Rivaroxaban Sandoz 10 mg, filmomhulde tabletten

Երկիր: Նիդերլանդեր

Լեզու: հոլանդերեն

Աղբյուրը: CBG-MEB (College ter Beoordeling van Geneesmiddelen)

Գնել հիմա

Ակտիվ բաղադրիչ:

RIVAROXABAN 10 mg/stuk

Հասանելի է:

Sandoz B.V. Veluwezoom 22 1327 AH ALMERE

INN (Միջազգային անվանումը):

RIVAROXABAN 10 mg/stuk

Դեղագործական ձեւ:

Filmomhulde tablet

Կազմը:

CELLULOSE, MICROKRISTALLIJN (E 460(i)) ; CROSCARMELLOSE NATRIUM (E 468) ; HYPROMELLOSE, Type 2910 (3 - 15 mPa.s) (E 464) ; IJZEROXIDE ROOD (E 172) ; LACTOSE 1-WATER ; MAGNESIUMSTEARAAT (E 470b) ; NATRIUMLAURILSULFAAT ; POLYETHYLEENGLYCOL (E 1521) ; SILICIUMDIOXIDE (E 551) ; TITAANDIOXIDE (E 171) ; ZONNEGEEL FCF (E 110), CELLULOSE, MICROKRISTALLIJN (E 460) ; CROSCARMELLOSE NATRIUM (E 468) ; HYPROMELLOSE, Type 2910 (3 - 15 mPa.s) (E 464) ; IJZEROXIDE ROOD (E 172) ; LACTOSE 1-WATER ; MAGNESIUMSTEARAAT (E 470b) ; NATRIUMLAURILSULFAAT (E 487) ; POLYETHYLEENGLYCOL (E 1521) ; SILICIUMDIOXIDE (E 551) ; TITAANDIOXIDE (E 171) ; ZONNEGEEL FCF (E 110)

Կառավարման երթուղին:

Oraal gebruik

Հաստատման ամսաթիվը:

2020-12-18

Տեղեկատվական թերթիկ

                                Sandoz B.V.
Page 1/7
Rivaroxaban Sandoz
®
10 mg, filmomhulde tabletten
RVG 125799
1313-V5
1.3.1.3 Bijsluiter
Mei 2023
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
RIVAROXABAN SANDOZ
® 10 MG, FILMOMHULDE TABLETTEN
rivaroxaban
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 [Nationally Completed Name] is and what it is used for
2.
What you need to know before you take [Nationally Completed Name]
3.
How to take [Nationally Completed Name]
4.
Possible side effects
5.
How to store [Nationally Completed Name]
6.
Contents of the pack and other information
1.
WHAT [NATIONALLY COMPLETED NAME] IS AND WHAT IT IS USED FOR
[
Nationally Completed Name] contains the active substance rivaroxaban
and is used in
adults to
−
prevent blood clots in the
veins after a hip or knee replacement operation. Your
doctor has prescribed this medicine for you because after an operation
you are at an
increased risk of getting blood clots.
−
treat blood clots in the veins of your legs (deep vein thrombosis) and
in the blood
vessels of your lungs (pulmonary embolism), and to prevent blood clots
from re-
occurring in the blood vessels of your legs and/or lungs.
[Nationally Completed Name] belongs to a group of medicines called
antithrombotic agents.
It works by blocking a blood clotting factor (factor Xa) and thus
reducing the tendency of
the blood to form clots.
2.
WHAT YOU NEED TO KNOW BEFORE YOU TAKE [NATIONALLY COMPLETED NAME]
DO NOT TAKE [NATIONALLY COMPLETED NAME]
•
if you are allergic to rivaroxaban or any of the o
                                
                                Կարդացեք ամբողջական փաստաթուղթը
                                
                            

Ապրանքի հատկությունները

                                Sandoz B.V.
Page 1/27
Rivaroxaban Sandoz 10 mg, filmomhulde tabletten
RVG 125799
1311-V4
1.3.1.1 Samenvatting van de Productkenmerken
Mei 2023
SUMMARY OF PRODUCT CHARACTERISTICS
1.
NAME OF THE MEDICINAL PRODUCT
Rivaroxaban Sandoz 10 mg, filmomhulde tabletten
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each film-coated tablet contains 10 mg of rivaroxaban.
Excipients with known effect:
Each film-coated tablet contains 46 mg of lactose (as monohydrate) and
0.081 mg of sunset
yellow FCF aluminium lake (E 110).
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet.
Peach coloured, round, biconvex film-coated tablets marked with
‘10’ on one side, with a
diameter of 6 mm
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Prevention of venous thromboembolism (VTE) in adult patients
undergoing elective hip or
knee
replacement surgery.
Treatment of deep vein thrombosis (DVT) and pulmonary embolism (PE),
and prevention
of recurrent DVT and PE in adults (see section 4.4 for
haemodynamically unstable PE
patients).
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
_Prevention of VTE in adult patients undergoing elective hip or knee
replacement surgery _
The recommended dose is 10 mg rivaroxaban taken orally once daily. The
initial dose should
be taken 6 to 10 hours after surgery, provided that haemostasis has
been established.
The duration of treatment depends on the individual risk of the
patient for venous
thromboembolism
which is determined by the type of orthopaedic surgery.
•
For patients undergoing major hip surgery, a treatment duration of 5
weeks is
recommended.
•
For patients undergoing major knee surgery, a treatment duration of 2
weeks is
recommended.
Sandoz B.V.
Page 2/27
Rivaroxaban Sandoz 10 mg, filmomhulde tabletten
RVG 125799
1311-V4
1.3.1.1 Samenvatting van de Productkenmerken
Mei 2023
If a dose is missed the patient should take rivaroxaban immediately
and then continue the
following day with once daily intake as before.
_Treatment of DVT, treatment of PE and pr
                                
                                Կարդացեք ամբողջական փաստաթուղթը