Envarsus

Country: Unjoni Ewropea

Lingwa: Ingliż

Sors: EMA (European Medicines Agency)

Ixtrih issa

Ingredjent attiv:

tacrolimus

Disponibbli minn:

Chiesi Farmaceutici S.p.A.

Kodiċi ATC:

L04AD02

INN (Isem Internazzjonali):

tacrolimus

Grupp terapewtiku:

Immunosuppressants

Żona terapewtika:

Graft Rejection

Indikazzjonijiet terapewtiċi:

Prophylaxis of transplant rejection in adult kidney or liver allograft recipients. Treatment of allograft rejection resistant to treatment with other immunosuppressive medicinal products in adult patients.

Sommarju tal-prodott:

Revision: 12

L-istatus ta 'awtorizzazzjoni:

Authorised

Data ta 'l-awtorizzazzjoni:

2014-07-18

Fuljett ta 'informazzjoni

                                41
B. PACKAGE LEAFLET
42
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
ENVARSUS 0.75 MG PROLONGED-RELEASE TABLETS
ENVARSUS 1 MG PROLONGED-RELEASE TABLETS
ENVARSUS 4 MG PROLONGED-RELEASE TABLETS
tacrolimus
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 Envarsus is and what it is used for
2.
What you need to know before you take Envarsus
3.
How to take Envarsus
4.
Possible side effects
5.
How to store Envarsus
6.
Contents of the pack and other information
1.
WHAT ENVARSUS IS AND WHAT IT IS USED FOR
Envarsus contains the active substance tacrolimus. It is an
immunosuppressant. Following your kidney
or liver transplant, your body’s immune system will try to reject
the new organ.
Envarsus is used to control your body’s immune response, enabling
your body to accept the
transplanted organ.
You may also be given Envarsus for an ongoing rejection of your
transplanted liver, kidney, heart or
other organ when any previous treatment you were taking was unable to
control this immune response
after your transplantation.
Envarsus is used in adults.
2.
WHAT YOU NEED TO KNOW BEFORE YOU TAKE ENVARSUS
DO NOT TAKE ENVARSUS
-
if you are allergic to tacrolimus or any of the other ingredients of
this medicine (listed in
section 6).
-
if you are allergic to sirolimus or to any macrolide-antibiotic (e.g.,
erythromycin,
clarithromycin, josamycin).
WARNINGS AND PRECAUTIONS
Envarsus contains the active substance tacrolimus presented in a
prolonged release formulation.
Envarsus is taken once daily and is
NOT
interchange
                                
                                Aqra d-dokument sħiħ
                                
                            

Karatteristiċi tal-prodott

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Envarsus 0.75 mg prolonged-release tablets
Envarsus 1 mg prolonged-release tablets
Envarsus 4 mg prolonged-release tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Envarsus 0.75 mg prolonged-release tablets
Each prolonged-release tablet contains 0.75 mg tacrolimus (as
monohydrate).
_Excipient with known effect _
Each tablet contains 41.7 mg lactose monohydrate.
Envarsus 1 mg prolonged-release tablets
Each prolonged-release tablet contains 1 mg tacrolimus (as
monohydrate).
_Excipient with known effect _
Each tablet contains 41.7 mg lactose monohydrate.
Envarsus 4 mg prolonged-release tablets
Each prolonged-release tablet contains 4 mg tacrolimus (as
monohydrate).
_ _
_Excipient with known effect _
Each tablet contains 104 mg lactose monohydrate.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Prolonged-release tablet.
Envarsus 0.75 mg prolonged-release tablets
Oval, white to off-white uncoated tablet, debossed with “0.75” on
one side and “TCS” on the other
side.
Envarsus 1 mg prolonged-release tablets
Oval, white to off-white uncoated tablet, debossed with “1” on one
side and “TCS” on the other side.
Envarsus 4 mg prolonged-release tablets
Oval, white to off-white uncoated tablet, debossed with “4” on one
side and “TCS” on the other side.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Prophylaxis of transplant rejection in adult kidney or liver allograft
recipients.
3
Treatment of allograft rejection resistant to treatment with other
immunosuppressive medicinal
products in adult patients.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Envarsus is a once-a-day oral formulation of tacrolimus. Tacrolimus
therapy requires careful
monitoring by adequately qualified and equipped personnel. This
medicinal product should only be
prescribed, and changes in immunosuppressive therapy be initiated, by
physicians experienced in
immunosuppressive therapy and the management of transplant patients.
I
                                
                                Aqra d-dokument sħiħ
                                
                            

Dokumenti f'lingwi oħra

Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Bulgaru 23-01-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Bulgaru 23-01-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Spanjol 23-01-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Spanjol 23-01-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Ċek 23-01-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Ċek 23-01-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Daniż 23-01-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Daniż 23-01-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Ġermaniż 23-01-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Ġermaniż 23-01-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Ġermaniż 31-07-2014
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Estonjan 23-01-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Estonjan 23-01-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Estonjan 31-07-2014
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Grieg 23-01-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Grieg 23-01-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Franċiż 23-01-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Franċiż 23-01-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Franċiż 31-07-2014
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Taljan 23-01-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Taljan 23-01-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Latvjan 23-01-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Latvjan 23-01-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Litwanjan 23-01-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Litwanjan 23-01-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Litwanjan 31-07-2014
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Ungeriż 23-01-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Ungeriż 23-01-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Ungeriż 31-07-2014
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Malti 23-01-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Malti 23-01-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Olandiż 23-01-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Olandiż 23-01-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Olandiż 31-07-2014
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Pollakk 23-01-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Pollakk 23-01-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Portugiż 23-01-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Portugiż 23-01-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Portugiż 31-07-2014
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Rumen 23-01-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Rumen 23-01-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Slovakk 23-01-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Slovakk 23-01-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Sloven 23-01-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Sloven 23-01-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Finlandiż 23-01-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Finlandiż 23-01-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Finlandiż 31-07-2014
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Svediż 23-01-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Svediż 23-01-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Norveġiż 23-01-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Norveġiż 23-01-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Iżlandiż 23-01-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Iżlandiż 23-01-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Kroat 23-01-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Kroat 23-01-2023

Fittex twissijiet relatati ma 'dan il-prodott

Ara l-istorja tad-dokumenti