Trulicity

Country: European Union

Language: English

Source: EMA (European Medicines Agency)

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Active ingredient:

dulaglutide

Available from:

Eli Lilly Nederland B.V.

ATC code:

A10BJ05

INN (International Name):

dulaglutide

Therapeutic group:

Drugs used in diabetes, Blood glucose lowering drugs, excl. insulins

Therapeutic area:

Diabetes Mellitus, Type 2

Therapeutic indications:

Trulicity is indicated for the treatment of patients 10 years and above with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exerciseas monotherapy when metformin is considered inappropriate due to intolerance or contraindicationsin addition to other medicinal products for the treatment of diabetes.For study results with respect to combinations, effects on glycaemic control and cardiovascular events, and the populations studied, see sections 4.4, 4.5 and 5.1.

Product summary:

Revision: 17

Authorization status:

Authorised

Authorization date:

2014-11-21

Patient Information leaflet

                                72
B. PACKAGE LEAFLET
73
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
TRULICITY 0.75 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN
TRULICITY 1.5 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN
TRULICITY 3 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN
TRULICITY 4.5 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN
dulaglutide
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, pharmacist or
nurse.
-
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, pharmacist or nurse.
This includes any possible
side effects not listed in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET
1.
What Trulicity is and what it is used for
2.
What you need to know before you use Trulicity
3.
How to use Trulicity
4.
Possible side effects
5.
How to store Trulicity
6.
Contents of the pack and other information
1.
WHAT TRULICITY IS AND WHAT IT IS USED FOR
Trulicity contains an active substance called dulaglutide and is used
to lower blood sugar (glucose) in
adults and children aged 10 years and above, with type 2 diabetes
mellitus and can help prevent heart
disease.
Type 2 diabetes is a condition in which your body does not make enough
insulin, and the insulin that
your body produces does not work as well as it should.
When this happens, sugar (glucose) builds up in the blood.
Trulicity is used:
-
on its own if your blood sugar is not properly controlled by diet and
exercise alone, and you
can’t take metformin (another diabetes medicine).
-
or with other medicines for diabetes when they are not enough to
control your blood sugar
levels. These other medicines may be medicines taken by mouth and/or
insulin given by
injection.
It is important to continue to follow the advice on diet and exercise
given to you by your doctor,
pharmac
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Trulicity 0.75 mg solution for injection in pre-filled pen
Trulicity 1.5 mg solution for injection in pre-filled pen
Trulicity 3 mg solution for injection in pre-filled pen
Trulicity 4.5 mg solution for injection in pre-filled pen
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Trulicity 0.75 mg solution for injection in pre-filled pen
Each pre-filled pen contains 0.75 mg of dulaglutide* in 0.5 ml
solution.
Trulicity 1.5 mg solution for injection in pre-filled pen
Each pre-filled pen contains 1.5 mg of dulaglutide* in 0.5 ml
solution.
Trulicity 3 mg solution for injection in pre-filled pen
Each pre-filled pen contains 3 mg of dulaglutide* in 0.5 ml solution.
Trulicity 4.5 mg solution for injection in pre-filled pen
Each pre-filled pen contains 4.5 mg of dulaglutide* in 0.5 ml
solution.
*produced in CHO cells by recombinant DNA technology.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Solution for injection.
Clear, colourless solution.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Type 2 Diabetes Mellitus
Trulicity is indicated for the treatment of patients 10 years and
above 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 cardiovascular events,
and the populations studied, see sections 4.4, 4.5 and 5.1.
3
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
_ _
Posology
_Adults _
_ _
_Monotherapy _
The recommended dose is 0.75 mg once weekly.
_Add-on therapy_
The recommended dose is 1.5 mg once weekly.
If needed,
•
the 1.5 mg dose can be increased after at least 4 weeks to 3 mg once
weekly.
•
the 3 mg dose can be increased after at least 4 weeks to 4.5 mg once
weekly.
The maximum dose is 4.5 mg once weekly.
_Paediatri
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 16-03-2023
Summary of Product characteristics Summary of Product characteristics Bulgarian 16-03-2023
Public Assessment Report Public Assessment Report Bulgarian 16-03-2023
Patient Information leaflet Patient Information leaflet Spanish 16-03-2023
Public Assessment Report Public Assessment Report Spanish 16-03-2023
Patient Information leaflet Patient Information leaflet Czech 16-03-2023
Public Assessment Report Public Assessment Report Czech 16-03-2023
Patient Information leaflet Patient Information leaflet Danish 16-03-2023
Public Assessment Report Public Assessment Report Danish 16-03-2023
Patient Information leaflet Patient Information leaflet German 16-03-2023
Public Assessment Report Public Assessment Report German 16-03-2023
Patient Information leaflet Patient Information leaflet Estonian 16-03-2023
Public Assessment Report Public Assessment Report Estonian 16-03-2023
Patient Information leaflet Patient Information leaflet Greek 16-03-2023
Public Assessment Report Public Assessment Report Greek 16-03-2023
Patient Information leaflet Patient Information leaflet French 16-03-2023
Public Assessment Report Public Assessment Report French 16-03-2023
Patient Information leaflet Patient Information leaflet Italian 16-03-2023
Public Assessment Report Public Assessment Report Italian 16-03-2023
Patient Information leaflet Patient Information leaflet Latvian 16-03-2023
Public Assessment Report Public Assessment Report Latvian 16-03-2023
Patient Information leaflet Patient Information leaflet Lithuanian 16-03-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 16-03-2023
Public Assessment Report Public Assessment Report Lithuanian 16-03-2023
Patient Information leaflet Patient Information leaflet Hungarian 16-03-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 16-03-2023
Public Assessment Report Public Assessment Report Hungarian 16-03-2023
Patient Information leaflet Patient Information leaflet Maltese 16-03-2023
Public Assessment Report Public Assessment Report Maltese 16-03-2023
Patient Information leaflet Patient Information leaflet Dutch 16-03-2023
Public Assessment Report Public Assessment Report Dutch 16-03-2023
Patient Information leaflet Patient Information leaflet Polish 16-03-2023
Public Assessment Report Public Assessment Report Polish 16-03-2023
Patient Information leaflet Patient Information leaflet Portuguese 16-03-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 16-03-2023
Public Assessment Report Public Assessment Report Portuguese 16-03-2023
Patient Information leaflet Patient Information leaflet Romanian 16-03-2023
Public Assessment Report Public Assessment Report Romanian 16-03-2023
Patient Information leaflet Patient Information leaflet Slovak 16-03-2023
Public Assessment Report Public Assessment Report Slovak 16-03-2023
Patient Information leaflet Patient Information leaflet Slovenian 16-03-2023
Summary of Product characteristics Summary of Product characteristics Slovenian 16-03-2023
Public Assessment Report Public Assessment Report Slovenian 16-03-2023
Patient Information leaflet Patient Information leaflet Finnish 16-03-2023
Public Assessment Report Public Assessment Report Finnish 16-03-2023
Patient Information leaflet Patient Information leaflet Swedish 16-03-2023
Public Assessment Report Public Assessment Report Swedish 16-03-2023
Patient Information leaflet Patient Information leaflet Norwegian 16-03-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 16-03-2023
Patient Information leaflet Patient Information leaflet Icelandic 16-03-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 16-03-2023
Patient Information leaflet Patient Information leaflet Croatian 16-03-2023
Public Assessment Report Public Assessment Report Croatian 16-03-2023

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