sofidexFor patientsAre you a clinician? Clinical site

Meds & supplements  ›  Pomalidomide

Medicine · Thalidomide Analog

Pomalidomide

Pomalidomide capsules are a thalidomide analogue indicated for the treatment of adult patients: in combination with dexamethasone, for patients with multiple myeloma (MM) who have received at least two prior therapies including…

Medication guideLabel updated 2026-01-30

Selected manufacturer label information, organised into consistent sections by Sofidex. Read the full label at DailyMed ↗

Boxed warning

WARNING: EMBRYO-FETAL TOXICITY and VENOUS AND ARTERIAL THROMBOEMBOLISM Embryo-Fetal Toxicity Pomalidomide is contraindicated in pregnancy. Pomalidomide is a thalidomide analogue. Thalidomide is a known human teratogen that causes severe birth defects or embryo-fetal death. In females of reproductive potential, obtain 2 negative pregnancy tests before starting pomalidomide treatment. Females of reproductive potential must use 2 forms of contraception or continuously abstain from heterosexual sex during and for 4 weeks after stopping pomalidomide treatment. Pomalidomide is only available through a restricted distribution program called PS-Pomalidomide REMS. Information about PS-Pomalidomide REMS is available at www.PS-PomalidomideREMS.com or by calling the REMS Call Center at 1-888-423-5436. Venous and Arterial Thromboembolism Deep venous thrombosis (DVT), pulmonary embolism (PE), myocardial infarction, and stroke occur in patients with multiple myeloma treated with pomalidomide. Prophylactic antithrombotic measures were employed in clinical trials. Thromboprophylaxis is recommended, and the choice of regimen should be based on assessment of the patient's underlying risk factors. WARNING: EMBRYO-FETAL TOXICITY and VENOUS AND ARTERIAL THROMBOEMBOLISM See full prescribing information for complete boxed warning EMBRYO-FETAL TOXICITY Pomalidomide is contraindicated in pregnancy. Thalidomide is a known human teratogen that causes severe life-threatening birth defects. For females of reproductive potential: Exclude pregnancy before start of treatment. Prevent pregnancy during treatment by the use of 2 reliable methods of contraception. Pomalidomide is available only through a restricted program called PS- Pomalidomide REMS. Antithrombotic prophylaxis is recommended.

Drug facts

Used for
  • in combination with dexamethasone, for patients with multiple myeloma (MM) who have received at least two prior therapies including lenalidomide and a proteasome inhibitor and have demonstrated disease progression on or within 60 days of completion of the last therapy . with AIDS-related Kaposi sarcoma (KS) after failure of highly active antiretroviral therapy (HAART) or in patients with KS who are HIV-negative. This indication is approved under accelerated approval based on overall response rate. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial(s) . 1.1 Multiple Myeloma Pomalidomide
  • in combination with dexamethasone, are indicated for adult patients with multiple myeloma (MM) who have received at least two prior therapies including lenalidomide and a proteasome inhibitor and have demonstrated disease progression on or within 60 days of completion of the last therapy. 1.2 Kaposi Sarcoma Pomalidomide capsules are indicated
  • for the treatment of: Adult patients with AIDS-related Kaposi sarcoma (KS) after failure of highly active antiretroviral therapy (HAART). Kaposi sarcoma (KS) in adult patients who are HIV-negative. This indication is approved under accelerated approval based on overall response rate . Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial(s).
How to take it
Take pomalidomide exactly as prescribed and follow all the instructions of PS-Pomalidomide REMS.

What it is used for

Pomalidomide capsules are a thalidomide analogue indicated for the treatment of adult patients: in combination with dexamethasone, for patients with multiple myeloma (MM) who have received at least two prior therapies including lenalidomide and a proteasome inhibitor and have demonstrated disease progression on or within 60 days of completion of the last therapy.

with AIDS-related Kaposi sarcoma (KS) after failure of highly active antiretroviral therapy (HAART) or in patients with KS who are HIV-negative. This indication is approved under accelerated approval based on overall response rate. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial(s).

1.1 Multiple Myeloma Pomalidomide, in combination with dexamethasone, are indicated for adult patients with multiple myeloma (MM) who have received at least two prior therapies including lenalidomide and a proteasome inhibitor and have demonstrated disease progression on or within 60 days of completion of the last therapy.

1.2 Kaposi Sarcoma Pomalidomide capsules are indicated for the treatment of: Adult patients with AIDS-related Kaposi sarcoma (KS) after failure of highly active antiretroviral therapy (HAART). Kaposi sarcoma (KS) in adult patients who are HIV-negative. This indication is approved under accelerated approval based on overall response rate.

Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial(s).

The most important thing to know

Before you begin taking pomalidomide capsules, you must read and agree to all of the instructions in PS-Pomalidomide REMS. For more information, call 1-888-423-5436 or go to www.PS-PomalidomideREMS.com. Before prescribing pomalidomide capsules, your healthcare provider will explain PS-Pomalidomide REMS to you and have you sign the Patient-Physician Agreement Form.

Pomalidomide capsules can cause serious side effects including: Possible birth defects (deformed babies) or death of an unborn baby. Females who are pregnant or who plan to become pregnant must not take pomalidomide capsules. Pomalidomide capsules are similar to the medicine thalidomide (THALOMID). We know thalidomide can cause severe life-threatening birth defects.

Pomalidomide capsules have not been tested in pregnant females. Pomalidomide capsules have harmed unborn animals in animal testing. Females must not get pregnant: o For at least 4 weeks before starting pomalidomide capsules o While taking pomalidomide capsules o During any breaks (interruptions) in your treatment with pomalidomide capsules o For at least 4 weeks after stopping pomalidomide capsules Females who can become pregnant: o Will have pregnancy tests weekly for 4 weeks, then every 4 weeks if your menstrual cycle is regular, or every 2 weeks if your menstrual cycle is irregular.

If you miss your period or have unusual bleeding, you will need to have a pregnancy test and receive counseling. o Must agree to use two acceptable forms of birth control at the same time, for at least 4 weeks before, while taking, during any breaks (interruptions) in your treatment, and for at least 4 weeks after stopping pomalidomide capsules.

o Talk with your healthcare provider to find out about options for acceptable forms of birth control that you may use to prevent pregnancy before, during, and after treatment with pomalidomide capsules. If you become pregnant while taking pomalidomide capsules, stop taking it right away and call your healthcare provider.

If your healthcare provider is not available, you can call the REMS Call Center at 1-888-423-5436. Healthcare providers and patients should report all cases of pregnancy to: o FDA MedWatch at 1-800-FDA-1088, and o REMS Call Center at 1-888-423-5436 There is a pregnancy exposure registry that monitors the outcomes of females who take pomalidomide capsules during pregnancy, or if their male partner takes pomalidomide capsules and they are exposed during pregnancy.

You can enroll in this registry by calling the REMS Call Center at the phone number listed above. Pomalidomide can pass into human semen: o Males, including those who have had a vasectomy, must always use a latex or synthetic condom during any sexual contact with a pregnant female or a female that can become pregnant while taking pomalidomide capsules, during any breaks (interruptions) in your treatment with pomalidomide capsules, and for 4 weeks after stopping pomalidomide capsules.

o Do not have unprotected sexual contact with a female who is or could become pregnant. Tell your healthcare provider if you do have unprotected sexual contact with a female who is or could become pregnant. o Do not donate sperm while taking pomalidomide capsules, during any breaks (interruptions) in your treatment, and for 4 weeks after stopping pomalidomide capsules.

If a female becomes pregnant with your sperm, the baby may be exposed to pomalidomide capsules and may be born with birth defects. Men, if your female partner becomes pregnant, you should call your healthcare provider right away. Blood clots in your arteries, veins, and lungs, heart attack, and stroke can happen if you take pomalidomide capsules.

Most people who take pomalidomide capsules will also take a blood thinner medicine to help prevent blood clots. Before taking pomalidomide capsules, tell your healthcare provider: o If you have had a blood clot in the past o If you have high blood pressure, smoke, or if you have been told you have a high level of fat in y

How to take it

Take pomalidomide exactly as prescribed and follow all the instructions of PS-Pomalidomide REMS. Swallow pomalidomide capsules whole with water 1 time a day. Do not break, chew, or open your capsules. Pomalidomide capsules may be taken with or without food. Take pomalidomide capsules at about the same time each day. If you are on hemodialysis, take pomalidomide capsules after hemodialysis, on hemodialysis days.

Do not open the pomalidomide capsules or handle them any more than needed. If you touch a broken pomalidomide capsule or the medicine in the capsule, wash the area of your body right away with soap and water. If you miss a dose of pomalidomide capsules and it has been less than 12 hours since your regular time, take it as soon as you remember.

If it has been more than 12 hours, just skip your missed dose. Do not take 2 doses at the same time. If you take too much pomalidomide, call your healthcare provider right away.

Side effects, and when to stop

Pomalidomide capsules can cause serious side effects, including: Low white blood cells (neutropenia), low platelets (thrombocytopenia), and low red blood cells (anemia) are common with pomalidomide capsules, but can also be serious. You may need a blood transfusion or certain medicines if your blood counts drop too low.

Your blood counts should be checked weekly for the first 8 weeks of treatment and monthly after that. Severe liver problems, including liver failure and death. Your healthcare provider should do blood tests to check your liver function during your treatment with pomalidomide capsules. Tell your healthcare provider right away if you develop any of the following symptoms of liver problems: o Yellowing of your skin or the white part of your eyes (jaundice) o Pain on the upper right side of your stomach area (abdomen) o Dark or brown (tea-colored) urine o Bleeding or bruising more easily than normal o Feeling very tired Severe allergic reactions and severe skin reactions can happen with pomalidomide capsules and may cause death.

Call your healthcare provider if you develop any of the following signs or symptoms during treatment with pomalidomide capsules: o a red, itchy, skin rash o peeling of your skin or blisters o severe itching o fever Get emergency medical help right away if you develop any of the following signs or symptoms during treatment with pomalidomide capsules: o swelling of your lips, mouth, tongue, or throat o a very fast heartbeat o trouble breathing or swallowing o you feel dizzy or faint o raised red areas on your skin (hives) Dizziness and confusion.

See “What should I avoid while taking pomalidomide capsules?” Nerve damage. Stop taking pomalidomide capsules and call your healthcare provider if you develop symptoms of nerve damage including: numbness, tingling, pain, burning sensation in your hands, legs, or feet. Risk of new cancers (malignancies). New cancers, including certain blood cancers (acute myelogenous leukemia or AML) have been seen in people who received pomalidomide capsules.

Talk with your healthcare provider about your risk of developing new cancers if you take pomalidomide capsules. Tumor lysis syndrome (TLS). TLS is caused by the fast breakdown of cancer cells. TLS can cause kidney failure and the need for dialysis treatment, abnormal heart rhythm, seizure, and sometimes death. Your healthcare provider may do blood tests to check you for TLS.

Your healthcare provider may tell you to stop taking pomalidomide capsules if you develop certain serious side effects during treatment. The most common side effects of pomalidomide capsules in people with Multiple Myeloma include: o tiredness and weakness o diarrhea o back pain o constipation o shortness of breath o fever o nausea o upper respiratory tract infection The most common side effects of pomalidomide capsules in people with KS include: o tiredness o nausea o diarrhea o constipation o abnormal kidney function tests o increased blood sugar o decreased phosphate and calcium in the blood o decreased albumin in the blood o rash.

See “Severe allergic reactions and severe skin reactions” above. These are not all the possible side effects of pomalidomide capsules. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

Who should not take it

Do not take pomalidomide capsules if you: are pregnant, plan to become pregnant, or become pregnant during treatment with pomalidomide capsules. are allergic to pomalidomide or any of the ingredients in pomalidomide capsules. See the end of this Medication Guide for a complete list of ingredients in pomalidomide capsules.

What to say before you start

Before you take pomalidomide capsules, tell your healthcare provider if you: smoke cigarettes. Pomalidomide capsules may not work as well in people who smoke have liver problems have kidney problems and are receiving hemodialysis treatment have any other medical conditions are breastfeeding. You should not breastfeed during treatment with pomalidomide capsules.

It is not known if pomalidomide passes into your breast milk and can harm your baby. Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. Pomalidomide capsules and other medicines may affect each other, causing serious side effects.

Talk with your healthcare provider before taking any new medicines. Know the medicines you take. Keep a list of them to show your healthcare provider and pharmacist.

What to avoid

Females: Do not get pregnant and do not breastfeed while taking pomalidomide capsules. Males: Do not donate sperm. Do not share pomalidomide capsules with other people. It may cause birth defects and other serious problems. Do not donate blood while you take pomalidomide capsules, during any breaks (interruptions) in your treatment, and for 4 weeks after stopping pomalidomide capsules.

If someone who is pregnant gets your donated blood, her baby may be exposed to pomalidomide capsules and may be born with birth defects. Pomalidomide capsules can cause dizziness and confusion. Avoid taking other medicines that may cause dizziness and confusion during treatment with pomalidomide capsules. Avoid situations that require you to be alert until you know how pomalidomide capsules affects you.

Storing it

Store pomalidomide capsules at room temperature between 68° to 77°F (20° to 25°C). Return any unused pomalidomide capsules to PS-Pomalidomide REMS by calling 1-888-423-5346. or your healthcare provider. Keep pomalidomide capsules and all medicines out of the reach of children.

Cite this page

NLM

sofidex [Internet]. Daloreum; c2026. Pomalidomide; [reviewed 2026 Aug 2; cited 2026 Nov 10]. Available from: https://sofidex.com/patients/medicines/pomalidomide

APA 7th

sofidex. (2026, August 2). Pomalidomide. Daloreum. Retrieved November 10, 2026, from https://sofidex.com/patients/medicines/pomalidomide

AMA 11th

Pomalidomide. sofidex. Reviewed August 2, 2026. Accessed November 10, 2026. https://sofidex.com/patients/medicines/pomalidomide

The cited date is today’s, because a citation records when you read the page. The reviewed date is when a clinician last checked it.