Rivaroxaban Sandoz 15 mg, filmomhulde tabletten

Země: Nizozemsko

Jazyk: nizozemština

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

Aktivní složka:

RIVAROXABAN 15 mg/stuk

Dostupné s:

Sandoz B.V. Veluwezoom 22 1327 AH ALMERE

ATC kód:

B01AF01

INN (Mezinárodní Name):

RIVAROXABAN 15 mg/stuk

Léková forma:

Filmomhulde tablet

Složení:

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 ALUMINIUMLAK (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 ALUMINIUMLAK (E 110),

Podání:

Oraal gebruik

Terapeutické oblasti:

Rivaroxaban

Přehled produktů:

Hulpstoffen: 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 ALUMINIUMLAK (E 110);

Datum autorizace:

2017-11-23

Informace pro uživatele

Sandoz B.V.
Rivaroxaban Sandoz 15 mg en 20 mg, filmomhulde tabletten
RVG 120075-6
1313-V16
1.3.1.3 Bijsluiter
Juni 2023
BIJSLUITER: INFORMATIE VOOR DE PATIËNT
RIVAROXABAN SANDOZ 15 MG, FILMOMHULDE TABLETTEN
RIVAROXABAN SANDOZ 20 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 brain (stroke) and other blood vessels in your
body if you have a
form of irregular heart rhythm called non-valvular atrial
fibrillation.
•
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] is used in children and adolescents below
18 years and with a
body weight of 30 kg or more to:
•
treat blood clots and prevent re-occurrence of blood clots in the
veins or in the blood
vessels of the lungs, following initial treatment of at least 5 days
with injectable medicines
used to treat blood clots.
[Nationally Completed Name] belongs

Charakteristika produktu

Sandoz B.V.
Rivaroxaban Sandoz 15 mg, filmomhulde tabletten
RVG 120075
1311-V12
1.3.1.1 Samenvatting van de Productkenmerken
Juni 2023
1.
NAAM VAN HET GENEESMIDDEL
Rivaroxaban Sandoz 15 mg, filmomhulde tabletten
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each film-coated tablet contains 15 mg of rivaroxaban.
Excipients with known effect
Each film-coated tablet contains 42.749 mg of lactose (as monohydrate)
and 0.114 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.
Light orange coloured, round, biconvex film-coated tablet marked with
‘15’ on one side, with a
diameter of 6 mm.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
_Adults _
Prevention of stroke and systemic embolism in adult patients with
non-valvular atrial
fibrillation with one or more risk factors, such as congestive heart
failure, hypertension, age ≥
75 years, diabetes mellitus, prior stroke or transient ischaemic
attack.
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.)
_Paediatric population _
Treatment of venous thromboembolism (VTE) and prevention of VTE
recurrence in children
and adolescents aged less than 18 years and weighing from 30 kg to 50
kg after at least 5 days
of initial parenteral anticoagulation treatment.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
_Prevention of stroke and systemic embolism in adults_
The recommended dose is 20 mg once daily, which is also the
recommended maximum dose.
Therapy with rivaroxaban should be continued long term provided the
benefit of prevention of
stroke and systemic embolism outweighs the risk of bleeding (see
section 4.4).
Sandoz B.V.
Rivaroxaban Sandoz 15 mg, filmomhulde tabletten
RVG 120075
1311-V12
1.3.1.1 Samenvatting van de Productkenmerken
Juni 2023
If a dose is missed the patient should take rivaroxaban immediately
and continue on the
following day with
the on