LENALIDOMIDE SANDOZ 5 mg HARD CAPSULES

Introduction

Package Leaflet: Information for the Patient

Lenalidomide Sandoz 2.5 mg hard capsules EFG

Lenalidomide Sandoz 5 mg hard capsules EFG

Lenalidomide Sandoz 10 mg hard capsules EFG

Lenalidomide Sandoz 15 mg hard capsules EFG

Lenalidomide Sandoz 20 mg hard capsules EFG

Lenalidomide Sandoz 25 mg hard capsules EFG

Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.

• Keep this leaflet, you may need to read it again.

If you have any further questions, ask your doctor or pharmacist.

• This medicine has been prescribed for you only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours.
• If you get any side effects, talk to your doctor, pharmacist, or nurse. This includes any possible side effects not listed in this leaflet. See section 4.

Contents of the pack and other information

1. What is Lenalidomide Sandoz and what is it used for
2. What you need to know before you take Lenalidomide Sandoz
3. How to take Lenalidomide Sandoz
4. Possible side effects
5. Storage of Lenalidomide Sandoz
6. Contents of the pack and other information

1. What is Lenalidomide Sandoz and what is it used for

What is Lenalidomide Sandoz

Lenalidomide Sandoz contains the active substance lenalidomide. This medicine belongs to a group of medicines that affect how the immune system works.

What Lenalidomide Sandoz is used for

Lenalidomide is used in adults to:

• Multiple myeloma.
• Myelodysplastic syndromes (MDS).
• Mantle cell lymphoma (MCL).
• Follicular lymphoma.

Multiple myeloma

Multiple myeloma is a type of cancer that affects a specific type of white blood cell called plasma cells. These cells build up in the bone marrow and multiply out of control. This can damage the bones and kidneys.

Multiple myeloma usually cannot be cured. However, the signs and symptoms can be greatly reduced or may disappear for a period of time. This is called a "remission".

Newly diagnosed multiple myeloma: in patients who have undergone a bone marrow transplant

Lenalidomide is used as maintenance treatment after recovering from a bone marrow transplant.

Newly diagnosed multiple myeloma: in patients who cannot be treated with a bone marrow transplant

Lenalidomide is taken with other medicines. These include:

• a chemotherapy medicine called "bortezomib",
• an anti-inflammatory called "dexamethasone",
• a chemotherapy medicine called "melphalan", and
• an immunosuppressant called "prednisone".

You will take these medicines when you start treatment and then continue to take lenalidomide alone.

If you are 75 years or older or have moderate to severe kidney problems, your doctor will monitor you closely before starting treatment.

Multiple myeloma: in patients previously treated

Lenalidomide is taken with an anti-inflammatory called "dexamethasone".

Lenalidomide may slow down the worsening of multiple myeloma symptoms. It has also been shown to delay the return of multiple myeloma after treatment.

Myelodysplastic syndromes (MDS)

MDS are a group of many different blood and bone marrow disorders. The blood cells become abnormal and do not work properly. Patients may experience a variety of signs and symptoms including low red blood cell count (anemia), the need for blood transfusions, and an increased risk of infection.

Lenalidomide is used alone to treat adult patients diagnosed with MDS, when all of the following apply:

• you need regular blood transfusions to treat low red blood cell counts ("transfusion-dependent anemia");
• you have a bone marrow cell abnormality called "isolated deletion 5q cytogenetic abnormality". This means your body does not produce enough healthy blood cells,
• other treatments you have used before are not suitable or have not worked well enough.

Lenalidomide may increase the number of healthy red blood cells your body produces by reducing the number of abnormal cells:

• this may reduce the number of blood transfusions you need. You may not need transfusions at all.

Mantle cell lymphoma (MCL)

MCL is a cancer of part of the immune system (lymph tissue). It affects a type of white blood cell called "B lymphocytes" or B cells. MCL is a disease in which B cells grow out of control and build up in lymph tissue, bone marrow, or blood. Lenalidomide is used alone to treat adult patients who have previously been treated with other medicines.

Follicular lymphoma (FL)

FL is a slow-growing cancer that affects B lymphocytes. These are a type of white blood cell that helps the body fight infection. When someone has FL, they may have too many of these B lymphocytes in their blood, bone marrow, lymph nodes, and spleen.

Lenalidomide is used with another medicine called "rituximab" to treat adult patients who have previously been treated for follicular lymphoma.

How lenalidomide works

Lenalidomide works by affecting the immune system and directly attacking the cancer.

It works in several ways:

• stops the growth of cancer cells,
• stops the growth of blood vessels in the cancer,
• stimulates part of the immune system to attack cancer cells.

2. What you need to know before you take Lenalidomide Sandoz

You must read the package leaflet of all medicines you are going to take in combination with Lenalidomide Sandoz before you start treatment with Lenalidomide Sandoz.

Do not take Lenalidomide Sandoz:

• if you are pregnant, think you may be pregnant or plan to become pregnant, as lenalidomide is expected to be harmful to the fetus(see section 2, "Pregnancy, breastfeeding, and contraception: information for women and men"),
• if you can become pregnant, unless you use effective contraception (see section 2, "Pregnancy, breastfeeding, and contraception: information for women and men"). If you can become pregnant, your doctor will record with each prescription that all necessary measures have been taken and will provide you with this confirmation,
• if you are allergic to lenalidomide or any of the other ingredients of this medicine listed in section 6. If you think you may be allergic, consult your doctor.

If any of these conditions apply to you, do not take lenalidomide. If you are in doubt, consult your doctor.

Warnings and precautions

Consult your doctor, pharmacist, or nurse before you start taking Lenalidomide Sandoz if:

• you have ever had blood clots; during treatment, you have a higher risk of getting blood clots in your veins and arteries,
• you have any signs of infection, such as cough or fever,
• you have or have had a viral infection, especially hepatitis B, varicella-zoster, or HIV. If you are in doubt, consult your doctor. Treatment with lenalidomide may cause the virus to become active again in patients who carry the virus, leading to the return of the infection. Your doctor should check if you have ever had a hepatitis B infection,
• you have kidney problems; your doctor may adjust your dose of lenalidomide,
• you have had a heart attack, have ever had a blood clot, or if you smoke, have high blood pressure, or high cholesterol levels,
• you have had an allergic reaction while using thalidomide (another medicine used to treat multiple myeloma), such as a skin rash, itching, swelling, dizziness, or breathing problems,
• you have experienced in the past a combination of any of the following symptoms: rash on the face or generalized, skin redness, high fever, flu-like symptoms, increased liver enzymes, blood abnormalities (eosinophilia), swollen lymph nodes (symptoms of a severe skin reaction called DRESS, drug reaction with eosinophilia and systemic symptoms; see also section 4 "Possible side effects").

If any of these conditions apply to you, inform your doctor before starting treatment.

At any time during or after treatment, contact your doctor or nurse immediately if you:

• have blurred vision, loss of vision, or double vision, difficulty speaking, weakness in an arm or leg, a change in the way you walk, or balance problems, numbness, decreased sensitivity, or loss of sensitivity, memory loss, or confusion. These may be symptoms of a serious and potentially life-threatening brain disease called progressive multifocal leukoencephalopathy (PML). If you have any of these symptoms before starting treatment with lenalidomide, inform your doctor if you notice any change in these symptoms.
• have shortness of breath, tiredness, dizziness, chest pain, faster heartbeat, or swelling in your legs or ankles. These may be symptoms of a serious condition called pulmonary hypertension (see section 4).

Tests and examinations

Before starting treatment with lenalidomide and during treatment, you will have regular blood tests, as lenalidomide may cause a decrease in the blood cells that help fight infections (white blood cells) and those involved in blood clotting (platelets).

Your doctor will ask you to have a blood test:

• before treatment,
• every week during the first 8 weeks of treatment,
• then at least every month.

You may be evaluated for signs of heart and lung problems before and during treatment with lenalidomide.

For patients with MDS taking lenalidomide

If you have MDS, you may be more likely to develop a more advanced disease called acute myeloid leukemia (AML). Additionally, it is not known how lenalidomide affects the chances of developing AML. Your doctor may therefore perform tests to detect signs that may predict a higher chance of developing AML during treatment with lenalidomide.

For patients with MCL taking lenalidomide

Your doctor will ask you to have a blood test:

• before treatment,
• every week during the first 8 weeks (2 cycles) of treatment,
• then every 2 weeks in cycles 3 and 4 (see section 3 "Treatment cycle" for more information),
• after that, at the start of each cycle,
• and at least once a month.

For patients with FL taking lenalidomide

Your doctor will ask you to have a blood test:

• before treatment,
• every week during the first 3 weeks (1 cycle) of treatment;
• then every 2 weeks in cycles 2 to 4 (see section 3 "Treatment cycle" for more information),
• after that, at the start of each cycle, and
• at least every month.

Your doctor may check if you have a high total tumor burden in your body, including the bone marrow. This could lead to a condition in which the tumors break down and produce unusual levels of chemicals in the blood, which can cause kidney failure (this condition is called "tumor lysis syndrome").

Your doctor may examine you to check for changes in your skin, such as red spots or skin rash.

Your doctor may adjust your dose of lenalidomide or interrupt your treatment, depending on the results of your blood tests and your overall condition. If you are a newly diagnosed patient, your doctor may also evaluate your treatment based on your age and other conditions you already have.

Blood donation

You must not donate blood during treatment or for at least 7 days after the end of treatment.

Children and adolescents

The use of lenalidomide is not recommended in children and adolescents under 18 years of age.

Elderly and patients with kidney problems

If you are 75 years or older or have moderate to severe kidney problems, your doctor will monitor you closely before starting treatment.

Other medicines and Lenalidomide Sandoz

Tell your doctor or nurse if you are taking, have recently taken, or might take any other medicines. This is because lenalidomide may affect how other medicines work. Also, some medicines may affect how lenalidomide works.

In particular, tell your doctor or nurse if you are taking any of the following medicines:

• some medicines used to prevent pregnancy, such as oral contraceptives, as they may stop working,
• some medicines used for heart problems, such as digoxin,
• some medicines used to thin the blood, such as warfarin.

Pregnancy, breastfeeding, and contraception: information for women and men

Pregnancy

Women taking lenalidomide

• Do not take lenalidomide if you are pregnant, as it is expected to be harmful to the fetus.
• Do not become pregnant while taking lenalidomide. You must use effective contraception if there is a possibility that you may become pregnant (see "Contraception").
• If you become pregnant during treatment with lenalidomide, stop treatment and inform your doctor immediately.

Men taking lenalidomide

• If your partner becomes pregnant while you are taking lenalidomide, inform your doctor immediately. It is recommended that your partner seeks medical advice.
• You must also use effective contraception (see "Contraception").

Breastfeeding

Do not breastfeed while taking lenalidomide, as it is not known whether lenalidomide passes into breast milk.

Contraception

For women taking lenalidomide

Before starting treatment, ask your doctor if you are able to become pregnant, even if you think it is unlikely.

If you can become pregnant

• you will have pregnancy tests under medical supervision (before each treatment, at least every 4 weeks during treatment, and for at least 4 weeks after the end of treatment) unless it has been confirmed that your fallopian tubes have been blocked (tubal ligation),

And

• you must use effective contraception from at least 4 weeks before starting treatment, during treatment, and for at least 4 weeks after the end of treatment. Your doctor will advise you on the most suitable contraceptive methods.

For men taking lenalidomide

Lenalidomide passes into human semen. If your partner is pregnant or may become pregnant and does not use effective contraception, you must use condoms during treatment and for at least 7 days after the end of treatment, even if you have had a vasectomy. Do not donate semen or sperm during treatment or for at least 7 days after the end of treatment.

Driving and using machines

Do not drive or use machines if you feel dizzy, tired, drowsy, have vertigo, or blurred vision after taking lenalidomide.

Lenalidomide Sandoz contains lactose and sodium

If your doctor has told you that you have an intolerance to some sugars, consult your doctor before taking this medicine.

This medicine contains less than 1 mmol of sodium (23 mg) per capsule; this is essentially "sodium-free".

3. How to Take Lenalidomide Sandoz

Lenalidomide should be administered by a healthcare professional with experience in the treatment of multiple myeloma, MDS, CMML, or MF.

• When lenalidomide is used to treat multiple myeloma in patients who cannot undergo a bone marrow transplant or have undergone other treatments before, it is taken with other medications (see section 1 "What is Lenalidomide Sandoz and what is it used for").
• When lenalidomide is used to treat multiple myeloma in patients who have undergone a bone marrow transplant or to treat patients with MDS or CMML, it is taken alone.
• When lenalidomide is used to treat follicular lymphoma, it is taken with another medication called "rituximab".

Follow the administration instructions for lenalidomide exactly as indicated by your doctor. In case of doubt, consult your doctor or pharmacist.

If you are taking lenalidomide with other medications, you should consult the package insert of those other medications for additional information on their use and effects.

Treatment Cycle

Lenalidomide is taken on certain days during a period of 3 weeks (21 days).

• A "treatment cycle" consists of 21 days.
• Depending on the day of the cycle, you will take one or more medications. However, some days you will not take any medication.
• After completing each 21-day cycle, you should start a new "cycle" for the next 21 days.

Or

Lenalidomide is taken on certain days during a period of 4 weeks (28 days).

• A "treatment cycle" consists of 28 days.
• Depending on the day of the cycle, you will take one or more medications. However, some days you will not take any medication.
• After completing each 28-day cycle, you should start a new "cycle" for the next 28 days.

How Much Lenalidomide Sandoz to Take

Before starting treatment, your doctor will indicate:

• what quantity of lenalidomide you should take,
• what quantity of other medications you should take with lenalidomide, if applicable;
• which days of the treatment cycle you should take each medication.

How and When to Take Lenalidomide Sandoz

• Swallow the capsules whole, preferably with water.
• Do not break, open, or chew the capsules. If the powder from a broken capsule comes into contact with the skin, wash the skin immediately and carefully with water and soap.
• Healthcare professionals, caregivers, and family members should wear disposable gloves when handling the blister or capsule. Afterwards, they should carefully remove the gloves to avoid skin exposure, place them in a sealable polyethylene plastic bag, and dispose of them according to local requirements. Then, they should wash their hands well with water and soap. Pregnant women or those who suspect they may be pregnant should not handle the blister or capsule.
• The capsules can be taken with or without food.
• You should take lenalidomide approximately at the same time on the scheduled days.

Taking this Medication

To remove the capsule from the blister:

• press only one end of the capsule so that it comes out through the foil.
• do not press in the center of the capsule as it may break.

Duration of Treatment with Lenalidomide Sandoz

Lenalidomide is taken in treatment cycles, each cycle lasting 21 or 28 days (see "Treatment Cycle" above). You should continue the treatment cycles until your doctor tells you to stop the treatment.

If you Take More Lenalidomide Sandoz than you Should

If you take more lenalidomide than prescribed, inform your doctor immediately.

In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service, phone: 91 562 04 20, indicating the medication and the amount ingested.

If you Miss a Dose of Lenalidomide Sandoz

If you forget to take lenalidomide at your usual time and

• less than 12 hours have passed: take the capsule immediately;
• more than 12 hours have passed: do not take the capsule. Take the next capsule the next day at the usual time.

If you have any other doubts about the use of this medication, ask your doctor or pharmacist.

4. Possible Adverse Effects

Like all medications, this medication can cause adverse effects, although not all people experience them.

If you experience any of the following serious adverse effects, stop treatment with lenalidomide and consult a doctor immediately, as you may require urgent medical treatment:

• Hives, rash, swelling of the eyes, mouth, or face, difficulty breathing or itching, which can be symptoms of severe allergic reactions called angioedema and anaphylactic reaction.
• Severe allergic reaction that can start as a rash in one area but spreads, causing significant skin loss throughout the body (Stevens-Johnson syndrome and/or toxic epidermal necrolysis).
• Widespread rash, high body temperature, increased liver enzymes, blood abnormalities (eosinophilia), swollen lymph nodes, and effects on other organs of the body (drug reaction with eosinophilia and systemic symptoms, also known as DRESS or drug hypersensitivity syndrome). See also section 2.

Consult your doctor immediately if you notice any of the following serious adverse effects:

• fever, chills, sore throat, cough, mouth ulcers, or any other symptom of infection, including in the bloodstream (sepsis),
• bleeding (bleeding) or bruising (bruising) not due to an injury,
• chest pain (thoracic) or leg pain,
• difficulty breathing,
• bone pain, muscle pain, confusion, or fatigue that may be due to high levels of calcium in the blood.

Lenalidomide may reduce the number of white blood cells that fight infections and also the cells in the blood that help blood to clot (platelets), which can cause bleeding disorders such as nosebleeds and bruising. Lenalidomide can also cause blood clots in the veins (thrombosis).

Other Adverse Effects

It is essential to note that a small number of patients may develop other types of cancer, and this risk may increase with treatment with lenalidomide. Therefore, your doctor should carefully evaluate the benefits and risks when prescribing lenalidomide.

Adverse effects very common(may affect more than 1 in 10 people):

• A decrease in the number of red blood cells, which can cause anemia, leading to fatigue and weakness.
• Skin rash, itching.
• Muscle cramps, muscle weakness, muscle pain, muscle discomfort, bone pain, joint pain, back pain, pain in the limbs.
• Generalized swelling, including swelling of the arms and legs.
• Weakness, fatigue.
• Fever and flu-like symptoms, including fever, muscle pain, headache, ear pain, and chills.
• Numbness, tingling, or a prickling sensation in the skin, pain in the hands or feet, dizziness, tremors.
• Decreased appetite, changes in taste.
• Increased pain, tumor size, or redness around the tumor.
• Weight loss.
• Constipation, diarrhea, nausea, vomiting, stomach pain, heartburn.
• Low levels of potassium, calcium, or sodium in the blood.
• Underactive thyroid function.
• Pain in the legs (which could be a symptom of thrombosis), chest pain, or difficulty breathing (which could be a symptom of blood clots in the lungs, called pulmonary embolism).
• Infections of all kinds, including sinusitis, pneumonia, and upper respiratory tract infections.
• Difficulty breathing.
• Blurred vision.
• Eye opacity (cataracts).
• Kidney problems, including kidney failure or inability to maintain normal kidney function.
• Abnormal liver function test results.
• High liver function test results.
• Changes in a blood protein that can cause swelling of the arteries (vasculitis).
• Increased blood sugar levels (diabetes).
• Decreased blood sugar levels.
• Headache.
• Nosebleeds.
• Dry skin.
• Stomach pain.
• Depression, mood changes, difficulty sleeping.
• Cough.
• Low blood pressure.
• A vague feeling of discomfort in the body, feeling unwell.
• Painful inflammation of the mouth, dry mouth.
• Dehydration.

Adverse effects common(may affect up to 1 in 10 people):

• Destruction of red blood cells (hemolytic anemia)
• Certain types of skin tumors.
• Bleeding from the gums, stomach, or intestines.
• Increased blood pressure, slow, fast, or irregular heartbeat.
• Increased levels of a substance released after normal or abnormal destruction of red blood cells.
• Increased levels of a protein that indicates inflammation in the body.
• Darkening of skin color; change in skin color due to internal bleeding, usually caused by bruising; skin inflammation caused by blood accumulation; bruising.
• Increased uric acid levels in the blood.
• Skin rash, redness of the skin, cracked skin, peeling or flaking of the skin, hives.
• Increased sweating, night sweats.
• Difficulty swallowing, sore throat, difficulty maintaining voice quality or changes in voice
• Runny nose.
• Strong increase or decrease in urine output compared to usual or inability to control urination.
• Blood in the urine.
• Difficulty breathing, especially when lying down (which could be a symptom of heart failure).
• Difficulty having an erection.
• Stroke, fainting, vertigo (inner ear disorder that causes a sensation of spinning), temporary loss of consciousness.
• Chest pain that spreads to the arms, neck, jaw, back, or stomach, sensation of sweating and shortness of breath, nausea or vomiting, which can be symptoms of a heart attack (myocardial infarction).
• Muscle weakness, lack of energy.
• Neck pain, chest pain.
• Chills.
• Swollen joints.
• Slower or blocked bile flow from the liver.
• Low levels of phosphate or magnesium in the blood.
• Difficulty speaking.
• Liver damage.
• Balance disturbance, difficulty moving.
• Deafness, ringing in the ears (tinnitus).
• Pain in the nerves, abnormal and unpleasant sensation, especially when touched.
• Excess iron in the body.
• Thirst.
• Confusion.
• Toothache.
• Fall that can cause injuries.

Adverse effects uncommon(may affect up to 1 in 100 people):

• Bleeding in the brain.
• Circulatory problems.
• Loss of vision.
• Loss of sexual desire (libido).
• Excretion of large amounts of urine with bone pain and weakness, which can be symptoms of a kidney disorder (Fanconi syndrome).
• Yellowing of the skin, mucous membranes, or eyes (jaundice), pale stools, dark urine, itching of the skin, rash, pain or swelling of the stomach; these can be symptoms of liver damage (liver failure).
• Stomach pain, abdominal swelling, or diarrhea, which can be symptoms of inflammation of the large intestine (colitis or typhlitis).
• Damage to kidney cells (called tubular necrosis).
• Changes in skin color, sensitivity to sunlight.
• Tumor lysis syndrome, which can cause metabolic complications during cancer treatment and sometimes even without treatment. These complications occur as a result of the breakdown products of dying cancer cells and can include: changes in blood biochemistry, high levels of potassium, phosphorus, uric acid, and low levels of calcium, which can cause changes in kidney function and heart rhythm, seizures, and sometimes death.
• Increased blood pressure in the blood vessels that supply the lungs (pulmonary hypertension).

Frequency Not Known(cannot be estimated from the available data):

• Sudden, mild, or severe pain in the upper abdomen and/or back that lasts for several days, possibly accompanied by nausea, vomiting, fever, and rapid pulse. These symptoms can be due to pancreatitis.
• Wheezing or whistling when breathing, difficulty breathing, or dry cough, which can be symptoms caused by inflammation of the lung tissue.
• Rare cases of muscle breakdown (pain, weakness, or swelling of the muscles) that can lead to kidney problems (rhabdomyolysis), some of which occur when lenalidomide is administered with a statin (a type of medication to lower cholesterol).
• A disease that affects the skin, caused by inflammation of small blood vessels, accompanied by joint pain and fever (leukocytoclastic vasculitis).
• Rupture of the stomach or intestine wall. This can lead to a severe infection. Inform your doctor if you have severe stomach pain, fever, nausea, vomiting, blood in the stool, or changes in bowel habits.
• Viral infections, including herpes zoster (also known as shingles, a viral disease that causes a painful rash with blisters) and the recurrence of hepatitis B infection (which can cause yellowing of the skin and eyes, dark urine, stomach pain on the right side, fever, and nausea or feeling sick).
• Rejection of solid organ transplants (such as kidney, heart).

Reporting Adverse Effects

If you experience any type of adverse effect, consult your doctor, pharmacist, or nurse, even if it is a possible adverse effect that is not listed in this package insert. You can also report them directly through the Spanish Medication Surveillance System for Human Use: https://www.notificaram.es. By reporting adverse effects, you can contribute to providing more information on the safety of this medication.

5. Storage of Lenalidomide Sandoz

Keep this medication out of the sight and reach of children.

Do not use this medication after the expiration date shown on the box and blister after "EXP". The expiration date is the last day of the month indicated.

This medication does not require special storage conditions.

Do not use this medication if you notice any damage or signs of damage to the packaging.

Medications should not be disposed of through wastewater or household waste. In case of doubt, ask your pharmacist how to dispose of the packaging and medications you no longer need. This will help protect the environment.

6. Package Contents and Additional Information

What Lenalidomide Sandoz contains

Lenalidomide Sandoz 2.5 mg hard capsules:

• The active ingredient is lenalidomide. Each capsule contains 2.5 mg of lenalidomide.
• The other excipients are:
• Capsule content: lactose, microcrystalline cellulose, sodium croscarmellose, and magnesium stearate.
• Capsule shell: gelatin, titanium dioxide (E 171), indigo carmine lake (E 132), and yellow iron oxide (E 172).

(E 132) and yellow iron oxide (E 172).

• Printing ink: shellac, propylene glycol, potassium hydroxide, and black iron oxide (E 172).

Lenalidomide Sandoz 5 mg hard capsules:

• The active ingredient is lenalidomide. Each capsule contains 5 mg of lenalidomide.
• The other excipients are:
• Capsule content: lactose, microcrystalline cellulose, sodium croscarmellose, and magnesium stearate.
• Capsule shell: gelatin and titanium dioxide (E 171).
• Printing ink: shellac, propylene glycol, potassium hydroxide, and black iron oxide (E 172).

Lenalidomide Sandoz 10 mg hard capsules:

• The active ingredient is lenalidomide. Each capsule contains 10 mg of lenalidomide.
• The other excipients are:
• Capsule content: lactose, microcrystalline cellulose, sodium croscarmellose, and magnesium stearate.
• Capsule shell: gelatin, titanium dioxide (E 171), indigo carmine lake (E 132), and yellow iron oxide (E 172).

(E 132) and yellow iron oxide (E 172).

• Printing ink: shellac, propylene glycol, potassium hydroxide, and black iron oxide (E 172).

Lenalidomide Sandoz 15 mg hard capsules:

• The active ingredient is lenalidomide. Each capsule contains 15 mg of lenalidomide.
• The other excipients are:
• Capsule content: lactose, microcrystalline cellulose, sodium croscarmellose, and magnesium stearate.
• Capsule shell: gelatin, titanium dioxide (E 171), and indigo carmine lake (E 132).

(E 132).

• Printing ink: shellac, propylene glycol, potassium hydroxide, and black iron oxide (E 172).

Lenalidomide Sandoz 20 mg hard capsules:

• The active ingredient is lenalidomide. Each capsule contains 20 mg of lenalidomide.
• The other excipients are:
• Capsule content: lactose, microcrystalline cellulose, sodium croscarmellose, and magnesium stearate.
• Capsule shell: gelatin, titanium dioxide (E 171), indigo carmine lake (E 132), and yellow iron oxide (E 172).

(E 132) and yellow iron oxide (E 172).

• Printing ink: shellac, propylene glycol, potassium hydroxide, and black iron oxide (E 172).

Lenalidomide Sandoz 25 mg hard capsules:

• The active ingredient is lenalidomide. Each capsule contains 25 mg of lenalidomide.
• The other excipients are:
• Capsule content: lactose, microcrystalline cellulose, sodium croscarmellose, and magnesium stearate.
• Capsule shell: gelatin and titanium dioxide (E 171).
• Printing ink: shellac, propylene glycol, potassium hydroxide, and black iron oxide (E 172).

Appearance and Package Contents

Lenalidomide Sandoz 2.5 mg hard capsules:

White opaque body and green to light green opaque cap, with an approximate length of 14.3 mm, marked with “L9NL” and “2.5”.

Lenalidomide Sandoz 5 mg hard capsules:

White opaque body and white opaque cap, with an approximate length of 18.0 mm, marked with “L9NL” and “5”.

Lenalidomide Sandoz 10 mg hard capsules:

Yellow opaque body and green to light green opaque cap, with an approximate length of 21.7 mm, marked with “L9NL” and “10”.

Lenalidomide Sandoz 15 mg hard capsules:

White opaque body and blue to light blue opaque cap, with an approximate length of 21.7 mm, marked with “L9NL” and “15”.

Lenalidomide Sandoz 20 mg hard capsules:

Blue to light blue opaque body and green to light green opaque cap, with an approximate length of 21.7 mm, marked with “L9NL” and “20”.

Lenalidomide Sandoz 25 mg hard capsules:

White opaque body and white opaque cap, with an approximate length of 21.7 mm, marked with “L9NL” and “25”.

The hard capsules are packaged in:

OPA/Al/PVC/Al blisters

OPA/Al/PVC/Al calendarized blisters.

OPA/Al/PVC/Al single-dose perforated blisters.

OPA/Al/PVC/Al single-dose perforated calendarized blisters.

Package sizes:

OPA/Al/PVC/Al blisters: packages containing 7, 14, 21, 28, 42 hard capsules.

OPA/Al/PVC/Al calendarized blisters: packages containing 7, 14, 21, 28, and 42 capsules, 1, 2, 3, 4, and 6 calendarized blisters of 7 hard capsules each.

OPA/Al/PVC/Al single-dose perforated blisters: packages containing 7 x 1, 14 x 1, 21 x 1, 28 x 1 hard capsules.

OPA/Al/PVC/Al single-dose perforated calendarized blisters: packages containing 7 x 1, 14 x 1, 21 x 1, 28 x 1 hard capsules.

Only some package sizes may be marketed.

Marketing Authorization Holder and Manufacturer

Marketing Authorization Holder

Sandoz Farmacéutica, S.A.

Centro Empresarial Parque Norte

Edificio Roble

C/ Serrano Galvache, 56

28033 Madrid

Spain

Manufacturer

Synthon B.V.

Microweg 22

6545 CM

Nijmegen

Netherlands

or

Synthon Hispania, S.L.

C/ Castelló, nº 1

Sant Boi de Llobregat

08830 Barcelona

Spain

or

Salutas Pharma GmbH

Otto-von-Guericke-Alle 1

39179 Barleben

Germany

This medicinal product is authorized in the Member States of the European Economic Area and in the United Kingdom (Northern Ireland) under the following names:

Germany:Lenalidomid HEXAL 2.5mg/5 mg/7.5 mg/10 mg/15 mg/20 mg/25 mg Hartkapseln

Croatia:Lenalidomid Sandoz 2.5 mg/10 mg/15 mg/25 mg hard capsules

Denmark:Lenalidomida Sandoz

Slovakia:Lenalidomid Sandoz 2.5 mg/5 mg/10 mg/15 mg/25 mg

Slovenia:Lenalidomid Sandoz 2.5 mg/5 mg/7.5 mg/10 mg/15 mg/20 mg/25 mg trde kapsule

Estonia:Lenalidomide Sandoz

Spain:Lenalidomida Sandoz 2.5 mg/5 mg/10 mg/15 mg/20 mg/25 mg hard capsules EFG

Finland:Lenalidomide Sandoz 2.5 mg/5 mg/7.5 mg/10 mg/15 mg/20 mg/25 mg kapselit, kovat

France:LENALIDOMIDE SANDOZ 2.5 mg/5 mg/7.5 mg/10 mg/15 mg/20 mg/25 mg, gélule

Greece:Lenalidomide/Sandoz

Netherlands:Lenalidomide Sandoz 2.5 mg/5 mg/7.5 mg/10 mg/15 mg/20 mg/25 mg, harde capsules

Iceland:Lenalidomide Sandoz 2.5 mg hard capsule

Italy:Lenalidomide Sandoz

Latvia:Lenalidomide Sandoz 2.5 mg/5 mg/10 mg/15 mg/25 mg cietas kapsulas

Norway:Lenalidomide Sandoz

Poland:Lenalidomide Sandoz

Romania:Lenalidomida Sandoz 2.5 mg/5 mg/7.5 mg/10 mg/15 mg/20 mg/25 mg capsule

Sweden:Lenalidomide Sandoz 2.5 mg/5 mg/7.5 mg/10 mg hårda kapslar

United Kingdom (Northern Ireland):Lenalidomide Sandoz 2.5 mg/5 mg/7.5 mg/10 mg/15 mg/20 mg/25 mg hard capsules

Date of last revision of this leaflet: 06/2023.

Detailed information on this medicinal product is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/