Zyprexa Velotab

Pays: Union européenne

Langue: anglais

Source: EMA (European Medicines Agency)

Achète-le

Ingrédients actifs:

olanzapine

Disponible depuis:

Eli Lilly Nederland B.V.

Code ATC:

N05AH03

DCI (Dénomination commune internationale):

olanzapine

Groupe thérapeutique:

Psycholeptics

Domaine thérapeutique:

Schizophrenia; Bipolar Disorder

indications thérapeutiques:

AdultsOlanzapine is indicated for the treatment of schizophrenia.Olanzapine is effective in maintaining the clinical improvement during continuation therapy in patients who have shown an initial treatment response.Olanzapine is indicated for the treatment of moderate to severe manic episode.In patients whose manic episode has responded to olanzapine treatment, olanzapine is indicated for the prevention of recurrence in patients with bipolar disorder.

Descriptif du produit:

Revision: 31

Statut de autorisation:

Authorised

Date de l'autorisation:

2000-02-03

Notice patient

                                39
B. PACKAGE LEAFLET
40
PACKAGE LEAFLET: INFORMATION FOR THE USER
ZYPREXA VELOTAB 5 MG ORODISPERSIBLE TABLETS
ZYPREXA VELOTAB 10 MG ORODISPERSIBLE TABLETS
ZYPREXA VELOTAB 15 MG ORODISPERSIBLE TABLETS
ZYPREXA VELOTAB 20 MG ORODISPERSIBLE TABLETS
olanzapine
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 or pharmacist.
-
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 ZYPREXA VELOTAB is and what it is used for
2.
What you need to know before you take ZYPREXA VELOTAB
3.
How to take ZYPREXA VELOTAB
4.
Possible side effects
5.
How to store ZYPREXA VELOTAB
6.
Contents of the pack and other information
1.
WHAT ZYPREXA VELOTAB IS AND WHAT IT IS USED FOR
ZYPREXA VELOTAB contains the active substance olanzapine. ZYPREXA
VELOTAB belongs to a
group of medicines called antipsychotics and is used to treat the
following conditions:
•
Schizophrenia, a disease with symptoms such as hearing, seeing or
sensing things which are not
there, mistaken beliefs, unusual suspiciousness, and becoming
withdrawn. People with this
disease may also feel depressed, anxious or tense.
•
Moderate to severe manic episodes, a condition with symptoms of
excitement or euphoria.
ZYPREXA VELOTAB has been shown to prevent recurrence of these symptoms
in patients with
bipolar disorder whose manic episode has responded to olanzapine
treatment.
2.
WHAT YOU NEED TO KNOW BEFORE YOU TAKE ZYPREXA VELOTAB
_ _
DO NOT TAKE ZYPREXA VELOTAB
•
If you are allergic (hypersensitive) to olanzapine or any of the other
ingredients of this medicine
(listed in section 6). An allergic reaction may be recognised as a
                                
                                Lire le document complet
                                
                            

Résumé des caractéristiques du produit

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
ZYPREXA VELOTAB 5 mg orodispersible tablets
ZYPREXA VELOTAB 10 mg orodispersible tablets
ZYPREXA VELOTAB 15 mg orodispersible tablets
ZYPREXA VELOTAB 20 mg orodispersible tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
ZYPREXA VELOTAB 5 mg orodispersible tablets
Each orodispersible tablet contains 5 mg olanzapine.
Excipients with known effect: Each orodispersible tablet contains
0.60 mg aspartame (E951),
0.1125 mg sodium methyl parahydroxybenzoate (E219),
0.0375 mg sodium propyl parahydroxybenzoate (E217).
ZYPREXA VELOTAB 10 mg orodispersible tablets
Each orodispersible tablet contains 10 mg olanzapine.
Excipients with known effect: Each orodispersible tablet contains
0.80 mg aspartame (E951),
0.15 mg sodium methyl parahydroxybenzoate (E219),
0.05 mg sodium propyl parahydroxybenzoate (E217).
ZYPREXA VELOTAB 15 mg orodispersible tablets
Each orodispersible tablet contains 15 mg olanzapine.
Excipients with known effect: Each orodispersible tablet contains
1.20 mg aspartame (E951),
0.225 mg sodium methyl parahydroxybenzoate (E219),
0.075 mg sodium propyl parahydroxybenzoate
(E217)
.
ZYPREXA VELOTAB 20 mg orodispersible tablets
Each orodispersible tablet contains 20 mg olanzapine.
Excipients with known effect: Each orodispersible tablet contains
1.60 mg aspartame (E951),
0.30 mg sodium methyl parahydroxybenzoate (E219),
0.10 mg sodium propyl parahydroxybenzoate (E217).
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Orodispersible tablet
Yellow, round, freeze dried, rapid-dispersing preparation to be placed
in the mouth or alternatively to
be dispersed in water or other suitable beverage for administration.
_ _
_ _
3
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
_Adults _
Olanzapine is indicated for the treatment of schizophrenia.
Olanzapine is effective in maintaining the clinical improvement during
continuation therapy in
patients who have shown an initial treatment response.
Olanzapine is indicated fo
                                
                                Lire le document complet
                                
                            

Documents dans d'autres langues

Notice patient Notice patient bulgare 27-02-2024
Rapport public d'évaluation Rapport public d'évaluation bulgare 03-07-2013
Notice patient Notice patient espagnol 27-02-2024
Rapport public d'évaluation Rapport public d'évaluation espagnol 03-07-2013
Notice patient Notice patient tchèque 27-02-2024
Rapport public d'évaluation Rapport public d'évaluation tchèque 03-07-2013
Notice patient Notice patient danois 27-02-2024
Rapport public d'évaluation Rapport public d'évaluation danois 03-07-2013
Notice patient Notice patient allemand 27-02-2024
Rapport public d'évaluation Rapport public d'évaluation allemand 03-07-2013
Notice patient Notice patient estonien 27-02-2024
Rapport public d'évaluation Rapport public d'évaluation estonien 03-07-2013
Notice patient Notice patient grec 27-02-2024
Notice patient Notice patient français 27-02-2024
Rapport public d'évaluation Rapport public d'évaluation français 03-07-2013
Notice patient Notice patient italien 27-02-2024
Rapport public d'évaluation Rapport public d'évaluation italien 03-07-2013
Notice patient Notice patient letton 27-02-2024
Rapport public d'évaluation Rapport public d'évaluation letton 03-07-2013
Notice patient Notice patient lituanien 27-02-2024
Rapport public d'évaluation Rapport public d'évaluation lituanien 03-07-2013
Notice patient Notice patient hongrois 27-02-2024
Rapport public d'évaluation Rapport public d'évaluation hongrois 03-07-2013
Notice patient Notice patient maltais 27-02-2024
Rapport public d'évaluation Rapport public d'évaluation maltais 03-07-2013
Notice patient Notice patient néerlandais 27-02-2024
Rapport public d'évaluation Rapport public d'évaluation néerlandais 03-07-2013
Notice patient Notice patient polonais 27-02-2024
Rapport public d'évaluation Rapport public d'évaluation polonais 03-07-2013
Notice patient Notice patient portugais 27-02-2024
Rapport public d'évaluation Rapport public d'évaluation portugais 03-07-2013
Notice patient Notice patient roumain 27-02-2024
Rapport public d'évaluation Rapport public d'évaluation roumain 03-07-2013
Notice patient Notice patient slovaque 27-02-2024
Rapport public d'évaluation Rapport public d'évaluation slovaque 03-07-2013
Notice patient Notice patient slovène 27-02-2024
Rapport public d'évaluation Rapport public d'évaluation slovène 03-07-2013
Notice patient Notice patient finnois 27-02-2024
Rapport public d'évaluation Rapport public d'évaluation finnois 03-07-2013
Notice patient Notice patient suédois 27-02-2024
Rapport public d'évaluation Rapport public d'évaluation suédois 03-07-2013
Notice patient Notice patient norvégien 27-02-2024
Notice patient Notice patient islandais 27-02-2024
Notice patient Notice patient croate 27-02-2024

Rechercher des alertes liées à ce produit

Afficher l'historique des documents