Rivastigmine 1 A Pharma

Country: European Union

Language: English

Source: EMA (European Medicines Agency)

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Active ingredient:

rivastigmine

Available from:

1 A Pharma GmbH

ATC code:

N06DA03

INN (International Name):

rivastigmine

Therapeutic group:

Psychoanaleptics,

Therapeutic area:

Alzheimer Disease; Dementia; Parkinson Disease

Therapeutic indications:

Symptomatic treatment of mild to moderately severe Alzheimer's dementia.Symptomatic treatment of mild to moderately severe dementia in patients with idiopathic Parkinson's disease.

Product summary:

Revision: 15

Authorization status:

Authorised

Authorization date:

2009-12-11

Patient Information leaflet

                                51
B. PACKAGE LEAFLET
52
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
RIVASTIGMINE 1 A PHARMA 1.5 MG HARD CAPSULES
RIVASTIGMINE 1 A PHARMA 3 MG HARD CAPSULES
RIVASTIGMINE 1 A PHARMA 4.5 MG HARD CAPSULES
RIVASTIGMINE 1 A PHARMA 6 MG HARD CAPSULES
rivastigmine
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 Rivastigmine 1 A Pharma is and what it is used for
2.
What you need to know before you take Rivastigmine 1 A Pharma
3.
How to take Rivastigmine 1 A Pharma
4.
Possible side effects
5.
How to store Rivastigmine 1 A Pharma
6.
Contents of the pack and other information
1.
WHAT RIVASTIGMINE 1 A PHARMA IS AND WHAT IT IS USED FOR
The active substance of Rivastigmine 1 A Pharma is rivastigmine.
Rivastigmine 1 A Pharma belongs to a class of substances called
cholinesterase inhibitors.
In patients with Alzheimer’s dementia or dementia due to
Parkinson’s disease, certain nerve cells die
in the brain, resulting in low levels of the neurotransmitter
acetylcholine (a substance that allows nerve
cells to communicate with each other). Rivastigmine works by blocking
the enzymes that break down
acetylcholine: acetylcholinesterase and butyrylcholinesterase. By
blocking these enzymes,
Rivastigmine 1 A Pharma allows levels of acetylcholine to be increased
in the brain, helping to reduce
the symptoms of Alzheimer’s disease and dementia associated with
Parkinson’s disease.
Rivastigmine 1 A Pharma is used for the treatment of adult patients
with mild to moderately severe
Alzheimer’s dementia, a progressive b
                                
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Summary of Product characteristics

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Rivastigmine 1 A Pharma 1.5 mg hard capsules
Rivastigmine 1 A Pharma 3 mg hard capsules
Rivastigmine 1 A Pharma 4.5 mg hard capsules
Rivastigmine 1 A Pharma 6 mg hard capsules
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each capsule contains rivastigmine hydrogen tartrate corresponding to
1.5 mg rivastigmine.
Each capsule contains rivastigmine hydrogen tartrate corresponding to
3 mg rivastigmine.
Each capsule contains rivastigmine hydrogen tartrate corresponding to
4.5 mg rivastigmine.
Each capsule contains rivastigmine hydrogen tartrate corresponding to
6 mg rivastigmine.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Hard capsule
Off-white to slightly yellow powder in a capsule with yellow cap and
yellow body, with red imprint
“RIV 1.5 mg” on the body.
Off-white to slightly yellow powder in a capsule with orange cap and
orange body, with red imprint
“RIV 3 mg” on the body.
Off-white to slightly yellow powder in a capsule with red cap and red
body, with white imprint
“RIV 4.5 mg” on the body.
Off-white to slightly yellow powder in a capsule with red cap and
orange body, with red imprint
“RIV 6 mg” on the body.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Symptomatic treatment of mild to moderately severe Alzheimer’s
dementia.
Symptomatic treatment of mild to moderately severe dementia in
patients with idiopathic Parkinson’s
disease.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Treatment should be initiated and supervised by a physician
experienced in the diagnosis and
treatment of Alzheimer’s dementia or dementia associated with
Parkinson’s disease. Diagnosis should
be made according to current guidelines. Therapy with rivastigmine
should only be started if a
caregiver is available who will regularly monitor intake of the
medicinal product by the patient.
Posology
Rivastigmine should be administered twice a day, with morning and
evening meals. The capsules
should be swallowed whol
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 21-06-2023
Summary of Product characteristics Summary of Product characteristics Bulgarian 21-06-2023
Public Assessment Report Public Assessment Report Bulgarian 21-07-2013
Patient Information leaflet Patient Information leaflet Spanish 21-06-2023
Public Assessment Report Public Assessment Report Spanish 21-07-2013
Patient Information leaflet Patient Information leaflet Czech 21-06-2023
Public Assessment Report Public Assessment Report Czech 21-07-2013
Patient Information leaflet Patient Information leaflet Danish 21-06-2023
Public Assessment Report Public Assessment Report Danish 21-07-2013
Patient Information leaflet Patient Information leaflet German 21-06-2023
Public Assessment Report Public Assessment Report German 21-07-2013
Patient Information leaflet Patient Information leaflet Estonian 21-06-2023
Public Assessment Report Public Assessment Report Estonian 21-07-2013
Patient Information leaflet Patient Information leaflet Greek 21-06-2023
Public Assessment Report Public Assessment Report Greek 21-07-2013
Patient Information leaflet Patient Information leaflet French 21-06-2023
Public Assessment Report Public Assessment Report French 21-07-2013
Patient Information leaflet Patient Information leaflet Italian 21-06-2023
Public Assessment Report Public Assessment Report Italian 21-07-2013
Patient Information leaflet Patient Information leaflet Latvian 21-06-2023
Public Assessment Report Public Assessment Report Latvian 21-07-2013
Patient Information leaflet Patient Information leaflet Lithuanian 21-06-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 21-06-2023
Public Assessment Report Public Assessment Report Lithuanian 21-07-2013
Patient Information leaflet Patient Information leaflet Hungarian 21-06-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 21-06-2023
Public Assessment Report Public Assessment Report Hungarian 21-07-2013
Patient Information leaflet Patient Information leaflet Maltese 21-06-2023
Public Assessment Report Public Assessment Report Maltese 21-07-2013
Patient Information leaflet Patient Information leaflet Dutch 21-06-2023
Public Assessment Report Public Assessment Report Dutch 21-07-2013
Patient Information leaflet Patient Information leaflet Polish 21-06-2023
Public Assessment Report Public Assessment Report Polish 21-07-2013
Patient Information leaflet Patient Information leaflet Portuguese 21-06-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 21-06-2023
Public Assessment Report Public Assessment Report Portuguese 21-07-2013
Patient Information leaflet Patient Information leaflet Romanian 21-06-2023
Public Assessment Report Public Assessment Report Romanian 21-07-2013
Patient Information leaflet Patient Information leaflet Slovak 21-06-2023
Public Assessment Report Public Assessment Report Slovak 21-07-2013
Patient Information leaflet Patient Information leaflet Slovenian 21-06-2023
Summary of Product characteristics Summary of Product characteristics Slovenian 21-06-2023
Public Assessment Report Public Assessment Report Slovenian 21-07-2013
Patient Information leaflet Patient Information leaflet Finnish 21-06-2023
Public Assessment Report Public Assessment Report Finnish 21-07-2013
Patient Information leaflet Patient Information leaflet Swedish 21-06-2023
Public Assessment Report Public Assessment Report Swedish 21-07-2013
Patient Information leaflet Patient Information leaflet Norwegian 21-06-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 21-06-2023
Patient Information leaflet Patient Information leaflet Icelandic 21-06-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 21-06-2023
Patient Information leaflet Patient Information leaflet Croatian 21-06-2023

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