Somatropin Biopartners

Country: European Union

Language: English

Source: EMA (European Medicines Agency)

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Active ingredient:

somatropin

Available from:

BioPartners GmbH

ATC code:

H01AC01

INN (International Name):

somatropin

Therapeutic group:

Pituitary and hypothalamic hormones and analogues, Somatropin and somatropin agonists

Therapeutic area:

Growth

Therapeutic indications:

Somatropin Biopartners is indicated for the replacement therapy of endogenous growth hormone in adults with childhood- or adult-onset growth-hormone deficiency (GHD).Adult-onset: Patients with GHD in adulthood are defined as patients with known hypothalamic-pituitary pathology and at least one additional known deficiency of a pituitary hormone excluding prolactin. These patients should undergo a single dynamic test in order to diagnose or exclude a GHD.Childhood-onset: In patients with childhood-onset isolated GHD (no evidence of hypothalamic-pituitary disease or cranial irradiation), two dynamic tests should be performed after completion of growth, except for those having low insulin-like-growth-factor-I (IGF-I) concentrations (< -2 standard-deviation score (SDS)), who may be considered for one test. The cut-off point of the dynamic test should be strict.

Product summary:

Revision: 3

Authorization status:

Withdrawn

Authorization date:

2013-08-05

Patient Information leaflet

                                81
B. PACKAGE LEAFLET
Medicinal product no longer authorised
82
PACKAGE LEAFLET: INFORMATION FOR THE USER
SOMATROPIN BIOPARTNERS 2 MG POWDER AND SOLVENT FOR PROLONGED-RELEASE
SUSPENSION FOR INJECTION
SOMATROPIN BIOPARTNERS 4 MG POWDER AND SOLVENT FOR PROLONGED-RELEASE
SUSPENSION FOR INJECTION
SOMATROPIN BIOPARTNERS 7 MG POWDER AND SOLVENT FOR PROLONGED-RELEASE
SUSPENSION FOR INJECTION
FOR ADULTS
Somatropin
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, 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 Somatropin Biopartners is and what it is used for
2.
What you need to know before you use Somatropin Biopartners
3.
How to use Somatropin Biopartners
4.
Possible side effects
5.
How to store Somatropin Biopartners
6.
Contents of the pack and other information
1.
WHAT SOMATROPIN BIOPARTNERS IS AND WHAT IT IS USED FOR
Somatropin Biopartners contains human growth hormone, also called
somatropin. Growth hormone
regulates the growth and development of cells.
This medicine is used to treat adults with a lack (deficiency) of
growth hormone who
-
already had growth hormone deficiency when they were children or
-
do not have enough growth hormone during adulthood.
2.
WHAT YOU NEED TO KNOW BEFORE YOU USE SOMATROPIN BIOPARTNERS
DO NOT USE SOMATROPIN BIOPARTNERS
-
if you are allergic to somatropin or any of the other ingr
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
Medicinal product no longer authorised
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
Somatropin Biopartners 2 mg powder and solvent for prolonged-release
suspension for injection
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
One vial delivers 2 mg of somatropin* (corresponding to 6 IU).
_ _
After reconstitution, 0.2 mL of suspension contains 2 mg somatropin
(10 mg/mL).
_ _
*produced in Saccharomyces cerevisiae by recombinant DNA technology
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Powder and solvent for prolonged-release suspension for injection.
White or almost white powder. The solvent is a clear, oily liquid.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Somatropin Biopartners is indicated for the replacement therapy of
endogenous growth hormone in
adults with childhood- or adult-onset growth hormone deficiency (GHD).
Adult-onset: Patients with GHD in adulthood are defined as patients
with known
hypothalamic-pituitary pathology and at least one additional known
deficiency of a pituitary hormone
excluding prolactin. These patients should undergo a single dynamic
test in order to diagnose or
exclude a GHD.
Childhood-onset: In patients with childhood-onset isolated GHD (no
evidence of
hypothalamic-pituitary disease or cranial irradiation), two dynamic
tests should be performed after
completion of growth, except for those having low insulin-like growth
factor-I (IGF-I) concentrations
(< -2 standard deviation score (SDS)), who may be considered for one
test. The cut-off point of the
dynamic test should be strict.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Diagnosis and therapy with this medicinal product should be initiated
and monitored by physicians
adequately experienced in the diagnosis and man
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 27-04-2017
Summary of Product characteristics Summary of Product characteristics Bulgarian 27-04-2017
Public Assessment Report Public Assessment Report Bulgarian 01-12-2017
Patient Information leaflet Patient Information leaflet Spanish 27-04-2017
Public Assessment Report Public Assessment Report Spanish 01-12-2017
Patient Information leaflet Patient Information leaflet Czech 27-04-2017
Public Assessment Report Public Assessment Report Czech 01-12-2017
Patient Information leaflet Patient Information leaflet Danish 27-04-2017
Public Assessment Report Public Assessment Report Danish 01-12-2017
Patient Information leaflet Patient Information leaflet German 27-04-2017
Public Assessment Report Public Assessment Report German 01-12-2017
Patient Information leaflet Patient Information leaflet Estonian 27-04-2017
Public Assessment Report Public Assessment Report Estonian 01-12-2017
Patient Information leaflet Patient Information leaflet Greek 27-04-2017
Public Assessment Report Public Assessment Report Greek 01-12-2017
Patient Information leaflet Patient Information leaflet French 27-04-2017
Public Assessment Report Public Assessment Report French 01-12-2017
Patient Information leaflet Patient Information leaflet Italian 27-04-2017
Public Assessment Report Public Assessment Report Italian 01-12-2017
Patient Information leaflet Patient Information leaflet Latvian 27-04-2017
Public Assessment Report Public Assessment Report Latvian 01-12-2017
Patient Information leaflet Patient Information leaflet Lithuanian 27-04-2017
Summary of Product characteristics Summary of Product characteristics Lithuanian 27-04-2017
Public Assessment Report Public Assessment Report Lithuanian 01-12-2017
Patient Information leaflet Patient Information leaflet Hungarian 27-04-2017
Summary of Product characteristics Summary of Product characteristics Hungarian 27-04-2017
Public Assessment Report Public Assessment Report Hungarian 01-12-2017
Patient Information leaflet Patient Information leaflet Maltese 27-04-2017
Public Assessment Report Public Assessment Report Maltese 01-12-2017
Patient Information leaflet Patient Information leaflet Dutch 27-04-2017
Public Assessment Report Public Assessment Report Dutch 01-12-2017
Patient Information leaflet Patient Information leaflet Polish 27-04-2017
Public Assessment Report Public Assessment Report Polish 01-12-2017
Patient Information leaflet Patient Information leaflet Portuguese 27-04-2017
Summary of Product characteristics Summary of Product characteristics Portuguese 27-04-2017
Public Assessment Report Public Assessment Report Portuguese 01-12-2017
Patient Information leaflet Patient Information leaflet Romanian 27-04-2017
Public Assessment Report Public Assessment Report Romanian 01-12-2017
Patient Information leaflet Patient Information leaflet Slovak 27-04-2017
Public Assessment Report Public Assessment Report Slovak 01-12-2017
Patient Information leaflet Patient Information leaflet Slovenian 27-04-2017
Summary of Product characteristics Summary of Product characteristics Slovenian 27-04-2017
Public Assessment Report Public Assessment Report Slovenian 01-12-2017
Patient Information leaflet Patient Information leaflet Finnish 27-04-2017
Public Assessment Report Public Assessment Report Finnish 01-12-2017
Patient Information leaflet Patient Information leaflet Swedish 27-04-2017
Public Assessment Report Public Assessment Report Swedish 01-12-2017
Patient Information leaflet Patient Information leaflet Norwegian 27-04-2017
Summary of Product characteristics Summary of Product characteristics Norwegian 27-04-2017
Patient Information leaflet Patient Information leaflet Icelandic 27-04-2017
Summary of Product characteristics Summary of Product characteristics Icelandic 27-04-2017
Patient Information leaflet Patient Information leaflet Croatian 27-04-2017
Public Assessment Report Public Assessment Report Croatian 01-12-2017

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