Veklury® (remdesivir)
Treatment Interruption

Veklury® (remdesivir)

Treatment Interruption

This document summarizes available information regarding Veklury® (remdesivir [RDV]) and treatment interruption or missed doses.

Some data may be outside of the US FDA-approved Prescribing Information. In providing this data, Gilead Sciences, Inc. is not making any representation as to its clinical relevance or to the use of any Gilead product(s). For information about the approved conditions of use of any Gilead drug product, please consult the FDA approved prescribing information.

The full indication, important safety information, and boxed warnings are available at:  www.gilead.com/-/media/files/pdfs/medicines/covid-19/veklury/veklury_pi.  

Available Data in Treatment Interruption or Missed Doses

There are no data regarding treatment interruption or missed dose management for RDV, including stopping, re-starting, or resuming RDV.

Literature Search

A literature search was conducted in Ovid MEDLINE and Embase databases for studies published between 1946 and 5 February 2025 using the search terms of Veklury, remdesivir, treatment interruption, missed dose, adherence and related search terms. No relevant citations were found.

Abbreviations

RDV=remdesivir
 

Product Label

For the full indication, important safety information, and boxed warning(s), please refer to the Veklury US Prescribing Information available at:
www.gilead.com/-/media/files/pdfs/medicines/covid-19/veklury/veklury_pi

Follow Up

For any additional questions, please contact Gilead Medical Information at:

☎1‐866‐MEDI‐GSI (1‐866‐633‐4474) or   www.askgileadmedical.com

Adverse Event Reporting

Please report all adverse events to:

Gilead Global Patient Safety ☎ 1-800-445-3235, option 3 or
 www.gilead.com/utility/contact/report-an-adverse-event

FDA MedWatch Program by ☎ 1-800-FDA-1088 or MedWatch, FDA, 5600 Fishers Ln, Rockville, MD 20852 or   www.accessdata.fda.gov/scripts/medwatch

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