Jinarc

Land: Europeiska unionen

Språk: engelska

Källa: EMA (European Medicines Agency)

Köp det nu

Bipacksedel Bipacksedel (PIL)
21-10-2022
Produktens egenskaper Produktens egenskaper (SPC)
21-10-2022

Aktiva substanser:

Tolvaptan

Tillgänglig från:

Otsuka Pharmaceutical Netherlands B.V.

ATC-kod:

C03XA01

INN (International namn):

tolvaptan

Terapeutisk grupp:

Diuretics,

Terapiområde:

Polycystic Kidney, Autosomal Dominant

Terapeutiska indikationer:

Jinarc is indicated to slow the progression of cyst development and renal insufficiency of autosomal dominant polycystic kidney disease (ADPKD) in adults with CKD stage 1 to 3 at initiation of treatment with evidence of rapidly progressing disease.

Produktsammanfattning:

Revision: 20

Bemyndigande status:

Authorised

Tillstånd datum:

2015-05-27

Bipacksedel

                                60
B. PACKAGE LEAFLET
61
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
JINARC 15 MG TABLETS
JINARC 30 MG TABLETS
JINARC 45 MG TABLETS
JINARC 60 MG TABLETS
JINARC 90 MG TABLETS
Tolvaptan
This medicine is subject to additional monitoring. This will allow
quick identification of new safety
information. You can help by reporting any side effects you may get.
See the end of section 4 for how to
report side effects.
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 Jinarc is and what it is used for
2.
What you need to know before you take Jinarc
3.
How to take Jinarc
4.
Possible side effects
5.
How to store Jinarc
6.
Contents of the pack and other information
1.
WHAT JINARC IS AND WHAT IT IS USED FOR
Jinarc contains the active substance tolvaptan which blocks the effect
of vasopressin, a hormone
involved in the formation of cysts in the kidneys of ADPKD patients.
By blocking the effect of
vasopressin, Jinarc slows the development of kidney cysts in patients
with ADPKD, reduces symptoms
of the disease and increases urine production.
Jinarc is a medicine used to treat a disease called “autosomal
dominant polycystic kidney disease”
(ADPKD). This disease causes growth of fluid-filled cysts in the
kidneys, which put pressure on
surrounding tissues and reduce kidney function, possibly leading to
kidney failure. Jinarc is used to treat
ADPKD in adults with chronic kidney disease (CKD) stages 1 to 4 with
evidence of rapidly progressing
disease.
2.
WHAT YOU NEED TO KNOW BEFORE YOU TAKE JINARC
DO NOT TAKE JINA
                                
                                Läs hela dokumentet
                                
                            

Produktens egenskaper

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
This medicinal product is subject to additional monitoring. This will
allow quick identification of
new safety information. Healthcare professionals are asked to report
any suspected adverse reactions.
See section 4.8 for how to report adverse reactions.
1.
NAME OF THE MEDICINAL PRODUCT
Jinarc 15 mg tablets
Jinarc 30 mg tablets
Jinarc 45 mg tablets
Jinarc 60 mg tablets
Jinarc 90 mg tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Jinarc 15 mg tablets
Each tablet contains 15 mg of tolvaptan.
Excipient(s) with known effect
Each 15 mg tablet contains approximately 35 mg lactose (as
monohydrate).
Jinarc 30 mg tablets
Each tablet contains 30 mg of tolvaptan.
Excipient(s) with known effect
Each 30 mg tablet contains approximately 70 mg lactose (as
monohydrate).
Jinarc 45 mg tablets
Each tablet contains 45 mg of tolvaptan.
Excipient(s) with known effect
Each 45 mg tablet contains approximately 12 mg lactose (as
monohydrate).
Jinarc 60 mg tablets
Each tablet contains 60 mg of tolvaptan.
Excipient(s) with known effect
Each 60 mg tablet contains approximately 16 mg lactose (as
monohydrate).
Jinarc 90 mg tablets
Each tablet contains 90 mg of tolvaptan.
Excipient(s) with known effect
Each 90 mg tablet contains approximately 24 mg lactose (as
monohydrate).
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Tablet
Jinarc 15 mg tablets
Blue, triangular (major axis: 6.58 mm, minor axis: 6.20 mm),
shallow-convex, debossed with
“OTSUKA” and “15” on one side.
Jinarc 30 mg tablets
Blue, round (diameter: 8 mm), shallow-convex, debossed with
“OTSUKA” and “30” on one side.
3
Jinarc 45 mg tablets
Blue, square (6.8 mm on a side, major axis 8.2 mm), shallow-convex,
debossed with “OTSUKA” and
“45” on one side
Jinarc 60 mg tablets
Blue, modified rectangular (major axis 9.9 mm, minor axis 5.6 mm),
shallow-convex, debossed with
“OTSUKA” and “60” on one side
Jinarc 90 mg tablets
Blue, pentagonal (major axis 9.7 mm, minor axis 9.5 mm),
shallo
                                
                                Läs hela dokumentet
                                
                            

Dokument på andra språk

Bipacksedel Bipacksedel bulgariska 21-10-2022
Produktens egenskaper Produktens egenskaper bulgariska 21-10-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport bulgariska 31-08-2018
Bipacksedel Bipacksedel spanska 21-10-2022
Produktens egenskaper Produktens egenskaper spanska 21-10-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport spanska 31-08-2018
Bipacksedel Bipacksedel tjeckiska 21-10-2022
Produktens egenskaper Produktens egenskaper tjeckiska 21-10-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport tjeckiska 31-08-2018
Bipacksedel Bipacksedel danska 21-10-2022
Produktens egenskaper Produktens egenskaper danska 21-10-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport danska 31-08-2018
Bipacksedel Bipacksedel tyska 21-10-2022
Produktens egenskaper Produktens egenskaper tyska 21-10-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport tyska 31-08-2018
Bipacksedel Bipacksedel estniska 21-10-2022
Produktens egenskaper Produktens egenskaper estniska 21-10-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport estniska 31-08-2018
Bipacksedel Bipacksedel grekiska 21-10-2022
Produktens egenskaper Produktens egenskaper grekiska 21-10-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport grekiska 31-08-2018
Bipacksedel Bipacksedel franska 21-10-2022
Produktens egenskaper Produktens egenskaper franska 21-10-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport franska 31-08-2018
Bipacksedel Bipacksedel italienska 21-10-2022
Produktens egenskaper Produktens egenskaper italienska 21-10-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport italienska 31-08-2018
Bipacksedel Bipacksedel lettiska 21-10-2022
Produktens egenskaper Produktens egenskaper lettiska 21-10-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport lettiska 31-08-2018
Bipacksedel Bipacksedel litauiska 21-10-2022
Produktens egenskaper Produktens egenskaper litauiska 21-10-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport litauiska 31-08-2018
Bipacksedel Bipacksedel ungerska 21-10-2022
Produktens egenskaper Produktens egenskaper ungerska 21-10-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport ungerska 31-08-2018
Bipacksedel Bipacksedel maltesiska 21-10-2022
Produktens egenskaper Produktens egenskaper maltesiska 21-10-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport maltesiska 31-08-2018
Bipacksedel Bipacksedel nederländska 21-10-2022
Produktens egenskaper Produktens egenskaper nederländska 21-10-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport nederländska 31-08-2018
Bipacksedel Bipacksedel polska 21-10-2022
Produktens egenskaper Produktens egenskaper polska 21-10-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport polska 31-08-2018
Bipacksedel Bipacksedel portugisiska 21-10-2022
Produktens egenskaper Produktens egenskaper portugisiska 21-10-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport portugisiska 31-08-2018
Bipacksedel Bipacksedel rumänska 21-10-2022
Produktens egenskaper Produktens egenskaper rumänska 21-10-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport rumänska 31-08-2018
Bipacksedel Bipacksedel slovakiska 21-10-2022
Produktens egenskaper Produktens egenskaper slovakiska 21-10-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport slovakiska 31-08-2018
Bipacksedel Bipacksedel slovenska 21-10-2022
Produktens egenskaper Produktens egenskaper slovenska 21-10-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport slovenska 31-08-2018
Bipacksedel Bipacksedel finska 21-10-2022
Produktens egenskaper Produktens egenskaper finska 21-10-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport finska 31-08-2018
Bipacksedel Bipacksedel svenska 21-10-2022
Produktens egenskaper Produktens egenskaper svenska 21-10-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport svenska 31-08-2018
Bipacksedel Bipacksedel norska 21-10-2022
Produktens egenskaper Produktens egenskaper norska 21-10-2022
Bipacksedel Bipacksedel isländska 21-10-2022
Produktens egenskaper Produktens egenskaper isländska 21-10-2022
Bipacksedel Bipacksedel kroatiska 21-10-2022
Produktens egenskaper Produktens egenskaper kroatiska 21-10-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport kroatiska 31-08-2018

Sök varningar relaterade till denna produkt

Visa dokumenthistorik