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Hematologic Risk Evaluation and Mitigation Strategies

Risk Evaluation and Mitigation Strategies (REMS) are safety programs to manage the serious risks that can arise from certain drugs or biological products. If a drug or biological product has a high risk, REMS are established by the U.S. Food and Drug Administration (FDA) to ensure that the benefits of the drug will outweigh the risks. There are a number of hematologic therapies that require REMS. ASH is providing the following information to keep physicians apprised of the resources available for hematology-related REMS programs.

The  provides background about REMS and the therapies that require them. 

  • View the newly launched , an interactive web-based tool that allows for analysis and visualization of the REMS data files.

The following list provides information about the hematologic therapies that require REMS and links for providers about their respective REMS programs.

Belantamab Mafodotin (Blenrep)

Visit the website on Duvelisib REMS or a PDF of information from the FDA.

Duvelisib (Copiktra)

Visit the website on Duvelisib REMS or a PDF of information from the FDA.

Darbepoetin (Aranesp)

On April 13, 2017 the FDA announced the elimination of the REMS for .

Epoetin Alfa (Epogen)

On April 13, 2017 the FDA announced the elimination of the REMS for .

Pomalidomide (Pomalyst)

Visit the  website on Pomalidomide REMS or  a PDF of information from the FDA.

Lenalidomide (Revlimid)

Visit the  website on Lenlidomide REMS or  a PDF of information from the FDA.

Thalidomide (Thalomid)

Visit the  website on Thalidomide REMS or  a PDF of information from the FDA.

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