Lantus

Country: European Union

Language: English

Source: EMA (European Medicines Agency)

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Active ingredient:

insulin glargine

Available from:

sanofi-aventis Deutschland GmbH

ATC code:

A10AE04

INN (International Name):

insulin glargine

Therapeutic group:

Drugs used in diabetes

Therapeutic area:

Diabetes Mellitus

Therapeutic indications:

Treatment of diabetes mellitus in adults, adolescents and children aged two years and above

Product summary:

Revision: 40

Authorization status:

Authorised

Authorization date:

2000-06-09

Patient Information leaflet

                                35
B. PACKAGE LEAFLET
36
PACKAGE LEAFLET: INFORMATION FOR THE USER
LANTUS 100 UNITS/ML SOLUTION FOR INJECTION IN A VIAL
Insulin glargine
_ _
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, 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 or pharmacist. This
includes any possible side
effects not listed in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET
1.
What Lantus is and what it is used for
2.
What you need to know before you use Lantus
3.
How to use Lantus
4.
Possible side effects
5.
How to store Lantus
6.
Contents of the pack and other information
1.
WHAT LANTUS IS AND WHAT IT IS USED FOR
Lantus contains insulin glargine. This is a modified insulin, very
similar to human insulin.
Lantus is used to treat diabetes mellitus in adults, adolescents and
children aged 2 years and above.
Diabetes mellitus is a disease where your body does not produce enough
insulin to control the level of
blood sugar. Insulin glargine has a long and steady
blood-sugar-lowering action.
2.
WHAT YOU NEED TO KNOW BEFORE YOU USE LANTUS
DO NOT USE LANTUS
-
If you are allergic to insulin glargine or any of the other
ingredients of this medicine (listed in
section 6).
WARNINGS AND PRECAUTIONS
Talk to your doctor, pharmacist or nurse before using Lantus.
Follow closely the instructions for posology, monitoring (blood and
urine tests), diet and physical
activity (physical work and exercise) as discussed with your doctor.
If your blood sugar is too low (hypoglycaemia), follow the guidance
for hypoglycaemia (see box at the
end of this leaflet).
Skin changes at the injection site
The injection site should be rotated to prevent skin changes such as
lumps under the skin. The insulin
may not wor
                                
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Summary of Product characteristics

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Lantus 100 units/ml solution for injection in a vial
Lantus 100 units/ml solution for injection in a cartridge
Lantus SoloStar 100 units/ml solution for injection in a pre-filled
pen
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each ml contains 100 units insulin glargine* (equivalent to 3.64 mg).
Lantus 100 units/ml solution for injection in a vial
Each vial contains 5 ml of solution for injection, equivalent to 500
units, or 10 ml of solution for
injection, equivalent to 1000 units.
Lantus 100 units/ml solution for injection in a cartridge, Lantus
SoloStar 100 units/ml solution for
injection in a pre-filled pen
Each cartridge or pen contains 3 ml of solution for injection,
equivalent to 300 units.
*Insulin glargine is produced by recombinant DNA technology in
_Escherichia coli_
.
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
Treatment of diabetes mellitus in adults, adolescents and children
aged 2 years and above.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
Lantus contains insulin glargine, an insulin analogue, and has a
prolonged duration of action.
Lantus should be administered once daily at any time but at the same
time each day.
_ _
The dose regimen (dose and timing) should be individually adjusted. In
patients with type 2 diabetes
mellitus, Lantus can also be given together with orally active
antidiabetic medicinal products.
The potency of this medicinal product is stated in units. These units
are exclusive to Lantus and are not
the same as IU or the units used to express the potency of other
insulin analogues (see section 5.1).
_ _
_Special population _
_Elderly population (≥65 years old) _
In the elderly, progressive deterioration of renal function may lead
to a steady decrease in insulin
requirements.
3
_Renal impairment _
In patients with renal impairment, insulin requirements may be
d
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 10-07-2023
Summary of Product characteristics Summary of Product characteristics Bulgarian 10-07-2023
Public Assessment Report Public Assessment Report Bulgarian 14-08-2012
Patient Information leaflet Patient Information leaflet Spanish 10-07-2023
Public Assessment Report Public Assessment Report Spanish 14-08-2012
Patient Information leaflet Patient Information leaflet Czech 10-07-2023
Public Assessment Report Public Assessment Report Czech 14-08-2012
Patient Information leaflet Patient Information leaflet Danish 10-07-2023
Public Assessment Report Public Assessment Report Danish 14-08-2012
Patient Information leaflet Patient Information leaflet German 10-07-2023
Public Assessment Report Public Assessment Report German 14-08-2012
Patient Information leaflet Patient Information leaflet Estonian 10-07-2023
Public Assessment Report Public Assessment Report Estonian 14-08-2012
Patient Information leaflet Patient Information leaflet Greek 10-07-2023
Public Assessment Report Public Assessment Report Greek 14-08-2012
Patient Information leaflet Patient Information leaflet French 10-07-2023
Public Assessment Report Public Assessment Report French 14-08-2012
Patient Information leaflet Patient Information leaflet Italian 10-07-2023
Public Assessment Report Public Assessment Report Italian 14-08-2012
Patient Information leaflet Patient Information leaflet Latvian 10-07-2023
Public Assessment Report Public Assessment Report Latvian 14-08-2012
Patient Information leaflet Patient Information leaflet Lithuanian 10-07-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 10-07-2023
Public Assessment Report Public Assessment Report Lithuanian 14-08-2012
Patient Information leaflet Patient Information leaflet Hungarian 10-07-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 10-07-2023
Public Assessment Report Public Assessment Report Hungarian 14-08-2012
Patient Information leaflet Patient Information leaflet Maltese 10-07-2023
Public Assessment Report Public Assessment Report Maltese 14-08-2012
Patient Information leaflet Patient Information leaflet Dutch 10-07-2023
Public Assessment Report Public Assessment Report Dutch 14-08-2012
Patient Information leaflet Patient Information leaflet Polish 10-07-2023
Public Assessment Report Public Assessment Report Polish 14-08-2012
Patient Information leaflet Patient Information leaflet Portuguese 10-07-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 10-07-2023
Public Assessment Report Public Assessment Report Portuguese 14-08-2012
Patient Information leaflet Patient Information leaflet Romanian 10-07-2023
Public Assessment Report Public Assessment Report Romanian 14-08-2012
Patient Information leaflet Patient Information leaflet Slovak 10-07-2023
Public Assessment Report Public Assessment Report Slovak 14-08-2012
Patient Information leaflet Patient Information leaflet Slovenian 10-07-2023
Summary of Product characteristics Summary of Product characteristics Slovenian 10-07-2023
Public Assessment Report Public Assessment Report Slovenian 14-08-2012
Patient Information leaflet Patient Information leaflet Finnish 10-07-2023
Public Assessment Report Public Assessment Report Finnish 14-08-2012
Patient Information leaflet Patient Information leaflet Swedish 10-07-2023
Public Assessment Report Public Assessment Report Swedish 14-08-2012
Patient Information leaflet Patient Information leaflet Norwegian 10-07-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 10-07-2023
Patient Information leaflet Patient Information leaflet Icelandic 10-07-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 10-07-2023
Patient Information leaflet Patient Information leaflet Croatian 10-07-2023

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