Humira 40mg0.8ml solution for injection vials

Land: Storbritannia

Språk: engelsk

Kilde: MHRA (Medicines & Healthcare Products Regulatory Agency)

Aktiv ingrediens:

Adalimumab

Tilgjengelig fra:

AbbVie Ltd

ATC-kode:

L04AB04

INN (International Name):

Adalimumab

Dosering :

50mg/1ml

Legemiddelform:

Solution for injection

Administreringsrute:

Subcutaneous

Klasse:

No Controlled Drug Status

Resept typen:

Valid as a prescribable product

Produkt oppsummering:

BNF: ; GTIN: 5013158781405

Informasjon til brukeren

1
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
HUMIRA 40 MG/0.8 ML SOLUTION FOR INJECTION
adalimumab
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOUR CHILD STARTS USING THIS
MEDICINE BECAUSE IT CONTAINS
IMPORTANT INFORMATION.

Keep this leaflet. You may need to read it again.

Your doctor will also give you a Patient Alert Card, which contains
important safety information
that you need to be aware of before your child is given Humira and
during treatment with Humira.
Keep this Patient Alert Card with you or your child.

If you have any further questions, please ask your doctor or
pharmacist.

This medicine has been prescribed for your child only. Do not pass it
on to others. It may harm
them, even if their signs of illness are the same as your child's.

If your child gets any side effects, talk to your child’s doctor or
pharmacist. This includes any
possible side effects not listed in this leaflet (see section 4).
WHAT IS IN THIS LEAFLET
1.
What Humira is and what it is used for
2.
What you need to know before your child uses Humira
3.
How to use Humira
4.
Possible side effects
5.
How to store Humira
6.
Contents of the pack and other information
1.
WHAT HUMIRA IS AND WHAT IT IS USED FOR
Humira contains the active substance adalimumab.
Humira is intended for the treatment of the inflammatory diseases
described below:

Polyarticular juvenile idiopathic arthritis

Enthesitis-related arthritis

Paediatric plaque psoriasis

Adolescent hidradenitis suppurativa

Paediatric Crohn’s disease

Paediatric uveitis
The active ingredient in Humira, adalimumab, is a human monoclonal
antibody. Monoclonal antibodies
are proteins that attach to a specific target.
The target of adalimumab is a protein called tumour necrosis factor
(TNFα), which is involved in the
immune (defence) system and is present at increased levels in the
inflammatory diseases listed above. By
attaching to TNFα, Humira decreases the process of inflammation in
these diseases.
Polyarticular juvenile idiopathic arthritis and e

Preparatomtale

OBJECT 1
HUMIRA 40 MG/0.8 ML VIAL FOR PAEDIATRIC USE
Summary of Product Characteristics Updated 02-May-2018 | AbbVie
Limited
1. Name of the medicinal product
Humira 40 mg/0.8 ml solution for injection
2. Qualitative and quantitative composition
Each 0.8 ml single dose vial contains 40 mg of adalimumab.
Adalimumab is a recombinant human monoclonal antibody produced in
Chinese Hamster Ovary cells.
For the full list of excipients, see section 6.1.
3. Pharmaceutical form
Solution for injection. (injection)
Clear, colourless solution.
4. Clinical particulars
4.1 Therapeutic indications
Juvenile idiopathic arthritis
_Polyarticular juvenile idiopathic arthritis_
Humira in combination with methotrexate is indicated for the treatment
of active polyarticular juvenile
idiopathic arthritis, in patients from the age of 2 years who have had
an inadequate response to one or
more disease-modifying anti-rheumatic drugs (DMARDs). Humira can be
given as monotherapy in case
of intolerance to methotrexate or when continued treatment with
methotrexate is inappropriate (for the
efficacy in monotherapy see section 5.1). Humira has not been studied
in patients aged less than 2 years.
_Enthesitis-related arthritis_
Humira is indicated for the treatment of active enthesitis-related
arthritis in patients, 6 years of age and
older, who have had an inadequate response to, or who are intolerant
of, conventional therapy (see section
5.1).
Paediatric plaque psoriasis
Humira is indicated for the treatment of severe chronic plaque
psoriasis in children and adolescents from
4 years of age who have had an inadequate response to or are
inappropriate candidates for topical therapy
and phototherapies.
Paediatric Crohn's disease
Humira is indicated for the treatment of moderately to severely active
Crohn's disease in paediatric
patients (from 6 years of age) who have had an inadequate response to
conventional therapy including
primary nutrition therapy and a corticosteroid and/or an
immunomodulator, or who are intolerant to or
have contraindications for