Land: Verenigd Koninkrijk
Taal: Engels
Bron: MHRA (Medicines & Healthcare Products Regulatory Agency)
Atosiban acetate
Ferring Pharmaceuticals Ltd
G02CX01
Atosiban acetate
7.5mg/1ml
Solution for injection
Intravenous
No Controlled Drug Status
Valid as a prescribable product
BNF: 07010300; GTIN: 5015919824109
= No print area = Folding line =Perforation Fiber direction Pharmacode is centered 87,5 mm from the top Drawring E-MS-3056 Size 180x500mm 2009052819 Title: Leaflet TRACTOCILE sol inj 7.5mg/ml vial 1x 0.9ml GB/IE Document: Artwork Code No: E-2009052819.01 Supersedes: NA 1 Packaging coordinator Nathalie Chateau +41 58 301 08 21 FERRING International Center SA Ch. de la Vergognausaz 50 1162 St-Prex Switzerland Ferring item number 2009052819 E-MS- number E-MS-3056 Pharma code 1828 Comments: NA 3 M&S country Country: All text is according to the National Registration Documentation. Printers proof proofread/approved by responsible regulatory person Variable Datas (english translation) Line 1 : Line 2 : Line 3 : Name Date Signature 2 Supplier Order number: 4314888 Eson Pac Denmark Hørskætten 26-28 2630 Taastrup Denmark Date 2013.06.03 Proof version 2 Braille Braille Perforation vignette other Format (mm) 180x500 Colours and Varnish NA NA NA NA Black NA NA Comments: NA 4 Ferring Reviewers Packaging Support Approval Date Comments: Change / Review log Version No. Effective Date Reason for the Change / Revision 01 New document Lees het volledige document
OBJECT 1 TRACTOCILE 7.5 MG/ML SOLUTION FOR INJECTION Summary of Product Characteristics Updated 21-Jun-2013 | Ferring Pharmaceuticals Ltd 1. Name of the medicinal product Tractocile 6.75 mg/0.9 ml solution for injection 2. Qualitative and quantitative composition Each vial of 0.9 ml solution contains 6.75 mg atosiban (as acetate). For a full list of excipients, see section 6.1. 3. Pharmaceutical form Solution for injection (injection). Clear, colourless solution without particles. 4. Clinical particulars 4.1 Therapeutic indications Tractocile is indicated to delay imminent pre-term birth in pregnant adult women with: − regular uterine contractions of at least 30 seconds duration at a rate of ≥ 4 per 30 minutes − a cervical dilation of 1 to 3 cm (0-3 for nulliparas) and effacement of ≥ 50% − a gestational age from 24 until 33 completed weeks − a normal foetal heart rate 4.2 Posology and method of administration Posology Treatment with Tractocile should be initiated and maintained by a physician experienced in the treatment of pre-term labour. Tractocile is administered intravenously in three successive stages: an initial bolus dose (6.75 mg), performed with Tractocile 6.75 mg/0.9 ml solution for injection, immediately followed by a continuous high dose infusion (loading infusion 300 micrograms/min) of Tractocile 37.5 mg/5 ml concentrate for solution for infusion during three hours, followed by a lower dose of Tractocile 37.5 mg/5 ml concentrate for solution for infusion (subsequent infusion 100 micrograms/min) up to 45 hours. The duration of the treatment should not exceed 48 hours. The total dose given during a full course of Tractocile therapy should preferably not exceed 330.75 mg of atosiban. Intravenous therapy using the initial bolus injection should be started as soon as possible after diagnosis of pre-term labour. Once the bolus has been injected, proceed with the infusion (See Summary of Product Characteristics of Tractocile 37.5 mg/5 ml, concentrate for solution for infusion). In the case of Lees het volledige document