Brevoxyl

Generic Name: benzoyl peroxide topical (BEN zoyl per OX ide)

Brand Names: Acne Treatment, Acne-Clear, Benzac AC, Benzac W, Benzashave 10, Benzashave 5, BenzEFoam, Benziq, Benziq Wash, BPO Foaming Cloths, Brevoxyl, Brevoxyl Acne Wash Kit, Brevoxyl-4 Creamy Wash Complete Pack, Brevoxyl-8 Creamy Wash Complete Pack, Breze, Clearplex, Clearskin, Clinac BPO, Desquam-E, Desquam-X 10, Desquam-X 5, Desquam-X Wash, Fostex Bar 10%, Fostex Gel 10%, Fostex Wash 10%, Inova, Lavoclen-4, Lavoclen-8, Loroxide, NeoBenz Micro, Neutrogena Acne Mask, Neutrogena On Spot Acne Treatment, Oscion, Oscion Cleanser, Oxy 10 Balance, Oxy Balance, Oxy Daily Wash Chill Factor, Oxy-10, Pacnex, PanOxyl, Panoxyl 10, Panoxyl 5, Panoxyl Aqua Gel, PanOxyl Maximum Strength Foaming Acne Wash, Persa-Gel, Seba-Gel, SoluCLENZ Rx, Triaz, Triaz Cleanser, Zaclir

What is Brevoxyl (benzoyl peroxide topical)?

Benzoyl peroxide has an antibacterial effect. It also has a mild drying effect, which allows excess oils and dirt to be easily washed away from the skin.

Benzoyl peroxide topical (for the skin) is used to treat acne.

Benzoyl peroxide topical may also be used for purposes not listed in this medication guide.

What is the most important information I should know about Brevoxyl (benzoyl peroxide topical)?

There are many brands and forms of benzoyl peroxide available and not all brands are listed on this leaflet.

Do not use benzoyl peroxide topical while you are also using tretinoin (Altinac, Avita, Renova, Retin-A, Tretin-X). Using these medications together could cause severe skin irritation.

Use this medication exactly as directed on the label, or as prescribed by your doctor. Do not use it in larger amounts or for longer than recommended.

Avoid getting this medication in your mouth or eyes. If it does get into any of these areas, rinse with water. Do not use benzoyl peroxide topical on sunburned, windburned, dry, chapped, irritated, or broken skin. Also avoid using benzoyl peroxide topical on wounds or on areas of eczema. Wait until these conditions have healed before using this medication.

Avoid using skin products that can cause irritation, such as harsh soaps, shampoos, or skin cleansers, hair coloring or permanent chemicals, hair removers or waxes, or skin products with alcohol, spices, astringents, or lime. Do not use other medicated skin products unless your doctor has told you to.

Benzoyl peroxide may bleach hair or fabrics. Avoid allowing this medication to come into contact with your hair or clothing.

It may take several weeks before your symptoms improve. Keep using the medication as directed and tell your doctor if your symptoms do not improve.

What should I discuss with my healthcare provider before using Brevoxyl (benzoyl peroxide topical)?

Do not use benzoyl peroxide topical while you are also using tretinoin (Altinac, Avita, Renova, Retin-A, Tretin-X). Using these medications together could cause severe skin irritation. FDA pregnancy category C. It is not known whether benzoyl peroxide topical will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medication. It is not known whether benzoyl peroxide passes into breast milk or if it could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.

How should I use Brevoxyl (benzoyl peroxide topical)?

Use exactly as directed on the label, or as prescribed by your doctor. Do not use in larger or smaller amounts or for longer than recommended.

Wash your hands before and after applying this medication. Shake the lotion well just before each use.

Clean and pat dry the skin to be treated. Apply benzoyl peroxide in a thin layer and rub in gently.

Do not cover the treated skin area unless your doctor has told you to.

Benzoyl peroxide topical is usually applied one to three times daily. Follow your doctor's instructions.

Benzoyl peroxide may bleach hair or fabrics. Avoid allowing this medication to come into contact with your hair or clothing.

It may take several weeks before your symptoms improve. Keep using the medication as directed and tell your doctor if your symptoms do not improve.

Store at room temperature away from moisture and heat.

What happens if I miss a dose?

Use the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not use extra medicine to make up the missed dose.

What happens if I overdose?

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

What should I avoid while using Brevoxyl (benzoyl peroxide topical)?

Avoid getting this medication in your mouth or eyes. If it does get into any of these areas, rinse with water. Do not use benzoyl peroxide topical on sunburned, windburned, dry, chapped, irritated, or broken skin. Also avoid using benzoyl peroxide topical on wounds or on areas of eczema. Wait until these conditions have healed before using this medication.

Avoid using skin products that can cause irritation, such as harsh soaps, shampoos, or skin cleansers, hair coloring or permanent chemicals, hair removers or waxes, or skin products with alcohol, spices, astringents, or lime. Do not use other medicated skin products unless your doctor has told you to.

Avoid using sunscreen containing PABA on the same skin treated with benzoyl peroxide, or skin discoloration may occur.

Brevoxyl (benzoyl peroxide topical) side effects

Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Stop using benzoyl peroxide and call your doctor at once if you have severe stinging or burning of your skin.

Less serious side effects may include:

• 
  

  mild stinging or burning;

  
  


• 
  

  itching or tingly feeling;

  
  


• 
  

  skin dryness, peeling, or flaking; or

  
  


• 
  

  redness or other irritation.

  
  

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

What other drugs will affect Brevoxyl (benzoyl peroxide topical)?

It is not likely that other drugs you take orally or inject will have an effect on topically applied benzoyl peroxide topical. But many drugs can interact with each other. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor.

More Brevoxyl resources

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

• Brevoxyl Gel MedFacts Consumer Leaflet (Wolters Kluwer)


• Brevoxyl Topical Advanced Consumer (Micromedex) - Includes Dosage Information


• Acne Treatment Cream MedFacts Consumer Leaflet (Wolters Kluwer)


• BenzEFoam Foam MedFacts Consumer Leaflet (Wolters Kluwer)


• Benzac AC Wash MedFacts Consumer Leaflet (Wolters Kluwer)


• Benzefoam Prescribing Information (FDA)


• Benzefoam Ultra Prescribing Information (FDA)


• Brevoxyl Creamy Wash Prescribing Information (FDA)


• Desquam-X Wash Prescribing Information (FDA)


• Inova Pads MedFacts Consumer Leaflet (Wolters Kluwer)


• NeoBenz Micro Wash Plus Pack Cream MedFacts Consumer Leaflet (Wolters Kluwer)


• Neobenz Micro SD Prescribing Information (FDA)


• Neobenz Micro Wash Plus Pack Prescribing Information (FDA)


• Oxy Balance Topical Advanced Consumer (Micromedex) - Includes Dosage Information


• Pacnex LP Prescribing Information (FDA)


• PanOxyl Bar MedFacts Consumer Leaflet (Wolters Kluwer)


• Triaz Cloths MedFacts Consumer Leaflet (Wolters Kluwer)


• Triazolam Monograph (AHFS DI)

Compare Brevoxyl with other medications

• Acne
• Perioral Dermatitis

Where can I get more information?

• Your pharmacist can provide more information about benzoyl peroxide topical.

See also: Brevoxyl side effects (in more detail)

DexPak Tablets (Dose Pack)

Pronunciation: dex-a-METH-a-sone
Generic Name: Dexamethasone
Brand Name: Examples include Decadron Dose Pack and DexPak

DexPak is used for:

Treating certain conditions associated with decreased adrenal gland function. It is also used to treat severe inflammation due to certain conditions, including severe asthma, severe allergies, rheumatoid arthritis, ulcerative colitis, certain blood disorders, lupus, multiple sclerosis, and certain eye and skin conditions. It may also be used for other conditions as determined by your doctor.

DexPak is a corticosteroid. It works by decreasing or preventing tissues from responding to inflammation. It also modifies the body's response to certain immune stimulation.

Do NOT use DexPak if:

• you are allergic to any ingredient in DexPak


• you have a systemic fungal infection


• you are taking mifepristone

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

Before using DexPak:

Some medical conditions may interact with DexPak. 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 scheduled for a vaccination with a live virus vaccine (eg, smallpox)


• if you have an underactive thyroid, liver or kidney problems, diabetes, or ulcerative colitis


• if you have heart problems, esophagitis, gastritis, stomach obstruction or perforation, or an ulcer


• if you have a history of mental problems (eg, depression), glaucoma, cataracts, or other eye problems


• if you have a herpes infection in your eye or any other type of infection (bacterial, fungal, or viral); have or recently had tuberculosis (TB) or tested positive for TB, measles, or chickenpox

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

• Barbiturates (eg, phenobarbital), carbamazepine, hydantoins (eg, phenytoin), or rifampin because they may decrease DexPak's effectiveness


• Clarithromycin, azole antifungals (eg, ketoconazole), steroidal contraceptives (eg, desogestrel), or troleandomycin because because weakness, confusion, muscle aches, joint pain, or low blood sugar, may occur


• Methotrexate or ritodrine because the risk of their side effects may be increased by DexPak


• Hydantoins (eg, phenytoin),mifepristone, or live vaccines because their effectiveness may be decreased by DexPak


• Anticoagulants (eg, warfarin) or aspirin because their actions and side effects may be increased or decreased by DexPak

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

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

• Take DexPak by mouth with food.


• DexPak is a dose pack. Unless otherwise directed by your doctor, follow the instructions on the pack for taking DexPak.


• If you miss a dose of DexPak, 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 DexPak.

Important safety information:

• DexPak 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.


• Tell your doctor or dentist that you take DexPak before you receive any medical or dental care, emergency care, or surgery.


• DexPak may cause an elevation in blood pressure, salt and water retention, and increased potassium loss. You may need to restrict the use of salt and take a calcium supplement.


• DexPak can cause calcium loss and promote the development of osteoporosis. Take adequate calcium and vitamin D supplements.


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


• Caution is advised when using DexPak in CHILDREN; they may be more sensitive to its effects.


• Corticosteroids may affect growth rate in CHILDREN and teenagers in some cases. They may need regular growth checks while they take DexPak.


• PREGNANCY and BREAST-FEEDING: It is not known if DexPak can cause harm to the fetus. If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using DexPak while you are pregnant. DexPak is found in breast milk. Do not breast-feed while taking DexPak.

Possible side effects of DexPak:

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:

Difficulty sleeping; feeling of a whirling motion; increased appetite; increased sweating; indigestion; mood changes; nervousness.

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); appetite loss; black, tarry stools; changes in menstrual periods; convulsions; depression; diarrhea; dizziness; exaggerated sense of well-being; fever; general body discomfort; headache; increased pressure in the eye; joint or muscle pain; mood swings; muscle weakness; personality changes; prolonged sore throat, cold, or fever; puffing of the face; severe nausea or vomiting; swelling of feet or legs; unusual weight gain; vomiting material that looks like coffee grounds; weakness; weight loss.

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: DexPak 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.

Proper storage of DexPak:

Store DexPak 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 DexPak out of the reach of children and away from pets.

General information:

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


• DexPak 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 DexPak. 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 DexPak resources

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

Compare DexPak with other medications

• Addison's Disease
• Adrenal Insufficiency
• Adrenocortical Insufficiency
• Adrenogenital Syndrome
• Ankylosing Spondylitis
• Aspiration Pneumonia
• Asthma
• Asthma, acute
• Atopic Dermatitis
• Bronchopulmonary Dysplasia
• Bursitis
• Cerebral Edema
• Chorioretinitis
• Croup
• Cushing's Syndrome
• Dermatitis Herpetiformis
• Eczema
• Epicondylitis, Tennis Elbow
• Erythroblastopenia
• Evan's Syndrome
• Gouty Arthritis
• Hay Fever
• Hemolytic Anemia
• Hypercalcemia of Malignancy
• Idiopathic Thrombocytopenic Purpura
• Inflammatory Bowel Disease
• Inflammatory Conditions
• Iridocyclitis
• Iritis
• Juvenile Rheumatoid Arthritis
• Keratitis
• Leukemia
• Loeffler's Syndrome
• Lymphoma
• Meningitis, Haemophilus influenzae
• Meningitis, Listeriosis
• Meningitis, Meningococcal
• Meningitis, Pneumococcal
• Mountain Sickness / Altitude Sickness
• Multiple Myeloma
• Multiple Sclerosis
• Mycosis Fungoides
• Nausea/Vomiting, Chemotherapy Induced
• Neurosarcoidosis
• Pemphigus
• Psoriatic Arthritis
• Pulmonary Tuberculosis
• Rheumatoid Arthritis
• Sarcoidosis
• Seborrheic Dermatitis
• Shock
• Synovitis
• Systemic Lupus Erythematosus
• Thrombocytopenia
• Toxic Epidermal Necrolysis
• Tuberculous Meningitis
• Ulcerative Colitis
• Uveitis, Posterior

DryMax AF Syrup

Pronunciation: SOO-doe-e-FED-rin/KLOR-fen-IR-a-meen/KLOE-fe-DYE-a-nol
Generic Name: Pseudoephedrine/Chlorpheniramine/Chlophedianol
Brand Name: DryMax AF

DryMax AF Syrup is used for:

Relieving symptoms of sinus congestion, runny nose, sneezing, itchy nose or throat, itchy or watery eyes, and cough due to colds, hay fever, and other upper respiratory allergies. It may also be used for other conditions as determined by your doctor.

DryMax AF Syrup is a decongestant, antihistamine, and cough suppressant combination. The decongestant works by constricting blood vessels and reducing swelling in the nasal passages. The antihistamine works by blocking the action of histamine, which helps reduce symptoms such as watery eyes and sneezing. The cough suppressant works in the brain to help decrease the cough reflex to reduce a dry cough.

Do NOT use DryMax AF Syrup if:

• you are allergic to any ingredient in DryMax AF Syrup


• you have severe or uncontrolled high blood pressure, severe heart blood vessel disease, rapid heartbeat, or severe heart problems


• you are unable to urinate or are having an asthma attack


• you are taking droxidopa or sodium oxybate (GHB), or you have taken furazolidone or a monoamine oxidase inhibitor (MAOI) (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 DryMax AF Syrup:

Some medical conditions may interact with DryMax AF Syrup. 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 adrenal gland problems (eg, adrenal gland tumor), heart problems (eg, fast, slow, or irregular heartbeat; heart disease), high or low blood pressure, low blood volume, diabetes, blood vessel problems, stroke, glaucoma or increased pressure in the eye, seizures, mental or mood problems (eg, depression), thyroid problems, or trouble sleeping


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


• if you have a history of stomach or bowel ulcers; a blockage of your stomach, bladder, or bowels ; an enlarged prostate or other prostate problems; kidney problems; or trouble urinating


• if you take medicine for high blood pressure or depression

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

• Digoxin or droxidopa because the risk of irregular heartbeat or heart attack may be increased


• Beta-blockers (eg, propranolol), furazolidone, linezolid, MAOIs (eg, phenelzine), selective serotonin reuptake inhibitors (SSRIs) (eg, citalopram, fluoxetine), sodium oxybate (GHB), or urinary alkalinizers (eg, sodium bicarbonate) because they may increase the risk of DryMax AF Syrup's side effects


• Bromocriptine or hydantoins (eg, phenytoin) because the risk of their side effects may be increased by DryMax AF Syrup


• Guanadrel, guanethidine, mecamylamine, methyldopa, or reserpine because their effectiveness may be decreased by DryMax AF Syrup

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

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

• Take DryMax AF Syrup by mouth with or without food. If stomach upset occurs, take with food to reduce stomach irritation.


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


• Take DryMax AF Syrup with a full glass of water (8 oz/240 mL).


• If you miss a dose of DryMax AF Syrup and you are taking it regularly, 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 DryMax AF Syrup.

Important safety information:

• DryMax AF Syrup may cause drowsiness, dizziness, or blurred vision. These effects may be worse if you take it with alcohol or certain medicines. Use DryMax AF Syrup 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 using DryMax AF Syrup.


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


• Do not take diet or appetite control medicines while you take DryMax AF Syrup without checking with your doctor.


• DryMax AF Syrup has a decongestant, antihistamine, and cough suppressant in it. Before you start any new medicine, check the label to see if it has a decongestant, antihistamine, or cough suppressant in it too. If it does or if you are not sure, check with your doctor or pharmacist.


• Do not use DryMax AF Syrup for a cough with a lot of mucus. Do not use it for a long-term cough (eg, caused by asthma, emphysema, smoking). However, you may use it for these conditions if your doctor tells you to.


• Do NOT take more than the recommended dose or use for longer than recommended without checking with your doctor.


• If new symptoms occur, or if cough or nasal congestion persists for more than 1 week, goes away and returns, or occurs along with a fever, rash, or persistent headache, check with your doctor. A persistent cough may be a sign of a serious condition.


• DryMax AF Syrup may cause you to become sunburned more easily. Avoid the sun, sunlamps, or tanning booths until you know how you react to DryMax AF Syrup. Use a sunscreen or wear protective clothing if you must be outside for more than a short time.


• DryMax AF Syrup may interfere with skin allergy tests. If you are scheduled for a skin test, talk to your doctor. You may need to stop taking DryMax AF Syrup for a few days before the tests.


• Tell your doctor or dentist that you take DryMax AF Syrup before you receive any medical or dental care, emergency care, or surgery.


• Use DryMax AF Syrup with caution in the ELDERLY; they may be more sensitive to its effects, especially confusion, drowsiness, dizziness, dry mouth, nervousness, sleeplessness, and trouble urinating.


• Caution is advised when using DryMax AF Syrup in CHILDREN; they may be more sensitive to its effects, especially excitability.


• DryMax AF Syrup should not be used in CHILDREN younger than 6 years old without first checking with the child's doctor; 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 using DryMax AF Syrup while you are pregnant. Some ingredients of DryMax AF Syrup are found in breast milk. Do not breast-feed while taking DryMax AF Syrup.

Possible side effects of DryMax AF Syrup:

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; diarrhea; dizziness; drowsiness; dry mouth, nose, or throat; excitability; headache; increased sweating; loss of appetite; nausea; trouble sleeping; upset stomach; vomiting; 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); difficulty urinating or inability to urinate; fast or irregular heartbeat; fever, chills, or persistent sore throat; flushing or redness of the face; hallucinations; loss of coordination; mental or mood changes (eg depression, nervousness); numbness or tingling; seizures; severe dryness of mouth, nose, or throat; severe or persistent dizziness, drowsiness, light-headedness, or headache; severe or persistent trouble sleeping; shortness of breath; tremor; unusual bruising or bleeding; unusual tiredness or weakness; vision problems (eg, double vision, severe or persistent blurred vision).

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.

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; flushing; hallucinations; mental or mood changes; muscle spasms; seizures; severe dizziness, light-headedness, or headache; severe drowsiness; trouble breathing; unusual eye movements; unusually fast, slow, or irregular heartbeat; vomiting.

Proper storage of DryMax AF Syrup:

Store DryMax AF Syrup 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 DryMax AF Syrup out of the reach of children and away from pets.

General information:

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


• DryMax AF Syrup 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 DryMax AF Syrup. 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.

Klostenal

Klostenal may be available in the countries listed below.

Ingredient matches for Klostenal

Beclometasone

Beclometasone 17α,21-dipropionate (a derivative of Beclometasone) is reported as an ingredient of Klostenal in the following countries:

• Italy

International Drug Name Search

Carboplan

Carboplan may be available in the countries listed below.

Ingredient matches for Carboplan

Carboplatin

Carboplatin is reported as an ingredient of Carboplan in the following countries:

• Greece

International Drug Name Search

Zeta N

Zeta N may be available in the countries listed below.

Ingredient matches for Zeta N

Usnic Acid

Usnic Acid is reported as an ingredient of Zeta N in the following countries:

• Italy

Zinc Sulfate

Zinc Sulfate is reported as an ingredient of Zeta N in the following countries:

• Italy

International Drug Name Search

Bromday

Pronunciation: BROME-fen-ak
Generic Name: Bromfenac
Brand Name: Examples include Bromday and Xibrom

Bromday is used for:

Treating eye pain and swelling in patients who have recently had surgery to remove cataracts. It may also be used for other conditions as determined by your doctor.

Bromday is a nonsteroidal anti-inflammatory drug (NSAID) eye drop. It works by blocking the production of prostaglandin, a substance that causes inflammation (redness, swelling, irritation).

Do NOT use Bromday if:

• you are allergic to any ingredient in Bromday


• you are in late pregnancy

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

Before using Bromday:

Some medical conditions may interact with Bromday. 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 sulfites, aspirin or any medicine containing aspirin, an NSAID (eg, ibuprofen), or a phenylacetic acid derivative


• if you have asthma, diabetes, bleeding problems, or rheumatoid arthritis


• if you have other eye problems (eg, dry eye syndrome, cornea problems), have had complicated eye surgery, or have had repeated eye surgeries within a short period of time

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

• Anticoagulants (eg, warfarin) or heparin because the risk of bleeding may be increased


• Corticosteroids (eg, prednisolone) because healing may be slowed or delayed

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

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

• To use Bromday, 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. Do not blink. Remove excess medicine around your eye with a clean 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 your eye. Keep the container tightly closed.


• Do not wear contact lenses while you are using Bromday. Sterilize contact lenses according to the manufacturer's directions and check with your doctor before using them.


• If you are using another medicine that you put in your eye, use Bromday at least 5 minutes before or after using the other medicine.


• If you miss a dose of Bromday, 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 Bromday.

Important safety information:

• Do not exceed the recommended dose or use Bromday for longer than prescribed without checking with your doctor.


• If your symptoms do not improve within 14 days or if they become worse, check with your doctor.


• Check with your doctor if you have an eye wound or irritation that does not heal.


• Bromday contains sulfites, which can cause allergic reactions in certain individuals. Asthma patients may be at higher risk of these allergic reactions. If you have previously had allergic reactions to sulfites, contact your doctor or pharmacist before using Bromday.


• Bromday should be used with caution in CHILDREN younger than 18 years of age; safety and effectiveness in these children have not been confirmed.


• PREGNANCY and BREAST-FEEDING: Bromday may cause harm to the fetus. If you think you may be pregnant, contact your doctor. You will need to discuss the benefits and risks of using Bromday while you are pregnant. Avoid use of Bromday during late pregnancy. It is not known if Bromday is found in breast milk. If you are or will be breast-feeding while you use Bromday, check with your doctor. Discuss any possible risks to your baby.

Possible side effects of Bromday:

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:

Eye burning, irritation, itching, pain, redness, stinging, or swelling; headache; unusual feeling in the eye.

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); severe eye burning, irritation, itching, redness, stinging, or swelling; unusual bleeding of the eye; 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: Bromday 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.

Proper storage of Bromday:

Store Bromday 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 Bromday out of the reach of children and away from pets.

General information:

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


• Bromday 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 Bromday. 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 Bromday resources

• Bromday Side Effects (in more detail)
• Bromday Use in Pregnancy & Breastfeeding
• Bromday Drug Interactions
• Bromday Support Group
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• Bromday Prescribing Information (FDA)


• Bromday Consumer Overview


• Bromday Advanced Consumer (Micromedex) - Includes Dosage Information


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