Archive for the ‘antibiotics/antineoplastics’ Category

Valstar

Valstar

Valstar is used for:

Treating certain types of bladder cancer in certain patients.

Valstar is an anthracycline cytotoxic agent. It works by preventing the cancer cell from reproducing, which results in death of the cancer cell.

Do NOT use Valstar if:

Contact your doctor or health care provider right away if any of these apply to you.

Before using Valstar :

Some medical conditions may interact with Valstar . Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

Some MEDICINES MAY INTERACT with Valstar . Because little, if any, of Valstar is absorbed into the blood, the risk of it interacting with another medicine is low.

Ask your health care provider if Valstar may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Valstar :

Use Valstar as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Ask your health care provider any questions you may have about how to use Valstar .

Important safety information:

Possible side effects of Valstar :

All medicines may cause side effects, but many people have no, or minor, side effects.

Bladder pain or spasm; burning or discomfort of the urethra; headache; irritable bladder symptoms (eg, frequent or painful urination, urgent need to urinate); loss of bladder control; mild dizziness, weakness, or tiredness; nausea; stomach pain.

Severe allergic reactions (difficulty breathing; hives; itching; rash; swelling of the mouth, face, lips, or tongue; tightness in the chest); blood in the urine; chest pain; fever; inability to urinate; persistent red discoloration of the urine; severe or persistent bladder pain or spasms; severe or persistent painful urination, trouble urinating, or urinary urgency.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects at

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center (

Valstar is usually handled and stored by a health care provider. If you are using Valstar at home, store Valstar as directed by your pharmacist or health care provider. Keep Valstar out of the reach of children and away from pets.

General information:

This information is a summary only. It does not contain all information about Valstar . If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

More Valstar resources

Compare Valstar with other medications for the treatment of:

Nipent

Nipent

The use of doses higher than specified by the manufacturer of Nipent is not recommended. Severe kidney, liver, lung, and central nervous system problems (toxicities) have occurred in some studies when using higher than recommended doses. Nipent is not recommended for use with fludarabine. The use of pentostatin in combination with fludarabine has caused severe lung problems; in some cases, this has led to death. Ask your doctor or pharmacist for more information.

Nipent is used for:

Treating certain types of cancer.

Nipent is an antineoplastic. How it prevents growth of cancer cells is unknown.

Do NOT use Nipent if:

Contact your doctor or health care provider right away if any of these apply to you.

Before using Nipent :

Some medical conditions may interact with Nipent . Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

Some MEDICINES MAY INTERACT with Nipent . Tell your health care provider if you are taking any other medicines, especially any of the following:

This may not be a complete list of all interactions that may occur. Ask your health care provider if Nipent may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Nipent :

Use Nipent as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Ask your health care provider any questions you may have about how to use Nipent .

Important safety information:

Possible side effects of Nipent :

All medicines may cause side effects, but many people have no, or minor, side effects.

Diarrhea; fatigue; headache; loss of appetite; muscle pain; nausea; vomiting; weakness.

Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); chills; cough; eye pain or changes in vision; fever; hoarseness; itching; pain, redness, or swelling at the injection site; sore throat; sores on the mouth or lips; unusual bruising or bleeding; unusual tiredness or weakness

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects at

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center (

Nipent is usually handled and stored by a health care provider. If you are using Nipent at home, store Nipent as directed by your pharmacist or health care provider.

General information:

This information is a summary only. It does not contain all information about Nipent . If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

More Nipent resources

Compare Nipent with other medications for the treatment of:

Mutamycin

Mutamycin

Mutamycin may cause bone marrow suppression, which may cause severe blood problems such as low platelet levels (thrombocytopenia) and low white blood cell levels (leukopenia). These blood problems may increase your risk of developing severe bleeding or a severe and possibly fatal infection. Mutamycin may also increase your risk of developing hemolytic uremic syndrome (HUS), which may cause problems such as hemolytic anemia, low platelet count, and permanent kidney failure. HUS may occur at any time during treatment. Higher doses may increase your risk for developing this side effect. Blood transfusions may make the symptoms of this syndrome worse. Notify your doctor immediately if you develop symptoms of an infection (eg, fever, chills, persistent sore throat), fatigue, unusual bleeding or bruising, or a change in the amount of urine produced.

Mutamycin is used for:

Treating cancer of the stomach or pancreas in combination with other medicines. It may also be used to reduce the severity of these cancers when they have not responded to other treatments. It may also be used for other conditions as determined by your doctor.

Mutamycin is an antibiotic that has been shown to have action against tumors. It works by blocking growth of the cancer cell.

Do NOT use Mutamycin if:

Contact your doctor or health care provider right away if any of these apply to you.

Before using Mutamycin :

Some medical conditions may interact with Mutamycin . Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

Some MEDICINES MAY INTERACT with Mutamycin . Tell your health care provider if you are taking any other medicines, especially any of the following:

This may not be a complete list of all interactions that may occur. Ask your health care provider if Mutamycin may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Mutamycin :

Use Mutamycin as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Ask your health care provider any questions you may have about how to use Mutamycin .

Important safety information:

Possible side effects of Mutamycin :

All medicines may cause side effects, but many people have no, or minor, side effects.

Hair loss; loss of appetite; nausea; vomiting.

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); chest pain; decreased urination; dizziness; dry cough; fever, chills, or sore throat; pain, redness, or swelling at the injection site; shortness of breath; sores or swelling of the mouth, lips, hands, or feet; unusual bruising or bleeding; unusual tiredness or weakness.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects at

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center (

Mutamycin is usually handled and stored by a health care provider. If you are using Mutamycin at home, store Mutamycin as directed by your pharmacist or health care provider.

General information:

This information is a summary only. It does not contain all information about Mutamycin . If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

More Mutamycin resources

Compare Mutamycin with other medications for the treatment of:

Mithracin

Mithracin

Generic Name: plicamycin (plih CA my sin)

What is Mithracin (plicamycin)?

Plicamycin is a cancer (antineoplastic) medication. Plicamycin interferes with the growth of cancer cells and slows their growth and spread in the body.

Plicamycin is used to treat cancer of the testicles. Plicamycin is also used in the treatment of treat too much calcium in the blood (hypercalcemia) and too much calcium in the urine (hypercalciuria) associated with a variety of advanced forms of cancer.

Plicamycin may also be used for purposes other than those listed in this medication guide.

What is the most important information I should know about Mithracin (plicamycin)?

Plicamycin should only be administered under the supervision of a qualified healthcare provider experienced in the use of cancer chemotherapeutic agents.

Serious side effects have been reported with the use of plicamycin including: allergic reactions (difficulty breathing; closing of the throat; swelling of the lips, tongue, or face; or hives); decreased bone marrow function and blood problems (extreme fatigue; easy bruising or bleeding; black, bloody or tarry stools; fever or chills; or signs of infection such as fever; chills, or sore throat); severe nausea, vomiting, diarrhea, and loss of appetite; and others. Talk to your doctor about the possible side effects from treatment with plicamycin.

Plicamycin should not be used in women who are or may become pregnant.

Who should not take Mithracin (plicamycin)?

Before taking plicamycin, tell your doctor if you have

bone marrow problems; or

a bleeding disorder.

You may not be able to take plicamycin, or you may require a dosage adjustment or special monitoring during treatment if you have any of the conditions listed above.

Plicamycin is in the FDA pregnancy category X. This means that plicamycin is known to cause birth defects in an unborn baby. Plicamycin may also affect egg production in women and sperm production in men. Do not take plicamycin if you are pregnant or could become pregnant during treatment. Contraceptive measures are recommended during treatment with plicamycin. It is not known whether plicamycin passes into breast milk. Do not take plicamycin without first talking to your doctor if you are breast feeding a baby.

How should I take Mithracin (plicamycin)?

Plicamycin should only be administered under the supervision of a qualified healthcare provider experienced in the use of cancer chemotherapeutic agents.

Your doctor will determine the correct amount and frequency of treatment with plicamycin depending upon the type of cancer being treated and other factors. Talk to your doctor if you have any questions or concerns regarding the treatment schedule.

Your doctor will probably want you to have regularly scheduled blood tests and other medical evaluations during treatment with plicamycin to monitor progress and side effects.

Your healthcare provider will store cladribine as directed by the manufacturer. If you are storing cladribine, follow the directions provided by your healthcare provider.

What happens if I miss a dose?

Contact your doctor if you miss a dose of plicamycin injection.

What happens if I overdose?

If for any reason an overdose of plicamycin is suspected, seek emergency medical attention or contact your healthcare provider immediately.

Symptoms of a plicamycin overdose tend to be similar to side effects caused by the medication, although often more severe.

What should I avoid while taking Mithracin (plicamycin)?

Plicamycin can lower the activity of your immune system making you susceptible to infections. Avoid contact with people who have colds, the flu, or other contagious illnesses and do not receive vaccines that contain live strains of a virus (e.g., live oral polio vaccine) during treatment with plicamycin. In addition, avoid contact with individuals who have recently been vaccinated with a live vaccine. There is a chance that the virus can be passed on to you.

Mithracin (plicamycin) side effects

If you experience any of the following serious side effects, seek emergency medical attention or contact your doctor immediately:

an allergic reaction (shortness of breath; closing of your throat; difficulty breathing; swelling of your lips, face, or tongue; or hives);

blood in the urine;

black or tarry stools;

signs of infection such as fever; chills, or sore throat;

nose bleed (epistaxis) or vomiting blood (hematemesis); or

unusual bleeding or bruising.

Other less serious side effects may be more likely to occur. Talk to your doctor if you experience:

nausea, vomiting, diarrhea, or decreased appetite;

mouth sores;

drowsiness and extremely deep sleep;

a general discomfort or uneasiness;

headache or depression;

a rash; or

facial flushing..

Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome.

What other drugs will affect Mithracin (plicamycin)?

Do not receive “live” vaccines during treatment with plicamycin. Administration of a live vaccine may be dangerous during treatment with plicamycin.

Other drugs may interact with plicamycin. Talk to your doctor and pharmacist before taking any other prescription or over-the-counter medicines, including herbal products, during treatment with plicamycin.

Idamycin PFS

Idamycin PFS

Idamycin PFS must be given slowly and directly into a vein (intravenously) along with other IV fluids. Do not inject Idamycin PFS into the muscle (intramuscularly) or just beneath the skin (subcutaneously). If Idamycin PFS accidentally leaks into surrounding tissue, the skin and/or muscle may be severely damaged. Notify the doctor immediately if redness, pain, or swelling occurs at (or around) the injection site.

Idarubicin may cause heart problems (including heart failure) or bone marrow suppression, making it hard to fight off infections. Notify your doctor immediately if you develop an irregular heartbeat, trouble breathing, swelling of the hands or feet, easy bruising or bleeding, or signs of infection, such as fever, unusual fatigue, or persistent sore throat. People with heart conditions or people who have been treated with similar drugs (anthracyclines) are at greater risk for heart problems.

Idamycin PFS is used for:

Treating certain types of cancer (eg, acute myeloid leukemia). It is used along with other medicines. It may also be used for other conditions as determined by your doctor.

Idamycin PFS is a cytotoxic agent. It works by inhibiting activities of the cancer cell necessary for life and growth. This prevents the cancer cell from reproducing and results in death of the cancer cell.

Do NOT use Idamycin PFS if:

Contact your doctor or health care provider right away if any of these apply to you.

Before using Idamycin PFS :

Some medical conditions may interact with Idamycin PFS . Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

Some MEDICINES MAY INTERACT with Idamycin PFS . However, no specific interactions with Idamycin PFS are known at this time.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Idamycin PFS may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Idamycin PFS :

Use Idamycin PFS as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Ask your health care provider any questions you may have about how to use Idamycin PFS .

Important safety information:

Possible side effects of Idamycin PFS :

All medicines may cause side effects, but many people have no, or minor, side effects.

Cramps; diarrhea; fever; hair loss; headache; hives; nausea; rash; stomach pain; swelling of mucous membranes; vomiting.

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); changes in vision; chest pain; dizziness; fainting; infection (fever, chills, cough, sore throat); irregular heartbeat; numbness of an arm or leg; pain, redness, or swelling at the injection site; seizure; serious heart problems (eg, heart failure, serious irregular heartbeat, heart attack); severe stomach pain; sharp or crushing chest pain; sores on the mouth or lips; sudden leg pain; sudden severe headache; sudden shortness of breath; swelling of the feet, legs, or ankles; unusual bruising or bleeding; weakness.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects at

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center (

Idamycin PFS is usually handled and stored by a health care provider. If you are using Idamycin PFS at home, store Idamycin PFS as directed by your pharmacist or health care provider. Keep Idamycin PFS out of the reach of children and away from pets.

General information:

This information is a summary only. It does not contain all information about Idamycin PFS . If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

More Idamycin PFS resources

Compare Idamycin PFS with other medications for the treatment of:

Idamycin

Idamycin

Generic Name: idarubicin (EYE da ROO bi sin)

What is Idamycin (idarubicin)?

Idarubicin is a cancer (antineoplastic) medication. Idarubicin interferes with the growth of cancer cells and slows their growth and spread in the body.

Idarubicin is used to treat a type of blood cancer (acute myeloid leukemia -AML) in adults .

Idarubicin may also be used for purposes other than those listed in this medication guide.

What is the most important information I should know about Idamycin (idarubicin)?

Idarubicin should only be administered under the supervision of a qualified healthcare provider experienced in the use of cancer chemotherapeutic agents.

Serious side effects have been reported with the use of idarubicin including: allergic reactions (difficulty breathing; closing of the throat; swelling of the lips, tongue, or face; or hives); severe heart damage with prolonged use; decreased bone marrow function and blood problems (extreme fatigue; easy bruising or bleeding; black, bloody or tarry stools; fever or chills; or signs of infection); severe nausea, vomiting, diarrhea, and loss of appetite; and others.Talk to your doctor about the possible side effects from treatment with idarubicin.

What should I discuss with my healthcare provider before using Idamycin (idarubicin)?

Do not use idarubicin without first talking to your doctor if you have

heart disease;

poor bone marrow function;

received radiation therapy that encompassed the heart; or

previously received treatment with doxorubicin (Adriamycin, Rubex), doxorubicin liposomal (Doxil), daunorubicin (Cerubidine), daunorubicin liposomal (Daunoxome), idarubicin (Idamycin), or mitoxantrone (Novantrone).

The use of idarubicin may be dangerous if you have any of the conditions listed above.

Idarubicin is in the FDA pregnancy category D. This means that idarubicin is known to be harmful to an unborn baby. Do not use idarubicin without first talking to your doctor if you are pregnant or could become pregnant during treatment. Discuss with your doctor the appropriate use of birth control during treatment with idarubicin if necessary. Because of the potential for serious side effects in a nursing infant, breast-feeding should be avoided during treatment with idarubicin. The safety and effectiveness of idarubicin in children has not been established.

How should I use Idamycin (idarubicin)?

Idarubicin should only be administered under the supervision of a qualified healthcare provider experienced in the use of cancer chemotherapeutic agents.

Your doctor will determine the correct amount and frequency of treatment with idarubicin depending upon the type of cancer being treated and other factors. Talk to your doctor if you have any questions or concerns regarding the treatment schedule.

Your doctor will probably want you to have regularly scheduled blood tests and other medical evaluations during treatment with idarubicin to monitor progress and side effects.

Skin accidentally exposed to idarubicin should be rinsed thoroughly with soap and warm water.

Your healthcare provider will store idarubicin as directed by the manufacturer. If you are storing idarubicin at home, follow the directions provided by your healthcare provider.

What happens if I miss a dose?

Contact your doctor if you miss a dose of idarubicin.

What happens if I overdose?

If for any reason an overdose of idarubicin is suspected, seek emergency medical attention or contact your healthcare provider immediately.

Symptoms of a idarubicin overdose tend to be similar to side effects caused by the medication, although often more severe.

What should I avoid while using Idamycin (idarubicin)?

Skin accidentally exposed to idarubicin should be rinsed thoroughly with soap and warm water.

Do not receive “live” vaccines during treatment with idarubicin. Administration of a live vaccine may be dangerous during treatment with idarubicin.

Idamycin (idarubicin) side effects

If you experience any of the following serious side effects from idarubicin, contact your doctor immediately:

an allergic reaction (including difficulty breathing; closing of the throat; swelling of the lips, tongue, or face; or hives);

decreased bone marrow function and blood problems (extreme fatigue; easy bruising or bleeding; black, bloody or tarry stools; or fever, chills, or signs of infection);

congestive heart failure (difficulty breathing, fluid retention, chest pain);

irregular heartbeats;

tissue or vein reactions near the site of administration;

liver damage (abdominal pain, yellowing of the skin or eyes);

severe nausea, vomiting, diarrhea, and loss of appetite;

inflamation and sores inside the mouth, throat, or intestines;

fever, chills, or other signs of infection;

numbness, tingling, or difficult movement of a body part;

seizures; or

increased levels of uric acid in the body (joint pain and stiffness).

Other, less serious side effects may be more likely to occur. Continue taking idarubicin and talk to your doctor if you experience:

facial flushing during administration;

eye irritation or tearing;

darkening of the nail beds and skin folds;

temporary hair loss; or

red colored urine for 1 or 2 days following a dose.

Some breast cancer patients developed a second cancer (leukemia) after treatment with idarubicin. Idarubicin may cause premature menopause.

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

What other drugs will affect Idamycin (idarubicin)?

Do not use idarubicin without first talking to your doctor if you have had previous treatment with doxorubicin (Adriamycin, Rubex), doxorubicin liposomal (Doxil), daunorubicin (Cerubidine), daunorubicin liposomal (Daunoxome), idarubicin (Idamycin), or mitoxantrone (Novantrone). Because there is a maximum amount of these medications that should be administered to an individual, you may not be able to use idarubicin.

Before using idarubicin, tell your doctor if you are taking any of the following medicines.

paclitaxel (Taxol);

cimetidine (Tagamet, Tagamet HB, others);

progesterone (Prometrium);

verapamil (Calan, Calan SR, Covera-HS, Isoptin, Isoptin SR, Verelan, Verelan PM, others)

cyclosporine (Gengraf, Neoral, Sandimmune);

cyclophosphamide (Cytoxan, Cytoxan Lyophilized, Neosar);

phenobarbital;

phenytoin (Dilantin); or

streptozocin (Zanosar).

You may not be able to take idarubicin, or you may require a dosage adjustment or special monitoring during treatment if you are taking any of the medicines listed above.

Do not receive “live” vaccines during treatment with idarubicin. Administration of a live vaccine may be dangerous during treatment with idarubicin.

Drugs other than those listed here may also interact with idarubicin. Talk to your doctor and pharmacist before taking any other prescription or over-the-counter medicines, including vitamins, minerals, and herbal products, during treatment with idarubicin.

Ellence

Ellence

Generic Name: epirubicin (EP i ROO bi sin)

What is Ellence?

Ellence is a cancer medication that interferes with the growth of cancer cells and slows their growth and spread in the body. The exact way it works is not fully understood.

Ellence is used to treat certain types of breast cancer following surgery. It may also be used to treat other cancers.

Ellence may also be used for other purposes not listed in this medication guide.

Important information about Ellence

Before you are treated with Ellence, tell your doctor about all other cancer medications and treatments you have received, including radiation. You should not receive Ellence if you have an untreated or uncontrolled infection (including mouth sores), severe liver or heart problems, or if you have recently had a heart attack.

You should not receive Ellence if you are allergic to epirubicin or similar medications (Cerubidine, Adriamycin, Idamycin, Novantrone).

Before you receive Ellence, tell your doctor if you have liver or kidney disease, congestive heart failure, a history of heart disease or heart attack, or a weak immune system caused by prior cancer treatments.

Do not receive Ellence without telling your doctor if you are pregnant. Ellence could harm the unborn baby. Use effective birth control, and tell your doctor if you become pregnant during treatment.

If a man fathers a child while receiving Ellence, the baby may have birth defects. Use a condom to prevent pregnancy during your treatment.

Some people being treated with Ellence have developed secondary cancers such as leukemia. Talk with your doctor about your individual risk.

Before I receive Ellence

Tell your doctor about all other cancer medications and treatments you have received, including radiation. You should not use Ellence if you are allergic to epirubicin or similar medications (Cerubidine, Adriamycin, Idamycin, Novantrone), or if you have:

an untreated or uncontrolled infection (including mouth sores);

severe liver disease;

severe heart problems; or

if you have recently had a heart attack.

If you have certain conditions, you may need a dose adjustment or special tests to safely receive this medication. Before you receive Ellence, tell your doctor if you have:

a weak immune system caused by prior cancer treatments;

heart disease;

congestive heart failure; or

if you have ever had a heart attack.

Some people being treated with Ellence have developed secondary cancers such as leukemia. Talk with your doctor about your individual risk.

FDA pregnancy category D. This medication can cause harm to an unborn baby. Do not receive Ellence without telling your doctor if you are pregnant. It could harm the unborn baby. Use effective birth control, and tell your doctor if you become pregnant during treatment.

If a man fathers a child while receiving Ellence, the baby may have birth defects. Use a condom to prevent pregnancy during your treatment.

It is not known whether Ellence passes into breast milk or if it could harm a nursing baby. Do not receive this medication without telling your doctor if you are breast-feeding a baby.

How is Ellence given?

Ellence is given as an injection through a needle placed into a vein. You will receive this injection in a clinic or hospital setting. The medicine must be given slowly through an IV infusion, and can take at least 15 minutes to complete.

Ellence is usually given together with other cancer medications. Follow your doctor’s instructions about your specific treatment schedule.

You may also receive medications to prevent nausea, vomiting, or infections.

If any of this medication accidentally gets on your skin, wash it thoroughly with soap and warm water.

Ellence can lower blood cells that help your body fight infections. This can make it easier for you to bleed from an injury or get sick from being around others who are ill. To be sure your blood cells do not get too low, your blood will need to be tested on a regular basis. Your heart and liver function may also need to be tested. Do not miss any scheduled appointments.

What happens if I miss a dose?

Contact your doctor if you miss a dose of Ellence.

What happens if I overdose?

Seek emergency medical attention if you think you have received too much of this medicine.

Overdose symptoms may include mouth sores, cold feeling, bloody or black stools, coughing up blood, urinating less than usual, or weak or shallow breathing.

What should I avoid while receiving Ellence?

Avoid being near people who have colds, the flu, or other contagious illnesses. Contact your doctor at once if you develop signs of infection.

Ellence side effects

Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Call your doctor at once if you have a serious side effect such as:

feeling short of breath, even with mild exertion;

swelling, rapid weight gain;

severe burning, stinging, pain, swelling, redness, or skin changes around the IV needle;

white patches or sores inside your mouth or on your lips;

severe vomiting, thirst, and hot dry skin;

fever, chills, body aches, flu symptoms, or signs of infection;

slow or uneven heart rate, weak pulse;

confusion, fainting;

muscle weakness, tingly feeling;

urinating less than usual or not at all; or

easy bruising or bleeding, unusual weakness.

Less serious side effects may include:

red colored urine for 1 or 2 days after receiving the medication;

nausea, vomiting, diarrhea;

tired feeling;

hair loss;

changes in your menstrual periods;

warmth, redness, or tingly feeling under your skin;

darkening of your skin or nails; or

mild itching or skin rash.

This is not a complete list of side effects and others may occur. Tell your doctor about any unusual or bothersome side effect. You may report side effects to FDA at 1-800-FDA-1088.

What other drugs will affect Ellence?

The following drugs can interact with Ellence. Tell your doctor if you are using any of these:

paclitaxel (Taxol, Onxol);

docetaxel (Taxotere);

cimetidine (Tagamet); or

a calcium channel blocker such as amlodipine (Norvasc), diltiazem (Tiazac, Cartia, Cardizem), felodipine (Plendil), nicardipine (Cardene), nifedipine (Procardia, Adalat), nimodipine (Nimotop), nisoldipine (Sular), or verapamil (Calan, Covera, Isoptin, Verelan).

This list is not complete and there may be other drugs that can interact with Ellence. Tell your doctor about all your prescription and over-the-counter medications, vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start a new medication without telling your doctor.

Doxil

Doxil

Doxil is for intravenous (IV) use only. If Doxil accidentally leaks into surrounding tissue, the skin or muscle may be severely damaged. Notify your doctor immediately if redness, pain, or swelling at or around the injection site occur. Doxil may cause heart problems (eg, heart failure) or bone marrow suppression. Notify your doctor immediately if you develop an irregular heartbeat, trouble breathing, swelling of the hands or feet, easy bruising or bleeding, a dry cough, or signs of an infection (eg, fever, unusual tiredness, persistent sore throat). Heart problems may occur during therapy or sometimes months to years after receiving Doxil . The risk of developing heart problems varies depending on your dose and condition. The risk may be increased if you have a history of radiation therapy or if you are using cyclophosphamide. Tell your doctor if you have liver problems because your dose will have to be decreased. Your doctor will closely monitor you while you are using Doxil .

Doxil is used for:

Treating advanced ovarian cancer and AIDS-related Kaposi sarcoma in certain patients. It is also used with another medicine to treat a type of bone marrow cancer (multiple myeloma) in certain patients.

Doxil is an antineoplastic antibiotic. It works by killing cancer cells.

Do NOT use Doxil if:

Contact your doctor or health care provider right away if any of these apply to you.

Before using Doxil :

Some medical conditions may interact with Doxil . Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

Some MEDICINES MAY INTERACT with Doxil . Tell your health care provider if you are taking any other medicines, especially any of the following:

This may not be a complete list of all interactions that may occur. Ask your health care provider if Doxil may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Doxil :

Use Doxil as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Ask your health care provider any questions you may have about how to use Doxil .

Important safety information:

Possible side effects of Doxil :

All medicines may cause side effects, but many people have no, or minor, side effects.

Diarrhea; hair loss; loss of appetite; nausea; pain, redness, or swelling at the injection site; red-colored urine 1 to 2 days after receiving Doxil ; tiredness; vomiting; weakness.

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); back pain; bleeding or bruising; chest pain; cough; dizziness; fainting; flushing; hand-foot syndrome (tingling, burning, redness, swelling, flaking, small blisters or small sores on the palms of hands or sores of feet); headache; irregular or fast heartbeat; loose or bloody stools; rectal bleeding or irritation; serious infection (fever, chills, persistent sore throat); shortness of breath; sores in the mouth or on the lips; sudden weight gain; swelling of the face or ankles; tightness in the chest and throat; unusual tiredness.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects at

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center (

Doxil is usually handled and stored by a health care provider. If you are using Doxil at home, store Doxil as directed by your pharmacist or health care provider. Keep Doxil out of the reach of children and away from pets.

General information:

This information is a summary only. It does not contain all information about Doxil . If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

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DaunoXome

DaunoXome

DaunoXome may cause heart problems, including heart failure, or bone marrow depression, making it hard to fight off infection. Notify your doctor immediately if you develop chest pain, an irregular heartbeat, trouble breathing, swelling of the hands or feet, easy bruising or bleeding, or signs of infection, such as fever, unusual fatigue, or persistent sore throat. Tell your doctor if you have liver problems or heart problems, or have had chest x-rays before starting treatment with DaunoXome . You may require smaller doses of DaunoXome or different treatment. DaunoXome can cause a reaction including back pain, flushing, and chest tightness. Notify your doctor immediately if you experience any of these symptoms.

DaunoXome is used for:

Treating advanced AIDS-related Kaposi sarcoma. It may also be used for other conditions as determined by your doctor.

DaunoXome is a cytotoxic agent. It works by preventing the cancer cell from reproducing, which results in death of the cancer cell.

Do NOT use DaunoXome if:

Contact your doctor or health care provider right away if any of these apply to you.

Before using DaunoXome :

Some medical conditions may interact with DaunoXome . Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

Some MEDICINES MAY INTERACT with DaunoXome . Tell your health care provider if you are taking any other medicines, especially any of the following:

This may not be a complete list of all interactions that may occur. Ask your health care provider if DaunoXome may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use DaunoXome :

Use DaunoXome as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Ask your health care provider any questions you may have about how to use DaunoXome .

Important safety information:

Possible side effects of DaunoXome :

All medicines may cause side effects, but many people have no, or minor, side effects.

Diarrhea; hair loss; loss of appetite; mouth pain; nausea; sore throat; stomach pain; tiredness; weakness.

Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); back pain; black, tarry stools; blood in the stools; chest pain; chills; cough or sore throat; excessive bleeding; fever; flushing; irregular heartbeat; pain, redness, or swelling at the injection site; shortness of breath; sores on the mouth or lips; unusual bruising or bleeding.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects at

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center (

DaunoXome is usually handled and stored by a health care provider. If you are using DaunoXome at home, store DaunoXome as directed by your pharmacist or health care provider. Keep DaunoXome out of the reach of children and away from pets.

General information:

This information is a summary only. It does not contain all information about DaunoXome . If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

More DaunoXome resources

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Cosmegen

Cosmegen

Cosmegen is very toxic. Do not inhale the dust or vapors of Cosmegen . Do not get Cosmegen in your eyes, nose, mouth, or onto your skin. Do not come into contact with Cosmegen if you are pregnant. Cosmegen is given through a vein. If Cosmegen leaks out of the vein (extravasation), severe damage to the area around the injection site will occur. Tell your doctor or health care provider immediately if you notice any discomfort, pain, or redness at the injection site.

Cosmegen is used for:

Treating certain types of cancer. It may be used alone or with other medicines.

Cosmegen is an antineoplastic. It works by killing certain cancer cells.

Do NOT use Cosmegen if:

Contact your doctor or health care provider right away if any of these apply to you.

Before using Cosmegen :

Some medical conditions may interact with Cosmegen . Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

Some MEDICINES MAY INTERACT with Cosmegen . However, no specific interactions with Cosmegen are known at this time.

Ask your health care provider if Cosmegen may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Cosmegen :

Use Cosmegen as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Ask your health care provider any questions you may have about how to use Cosmegen .

Important safety information:

Possible side effects of Cosmegen :

All medicines may cause side effects, but many people have no, or minor, side effects.

Acne; hair loss; lack of energy; loss of appetite; mild nausea or vomiting; stomach pain; tiredness; weakness.

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); black, tarry, or bloody stools; chest pain; dark urine; diarrhea; fever, chills, or sore throat; flushing; leg pain or swelling; muscle pain or aches; pale stools; redness, swelling, pain, or blistering near the injection site; severe or persistent nausea or vomiting; shortness of breath; swelling, sores, or ulcers of the mouth or lips; trouble swallowing; unusual bruising or bleeding; unusual tiredness or weakness; yellowing of the skin or eyes.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects at

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center (

Cosmegen is usually handled and stored by a health care provider. If you are using Cosmegen at home, store Cosmegen as directed by your pharmacist or health care provider.

General information:

This information is a summary only. It does not contain all information about Cosmegen . If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

More Cosmegen resources

Compare Cosmegen with other medications for the treatment of:

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