Archive for the ‘miscellaneous antineoplastics’ Category

Zolinza

Zolinza

Generic Name: vorinostat (vor IN o stat)

What is Zolinza?

Zolinza is used to treat skin problems caused by cutaneous T-cell lymphoma.

Zolinza is usually given after other treatments have been tried without successful treatment of symptoms.

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

Important information about Zolinza

Do not use Zolinza without telling your doctor if you are pregnant. It could cause harm to the unborn baby. Use an effective form of birth control, and tell your doctor if you become pregnant during treatment. Drink at least 2 liters of water each day to keep from getting dehydrated while you are taking Zolinza. Tell your doctor if you have severe vomiting or diarrhea during treatment.

Call your doctor at once if you have symptoms of bleeding in your stomach or intestines. This includes black, bloody, or tarry stools, or coughing up blood or vomit that looks like coffee grounds.

Do not crush or open a Zolinza capsule. Swallow the pill whole. The medicine inside the capsule can be dangerous if it gets in your eyes, mouth, or nose, or on your skin. If contact occurs, wash the skin area with soap and water or rinse the eyes thoroughly with plain water. If you must handle a broken capsule, ask your doctor or pharmacist how to safely dispose of it.

To be sure Zolinza is not causing harmful effects, your blood will need to be tested on a regular basis. Your kidney function may also need to be tested. Do not miss any scheduled visits to your doctor.

Before taking Zolinza

Do not use Zolinza if you are allergic to vorinostat.

Before using Zolinza, tell your doctor if you are allergic to any drugs, or if you have:

diabetes;

liver disease;

kidney disease;

an electrolyte imbalance (such as high or low potassium levels);

a personal or family history of “Long QT syndrome”;

a history of stroke or blood clot; or

if you have recently been vomiting or had diarrhea.

If you have any of these conditions, you may not be able to use Zolinza, or you may need a dosage adjustment or special tests during treatment.

FDA pregnancy category D. Zolinza can cause harm to an unborn baby. Do not use Zolinza without your doctor’s consent if you are pregnant. Tell your doctor if you become pregnant during treatment. Use an effective form of birth control while you are using Zolinza. It is not known whether Zolinza passes into breast milk or if it could harm a nursing baby. Do not use Zolinza without telling your doctor if you are breast-feeding a baby.

How should I take Zolinza?

Take Zolinza exactly as it was prescribed for you. Do not take the medication in larger amounts, or take it for longer than recommended by your doctor. Follow the directions on your prescription label.

Your doctor may occasionally change your dose to make sure you get the best results from this medication.

Zolinza is usually taken once daily with food. Drink at least 2 liters of water each day to keep from getting dehydrated while you are taking Zolinza. Tell your doctor if you have severe vomiting or diarrhea during treatment. Do not crush or open a Zolinza capsule. Swallow the pill whole. The medicine inside the capsule can be dangerous if it gets in your eyes, mouth, or nose, or on your skin. If contact occurs, wash the skin area with soap and water or rinse the eyes thoroughly with plain water. If you must handle a broken capsule, ask your doctor or pharmacist how to safely dispose of it.

To be sure this medication is not causing harmful effects, your blood will need to be tested on a regular basis. Your kidney function may also need to be tested. Do not miss any scheduled visits to your doctor.

Store Zolinza at room temperature away from moisture and heat.

What happens if I miss a dose?

Take the missed dose as soon as you remember. If it is almost time for your next dose, skip the missed dose and take the medicine at your next regularly scheduled time. Do not take extra medicine to make up the missed dose.

What happens if I overdose?

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

Symptoms of a Zolinza overdose are not known.

What should I avoid while taking Zolinza?

Avoid becoming overheated or dehydrated during exercise and in hot weather. Drink at least 2 liters of water each day while you are taking Zolinza.

Zolinza 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. Stop using Zolinza and call your doctor at once if you have any of these serious side effects:

sudden shortness of breath, chest pain that gets worse with breathing, coughing up blood, fainting;

pain or swelling in one or both legs;

pale skin, easy bruising or bleeding, unusual weakness;

black, bloody, or tarry stools;

severe or prolonged vomiting or diarrhea;

increased thirst or urination;

dry mouth, confusion, nausea, vomiting, feeling light-headed, fainting, decreased sweating, and hot, dry skin;

Continue taking Zolinza and talk with your doctor if you have any of these less serious side effects:

nausea, vomiting, diarrhea, constipation;

headache, tired feeling;

loss of appetite;

dry mouth, changes in the way things taste;

weight loss;

chills;

hair loss; or

muscle spasms.

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. You may report side effects to FDA at 1-800-FDA-1088.

What other drugs will affect Zolinza?

Before taking Zolinza, tell your doctor if you are using any of the following drugs:

valproic acid; or

a blood thinner such as warfarin (Coumadin).

If you are using any of these drugs, you may not be able to use Zolinza, or you may need dosage adjustments or special tests during treatment.

There may be other drugs not listed that can affect Zolinza. Tell your doctor about all the prescription and over-the-counter medications you use. This includes vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start using a new medication without telling your doctor.

Visudyne

Visudyne

Visudyne is used for:

Treating macular degeneration, pathologic myopia, and presumed histoplasmosis infection of the eye. It may also be used for other conditions as determined by your doctor.

It works by causing clotting in the blood vessels of the eye, which decreases damage already done in the eye.

Do NOT use Visudyne if:

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

Before using Visudyne :

Some medical conditions may interact with Visudyne . 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 Visudyne . 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 Visudyne 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 Visudyne :

Use Visudyne 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 Visudyne .

Important safety information:

Possible side effects of Visudyne :

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

Blurred vision or other vision changes; headache; mild discomfort or redness at the injection site.

Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); pain or swelling at the injection site; sensitivity to bright light lasting more than 5 days after your dose; severe vision changes or vision loss; skin rash or severe sunburn.

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 (

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

Compare Visudyne with other medications for the treatment of:

Trisenox

Trisenox

A severe and sometimes fatal side effect called retinoic acid-acute promyelocytic leukemia (RA-APL) or APL differentiation syndrome has been reported with use of Trisenox in some patients. Contact your doctor immediately if you experience fever, shortness of breath, tightness in the chest, or weight gain.

Use of Trisenox may increase your risk for serious and even fatal heart problems, including irregular heartbeat or heart block. Your risk may be higher if you are taking medicine that may also increase your risk for irregular heartbeat or certain types of diuretics (potassium-wasting), or if you have a history of irregular heartbeat or electrocardiogram (ECG) abnormalities, congestive heart failure, or low blood levels of potassium or magnesium.

Lab tests, including an ECG, blood electrolyte levels, and creatinine levels, should be performed before and during use of Trisenox to monitor your progress and to check for side effects. Contact your doctor immediately if you experience fainting of fast or irregular heartbeat.

Trisenox is used for:

Treating a certain type of cancer (APL) in certain patients. It may also be used for other conditions as determined by your doctor.

Trisenox is a chemotherapy agent. The way it works is not completely understood. It may work by blocking the growth of cancer cells.

Do NOT use Trisenox if:

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

Before using Trisenox :

Some medical conditions may interact with Trisenox . 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 Trisenox . 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 Trisenox 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 Trisenox :

Use Trisenox 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 Trisenox .

Important safety information:

Possible side effects of Trisenox :

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

Agitation; blurred vision; chills; constipation; cough; darkening of skin; diarrhea; dizziness; drowsiness; dry eyes, mouth, or skin; earache; eye pain or irritation; flushing; headache; increased sweating; indigestion; loss of appetite; mouth sores; muscle, joint, or bone pain; nausea; nosebleed; numbness or tingling of the skin; pain, swelling, or redness at the injection site; pale skin; postnasal drip; ringing in the ears; skin lesions; sore throat; stomach pain, tenderness, or bloating; swelling of the eyelid; tiredness; trouble sleeping; vomiting; weakness; weight loss.

Severe allergic reactions (rash; hives; itching, difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); anxiety, confusion, or depression; black or bloody stools; bleeding between menstrual periods; chest pain; convulsions; decreased urination; fainting; fast heartbeat; fever; increased thirst or urination; irregular heart rate; loss of bowel or bladder control; loss of consciousness; rapid breathing; seizures; severe dizziness; severe weakness; skin shedding at the injection site; spitting up of blood; sudden weight gain; swelling of ankles, feet, or hands; tremors; trouble breathing; unusual bruising or bleeding; vaginal bleeding; wheezing.

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 (

Store Trisenox at 77 degrees F (25 degrees C). Storage between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Do not freeze. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Trisenox 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 Trisenox . 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 Trisenox resources

Compare Trisenox with other medications for the treatment of:

Torisel

Torisel

Generic Name: temsirolimus (TEM sir OH li mus)

What is Torisel?

Torisel is a cancer medication. It slows the growth and spread of cancer cells in the body.

Torisel is used to treat cancer of the kidneys, also called renal cell carcinoma.

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

Important information about Torisel

FDA pregnancy category D. Torisel can cause harm to an unborn baby. Do not receive this medication without telling your doctor if you are pregnant. Use an effective form of birth control while you are using this medication and for at least 3 months after your treatment ends.

If a man fathers a child while using Torisel, the baby may have birth defects. Use a condom to prevent pregnancy during your treatment. Continue using condoms for at least 3 months after you stop using Torisel.

Torisel can lower the blood cells that help your body fight infections. Avoid contact with people who have colds, the flu, or other contagious illnesses. Do not receive any vaccines. Contact your doctor immediately if you develop signs of infection.

Before receiving Torisel

You should not use Torisel if you are allergic to temsirolimus.

If you have any of these other conditions, you may need a dose adjustment or special tests to safely use this medication:

high cholesterol or triglycerides;

diabetes;

a history of head injury, stroke, or brain tumor; or

if you are allergic to sirolimus (Rapamune).

FDA pregnancy category D. Torisel can cause harm to an unborn baby. Do not receive Torisel without telling your doctor if you are pregnant. Tell your doctor if you become pregnant during treatment. Use an effective form of birth control while you are using Torisel and for at least 3 months after your treatment ends.

If a man fathers a child while using this medication, the baby may have birth defects. Use a condom to prevent pregnancy during your treatment. Continue using condoms for at least 3 months after you stop using Torisel.

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

How is Torisel given?

Torisel 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 up to 1 hour to complete.

Torisel is usually given once each week unless your cancer progresses or you have serious side effects from the medication.

You may receive other medications before your Torisel infusion. These medications will help prevent certain side effects.

Torisel can lower the 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 kidney function may also need to be tested. Do not miss any scheduled visits to your doctor.

If you need to have any type of surgery, tell the surgeon ahead of time that you are using Torisel. Temsirolimus can make it harder for wounds to heal, and you may need to stop using the medicine for a short time.

What happens if I miss a dose?

Call your doctor if you miss an appointment for your Torisel injection.

What happens if I overdose?

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

Overdose symptoms may include black or bloody stools, severe stomach pain, confusion, unusual thoughts or behavior, sudden numbness or weakness, sudden headache, problems with vision or speech, pain or swelling in one or both legs, or seizure (convulsions).

What should I avoid while receiving Torisel?

Avoid contact with people who have colds, the flu, or other contagious illnesses. Contact your doctor immediately if you develop signs of infection.

Do not receive a “live” vaccine while you are being treated with Torisel, and avoid coming into contact with anyone who has recently received a live vaccine. There is a chance that the virus could be passed on to you.

Grapefruit and grapefruit juice may interact with Torisel and lead to potentially dangerous effects. Discuss the use of grapefruit products with your doctor. Do not increase or decrease the amount of grapefruit products in your diet without first talking to your doctor.

Torisel side effects

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

chest pain;

cough, feeling short of breath;

warmth, redness, or tingly feeling under your skin;

increased thirst, hunger, or urination;

black, bloody, or tarry stools;

fever, severe stomach pain;

urinating less than usual or not at all;

drowsiness, confusion, mood changes, loss of appetite, nausea and vomiting;

swelling, weight gain; or

pale skin, easy bruising or bleeding, weakness.

Less serious Torisel side effects include:

minor skin rash; or

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

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 Torisel?

Before receiving Torisel, tell your doctor if you are using any of the following drugs:

dexamethasone (Decadron, Hexadrol);

rifabutin (Mycobutin);

rifampin (Rifadin, Rimactane, Rifater);

St. John’s wort;

sunitinib (Sutent);

a blood thinner such as warfarin (Coumadin);

insulin or diabetes medications you take by mouth;

an antibiotic such as clarithromycin (Biaxin), telithromycin (Ketek) and others;

an antifungal medication such as itraconazole (Sporanox), ketoconazole (Nizoral), or voriconazole (Vfend);

HIV/AIDS medicine such as atazanavir (Reyataz), indinavir (Crixivan), nelfinavir (Viracept), ritonavir (Norvir), or saquinavir (Invirase, Fortovase); or

seizure medication such as carbamazepine (Carbatrol, Tegretol), phenytoin (Dilantin), or phenobarbital (Luminal, Solfoton).

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

Tice BCG Vaccine

Tice BCG Vaccine

Generic Name: BCG (bee cee jee)

What is Tice BCG Vaccine (BCG)?

BCG (Bacillus Calmette and Guérin) is made using the organisms of a bacteria.

This medication is injected directly into the bladder, where it causes inflammation and increases certain white blood cells known as natural killer cells. These killer cells act to destroy invading cells such as tumor cells in the bladder.

BCG is used to treat bladder cancer that is localized (has not spread to other parts of the body).

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

What is the most important information I should know about Tice BCG Vaccine (BCG)?

You should not be treated with this medication if you are allergic to BCG, or if you have tuberculosis, a fever, a bladder infection, blood in your urine, or a weak immune system (caused by certain drugs or disease such as AIDS, leukemia, or lymphoma).

You should also not receive BCG if you have had a bladder biopsy, surgery, or catheter within the past 14 days.

Before you receive BCG, tell your doctor if you are allergic to latex rubber, or if you have myasthenia gravis, a pacemaker or other artificial heart device, an artificial joint or other prosthetic, or any type of infection (including HIV).

Also tell your doctor if you have ever had tuberculosis, bypass surgery, or an aneurysm (dilated blood vessel), or if you currently need to have an organ transplant (kidney, liver, heart, etc).

Your doctor may ask you to drink extra fluids for several hours after your BCG treatment to help flush out your bladder. Follow your doctor’s instructions about the type and amount of liquids you should drink.

Call your doctor right away if you have a fever after receiving BCG, especially if the fever lasts for several hours or longer. Antibiotics can make BCG less effective and should be avoided during your treatment with BCG. If you have an infection that must be treated with an antibiotic, you may need to stop receiving BCG for a short time. Follow your doctor’s instructions and be sure to tell any other doctor who treats you that you are receiving BCG.

What should I discuss with my health care provider before I receive Tice BCG Vaccine (BCG)?

You should not receive this medication if you are allergic to BCG, or if you have:

tuberculosis;

a weak immune system from diseases such as AIDS, leukemia, or lymphoma;

fever, a bladder infection, or blood in your urine;

if you are using steroids or receiving chemotherapy or radiation treatments; or

if you have had a bladder biopsy, surgery, or catheter within the past 14 days.

Before you receive BCG, tell your doctor if you are allergic to latex rubber, or if you have:

any type of bacterial, fungal, or viral infection (including HIV);

myasthenia gravis;

a pacemaker or other artificial heart device;

an artificial joint or other prosthetic;

a history of aneurysm (dilated blood vessel);

if you have ever had bypass surgery;

if you have ever had tuberculosis; or

if you need to have an organ transplant (kidney, liver, heart, etc).

If you have any of these conditions, you may need a dose adjustment or special tests to safely receive BCG.

FDA pregnancy category C. This medication may be harmful to an unborn baby. Before you receive BCG, tell your doctor if you are pregnant. Use effective birth control, and tell your doctor if you become pregnant during treatment. It is not known whether BCG passes into breast milk or if it could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.

How is BCG given?

BCG is a freeze-dried product that is mixed with saline and other diluents (liquids) in an amount equal to approximately 8 ounces. This liquid mixture is injected directly into the bladder using a catheter inserted into the urethra (the tube for passing urine out of your bladder). You will receive this medication in a clinic or hospital setting.

This medication is usually given once every week for 6 weeks, and then given every 3 to 6 months for up to 2 years. Follow your doctor’s instructions about your specific dosing schedule.

After BCG is placed into the bladder, you will need hold the medication in your bladder as long as possible up to 2 hours. During that time you may be encouraged to lie down or stay relaxed.

For at least 6 hours after you are treated with BCG, your urine will still contain some of the medication and the bacteria it is made from. To prevent the spread of this bacteria, use a toilet rather than a urinal, and sit on the toilet while urinating.

Before you flush the toilet, disinfect the urine with household bleach in an amount that is approximately equal to how much you have urinated. Pour the bleach into the toilet in which you urinated, let it stand for 15 minutes and then flush.

Your doctor may ask you to drink extra fluids for several hours after your BCG treatment to help flush out your bladder. Follow your doctor’s instructions about the type and amount of liquids you should drink.

Call your doctor right away if you have a fever after receiving BCG, especially if the fever lasts for several hours or longer.

Being treated with BCG can cause you to have unusual results with certain medical tests. Tell any doctor who treats you that you are using BCG.

What happens if I miss a dose?

Call your doctor for instructions if you miss an appointment for your BCG treatment.

What happens if I overdose?

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

Overdose symptoms may include signs of an infection, such as fever, chills, body aches, weakness, or other flu symptoms.

What should I avoid while receiving Tice BCG Vaccine (BCG)?

Antibiotics can make BCG less effective and should be avoided during your treatment with BCG. If you have an infection that must be treated with an antibiotic, you may need to stop receiving BCG for a short time. Follow your doctor’s instructions and be sure to tell any other doctor who treats you that you are receiving BCG.

Tice BCG Vaccine (BCG) 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. Report any side effects to your doctor. Some side effects may be serious, including:

fever, chills, cough, body aches, joint pain, weakness, vomiting, or other flu symptoms;

nausea, vomiting, stomach pain, jaundice (yellowing of your skin or eyes);

pain or burning when you urinate;

difficult urination;

more frequent or urgent urinating;

blood in your urine, lower back pain;

pain or swelling in your testicles;

easy bruising or bleeding;

eye pain, redness, watering, severe burning or itching; or

vision changes, increased sensitivity to light.

Less serious side effects may include:

mild nausea, stomach pain, or loss of appetite;

mild bladder or groin pain;

urine leakage or incontinence;

diarrhea, constipation;

headache;

mild skin rash;

dizziness, tired feeling; or

tissue particles in your urine (not blood).

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 Tice BCG Vaccine (BCG)?

Before you receive BCG, tell your doctor if you are taking an antibiotic, or if you are using any drugs that weaken your immune system, such as:

cancer medicine or radiation;

cyclosporine (Neoral, Sandimmune, Gengraf);

sirolimus (Rapamune), tacrolimus (Prograf);

basiliximab (Simulect), efalizumab (Raptiva), muromonab-CD3 (Orthoclone);

mycophenolate mofetil (CellCept);

azathioprine (Imuran), leflunomide (Arava), etanercept (Enbrel); or

steroids such as prednisone, fluticasone (Advair), mometasone (Asmanex, Nasonex), dexamethasone (Decadron, Hexadrol) and others.

This list is not complete and there may be other drugs that can interact with BCG. 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.

Tice BCG

Tice BCG

Tice BCG contains live bacteria. It must be prepared, handled, and disposed of as biohazard material. Serious infections have been reported by health care providers after accidental needle sticks during preparation and handling of Tice BCG . Patients with weakened immune systems have become infected when their injection medicines are prepared in the same area as Tice BCG . Serious, sometimes fatal, infections have also occurred in patients receiving Tice BCG through a catheter.

Tice BCG is used for:

Treating cancer of the bladder.

Tice BCG is a strain of bacteria. How it works is not fully known. It is thought to stimulate the immune system.

Do NOT use Tice BCG if:

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

Before using Tice BCG :

Some medical conditions may interact with Tice BCG . 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 Tice BCG . 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 Tice BCG 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 Tice BCG :

Use Tice BCG 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 Tice BCG .

Important safety information:

Possible side effects of Tice BCG :

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

Diarrhea; increased pain or frequency of urination; loss of appetite; nausea; stomach pain.

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); blood in urine; burning or pain when urinating; chills; cough; fever; flu-like symptoms; frequent or urgent urination; general feeling of discomfort; joint pain; tiredness; vomiting.

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 (

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

TheraCys

TheraCys

TheraCys contains live bacteria. It must be prepared, handled, and disposed of as biohazard material. Serious infections have been reported by health care providers after accidental needle sticks during preparation and handling of TheraCys . Patients with weakened immune systems have become infected when their injection medicines are prepared in the same area as TheraCys . Serious, sometimes fatal, infections have also occurred in patients receiving TheraCys through a catheter.

TheraCys is used for:

Treating cancer of the bladder.

TheraCys is a strain of bacteria. How it works is not fully known. It is thought to stimulate the immune system.

Do NOT use TheraCys if:

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

Before using TheraCys :

Some medical conditions may interact with TheraCys . 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 TheraCys . 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 TheraCys 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 TheraCys :

Use TheraCys 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 TheraCys .

Important safety information:

Possible side effects of TheraCys :

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

Diarrhea; increased pain or frequency of urination; loss of appetite; nausea; stomach pain.

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); blood in urine; burning or pain when urinating; chills; cough; fever; flu-like symptoms; frequent or urgent urination; general feeling of discomfort; joint pain; tiredness; vomiting.

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 (

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

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Thalomid

Thalomid

Generic Name: thalidomide (tha LID o mide)

What is Thalomid?

Thalomid affects the immune system. It helps promote immune responses to prevent inflammation in the body.

Thalomid is used to treat and prevent the debilitating and disfiguring skin sores caused by erythema nodosum leprosum (ENL), an inflammatory complication of leprosy. It is also used together with another medicine called dexamethasone to treat multiple myeloma (bone marrow cancer).

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

Important information about Thalomid

Thalomid can cause severe, life-threatening birth defects or death of a baby if the mother or the father is taking this medication at the time of conception or during pregnancy. Even one dose of Thalomid can cause major birth defects of the baby’s arms and legs, bones, ears, eyes, face, and heart. Never use thalidomide if you are pregnant.

For Women: You will be required to use two reliable forms of birth control beginning 4 weeks before you start taking Thalomid and ending 4 weeks after you stop taking it. Any woman who has not had a hysterectomy or has not been in menopause for at least 24 months in a row must agree in writing to use birth control before, during, and after taking Thalomid. Even women with fertility problems are required to use birth control while taking this medication. You must also have a negative pregnancy test within 24 hours before you start Thalomid treatment. While you are taking Thalomid, you will need to have a pregnancy test weekly during the first month of treatment, and then every 4 weeks thereafter.

Stop using Thalomid and call your doctor at once if you quit using birth control, if your period is late, or if you think you might be pregnant.

For Men: You must not cause a woman to become pregnant while you are taking Thalomid because the medicine may affect your sperm and cause birth defects in the baby. You must agree in writing to always use latex condoms when having sex with a woman who is able to get pregnant, even if you have had a vasectomy. Avoid ejaculating without a condom because thalidomide can be passed in your sperm.

Thalomid is available only under a special program called “System for Thalidomide Education and Prescribing Safety” (S.T.E.P.S.). You must be registered in the program and sign documents stating that you understand the dangers of this medication and that you agree to use birth control as required by the program. For patients between 12 and 18 years, a parent or legal guardian must read and sign all written requirements for the S.T.E.P.S. program.

Do not donate blood or sperm while you are using Thalomid. Avoid exposing another person to your blood or semen through casual or sexual contact.

Before taking Thalomid

Before taking Thalomid, tell your doctor if you have:

a history of stroke or blood clots;

heart disease;

HIV or AIDS;

epilepsy or seizures;

a weak immune system; or

nerve problems, such as numbness or tingling in your hands or feet.

If you have any of these conditions, you may not be able to take thalidomide, or you may need a dosage adjustment or special tests during treatment.

Thalomid can cause severe, life-threatening birth defects or death of a baby if the mother or the father is taking this medication at the time of conception or during pregnancy. Even one dose of Thalomid can cause major birth defects of the baby’s arms and legs, bones, ears, eyes, face, and heart. Never use Thalomid if you are pregnant. It is not known if thalidomide passes into breast milk or if it could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.

For Women: You will be required to use two reliable forms of birth control beginning 4 weeks before you start taking thalidomide and ending 4 weeks after you stop taking it. Any woman who has not had a hysterectomy or has not been in menopause for at least 24 months in a row must agree in writing to use birth control before, during, and after taking Thalomid. Even women with fertility problems are required to use birth control while taking this medication. You must also have a negative pregnancy test within 24 hours before you start thalidomide treatment. While you are taking Thalomid, you will need to have a pregnancy test weekly during the first month of treatment, and then every 4 weeks thereafter.

The birth control method you use must be proven highly effective: hormonal birth control (pills, implants, or injections), an intrauterine device (IUD), a tubal ligation, or a sexual partner’s vasectomy. The extra form of birth control you use must be a barrier method such as a latex condom, a diaphragm, or a cervical cap.

Stop using thalidomide and call your dotor at once if you quit using birth control, if your period is late, or if you think you might be pregnant.

For Men: You must not cause a woman to become pregnant while you are taking Thalomid because the medicine may affect your sperm and cause birth defects in the baby. You must agree in writing to always use latex condoms when having sex with a woman who is able to get pregnant, even if you have had a vasectomy. Avoid ejaculating without a condom because Thalomid can be passed in your sperm.

Thalomid is available only under a special program called “System for Thalidomide Education and Prescribing Safety” (S.T.E.P.S.). You must be registered in the program and sign documents stating that you understand the dangers of this medication and that you agree to use birth control as required by the program. For patients between 12 and 18 years, a parent or legal guardian must read and sign all written requirements for the S.T.E.P.S. program. Do not give this medicine to a child younger than 12 years old.

How should I take Thalomid?

While you are using Thalomid, you will be required to be listed on a patient registry and participate in occasional telephone surveys. You will be limited to a 28-day supply of thalidomide each time your prescription is refilled. You may continue getting refills only if you participate fully in the S.T.E.P.S. program and commit to all agreements.

Take Thalomid exactly as it was prescribed for you. Do not take the medication in larger amounts, or take it for longer than recommended by your doctor. Your doctor may occasionally change your dose to make sure you get the best results from this medication.

Take each dose with a full glass of water.

Swallow the capsule whole, without breaking it open.

Thalomid is usually taken at bedtime. Take the medicine on an empty stomach, at least 1 hour after eating a meal.

To be sure Thalomid is helping your condition, your progress will need to be checked on a regular basis. It is important that you not miss any scheduled visits to your doctor.

You must not donate blood or sperm while you are using thalidomide. Avoid exposing another person to your blood or semen through casual or sexual contact.

This medication comes with patient instructions for safe and effective use. Follow these directions carefully. Never give Thalomid to another person, even if he or she has the same disorder for which you are being treated.

Store Thalomid at room temperature away from moisture and heat. Keep each capsule in its blister pack until you are ready to take it.

Do not allow another person to handle your medicine without wearing disposable gloves. Caregivers should avoid handling broken capsules or inhaling the powder from a damaged capsule.

What happens if I miss a dose?

Take the missed dose as soon as you remember. If it is almost time for the next dose, skip the missed dose and take only the next regularly scheduled dose. Do not take extra medicine to make up the missed dose.

What happens if I overdose?

Seek emergency medical attention if you think you have used too much of this medicine. An overdose of Thalomid is not expected to produce life-threatening symptoms.

What should I avoid while taking Thalomid?

Thalomid can cause side effects that may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be awake and alert. Avoid drinking alcohol, which can increase some of the side effects of Thalomid.

Avoid using other medicines that make you sleepy (such as cold medicine, pain medication, muscle relaxers, and medicine for seizures, depression or anxiety). They can add to sleepiness caused by Thalomid.

What are the possible side effects of Thalomid?

Stop using this medicine and get emergency medical help if you have any of these signs of an allergic reaction to Thalomid: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.

Call your doctor at once if you have any of these serious side effects:

chest pain, sudden shortness of breath, coughing up blood;

pain or swelling in your arm, thigh, or calf;

easy bruising, unusual bleeding or weakness;

slow heartbeats, shallow breathing;

feeling light-headed, fainting;

fever, chills, body aches, flu symptoms;

a red, blistering, peeling skin rash;

red, raised skin rash (especially if you also have fever, fast heart rate, and dizziness or fainting);

numbness, burning, pain, or tingly feeling; or

seizure (convulsions).

Other less serious Thalomid side effects are more likely to occur, such as:

feeling drowsy or sleepy;

anxiety, confusion, tremors or shaking;

bone pain, muscle weakness;

sleep problems (insomnia); or

nausea, constipation, loss of appetite.

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 Thalomid?

If you use hormonal birth control (pills, implants, injections) to prevent pregnancy: There are certain drugs that can make hormonal birth control less effective in your body. Below is a list of some of these drugs. This list may not include all drugs with the potential to affect hormonal birth control.

HIV medicines such as tipranavir (Aptivus), indinavir (Crixivan), saquinavir (Invirase), lopinavir/ritonavir (Kaletra), fosamprenavir (Lexiva), ritonavir (Norvir), atazanavir (Reyataz), or nelfinavir (Viracept);

griseofulvin (Gris-PEG, Grifulvin V, Grisactin, or Fulvicin);

rifampin (Rimactane, Rifadin);

rifabutin (Mycobutin);

phenytoin (Dilantin); or

carbamazepine (Tegretol).

If you rely on hormonal contraception as one of the two forms of birth control during your treatment with Thalomid, tell your doctor about all other medicines you use. You may also need to replace your hormonal birth control method with another effective form of contraception. Not having sexual intercourse (abstinence) is the most effective method of preventing pregnancy.

There may be other drugs not listed that can affect Thalomid. Tell your doctor about all the prescription and over-the-counter medications you use. This includes vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start using a new medication without telling your doctor.

Targretin

Targretin

Targretin may cause serious birth defects if used by a pregnant woman. Women who are pregnant or who may become pregnant during treatment must not use Targretin .

Women must have a negative pregnancy test within 1 week of starting Targretin and must take a pregnancy test every month while taking Targretin . Two effective forms of birth control (eg, condoms, diaphragms, cervical caps, IUDs, spermicides) must be used for 1 month before starting Targretin , during the use of Targretin , and for 1 month after stopping Targretin . If pregnancy occurs before, during, or within 1 month after treatment with Targretin , notify your doctor immediately.

Men with partners who are pregnant, are possibly pregnant, or could become pregnant must use a latex condom while taking Targretin and for at least 1 month after the last dose is taken.

Targretin is used for:

Treating skin conditions caused by certain cancers in patients who have not responded to other treatments.

Targretin is a retinoid. It works by inhibiting the growth of some cancer cells.

Do NOT use Targretin if:

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

Before using Targretin :

Some medical conditions may interact with Targretin . 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 Targretin . 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 Targretin 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 Targretin :

Use Targretin 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 Targretin .

Important safety information:

Possible side effects of Targretin :

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

Diarrhea; dizziness; dry skin; headache; loss of appetite; nausea; trouble sleeping; weakness.

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); bloating or swelling of ankles, feet, or hands; changes in vision; chest pain; chills; confusion; dark urine or pale stools; fever; severe stomach or back pain with continuing nausea or vomiting; red, swollen, or blistered skin; sore throat; unusual fatigue; 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 (

Store Targretin between 36 and 77 degrees F (2 and 25 degrees C). Do not freeze. Store away from excessive heat, moisture, and light. Do not store in the bathroom. Keep Targretin 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 Targretin . 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 Targretin resources

Compare Targretin with other medications for the treatment of:

Sotret

Sotret

Generic Name: isotretinoin (oral) (EYE so TRET i noyn)

What is isotretinoin?

Isotretinoin is a form of vitamin A. It reduces the amount of oil released by oil glands in your skin, and helps your skin renew itself more quickly.

Isotretinoin is used to treat severe nodular acne that has not responded to other treatments, including antibiotics.

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

What is the most important information I should know about isotretinoin?

Isotretinoin can cause severe, life-threatening birth defects. Never use isotretinoin if you are pregnant.

Women of child-bearing potential must agree in writing to use two specific forms of birth control and have regular pregnancy tests before, during, and after taking isotretinoin.

Isotretinoin is available only under a special program called iPLEDGE. It is dangerous to try and purchase isotretinoin on the Internet or from vendors outside of the United States.

Do not take vitamin supplements containing vitamin A while you are taking isotretinoin. Do not donate blood while taking isotretinoin and for at least 30 days after you stop taking it.

What should I discuss with my healthcare provider before taking isotretinoin?

Isotretinoin is available only under a special program called iPLEDGE. You must be registered in the program and sign documents stating that you understand the dangers of this medication and that you agree to use birth control as required by the program. Ask your doctor or call the drug maker if you have questions about the program or the written requirements.

It is dangerous to try and purchase isotretinoin on the Internet or from vendors outside of the United States. The sale and distribution of isotretinoin outside of the iPLEDGE program violates the regulations of the U.S. Food and Drug Administration for the safe use of this medication.

Do not use this medication if you are allergic to isotretinoin or to parabens, or if you are pregnant or may become pregnant.

If you have any of these other conditions, you may need a dose adjustment or special tests to safely take isotretinoin:

a personal or family history of depression or mental illness;

heart disease, high cholesterol or triglycerides;

osteoporosis or other bone disorders;

diabetes;

asthma;

an eating disorder (anorexia nervosa); or

For Women: Unless you have had your uterus and ovaries removed (total hysterectomy) or have been in menopause for at least 12 months in a row, you are considered to be of child-bearing potential.

Even women who have had their tubes tied are required to use birth control while taking isotretinoin.

You must have a negative pregnancy test 30 days before you start taking isotretinoin. A pregnancy test is also required before each prescription is refilled, right after you take your last dose of isotretinoin, and again 30 days later. All pregnancy testing is required by the iPLEDGE program.

You must agree in writing to use two specific forms of birth control beginning 30 days before you start taking isotretinoin and ending 30 days after you stop taking it. Both a primary and a secondary form of birth control must be used together.

Primary forms of birth control include:

tubal ligation (tubes tied);

vasectomy of the male sexual partner;

an IUD (intrauterine device);

estrogen-containing birth control pills (not mini-pills); and

hormonal birth control patches, implants, injections, or vaginal ring.

Secondary forms of birth control include:

a male latex condom plus spermicidal foam or gel;

a diaphragm plus spermicidal foam or gel;

a cervical cap plus spermicidal foam or gel; and

a vaginal sponge containing spermicide.

Stop using isotretinoin and call your doctor at once if you have unprotected sex, if you quit using birth control, if your period is late, or if you think you might be pregnant. If you get pregnant while taking isotretinoin, call the iPLEDGE pregnancy registry at 1-866-495-0654.

It is not known whether isotretinoin passes into breast milk. Do not take isotretinoin without first talking to your doctor if you are breast-feeding a baby.

How should I take isotretinoin?

Take this medication exactly as it was prescribed for you. Do not take the medication in larger amounts, or take it for longer than recommended by your doctor. Follow the directions on your prescription label.

Each prescription of isotretinoin must be filled within 7 days of the date it was prescribed by your doctor. You will receive no more than a 30-day supply of isotretinoin at one time.

Always take isotretinoin with a full glass of water to prevent the capsule from melting in your esophagus (food pipe), causing irritation. Do not chew or suck on the capsule. Swallow it as quickly as possible. Take isotretinoin with food or milk. Take this medication for the entire length of time prescribed by your doctor. Your acne may seem to get worse at first, but should then begin to improve.

To be sure this medication is not causing harmful effects, your blood may need to be tested on a regular basis. Your liver function may also need to be tested. Do not miss any scheduled visits to your doctor.

Never share this medicine with another person, even if they have the same symptoms you have. Store isotretinoin at room temperature away from moisture, heat, and light.

What happens if I miss a dose?

Skip the missed dose and take the medicine at your next regularly scheduled time. Do not take extra medicine to make up the missed dose.

What happens if I overdose?

Seek emergency medical attention if you think you have used too much of this medicine. Overdose symptoms may include headache, dizziness, vomiting, stomach pain, warmth or tingling under the skin, swelling of the lips, and loss of balance or coordination.

What should I avoid while taking isotretinoin?

Do not take vitamin supplements containing vitamin A while you are taking isotretinoin. Do not donate blood while taking isotretinoin and for at least 30 days after you stop taking it. Donated blood that is later given to pregnant woman could lead to birth defects in her baby if the blood contains any level of isotretinoin.

Do not use wax hair removers or have dermabrasion or laser skin treatments while you are taking isotretinoin and for at least 6 months after you stop taking it. Scarring may result.

Avoid exposure to sunlight or artificial UV rays (sunlamps or tanning beds). Isotretinoin can make your skin more sensitive to sunlight and sunburn may result. Isotretinoin can cause side effects that may impair your vision, especially at night. Be careful if you drive or do anything that requires you to see clearly.

Isotretinoin 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. Stop using isotretinoin and call your doctor at once if you have any of these serious side effects:

depressed mood, trouble concentrating, sleep problems, crying spells, aggression or agitation, changes in behavior, hallucinations, thoughts of suicide or hurting yourself;

sudden numbness or weakness, especially on one side of the body;

blurred vision, sudden and severe headache or pain behind your eyes, sometimes with vomiting;

hearing problems, hearing loss, or ringing in your ears;

seizure (convulsions);

severe pain in your upper stomach spreading to your back, nausea and vomiting, fast heart rate;

loss of appetite, dark urine, clay-colored stools, jaundice (yellowing of the skin or eyes);

severe diarrhea, rectal bleeding, black, bloody, or tarry stools;

fever, chills, body aches, flu symptoms, purple spots under your skin, easy bruising or bleeding; or

joint stiffness, bone pain or fracture.

Less serious side effects may include:

joint pain, back pain;

feeling dizzy, drowsy, or nervous;

dryness of the lips, mouth, nose, or skin; or

cracking or peeling skin, itching, rash, changes in your fingernails or toenails.

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 isotretinoin?

Before taking isotretinoin, tell your doctor if you are also taking:

steroids (prednisone and others);

seizure medication such phenytoin (Dilantin); or

a tetracycline antibiotic such as demeclocycline (Declomycin), doxycycline (Doryx, Vibramycin), minocycline (Minocin), or tetracycline (Brodspec, Sumycin, Tetracap).

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

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