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Lenalidomide

Lenalidomide is an active ingredient of the class «immunosuppressive drug».

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Pair of enantiomers

Informational only — not medical advice. Ask a doctor or pharmacist; never change a dose on your own.

Boxed warning (US label)

EMBRYO-FETAL TOXICITY, HEMATOLOGIC TOXICITY, and VENOUS and ARTERIAL THROMBOEMBOLISM Embryo-Fetal Toxicity Do not use REVLIMID during pregnancy.

What it is used for

REVLIMID is a thalidomide analogue indicated for the treatment of adult patients with: • Multiple myeloma (MM), in combination with dexamethasone. • MM, as maintenance following autologous hematopoietic stem cell transplantation (auto-HSCT). • Transfusion-dependent anemia due to low- or…

US label

Multiple myeloma Revlimid as monotherapy is indicated for the maintenance treatment of adult patients with newly diagnosed multiple myeloma who have undergone autologous stem cell transplantation.

EMA

How it works

Class: immunosuppressive drug

Common side effects

The following clinically significant adverse reactions are described in detail in other sections of the prescribing information: o Embryo-Fetal Toxicity o Hematologic Toxicity o Venous and Arterial Thromboembolism o Increased Mortality in Patients with CLL o Second Primary Malignancies o Increased Mortality in…

US label

Who should not take it

Pregnancy ( Boxed Warning, 4.1, 5.1, 8.1 ). • Demonstrated severe hypersensitivity to lenalidomide. 4.1 Pregnancy REVLIMID can cause fetal harm when administered to a pregnant female.

US label

Pregnancy and breastfeeding

Exposure Registry There is a pregnancy exposure registry that monitors pregnancy outcomes in females exposed to REVLIMID during pregnancy as well as female partners of male patients who are exposed to REVLIMID. This registry is also used to understand the…

Excerpts from the US prescribing label (public domain), copied without changes.

Interactions

Recorded interactions from open sources (Wikidata, US labels). The list is not complete — ask a pharmacist.

Brand names

United States

Revlimid

European Union

Lenalidomide Accord · Lenalidomide Krka d.d. Novo mesto (previously Lenalidomide Krka) · Lenalidomide Krka (previously Lenalidomide Krka d.d. Novo mesto) · Lenalidomide Mylan · Revlimid

Canada

Apo-Lenalidomide · Eugia-Lenalidomide · Jamp Lenalidomide · Nat-Lenalidomide · Reddy-Lenalidomide · Revlimid · Sandoz Lenalidomide · Taro-Lenalidomide

Other trade names

Lenalidomide krka d.d.

Approval status

US Food and Drug Administration
prescription · since 2005
European Medicines Agency
authorised · since 2007
Health Canada
prescription · marketed
First approval anywhere
2005

Codes

ATC
L04AX04, L04AX07
RxNorm CUI
342369
ChEMBL
CHEMBL848
PubChem CID
216326
UNII
F0P408N6V4
Wikidata
Q425681

Frequently asked questions

What is Lenalidomide used for?

Lenalidomide is used for: Chronic myelomonocytic leukemia, Chronic lymphocytic leukemia, Non-Hodgkin lymphoma, Central nervous system lymphoma, Myelofibrosis, Waldenström macroglobulinemia, Mature T-cell and NK-cell lymphoma, and Lymphoblastic leukemia.

What kind of medicine is Lenalidomide?

Lenalidomide is an active ingredient of the class «immunosuppressive drug».

What are the brand names of Lenalidomide?

Brand names of Lenalidomide include Revlimid, Lenalidomide Accord, Lenalidomide Krka d.d. Novo mesto (previously Lenalidomide Krka), Lenalidomide Krka (previously Lenalidomide Krka d.d. Novo mesto), Lenalidomide Mylan, Apo-Lenalidomide, Eugia-Lenalidomide, and Jamp Lenalidomide.

Medicines in the same class

Sources and licences

Updated November 15, 2026