Monday, 28 May 2012

clopidogrel



kloe-PID-oh-grel


Oral route(Tablet)

Clopidogrel hydrogen sulfate effectiveness is dependent on its activation to an active metabolite by CYP2C19. In patients who are CYP2C19 poor metabolizers, clopidogrel at recommended doses forms less of that metabolite and has a smaller effect on platelet function. Compared with normal metabolizers, poor CYP2C19 metabolizers with acute coronary syndrome or undergoing percutaneous coronary intervention treated with clopidogrel at recommended doses exhibit higher cardiovascular event rates. Tests are available to identify a patient's CYP2C19 genotype; these tests can be help determine therapeutic strategy. Consider alternative treatment or treatment strategies in CYP2C19 poor metabolizers .



Commonly used brand name(s)

In the U.S.


  • Plavix

Available Dosage Forms:


  • Tablet

Therapeutic Class: Platelet Aggregation Inhibitor


Pharmacologic Class: ADP-Induced Aggregation Inhibitor


Uses For clopidogrel


Clopidogrel is used alone or together with aspirin to lessen the chance of heart attack, stroke, or other serious problems with your heart or blood vessels. It is given to patients who have already had a heart attack or severe chest pain, stroke, or to people with other blood circulation problems that could lead to a stroke or heart attack.


A heart attack or stroke may occur when a blood vessel in the heart or brain is blocked by a blood clot. Clopidogrel reduces the chance that a harmful blood clot will form by preventing certain cells in the blood from clumping together. This effect of clopidogrel may also increase the chance of serious bleeding in some people.


clopidogrel is available only with your doctor's prescription.


Before Using clopidogrel


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 clopidogrel, the following should be considered:


Allergies


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


Appropriate studies have not been performed on the relationship of age to the effects of clopidogrel in the pediatric population. 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 clopidogrel in the elderly.


Pregnancy








Pregnancy CategoryExplanation
All TrimestersBAnimal 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 clopidogrel, 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 clopidogrel 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.


  • Aceclofenac

  • Acemetacin

  • Acenocoumarol

  • Alclofenac

  • Alteplase, Recombinant

  • Apazone

  • Argatroban

  • Benoxaprofen

  • Bivalirudin

  • Bromfenac

  • Bufexamac

  • Carprofen

  • Cilostazol

  • Cimetidine

  • Citalopram

  • Clometacin

  • Clonixin

  • Dabigatran Etexilate

  • Dalteparin

  • Danaparoid

  • Desirudin

  • Desvenlafaxine

  • Dexketoprofen

  • Diclofenac

  • Diflunisal

  • Dipyrone

  • Drotrecogin Alfa

  • Droxicam

  • Duloxetine

  • Enoxaparin

  • Escitalopram

  • Esomeprazole

  • Etodolac

  • Etofenamate

  • Etravirine

  • Felbamate

  • Felbinac

  • Fenbufen

  • Fenoprofen

  • Fentiazac

  • Floctafenine

  • Fluconazole

  • Flufenamic Acid

  • Fluoxetine

  • Flurbiprofen

  • Fluvoxamine

  • Fondaparinux

  • Heparin

  • Ibuprofen

  • Indomethacin

  • Indoprofen

  • Isoxicam

  • Ketoconazole

  • Ketoprofen

  • Ketorolac

  • Lepirudin

  • Lornoxicam

  • Meclofenamate

  • Mefenamic Acid

  • Meloxicam

  • Milnacipran

  • Nabumetone

  • Naproxen

  • Nefazodone

  • Niflumic Acid

  • Nimesulide

  • Omeprazole

  • Oxaprozin

  • Oxyphenbutazone

  • Paroxetine

  • Phenindione

  • Phenprocoumon

  • Phenylbutazone

  • Pirazolac

  • Piroxicam

  • Pirprofen

  • Propyphenazone

  • Proquazone

  • Protein C, Human

  • Rabeprazole

  • Rivaroxaban

  • Sertraline

  • Sulindac

  • Suprofen

  • Tenidap

  • Tenoxicam

  • Tiaprofenic Acid

  • Ticlopidine

  • Tinzaparin

  • Tolmetin

  • Venlafaxine

  • Voriconazole

  • Warfarin

  • Zomepirac

Using clopidogrel 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.


  • Amiodarone

  • Amlodipine

  • Diltiazem

  • Ginkgo

  • Nifedipine

  • Nisoldipine

  • Phenytoin

  • Vitamin A

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


  • Bleeding, pathological and active (e.g., from peptic ulcers or head injury)—Should not be used in patients with this condition.

  • CYP2C19 (a liver enzyme) deficiency—clopidogrel may not work well in patients who have this condition.

  • Stroke, recent or

  • Transient ischemic attack (TIA) or "mini-stroke", recent—The chance of major bleeding may be increased. Talk with your doctor if you have concerns about this.

Proper Use of clopidogrel


Take clopidogrel exactly as directed by your doctor. Clopidogrel will not work properly if you take less of it than directed. Taking more clopidogrel than directed may increase the chance of serious side effects without increasing the helpful effects.


clopidogrel comes with a Medication Guide. It is very important that you read and understand this information. Be sure to ask your doctor about anything you do not understand.


You may take clopidogrel with or without food.


If you are also taking omeprazole (Prilosec®), do not use it at the same time that you take clopidogrel. Talk with your doctor about using a different antacid.


If you are using clopidogrel for a condition called acute coronary syndrome, your doctor may tell you to take aspirin while you are using clopidogrel. In this case, do not change the dose or stop taking the aspirin without talking to your doctor first.


Dosing


The dose of clopidogrel 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 clopidogrel. If your dose is different, do not change it unless your doctor tells you to do so.


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


  • For oral dosage form (tablets):
    • For prevention of blood clots after unstable angina (chest pain) or non-ST-elevation myocardial infarction (a type of heart attack):
      • Adults—At first, 300 milligrams (mg) taken as a single dose. Then, 75 mg once a day. Your doctor may also give you aspirin (75 to 325 mg once a day) to be taken together with clopidogrel.

      • Children—Use and dose must be determined by your doctor.


    • For prevention of blood clots after ST-elevation myocardial infarction or STEMI (a type of heart attack):
      • Adults—75 milligrams (mg) once a day. Your doctor may also give you aspirin (75 to 325 mg once a day) to be taken together with clopidogrel.

      • Children—Use and dose must be determined by your doctor.


    • For prevention of blood clots after a recent heart attack, stroke, or in patients with peripheral artery disease:
      • Adults—75 milligrams (mg) once a day.

      • Children—Use and dose must be determined by your doctor.



Missed Dose


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


Storage


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


Keep out of the reach of children.


Do not keep outdated medicine or medicine no longer needed.


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


Precautions While Using clopidogrel


It is very important that your doctor check your progress at regular visits. This will allow your doctor to see if the medicine is working properly and to decide if you should continue to take it. Blood tests may be needed to check for unwanted effects.


Your doctor may do a genetic test before prescribing clopidogrel to determine if you have a deficiency in a liver enzyme called CYP2C19. clopidogrel may not work well for you if you have this condition.


Tell all medical doctors, dentists, nurses, and pharmacists you go to that you are taking clopidogrel. Clopidogrel may increase the risk of serious bleeding during a surgery, other medical procedures (e.g., coronary stent procedure), or some kinds of dental work. You may need to stop using clopidogrel at least 5 days before a surgery, medical procedure, or dental work. Do not stop taking your medicine without your doctor's permission.


While you are using clopidogrel, if you have any kind of bleeding, it may take longer than usual to stop, especially if you hurt yourself. Stay away from rough sports or other situations where you could be bruised, cut, or injured. Be careful when using sharp objects, including razors and fingernail clippers.


clopidogrel may increase your chance of bleeding or bruising. Check with your doctor right away if you notice any unusual bleeding or bruising; black, tarry stools; blood in the urine or stools; or pinpoint red spots on your skin. Avoid picking your nose. If you need to blow your nose, blow it gently.


Do not change your dose or stop taking clopidogrel without checking first with your doctor.


Check with your doctor right away if you have the following symptoms: change in mental status, dark or bloody urine, difficulty with speaking, fever, pale color of the skin, pinpoint red spots on the skin, seizures, weakness, yellow eyes or skin. These maybe symptoms of a rare and serious condition called thrombotic thrombocytopenic purpura (TTP).


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.


clopidogrel 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:


More common
  • Chest pain

  • collection of blood under the skin

  • deep, dark purple bruise

  • itching, pain, redness, or swelling

  • pain in general

  • red or purple spots on the skin, varying in size from pinpoint to large bruises

Less common
  • Nosebleed

  • painful or difficult urination

  • shortness of breath

  • vomiting of blood or material that looks like coffee grounds

Rare
  • Black, tarry stools

  • blistering, flaking, or peeling of the skin

  • blood in the urine or stools

  • confusion

  • fever, chills, or sore throat

  • headache (sudden, severe)

  • nausea or vomiting

  • stomach pain (severe)

  • ulcers, sores, or white spots in the mouth

  • unusual bleeding or bruising

  • weakness (sudden)

Incidence not known
  • Abdominal or stomach cramps or swelling

  • back pain or backaches

  • blurred vision

  • change in mental status

  • cough or hoarseness

  • dark urine

  • difficulty with breathing or swallowing

  • difficulty with speaking

  • dizziness

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

  • fast heartbeat

  • feeling of discomfort

  • general feeling of tiredness or weakness

  • hives

  • inflammation of the joints

  • itching

  • light-colored stools

  • lower back or side pain

  • muscle aches

  • pale color of the skin

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

  • rash

  • reddening of the skin, especially around the ears

  • seizures

  • sweating

  • swelling of the eyes, face, or inside of the nose

  • swollen lymph glands

  • swollen or painful glands

  • tightness in the chest

  • unusual tiredness or weakness

  • upper right abdominal or stomach pain

  • watery or bloody diarrhea

  • wheezing

  • yellow eyes or skin

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:


Incidence not known
  • Bad, unusual, or unpleasant (after) taste

  • bloating

  • change in taste

  • constipation

  • diarrhea

  • difficulty with moving

  • headache

  • hives or welts

  • indigestion

  • loss of appetite

  • muscle pain or stiffness

  • noisy breathing

  • pain in the joints

  • pains in the stomach, side, or abdomen, possibly radiating to the back

  • redness, soreness, or itching skin

  • seeing, hearing, or feeling things that are not there

  • skin blisters

  • sores, welting, or blisters

  • swelling or inflammation of the mouth

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


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

See also: clopidogrel 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.


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More clopidogrel resources


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


  • Clopidogrel Prescribing Information (FDA)

  • Clopidogrel MedFacts Consumer Leaflet (Wolters Kluwer)

  • Clopidogrel Professional Patient Advice (Wolters Kluwer)

  • Clopidogrel Bisulfate Monograph (AHFS DI)

  • Plavix Prescribing Information (FDA)

  • Plavix Consumer Overview



Compare clopidogrel with other medications


  • Acute Coronary Syndrome
  • Acute Coronary Syndrome, Prophylaxis
  • Heart Attack
  • Ischemic Stroke
  • Ischemic Stroke, Prophylaxis
  • Percutaneous Coronary Intervention
  • Peripheral Arterial Disease
  • Platelet Aggregation Inhibition
  • Transient Ischemic Attack

Saturday, 26 May 2012

Brucellosis Medications


Definition of Brucellosis: Brucellosis is a disease caused by contact with animals carrying the Brucella bacteria.

Drugs associated with Brucellosis

The following drugs and medications are in some way related to, or used in the treatment of Brucellosis. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.

Learn more about Brucellosis





Drug List:

Friday, 25 May 2012

Clear Away Wart Removal System Topical


Generic Name: salicylic acid (Topical route)


sal-i-SIL-ik AS-id


Commonly used brand name(s)

In the U.S.


  • Akurza

  • Aliclen

  • Avosil

  • Betasal

  • Compound W

  • Corn Removing

  • Dermarest Psoriasis

  • DHS Sal

  • Drytex

  • Duofilm

  • Duoplant

  • Durasal

  • Freezone

  • Fung-O

  • Gets-It Corn/Callus Remover

  • Gordofilm

  • Hydrisalic

  • Ionil

  • Ionil Plus

  • Keralyt

  • Keralyt Scalp

  • Lupicare

  • Mediplast

  • Mg217 Sal-Acid

  • Mosco Corn & Callus Remover

  • Neutrogena

  • Occlusal-HP

  • Off-Ezy

  • Oxy Balance

  • P & S

  • Palmer's Skin Success Acne Cleanser

  • Propa pH

  • Salac

  • Sal-Acid Plaster

  • Salactic Film

  • Salex

  • Salitop

  • Salkera

  • Sal-Plant Gel

  • Salvax

  • Seba-Clear

  • Stri-Dex

  • Thera-Sal

  • Therasoft Anti-Acne

  • Tinamed

  • Ti-Seb

  • Virasal

  • Wart-Off Maximum Strength

  • Zapzyt

In Canada


  • Acnex

  • Acnomel Acne Mask

  • Clear Away Wart Removal System

  • Compound W One-Step Wart Remover

  • Compound W Plus

  • Dr. Scholl's Clear Away One Step Plantar Wart Remover

  • Dr. Scholl's Cushlin Ultra Slim Callus Removers

  • Dr. Scholl's Cushlin Ultra Slim Corn Removers

  • Duoforte 27

  • Freezone - One Step Callus Remover Pad

  • Freezone - One Step Corn Remover Pad

Available Dosage Forms:


  • Soap

  • Lotion

  • Liquid

  • Foam

  • Ointment

  • Gel/Jelly

  • Solution

  • Cream

  • Pad

  • Paste

  • Shampoo

  • Dressing

  • Stick

Therapeutic Class: Antiacne


Pharmacologic Class: NSAID


Chemical Class: Salicylate, Non-Aspirin


Uses For Clear Away Wart Removal System


Salicylic acid is used to treat many skin disorders, such as acne, dandruff, psoriasis, seborrheic dermatitis of the skin and scalp, calluses, corns, common warts, and plantar warts, depending on the dosage form and strength of the preparation.


Some of these preparations are available only with your doctor's prescription.


Before Using Clear Away Wart Removal System


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


Allergies


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


Pediatric


Young children may be at increased risk of unwanted effects because of increased absorption of salicylic acid through the skin. Also, young children may be more likely to get skin irritation from salicylic acid. Salicylic acid should not be applied to large areas of the body, used for long periods of time, or used under occlusive dressing (air-tight covering, such as kitchen plastic wrap) in infants and children. Salicylic acid should not be used in children younger than 2 years of age.


Geriatric


Elderly people are more likely to have age-related blood vessel disease. This may increase the chance of problems during treatment with this medicine.


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 this medicine, 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 this medicine 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.


  • Abciximab

  • Argatroban

  • Bivalirudin

  • Cilostazol

  • Citalopram

  • Clovoxamine

  • Dabigatran Etexilate

  • Dipyridamole

  • Escitalopram

  • Femoxetine

  • Flesinoxan

  • Fluoxetine

  • Fluvoxamine

  • Fondaparinux

  • Heparin

  • Lepirudin

  • Nefazodone

  • Paroxetine

  • Protein C

  • Rivaroxaban

  • Sertraline

  • Sibutramine

  • Ticlopidine

  • Tirofiban

  • Vilazodone

  • Zimeldine

Using this medicine 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.


  • Acenocoumarol

  • Anisindione

  • Ardeparin

  • Azilsartan Medoxomil

  • Azosemide

  • Bemetizide

  • Bendroflumethiazide

  • Benzthiazide

  • Bumetanide

  • Buthiazide

  • Candesartan Cilexetil

  • Certoparin

  • Chlorothiazide

  • Chlorthalidone

  • Clopamide

  • Cyclopenthiazide

  • Dalteparin

  • Danaparoid

  • Dicumarol

  • Enoxaparin

  • Eprosartan

  • Ethacrynic Acid

  • Furosemide

  • Hydrochlorothiazide

  • Hydroflumethiazide

  • Indapamide

  • Irbesartan

  • Losartan

  • Methyclothiazide

  • Metolazone

  • Nadroparin

  • Olmesartan Medoxomil

  • Parnaparin

  • Phenindione

  • Phenprocoumon

  • Piretanide

  • Polythiazide

  • Probenecid

  • Reviparin

  • Tamarind

  • Tasosartan

  • Telmisartan

  • Tinzaparin

  • Torsemide

  • Trichlormethiazide

  • Valsartan

  • Warfarin

  • Xipamide

Interactions with Food/Tobacco/Alcohol


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


Other Medical Problems


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


  • Blood vessel disease

  • Diabetes mellitus (sugar diabetes)—Use of this medicine may cause severe redness or ulceration, especially on the hands or feet

  • Inflammation, irritation, or infection of the skin—Use of this medicine may cause severe irritation if applied to inflamed, irritated, or infected area of the skin

  • Influenza (flu) or

  • Varicella (chicken pox)—This medicine should not be used in children and teenagers with the flu or chicken pox. There is a risk of Reye's syndrome.

  • Kidney disease or

  • Liver disease—Using this medicine for a long time over large areas could result in unwanted effects

Proper Use of salicylic acid

This section provides information on the proper use of a number of products that contain salicylic acid. It may not be specific to Clear Away Wart Removal System. Please read with care.


It is very important that you use this medicine only as directed. Do not use more of it, do not use it more often, and do not use it for a longer time than recommended on the label, unless otherwise directed by your doctor. To do so may increase the chance of absorption through the skin and the chance of salicylic acid poisoning.


If your doctor has ordered an occlusive dressing (airtight covering, such as kitchen plastic wrap) to be applied over this medicine, make sure you know how to apply it. Since an occlusive dressing will increase the amount of medicine absorbed through your skin and the possibility of salicylic acid poisoning, use it only as directed. If you have any questions about this, check with your doctor.


Keep this medicine away from the eyes and other mucous membranes, such as the mouth and inside of the nose. If you should accidentally get some in your eyes or on other mucous membranes, immediately flush them with water for 15 minutes.


To use the cream, lotion, or ointment form of salicylic acid:


  • Apply enough medicine to cover the affected area, and rub in gently.

To use the gel form of salicylic acid:


  • Before using salicylic acid gel, apply wet packs to the affected areas for at least 5 minutes. If you have any questions about this, check with your health care professional.

  • Apply enough gel to cover the affected areas, and rub in gently.

To use the pad form of salicylic acid:


  • Wipe the pad over the affected areas.

  • Do not rinse off medicine after treatment.

To use the plaster form of salicylic acid for warts, corns, or calluses:


  • This medicine comes with patient instructions. Read them carefully before using.

  • Do not use this medicine on irritated skin or on any area that is infected or reddened. Also, do not use this medicine if you are a diabetic or if you have poor blood circulation.

  • Do not use this medicine on warts with hair growing from them or on warts on the face, in or on the genital (sex) organs, or inside the nose or mouth. Also do not use on moles or birthmarks. To do so may cause severe irritation.

  • Wash the area to be treated and dry thoroughly. Warts may be soaked in warm water for 5 minutes before drying.

  • Cut the plaster to fit the wart, corn, or callus and apply.

  • For corns and calluses:
    • Repeat every 48 hours as needed for up to 14 days, or as directed by your doctor, until the corn or callus is removed.

    • Corns or calluses may be soaked in warm water for 5 minutes to help in their removal.


  • For warts:
    • Depending on the product, either:
      • Apply plaster and repeat every 48 hours as needed, or
        • Apply plaster at bedtime, leave in place for at least 8 hours, remove plaster in the morning, and repeat every 24 hours as needed.



    • Repeat for up to 12 weeks as needed, or as directed by your doctor, until wart is removed.


  • If discomfort gets worse during treatment or continues after treatment, or if the wart spreads, check with your doctor.

To use the shampoo form of salicylic acid:


  • Before applying this medicine, wet the hair and scalp with lukewarm water. Apply enough medicine to work up a lather and rub well into the scalp for 2 or 3 minutes, then rinse. Apply the medicine again and rinse thoroughly.

To use the soap form of salicylic acid:


  • Work up a lather with the soap, using hot water, and scrub the entire affected area with a washcloth or facial sponge or mitt.

  • If you are to use this soap in a foot bath, work up rich suds in hot water and soak the feet for 10 to 15 minutes. Then pat dry without rinsing.

To use the topical solution form of salicylic acid for acne:


  • Wet a cotton ball or pad with the topical solution and wipe the affected areas.

  • Do not rinse off medicine after treatment.

To use the topical solution form of salicylic acid for warts, corns, or calluses:


  • This medicine comes with patient instructions. Read them carefully before using.

  • This medicine is flammable. Do not use it near heat or open flame or while smoking.

  • Do not use this medicine on irritated skin or on any area that is infected or reddened. Also, do not use this medicine if you are a diabetic or if you have poor blood circulation.

  • Do not use this medicine on warts with hair growing from them or on warts on the face, in or on the genital (sex) organs, or inside the nose or mouth. Also do not use on moles or birthmarks. To do so may cause severe irritation.

  • Avoid breathing in the vapors from the medicine.

  • Wash the area to be treated and dry thoroughly. Warts may be soaked in warm water for 5 minutes before drying.

  • Apply the medicine one drop at a time to completely cover each wart, corn, or callus. Let dry.

  • For warts—Repeat one or two times a day as needed for up to 12 weeks, or as directed by your doctor, until wart is removed.

  • For corns and calluses—Repeat one or two times a day as needed for up to 14 days, or as directed by your doctor, until the corn or callus is removed.

  • Corns and calluses may be soaked in warm water for 5 minutes to help in their removal.

  • If discomfort gets worse during treatment or continues after treatment, or if the wart spreads, check with your doctor.

Unless your hands are being treated, wash them immediately after applying this medicine to remove any medicine that may be on them.


Dosing


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


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


  • For cream dosage form:
    • For corns and calluses:
      • Adults and children—Use the 2 to 10% cream as needed. Use the 25 to 60% cream one time every three to five days.



  • For gel dosage form:
    • For acne:
      • Adults and children—Use the 0.5 to 5% gel one time a day.


    • For psoriasis:
      • Adults and children—Use the 5% gel one time a day.


    • For common warts:
      • Adults and children—Use the 5 to 26% gel one time a day.



  • For lotion dosage form:
    • For acne:
      • Adults and children—Use the 1 to 2% lotion one to three times a day.


    • For dandruff and antiseborrhic dermatitis of the scalp:
      • Adults and children—Use the 1.8 to 2% lotion on the scalp one or two times a day.



  • For ointment dosage form:
    • For acne:
      • Adults and children—Use the 3 to 6% ointment as needed.


    • For psoriasis and seborrheic dermatitis:
      • Adults and children—Use the 3 to 10% ointment as needed.


    • For common warts:
      • Adults and children—Use the 3 to 10% ointment as needed. Use the 25 to 60% ointment one time every three to five days.



  • For pads dosage form:
    • For acne:
      • Adults and children—Use one to three times a day.



  • For plaster dosage form:
    • For corns, calluses, common warts, or plantar warts:
      • Adults and children—Use one time a day or one time every other day.



  • For shampoo dosage form:
    • For dandruff or seborrheic dermatitis of the scalp:
      • Adults and children—Use on the scalp one or two times a week.



  • For soap dosage form:
    • For acne:
      • Adults and children—Use as needed.



  • For topical solution dosage form:
    • For acne:
      • Adults and children—Use the 0.5 to 2% topical solution one to three times a day.


    • For common warts and plantar warts:
      • Adults and children—Use the 5 to 27% topical solution one or two times a day.


    • For corns and calluses:
      • Adults and children—Use the 12 to 27% topical solution one or two times a day.



Missed Dose


If you miss a dose of this medicine, apply it as soon as possible. However, if it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule.


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.


Precautions While Using Clear Away Wart Removal System


When using salicylic acid, do not use any of the following preparations on the same affected area as this medicine, unless otherwise directed by your doctor:


  • Abrasive soaps or cleansers

  • Alcohol-containing preparations

  • Any other topical acne preparation or preparation containing a peeling agent (for example, benzoyl peroxide, resorcinol, sulfur, or tretinoin [vitamin A acid])

  • Cosmetics or soaps that dry the skin

  • Medicated cosmetics

  • Other topical medicine for the skin

To use any of the above preparations on the same affected area as salicylic acid may cause severe irritation of the skin.


Check with your doctor right away if you have nausea, vomiting, dizziness, loss of hearing, tinnitus, lethargy hyperpnea, diarrhea, and psychic disturbances. These could be symptoms of a serious condition called salicylate toxicity, especially in children under 12 years of age and patients with kidney or liver problems.


Clear Away Wart Removal System 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 as soon as possible if any of the following side effects occur:


Less common or rare
  • Skin irritation not present before use of this medicine (moderate or severe)

Frequency not known
  • Dryness and peeling of skin

  • flushing

  • redness of skin

  • unusually warm skin

Symptoms of salicylic acid poisoning
  • Confusion

  • diarrhea

  • dizziness

  • fast or deep breathing

  • headache (severe or continuing)

  • hearing loss

  • lightheadedness

  • nausea

  • rapid breathing

  • ringing or buzzing in ears (continuing)

  • severe drowsiness

  • stomach pain

  • vomiting

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
  • Skin irritation not present before use of this medicine (mild)

  • stinging

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.



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.


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  • Clear Away Wart Removal System Topical Use in Pregnancy & Breastfeeding
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Compare Clear Away Wart Removal System Topical with other medications


  • Acne
  • Dermatological Disorders
  • Warts

Nurofen Express 256 mg Tablets





1. Name Of The Medicinal Product



Nurofen Express 256 mg Tablets


2. Qualitative And Quantitative Composition



Ibuprofen 200 mg (as sodium dihydrate).



Also contains the following excipients:



carmellose sodium



xylitol



sucrose



For a full list of excipients, see Section 6.1.



3. Pharmaceutical Form



Tablet



A white to off-white, biconvex, round, sugar coated tablet printed with an identifying logo in black on one face.



4. Clinical Particulars



4.1 Therapeutic Indications



For the symptomatic relief of mild to moderate pain, such as headache, backache, period pain, dental pain, neuralgia, rheumatic and muscular pain, migraine, cold and flu symptoms, sore throat and fever.



4.2 Posology And Method Of Administration



For oral administration and short-term use only.



Adults, the elderly and children over 12 years:



The lowest effective dose should be used for the shortest duration necessary to relieve symptoms. The patient should consult a doctor if symptoms persist or worsen, or if the product is required for more than 10 days.



Adults and children over 12 years: Initial dose, 200mg to 400mg, up to three times a day as required.



Leave at least four hours between doses and do not take more than 1200mg in any 24 hour period.



Not for use by children under 12 years of age.



Elderly: No special dosage modifications are required (see Section 4.4).



4.3 Contraindications



Patients with a known hypersensitivity to ibuprofen or any other constituent of the medicinal product.



Patients who have previously shown hypersensitivity reactions (e.g. asthma, rhinitis, angioderma or urticaria) in response to aspirin or other non steroidal anti-inflammatory drugs.



Active or history of recurrent peptic ulcer/haemorrhage (two or more distinct episodes of proven ulceration or bleeding).



History of gastrointestinal bleeding or perforation, related to previous NSAIDs therapy.



Patients with severe hepatic failure, severe renal failure or severe heart failure. See also section 4.4.



Patients with rare hereditary problems of fructose intolerance, glucose-galatose malabsorption or sucrase-isomaltase insufficiency should not take this medicine.



Use with concomitant NSAIDs, including cyclo-oxygenase-2 specific inhibitors – increased risk of adverse reactions (see section 4.5).



During the last trimester of pregnancy as there is a risk of premature closure of the foetal ductus arteriosus with possible persistent pulmonary hypertension. The onset of labour may be delayed and the duration increased with an increased bleeding tendency in both mother and child (see Section 4.6).



4.4 Special Warnings And Precautions For Use



Undesirable effects may be minimised by using the lowest effective dose for the shortest possible duration necessary to control symptoms (see GI and cardiovascular risks below).



The elderly have an increased frequency of adverse reactions to NSAIDs, especially gastrointestinal bleeding and perforation, which may be fatal.



Respiratory:



Bronchospasm may be precipitated in patients suffering from, or with a history of, bronchial asthma or allergic disease.



Other NSAIDs:



The use of ibuprofen with concomitant NSAIDs including cyclooxygenase-2 selective inhibitors should be avoided (see section 4.5).



SLE and mixed connective tissue disease:



Systemic lupus erythematosus and mixed connective tissue disease –increased risk of aseptic meningitis (see section 4.8).



Renal:



Renal impairment as renal function may further deteriorate (see sections 4.3 and 4.8).



Hepatic:



Hepatic dysfunction (see sections 4.3 and 4.8).



Cardiovascular and cerebrovascular effects



Caution (discussion with doctor or pharmacist) is required prior to starting treatment in patients with a history of hypertension and/or heart failure as fluid retention, hypertension and oedema have been reported in association with NSAID therapy.



Clinical trial and epidemiological data suggest that the use of ibuprofen, particularly at high doses (2400 mg daily) and in long-term treatment may be associated with a small increased risk of arterial thrombotic events (for example myocardial infarction or stroke). Overall, epidemiological studies do not suggest that low dose ibuprofen (e.g.



Impaired female fertility:



There is some evidence that drugs which inhibit cyclooxygenase/prostaglandin synthesis may cause impairment of female fertility by an effect on ovulation. This is reversible on withdrawal of treatment.



Gastrointestinal:



NSAIDs should be given with care to patients with a history of gastrointestinal disease (ulcerative colitis, Crohn's disease) as these conditions may be exacerbated (see section 4.8).



GI bleeding, ulceration or perforation, which can be fatal has been reported with all NSAIDs at anytime during treatment, with or without warning symptoms or a previous history of GI events.



The risk of GI bleeding, ulceration or perforation is higher with increasing NSAID doses, in patients with a history of ulcer, particularly if complicated with haemorrhage or perforation (see section 4.3), and in the elderly. These patients should commence treatment on the lowest dose available.



Patients with a history of GI toxicity, particularly the elderly, should report any unusual abdominal symptoms (especially GI bleeding) particularly in the initial stages of treatment.



Caution should be advised in patients receiving concomitant medications which could increase the risk of ulceration or bleeding, such as oral corticosteroids, anticoagulants such as warfarin, selective serotonin-reuptake inhibitors or anti-platelet agents such as aspirin (see section 4.5).



When GI bleeding or ulceration occurs in patients receiving ibuprofen, the treatment should be withdrawn.



Dermatological:



Serious skin reactions, some of them fatal, including exfoliative dermatitis, Stevens-Johnson syndrome and toxic epidermal necrolysis, have been reported very rarely in association with the use of NSAIDs (see section 4.8). Patients appear to be at highest risk of these reactions early in the course of therapy, the onset of the reaction occurring in the majority of cases within the first month of treatment. Ibuprofen should be discontinued at the first appearance of skin rash, mucosal lesions, or any other sign of hypersensitivity.



Each tablet contains 24.3 mg (approximately 1.06 mmol) sodium. This should be considered in patients whose overall intake of sodium must be markedly restricted.



The label will include:



Read the enclosed leaflet before taking this product



Do not take if you:



• have (or have had two or more episodes of ) a stomach ulcer, perforation or bleeding



• are allergic to ibuprofen, to any of the ingredients, or to aspirin or other painkillers



• are taking other NSAID pain killers or aspirin with a daily dose above 75mg



Speak to a pharmacist or your doctor before taking if you:



• have or have had asthma, diabetes, high cholesterol, high blood pressure, a stroke, heart, liver, kidney or bowel problems



• are a smoker



• are pregnant



• are on a restricted sodium intake



If symptoms persist or worsen, or if new symptoms occur, consult your doctor or pharmacist.



4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction



Ibuprofen (like other NSAIDs) should not be used in combination with:



Aspirin: Unless low-dose aspirin (not above 75mg daily) has been advised by a doctor as this may increase the risk of adverse reactions (see section 4.4).



Experimental data suggest that ibuprofen may inhibit the effect of low dose aspirin on platelet aggregation when they are dosed concomitantly. However, the limitations of these data and the uncertainties regarding extrapolation of ex vivo data to the clinical situation imply that no firm conclusions can be made for regular ibuprofen use, and no clinically relevant effect is considered to be likely for occasional ibuprofen use (see section 5.1).



Other NSAIDs , including cyclooxygenase-2 selective inhibitors: Avoid concomitant use of two or more NSAIDs as this may (see section 4.4).



Ibuprofen should be used with caution in combination with:



Corticosteroids: as these may increase the risk of gastrointestinal ulceration or bleeding (see Section 4.4)



• Antihypertensives and diuretics: since NSAIDs may diminish the effects of these drugs. Diuretics can increase the risk of nephrotoxicity of NSAIDs.



Anticoagulants. NSAIDs may enhance the effects of anti-coagulants, such as warfarin (see section 4.4).



Antiplatelet agents and selective serotonin reuptake inhibitors (SSRIs): These can increase the risk of gastrointestinal bleeding. (see section 4.4).



Cardiac glycosides: NSAIDs may exacerbate cardiac failure, reduce GFR and increase plasma glycoside levels.



Lithium: There is evidence for potential increase in plasma levels of lithium.



Methotrexate: There is evidence for the potential increase in plasma levels of methotrexate.



Ciclosporin: Increased risk of nephrotoxicity.



Mifepristone: NSAIDs should not be used for 8-12 days after mifepristone administration as NSAIDs can reduce the effect of mifepristone.



Tacrolimus: Possible increased risk of nephrotoxicity when NSAIDs are given with tacrolimus.



Zidovudine: Increased risk of haematological toxicity when NSAIDs are given with zidovudine. There is evidence of an increased risk haemarthroses and haematoma in HIV (+) haemophiliacs receiving concurrent treatment with zidovudine and ibuprofen.



Quinolone antibiotics: Animal data indicate that NSAIDs can increase the risk of convulsions associated with quinolone antibiotics. Patients taking NSAIDs and quinolones may have an increased risk of developing convulsions.



4.6 Pregnancy And Lactation



No specific studies have been conducted with sodium ibuprofen.



Whilst no teratogenic effects have been demonstrated with ibuprofen acid in animal experiments, the use of the product during pregnancy should, if possible, be avoided during the first 6 months of pregnancy. It should not be used for the last trimester of pregnancy as there is a risk of premature closure of the foetal ductus arteriosus with possible persistent pulmonary hypertension. The onset of labour may be delayed and duration increased with an increased bleeding tendency in both mother and child. (See Section 4.3 Contraindications).



In limited studies, ibuprofen appears in the breast milk in very low concentration and is unlikely to affect the breast-fed infant adversely.



See section 4.4 regarding female fertility.



4.7 Effects On Ability To Drive And Use Machines



None expected at recommended dose and duration of therapy.



4.8 Undesirable Effects



Hypersensitivity reactions have been reported and these may consist of



a) non-specific allergic reactions and anaphylaxis;



b) respiratory tract reactivity e.g. asthma, aggravated asthma, bronchospasm, dyspnoea;



c) various skin reactions e.g. pruritus, urticaria, angioedema and more rarely exfoliative and bullous dermatoses (including epidermal necrolysis and erythema multiforme).



The list of the following adverse effects relates to those experienced with ibuprofen at OTC doses, for short-term use. In the treatment of chronic conditions, under long-term treatment, additional adverse effects may occur.



Hypersensitivity reactions:



Uncommon: Hypersensitivity reactions with urticaria and pruritis.



Very rare: severe hypersensitivity reactions. Symptoms could be facial, tongue and larynx swelling, dysponoea, tachycardia, hypotension, (anaphylaxis, angioedema or severe shock).



Exacerbation of asthma and bronchospasm.



Gastrointestinal disorders:



The most commonly observed adverse events are gastrointestinal in nature.



Uncommon: abdominal pain, nausea, dyspepsia.



Rare: Diarrhoea, flatulence, constipation and vomiting.



Very rare: peptic ulcer, perforation or gastrointestinal haemorrhage, melaena, haematemesis, sometimes fatal, particularly in the elderly (see section 4.4). Ulcerative stomatitis, gastritis.



Exacerbation of colitis and Crohn's disease (see section 4.4).



Nervous System:



Uncommon: Headache.



Very rare: Aseptic meningitis – single cases have been reported.



Renal:



Very rare: Acute renal failure, papillary necrosis, especially in long-term use, associated with increased serum urea and oedema.



Hepatic:



Very rare: liver disorders.



Blood:



Very rare: Haematopoietic disorders (anaemia, leucopenia, thrombocytopenia, pancytopenia, agranulocytosis). First signs are fever, sore throat, superficial mouth ulcers, flu-like symptoms, severe exhaustion, unexplained bleeding and bruising.



Dermatological:



Very rare: Severe forms of skin reactions such as bullous reaction, including Stevens-Johnson Syndrome, erythema multiform and toxic epidermal necrolysis can occur.



Uncommon: Various skin rashes.



Immune System:



In patients with existing auto-immune disorders (such as systemic lupus erythematosus, mixed connective tissue disease) during treatment with ibuprofen, single cases of symptoms of aseptic meningitis, such as stiff neck, headache, nausea, vomiting, fever or disorientation have been observed (see section 4.4).



Cardiovascular and Cerebrovascular:



Oedema, hypertension and cardiac failure have been reported in association with NSAID treatment.



Clinical trial and epidemiological data suggest that use of ibuprofen (particularly at high doses (2400mg daily) and in long-term treatment may be associated with a small increased risk of arterial thrombotic events (for example myocardial infarction or stroke) (see section 4.4).



4.9 Overdose



In children ingestion of more than 400 mg/kg may cause symptoms. In adults the dose response effect is less clear cut. The half-life in overdose is 1.5-3 hours.



Symptoms – Most patients who have ingested clinically important amounts of NSAIDs will develop no more than nausea, vomiting, epigastric pain, or more rarely diarrhoea. Tinnitus, headache and gastrointestinal bleeding are also possible. In more serious poisoning, toxicity is seen in the central nervous system, manifesting as drowsiness, occasionally excitation and disorientation or coma. Occasionally patients develop convulsions. In serious poisoning metabolic acidosis may occur and the prothrombin time/ INR may be prolonged, probably due to interference with the actions of circulating clotting factors. Acute renal failure and liver damage may occur. Exacerbation of asthma is possible in asthmatics.



Management – Management should be symptomatic and supportive and include the maintenance of a clear airway and monitoring of cardiac and vital signs until stable. Consider oral administration of activated charcoal if the patient presents within 1 hour of ingestion of a potentially toxic amount. If frequent or prolonged, convulsions should be treated with intravenous diazepam or lorazepam. Give bronchodilators for asthma.



5. Pharmacological Properties



5.1 Pharmacodynamic Properties



Pharmacotherapeutic group: propionic acid derivative



ATC Code: M01A E01



Ibuprofen is an NSAID that has demonstrated its efficacy in the common animal experimental inflammation models by inhibition of prostaglandin synthesis. In humans, ibuprofen reduces inflammatory pain, swellings and fever. Furthermore, ibuprofen reversibly inhibits platelet aggregation.



The clinical efficacy of ibuprofen has been demonstrated in pain associated with headache, toothache and dysmenorrhoea and fever; furthermore in patients with pain and fever associated with cold and flu and in pain models such as sore throat, muscular pain or soft tissue injury and backache.



A study in dental pain has shown that patients experienced statistically significant pain relief in 15 minutes after the administration of 2 x Nurofen Express 256 mg Tablets, compared with placebo. In this study, significantly more patients achieved meaningful pain relief after administration of 2 x Nurofen Express 256 mg Tablets than after administration of paracetamol tablets (96.3% vs 67.9%). These patients also achieved significantly greater reduction in pain intensity and greater pain relief over 6 hours compared with patients receiving paracetamol. Using measures of distractibility, patients receiving sodium ibuprofen experienced significantly greater benefit than those receiving placebo.



Clinical evidence demonstrates that ibuprofen, in the form of salts such as ibuprofen sodium and ibuprofen lysine, acts significantly faster than standard ibuprofen acid tablets for the relief of mild-moderate pain.



Clinical evidence demonstrates that when 400mg of ibuprofen is taken the pain relieving effects can last for up to 8 hours.



Experimental data suggest that ibuprofen may inhibit the effect of low dose aspirin on platelet aggregation when they are dosed concomitantly. In one study, when a single dose of ibuprofen 400mg was taken within 8 h before or within 30 min after immediate release aspirin dosing (81mg), a decreased effect of ASA on the formation of thromboxane or platelet aggregation occurred. However, the limitations of these data and the uncertainties regarding extrapolation of ex vivo data to the clinical situation imply that no firm conclusions can be made for regular ibuprofen use, and no relevant effect is considered to be likely for occasional ibuprofen use.



5.2 Pharmacokinetic Properties



Ibuprofen is well absorbed from the gastrointestinal tract. Ibuprofen is extensively bound to plasma proteins. Ibuprofen diffuses into the synovial fluid.



Maximum plasma concentrations of ibuprofen are reached 45 minutes after ingestion if taken on an empty stomach. When taken with food, peak plasma concentration of ibuprofen occurs 1 - 2 hours after administration. However, ibuprofen is more rapidly absorbed from the gastrointestinal tract following the administration of Nurofen Express 256mg Tablets, with peak plasma concentration occurring approximately 35 minutes after administration when taken on an empty stomach.



Ibuprofen is metabolised in the liver to two major metabolites with primary excretion via the kidneys, either as such or as major conjugates, together with a negligible amount of unchanged ibuprofen. Excretion by the kidney is both rapid and complete.



Elimination half-life is approximately 2 hours.



No significant differences in pharmacokinetic profile are observed in the elderly.



In limited studies, ibuprofen appears in the breast milk in very low concentrations.



5.3 Preclinical Safety Data



No relevant information, additional to that contained elsewhere in the SPC.



6. Pharmaceutical Particulars



6.1 List Of Excipients



Tablet core



Croscarmellose sodium (E468)



Xylitol (E967)



Microcrystalline cellulose (E460)



Magnesium stearate (E572)



Colloidal anhydrous silica (E551)



Coating ingredients



Carmellose sodium (E466),



Talc (E553b),



Acacia spray dried (E414),



Sucrose,



Titanium dioxide (E171),



Macrogol 6000 powder,



Tablet printing



Opacode S-1-27794 Black Printing Ink



Industrial Methylated Spirits



The ink contains the following residual materials after application: shellac (E904), iron oxide black (E172), propylene glycol.



6.2 Incompatibilities



Not applicable.



6.3 Shelf Life



2 years.



6.4 Special Precautions For Storage



Store in the original package.



6.5 Nature And Contents Of Container



A push through laminate blister tray consisting of opaque, white 250 micron PVC with 40 gsm polyvinylidene chloride (PVdC), heat-sealed to 20 micron aluminium foil.



The blister trays are packed into either a cardboard carton or a plastic, moulded acrylonitrile butadiene styrene (ABS) case.



Each carton will contain 2, 3, 4, 5, 6, 8, 10, 12, 14, 15, 16 tablets



Not all packs will be marketed.



6.6 Special Precautions For Disposal And Other Handling



Not applicable.



7. Marketing Authorisation Holder



Reckitt Benckiser (UK) Ltd, Dansom Lane, Hull HU8 7DS UK



8. Marketing Authorisation Number(S)



00063/0372



9. Date Of First Authorisation/Renewal Of The Authorisation



03/06/2008



10. Date Of Revision Of The Text



24/08/2010



11 DOSIMETRY


(IF APPLICABLE)



12 INSTRUCTIONS FOR PREPARATION OF RADIOPHARMACEUTICALS


(IF APPLICABLE)




Wednesday, 23 May 2012

chondroitin


Generic Name: chondroitin (KON droy tin)

Brand names: OptiFlex-C


What is chondroitin?

The use of chondroitin in cultural and traditional settings may differ from concepts accepted by current Western medicine. When considering the use of herbal/health supplements, consultation with a primary health care professional is advisable. Additionally, consultation with a practitioner trained in the uses of herbal/health supplements may be beneficial, and coordination of treatment among all health care providers involved may be advantageous.


Chondroitin is also known as chondroitin sulfate, chondroitin sulfuric acid, and chonsurid.


Chondroitin has been used for the alleviation of the symptoms of arthritis.


It has been reported that chondroitin may be involved in the production of cartilage that is important for healthy joints.


Chondroitin has not been evaluated by the FDA for safety, effectiveness, or purity. All potential risks and/or advantages of chondroitin may not be known. Additionally, there are no regulated manufacturing standards in place for these compounds. There have been instances where herbal/health supplements have been sold which were contaminated with toxic metals or other drugs. Herbal/health supplements should be purchased from a reliable source to minimize the risk of contamination.


Chondroitin may also have uses other than those listed in this product guide.


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


Chondroitin has not been evaluated by the FDA for safety, effectiveness, or purity. All potential risks and/or advantages of chondroitin may not be known. Additionally, there are no regulated manufacturing standards in place for these compounds. There have been instances where herbal/health supplements have been sold which were contaminated with toxic metals or other drugs. Herbal/health supplements should be purchased from a reliable source to minimize the risk of contamination.


Who should not take chondroitin?


Before taking chondroitin, talk to your doctor, pharmacist, or health care professional if you have any other medical conditions, allergies, or if you take other medicines or other herbal/health supplements. Chondroitin may not be recommended in some situations.


Do not take chondroitin without first talking to your doctor if you are pregnant or could become pregnant. Do not take chondroitin without first talking to your doctor if you are breast-feeding a baby. There is no information available regarding the use of chondroitin by children. Do not give any herbal/health supplement to a child without first talking to the child's doctor.

How should I take chondroitin?


The use of chondroitin in cultural and traditional settings may differ from concepts accepted by current Western medicine. When considering the use of herbal/health supplements, consultation with a primary health care professional is advisable. Additionally, consultation with a practitioner trained in the uses of herbal/health supplements may be beneficial, and coordination of treatment among all health care providers involved may be advantageous.


If you choose to take chondroitin, use it as directed on the package or as directed by your doctor, pharmacist, or other health care provider.


Chondroitin is often combined with glucosamine in the treatment of the symptoms of arthritis.


Different formulations of chondroitin are available to be used internally (orally).


Do not use different formulations (e.g., tablets and powder) of chondroitin at the same time, unless specifically directed to do so by a health care professional. Using different formulations together increases the risk of an overdose of chondroitin.

Although chondroitin may be readily available for use, it is important to consult with your doctor regarding traditional treatments for arthritis, to maintain proper body weight, and to continue with an exercise regimen as directed.


Store chondroitin as directed on the package. In general, chondroitin should be protected from light and moisture and stored in a sealed container.


What happens if I miss a dose?


Skip the missed dose if it is almost time for your next scheduled dose. Do not use extra chondroitin 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 taking chondroitin?


Follow your healthcare provider's instructions about any restrictions on food, beverages, or activity.


Chondroitin side effects


Although uncommon, allergic reactions to chondroitin have been reported. Stop taking chondroitin and seek emergency medical attention if you experience symptoms of a serious allergic reaction including difficulty breathing; closing of your throat; swelling of your lips, tongue, or face; or hives.

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 chondroitin?


Interactions between chondroitin and other prescription or over-the-counter medicines or herbal/health supplements have not been reported. Talk to your doctor, pharmacist, or health care professional before taking chondroitin if you are taking any other medicines or supplements.



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  • 0 Reviews for Chondroitin - Add your own review/rating


  • Chondroitin Natural MedFacts for Professionals (Wolters Kluwer)

  • Chondroitin Natural MedFacts for Consumers (Wolters Kluwer)



Compare chondroitin with other medications


  • Osteoarthritis
  • Rheumatoid Arthritis


Where can I get more information?


  • Consult with a licensed healthcare professional before using any herbal/health supplement. Whether you are treated by a medical doctor or a practitioner trained in the use of natural medicines/supplements, make sure all your healthcare providers know about all of your medical conditions and treatments.


Tuesday, 22 May 2012

Maalox Anti-Gas


Generic Name: simethicone (Oral route)

sye-METH-i-kone

Commonly used brand name(s)

In the U.S.


  • Alka-Seltzer Anti-Gas

  • Anti-Gas Ultra Strength

  • Baby Gasz

  • Equilizer Gas Relief

  • Gas Aid Maximum Strength

  • Gas-X

  • Genasyme

  • Maalox Anti-Gas

  • Mylanta Gas

  • Mylicon

  • Mytab Gas

  • Phazyme

In Canada


  • Ovol

  • Phazyme Liquid Gas Relief, Maximum Strength

Available Dosage Forms:


  • Tablet, Chewable

  • Liquid

  • Capsule

  • Syrup

  • Suspension

  • Tablet

  • Solution

  • Capsule, Liquid Filled

Therapeutic Class: Antiflatulent


Uses For Maalox Anti-Gas


Simethicone is used to relieve the painful symptoms of too much gas in the stomach and intestines.


Simethicone may also be used for other conditions as determined by your doctor.


Simethicone is available without a prescription.


Once a medicine has been approved for marketing for a certain use, experience may show that it is also useful for other medical problems. Although these uses are not included in product labeling, simethicone is used in certain patients before the following tests:


  • Before a gastroscopy

  • Before a radiography of the bowel

Before Using Maalox Anti-Gas


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


Allergies


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


Pediatric


This medicine has been tested in children and, in effective doses, has not been shown to cause different side effects or problems than it does in adults.


Geriatric


Many medicines have not been studied specifically in older people. Therefore, it may not be known whether they work exactly the same way they do in younger adults. There is no specific information comparing use of simethicone in the elderly with use in other age groups.


Interactions with Medicines


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


Interactions with Food/Tobacco/Alcohol


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


Proper Use of simethicone

This section provides information on the proper use of a number of products that contain simethicone. It may not be specific to Maalox Anti-Gas. Please read with care.


For effective use of simethicone:


  • Follow your doctor's instructions if this medicine was prescribed.

  • Follow the manufacturer's package directions if you are treating yourself.

Take this medicine after meals and at bedtime for best results.


For patients taking the chewable tablet form of this medicine:


  • It is important that you chew the tablets thoroughly before you swallow them. This is to allow the medicine to work faster and more completely.

For patients taking the oral liquid form of this medicine:


  • This medicine is to be taken by mouth even if it comes in a dropper bottle. The amount you should take is to be measured with the specially marked dropper or measuring spoon.

Avoid foods that seem to increase gas. Chew food thoroughly and slowly. Reduce air swallowing by avoiding fizzy, carbonated drinks. Do not smoke before meals. Develop regular bowel habits and exercise regularly. Make certain your health care professional knows if you are on a low-sodium, low-sugar, or any other special diet. Most medicines contain more than their active ingredient.


Dosing


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


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


  • For symptoms of too much gas:
    • For oral dosage forms (capsules or tablets):
      • Adults and teenagers—Usual dose is 60 to 125 milligrams (mg) four times a day, after meals and at bedtime. The dose should not be more than 500 mg in twenty-four hours.

      • Children—Dose must be determined by the doctor.


    • For oral dosage form (chewable tablets):
      • Adults and teenagers—Usual dose is 40 to 125 mg four times a day, after meals and at bedtime or the dose may be 150 mg three times a day, after meals. The dose should not be more than 500 mg in twenty-four hours.

      • Children—Dose must be determined by the doctor.


    • For oral dosage form (suspension):
      • Adults and teenagers—Usual dose is 40 to 95 mg four times a day, after meals and at bedtime. The dose should not be more than 500 mg in twenty-four hours.

      • Children—Dose must be determined by the doctor.



Missed Dose


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


Storage


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


Keep out of the reach of children.


Do not keep outdated medicine or medicine no longer needed.


Maalox Anti-Gas Side Effects


There have not been any common or important side effects reported with this medicine. However, if you notice any side effects, check with your doctor.



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 Maalox Anti-Gas resources


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


  • Maalox Anti-Gas Chewable Tablets MedFacts Consumer Leaflet (Wolters Kluwer)

  • Maalox Anti-Gas Concise Consumer Information (Cerner Multum)

  • Simethicone Professional Patient Advice (Wolters Kluwer)

  • Simethicone Monograph (AHFS DI)

  • Bicarsim MedFacts Consumer Leaflet (Wolters Kluwer)

  • Gas-X Extra Strength MedFacts Consumer Leaflet (Wolters Kluwer)

  • Gas-X Infant Drops Liquid Drops MedFacts Consumer Leaflet (Wolters Kluwer)

  • Genasyme Suspension MedFacts Consumer Leaflet (Wolters Kluwer)



Compare Maalox Anti-Gas with other medications


  • Endoscopy or Radiology Premedication
  • Functional Gastric Disorder
  • Gas
  • Postoperative Gas Pains

Sunday, 20 May 2012

Cipro



Pronunciation: SIP-roe-FLOX-a-sin
Generic Name: Ciprofloxacin
Brand Name: Cipro

Cipro is associated with an increased risk of tendon problems. These include pain, swelling, inflammation, and possible breakage of tendons. The risk of tendon problems is greater in patients who are older than 60 years, patients who take corticosteroids (eg, prednisone), and in those who have received kidney, heart, or lung transplants. The Achilles tendon in the back of the foot/ankle is most often affected. However, problems may also occur in other tendons (eg, in the shoulder, arm, hand). Problems may occur while you take Cipro or up to several months after you stop taking it.


Signs of tendon problems may include pain, soreness, redness, or swelling of a tendon or joint; bruising right after an injury in a tendon area; hearing or feeling a snap or pop in a joint or tendon area; or inability to move or bear weight on a joint or tendon area. Tell your doctor right away if you experience any of these symptoms while you take Cipro or within several months after you stop taking it.


Cipro may worsen muscle weakness and breathing problems in patients with myasthenia gravis. Do not take Cipro if you have a history of myasthenia gravis.





Cipro is used for:

Treating bacterial infections. It may also be used to prevent or slow anthrax after exposure.


Cipro is a fluoroquinolone antibiotic used to kill sensitive bacteria. It works by stopping the production of essential proteins needed by the bacteria to survive.


Do NOT use Cipro if:


  • you are allergic to any ingredient in Cipro or to any other fluoroquinolone (eg, levofloxacin)

  • you have a history of myasthenia gravis

  • you are taking tizanidine or you have recently received a live oral typhoid vaccine

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



Before using Cipro:


Some medical conditions may interact with Cipro. 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 stomach infection, liver problems, brain or nervous system problems, increased pressure in the brain, Alzheimer disease, brain blood vessel problems, muscle problems (eg, myasthenia gravis), or a history of seizures

  • if you have a history of severe or persistent diarrhea, skin sensitivity to the sun, low blood potassium levels, heart problems, or irregular heartbeat (eg, QT prolongation), or if you have a family member with a history of irregular heartbeat

  • if you have a history of joint or tendon problems; rheumatoid arthritis; kidney problems or decreased kidney function; or a heart, kidney, or lung transplant

  • if you take corticosteroids (eg, prednisone) or you participate in strenuous physical work or exercise

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


  • Antiarrhythmics (eg, amiodarone, quinidine) because the risk of serious side effects, including irregular heartbeat, may be increased

  • Corticosteroids (eg, prednisone) because they may increase the risk of tendon problems

  • Diuretics (eg, furosemide, hydrochlorothiazide), metoclopramide, nonsteroidal anti-inflammatory drugs (NSAIDs) (eg, ibuprofen), or probenecid because they may increase the risk of Cipro's side effects

  • Anticoagulants (eg, warfarin), antipsychotics (eg, clozapine), cyclosporine, methotrexate, monoamine oxidase inhibitors (MAOIs) (eg, phenelzine), serotonin-norepinephrine reuptake inhibitors (SNRIs) (eg, duloxetine), sulfonylureas (eg, glyburide), theophylline, tizanidine, tricyclic antidepressants (eg, amitriptyline), or xanthines (eg, caffeine) because the risk of their side effects may be increased by Cipro

  • Hydantoins (eg, phenytoin) or live oral typhoid vaccine because their effectiveness may be decreased by Cipro

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


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


  • An extra patient leaflet may be available with Cipro. Talk to your pharmacist if you have questions about this information.

  • Take Cipro by mouth with or without food. The preferred dosing time is 2 hours after a meal.

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

  • Drinking extra fluids while you are taking Cipro is recommended. Check with your doctor for instructions.

  • If you also take any products containing magnesium, aluminum, calcium, iron, or zinc (eg, antacids, quinapril, vitamins/minerals); didanosine; sucralfate; or bismuth subsalicylate, do not take them within 6 hours before or 2 hours after taking Cipro. Check with your doctor if you have questions.

  • If you also take sevelamer, do not take it within 4 hours before or after taking Cipro. Check with your doctor if you have questions.

  • Cipro works best if it is taken at the same time each day.

  • To clear up your infection completely, take Cipro for the full course of treatment. Keep taking it even if you feel better in a few days.

  • Avoid taking Cipro with milk or milk products (eg, calcium-enriched juice, yogurt) by themselves. However, taking Cipro as part of a full meal that contains milk or milk products is permitted.

  • Do not miss any doses. If you miss a dose of Cipro, 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 Cipro.



Important safety information:


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

  • Be sure to use Cipro for the full course of treatment. If you do not, the medicine may not clear up your infection completely. The bacteria could also become less sensitive to this or other medicines. This could make the infection harder to treat in the future.

  • Long-term or repeated use of Cipro may cause a second infection. Tell your doctor if signs of a second infection occur. Your medicine may need to be changed to treat this.

  • Cipro only works against bacteria; it does not treat viral infections (eg, the common cold).

  • Avoid large amounts of food or drink that have caffeine (eg, coffee, tea, cocoa, cola, chocolate).

  • Tell your doctor right away if you experience pain or swelling of a tendon or weakness or loss of use of a joint area. Rest the area and avoid exercise until further instruction from your doctor.

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

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

  • Mild diarrhea is common with antibiotic use. However, a more serious form of diarrhea (pseudomembranous colitis) may rarely occur. This may develop while you use the antibiotic or within several months after you stop using it. Contact your doctor right away if stomach pain or cramps, severe diarrhea, or bloody stools occur. Do not treat diarrhea without first checking with your doctor.

  • Use Cipro with caution in the ELDERLY; they may be more sensitive to its effects (eg, tendon problems), especially if they take corticosteroids (eg, prednisone). They may also be more sensitive to other effects (eg, irregular heartbeat).

  • Cipro should be used with extreme caution in CHILDREN younger than 18 years; they may be more sensitive to its effects, especially joint and tendon problems.

  • PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of taking Cipro while you are pregnant. Cipro is found in breast milk. Do not breast-feed while taking Cipro.


Possible side effects of Cipro:


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



Diarrhea; dizziness; headache; loss of appetite; nausea; stomach upset; vomiting.



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); bloody or tarry stools; burning, numbness, tingling, pain, or weakness of the arms, hands, legs, or feet; chest pain; dark urine or unusual change in the amount of urine; fainting; fever, chills, or unusual cough; hallucinations; inability to move or bear weight on a joint or tendon area; irregular heartbeat; loss of consciousness; moderate to severe sunburn; mood or mental changes (eg, new or worsening anxiety, agitation, confusion, depression, restlessness, sleeplessness); muscle pain or weakness; pain, soreness, redness, swelling, weakness, or bruising of a tendon or joint area; pale stools; persistent sore throat; red, swollen, blistered, or peeling skin; seizures; severe or persistent diarrhea; severe or persistent dizziness; shortness of breath or trouble breathing; stomach cramps or pain; suicidal thoughts or actions; tremors; unusual bruising or bleeding; unusual fatigue; vaginal yeast infection; vision changes; 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: Cipro 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 Cipro:

Store Cipro 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. Do not store in the bathroom. Keep Cipro out of the reach of children and away from pets.


General information:


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

  • Cipro 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 Cipro. 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 Cipro resources


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


Compare Cipro with other medications


  • Anthrax
  • Anthrax Prophylaxis
  • Bacteremia
  • Bacterial Infection
  • Bladder Infection
  • Bone infection
  • Bronchitis
  • Chancroid
  • Cholera
  • Crohn's Disease
  • Cutaneous Bacillus anthracis
  • Diverticulitis
  • Epididymitis, Sexually Transmitted
  • Febrile Neutropenia
  • Gonococcal Infection, Disseminated
  • Gonococcal Infection, Uncomplicated
  • Granuloma Inguinale
  • Infection Prophylaxis
  • Infectious Diarrhea
  • Intraabdominal Infection
  • Joint Infection
  • Kidney Infections
  • Meningococcal Meningitis Prophylaxis
  • Mycobacterium avium-intracellulare, Treatment
  • Nosocomial Pneumonia
  • Peritonitis
  • Plague
  • Pneumonia
  • Pneumonia with Cystic Fibrosis
  • Prostatitis
  • Rabbit Fever
  • Salmonella Enteric Fever
  • Salmonella Gastroenteritis
  • Shigellosis
  • Sinusitis
  • Skin Infection
  • Traveler's Diarrhea
  • Tuberculosis, Active
  • Typhoid Fever
  • Urinary Tract Infection