Intended for licensed healthcare professionals located in the United Kingdom and Republic of Ireland only

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▼ This medicine is subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse events.

Frequently Asked Questions

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FAQ categories

Adverse reactions Dosing and administration Efficacy data Pharmacodynamics and pharmacokinetics Pregnancy and breastfeeding Prescribing information Product details and authorisation Special warnings and precautions for use Storage

Storage

How long is the shelf life for PEMAZYRE®?

The shelf life of PEMAZYRE is 4 years.1

    Reference
  1. PEMAZYRE® (pemigatinib) Summary of Product Characteristics.
How should PEMAZYRE® be stored?

Store PEMAZYRE out of sight and reach of children. PEMAZYRE does not require any special storage conditions.1

    Reference
  1. PEMAZYRE® (pemigatinib) Summary of Product Characteristics.

Can't find the answers you need?

Contact us
Privacy Policy Cookie Policy Terms of Use If you would like to request further medical information, please visit:
https://www.incyteglobalmedicalinformation.com/
Marketing authorisation holder:
United Kingdom
Incyte Biosciences UK Ltd,
First Floor Q1, The Square,
Randalls Way, Leatherhead,
KT22 7TW, UK

Republic of Ireland
Incyte Biosciences Distribution B.V.
Paasheuvelweg 25,
1105 BP Amsterdam, Netherlands

UNITED KINGDOM
Adverse events should be reported. Reporting forms and information can be found at: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store. Adverse events should also be reported to Incyte by calling 00‑800‑0002‑7423.

REPUBLIC OF IRELAND
Adverse events should be reported.Reporting forms and information can be found at HPRA Pharmacovigilance: www.hpra.ie. Adverse events should also be reported to Incyte immediately by phoning the Toll-free phone number 1800‑456‑748.

▼ 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.

This medicinal product has been authorised under a 'conditional approval' scheme. This means that further evidence on this medicinal product is awaited.

IE/PEMA/P/25/0010
Date of preparation: January 2025
Developed and funded by Incyte Biosciences International Sàrl.
© 2025, Incyte. All rights reserved.
PEMAZYRE, the PEMAZYRE logo and the Incyte logo are registered trademarks of Incyte.

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