Dacarbazine

Pronunciation: da-KAR-ba-zeen
Generic Name: Dacarbazine
Brand Name: DTIC-Dome

Dacarbazine can cause severe, even fatal, liver problems (hepatic necroses), or a decrease in the formation of new blood cells (hemopoietic depression). It has also caused cancer and birth defects in laboratory animals. Notify your doctor immediately if you develop symptoms of an infection (eg, persistent sore throat or fever), easy bruising or bleeding, nausea, dark urine, unusual fatigue, yellowing of the eyes or skin, or stomach pain. Your doctor will monitor you closely while you are using Dacarbazine.

Dacarbazine is used for:

Treating certain cancers (eg, advanced skin cancer) and Hodgkin disease. It may be used with other medicines. It may also be used for other conditions as determined by your doctor.

Dacarbazine is an antineoplastic agent. It is not known exactly how Dacarbazine works. It may block the growth of cancer cells.

Do NOT use Dacarbazine if:

• you are allergic to any ingredient in Dacarbazine


• you have shingles or chickenpox

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

Before using Dacarbazine:

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

• if you are pregnant, planning to become pregnant, or are breast-feeding


• if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement


• if you have allergies to medicines, foods, or other substances


• if you have a blood disease, an infection, or liver or kidney problems

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

This may not be a complete list of all interactions that may occur. Ask your health care provider if Dacarbazine 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 Dacarbazine:

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

• Dacarbazine will be administered as an injection at your doctor's office, hospital, or clinic.


• If Dacarbazine contains particles or is discolored, or if the vial is cracked or damaged in any way, do not use it.


• If nausea, vomiting, or loss of appetite occurs, ask your doctor or pharmacist for ways to lessen these effects.


• Keep this product, as well as syringes and needles, out of the reach of children and away from pets. Do not reuse needles, syringes, or other materials. Dispose of properly after use. Ask your doctor or pharmacist to explain local regulations for proper disposal.


• If you miss a dose of Dacarbazine, contact your doctor immediately.

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

Important safety information:

• Dacarbazine may lower your body's ability to fight infection. Prevent infection by avoiding contact with people with colds or other infections. Notify your doctor of any signs of infection, including fever, sore throat, rashes, or chills.


• Dacarbazine may reduce the number of clot-forming cells (platelets) in your blood. To prevent bleeding, avoid situations in which bruising or injury may occur. Report any unusual bleeding, bruising, blood in stools, or dark, tarry stools to your doctor.


• Use of Dacarbazine may increase the risk of developing a second cancer. Discuss any questions or concerns with your doctor.


• Avoid vaccination with live virus vaccines (eg, measles, mumps, oral polio) while you are taking Dacarbazine. Vaccinations may be less effective.


• LAB TESTS, including blood cell counts and liver function tests, may be performed to monitor your progress or to check for side effects. Be sure to keep all doctor and lab appointments.


• PREGNANCY and BREAST-FEEDING: If you become pregnant, discuss with your doctor the benefits and risks of using Dacarbazine during pregnancy. It is unknown if Dacarbazine is excreted in breast milk. Do not breast-feed while taking Dacarbazine.

Possible side effects of Dacarbazine:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Facial flushing, numbness, or tingling; loss of appetite; metallic taste in mouth; muscle pain or weakness; nausea; temporary hair loss; vomiting.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); dark urine; fever, chills, or sore throat; joint pain; pain, redness, or swelling at injection site; severe nausea and vomiting; stomach pain; unusual bruising or bleeding; unusual tiredness or weakness; yellowing of 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. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

See also: Dacarbazine side effects (in more detail)

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center (http://www.aapcc.org ), or emergency room immediately.

Proper storage of Dacarbazine:

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

General information:

• If you have any questions about Dacarbazine, please talk with your doctor, pharmacist, or other health care provider.


• Dacarbazine is to be used only by the patient for whom it is prescribed. Do not share it with other people.


• If your symptoms do not improve or if they become worse, check with your doctor.


• Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Dacarbazine. 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.

Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Dacarbazine resources

• Dacarbazine Side Effects (in more detail)
• Dacarbazine Use in Pregnancy & Breastfeeding
• Dacarbazine Drug Interactions
• Dacarbazine Support Group
• 0 Reviews for Dacarbazine - Add your own review/rating

• Dacarbazine Prescribing Information (FDA)


• Dacarbazine Monograph (AHFS DI)


• Dacarbazine Professional Patient Advice (Wolters Kluwer)


• dacarbazine Concise Consumer Information (Cerner Multum)


• dacarbazine Intravenous, Injection Advanced Consumer (Micromedex) - Includes Dosage Information

Compare Dacarbazine with other medications

• Hodgkin's Lymphoma
• Melanoma

Cicloral

Cicloral may be available in the countries listed below.

Ingredient matches for Cicloral

Ciclosporin

Ciclosporin is reported as an ingredient of Cicloral in the following countries:

• Australia

International Drug Name Search

Bicitra

Pronunciation: SIH-trik AS-id/SOE-dee-um SIH-trayt
Generic Name: Citric Acid/Sodium Citrate
Brand Name: Examples include Cytra-2 and Oracit

Bicitra is used for:

Treating metabolic acidosis and certain kidney problems (eg, kidney stones). It may also be used for other conditions as determined by your doctor.

Bicitra is an alkalinizing agent. It works by neutralizing excess acid in the blood and urine.

Do NOT use Bicitra if:

• you are allergic to any ingredient in Bicitra


• you have aluminum toxicity, untreated Addison disease, low or no urine production, high blood potassium, congestive heart failure, heart damage, or severe kidney problems, or if you are dehydrated

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

Before using Bicitra:

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

• if you are pregnant, planning to become pregnant, or are breast-feeding


• if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement


• if you have allergies to medicines, foods, or other substances


• if you are taking aluminum salts (eg, aluminum hydroxide), amphetamines or lithium


• if you have a history of kidney disease, heart disease, electrolyte/mineral imbalances (eg, high potassium levels), Addison disease, or stomach problems (eg, ulcer disease)


• if you have high blood pressure, a urinary tract infection, or toxemia, or you are on a sodium-restricted diet

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

• Aluminum salts (eg, aluminum hydroxide) because the risk of severe aluminum toxicity may be increased


• Anorexiants (eg, phentermine) or sympathomimetics (eg, pseudoephedrine) because side effects may be increased by Bicitra


• Lithium or tetracyclines (eg, doxycycline) because effectiveness may be decreased by Bicitra

This may not be a complete list of all interactions that may occur. Ask your health care provider if Bicitra 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 Bicitra:

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

• Take Bicitra after meals and at bedtime, unless directed otherwise by your health care provider.


• Shake well before using.


• Use a measuring device marked for medicine dosing. Ask your pharmacist for help if you are unsure of how to measure your dose.


• Mix Bicitra with water before swallowing. Follow with additional water, if desired.


• If you miss a dose of Bicitra, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

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

Important safety information:

• LAB TESTS, including blood electrolyte and bicarbonate levels, may be performed to monitor your progress or to check for side effects. Be sure to keep all doctor and lab appointments.


• Use Bicitra with caution in CHILDREN younger than 2 years of age because they may be more sensitive to its effects.


• PREGNANCY and BREAST-FEEDING: If you become pregnant while taking Bicitra, discuss with your doctor the benefits and risks of using Bicitra during pregnancy. It is unknown if Bicitra is excreted in breast milk. If you are or will be breast-feeding while you are using Bicitra, check with your doctor or pharmacist to discuss the risks to your baby.

Possible side effects of Bicitra:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Diarrhea; loose stools; nausea; upset stomach; vomiting.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); black, tarry stools; confusion; severe stomach pain; tingling of hands or feet; vomit that looks like coffee grounds; 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. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

See also: Bicitra side effects (in more detail)

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include diarrhea; nausea; seizures; vomiting.

Proper storage of Bicitra:

Store Bicitra at room temperature, between 68 and 77 degrees F (20 and 25 degrees C), in a tightly closed container. Store away from heat, moisture, and light. Do not freeze. Keep Bicitra out of the reach of children and away from pets.

General information:

• If you have any questions about Bicitra, please talk with your doctor, pharmacist, or other health care provider.


• Bicitra is to be used only by the patient for whom it is prescribed. Do not share it with other people.


• If your symptoms do not improve or if they become worse, check with your doctor.


• Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Bicitra. 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.

Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Bicitra resources

• Bicitra Side Effects (in more detail)
• Bicitra Use in Pregnancy & Breastfeeding
• Bicitra Drug Interactions
• Bicitra Support Group
• 0 Reviews for Bicitra - Add your own review/rating

• Bicitra Concise Consumer Information (Cerner Multum)

Compare Bicitra with other medications

• Urinary Alkalinization
• Urinary Tract Stones

Babee Teething

Generic Name: benzocaine (Oral route, Oromucosal route)

BEN-zoe-kane

Commonly used brand name(s)

In the U.S.

• Anbesol


• Babee Teething


• Benzodent


• Benz-O-Sthetic


• Bi-Zets/Benzo-Troches


• Dentemp's


• Dent-O-Kain/20


• Detane


• Gumsol


• HAD


• Hurricaine


• Hurricane Spray Kit


• Kank-A Soft Brush


• Larynex


• Miradyne-3


• Mycinette


• Orabase-B


• Oracaine


• Ora film


• Orajel


• OraMagic Plus


• Orasol


• Red Cross Canker Sore


• Thorets


• Trocaine


• Zetts


• Zilactin


• Zilactin-B

In Canada

• Anbesol Extra Strength


• Anbesol Liquid


• Baby Anbesol


• Baby Orajel


• Baby Orajel Liquid


• Maximum Strength Orajel Pm


• Orajel Extra Strength

Available Dosage Forms:

• Liquid


• Gel/Jelly


• Solution


• Lozenge/Troche


• Film


• Lotion


• Ointment


• Powder for Suspension


• Cream


• Tablet, Disintegrating


• Swab


• Spray


• Gum


• Paste

Therapeutic Class: Anesthetic, Local

Chemical Class: Amino Ester

Uses For Babee Teething

Benzocaine lozenges are used to relieve pain and irritation caused by sore throat, sore mouth, or canker sores.

This medicine is available without a prescription; however, your doctor may have special instructions on the proper use and dose for your medical problem.

Before Using Babee Teething

In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For this medicine, the following should be considered:

Allergies

Tell your doctor if you have ever had any unusual or allergic reaction to this medicine or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.

Pediatric

No information is available on the relationship of age to the effects of benzocaine lozenges in the pediatric population. Safety and efficacy have not been established in children below 5 years of age.

Geriatric

No information is available on the relationship of age to the effects of benzocaine in geriatric patients.

Interactions with Medicines

Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. Tell your healthcare professional if you are taking any other prescription or nonprescription (over-the-counter [OTC]) medicine.

Interactions with Food/Tobacco/Alcohol

Certain medicines should not be used at or around the time of eating food or eating certain types of food since interactions may occur. Using alcohol or tobacco with certain medicines may also cause interactions to occur. Discuss with your healthcare professional the use of your medicine with food, alcohol, or tobacco.

Other Medical Problems

The presence of other medical problems may affect the use of this medicine. Make sure you tell your doctor if you have any other medical problems, especially:

• Infection in or around your mouth or


• Large sores in or around your mouth—The chance of side effects may be increased.

Proper Use of benzocaine

This section provides information on the proper use of a number of products that contain benzocaine. It may not be specific to Babee Teething. Please read with care.

Use this medicine exactly as directed by your doctor. Do not use more of this medicine, do not use it more often, and do not use it for a longer time than directed. To do so may increase the chance of absorption into the body and the risk of side effects.

This medicine should be used only for problems being treated by your doctor or conditions listed in the package directions. Check with your doctor before using it for other problems, especially if you think that an infection may be present.

Do not use this medicine for more than 2 days without checking first with your doctor.

Dosing

The dose of this medicine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so.

The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.

• For oral dosage form (lozenges):
  
  • For sore throat and mouth pain:
    
    • Adults, teenagers, and children 5 years of age and older—One lozenge, dissolved slowly in the mouth every 2 hours as needed.
    
    
    • Children younger than 5 years of age—Use is not recommended.
    
    
  
  

Missed Dose

If you miss a dose of this medicine, take it as soon as possible. However, if it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not double doses.

Storage

Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing.

Keep out of the reach of children.

Do not keep outdated medicine or medicine no longer needed.

Ask your healthcare professional how you should dispose of any medicine you do not use.

Precautions While Using Babee Teething

If your condition does not improve within 7 days, or if it becomes worse, check with your doctor.

Call your doctor right away if you start to have a severe sore throat or sore throat that occurs with a high fever, headache, nausea, or vomiting. These maybe signs of an infection.

Babee Teething Side Effects

Along with its needed effects, a medicine may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.

Check with your doctor immediately if any of the following side effects occur:

Incidence not known

• Headache


• high fever


• nausea


• vomiting


• worsening of pain, redness, swelling, or irritation in or around the mouth

Other side effects not listed may also occur in some patients. If you notice any other effects, check with your healthcare professional.

Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.

See also: Babee Teething side effects (in more detail)

The information contained in the Thomson Reuters Micromedex products as delivered by Drugs.com is intended as an educational aid only. It is not intended as medical advice for individual conditions or treatment. It is not a substitute for a medical exam, nor does it replace the need for services provided by medical professionals. Talk to your doctor, nurse or pharmacist before taking any prescription or over the counter drugs (including any herbal medicines or supplements) or following any treatment or regimen. Only your doctor, nurse, or pharmacist can provide you with advice on what is safe and effective for you.

The use of the Thomson Reuters Healthcare products is at your sole risk. These products are provided "AS IS" and "as available" for use, without warranties of any kind, either express or implied. Thomson Reuters Healthcare and Drugs.com make no representation or warranty as to the accuracy, reliability, timeliness, usefulness or completeness of any of the information contained in the products. Additionally, THOMSON REUTERS HEALTHCARE MAKES NO REPRESENTATION OR WARRANTIES AS TO THE OPINIONS OR OTHER SERVICE OR DATA YOU MAY ACCESS, DOWNLOAD OR USE AS A RESULT OF USE OF THE THOMSON REUTERS HEALTHCARE PRODUCTS. ALL IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE OR USE ARE HEREBY EXCLUDED. Thomson Reuters Healthcare does not assume any responsibility or risk for your use of the Thomson Reuters Healthcare products.

More Babee Teething resources

• Babee Teething Side Effects (in more detail)
• Babee Teething Use in Pregnancy & Breastfeeding
• Babee Teething Support Group
• 0 Reviews · Be the first to review/rate this drug

Covospor

Covospor may be available in the countries listed below.

Ingredient matches for Covospor

Clotrimazole

Clotrimazole is reported as an ingredient of Covospor in the following countries:

• South Africa

International Drug Name Search

Risperidone Orally Disintegrating Tablets

Pronunciation: ris-PER-i-done
Generic Name: Risperidone
Brand Name: Risperdal M-Tab

Risperidone Orally Disintegrating Tablets are an atypical antipsychotic. It may increase the risk of death when used to treat mental problems caused by dementia in elderly patients. Most of the deaths were linked to heart problems or infection. Risperidone Orally Disintegrating Tablets are not approved to treat mental problems caused by dementia.

Risperidone Orally Disintegrating Tablets are used for:

Treating schizophrenia or bipolar disorder. It is used to treat irritability caused by autistic disorder. It may also be used for other conditions as determined by your doctor.

Risperidone Orally Disintegrating Tablets are an atypical antipsychotic. It works by affecting certain substances in the brain.

Do NOT use Risperidone Orally Disintegrating Tablets if:

• you are allergic to any ingredient in Risperidone Orally Disintegrating Tablets

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

Before using Risperidone Orally Disintegrating Tablets:

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

• if you are pregnant, planning to become pregnant, or are breast-feeding


• if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement


• if you have allergies to medicines, foods, or other substances


• if you have a history of seizures, heart problems (eg, heart failure, slow or irregular heartbeat), abnormal electrocardiogram (ECG), heart attack, stroke, blood vessel problems, high or low blood pressure, high cholesterol or triglyceride levels, or low white blood cell levels


• if you have a history of kidney or liver problems, stomach or bowel problems (eg, narrowing, blockage), neuroleptic malignant syndrome (NMS), suicidal thoughts or attempts, or alcohol abuse or dependence


• if you have diabetes or are very overweight, or if a family member has had diabetes


• if you have Alzheimer disease, dementia, phenylketonuria, Parkinson disease, or esophagus problems (eg, trouble swallowing)


• if you have had high blood prolactin levels or a history of certain types of cancer (eg, breast, pancreas, pituitary, brain), or if you are at risk for breast cancer


• if you are dehydrated, drink alcohol, or will be exposed to very high or very low temperatures

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

• Alpha-blockers (eg, doxazosin) or medicine for high blood pressure because the risk of low blood pressure and fainting may be increased


• Anticholinergics (eg, scopolamine) because the risk of overheating may be increased


• Tramadol because the risk of seizures may be increased


• Clozapine or selective serotonin reuptake inhibitors (SSRIs) (eg, fluoxetine, paroxetine) because they may increase the risk of Risperidone Orally Disintegrating Tablets's side effects


• Carbamazepine, phenobarbital, phenytoin, or rifampin because they may decrease Risperidone Orally Disintegrating Tablets's effectiveness


• Dopamine receptor agonists (eg, pramipexole) or levodopa because their effectiveness may be decreased by Risperidone Orally Disintegrating Tablets

This may not be a complete list of all interactions that may occur. Ask your health care provider if Risperidone Orally Disintegrating Tablets 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 Risperidone Orally Disintegrating Tablets:

Use Risperidone Orally Disintegrating Tablets as directed by your doctor. Check the label on the medicine for exact dosing instructions.

• Take Risperidone Orally Disintegrating Tablets by mouth with or without food.


• Do not remove the blister from the outer pouch until you are ready to take Risperidone Orally Disintegrating Tablets. Make sure that your hands are dry when you open the blister pack. Do not push the tablet through the foil. Peel back the foil on the blister pack, place the tablet on your tongue, and allow it to dissolve. The tablet dissolves quickly and can be swallowed with saliva. Risperidone Orally Disintegrating Tablets may be taken with or without water. Take the tablet immediately after opening the blister pack. Do not store the removed tablet for future use.


• Do not break, chew, or swallow the tablet whole.


• Take Risperidone Orally Disintegrating Tablets on a regular schedule to get the most benefit from it. Taking Risperidone Orally Disintegrating Tablets at the same time each day will help you remember to take it.


• Continue to take Risperidone Orally Disintegrating Tablets even if you feel well. Do not miss any doses.


• If you miss a dose of Risperidone Orally Disintegrating Tablets, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Risperidone Orally Disintegrating Tablets.

Important safety information:

• Risperidone Orally Disintegrating Tablets may cause drowsiness, dizziness, light-headedness, or blurred vision. These effects may be worse if you take it with alcohol or certain medicines. Use Risperidone Orally Disintegrating Tablets with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.


• Do not drink alcohol while you are taking Risperidone Orally Disintegrating Tablets.


• Check with your doctor before taking medicines that may cause drowsiness (eg, sleep aids, muscle relaxers) while you are using Risperidone Orally Disintegrating Tablets; it may add to their effects. Ask your pharmacist if you have questions about which medicines may cause drowsiness.


• Risperidone Orally Disintegrating Tablets may cause dizziness, light-headedness, or fainting; alcohol, hot weather, exercise, or fever may increase these effects. To prevent them, sit up or stand slowly, especially in the morning. Sit or lie down at the first sign of any of these effects.


• Do not become overheated in hot weather or while you are being active; heatstroke may occur.


• Patients who have bipolar (manic-depressive) illness, or if their family members have had it, may be at increased risk for suicidal thoughts or actions. Watch patients who take Risperidone Orally Disintegrating Tablets closely. Contact the doctor at once if new, worsened, or sudden symptoms such as anxious, restless, or irritable behavior; depressed mood; panic attacks; or any unusual change in mood or behavior occur. Contact the doctor right away if any signs of suicidal thoughts or actions occur.


• Risperidone Orally Disintegrating Tablets may raise your blood sugar. High blood sugar may make you feel confused, drowsy, or thirsty. It can also make you flush, breathe faster, or have a fruit-like breath odor. If these symptoms occur, tell your doctor right away.


• Diabetes patients - Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.


• Risperidone Orally Disintegrating Tablets may lower the ability of your body to fight infection. Avoid contact with people who have colds or infections. Tell your doctor if you notice signs of infection like fever, sore throat, rash, or chills.


• NMS is a possibly fatal syndrome that can be caused by Risperidone Orally Disintegrating Tablets. Symptoms may include fever; stiff muscles; confusion; abnormal thinking; fast or irregular heartbeat; or sweating. Contact your doctor at once if you have any of these symptoms.


• Risperidone Orally Disintegrating Tablets contains phenylalanine. If you must have a diet that is low in phenylalanine, check with your doctor before using Risperidone Orally Disintegrating Tablets.


• Some patients who take Risperidone Orally Disintegrating Tablets may develop muscle movements that they cannot control. This is more likely to happen in elderly patients, especially women. The chance that this will happen or that it will become permanent is greater in those who take Risperidone Orally Disintegrating Tablets in higher doses or for a long time. Muscle problems may also occur after short-term treatment with low doses. Tell your doctor at once if you have muscle problems with your arms; legs; or your tongue, face, mouth, or jaw (eg, tongue sticking out, puffing of cheeks, mouth puckering, chewing movements) while taking Risperidone Orally Disintegrating Tablets.


• Risperidone Orally Disintegrating Tablets may increase the amount of a certain hormone (prolactin) in your blood. Symptoms may include enlarged breasts, missed menstrual period, decreased sexual ability, or nipple discharge. Contact your doctor right away if you experience any of these symptoms.


• Risperidone Orally Disintegrating Tablets may rarely cause a prolonged, painful erection. This could happen even when you are not having sex. If this is not treated right away, it could lead to permanent sexual problems such as impotence. Contact your doctor right away if this happens.


• Lab tests, including fasting blood glucose and complete blood cell counts, may be performed while you use Risperidone Orally Disintegrating Tablets. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.


• Risperidone Orally Disintegrating Tablets may cause weight gain. Your weight may need to be monitored while you take Risperidone Orally Disintegrating Tablets.


• Use Risperidone Orally Disintegrating Tablets with caution in the ELDERLY; they may be more sensitive to its effects, especially dizziness when standing or uncontrolled muscles movements.


• Risperidone Orally Disintegrating Tablets should be used with extreme caution in CHILDREN younger than 5 years old; safety and effectiveness in these children have not been confirmed.


• PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of taking Risperidone Orally Disintegrating Tablets while you are pregnant. Using Risperidone Orally Disintegrating Tablets during the third trimester may result in uncontrolled muscle movements or withdrawal symptoms in the newborn. Discuss any questions or concerns with your doctor. Risperidone Orally Disintegrating Tablets are found in breast milk. Do not breast-feed while taking Risperidone Orally Disintegrating Tablets.

Possible side effects of Risperidone Orally Disintegrating Tablets:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Anxiety; constipation; cough; diarrhea; dizziness; drowsiness; dry mouth; fatigue; headache; increased appetite; increased saliva production; indigestion; light-headedness; nausea; restlessness; runny nose; stomach pain or upset; trouble sleeping; vomiting; weight gain.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing or swallowing; tightness in the chest; swelling of the mouth, face, lips, or tongue; unusual hoarseness); abnormal thoughts; confusion; drooling; fainting; fast or irregular heartbeat; fever, chills, or persistent sore throat; inability to control urination; increased sweating; new or worsening mental or mood changes (eg, aggression, agitation, depression, severe anxiety); seizures; severe dizziness; stiff or rigid muscles; suicidal thoughts or attempts; symptoms of high blood sugar (eg, increased thirst, hunger, or urination; unusual weakness); tremor; trouble concentrating, speaking, or swallowing; trouble sitting still; trouble walking or standing; uncontrolled muscle movements (eg, arm or leg movements, twitching of the face or tongue, jerking or twisting); unusual bruising; vision changes.

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. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

See also: Risperidone side effects (in more detail)

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include fast or irregular heartbeat; severe drowsiness or dizziness; unusual muscle movements.

Proper storage of Risperidone Orally Disintegrating Tablets:

Store Risperidone Orally Disintegrating Tablets between 59 and 77 degrees F (15 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Risperidone Orally Disintegrating Tablets out of the reach of children and away from pets.

General information:

• If you have any questions about Risperidone Orally Disintegrating Tablets, please talk with your doctor, pharmacist, or other health care provider.


• Risperidone Orally Disintegrating Tablets are to be used only by the patient for whom it is prescribed. Do not share it with other people.


• If your symptoms do not improve or if they become worse, check with your doctor.


• Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Risperidone Orally Disintegrating Tablets. 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.

Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Risperidone resources

• Risperidone Side Effects (in more detail)
• Risperidone Use in Pregnancy & Breastfeeding
• Drug Images
• Risperidone Drug Interactions
• Risperidone Support Group
• 102 Reviews for Risperidone - Add your own review/rating

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Calcihexal

Calcihexal may be available in the countries listed below.

Ingredient matches for Calcihexal

Calcitonin

Calcitonin is reported as an ingredient of Calcihexal in the following countries:

• Germany

International Drug Name Search

Better Bladder Control

Generic Name: lytta vesicatoria, causticum, equisetum arvense top and ferrum phosphoricum granule

Dosage Form: FOR ANIMAL USE ONLY
Better Bladder Control

Relieves incontinence and strengthens bladder

Indications: Homeopathic remedy for the relief of incontinence in pets and bladder strengthening.

Dosage: Sprinkle granules directly into the mouth and hold closed briefly. Initial dose: every 30 minutes for up to 10 doses. Thereafter, 3 times daily. Cats and dogs under 20 lbs:1 large pinch. Dogs 20-50 lbs: 2 pinches. Dogs over 50 lbs:1/4 cap granules. May be used with PetAlive UTI-Free™.

Caution: Consult your vet if symptoms persist or worsen. Keep this and all medicines from the reach of children.

Ingredients: Each dose contains equal parts of Cantharis (30C) (HPUS), Causticum (6C ) (HPUS), Equisetum (6C) (HPUS), Ferrum phos (6C) (HPUS)

Sucrose (inactive ingredient).

Enter section text here

Contains no gluten, artificial flavors, colors or preservatives

Better Bladder Control  Better Bladder Control  granule

Product Information Product Type OTC ANIMAL DRUG NDC Product Code (Source) 68647-184 Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LYTTA VESICATORIA (LYTTA VESICATORIA) LYTTA VESICATORIA 30 [hp_C]  in 50 mg CAUSTICUM (CAUSTICUM) CAUSTICUM 6 [hp_C]  in 50 mg EQUISETUM ARVENSE TOP (EQUISETUM ARVENSE TOP) EQUISETUM ARVENSE TOP 6 [hp_C]  in 50 mg FERRUM PHOSPHORICUM (FERRUM PHOSPHORICUM) FERRUM PHOSPHORICUM 6 [hp_C]  in 50 mg

Inactive Ingredients Ingredient Name Strength SUCROSE 1   in 20000 mg

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 68647-184-10 20000 mg In 1 BOTTLE, GLASS None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		01/01/2010

Labeler - Feelgood Health (538418296)

Establishment
Name	Address	ID/FEI	Operations
W Last		567284153	manufacture

Revised: 06/2010Feelgood Health

Terry White Chemists Sotalol

Terry White Chemists Sotalol may be available in the countries listed below.

Ingredient matches for Terry White Chemists Sotalol

Sotalol

Sotalol hydrochloride (a derivative of Sotalol) is reported as an ingredient of Terry White Chemists Sotalol in the following countries:

• Australia

International Drug Name Search