Angeliq

Pronunciation: droe-SPYE-re-none/ES-tra-DYE-ol
Generic Name: Drospirenone/Estradiol
Brand Name: Angeliq

Estrogen, alone or in combination with progestin hormones, should not be used to prevent heart disease or dementia. Estrogen taken alone or in combination with progestin may increase the risk of heart disease (including heart attacks), stroke, serious blood clots in the lung (pulmonary embolism) or leg (deep venous thrombosis), breast cancer, or dementia. These risks appear to depend on the length of time Angeliq is used and the amount of estrogen per dose. Therefore, Angeliq should be used for the shortest possible length of time at the lowest effective dose so you obtain the benefits and minimize the chance of serious side effects from long-term treatment. Discuss any questions or concerns with your doctor.

Angeliq is used for:

Treating certain moderate to severe symptoms of menopause (eg, hot flashes; dryness, itching, and burning in or around the vagina). It may also be used for other conditions as determined by your doctor.

Angeliq is a combination of progestin and estrogen hormones. It works by replacing natural progestin and estrogen in women who can no longer produce enough of these hormones.

Do NOT use Angeliq if:

• you are allergic to any ingredient in Angeliq


• you are pregnant or think you may be pregnant


• you have kidney, liver, or adrenal gland problems


• you have a history of blood clots (eg, in the lungs, legs, eyes); endometrial, cervical, or vaginal cancer; estrogen-dependent growths; undiagnosed abnormal vaginal bleeding; or breast cancer


• you have had recent (within the past year) bleeding in the brain, stroke, heart attack, or other serious blood vessel problems

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

Before using Angeliq:

Some medical conditions may interact with Angeliq. 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 had your uterus removed (hysterectomy), or you have a history of endometriosis, growths in the uterus, uterine fibroids, abnormal mammograms, or lumps in the breast


• if you have a history of asthma, heart problems (eg, heart failure), high blood pressure, blood problems (eg porphyria), blood vessel problems, heart attack, stroke, high cholesterol or lipid levels, diabetes, depression, dementia, gallbladder problems, pancreas problems, cancer, growths in the liver, lupus, migraine headaches, seizures, or underactive thyroid


• if you have high blood potassium levels, low blood sodium levels, or abnormal blood calcium levels


• if you have a history of fluid retention (swelling) or tobacco use, or if you are very overweight


• if a member of your family has ever had a blood clot (eg, in the lung or leg)


• if you have a history of jaundice (yellowing of the eyes or skin) caused by pregnancy or estrogen use


• if you will be confined to a bed or chair for an extended period of time (eg, because of surgery or a long airplane ride)

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

• Troleandomycin because the risk of jaundice (yellowing of the skin of eyes) and liver problems may be increased


• Angiotensin-converting enzyme (ACE) inhibitors (eg, lisinopril), angiotensin receptor blockers (eg, valsartan), heparin, nonsteroidal anti-inflammatory drugs (NSAIDs) (eg, ibuprofen), potassium sparing diuretics (eg, triamterene), or potassium supplements because the risk of high potassium levels in the blood may be increased


• Azole antifungals (eg, ketoconazole), HIV protease inhibitors (eg, ritonavir), or macrolide antibiotics (eg, erythromycin) because they may increase the risk of Angeliq's side effects


• Barbiturates (eg, phenobarbital), carbamazepine, griseofulvin, hydantoins (eg, phenytoin), penicillins (eg, amoxicillin), rifampin, St. John's wort, or tetracyclines (eg, doxycycline) because they may decrease Angeliq's effectiveness


• Corticosteroids (eg, prednisone) because the risk of their side effects may be increased by Angeliq


• Lamotrigine or thyroid hormones (eg, levothyroxine) because their effectiveness may be decreased by Angeliq

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

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

• An extra patient leaflet is available with Angeliq. Talk to your pharmacist if you have questions about this information.


• Take Angeliq by mouth with or without food.


• Grapefruit and grapefruit juice may increase the risk of side effects from Angeliq. Talk to your doctor before including grapefruit or grapefruit juice in your diet while taking Angeliq.


• Take Angeliq on a regular schedule to get the most benefit from it.


• Taking Angeliq at the same time each day will help you remember to take it.


• Continue to take Angeliq even if you feel well. Do not miss any doses.


• If you miss a dose of Angeliq, 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 Angeliq.

Important safety information:

• Angeliq may cause dizziness. This effect may be worse if you take it with alcohol or certain medicines. Use Angeliq with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.


• Check with your doctor before you use a salt substitute or a product that has potassium in it.


• Angeliq may increase the risk of stroke, heart attack, blood clots, high blood pressure, or similar problems. The risk may be greater if you smoke.


• Tell your doctor or dentist that you take Angeliq before you receive any medical or dental care, emergency care, or surgery. Angeliq should be discontinued at least 4 to 6 weeks before surgery or at any time you will be confined to a bed or chair for a long period of time (eg, a long plane flight). Talk to your doctor about the safe use of Angeliq if any of these conditions apply to you.


• Angeliq may cause dark skin patches on your face (melasma). Exposure to the sun may make these patches darker. Ask your doctor whether you should use sunscreen or wear protective clothing when your skin is exposed to the sun, sunlamps, or tanning booths.


• If you wear contact lenses and you develop problems with them or your vision, contact your doctor as soon as possible.


• Angeliq may interfere with certain lab tests. Be sure your doctor and lab personnel know you are taking Angeliq.


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


• You should talk to your doctor regularly to determine whether or not you still need to take Angeliq.


• Lab tests, including mammograms, Pap smears, blood pressure, and blood potassium levels, may be performed while you use Angeliq. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.


• You should perform monthly self-breast exams and receive yearly breast exams from your doctor while you are taking Angeliq. Talk with your doctor if you are unsure how to properly perform a self-breast exam. Report any lumps to your doctor right away.


• Use Angeliq with caution in the ELDERLY; they may be more sensitive to its effects.


• Angeliq should not be used in CHILDREN; safety and effectiveness in children have not been confirmed.


• PREGNANCY and BREAST-FEEDING: Do not use Angeliq if you are pregnant. If you think you may be pregnant, contact your doctor right away. Angeliq is found in breast milk. If you are or will be breast-feeding while you use Angeliq, check with your doctor. Discuss any possible risks to your baby.

Possible side effects of Angeliq:

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:

Back pain; breast tenderness, pain, or enlargement; headache; mild hair loss; nausea; nervousness; stomach cramps, bloating, or pain; vaginal spotting or breakthrough bleeding; vomiting; weight changes.

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

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue; unusual hoarseness); calf pain, swelling, or tenderness; chest pain; confusion; discharge from the nipples; fainting; irregular heartbeat; lumps in the breast; mental or mood changes (eg, depression, irritability, memory loss); numbness of an arm or leg; one-sided weakness; severe or persistent dizziness or stomach pain; severe or persistent breast pain; severe, persistent, or recurring abnormal vaginal bleeding; speech changes (eg, slurred speech); sudden severe headache, nausea, or vomiting; sudden shortness of breath; sudden weight gain; swelling of the hands or feet; unusual vaginal discharge, itching, or odor; vision changes (eg, double vision, sudden vision loss); 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. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

See also: Angeliq 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 severe or persistent nausea; severe or unusual vaginal bleeding.

Proper storage of Angeliq:

Store Angeliq at room temperature, between 68 and 77 degrees F (20 and 20 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Angeliq out of the reach of children and away from pets.

General information:

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


• Angeliq 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 Angeliq. 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 Angeliq resources

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

• Angeliq Prescribing Information (FDA)


• Angeliq Advanced Consumer (Micromedex) - Includes Dosage Information


• Angeliq Consumer Overview

Compare Angeliq with other medications

• Postmenopausal Symptoms

Tylenol Flu No Drowsiness

Pronunciation: a-seet-a-MIN-oh-fen/dex-troe-meth-OR-fan/sue-doe-eh-FED-rin
Generic Name: Acetaminophen/Dextromethorphan/Pseudoephedrine
Brand Name: Examples include Contac Severe Cold/Flu No-Drowsiness and Tylenol Flu No Drowsiness

Tylenol Flu No Drowsiness is used for:

Relieving pain, congestion, and cough due to colds, flu, or hay fever. It may also be used for other conditions as determined by your doctor.

Tylenol Flu No Drowsiness is an analgesic, decongestant, and cough suppressant combination. It works by constricting blood vessels and reducing swelling in the nasal passages, which helps you breathe more easily. The analgesic and cough suppressant work in the brain to decrease pain and reduce the cough reflex.

Do NOT use Tylenol Flu No Drowsiness if:

• you are allergic to any ingredient in Tylenol Flu No Drowsiness


• you have severe high blood pressure, rapid heartbeat, or other severe heart problems (eg, heart blood vessel disease)


• you have taken furazolidone or a monoamine oxidase (MAO) inhibitor (eg, phenelzine) within the last 14 days

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

Before using Tylenol Flu No Drowsiness:

Some medical conditions may interact with Tylenol Flu No Drowsiness. 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 glaucoma, an enlarged prostate gland or other prostate problems, heart problems, diabetes, high blood pressure, blood vessel problems, adrenal gland problems, an overactive thyroid, seizures, stroke, or liver problems, or if you consume more than 3 alcohol-containing drinks per day


• if you have a history of asthma, chronic cough, chronic obstructive pulmonary disease (COPD), or other lung problems (eg, chronic bronchitis, emphysema), or if your cough produces large amounts of mucus

Some MEDICINES MAY INTERACT with Tylenol Flu No Drowsiness. Tell your health care provider if you are taking any other medicines, especially any of the following:

• Beta-blockers (eg, propranolol), COMT inhibitors (eg, tolcapone), furazolidone, indomethacin, isoniazid, MAO inhibitors (eg, phenelzine), or tricyclic antidepressants (eg, amitriptyline) because the risk of side effects from Tylenol Flu No Drowsiness may be increased


• Anticoagulants (eg, warfarin), digoxin, or droxidopa because the risk of side effects such as bleeding, irregular heartbeat, or heart attack may be increased


• Bromocriptine because the risk of side effects may be increased by Tylenol Flu No Drowsiness


• Guanadrel, guanethidine, mecamylamine, methyldopa, or reserpine because their effectiveness may be decreased by Tylenol Flu No Drowsiness

This may not be a complete list of all interactions that may occur. Ask your health care provider if Tylenol Flu No Drowsiness 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 Tylenol Flu No Drowsiness:

Use Tylenol Flu No Drowsiness as directed by your doctor. Check the label on the medicine for exact dosing instructions.

• Tylenol Flu No Drowsiness may be taken with or without food.


• If you miss a dose of Tylenol Flu No Drowsiness, 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 Tylenol Flu No Drowsiness.

Important safety information:

• Tylenol Flu No Drowsiness may cause dizziness or drowsiness. Do not drive, operate machinery, or do anything else that could be dangerous until you know how you react to Tylenol Flu No Drowsiness. Using Tylenol Flu No Drowsiness alone, with certain other medicines, or with alcohol may lessen your ability to drive or perform other potentially dangerous tasks.


• Do not take appetite suppressants while you are taking Tylenol Flu No Drowsiness without checking with your doctor.


• Tylenol Flu No Drowsiness contains acetaminophen and pseudoephedrine. Before you begin taking any new prescription or nonprescription medicine, read the ingredients to see if it also contains acetaminophen or pseudoephedrine. If it does or if you are uncertain, contact your doctor or pharmacist.


• Do NOT exceed the recommended dose or take Tylenol Flu No Drowsiness for longer than prescribed without checking with your doctor.


• If your symptoms do not improve within 5 to 7 days or if they become worse, check with your doctor.


• Tylenol Flu No Drowsiness may cause liver damage. If you consume 3 or more alcohol-containing drinks every day, ask your doctor if you should take Tylenol Flu No Drowsiness or other pain relievers/fever reducers. Alcohol use combined with Tylenol Flu No Drowsiness may increase your risk for liver damage.


• Tylenol Flu No Drowsiness may interfere with certain lab test results. Make sure that all of your doctors and lab personnel know that you are taking Tylenol Flu No Drowsiness.


• Before you have any medical or dental treatments, emergency care, or surgery, tell the doctor or dentist that you are using Tylenol Flu No Drowsiness.


• Use Tylenol Flu No Drowsiness with caution in the ELDERLY because they may be more sensitive to its effects.


• Caution is advised when using Tylenol Flu No Drowsiness in CHILDREN because they may be more sensitive to its effects.


• PREGNANCY and BREAST-FEEDING: If you become pregnant while taking Tylenol Flu No Drowsiness, discuss with your doctor the benefits and risks of using Tylenol Flu No Drowsiness during pregnancy. It is unknown if Tylenol Flu No Drowsiness is excreted in breast milk. Do not breast-feed while taking Tylenol Flu No Drowsiness.

Possible side effects of Tylenol Flu No Drowsiness:

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:

Dizziness; excitability; headache; nausea; nervousness or anxiety; trouble sleeping; weakness.

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); difficulty urinating; fast or irregular heartbeat; hallucinations; seizures; severe dizziness, lightheadedness, or headache; stomach pain; tremor; 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: Tylenol Flu No Drowsiness 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 blurred vision; confusion; hallucinations; seizures; severe dizziness, lightheadedness, or headache; severe drowsiness; stomach pain; unusually fast, slow, or irregular heartbeat; vomiting; yellowing of skin or eyes.

Proper storage of Tylenol Flu No Drowsiness:

Store Tylenol Flu No Drowsiness at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Tylenol Flu No Drowsiness out of the reach of children and away from pets.

General information:

• If you have any questions about Tylenol Flu No Drowsiness, please talk with your doctor, pharmacist, or other health care provider.


• Tylenol Flu No Drowsiness 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 Tylenol Flu No Drowsiness. 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 Tylenol Flu No Drowsiness resources

• Tylenol Flu No Drowsiness Side Effects (in more detail)
• Tylenol Flu No Drowsiness Use in Pregnancy & Breastfeeding
• Tylenol Flu No Drowsiness Drug Interactions
• Tylenol Flu No Drowsiness Support Group
• 1 Review for Tylenol Flu No Drowsiness - Add your own review/rating

Compare Tylenol Flu No Drowsiness with other medications

• Cold Symptoms

Pilocar Drops

Pronunciation: pye-loe-KAR-peen
Generic Name: Pilocarpine
Brand Name: Examples include Isopto Carpine and Piloptic

Pilocar Drops are used for:

Treating certain types of glaucoma (increased pressure in the eye) alone or in combination with other medicines. It may also be used to reverse the effects of other medicines used during eye surgeries or examinations. It may also be used for other conditions as determined by your doctor.

Pilocar Drops are a direct-acting miotic. It works by lowering the fluid pressure inside the eyeball by increasing fluid drainage from the eyeball. It also causes the pupils to constrict or get smaller (miosis).

Do NOT use Pilocar Drops if:

• you are allergic to any ingredient in Pilocar Drops


• you have a certain type of glaucoma (eg, pupillary block glaucoma), eye inflammation, or a severe eye infection

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

Before using Pilocar Drops:

Some medical conditions may interact with Pilocar Drops. 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 detached retina, an eye infection, or chronic obstructive pulmonary disease


• if you have had a heart attack

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

Ask your health care provider if Pilocar Drops 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 Pilocar Drops:

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

• Pilocar Drops are only for the eye. Do not get it in your nose or mouth.


• To use Pilocar Drops in the eye, first, wash your hands. Tilt your head back. Using your index finger, pull the lower eyelid away from the eye to form a pouch. Drop the medicine into the pouch and gently close your eyes. Immediately use your finger to apply pressure to the inside corner of the eyelid for 1 to 2 minutes. Do not blink. Remove excess medicine around your eye with a clean, dry tissue, being careful not to touch your eye. Wash your hands to remove any medicine that may be on them.


• To prevent germs from contaminating your medicine, do not touch the applicator tip to any surface, including the eye. Keep the container tightly closed.


• If you miss a dose of Pilocar Drops, use 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 use 2 doses at once.

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

Important safety information:

• Pilocar Drops may cause blurred vision. These effects may be worse if you take it with alcohol or certain medicines. Use Pilocar Drops with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.


• Pilocar Drops may cause harm if it is swallowed. If you may have taken it by mouth, contact your poison control center or emergency room right away.


• PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Pilocar Drops while you are pregnant. It is not known if Pilocar Drops are found in breast milk. If you are or will be breast-feeding while you use Pilocar Drops, check with your doctor. Discuss any possible risks to your baby.

Possible side effects of Pilocar Drops:

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:

Blurred vision; change in vision; eyelid twitching; headache at the temples or around the eyes; increased tearing; nearsightedness; redness or swelling of the eye; temporary stinging or burning.

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

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); detachment of the retina; fast or abnormal heartbeat; increase in blood pressure; poor vision at night.

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: Pilocar 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 asthma; blurred vision; diarrhea; fainting; increased saliva; increased sweating; irregular heartbeat; vomiting.

Proper storage of Pilocar Drops:

Store Pilocar Drops at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Pilocar Drops out of the reach of children and away from pets.

General information:

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


• Pilocar Drops 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 Pilocar Drops. 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 Pilocar resources

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

Compare Pilocar with other medications

• Glaucoma
• Intraocular Hypertension

Sheerdesenz Desensitizing Treatment

Generic Name: potassium nitrate

Dosage Form: dental film
Product Information

[Patient Kit Information Panel]

TO REORDER: 1.877.236.4408

www.caogroup.com

PACKAGE CONTENTS: 4) desensitizing treatments

See package insert for dosage information. Rx Only. Dispose of properly after use. For complete safety information see product MSDS. Do not use if the packaging has been damaged, or if the safety seals are found to be broken.

REORDER #: 006-00104

Manufactured by CAO (China) Medical Equipment Co., Ltd. for CAO Group, Inc.

4628 West Skyhawk Drive

West Jordan, UT 84084

U.S.A.

877-236-4408 (tel)

801-256-9287 (fax)

www.caogroup.com

Expiration date:

MADE IN CHINA

[Side panels for the Patient Pack]

SheerDesenZ

Active Ingredient: Potassium nitrate, 12mg/film

Other Ingredients: Proprietary polymer, water/eau, xylitol, glycerin, poly(acrylic acid), peppermint oil, sucralose, potassium hydroxide

NDC#: 1406000304

[Front side of patient instruction card]

SheerDesenZ

Desensitizing Treatment

Simple.Comfort.Now

Disclaimer: CAO Group believes this information to be accurate and is offered only for the benefit of its customers for use of the product under proscribed conditions. This document is not to eb considered a warranty or guarantee of product performance, and CAO Group is not legally bound to such claims based on this document.

Shelf Life: 2 years

Manufactured by CAO (China) Medical Equipment Co., Ltd. for CAO Group, Inc.

4628 West Skyhawk Drive

West Jordan, UT 84084 U.S.A.

www.caogroup.com


13 Sept 2010

SAL-CSG010B.1

[Back panel of patient guide]

Sheer DesenZ

Desensitizing Treatment

Wear 01:00:00

Description

Sheer DesenZ™ desensitizing treatment is an easy, fast way to relieve oral pain and discomfort associated with dental procedures or even the hot/cold thermal changes teeth may experience. The thin, flexible film stays where it is placed molding to the teeth and gums to deliver relief exactly where it is needed. Yet it is easily removed when comfort is achieved.

Counter Indications

• Do not smoke while wearing the film.

• Avoid eating while wearing the film.

• Flush with copious amounts of water if accidentally placed in eye.

• Keep out of reach of young children.

• Avoid contact with clothing.

Instructions

1. Use enclosed tool to cut wrapper open.
   


2. Remove shrink wrap from tray. Carefully remove film from tray. The sticky gel side faces up. Position the film so it is centered on the arch. Firmly apply the film to the teeth, with the edge of the film just extending onto the gums.


3. Starting at the front teeth, wrap the film around the edge of the teeth and onto the back side of the teeth. Use your fingers to firmly mold the film to your teeth.


4. Remove the smaller film and position it over the premolars and molars on one side of your mouth. Apply the smaller piece as described above.


5. Wear for a maximum of one hour, or until sensitivity is gone. Repeat as directed by your dental professional.


6. To remove, grasp corner of film and begin to loosen away from teeth.


7. If film becomes difficult to remove, rinse with water.


8. Continue removing film from all surfaces. The film may come away in pieces; this is normal.


9. Brush teeth and gums to remove any remaining gel.
   

[Complete Instructions Back Page]

Caution: Federal law restricts this device to sale by or on the order of a licensed professional.

Disclaimer: CAO Group believes this information to be accurate and is offered only for the benefit of its customers for use of the product under proscribed conditions. This document is not to be considered a warranty or guarantee of product performance, and CAO Group is not legally bound to such claims based on this document.

Manufactured by CAO (China) Medical Equipment Co,. Ltd. for

CAO Group, Inc.

P 877.236.4408 F 801.256.9287

4628 West Skyhawk Drive, West Jordan, UT 84084-4501 U.S.A.

www.caogroup.com

13 Sept 2010

SAL-CAI010 B.1

[Immediate Package]

SheerDesenZ

Desensitizing Treatment


See carton for complete instructions and information. Keep out of reach of children.


For one-time use only.


CAO Group, Inc.


LOT#: [######]


EXP: [MMM YYYY]

[Patient Kit Principal Display Panel]

SheerDesenZ

Desensitizing Treatment

Patient Treatment Kit


Simple.Comfort.Now


Net Qty: 8) 0.4 gram films

Active Ingredient: Potassium nitrate, 12mg/film

SHEERDESENZ  DESENSITIZING TREATMENT potassium nitrate  film

Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 14060-003 Route of Administration DENTAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength potassium nitrate (nitrate ion) potassium nitrate 12 mg

Inactive Ingredients Ingredient Name Strength Water 99 mg Potassium hydroxide 0.4 mg Glycerin 40 mg Xylitol 86 mg

Product Characteristics Color      Score      Shape Size Flavor PEPPERMINT (Peppermint Oil) Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 14060-003-04 4 TRAY In 1 PACKAGE contains a TRAY 1 3 FILM In 1 TRAY This package is contained within the PACKAGE (14060-003-04)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		09/01/2010

Labeler - CAO Group, Inc. (102422578)

Revised: 10/2010CAO Group, Inc.

vardenafil

var-DEN-a-fil

Commonly used brand name(s)

In the U.S.

• Levitra


• Staxyn

Available Dosage Forms:

• Tablet


• Tablet, Disintegrating

Therapeutic Class: Erectile Dysfunction Agent

Pharmacologic Class: Phosphodiesterase Type 5 Inhibitor

Uses For vardenafil

Vardenafil is used to treat men who have erectile dysfunction (also called sexual impotence). Vardenafil belongs to a group of medicines called phosphodiesterase 5 (PDE5) inhibitors. These medicines prevent an enzyme called phosphodiesterase type-5 from working too quickly. The penis is one of the areas where this enzyme works.

Erectile dysfunction is a condition where the penis does not harden and expand when a man is sexually excited, or when he cannot keep an erection. When a man is sexually stimulated, his body's normal response is to increase blood flow to his penis to produce an erection. By controlling the enzyme, vardenafil helps to maintain an erection after the penis is stroked by increasing blood flow to the penis. Without physical action to the penis, such as that occurring during sexual intercourse, vardenafil will not work to cause an erection.

vardenafil is available only with your doctor's prescription.

Before Using vardenafil

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 vardenafil, the following should be considered:

Allergies

Tell your doctor if you have ever had any unusual or allergic reaction to vardenafil 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

Vardenafil is not indicated for use in children. Safety and efficacy have not been established.

Geriatric

Appropriate studies performed to date have not demonstrated geriatric-specific problems that would limit the usefulness of vardenafil in the elderly.

Pregnancy

	Pregnancy Category	Explanation
All Trimesters	B	Animal studies have revealed no evidence of harm to the fetus, however, there are no adequate studies in pregnant women OR animal studies have shown an adverse effect, but adequate studies in pregnant women have failed to demonstrate a risk to the fetus.

Breast Feeding

There are no adequate studies in women for determining infant risk when using this medication during breastfeeding. Weigh the potential benefits against the potential risks before taking this medication while breastfeeding.

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. When you are taking vardenafil, it is especially important that your healthcare professional know if you are taking any of the medicines listed below. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive.

Using vardenafil with any of the following medicines is not recommended. Your doctor may decide not to treat you with this medication or change some of the other medicines you take.

• Cisapride


• Dronedarone


• Erythrityl Tetranitrate


• Fluconazole


• Isosorbide Dinitrate


• Isosorbide Mononitrate


• Mesoridazine


• Nitroglycerin


• Pentaerythritol Tetranitrate


• Pimozide


• Posaconazole


• Sparfloxacin


• Thioridazine

Using vardenafil with any of the following medicines is usually not recommended, but may be required in some cases. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines.

• Acecainide


• Amiodarone


• Amitriptyline


• Amoxapine


• Apomorphine


• Arsenic Trioxide


• Asenapine


• Astemizole


• Azimilide


• Azithromycin


• Boceprevir


• Bretylium


• Chloroquine


• Chlorpromazine


• Ciprofloxacin


• Citalopram


• Clomipramine


• Clozapine


• Crizotinib


• Dasatinib


• Desipramine


• Disopyramide


• Dofetilide


• Dolasetron


• Flecainide


• Gatifloxacin


• Granisetron


• Halofantrine


• Haloperidol


• Ibutilide


• Iloperidone


• Imipramine


• Lapatinib


• Levofloxacin


• Lopinavir


• Lumefantrine


• Mefloquine


• Methadone


• Moricizine


• Moxifloxacin


• Nilotinib


• Norfloxacin


• Nortriptyline


• Octreotide


• Ofloxacin


• Ondansetron


• Paliperidone


• Pazopanib


• Perflutren Lipid Microsphere


• Procainamide


• Prochlorperazine


• Promethazine


• Propafenone


• Protriptyline


• Quetiapine


• Quinidine


• Quinine


• Ranolazine


• Salmeterol


• Saquinavir


• Sematilide


• Sodium Phosphate


• Sodium Phosphate, Dibasic


• Sodium Phosphate, Monobasic


• Solifenacin


• Sorafenib


• Sotalol


• Sunitinib


• Tedisamil


• Telaprevir


• Telithromycin


• Terfenadine


• Tetrabenazine


• Toremifene


• Trazodone


• Trifluoperazine


• Trimipramine


• Vandetanib


• Vemurafenib


• Voriconazole


• Ziprasidone

Using vardenafil with any of the following medicines may cause an increased risk of certain side effects, but using both drugs may be the best treatment for you. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines.

• Alfuzosin


• Amprenavir


• Bunazosin


• Doxazosin


• Indinavir


• Itraconazole


• Phenoxybenzamine


• Phentolamine


• Prazosin


• Tamsulosin


• Terazosin


• Trimazosin


• Urapidil

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 vardenafil. Make sure you tell your doctor if you have any other medical problems, especially:

• Abnormal penis, including curved penis and birth defects of the penis—Chance of problems occurring may be increased and vardenafil should be used with caution in these patients.

• Age greater than 50 years or


• Coronary artery disease or


• Diabetes or


• Hyperlipidemia (excess of lipids in the blood) or


• Hypertension (high blood pressure) or


• Low cup to disc ratio (eye condition also called "crowded disc") or


• Smoking—These conditions may increase risk for a serious eye problem called non-arteritic ischemic optic neuropathy or NAION.

• Angina (reoccurring chest pain) or


• Arrhythmia (irregular heartbeat) or


• Heart attack (within the last 6 months) or


• Heart failure, severe or


• Hypertension (high blood pressure), uncontrolled or


• Hypotension (low blood pressure) or


• Kidney disease, severe or


• Liver disease, severe or


• Retinal disorders (eye problem) or


• Retinitis pigmentosa (an inherited eye disorder) or


• Stroke, recent history of—Should not be used in patients with these conditions.

• Bleeding disorders or


• Stomach ulcers—Chance of problems occurring may be increased; it is not known if the medicine is safe for use in these patients.

• Bone marrow cancer or


• Leukemia (blood related cancer) or


• Multiple myeloma (blood related cancer) or


• Sickle-cell anemia (blood disorder)—Vardenafil should be used with caution in these patients as problems with prolonged erection of the penis may occur.

• Fructose intolerance—The orally disintegrating tablet contains sorbitol, which can make this condition worse.

• Heart blood flow problems—These conditions may cause you to be more sensitive to vardenafil.

• Heart disease, underlying—Chance of low blood pressure occurring is greater; vardenafil should be used carefully in these patients.

• Kidney disease or


• Liver disease—Chance of problems occurring may be increased. Lower starting doses may be used and doses increased as needed and as tolerated.

• NAION (serious eye condition) in one or both eyes, history of—May increase your chance of getting NAION again.

• Phenylketonuria (PKU)—The orally disintegrating tablet contains phenylalanine, which can make this condition worse.

• QT prolongation (rare heart condition), or history of—Use with caution. May make this condition worse.

Proper Use of vardenafil

Use vardenafil exactly as directed by your doctor. Do not use more of it and do not use it more often than your doctor ordered. If too much is used, the chance of side effects or other problems is increased.

Special patient instructions come with vardenafil. Read the directions carefully before you start using vardenafil and each time you get a refill of your medicine.

You may take vardenafil with or without food.

vardenafil usually begins to work within 60 minutes after taking it. It continues to work for up to 4 hours. Stimulation is required for an erection. If you have any questions about the use and benefits of vardenafil ask your doctor.

If you are using the disintegrating tablet, make sure your hands are dry before you handle the tablet. Do not open the blister pack that contains the tablet until you are ready to take it. Remove the tablet from the blister pack by peeling back the foil, then taking the tablet out. Do not push the tablet through the foil. Place the tablet on your tongue. It should melt quickly. The tablet should be taken without liquids. Do not break, crush, or chew it.

Use only the brand of vardenafil that your doctor prescribed. Different brands may not work the same way.

Dosing

The dose of vardenafil 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 vardenafil. 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 treatment of erectile dysfunction (as needed):
  
  • For oral dosage form (disintegrating tablets):
    
    • Adults—10 milligrams (mg) as a single dose, no more than once a day, taken 1 hour before you think sexual activity may occur.
    
    
    • Children—Use is not recommended.
    
    
  
  
  • For oral dosage form (tablets):
    
    • Adults 65 years of age and older—5 milligrams (mg) as a single dose no more than once a day, 1 hour before sexual intercourse. Your doctor may change your dose if needed.
    
    
    • Adults up to 65 years of age—10 mg as a single dose no more than once a day, 1 hour before sexual activity. Your doctor may change your dose if needed.
    
    
    • Children—Use is not recommended.
    
    
  
  

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 vardenafil

It is important that you tell all of your doctors that you take vardenafil. If you need emergency medical care for a heart problem, it is important that your doctor knows when you last took vardenafil.

Levitra® also contains vardenafil. If you take too much vardenafil or take it together with these medicines, the chance for side effects will be higher.

If you experience a prolonged or painful erection for 4 hours or more, contact your doctor immediately. This condition may require prompt medical treatment to prevent serious and permanent damage to your penis.

vardenafil does not protect you against sexually transmitted diseases. Use protective measures and ask your doctor if you have any questions about this.

It is important to tell your doctor about any heart problems you may have now or may have had in the past. vardenafil can cause serious side effects in patients with heart problems.

Do not use vardenafil if you are also using a nitrate medicine, often used to treat angina (chest pain). Nitrate medicines include nitroglycerin, isosorbide, Imdur®, Nitro-Bid®, Nitrostat®, Nitro-Dur®, Transderm Nitro®, Nitrol® Ointment, and Nitrolingual® Spray. Some illegal ("street") drugs called "poppers" (such as amyl nitrate, butyl nitrate, or nitrite) also contain nitrates.

Do not drink excessive amounts of alcohol (e.g., 5 glasses of wine or 5 shots of whiskey) when taking vardenafil. When taken in excess, alcohol can increase your chances of getting a headache or getting dizzy, increase your heart rate, or lower your blood pressure.

If you have sudden loss of vision in one or both eyes, stop using vardenafil and contact your doctor right away.

Stop using vardenafil and check with your doctor right away if you have sudden decrease in hearing or loss of hearing, which may be accompanied by dizziness and ringing in the ears.

Do not eat grapefruit or drink grapefruit juice while you are using vardenafil.

Do not take other medicines unless they have been discussed with your doctor. This includes prescription or nonprescription (over-the-counter [OTC]) medicines and herbal or vitamin supplements.

vardenafil 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:

Less common

• Arm, back, or jaw pain


• blindness


• blurred vision


• chest pain or discomfort


• chest tightness or heaviness


• chills


• cold sweats


• confusion


• decreased vision


• difficult or labored breathing


• difficulty with swallowing


• dizziness


• dizziness, faintness, or lightheadedness when getting up from a lying or sitting position


• eye pain


• fainting


• fast, irregular, pounding, or racing heartbeat or pulse


• headache


• hives


• itching


• nausea


• nervousness


• pain or discomfort in the arms, jaw, back, or neck


• pounding in the ears


• puffiness or swelling of the eyelids or around the eyes, face, lips, or tongue


• shortness of breath


• skin rash


• slow or fast heartbeat


• sweating


• tearing


• tightness in the chest


• unusual tiredness or weakness


• vomiting


• wheezing

Incidence not known

• Hearing loss

Some side effects may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:

More common

• Feeling of warmth and redness of the face, neck, arms, and occasionally, upper chest


• sneezing


• stuffy nose

Less common

• Abnormal ejaculation


• abdominal or stomach pain


• abnormal vision


• acid or sour stomach


• back pain


• belching


• bloody nose


• body aches or pain


• burning feeling in the chest or stomach


• burning, crawling, itching, numbness, prickling, "pins and needles", or tingling feelings


• changes in color vision


• changes in vision


• congestion


• cough


• diarrhea


• difficulty seeing at night


• difficulty with moving


• difficulty with swallowing


• dim vision


• dry mouth


• dryness or soreness of the throat


• excessive muscle tone


• eye pain


• face swelling


• fast heartbeat


• feeling of constant movement of self or surroundings


• fever


• general feeling of discomfort or illness


• heartburn


• hoarseness


• increased redness of the eye


• increased sensitivity of the eyes to sunlight


• indigestion


• itching skin


• joint pain


• lack or loss of strength


• loss of appetite


• muscle aches and pains


• muscle cramping


• muscle stiffness


• muscle tension or tightness


• neck pain


• pain


• pain or burning in the throat


• runny nose


• sensation of spinning


• shivering


• sleepiness or unusual drowsiness


• sleeplessness


• sore throat


• sores, ulcers, or white spots on the lips or tongue or inside the mouth


• stomach discomfort, upset, or pain


• swollen joints


• tender, swollen glands in the neck


• tenderness in the stomach area


• trouble with sleeping


• trouble with swallowing


• unable to sleep


• voice changes


• watery eyes

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: vardenafil 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 vardenafil resources

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

• Vardenafil MedFacts Consumer Leaflet (Wolters Kluwer)


• Levitra Prescribing Information (FDA)


• Levitra Monograph (AHFS DI)


• Levitra Consumer Overview


• Staxyn Prescribing Information (FDA)


• Staxyn Orally Disintegrating Tablets MedFacts Consumer Leaflet (Wolters Kluwer)


• Staxyn Consumer Overview

Compare vardenafil with other medications

• Erectile Dysfunction

Cartia XT 24-Hour Sustained-Release Beads Capsules

Pronunciation: dil-TYE-a-zem
Generic Name: Diltiazem
Brand Name: Examples include Cardizem CD and Cartia XT

Cartia XT 24-Hour Sustained-Release Beads Capsules are used for:

Treating high blood pressure and chronic stable angina (chest pain). It may be used alone or in combination with other medicines. It may also be used for other conditions as determined by your doctor.

Cartia XT 24-Hour Sustained-Release Beads Capsules are a calcium channel blocker. It works by relaxing (dilating) your blood vessels, lowering blood pressure, and decreasing heart rate, which lowers the workload of the heart. It also dilates coronary arteries, which increases blood flow to the heart.

Do NOT use Cartia XT 24-Hour Sustained-Release Beads Capsules if:

• you are allergic to any ingredient in Cartia XT 24-Hour Sustained-Release Beads Capsules


• you have certain heart problems (eg, sick sinus syndrome, second- or third-degree heart block) and do not have a pacemaker, you have very low blood pressure, or you have fluid buildup in the lungs during or soon after a heart attack


• you are taking erythromycin

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

Before using Cartia XT 24-Hour Sustained-Release Beads Capsules:

Some medical conditions may interact with Cartia XT 24-Hour Sustained-Release Beads Capsules. 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 heart failure, a recent heart attack with lung congestion, heart block, a very slow heart rate, or other heart problems; low blood pressure; certain stomach or intestine problems (eg, narrowing); liver disease; or kidney problems


• if you are taking other medicines for high blood pressure or heart conditions

Some MEDICINES MAY INTERACT with Cartia XT 24-Hour Sustained-Release Beads Capsules. Tell your health care provider if you are taking any other medicines, especially any of the following:

• Antiarrhythmics (eg, amiodarone, dronedarone), cimetidine, clonidine, HIV protease inhibitors (eg, atazanavir, indinavir), or tricyclic antidepressants (eg, amitriptyline) because they may increase the risk of Cartia XT 24-Hour Sustained-Release Beads Capsules's side effects, such as heart rhythm problems


• Moricizine or rifamycins (eg, rifampin) because they may decrease Cartia XT 24-Hour Sustained-Release Beads Capsules's effectiveness


• Benzodiazepines (eg, alprazolam), beta-blockers (eg, propranolol), buspirone, carbamazepine, cilostazol, cisapride, colchicine, corticosteroids (eg, hydrocortisone), cyclosporine, digoxin, everolimus, fentanyl, HMG-CoA reductase inhibitors (eg, simvastatin), hydantoins (eg, phenytoin), lurasidone, macrolide antibiotics (eg, erythromycin), macrolide immunosuppressants (eg, tacrolimus), nifedipine, quinidine, ranolazine, theophylline, or vasopressin antagonists (eg, tolvaptan) because the risk of their side effects, some potentially life-threatening, may be increased by Cartia XT 24-Hour Sustained-Release Beads Capsules

This may not be a complete list of all interactions that may occur. Ask your health care provider if Cartia XT 24-Hour Sustained-Release Beads Capsules 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 Cartia XT 24-Hour Sustained-Release Beads Capsules:

Use Cartia XT 24-Hour Sustained-Release Beads Capsules as directed by your doctor. Check the label on the medicine for exact dosing instructions.

• Take Cartia XT 24-Hour Sustained-Release Beads Capsules by mouth with or without food.


• Swallow Cartia XT 24-Hour Sustained-Release Beads Capsules whole. Do not open, break, crush, or chew before swallowing.


• Taking Cartia XT 24-Hour Sustained-Release Beads Capsules at the same time each day will help you remember to take it.


• Continue to take Cartia XT 24-Hour Sustained-Release Beads Capsules even if you feel well. Do not miss any doses.


• If you miss a dose of Cartia XT 24-Hour Sustained-Release Beads Capsules, 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 Cartia XT 24-Hour Sustained-Release Beads Capsules.

Important safety information:

• Cartia XT 24-Hour Sustained-Release Beads Capsules may cause dizziness, lightheadedness, or drowsiness. These effects may be worse if you take it with alcohol or certain medicines. Use Cartia XT 24-Hour Sustained-Release Beads Capsules with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.


• Cartia XT 24-Hour Sustained-Release Beads Capsules may cause dizziness, lightheadedness, 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.


• Cartia XT 24-Hour Sustained-Release Beads Capsules may cause you to become sunburned more easily. Avoid the sun, sunlamps, or tanning booths until you know how you react to Cartia XT 24-Hour Sustained-Release Beads Capsules. Use a sunscreen or wear protective clothing if you must be outside for more than a short time.


• Patients who take medicine for high blood pressure often feel tired or run down for a few weeks after starting treatment. Be sure to take your medicine even if you may not feel "normal." Tell your doctor if you develop any new symptoms.


• Do not suddenly stop taking Cartia XT 24-Hour Sustained-Release Beads Capsules. Your condition may get worse if you suddenly stop taking it. If you need to stop Cartia XT 24-Hour Sustained-Release Beads Capsules or add a new medicine, your doctor will gradually lower your dose.


• Tell your doctor or dentist that you take Cartia XT 24-Hour Sustained-Release Beads Capsules before you receive any medical or dental care, emergency care, or surgery.


• Be sure to have your blood pressure checked regularly while taking Cartia XT 24-Hour Sustained-Release Beads Capsules.


• Lab tests, including blood pressure, electrocardiogram (ECG), and heart rate, may be performed while you use Cartia XT 24-Hour Sustained-Release Beads Capsules. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.


• Use Cartia XT 24-Hour Sustained-Release Beads Capsules with caution in the ELDERLY; they may be more sensitive to its effects, especially swelling of the ankles, feet, or hands; dizziness; and slow heartbeat.


• Cartia XT 24-Hour Sustained-Release Beads Capsules should be used with extreme caution in CHILDREN; safety and effectiveness in 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 Cartia XT 24-Hour Sustained-Release Beads Capsules while you are pregnant. Cartia XT 24-Hour Sustained-Release Beads Capsules are found in breast milk. Do not breast-feed while taking Cartia XT 24-Hour Sustained-Release Beads Capsules.

Possible side effects of Cartia XT 24-Hour Sustained-Release Beads Capsules:

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:

Constipation; dizziness; facial flushing; headache; lightheadedness; tiredness; weakness.

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

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue; unusual hoarseness); chest pain; fainting; fast, slow, or irregular heartbeat; fever, chills, or sore throat; hallucinations; mental or mood changes; personality changes; reddened, blistered, or swollen skin; severe or persistent dizziness, lightheadedness, nausea, or vomiting; shortness of breath; sudden weight gain; swelling of the feet, ankles, or hands; symptoms of liver problems (eg, dark urine, pale stools, yellowing of the skin or eyes); tender, bleeding, or swollen gums; unusual bleeding or bruising; unusual or persistent tiredness or weakness; 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: Cartia XT 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 confusion; difficulty breathing, especially when lying down; dizziness; drowsiness; fainting; lightheadedness, especially when standing; loss of consciousness; nausea; nervousness; slurred speech; unusual weakness; very slow heart rate.

Proper storage of Cartia XT 24-Hour Sustained-Release Beads Capsules:

Store Cartia XT 24-Hour Sustained-Release Beads Capsules at room temperature, 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 Cartia XT 24-Hour Sustained-Release Beads Capsules out of the reach of children and away from pets.

General information:

• If you have any questions about Cartia XT 24-Hour Sustained-Release Beads Capsules, please talk with your doctor, pharmacist, or other health care provider.


• Cartia XT 24-Hour Sustained-Release Beads Capsules 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 Cartia XT 24-Hour Sustained-Release Beads Capsules. 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 Cartia XT resources

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

Compare Cartia XT with other medications

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• Atrial Fibrillation
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• Heart Failure
• High Blood Pressure
• Raynaud's Syndrome
• Supraventricular Tachycardia

Solarcaine Aloe Extra Gel

Pronunciation: L Y E-doe-cane
Generic Name: Lidocaine
Brand Name: Solarcaine Aloe Extra

Solarcaine Aloe Extra Gel is used for:

Temporarily relieving pain and itching associated with minor cuts, skin scrapes, minor burns (including sunburn), minor skin irritation, and insect bites.

Solarcaine Aloe Extra Gel is an anesthetic. It works by preventing nerves from transmitting painful impulses to the brain.

Do NOT use Solarcaine Aloe Extra Gel if:

• you are allergic to any ingredient in Solarcaine Aloe Extra Gel or to similar medications (eg, amide-type local anesthetics)


• there are signs of infection (eg, oozing, warmth, pain) or tissue damage in the affected area

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

Before using Solarcaine Aloe Extra Gel:

Some medical conditions may interact with Solarcaine Aloe Extra Gel. 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 had a severe allergic reaction (eg, severe rash, hives, difficulty breathing, dizziness) to any anesthetic medicine


• if you have heart, liver, or kidney problems

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

• Amiodarone, beta-blockers (eg, atenolol), cimetidine, or mexiletine because side effects, such as sluggishness, confusion, slow breathing, low blood pressure, or slow heartbeat, may occur

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

Use Solarcaine Aloe Extra Gel as directed by your doctor. Check the label on the medicine for exact dosing instructions.

• Wash and completely dry the affected area. Apply a thin layer of Solarcaine Aloe Extra Gel to the affected area. Gently rub the medicine in until it is evenly distributed.


• Wash your hands immediately after using Solarcaine Aloe Extra Gel, unless your hands are part of the treated area.


• Solarcaine Aloe Extra Gel is for external use only. Avoid contact with eyes. If contact occurs, wash out the eye at once with water or saline and protect it until the numbness is gone.


• Do not bandage or wrap the affected area, unless directed otherwise by your doctor.


• If you miss a dose of Solarcaine Aloe Extra Gel, use 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.

Ask your health care provider any questions you may have about how to use Solarcaine Aloe Extra Gel.

Important safety information:

• Solarcaine Aloe Extra Gel may cause harm if it is swallowed. If you may have taken it by mouth, contact your poison control center or emergency room right away.


• Solarcaine Aloe Extra Gel may cause a numbing effect at the application site. Do not scratch, rub, or expose the area to extreme hot or cold temperatures until the numbness is gone.


• Use caution when applying Solarcaine Aloe Extra Gel over large areas.


• Do not use more medicine, apply more often, or use for longer than prescribed. Your condition will not improve faster, but the risk of side effects may be increased.


• Tell your doctor or dentist that you take Solarcaine Aloe Extra Gel before you receive any medical or dental care, emergency care, or surgery.


• PREGNANCY and BREAST-FEEDING: It is not known if Solarcaine Aloe Extra Gel can cause harm to the fetus. If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Solarcaine Aloe Extra Gel while you are pregnant. It is not known if Solarcaine Aloe Extra Gel is found in breast milk after topical use. If you are or will be breast-feeding while you use Solarcaine Aloe Extra Gel, check with your doctor. Discuss any possible risks to your baby.

Possible side effects of Solarcaine Aloe Extra Gel:

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:

Redness or swelling at the application site.

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

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); excessive irritation; signs of infection in the affected area (eg, warmth, oozing, pain).

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: Solarcaine Aloe Extra 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. Solarcaine Aloe Extra Gel may be harmful if swallowed.

Proper storage of Solarcaine Aloe Extra Gel:

Store Solarcaine Aloe Extra Gel at room temperature, between 59 and 86 degrees F (15 and 30 degrees C), in a tightly closed container. Store away from heat, moisture, and light. Keep Solarcaine Aloe Extra Gel out of the reach of children and away from pets.

General information:

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


• Solarcaine Aloe Extra Gel 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.


• Discard unused medicine and packaging in the trash out of the reach of children and pets.


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

This information is a summary only. It does not contain all information about Solarcaine Aloe Extra Gel. 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 Solarcaine Aloe Extra resources

• Solarcaine Aloe Extra Side Effects (in more detail)
• Solarcaine Aloe Extra Use in Pregnancy & Breastfeeding
• 0 Reviews for Solarcaine Aloe Extra - Add your own review/rating

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