Pelmeg

País: União Europeia

Língua: inglês

Origem: EMA (European Medicines Agency)

Ingredientes ativos:

pegfilgrastim

Disponível em:

Mundipharma Corporation (Ireland) Limited

Código ATC:

L03AA13

DCI (Denominação Comum Internacional):

pegfilgrastim

Grupo terapêutico:

Immunostimulants,

Área terapêutica:

Neutropenia

Indicações terapêuticas:

To reduce the duration of neutropenia and the incidence of febrile neutropenia due to chemotherapy.

Resumo do produto:

Revision: 7

Status de autorização:

Authorised

Data de autorização:

2018-11-20

Folheto informativo - Bula

22
B. PACKAGE LEAFLET
23
PACKAGE LEAFLET: INFORMATION FOR THE USER
PELMEG 6 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
pegfilgrastim
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 symptoms 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 Pelmeg is and what it is used for
2.
What you need to know before you use Pelmeg
3.
How to use Pelmeg
4.
Possible side effects
5.
How to store Pelmeg
6.
Contents of the pack and other information
1.
WHAT PELMEG IS AND WHAT IT IS USED FOR
Pelmeg contains the active substance pegfilgrastim. Pegfilgrastim is a
protein produced by
biotechnology in bacteria called
_E. coli_
. It belongs to a group of proteins called cytokines, and is very
similar to a natural protein (granulocyte-colony stimulating factor)
produced by your own body.
Pelmeg is used in adult patients to reduce the duration of neutropenia
(low white blood cell count) and
the occurrence of febrile neutropenia (low white blood cell count with
a fever) which can be caused by
the use of cytotoxic chemotherapy (medicines that destroy rapidly
growing cells). White blood cells
are important as they help your body fight infection. These cells are
very sensitive to the effects of
chemotherapy which can cause the number of these cells in your body to
decrease. If white blood cells
fall to a low level there may not be enough left in the body to fight
bacteria and you may have an
increased risk of infection.
Your doctor has given you Pelmeg to encourage your bone marrow (part
of the bone which makes
blood cells) to produce more white blood cells that

Características técnicas

1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Pelmeg 6 mg solution for injection in pre-filled syringe
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each pre-filled syringe contains 6 mg of pegfilgrastim* in 0.6 mL
solution for injection. The
concentration is 10 mg/mL based on protein only**.
*Produced in
_Escherichia coli_
cells by recombinant DNA technology followed by conjugation with
polyethylene glycol (PEG).
** The concentration is 20 mg/mL if the PEG moiety is included.
The potency of this product should not be compared to the potency of
another pegylated or
nonpegylated protein of the same therapeutic class. For more
information, see section 5.1
Excipient with known effect
Each pre-filled syringe contains 30 mg sorbitol (E 420).
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Solution for injection
Clear, colourless solution for injection.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Reduction in the duration of neutropenia and the incidence of febrile
neutropenia in adult patients
treated with cytotoxic chemotherapy for malignancy (with the exception
of chronic myeloid leukaemia
and myelodysplastic syndromes).
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Pelmeg therapy should be initiated and supervised by physicians
experienced in oncology and/or
haematology.
Posology
One 6 mg dose (a single pre-filled syringe) of Pelmeg is recommended
for each chemotherapy cycle,
given at least 24 hours after cytotoxic chemotherapy.
Special populations
_Paediatric population _
The safety and efficacy of pegfilgrastim in children has not yet been
established. Currently available
data are described in sections 4.8, 5.1 and 5.2 but no recommendation
on a posology can be made.
3
_Patients with renal impairment _
No dose change is recommended in patients with renal impairment,
including those with end stage
renal disease.
Method of administration
Pelmeg is injected subcutaneously. The injections should be given into
the thigh, abdomen or upper
arm.
For instruction