MOVICOL®

Nom de l'organisation

Norgine BV

SRN

NL-MF-000009565

Statut du fabricant

Actif

Santé des certificats sur le portefeuille de ce fabricant.

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• CW999

  Do not take Movicol if your doctor has told you that you have: • a blockage in your intestine (gut obstruction, ileus) • a perforated gut wall •severe inflammatory bowel disease like ulcerative colitis, Crohn’s disease or toxic megacolon • an allergy to any of the ingredients of Movicol
• CW275

  If you are pregnant, trying to become pregnant or breastfeeding, ask your pharmacist or doctor for advice before taking Movicol.
• CW276

  There is a possibility that the absorption and consequently the effectiveness of any medicines taken orally could be reduced if taken at the same time as Movicol. Therefore, as a precautionary measure, any medicines should not be taken orally for one hour before, during and for one hour after taking Movicol. Please consult your doctor or pharmacist if you are taking, or have recently taken, any medicines, including medicines obtained without a prescription.
• CW999

  If you need to thicken fluids in order to swallow them safely, Movicol may counteract the effect of the thickener.
• CW999

  Talk to your doctor or pharmacist if you need 3 or more sachets daily for a prolonged period, especially if you have been advised to follow a low salt (sodium) diet.
• CW999

  Movicol contains sodium. Movicol contains 186.87 mg sodium (main component of cooking/table salt) per sachet. This is equivalent to 9.3% of the recommended maximum daily dietary intake of sodium for an adult.
• CW135

  Keep out of the sight and reach of children.
• CW032

  Do not use Movicol after the expiry date on the sachet.

Marché principal en Allemagne ; disponible dans 1 pays au total.

Dénomination commerciale

MOVICOL®

Code d'UDI-DI

05012748605589

Basic UDI-DI

B-05012748605589

Numéro de référence/catalogue

77710016

Entité d'attribution

GS1

Catégorie de risque

Classe IIb

Législation applicable

MDD [Directive 93/42/CEE relative aux dispositifs médicaux]

Statut

Sur le marché

Quantité

1

Description complémentaire du produit

MOVICOL®, Lemon and Lime flavour, 13.8g Powder for Oral Solution (50 sachets)

URL des informations complémentaires

https://www.norgine.de/

Dimensions cliniques

• 13.8 grams per sachet

Nomenclature européenne des dispositifs médicaux — la classification produit UE attribuée à ce dispositif.

• G0401ORALLY ADMINISTERED DEVICES FOR THE THERAPY OF GASTRO-INTESTINAL DISORDERS