Mounjaro

Riik: Euroopa Liit

keel: inglise

Allikas: EMA (European Medicines Agency)

Osta kohe

Laadi alla Infovoldik (PIL)
29-05-2024
Laadi alla Toote omadused (SPC)
29-05-2024
Laadi alla Avaliku hindamisaruande (PAR)
21-02-2024

Toimeaine:

Tirzepatide

Saadav alates:

Eli Lilly Nederland B.V.

ATC kood:

A10BX16

INN (Rahvusvaheline Nimetus):

tirzepatide

Terapeutiline rühm:

Drugs used in diabetes

Terapeutiline ala:

Diabetes Mellitus, Type 2

Näidustused:

Mounjaro is indicated for the treatment of adults with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exercise- as monotherapy when metformin is considered inappropriate due to intolerance or contraindications- in addition to other medicinal products for the treatment of diabetes.For study results with respect to combinations, effects on glycaemic control and the populations studied, see sections 4.4, 4.5 and 5.1.

Toote kokkuvõte:

Revision: 3

Volitamisolek:

Authorised

Loa andmise kuupäev:

2022-09-15

Infovoldik

                                143
B. PACKAGE LEAFLET
144
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
MOUNJARO 2.5 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN
MOUNJARO 5 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN
MOUNJARO 7.5 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN
MOUNJARO 10 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN
MOUNJARO 12.5 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN
MOUNJARO 15 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN
tirzepatide
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 USING 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, nurse 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, nurse or pharmacist.
This includes any possible
side effects not listed in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET
1.
What Mounjaro is and what it is used for
2.
What you need to know before you use Mounjaro
3.
How to use Mounjaro
4.
Possible side effects
5.
How to store Mounjaro
6.
Contents of the pack and other information
1.
WHAT MOUNJARO IS AND WHAT IT IS USED FOR
Mounjaro contains an active substance called tirzepatide and is used
to treat adults with type 2
diabetes mellitus. Mounjaro reduces the level of sugar in the body
only when the levels of sugar are
high.
Mounjaro is also used to treat adults with obesity or overweight (with
BMI of at least 27 kg/m
2
).
Mounjaro influences appetite regulation, which may help you eat less
food and reduce your body
weight.
In type 2 diabetes, Mounjaro is used:
-
on its own when you can’t take metformin (another diabetes
medicine).
-
with other medicines for diabetes when 
                                
                                Lugege kogu dokumenti
                                
                            

Toote omadused

                                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
Mounjaro 2.5 mg solution for injection in pre-filled pen
Mounjaro 5 mg solution for injection in pre-filled pen
Mounjaro 7.5 mg solution for injection in pre-filled pen
Mounjaro 10 mg solution for injection in pre-filled pen
Mounjaro 12.5 mg solution for injection in pre-filled pen
Mounjaro 15 mg solution for injection in pre-filled pen
Mounjaro 2.5 mg solution for injection in vial
Mounjaro 5 mg solution for injection in vial
Mounjaro 7.5 mg solution for injection in vial
Mounjaro 10 mg solution for injection in vial
Mounjaro 12.5 mg solution for injection in vial
Mounjaro 15 mg solution for injection in vial
Mounjaro 2.5 mg/dose KwikPen solution for injection in pre-filled pen
Mounjaro 5 mg/dose KwikPen solution for injection in pre-filled pen
Mounjaro 7.5 mg/dose KwikPen solution for injection in pre-filled pen
Mounjaro 10 mg/dose KwikPen solution for injection in pre-filled pen
Mounjaro 12.5 mg/dose KwikPen solution for injection in pre-filled pen
Mounjaro 15 mg/dose KwikPen solution for injection in pre-filled pen
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Pre-filled pen, single-dose
_Mounjaro 2.5 mg solution for injection in pre-filled pen _
Each pre-filled pen contains 2.5 mg of tirzepatide in 0.5 ml solution
(5 mg/ml).
_Mounjaro 5 mg solution for injection in pre-filled pen _
Each pre-filled pen contains 5 mg of tirzepatide in 0.5 ml solution
(10 mg/ml).
_Mounjaro 7.5 mg solution for injection in pre-filled pen _
Each pre-filled pen contains 7.5 mg of tirzepatide in 0.5 ml solution
(15 mg/ml).
_Mounjaro 10 mg solution for injection in pre-filled pen _
Each pre-filled pen contains 10 mg of tirzepatide in 0.5 ml solution
(20 mg/ml).
_Mounjaro 12.5 mg solution for injection in p
                                
                                Lugege kogu dokumenti
                                
                            

Dokumendid teistes keeltes

Infovoldik Infovoldik bulgaaria 29-05-2024
Toote omadused Toote omadused bulgaaria 29-05-2024
Avaliku hindamisaruande Avaliku hindamisaruande bulgaaria 21-02-2024
Infovoldik Infovoldik hispaania 29-05-2024
Toote omadused Toote omadused hispaania 29-05-2024
Avaliku hindamisaruande Avaliku hindamisaruande hispaania 21-02-2024
Infovoldik Infovoldik tšehhi 29-05-2024
Toote omadused Toote omadused tšehhi 29-05-2024
Avaliku hindamisaruande Avaliku hindamisaruande tšehhi 21-02-2024
Infovoldik Infovoldik taani 29-05-2024
Toote omadused Toote omadused taani 29-05-2024
Avaliku hindamisaruande Avaliku hindamisaruande taani 21-02-2024
Infovoldik Infovoldik saksa 29-05-2024
Toote omadused Toote omadused saksa 29-05-2024
Avaliku hindamisaruande Avaliku hindamisaruande saksa 21-02-2024
Infovoldik Infovoldik eesti 29-05-2024
Toote omadused Toote omadused eesti 29-05-2024
Avaliku hindamisaruande Avaliku hindamisaruande eesti 21-02-2024
Infovoldik Infovoldik kreeka 29-05-2024
Toote omadused Toote omadused kreeka 29-05-2024
Avaliku hindamisaruande Avaliku hindamisaruande kreeka 21-02-2024
Infovoldik Infovoldik prantsuse 29-05-2024
Toote omadused Toote omadused prantsuse 29-05-2024
Avaliku hindamisaruande Avaliku hindamisaruande prantsuse 21-02-2024
Infovoldik Infovoldik itaalia 29-05-2024
Toote omadused Toote omadused itaalia 29-05-2024
Avaliku hindamisaruande Avaliku hindamisaruande itaalia 21-02-2024
Infovoldik Infovoldik läti 29-05-2024
Toote omadused Toote omadused läti 29-05-2024
Avaliku hindamisaruande Avaliku hindamisaruande läti 21-02-2024
Infovoldik Infovoldik leedu 29-05-2024
Toote omadused Toote omadused leedu 29-05-2024
Avaliku hindamisaruande Avaliku hindamisaruande leedu 21-02-2024
Infovoldik Infovoldik ungari 29-05-2024
Toote omadused Toote omadused ungari 29-05-2024
Avaliku hindamisaruande Avaliku hindamisaruande ungari 21-02-2024
Infovoldik Infovoldik malta 29-05-2024
Toote omadused Toote omadused malta 29-05-2024
Avaliku hindamisaruande Avaliku hindamisaruande malta 21-02-2024
Infovoldik Infovoldik hollandi 29-05-2024
Toote omadused Toote omadused hollandi 29-05-2024
Avaliku hindamisaruande Avaliku hindamisaruande hollandi 21-02-2024
Infovoldik Infovoldik poola 29-05-2024
Toote omadused Toote omadused poola 29-05-2024
Avaliku hindamisaruande Avaliku hindamisaruande poola 21-02-2024
Infovoldik Infovoldik portugali 29-05-2024
Toote omadused Toote omadused portugali 29-05-2024
Avaliku hindamisaruande Avaliku hindamisaruande portugali 21-02-2024
Infovoldik Infovoldik rumeenia 29-05-2024
Toote omadused Toote omadused rumeenia 29-05-2024
Avaliku hindamisaruande Avaliku hindamisaruande rumeenia 21-02-2024
Infovoldik Infovoldik slovaki 29-05-2024
Toote omadused Toote omadused slovaki 29-05-2024
Avaliku hindamisaruande Avaliku hindamisaruande slovaki 21-02-2024
Infovoldik Infovoldik sloveeni 29-05-2024
Toote omadused Toote omadused sloveeni 29-05-2024
Avaliku hindamisaruande Avaliku hindamisaruande sloveeni 21-02-2024
Infovoldik Infovoldik soome 29-05-2024
Toote omadused Toote omadused soome 29-05-2024
Avaliku hindamisaruande Avaliku hindamisaruande soome 21-02-2024
Infovoldik Infovoldik rootsi 29-05-2024
Toote omadused Toote omadused rootsi 29-05-2024
Avaliku hindamisaruande Avaliku hindamisaruande rootsi 21-02-2024
Infovoldik Infovoldik norra 29-05-2024
Toote omadused Toote omadused norra 29-05-2024
Infovoldik Infovoldik islandi 29-05-2024
Toote omadused Toote omadused islandi 29-05-2024
Infovoldik Infovoldik horvaadi 29-05-2024
Toote omadused Toote omadused horvaadi 29-05-2024
Avaliku hindamisaruande Avaliku hindamisaruande horvaadi 21-02-2024

Otsige selle tootega seotud teateid

Vaadake dokumentide ajalugu