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Lithuanian

English

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Lithuanian

Lapkricio 8­10 d.

English

11-12 January

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

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Lithuanian

Lapkricio 8­10 d.

English

8-10 November

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

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Lithuanian

1999 m. lapkricio 25 d.

English

25/11/1999 Renewal:

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

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Lithuanian

2000 m. lapkricio 29 d.

English

29th November 2000.

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

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Lithuanian

2002 m. lapkricio 12 d.

English

12 November 2002 Date of last renewal:

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

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Lithuanian

2002 m. lapkricio 20 d.

English

20 November 2002

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 9
Quality:

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Lithuanian

2006 m. lapkricio 20 d.

English

V. on 20 November 2006.

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

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Lithuanian

2001 m. lapkricio 20 d.) , cia (LL:

English

20 November 2001) , here (ALL:

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

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Lithuanian

kadangi Susitarimo II priedas buvo iš dalies pakeistas 1997 m. lapkricio 12 d. EEE jungtinio komiteto sprendimu Nr. 76/97 [1],

English

Whereas Annex II to the Agreement was amended by Decision of the EEA Joint Committee No 76/97 of 12 November 1997 (1);

Last Update: 2016-09-30
Subject: Unknown
Usage Frequency: 1
Quality:

Reference:

Lithuanian

Šios proceduros buvo pradetos 2004 m. lapkricio men.

English

Further to discussions at the CHMP October 2004 plenary meeting, the European Commission recommended that this public health issue on all aspects of cardiovascular safety including thrombotic events and cardio-renal events is the subject of Community referrals under Article 31 of Directive 2001/ 83/ EC, as amended regarding decentrally authorised products containing celecoxib, etoricoxib and lumiracoxib and subject to a review procedure under Article 18 of Council Regulation (EEC) No 2309/ 93, as amended regarding the centrally authorised products containing celecoxib (Onsenal), parecoxib (Dynastat/ Rayzon) and valdecoxib (Bextra/ Valdyn), which were started in November 2004.

Last Update: 2011-10-23
Subject: Medical
Usage Frequency: 1
Quality:

Reference:
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Lithuanian

1995 lapkricio 30 Paskutinio atnaujinimo data:

English

30 November 1995 Date of last renewal:

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

Reference:
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Lithuanian

1995 m. lapkricio 27 d.Paskutinio perregistravimo data:

English

27 November 1995 Date of latest renewal:

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

Reference:
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Lithuanian

1996 m. lapkricio 12 d.Europos Komisija suteik visoje Europos Sjungoje galiojanci preparato Hycamtin rinkodaros teis bendrovei,, SmithKline Beecham ".

English

The European Commission granted a marketing authorisation valid throughout the European Union for Hycamtin to SmithKline Beecham on 12 November 1996.

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

Reference:
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Lithuanian

1997 m. lapkricio 17 d.Paskutinio rinkodaros teiss atnaujinimo data:

English

17 November 1997 Date of latest renewal:

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

Reference:
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Lithuanian

1999 m. lapkricio 16 d.2003 m. sausio 15 d.10.

English

10 DATE OF REVISION 13/11/2007

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

Reference:
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Lithuanian

2000 m. lapkricio 16 d.Informacija apie vaisto skyrim pateikta ant isorins pakuots.

English

Information on the prescription status of this product may be found on the outer package.

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

Reference:
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Lithuanian

2000 m. lapkricio 16 d.Paskutins perregistracijos data:

English

16 November 2000 Date of last renewal:

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

Reference:
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Lithuanian

2002 m. lapkricio 12 d.Rinkodaros teiss atnaujinimo data:

English

12 November 2002 Date of last renewal:

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

Reference:
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Lithuanian

2003 m. lapkricio mn. traukta indikacija,, kontrastinis preparatas magnetinio rezonanso angiografijai atlikti ".

English

In June 2005, a MR procedure started for a type II variation to add the indication of " Contrast enhanced MRI of other body regions: liver, kidneys " and the following posology and method of administration/dosage:

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 1
Quality:

Reference:
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Lithuanian

2004 m. lapkricio 18 d.CHMP papras pateikti issami informacij apie si preparat saugum sirdies ir kraujagysli sistemai.

English

On 18 November 2004, the CHMP requested comprehensive cardiovascular safety information for these products.

Last Update: 2008-03-04
Subject: Medical
Usage Frequency: 3
Quality:

Reference:
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