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This website is intended for healthcare professionals in KSA and UAE only.
 The content provided is developed in accordance with local regulations and may not be applicable or compliant in other regions.

Reporting adverse events
Reporting adverse events
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Submitted by Site Factory admin on
Source URL Clinical Trials
https://clinicaltrials.gov/study/NCT01913808?term=NCT01913808&rank=1
Sort Order Clinical Trials
25
Category Clinical Trials
Iron Deficiency
Tile Image Clinical Trials
FEV-POST/ESP10 - NCT01913808
Disease Area Clinical Trials
Patient Blood Management

Report adverse events in the UK


Adverse events should be reported. Reporting forms and
information for United Kingdom can be found at https://
yellowcard.mhra.gov.uk/ or search for MHRA Yellow Card in the
Google Play or Apple App Store. Adverse events should also be
reported to Vifor Pharma Ltd. Tel: +44 1276 853633. E-
mail: medicalInfo_UK@viforpharma.com

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