CATAFLAM 50 Milligram Coated Tablets

Negara: Irlandia

Bahasa: Inggris

Sumber: HPRA (Health Products Regulatory Authority)

Beli Sekarang

Selebaran informasi Selebaran informasi (PIL)
06-12-2016
Karakteristik produk Karakteristik produk (SPC)
24-02-2018

Bahan aktif:

DICLOFENAC POTASSIUM

Tersedia dari:

Novartis Pharmaceuticals UK Ltd

Kode ATC:

M01AB05

INN (Nama Internasional):

DICLOFENAC POTASSIUM

Dosis:

50 Milligram

Bentuk farmasi:

Coated Tablets

Jenis Resep:

Product subject to prescription which may be renewed (B)

Area terapi:

Acetic acid derivatives and related substances

Status otorisasi:

Authorised

Tanggal Otorisasi:

1995-03-13

Karakteristik produk

                                SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
Cataflam 50mg Coated Tablets
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each tablet contains 50mg diclofenac potassium.
Each tablet also contains 67mg sucrose.
For a full list of excipients, see section 6.1_._
3 PHARMACEUTICAL FORM
Coated tablet (Tablet)
Circular, biconvex, reddish brown sugar coated tablets approximately
8.8mm diameter.
4 CLINICAL PARTICULARS
4.1 THERAPEUTIC INDICATIONS
Short-term treatment of all grades of pain and inflammation in the
following acute conditions:
Post-traumatic pain, inflammation and swelling, e.g. due to sprains.
Acute musculo-skeletal disorders such as periarthritis (for example
frozen shoulder), tendonitis, tenosynovitis,
bursitis.
Post operative pain, inflammation and swelling, e.g. following dental
or orthopaedic surgery.
Painful and/or inflammatory conditions in gynaecology, e.g. primary
dysmenorrhoea or adnexitis and associated
menorrhagia.
Migraine attacks.
Acute gout
Painful syndromes of the vertebral column.
Non-articular rheumatism.
As an adjuvant in severe painful inflammatory infections of the ear,
nose or throat, e.g. pharyngotonsillitis, otitis.
In keeping with general therapeutic principles, the underlying disease
should be treated with basic therapy, as
appropriate. Fever alone is not an indication.
4.2 POSOLOGY AND METHOD OF ADMINISTRATION
Undesirable effects may be minimised by using the lowest effective
dose for the shortest
duration necessary to control
symptoms (see section 4.4).
The tablets should be swallowed whole with liquid, preferably before
meals, and must not be divided or chewed.
H
E
A
L
T
H
P
R
O
D
U
C
T
S
R
E
G
U
L
A
T
O
R
Y
A
U
T
H
O
R
I
T
Y
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___

                                
                                Baca dokumen lengkapnya
                                
                            

Peringatan pencarian terkait dengan produk ini