 75 MG HARD CAPSULES
dabigatran etexilate
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 Sianta is and what it is used for
2.
What you need to know before you take Sianta
3.
How to take Sianta
4.
Possible side effects
5.
How to store Sianta
6.
Contents of the pack and other information
1.
WHAT SIANTA IS AND WHAT IT IS USED FOR
Sianta contains the active substance dabigatran etexilate and belongs
to a group of medicines called
anticoagulants. It works by blocking a substance in the body which is
involved in blood clot formation.
Sianta is used in adults to:
-
prevent the formation of blood clots in the veins after knee or hip
replacement surgery.
Sianta is used in children to:
-
treat blood clots and to prevent blood clots from reoccurring.
2.
WHAT YOU NEED TO KNOW BEFORE YOU TAKE SIANTA
DO NOT TAKE SIANTA
-
if you are allergic to dabigatran etexilate or any of the other
ingredients of this medicine (listed
in section 6).
-
if you have severely reduced kidney function.
-
if you are currently bleeding.
-
if you have a disease in an organ of the body that increases the risk
of serious bleeding (e.g.,
stomach ulcer, injury or bleeding in the brain, recent surgery of the
brain or eyes).
-
if you have an increased tendency to bleed. This may be inborn, of
unknown cause or due to
other medicines.
-
if you are taking medicines to prevent blood clotting (e.g. warfarin,
rivaroxaban, apixaban or
heparin), except when changing anticoagulant treatment, wh

পণ্য বৈশিষ্ট্য

1
1.
NAME OF THE MEDICINAL PRODUCT
Sianta 75 mg hard capsules
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each hard capsule contains 86.48 mg of dabigatran etexilate (as
mesilate) equivalent to 75 mg of
dabigatran etexilate.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Hard capsule.
Off white to pale yellow coloured pellets filled in white to off white
hard capsule size 2 (approx. 18.0
mm).
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Primary prevention of venous thromboembolic events
(VTE)
in adult patients who have undergone
elective total hip replacement surgery or total knee replacement
surgery.
Treatment of VTE and prevention of recurrent VTE in paediatric
patients from birth to less than
18 years of age.
For age appropriate dose forms, see section 4.2.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
Sianta capsules can be used in adults and paediatric patients aged 8
years or older who are able to
swallow the capsules whole.
There are other age appropriate dose forms for the treatment of
children below 8 years.
When changing between the formulations, the prescribed dose may need
to be altered. The dose
stated in the relevant dosing table of a formulation should be
prescribed based on the weight and age
of the child.
_PRIMARY PREVENTION OF _
_VTE _
_IN ORTHOPAEDIC SURGERY _
_ _
The recommended doses of dabigatran etexilate and the duration of
therapy for primary prevention
of VTE in orthopaedic surgery are shown in table 1.
2
TABLE 1:
DOSE RECOMMENDATIONS AND DURATION OF THERAPY FOR PRIMARY PREVENTION OF
VTE IN ORTHOPAEDIC SURGERY
TREATMENT
INITIATION ON THE DAY
OF SURGERY 1-4 HOURS
AFTER COMPLETED
SURGERY
MAINTENANCE
DOSE STARTING
ON THE FIRST
DAY AFTER
SURGERY
DURATION OF
MAINTENANCE
DOSE
Patients following elective
knee replacement surgery
single capsule of
110 mg dabigatran
etexilate
220
mg
dabigatran
etexilate
once
daily taken as 2
capsules of 110
mg
10 days
Patients following elective
hip replacement surgery
28-35 days
_DOSE REDUCTION RECOMMENDED _
Patients with mo