Thursday, 21 June 2012

TheraCys


Generic Name: BCG (bee cee jee)

Brand Names: TheraCys, Tice BCG Vaccine


What is TheraCys (BCG)?

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


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


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


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


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


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

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


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


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


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


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

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


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

  • tuberculosis;




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




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




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




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



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



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




  • myasthenia gravis;




  • a pacemaker or other artificial heart device;




  • an artificial joint or other prosthetic;




  • a history of aneurysm (dilated blood vessel);




  • if you have ever had bypass surgery;




  • if you have ever had tuberculosis; or




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



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


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

How is BCG given?


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


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


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


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

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


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


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

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


What happens if I miss a dose?


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


What happens if I overdose?


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

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


What should I avoid while receiving TheraCys (BCG)?


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

TheraCys (BCG) side effects


Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Report any side effects to your doctor. Some side effects may be serious, including:

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




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




  • pain or burning when you urinate;




  • difficult urination;




  • more frequent or urgent urinating;




  • blood in your urine, lower back pain;




  • pain or swelling in your testicles;




  • easy bruising or bleeding;




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




  • vision changes, increased sensitivity to light.



Less serious side effects may include:



  • mild nausea, stomach pain, or loss of appetite;




  • mild bladder or groin pain;




  • urine leakage or incontinence;




  • diarrhea, constipation;




  • headache;




  • mild skin rash;




  • dizziness, tired feeling; or




  • tissue particles in your urine (not blood).



This is not a complete list of side effects and others may occur. Tell your doctor about any unusual or bothersome side effect. You may report side effects to FDA at 1-800-FDA-1088.


What other drugs will affect TheraCys (BCG)?


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



  • cancer medicine or radiation;




  • cyclosporine (Neoral, Sandimmune, Gengraf);




  • sirolimus (Rapamune), tacrolimus (Prograf);




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




  • mycophenolate mofetil (CellCept);




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




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



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



More TheraCys resources


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


  • TheraCys MedFacts Consumer Leaflet (Wolters Kluwer)

  • BCG Vaccine Prescribing Information (FDA)

  • BCG Vaccine Advanced Consumer (Micromedex) - Includes Dosage Information

  • Theracys Advanced Consumer (Micromedex) - Includes Dosage Information



Compare TheraCys with other medications


  • Tuberculosis, Prophylaxis
  • Urinary Tract Tumors


Where can I get more information?


  • Your doctor or pharmacist can provide more information about BCG.

See also: TheraCys side effects (in more detail)


Tuesday, 19 June 2012

Maxinate


Generic Name: prenatal multivitamins (PRE nay tal VYE ta mins)

Brand Names: Advance Care Plus, Bright Beginnings, Cavan Folate, Cavan One, Cavan-Heme OB, Cenogen Ultra, CitraNatal Rx, Co Natal FA, Complete Natal DHA, Complete-RF, CompleteNate, Concept OB, Docosavit, Dualvit OB, Duet, Edge OB, Elite OB 400, Femecal OB, Folbecal, Folcaps Care One, Folivan-OB, Foltabs, Gesticare, Icar Prenatal, Icare Prenatal Rx, Inatal Advance, Infanate DHA, Kolnatal DHA, Lactocal-F, Marnatal-F, Maternity, Maxinate, Mission Prenatal, Multi-Nate 30, Multinatal Plus, Nata 29 Prenatal, Natachew, Natafort, Natelle, Neevo, Nestabs, Nexa Select with DHA, Novanatal, NovaStart, O-Cal Prenatal, OB Complete, OB Natal One, Ob-20, Obtrex DHA, OptiNate, Paire OB Plus DHA, PNV Select, PNV-Total, PR Natal 400, Pre-H-Cal, Precare, PreferaOB, Premesis Rx, PrenaCare, PrenaFirst, PrenaPlus, Prenatabs OBN, Prenatabs Rx, Prenatal 1 Plus 1, Prenatal Elite, Prenatal Multivitamins, Prenatal Plus, Prenatal S, Prenatal-U, Prenate Advanced Formula, Prenate DHA, Prenate Elite, Prenavite FC, PreNexa, PreQue 10, Previte Rx, PrimaCare, Pruet DHA, RE OB Plus DHA, Renate, RightStep, Rovin-NV, Se-Care, Se-Natal One, Se-Plete DHA, Se-Tan DHA, Select-OB, Seton ET, Strongstart, Stuart Prenatal with Beta Carotene, Tandem OB, Taron-BC, Tri Rx, TriAdvance, TriCare, Trimesis Rx, Trinate, Triveen-PRx RNF, UltimateCare Advance, Ultra-Natal, Vemavite PRX 2, VeNatal FA, Verotin-BY, Verotin-GR, Vinacal OR, Vinatal Forte, Vinate Advanced (New Formula), Vinate AZ, Vinate Care, Vinate Good Start, Vinate II (New Formula), Vinate III, Vinate One, Vitafol-OB, VitaNatal OB plus DHA, Vitaphil, Vitaphil Aide, Vitaphil Plus DHA, Vitaspire, Viva DHA, Vol-Nate, Vol-Plus, Vol-Tab Rx, Vynatal F.A., Zatean-CH, Zatean-PN


What are Maxinate (prenatal multivitamins)?

There are many brands and forms of prenatal vitamin available and not all brands are listed on this leaflet.


Prenatal vitamins are a combination of many different vitamins that are normally found in foods and other natural sources.


Prenatal vitamins are used to provide the additional vitamins needed during pregnancy. Minerals may also be contained in prenatal multivitamins.


Prenatal vitamins may also be used for purposes not listed in this medication guide.


What is the most important information I should know about prenatal vitamins?


There are many brands and forms of prenatal vitamin available and not all brands are listed on this leaflet.


Never take more than the recommended dose of a multivitamin. Avoid taking any other multivitamin product within 2 hours before or after you take your prenatal vitamins. Taking similar vitamin products together at the same time can result in a vitamin overdose or serious side effects.

Many multivitamin products also contain minerals such as calcium, iron, magnesium, potassium, and zinc. Minerals (especially taken in large doses) can cause side effects such as tooth staining, increased urination, stomach bleeding, uneven heart rate, confusion, and muscle weakness or limp feeling. Read the label of any multivitamin product you take to make sure you are aware of what it contains.


Seek emergency medical attention if you think you have used too much of this medicine. An overdose of vitamins A, D, E, or K can cause serious or life-threatening side effects and can also harm your unborn baby. Certain minerals contained in a prenatal multivitamin may also cause serious overdose symptoms or harm to the baby if you take too much.

Overdose symptoms may include stomach pain, vomiting, diarrhea, constipation, loss of appetite, hair loss, peeling skin, tingly feeling in or around your mouth, changes in menstrual periods, weight loss, severe headache, muscle or joint pain, severe back pain, blood in your urine, pale skin, and easy bruising or bleeding.


Do not take this medication with milk, other dairy products, calcium supplements, or antacids that contain calcium. Calcium may make it harder for your body to absorb certain ingredients of the multivitamin.

What should I discuss with my healthcare provider before taking prenatal vitamins?


Many vitamins can cause serious or life-threatening side effects if taken in large doses. Do not take more of this medication than directed on the label or prescribed by your doctor.

Before taking prenatal vitamins, tell your doctor about all of your medical conditions.


You may need to continue taking prenatal vitamins if you breast-feed your baby. Ask your doctor about taking this medication while breast-feeding.

How should I take prenatal vitamins?


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.


Never take more than the recommended dose of prenatal vitamins.

Many multivitamin products also contain minerals such as calcium, iron, magnesium, potassium, and zinc. Minerals (especially taken in large doses) can cause side effects such as tooth staining, increased urination, stomach bleeding, uneven heart rate, confusion, and muscle weakness or limp feeling. Read the label of any multivitamin product you take to make sure you are aware of what it contains.


Take your prenatal vitamin with a full glass of water.

Swallow the regular tablet or capsule whole. Do not break, chew, crush, or open it.


The chewable tablet must be chewed or allowed to dissolve in your mouth before swallowing. You may also allow the chewable tablet to dissolve in drinking water, fruit juice, or infant formula (but not milk or other dairy products). Drink this mixture right away.


Use prenatal vitamins regularly to get the most benefit. Get your prescription refilled before you run out of medicine completely.


Store at room temperature away from moisture and heat. Keep prenatal vitamins in their original container. Storing vitamins in a glass container can ruin the medication.

What happens if I miss a dose?


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


What happens if I overdose?


Seek emergency medical attention if you think you have used too much of this medicine. An overdose of vitamins A, D, E, or K can cause serious or life-threatening side effects and can also harm your unborn baby. Certain minerals contained in a prenatal multivitamin may also cause serious overdose symptoms or harm to the baby if you take too much.

Overdose symptoms may include stomach pain, vomiting, diarrhea, constipation, loss of appetite, hair loss, peeling skin, tingly feeling in or around your mouth, changes in menstrual periods, weight loss, severe headache, muscle or joint pain, severe back pain, blood in your urine, pale skin, and easy bruising or bleeding.


What should I avoid while taking prenatal vitamins?


Avoid taking any other multivitamin product within 2 hours before or after you take your prenatal vitamins. Taking similar vitamin products together at the same time can result in a vitamin overdose or serious side effects.

Avoid the regular use of salt substitutes in your diet if your multivitamin contains potassium. If you are on a low-salt diet, ask your doctor before taking a vitamin or mineral supplement.


Do not take this medication with milk, other dairy products, calcium supplements, or antacids that contain calcium. Calcium may make it harder for your body to absorb certain ingredients of the prenatal vitamin.

Prenatal vitamins 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.

When taken as directed, prenatal vitamins are not expected to cause serious side effects. Less serious side effects may include:



  • upset stomach;




  • headache; or




  • unusual or unpleasant taste in your mouth.



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 prenatal vitamins?


Vitamin and mineral supplements can interact with certain medications, or affect how medications work in your body. Before taking a prenatal vitamin, tell your doctor if you also use:



  • diuretics (water pills);




  • heart or blood pressure medications;




  • tretinoin (Vesanoid);




  • isotretinoin (Accutane, Amnesteen, Clavaris, Sotret);




  • trimethoprim and sulfamethoxazole (Cotrim, Bactrim, Gantanol, Gantrisin, Septra, TMP/SMX); or




  • an NSAID (non-steroidal anti-inflammatory drug) such as ibuprofen (Advil, Motrin), naproxen (Aleve, Naprosyn, Naprelan, Treximet), celecoxib (Celebrex), diclofenac (Cataflam, Voltaren), indomethacin (Indocin), meloxicam (Mobic), and others.



This list is not complete and other drugs may interact with prenatal vitamins. 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 Maxinate resources


  • Maxinate Use in Pregnancy & Breastfeeding
  • Maxinate Drug Interactions
  • Maxinate Support Group
  • 0 Reviews for Maxinate - Add your own review/rating


  • Cal-Nate MedFacts Consumer Leaflet (Wolters Kluwer)

  • CareNatal DHA MedFacts Consumer Leaflet (Wolters Kluwer)

  • CitraNatal 90 DHA MedFacts Consumer Leaflet (Wolters Kluwer)

  • CitraNatal Assure Prescribing Information (FDA)

  • CitraNatal Harmony Prescribing Information (FDA)

  • Concept DHA Prescribing Information (FDA)

  • Docosavit Prescribing Information (FDA)

  • Duet DHA with Ferrazone MedFacts Consumer Leaflet (Wolters Kluwer)

  • Folbecal MedFacts Consumer Leaflet (Wolters Kluwer)

  • Folcal DHA Prescribing Information (FDA)

  • Folcaps Care One Prescribing Information (FDA)

  • Gesticare DHA Prescribing Information (FDA)

  • Gesticare DHA MedFacts Consumer Leaflet (Wolters Kluwer)

  • Inatal Advance Prescribing Information (FDA)

  • Inatal Ultra Prescribing Information (FDA)

  • Multi-Nate DHA Prescribing Information (FDA)

  • Multi-Nate DHA Extra Prescribing Information (FDA)

  • MultiNatal Plus MedFacts Consumer Leaflet (Wolters Kluwer)

  • Natelle One Prescribing Information (FDA)

  • Neevo Caplets MedFacts Consumer Leaflet (Wolters Kluwer)

  • Neevo DHA MedFacts Consumer Leaflet (Wolters Kluwer)

  • OB Complete 400 MedFacts Consumer Leaflet (Wolters Kluwer)

  • Paire OB Plus DHA Prescribing Information (FDA)

  • PreNexa MedFacts Consumer Leaflet (Wolters Kluwer)

  • PreNexa Prescribing Information (FDA)

  • PreferaOB Prescribing Information (FDA)

  • Prenatal Plus Prescribing Information (FDA)

  • Prenatal Plus Iron Prescribing Information (FDA)

  • Prenate Elite Prescribing Information (FDA)

  • Prenate Elite MedFacts Consumer Leaflet (Wolters Kluwer)

  • Prenate Elite tablets

  • Prenate Essential Prescribing Information (FDA)

  • PrimaCare Advantage MedFacts Consumer Leaflet (Wolters Kluwer)

  • PrimaCare ONE capsules

  • PrimaCare One MedFacts Consumer Leaflet (Wolters Kluwer)

  • Renate DHA Prescribing Information (FDA)

  • Se-Natal 19 Chewable Tablets MedFacts Consumer Leaflet (Wolters Kluwer)

  • Se-Natal 19 Prescribing Information (FDA)

  • Tandem DHA Prescribing Information (FDA)

  • Tandem OB Prescribing Information (FDA)

  • TriAdvance Prescribing Information (FDA)

  • Triveen-One MedFacts Consumer Leaflet (Wolters Kluwer)

  • Triveen-PRx RNF Prescribing Information (FDA)

  • UltimateCare ONE NF Prescribing Information (FDA)

  • Ultra NatalCare MedFacts Consumer Leaflet (Wolters Kluwer)

  • Vinate AZ Prescribing Information (FDA)

  • Vitafol-One MedFacts Consumer Leaflet (Wolters Kluwer)

  • Zatean-CH Prescribing Information (FDA)



Compare Maxinate with other medications


  • Vitamin/Mineral Supplementation during Pregnancy/Lactation


Where can I get more information?


  • Your pharmacist can provide more information about prenatal vitamins.


Monday, 18 June 2012

Atridox


Generic Name: doxycycline (Subgingival route)

dox-i-SYE-kleen

Commonly used brand name(s)

In the U.S.


  • Atridox

Available Dosage Forms:


  • Kit

Therapeutic Class: Antibacterial


Chemical Class: Tetracycline (class)


Uses For Atridox


Doxycycline is used to help treat periodontal disease (a disease of your gums). Periodontal disease is caused by bacteria growing beneath the gum line. Doxycycline works by keeping the number of bacteria from growing. Lowering the amount of bacteria helps to reduce inflammation and swelling in your mouth, and the amount of bleeding around the teeth. Doxycycline is placed in deep gum pockets next to your teeth in order to reduce the depth of the pockets.


This medicine will be applied by your dentist or other oral health care professional.


Before Using Atridox


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


Use is not recommended in infants and children younger than 8 years of age. Tetracyclines, such as doxycycline, may cause permanent discoloration of teeth and slow down the growth of bones. The safety and effectiveness of doxycycline have not been established in children 8 years of age or older.


Geriatric


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


Pregnancy








Pregnancy CategoryExplanation
All TrimestersDStudies in pregnant women have demonstrated a risk to the fetus. However, the benefits of therapy in a life threatening situation or a serious disease, may outweigh the potential risk.

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 receiving 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 not recommended. Your doctor may decide not to treat you with this medication or change some of the other medicines you take.


  • Acitretin

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.


  • Digoxin

  • Isotretinoin

  • Methotrexate

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.


  • Desogestrel

  • Dienogest

  • Drospirenone

  • Estradiol Cypionate

  • Estradiol Valerate

  • Ethinyl Estradiol

  • Ethynodiol Diacetate

  • Etonogestrel

  • Fosphenytoin

  • Levonorgestrel

  • Medroxyprogesterone Acetate

  • Mestranol

  • Norelgestromin

  • Norethindrone

  • Norgestimate

  • Norgestrel

  • Penicillin G

  • Penicillin G Procaine

  • Penicillin V

  • Rifampin

  • Rifapentine

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:


  • Candidiasis (yeast infection) of the mouth, or history of—Use with caution. May make this condition worse.

  • Conditions with severe periodontal defects or

  • Dental implants or

  • Weak immune system (caused by diabetes, HIV infection, or patients receiving cancer or radiation treatments)—Atridox® has not been tested and evaluated in patients with these conditions.

Proper Use of Atridox


Doxycycline periodontal system is placed by your dentist into one or more deep gum pockets next to your teeth. A dental dressing or adhesive will be placed on top to help keep the system in place. The treatment may be repeated four months later.


The treatment period for the doxycycline periodontal system is seven days after your dentist inserts it. If the system comes loose or falls out before the 7 days are up, check with your dentist.


Doxycycline periodontal system does not have to be removed by the dentist; it will dissolve. The dental dressing or adhesive that holds the system in place may fall out naturally. However, if the dental dressing or adhesive is still present after 7 days, it should be removed by the dentist.


After the medicine is placed in your mouth, try to avoid any actions that may cause the medicine to come out. For example:


  • Do not brush around the teeth that have been treated for 7 days.

  • Do not use dental floss or any other cleaning tools that go between the teeth for 7 days after treatment.

Precautions While Using Atridox


It is very important that your dentist check your progress while you are receiving this medicine. Do not miss any dental appointments.


Using this medicine while you are pregnant (especially during the last half of your pregnancy) can harm your unborn baby. Use an effective form of birth control to keep from getting pregnant. If you think you have become pregnant while using the medicine, tell your doctor right away.


Check with your dentist as soon as possible if you have pain or swelling or other problems in the treated areas.


Oral contraceptives (birth control pills) containing estrogen may not work properly if you take them while you are using doxycycline periodontal system. To keep from getting pregnant, use another form of birth control (e.g., condoms, diaphragms, or contraceptive foams or jellies) while doxycycline periodontal system is in place. If you have any questions about this, check with your doctor.


For 7 days after receiving doxycycline periodontal system, do not floss or brush around the teeth that have been treated. Brushing or flossing may loosen the system or cause it to fall out.


Tetracyclines, such as doxycycline, may cause your skin to be more sensitive to sunlight than it is normally. Exposure to sunlight, even for brief periods of time, may cause a skin rash, itching, redness or other discoloration of the skin, or a severe sunburn. For a period of 7 days after receiving doxycycline periodontal system:


  • Stay out of direct sunlight, especially between the hours of 10:00 a.m. and 3:00 p.m., if possible.

  • Wear protective clothing, including a hat. Also, wear sunglasses.

  • Apply a sun block product that has a skin protection factor (SPF) of at least 15. Some patients may require a product with a higher SPF number, especially if they have a fair complexion. If you have any questions about this, check with your doctor.

  • Apply a sun block lipstick that has an SPF of at least 15 to protect your lips.

  • Do not use a sunlamp or tanning bed or booth.

You may still be sensitive to sunlight or sunlamps for 2 weeks to several months or more after the 7-day treatment period of doxycycline periodontal system. If you have a severe reaction, check with your dentist or doctor.


Atridox 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 or nurse immediately if any of the following side effects occur:


Less common
  • High blood pressure

  • looseness of tooth

  • tooth or gum pain (severe or continuing)

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
  • Common cold–like symptoms

  • gum discomfort, pain, or soreness

  • headache

  • pressure sensitivity of the tooth

  • toothache

Less common
  • Abdominal or stomach bloating or pelvic pain

  • cough

  • diarrhea

  • gum redness

  • indigestion, upset stomach, or stomachache

  • influenza-like symptoms

  • mouth pain or soreness

  • muscle aches

  • sensitivity of the tooth to heat or cold

  • shortness of breath

  • sleeplessness

  • sore throat

  • stuffy head, postnasal drip, or nasal congestion

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.


More Atridox resources


  • Atridox Use in Pregnancy & Breastfeeding
  • Drug Images
  • Atridox Drug Interactions
  • Atridox Support Group
  • 153 Reviews for Atridox - Add your own review/rating


  • Atridox Prescribing Information (FDA)



Compare Atridox with other medications


  • Acne
  • Actinomycosis
  • Amebiasis
  • Anthrax
  • Anthrax Prophylaxis
  • Bacterial Infection
  • Bartonellosis
  • Bronchitis
  • Brucellosis
  • Bullous Pemphigoid
  • Chlamydia Infection
  • Cholera
  • Cutaneous Bacillus anthracis
  • Ehrlichiosis
  • Enterocolitis
  • Epididymitis, Sexually Transmitted
  • Gastroenteritis
  • Granuloma Inguinale
  • Inclusion Conjunctivitis
  • Lyme Disease
  • Lyme Disease, Arthritis
  • Lyme Disease, Carditis
  • Lyme Disease, Erythema Chronicum Migrans
  • Lyme Disease, Neurologic
  • Lymphogranuloma Venereum
  • Malaria
  • Malaria Prevention
  • Melioidosis
  • Mycoplasma Pneumonia
  • Nongonococcal Urethritis
  • Ocular Rosacea
  • Ornithosis
  • Pelvic Inflammatory Disease
  • Pemphigoid
  • Pemphigus
  • Periodontitis
  • Plague
  • Pleural Effusion
  • Pneumonia
  • Proctitis
  • Prostatitis
  • Psittacosis
  • Rabbit Fever
  • Rheumatoid Arthritis
  • Rickettsial Infection
  • Rosacea
  • Skin Infection
  • STD Prophylaxis
  • Syphilis, Early
  • Syphilis, Latent
  • Tertiary Syphilis
  • Trachoma
  • Upper Respiratory Tract Infection
  • Urinary Tract Infection

Wednesday, 13 June 2012

Urea Suspension


Pronunciation: ue-REE-a
Generic Name: Urea
Brand Name: Umecta


Urea Suspension is used for:

Promoting the healing of certain conditions of the fingernails and toenails (eg, hyperkeratotic conditions). It may also be used to treat certain other skin conditions (eg, corns; calluses; rough, dry skin) as determined by your doctor.


Urea Suspension is a debriding agent. It works by helping to break down dead skin and pus, which helps to soften, loosen, and shed hard, scaly skin and nails.


Do NOT use Urea Suspension if:


  • you are allergic to any ingredient in Urea Suspension

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



Before using Urea Suspension:


Some medical conditions may interact with Urea Suspension. 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

Some MEDICINES MAY INTERACT with Urea Suspension. Because little, if any, of Urea Suspension is absorbed into the blood, the risk of it interacting with another medicine is low.


Ask your health care provider if Urea Suspension 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 Urea Suspension:


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


  • Wash your hands before and after using Urea Suspension unless your hands are part of the treated area.

  • Shake well before each use.

  • To use Urea Suspension on the skin, apply a small amount of Urea Suspension to the affected area as directed by your doctor. Rub it in completely until it is absorbed. If you get Urea Suspension on any skin that is not part of the treated area, wash it off thoroughly.

  • To use Urea Suspension on the nail, apply a small amount of Urea Suspension on the affected area as directed by your doctor. If you get Urea Suspension on any skin that is not part of the treated area, wash it off thoroughly.

  • You may cover the affected area unless directed otherwise by your doctor.

  • Use Urea Suspension on a regular schedule to get the most benefit from it.

  • If you miss a dose of Urea Suspension, 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 Urea Suspension.



Important safety information:


  • Urea Suspension is for external use only. Do not get it in your eyes, nose, mouth, or on your lips. If you get it in any of these areas, rinse right away with cool water.

  • Do not exceed the recommended dose, use for longer than prescribed, or use for other skin conditions without checking with your doctor.

  • If your symptoms do not get better or if they get worse, check with your doctor.

  • Do not apply to broken or severely irritated skin.

  • Talk with your doctor before you use any other medicines or cleansers on your skin.

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


Possible side effects of Urea Suspension:


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:



Mild skin irritation; temporary burning, stinging, or itching.



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); redness; severe or persistent burning or irritation.



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. Urea Suspension may be harmful if swallowed.


Proper storage of Urea Suspension:

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


General information:


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

  • Urea Suspension 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 Urea Suspension. 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 Urea resources


  • Urea Use in Pregnancy & Breastfeeding
  • Urea Support Group
  • 9 Reviews for Urea - Add your own review/rating


Compare Urea with other medications


  • Dermatological Disorders
  • Dry Skin
  • Pityriasis rubra pilaris

Tuesday, 12 June 2012

maprotiline


ma-PROE-ti-leen


Oral route(Tablet)

Antidepressants increased the risk of suicidal thinking and behavior in children, adolescents, and young adults in short-term studies with major depressive disorder (MDD) and other psychiatric disorders. Short term studies did not show an increase in the risk of suicidality with antidepressants compared to placebo in adults beyond age 24, and there was a reduction in risk with antidepressants compared to placebo in adults aged 65 and older. This risk must be balanced with the clinical need. Monitor patients closely for clinical worsening, suicidality, or unusual changes in behavior. Families and caregivers should be advised of the need for close observation and communication with the prescriber. Not approved for use in pediatric patients .



Commonly used brand name(s)

In the U.S.


  • Ludiomil

Available Dosage Forms:


  • Tablet

Therapeutic Class: Antidepressant


Pharmacologic Class: Antidepressant, Tetracyclic


Uses For maprotiline


Maprotiline is used to relieve mental depression, including anxiety that sometimes occurs with depression.


Maprotiline is available only with your doctor's 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 this use is not included in product labeling, maprotiline is used in certain patients with the following medical condition:


  • Chronic neurogenic pain (a certain type of pain that is continuing)

Before Using maprotiline


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 maprotiline, the following should be considered:


Allergies


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


Maprotiline must be used with caution in children with depression. Studies have shown occurrences of children thinking about suicide or attempting suicide in clinical trials for maprotiline. More study is needed to be sure maprotiline is safe and effective in children


Geriatric


Drowsiness, dizziness or lightheadedness; confusion; vision problems; dryness of mouth; constipation; and difficulty in urinating may be especially likely to occur in elderly patients, who are usually more sensitive than younger adults to the effects of maprotiline.


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


  • Brofaromine

  • Cisapride

  • Clorgyline

  • Furazolidone

  • Iproniazid

  • Isocarboxazid

  • Lazabemide

  • Linezolid

  • Methylene Blue

  • Metoclopramide

  • Moclobemide

  • Nialamide

  • Pargyline

  • Phenelzine

  • Procarbazine

  • Rasagiline

  • Selegiline

  • Toloxatone

  • Tranylcypromine

Using maprotiline 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.


  • Rasagiline

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


  • Alcohol abuse or

  • Seizure disorders (including epilepsy)—The risk of seizures may be increased

  • Asthma or

  • Difficult urination or

  • Enlarged prostate or

  • Glaucoma or

  • Mental illness (severe) or

  • Stomach or intestinal problems—Maprotiline may make the condition worse

  • Heart or blood vessel disease or

  • Overactive thyroid—Serious effects on your heart may occur

  • Liver disease—Higher blood levels of maprotiline may occur, increasing the chance of side effects

Proper Use of maprotiline


Take maprotiline only as directed by your doctor to benefit your condition as much as possible. Do not take more of it, do not take it more often, and do not take it for a longer time than your doctor ordered.


Sometimes maprotiline must be taken for up to two or three weeks before you begin to feel better. Your doctor should check your progress at regular visits.


Dosing


The dose of maprotiline 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 maprotiline. 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 depression:
      • Adults—At first, 25 milligrams (mg) taken one to three times a day. Your doctor may increase your dose as needed. However, the dose is usually not more than 150 mg a day, unless you are in the hospital. Some hospitalized patients may need higher doses.

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



Missed Dose


If you miss a dose of maprotiline, 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.


For once daily dosing at bedtime: Do not take the missed dose in the morning since it may cause disturbing side effects during waking hours. Instead, check with your doctor.


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 maprotiline


It is very important that your doctor check your progress at regular visits. This will allow your dosage to be changed if necessary and will help to reduce side effects.


maprotiline will add to the effects of alcohol and other CNS depressants (medicines that slow down the nervous system, possibly causing drowsiness). Some examples of CNS depressants are antihistamines or medicine for hay fever, other allergies, or colds; sedatives, tranquilizers, or sleeping medicine; prescription pain medicine or narcotics; barbiturates; medicine for seizures; or anesthetics, including some dental anesthetics. Check with your doctor before taking any of the above while you are using maprotiline .


Maprotiline may cause some people to be agitated, irritable or display other abnormal behaviors. It may also cause some people to have suicidal thoughts and tendencies or to become more depressed. If you or your caregiver notice any of these adverse effects, tell your doctor right away.


maprotiline may cause blurred vision, especially during the first few weeks of treatment. It may also cause some people to become drowsy or less alert than they are normally. If these effects occur, do not drive, use machines, or do anything else that could be dangerous if you are not alert or able to see well.


Dizziness, lightheadedness, or fainting may occur, especially when you get up from a lying or sitting position. Getting up slowly may help. If this problem continues or gets worse, check with your doctor.


Maprotiline may cause dryness of the mouth. For temporary relief, use sugarless gum or candy, melt bits of ice in your mouth, or use a saliva substitute. However, if your mouth continues to feel dry for more than 2 weeks, check with your medical doctor or dentist. Continuing dryness of the mouth may increase the chance of dental disease, including tooth decay, gum disease, and fungus infections.


Before having any kind of surgery, dental treatment, or emergency treatment, tell the medical doctor or dentist in charge that you are using maprotiline. Taking maprotiline together with medicines that are used during surgery or dental or emergency treatments may increase the CNS depressant effects.


Do not stop taking maprotiline without first checking with your doctor. Your doctor may want you to reduce gradually the amount you are taking before stopping completely. This will allow your body to adjust properly and will reduce the possibility of unwanted effects.


maprotiline 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:


More common
  • Skin rash, redness, swelling, or itching

Less common
  • Constipation (severe)

  • nausea or vomiting

  • shakiness or trembling

  • seizures (convulsions)

  • unusual excitement

  • weight loss

Rare
  • Breast enlargement—in males and females

  • confusion (especially in the elderly)

  • difficulty in urinating

  • fainting

  • hallucinations (seeing, hearing, or feeling things that are not there)

  • inappropriate secretion of milk—in females

  • irregular heartbeat (pounding, racing, skipping)

  • sore throat and fever

  • swelling of testicles

  • yellow eyes or skin

Symptoms of overdose
  • Convulsions (seizures)

  • dizziness (severe)

  • drowsiness (severe)

  • fast or irregular heartbeat

  • fever

  • muscle stiffness or weakness (severe)

  • restlessness or agitation

  • trouble in breathing

  • 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
  • Blurred vision

  • decreased sexual ability

  • dizziness or lightheadedness (especially in the elderly)

  • drowsiness

  • dryness of mouth

  • headache

  • increased or decreased sexual drive

  • tiredness or weakness

Less common
  • Constipation (mild)

  • diarrhea

  • heartburn

  • increased appetite and weight gain

  • increased sensitivity of skin to sunlight

  • increased sweating

  • trouble in sleeping

  • weight loss

After you stop using maprotiline, it may still produce some side effects that need attention. During this period of time, check with your doctor immediately if you notice the following side effects:


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: maprotiline side effects (in more detail)



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


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


More maprotiline resources


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


  • maprotiline Concise Consumer Information (Cerner Multum)

  • Maprotiline Prescribing Information (FDA)

  • Maprotiline MedFacts Consumer Leaflet (Wolters Kluwer)

  • Ludiomil Prescribing Information (FDA)

  • Maprotiline Hydrochloride Monograph (AHFS DI)



Compare maprotiline with other medications


  • Depression
  • Panic Disorder

Monday, 11 June 2012

Ircon



Pronunciation: EYE-urn
Generic Name: Iron
Brand Name: Examples include FeoSol and Ircon


Ircon is used for:

Supplementing iron in the diet and treating or preventing anemia (low red blood cell levels) due to low iron levels. It may also be used for other conditions as determined by your doctor.


Ircon is a mineral. It works by helping the body to make hemoglobin, which is found in red blood cells. Hemoglobin allows red blood cells to carry oxygen throughout the body, which helps to reduce the effects of anemia.


Do NOT use Ircon if:


  • you are allergic to any ingredient in Ircon

  • you have high levels of iron in the blood

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



Before using Ircon:


Some medical conditions may interact with Ircon. 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 colon problems, Crohn disease, or a peptic ulcer

  • if you have anemia not caused by iron deficiency, porphyria cutanea tarda, liver or kidney problems, thalassemia, or a history of alcohol abuse, or you have had multiple blood transfusions

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


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


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


  • Ircon is absorbed better on an empty stomach, but may be taken with food if it upsets your stomach.

  • Do not take antacids within 1 hour before or 2 hours after taking Ircon.

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

  • Do not lie down for 30 minutes after taking Ircon.

  • If you miss a dose of Ircon, 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 Ircon.



Important safety information:


  • Do not take large doses of vitamins (megadoses or megavitamin therapy) unless otherwise instructed by your doctor.

  • Accidental overdose of iron-containing products is a leading cause of fatal poisoning in children younger than 6 years of age. In case of accidental overdose, call a doctor or poison control center immediately.

  • Some of these products contain sulfites, which can cause allergic reactions in certain individuals (eg, asthma patients). If you have previously had allergic reactions to sulfites, contact your pharmacist to determine if the product you are taking contains sulfites.

  • Some of these products may contain tartrazine dye (FD&C Yellow No. 5), which can cause allergic reactions in certain patients. If you have previously had an allergic reaction to tartrazine, contact your pharmacist to determine if the medicine you are taking contains tartrazine.

  • Ircon may cause incorrect test results with kits used to check for blood in the stool or blood cholesterol. Check with your doctor if you are using either kind of test kit.

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

  • PREGNANCY and BREAST-FEEDING: If you become pregnant, discuss with your doctor the benefits and risks of using Ircon during pregnancy. If you are or will be breast-feeding while you are using Ircon, check with your doctor or pharmacist to discuss the risks to your baby.


Possible side effects of Ircon:


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



Constipation; diarrhea; nausea; stomach discomfort.



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); black, tarry stools; blood or streaks of blood in the stool; fever; sharp stomach pain; vomiting.



This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.


See also: Ircon 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. Accidental overdose of iron-containing products is a leading cause of fatal poisoning in children younger than 6 years of age. In case of accidental overdose, call a doctor or poison control center immediately. Symptoms may include loss of consciousness; nausea; seizures; stomach pain; tarry stools; tiredness; vomiting; weak, fast heartbeat.


Proper storage of Ircon:

Store Ircon at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat, moisture, and light. Keep Ircon out of the reach of children and away from pets.


General information:


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

  • Ircon 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 Ircon. 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 Ircon resources


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


  • Ircon Concise Consumer Information (Cerner Multum)

  • Femiron Advanced Consumer (Micromedex) - Includes Dosage Information



Compare Ircon with other medications


  • Anemia Associated with Chronic Renal Failure
  • Iron Deficiency Anemia
  • Vitamin/Mineral Supplementation and Deficiency
  • Vitamin/Mineral Supplementation during Pregnancy/Lactation

Saturday, 9 June 2012

Ipran




Ipran may be available in the countries listed below.


Ingredient matches for Ipran



Escitalopram

Escitalopram is reported as an ingredient of Ipran in the following countries:


  • Chile

  • Ecuador

International Drug Name Search