Olanzapine Glenmark

Country: European Union

Language: English

Source: EMA (European Medicines Agency)

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Active ingredient:

olanzapine

Available from:

Glenmark Arzneimittel GmbH

ATC code:

N05AH03

INN (International Name):

olanzapine

Therapeutic group:

Psycholeptics

Therapeutic area:

Schizophrenia; Bipolar Disorder

Therapeutic indications:

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.

Product summary:

Revision: 15

Authorization status:

Authorised

Authorization date:

2009-12-03

Patient Information leaflet

                                122
B. PACKAGE LEAFLET
123
PACKAGE LEAFLET: INFORMATION FOR THE USER
Olanzapine Glenmark 2.5 mg tablets
Olanzapine Glenmark 5 mg tablets
Olanzapine Glenmark 7.5 mg tablets
Olanzapine Glenmark 10 mg tablets
Olanzapine Glenmark 15 mg tablets
Olanzapine Glenmark 20 mg 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 Olanzapine Glenmark is and what it is used for
2.
What you need to know before you take Olanzapine Glenmark
3.
How to take Olanzapine Glenmark
4.
Possible side effects
5.
How to store Olanzapine Glenmark
6.
Contents of the pack and other information
1.
WHAT OLANZAPINE GLENMARK IS AND WHAT IT IS USED FOR
Olanzapine Glenmark contains the active substance olanzapine.
Olanzapine Glenmark belongs to a
group of medicines called antipsychotics.
Olanzapine Glenmark 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.
Olanzapine Glenmark 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 OLANZAPINE GLENMARK
DO NOT TAKE OLANZAPINE GLENMARK
-
if you are allergic (hypersensitive) to olanzapine or any of the other
ingredients of thi
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
_ _
_ _
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Olanzapine Glenmark 2.5 mg tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each tablet contains 2.5 mg olanzapine.
Excipient with known effect: Each tablet contains 0.23 mg of aspartame
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Tablet
Yellow coloured circular flat bevelled edge tablets with ‘A’
debossed on one side.
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 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 (see
section 5.1).
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
_Adults_
Schizophrenia: The recommended starting dose for olanzapine is 10
mg/day.
Manic episode: The starting dose is 15 mg as a single daily dose in
monotherapy or 10 mg daily in
combination therapy (see section 5.1).
Preventing recurrence in bipolar disorder: The recommended starting
dose is 10 mg/day. For patients
who have been receiving olanzapine for treatment of manic episode,
continue therapy for preventing
recurrence at the same dose. If a new manic, mixed, or depressive
episode occurs, olanzapine
treatment should be continued (with dose optimisation as needed), with
supplementary therapy to treat
mood symptoms, as clinically indicated.
During treatment for schizophrenia, manic episode and recurrence
prevention in bipolar disorder,
daily dosage may subsequently be adjusted on the basis of individual
clinical status within the range
5-20 mg/day. An increase to a dose greater than the recommended
starting dose is advised only after
appropriate clinical reassessment and should generally occur at
intervals of
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 20-12-2022
Summary of Product characteristics Summary of Product characteristics Bulgarian 20-12-2022
Public Assessment Report Public Assessment Report Bulgarian 26-08-2014
Patient Information leaflet Patient Information leaflet Spanish 20-12-2022
Public Assessment Report Public Assessment Report Spanish 26-08-2014
Patient Information leaflet Patient Information leaflet Czech 20-12-2022
Public Assessment Report Public Assessment Report Czech 26-08-2014
Patient Information leaflet Patient Information leaflet Danish 20-12-2022
Public Assessment Report Public Assessment Report Danish 26-08-2014
Patient Information leaflet Patient Information leaflet German 20-12-2022
Public Assessment Report Public Assessment Report German 26-08-2014
Patient Information leaflet Patient Information leaflet Estonian 20-12-2022
Public Assessment Report Public Assessment Report Estonian 26-08-2014
Patient Information leaflet Patient Information leaflet Greek 20-12-2022
Public Assessment Report Public Assessment Report Greek 26-08-2014
Patient Information leaflet Patient Information leaflet French 20-12-2022
Public Assessment Report Public Assessment Report French 26-08-2014
Patient Information leaflet Patient Information leaflet Italian 20-12-2022
Public Assessment Report Public Assessment Report Italian 26-08-2014
Patient Information leaflet Patient Information leaflet Latvian 20-12-2022
Public Assessment Report Public Assessment Report Latvian 26-08-2014
Patient Information leaflet Patient Information leaflet Lithuanian 20-12-2022
Summary of Product characteristics Summary of Product characteristics Lithuanian 20-12-2022
Public Assessment Report Public Assessment Report Lithuanian 26-08-2014
Patient Information leaflet Patient Information leaflet Hungarian 20-12-2022
Summary of Product characteristics Summary of Product characteristics Hungarian 20-12-2022
Public Assessment Report Public Assessment Report Hungarian 26-08-2014
Patient Information leaflet Patient Information leaflet Maltese 20-12-2022
Public Assessment Report Public Assessment Report Maltese 26-08-2014
Patient Information leaflet Patient Information leaflet Dutch 20-12-2022
Public Assessment Report Public Assessment Report Dutch 26-08-2014
Patient Information leaflet Patient Information leaflet Polish 20-12-2022
Public Assessment Report Public Assessment Report Polish 26-08-2014
Patient Information leaflet Patient Information leaflet Portuguese 20-12-2022
Summary of Product characteristics Summary of Product characteristics Portuguese 20-12-2022
Public Assessment Report Public Assessment Report Portuguese 26-08-2014
Patient Information leaflet Patient Information leaflet Romanian 20-12-2022
Public Assessment Report Public Assessment Report Romanian 26-08-2014
Patient Information leaflet Patient Information leaflet Slovak 20-12-2022
Public Assessment Report Public Assessment Report Slovak 26-08-2014
Patient Information leaflet Patient Information leaflet Slovenian 20-12-2022
Summary of Product characteristics Summary of Product characteristics Slovenian 20-12-2022
Public Assessment Report Public Assessment Report Slovenian 26-08-2014
Patient Information leaflet Patient Information leaflet Finnish 20-12-2022
Public Assessment Report Public Assessment Report Finnish 26-08-2014
Patient Information leaflet Patient Information leaflet Swedish 20-12-2022
Public Assessment Report Public Assessment Report Swedish 26-08-2014
Patient Information leaflet Patient Information leaflet Norwegian 20-12-2022
Summary of Product characteristics Summary of Product characteristics Norwegian 20-12-2022
Patient Information leaflet Patient Information leaflet Icelandic 20-12-2022
Summary of Product characteristics Summary of Product characteristics Icelandic 20-12-2022
Patient Information leaflet Patient Information leaflet Croatian 20-12-2022
Public Assessment Report Public Assessment Report Croatian 26-08-2014

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