Reconcile

Country: Kesatuan Eropah

Bahasa: Inggeris

Sumber: EMA (European Medicines Agency)

Beli sekarang

Risalah maklumat Risalah maklumat (PIL)
16-06-2021
Ciri produk Ciri produk (SPC)
16-06-2021
Laporan Penilaian Awam Laporan Penilaian Awam (PAR)
19-10-2016

Bahan aktif:

fluoxetine

Boleh didapati daripada:

Forte Healthcare Limited

Kod ATC:

QN06AB03

INN (Nama Antarabangsa):

fluoxetine

Kumpulan terapeutik:

Dogs

Kawasan terapeutik:

Psychoanaleptics

Tanda-tanda terapeutik:

As an aid in the treatment of separation-related disorders in dogs manifested by destruction and inappropriate behaviours (vocalisation and inappropriate defecation and / or urination) and only in combination with behavioural-modification techniques.

Ringkasan produk:

Revision: 14

Status kebenaran:

Authorised

Tarikh kebenaran:

2008-07-08

Risalah maklumat

                                14
B. PACKAGE LEAFLET
15
PACKAGE LEAFLET:
RECONCILE 8 MG CHEWABLE TABLETS FOR DOGS
RECONCILE 16 MG CHEWABLE TABLETS FOR DOGS
RECONCILE 32 MG CHEWABLE TABLETS FOR DOGS
RECONCILE 64 MG CHEWABLE TABLETS FOR DOGS
1.
NAME AND ADDRESS OF THE MARKETING AUTHORISATION HOLDER AND OF
THE MANUFACTURING AUTHORISATION HOLDER RESPONSIBLE FOR BATCH
RELEASE, IF DIFFERENT
Marketing authorisation holder:
FORTE Healthcare ltd
Cougar Lane
Naul
Co. Dublin
Ireland
Manufacturer responsible for batch release:
Tairgi Tread -Lia Baile na Sceilge Teo T/A Ballinskelligs
Veterinary Products,
Ballinskelligs,
Co. Kerry,
V23 XR52,
Ireland
2.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Reconcile 8 mg chewable tablets for dogs
Reconcile 16 mg chewable tablets for dogs
Reconcile 32 mg chewable tablets for dogs
Reconcile 64 mg chewable tablets for dogs
fluoxetine
3.
STATEMENT OF THE ACTIVE SUBSTANCE(S) AND OTHER INGREDIENT(S)
Each tablet contains:
Reconcile 8
mg: fluoxetine 8 mg (equivalent to 9.04 mg fluoxetine hydrochloride)
Reconcile 16mg: fluoxetine 16 mg (equivalent to 18.08mg fluoxetine
hydrochloride)
Reconcile 32 mg: fluoxetine 32 mg (equivalent to 36.16 mg fluoxetine
hydrochloride)
Reconcile 64 mg: fluoxetine 64 mg (equivalent to 72.34 mg fluoxetine
hydrochloride)
Speckled, tan to brown round chewable tablets, embossed on one side
with a number (as listed below):
Reconcile 8 mg tablets: 4203
Reconcile 16 mg tablets: 4205
Reconcile 32 mg tablets: 4207
Reconcile 64 mg tablets: 4209
4.
INDICATION(S)
16
As an aid in the treatment of separation-related disorders in dogs,
such as destruction and vocalisation
and inappropriate defaecation and/or urination. This product should
only be used in conjunction with a
behaviour modification programme recommended by your veterinary
surgeon.
5.
CONTRAINDICATIONS
Do not use in dogs weighing less than 4 kg.
Do not use in dogs with epilepsy or a history of seizures.
Do not use in case of hypersensitivity to fluoxetine or other
Selective Serotonin Re-Uptake Inhibitors
(SSRIs) or to any of the excipients.
6.
ADVERSE
                                
                                Baca dokumen lengkap
                                
                            

Ciri produk

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Reconcile 8 mg chewable tablets for dogs
Reconcile 16mg chewable tablets for dogs
Reconcile 32 mg chewable tablets for dogs
Reconcile 64 mg chewable tablets for dogs
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
ACTIVE SUBSTANCE:
Each tablet contains:
Reconcile 8
mg: Fluoxetine 8 mg (equivalent to 9.04 mg fluoxetine hydrochloride)
Reconcile 16mg: Fluoxetine 16 mg (equivalent to 18.08mg fluoxetine
hydrochloride)
Reconcile 32 mg: Fluoxetine 32 mg (equivalent to 36.16 mg fluoxetine
hydrochloride)
Reconcile 64 mg: Fluoxetine 64 mg (equivalent to 72.34 mg fluoxetine
hydrochloride)
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Chewable tablet.
Speckled, tan to brown round chewable tablets, embossed on one side
with a number (as listed below):
Reconcile 8 mg tablets: 4203
Reconcile 16 mg tablets: 4205
Reconcile 32 mg tablets: 4207
Reconcile 64 mg tablets: 4209
4.
CLINICAL PARTICULARS
4.1
TARGET SPECIES
Dogs
4.2
INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
As an aid in the treatment of separation-related disorders in dogs
manifested by destruction and
inappropriate behaviours (vocalisation and inappropriate defaecation
and/or urination) and only in
combination with behavioural modification techniques.
4.3
CONTRAINDICATIONS
Do not use in dogs weighing less than 4 kg.
Do not use in dogs with epilepsy or in dogs with a history of
seizures.
Do not use in case of hypersensitivity to fluoxetine or other
Selective Serotonin Re-Uptake Inhibitors
(SSRIs) or to any of the excipients.
4.4
SPECIAL WARNINGS FOR EACH TARGET SPECIES
None.
3
4.5
SPECIAL PRECAUTIONS FOR USE
Special precautions for use in animals
The safety of the product has not been established in dogs less than 6
months of age or weighing less than
4 kg.
Though rare, seizures may occur in dogs treated with Reconcile.
Treatment should be stopped if seizures
occur.
Special precautions to be taken by the person administering the
veterinary medicinal pr
                                
                                Baca dokumen lengkap
                                
                            

Dokumen dalam bahasa lain

Risalah maklumat Risalah maklumat Bulgaria 16-06-2021
Ciri produk Ciri produk Bulgaria 16-06-2021
Laporan Penilaian Awam Laporan Penilaian Awam Bulgaria 19-10-2016
Risalah maklumat Risalah maklumat Sepanyol 16-06-2021
Ciri produk Ciri produk Sepanyol 16-06-2021
Laporan Penilaian Awam Laporan Penilaian Awam Sepanyol 19-10-2016
Risalah maklumat Risalah maklumat Czech 16-06-2021
Ciri produk Ciri produk Czech 16-06-2021
Laporan Penilaian Awam Laporan Penilaian Awam Czech 19-10-2016
Risalah maklumat Risalah maklumat Denmark 16-06-2021
Ciri produk Ciri produk Denmark 16-06-2021
Laporan Penilaian Awam Laporan Penilaian Awam Denmark 19-10-2016
Risalah maklumat Risalah maklumat Jerman 16-06-2021
Ciri produk Ciri produk Jerman 16-06-2021
Laporan Penilaian Awam Laporan Penilaian Awam Jerman 19-10-2016
Risalah maklumat Risalah maklumat Estonia 16-06-2021
Ciri produk Ciri produk Estonia 16-06-2021
Laporan Penilaian Awam Laporan Penilaian Awam Estonia 19-10-2016
Risalah maklumat Risalah maklumat Greek 16-06-2021
Ciri produk Ciri produk Greek 16-06-2021
Laporan Penilaian Awam Laporan Penilaian Awam Greek 19-10-2016
Risalah maklumat Risalah maklumat Perancis 16-06-2021
Ciri produk Ciri produk Perancis 16-06-2021
Laporan Penilaian Awam Laporan Penilaian Awam Perancis 19-10-2016
Risalah maklumat Risalah maklumat Itali 16-06-2021
Ciri produk Ciri produk Itali 16-06-2021
Laporan Penilaian Awam Laporan Penilaian Awam Itali 19-10-2016
Risalah maklumat Risalah maklumat Latvia 16-06-2021
Ciri produk Ciri produk Latvia 16-06-2021
Laporan Penilaian Awam Laporan Penilaian Awam Latvia 19-10-2016
Risalah maklumat Risalah maklumat Lithuania 16-06-2021
Ciri produk Ciri produk Lithuania 16-06-2021
Laporan Penilaian Awam Laporan Penilaian Awam Lithuania 19-10-2016
Risalah maklumat Risalah maklumat Hungary 16-06-2021
Ciri produk Ciri produk Hungary 16-06-2021
Laporan Penilaian Awam Laporan Penilaian Awam Hungary 19-10-2016
Risalah maklumat Risalah maklumat Malta 16-06-2021
Ciri produk Ciri produk Malta 16-06-2021
Laporan Penilaian Awam Laporan Penilaian Awam Malta 19-10-2016
Risalah maklumat Risalah maklumat Belanda 16-06-2021
Ciri produk Ciri produk Belanda 16-06-2021
Laporan Penilaian Awam Laporan Penilaian Awam Belanda 19-10-2016
Risalah maklumat Risalah maklumat Poland 16-06-2021
Ciri produk Ciri produk Poland 16-06-2021
Laporan Penilaian Awam Laporan Penilaian Awam Poland 19-10-2016
Risalah maklumat Risalah maklumat Portugis 16-06-2021
Ciri produk Ciri produk Portugis 16-06-2021
Laporan Penilaian Awam Laporan Penilaian Awam Portugis 19-10-2016
Risalah maklumat Risalah maklumat Romania 16-06-2021
Ciri produk Ciri produk Romania 16-06-2021
Laporan Penilaian Awam Laporan Penilaian Awam Romania 19-10-2016
Risalah maklumat Risalah maklumat Slovak 16-06-2021
Ciri produk Ciri produk Slovak 16-06-2021
Laporan Penilaian Awam Laporan Penilaian Awam Slovak 19-10-2016
Risalah maklumat Risalah maklumat Slovenia 16-06-2021
Ciri produk Ciri produk Slovenia 16-06-2021
Laporan Penilaian Awam Laporan Penilaian Awam Slovenia 19-10-2016
Risalah maklumat Risalah maklumat Finland 16-06-2021
Ciri produk Ciri produk Finland 16-06-2021
Laporan Penilaian Awam Laporan Penilaian Awam Finland 19-10-2016
Risalah maklumat Risalah maklumat Sweden 16-06-2021
Ciri produk Ciri produk Sweden 16-06-2021
Laporan Penilaian Awam Laporan Penilaian Awam Sweden 19-10-2016
Risalah maklumat Risalah maklumat Norway 16-06-2021
Ciri produk Ciri produk Norway 16-06-2021
Risalah maklumat Risalah maklumat Iceland 16-06-2021
Ciri produk Ciri produk Iceland 16-06-2021
Risalah maklumat Risalah maklumat Croat 16-06-2021
Ciri produk Ciri produk Croat 16-06-2021
Laporan Penilaian Awam Laporan Penilaian Awam Croat 19-10-2016

Cari amaran yang berkaitan dengan produk ini

Lihat sejarah dokumen