Quofenix 300 mg powder for concentrate for solution for infusion

  • Name:

    Quofenix 300 mg powder for concentrate for solution for infusion

  • Company:
    info
  • Active Ingredients:

    Delafloxacin Meglumine

  • Legal Category:

    Product subject to medical prescription which may not be renewed (A)

Patient Information Leaflet Patient Information Leaflet last updated on medicines.ie: 03/12/20

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Summary of Product Characteristics last updated on medicines.ie: 3/12/2020
This medicinal product is subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse reactions. See section 4.8 for how to report adverse reactions.

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A. Menarini Pharmaceuticals Ireland Ltd

A

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When a pharmaceutical company changes any document, a new version is published on medicines.ie. For each version, we show the dates it was published on medicines.ie and the reasons for change.

Updated on 3 December 2020 PIL

Reasons for updating

  • Change to section 2 - what you need to know - warnings and precautions
  • Change to section 4 - possible side effects
  • Change to section 6 - date of revision

Free text change information supplied by the pharmaceutical company

The changes relate to the requested actions following the PRAC recommendation concerning the signal of “heart valve regurgitation, cervical artery dissection and aortic aneurysm and dissection” associated with Fluoroquinolones intake.

 The following sections are updated:

2.         What you need to know before you take Quofenix

Warnings and precautions

…Talk to your doctor or pharmacist or nurse before taking Quofenix if:

 

4.         Possible side effects

 

Updated on 3 December 2020 SPC

Reasons for updating

  • Change to section 4.4 - Special warnings and precautions for use
  • Change to section 4.8 - Undesirable effects
  • Change to section 10 - Date of revision of the text

Legal category: Product subject to medical prescription which may not be renewed (A)

Free text change information supplied by the pharmaceutical company

The changes relate to the requested actions following the PRAC recommendation concerning the signal of “heart valve regurgitation, cervical artery dissection and aortic aneurysm and dissection” associated with Fluoroquinolones intake.

The following sections are updated:

Section 4.4     Special warnings and precautions for use

 [..] 

Aortic dissection and aneurysm, and heart valve regurgitation/incompetence

Further information added.

 

Section 4.8     Undesirable effects

Cardiac disorders** 

Vascular disorders**   

** Cases of aortic aneurysm and dissection, sometimes complicated by rupture (including fatal ones), and of regurgitation/incompetence of any of the heart valves have been reported in patients receiving fluoroquinolones (see section 4.4).

 

Updated on 28 May 2020 SPC

Reasons for updating

  • New SPC for new product

Legal category: Product subject to medical prescription which may not be renewed (A)

Updated on 28 May 2020 PIL

Reasons for updating

  • New PIL for new product