Saturday, 28 July 2012

abarelix


Generic Name: abarelix (a BAR eh lix)

Brand Names: Plenaxis


What is abarelix?

Abarelix reduces the amount of testosterone produced in the body.


Abarelix is used in the palliative treatment of advanced prostate cancer.


Abarelix may also be used for purposes other than those listed in this medication guide.


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


In some cases, the use of abarelix has resulted in serious allergic reactions. An allergic reaction may occur after any injection of the medication, including, but not limited to the first dose. Patients should be observed in the doctor's office for at least 30 minutes following each dose so that immediate treatment of an allergic reaction can be obtained if needed.

Treatment with abarelix may become less effective over time in some patients. Monitoring blood levels of testosterone will be done on a regular basis with blood tests to monitor the effectiveness of the medication.


Abarelix is not intended for use by women. Abarelix is in the FDA pregnancy category X. This means that abarelix will cause birth defects in an unborn baby. Do not use this medication if you are pregnant or if you could become pregnant during treatment.

What should I discuss with my healthcare provider before using abarelix?


Before using abarelix, tell your doctor if you



  • have irregular heartbeats;



  • have liver problems;


  • have osteoporosis; or




  • weigh more than 225 pounds.



You may not be able to use abarelix, or you may require a dosage adjustment or special monitoring during treatment.


Abarelix is not intended for use by women. Abarelix is in the FDA pregnancy category X. This means that abarelix will cause birth defects in an unborn baby. Do not use this medication if you are pregnant or if you could become pregnant during treatment. Abarelix is not intended for use by women. It is not known whether abarelix passes into breast milk. Do not use this medication without first talking to your doctor if you are breast-feeding a baby.

How should I use abarelix?


Abarelix must be administered by a qualified healthcare provider.


Abarelix is administered as an injection into the muscle.


In some cases, the use of abarelix has resulted in serious allergic reactions. An allergic reaction may occur after any injection of the medication, including, but not limited to the first dose. Patients should be observed in the doctor's office for at least 30 minutes following each dose so that immediate treatment of an allergic reaction can be obtained if needed.

Treatment with abarelix may become less effective over time in some patients. Monitoring blood levels of testosterone will be done on a regular basis with blood tests to monitor the effectiveness of the medication.


It is important to use abarelix regularly to get the most benefit.


Abarelix vials for injection should be stored at room temperature away from moisture and heat.


What happens if I miss a dose?


Contact your doctor if you miss a dose of abarelix.


What happens if I overdose?


An overdose of abarelix is unlikely to occur. If you do suspect that an overdose has occurred, contact your doctor, hospital emergency room, or poison control center for advice.


What should I avoid while using abarelix?


There are no restrictions on food, beverages, or activities while using abarelix. Follow any special instructions given by your doctor.


Abarelix side effects


In some cases, the use of abarelix has resulted in serious allergic reactions. An allergic reaction may occur after any injection of the medication, including, but not limited to the first dose. Patients should be observed in the doctor's office for at least 30 minutes following each dose so that immediate treatment of an allergic reaction can be obtained if needed.

Other, less serious side effects may be more likely to occur. Talk to your doctor if you experience



  • hot flashes;




  • sleep disturbances;




  • breast enlargement or pain;




  • diarrhea or constipation;




  • swelling;




  • nausea;




  • dizziness;




  • headache;




  • fatigue; or




  • changes with or difficulty urinating.



Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome.


Abarelix Dosing Information


Usual Adult Dose for Prostate Cancer:

100 mg administered intramuscularly to the buttock on day 1, 15, 29 (week 4) and every 4 weeks thereafter.


What other drugs will affect abarelix?


It is not known whether abarelix will interact with other medicines. Talk to your doctor and pharmacist before taking any prescription or over-the-counter medicines, including herbal products during treatment with abarelix.



More abarelix resources


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


  • abarelix Intramuscular, Injection Advanced Consumer (Micromedex) - Includes Dosage Information

  • Abarelix Monograph (AHFS DI)

  • Abarelix MedFacts Consumer Leaflet (Wolters Kluwer)

  • Abarelix Professional Patient Advice (Wolters Kluwer)

  • Plenaxis Consumer Overview



Compare abarelix with other medications


  • Prostate Cancer


Where can I get more information?


  • Your pharmacist has additional information about abarelix written for health professionals that you may read.

What does my medication look like?


Abarelix is available with a prescription under the brand name Plenaxis as an injection. Other brand or generic formulations may also be available. Ask your pharmacist any questions you have about this medication, especially if it is new to you.


See also: abarelix side effects (in more detail)


Celluvisc 1.0% w / v, Eye drops, solution






Celluvisc



1.0 % w/v Eye drops, solution, unit dose


Carmellose sodium



Read all of this leaflet carefully because it contains important information for you.


This medicine is available without prescription. However, you still need to use Celluvisc carefully to get the best results from it.


  • Keep this leaflet. You may need to read it again.

  • Ask your pharmacist if you need more information or advice.

  • You must contact a doctor if your symptoms worsen or do not improve.

  • If any of the side effects gets serious, or if you notice any side effect not listed in this leaflet, please tell your doctor or pharmacist.




In this leaflet:


  • 1. What Celluvisc is and what it is used for

  • 2. Before you use Celluvisc

  • 3. How to use Celluvisc

  • 4. Possible side effects

  • 5. How to store Celluvisc

  • 6. Further information




What Celluvisc Is And What It Is Used For



Celluvisc is a tear substitute and contains the lubricant called carmellose sodium. It is used for the treatment of the symptoms of dry eye (such as soreness, burning, irritation or dryness).




Before You Use Celluvisc



Do not use Celluvisc


  • If you are allergic (hypersensitive) to carmellose sodium or any of the other ingredients of Celluvisc (see section 6 for a full list of ingredients).



Take special care with Celluvisc


  • If you wear contact lenses, these should be removed before using Celluvisc. The lenses can be put back again 15 minutes after you have applied your drops.



Using other medicines


Please tell your doctor or pharmacist if you are taking or have recently taken any other medicines, including medicines obtained without a prescription.


If you are using other eye drops, leave at least 15 minutes before putting in Celluvisc.




Pregnancy and breast-feeding



Celluvisc can be used during pregnancy and breast-feeding.




Driving and using machines



Celluvisc may cause short-lasting blurring of vision typically lasting 1 – 15 minutes. If you do experience temporary blurring, do not drive or use machines until your sight is clear.





How To Use Celluvisc



Celluvisc is for ocular use (applied on the eye).


Follow these instructions unless the pharmacist or your doctor gave you different advice.


The usual dose is 1-2 drops of Celluvisc in the affected eyes as needed.


Make sure that the single-dose container is intact before use. The solution should be used immediately after opening. To avoid contamination, do not let the open-end of the single-dose container touch your eye or anything else. Wash your hands before use.



  • 1. Tear one single-dose container from the strip.

  • 2. Hold the single-dose container upright (with the cap uppermost) and twist off the cap.

  • 3. Gently pull down the lower eyelid to form a pocket. Turn the single-dose container upside down and squeeze it to release one drop into each eye. Blink your eyes a few times.

Do not re-use the single-dose container even if there is some solution left.


If irritation, pain, redness or changes in vision occur or if you feel your condition is getting worse, stop taking this medicine and consult your doctor or pharmacist.



If you use more Celluvisc than you should


It will not cause you any harm. If you are worried, talk to your doctor or pharmacist.




If you forget to use Celluvisc


Apply your next dose as required or at the normal time as directed by your pharmacist or doctor. Do not take a double dose to make up for forgotten individual doses.



If you have any further questions on the use of this product, ask your doctor or pharmacist.




Possible Side Effects


Like all medicines, Celluvisc can cause side effects, although not everybody gets them.



The following side affects are known to occur, but the number of people likely to be affected is unknown:


  • Eye irritation, burning or stinging sensation,

  • Blurring of vision,

  • Increase in tear production (also known as tearing).


If any of the side effects gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.




How To Store Celluvisc


Keep out of the reach and sight of children.


Do not use Celluvisc after the expiry date which is stated on the single-dose container tab and the carton after EXP:. The expiry date refers to the last day of that month.


Do not store above 25°C.


Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help to protect the environment.




Further Information



What Celluvisc contains


  • The active substance is carmellose sodium 10 mg/ml.

  • The other ingredients are sodium chloride, sodium lactate, potassium chloride, calcium chloride and purified water.

The Ingredients in Celluvisc were designed to match your natural tear composition.




What Celluvisc looks like and contents of the pack



Celluvisc is an eye drop solution. It is presented as a clear, colourless to pale yellow solution in a small see-through (bubble-like) casing (known as a ‘single-dose container’). The single-dose container has a twist-off cap. Each single-dose container contains 0.4 ml of solution.


Each pack contains 5, 10, 20, 30, 40, 60 or 90 single-dose containers. Not all pack sizes may be marketed.




Marketing Authorisation Holder and Manufacturer



Allergan Pharmaceuticals Ireland

Westport

Co. Mayo

Ireland



For any information about this medicine, please contact the local representative of the Marketing Authorisation Holder.



Allergan Ltd

The Parkway

Marlow

Bucks

SL7 1YL

United Kingdom

Tel:+44 (0)1628 494026

e-mail:
uk_medinfo@allergan.com



This medicinal product is authorised in the Member States of the EEA under the following names:



Denmark : Celluvisc


Finland : Celluvisc 1.0% Silmätipat, liuos


Germany : Celluvisc 1% Augentropfen


Greece : Celluvisc 1.0% w/v Οφθαλμικές σταγόνες, διάλυμα


Ireland : Celluvisc 1.0% w/v Eye drops, solution, unit dose


Portugal : Celluvisc, colírio, solução a 1,0%.


Spain : Viscofresh 10 mg/ml Colirio en solución


UK : Celluvisc 1.0% w/v Eye drops, solution, unit dose





This leaflet was last approved in March 2008.



To listen to or request a copy of this leaflet in Braille, large print or audio please call, free of charge: 0800 198 5000 (UK only).



Please be ready to give the following information: Carmellose sodium 1.0% reference number PL 05179/0001.



This is a service provided by the Royal National Institute of Blind People.


© 2008 Allergan, Inc., Irvine CA 92612


Marks owned by Allergan, Inc.





Thursday, 26 July 2012

Proventil HFA


Generic Name: albuterol inhalation (al BYOO ter all)

Brand Names: Accuneb, ProAir HFA, Proventil, Proventil HFA, Ventolin HFA


What is Proventil HFA (albuterol inhalation)?

Albuterol is a bronchodilator that relaxes muscles in the airways and increases air flow to the lungs.


Albuterol inhalation is used to treat or prevent bronchospasm in people with reversible obstructive airway disease. Albuterol is also used to prevent exercise-induced bronchospasm.


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


What is the most important information I should know about Proventil HFA (albuterol inhalation)?


It is important to keep this medication on hand at all times. Get your prescription refilled before you run out of medicine completely. Keep using all of your other medications as prescribed by your doctor.


Call your doctor right away if you feel that this medicine is not working as well as usual, or if it makes your condition worse. If it seems like you need to use more of any of your medications in a 24-hour period, talk with your doctor.


Seek emergency medical attention if you think you have used too much of this medicine. An overdose of albuterol can be fatal. Extreme heat can cause the medicine canister to burst. Do not store your inhaler in your car on hot days. Do not throw an empty canister into open flame.

What should I discuss with my healthcare provider before using Proventil HFA (albuterol inhalation)?


You should not use this medication if you are allergic to albuterol.

If you have certain conditions, you may need a dose adjustment or special tests to safely use this medication. Before using albuterol, tell your doctor if you have:



  • heart disease, high blood pressure, or congestive heart failure;




  • a heart rhythm disorder;




  • a seizure disorder such as epilepsy;




  • diabetes; or




  • overactive thyroid.



If you have any of these conditions, you may not be able to use albuterol, or you may need a dose adjustment or special tests during treatment.


FDA pregnancy category C. This medication may be harmful to an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant during treatment. It is not known whether albuterol passes into breast milk or if it could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.

How should I use Proventil HFA (albuterol inhalation)?


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


Albuterol may increase the risk of asthma-related death. Use only the prescribed dose of this medicine and follow all patient instructions for safe use. Talk with your doctor about your individual risks and benefits of using albuterol.

When using the inhaler device for the first time, prime it by spraying 4 test sprays into the air, away from your face. Shake well before priming. Also prime the inhaler if you have not used it for 2 weeks or longer, or if you have dropped the inhaler.


The instructions below are for standard use of the inhaler and nebulizer devices. Your doctor may want you to use your device differently. Use only the inhaler device provided with your medicine or you may not get the correct dose.

To use the inhaler:


  • Shake the canister well just before each spray.

  • Uncap the mouthpiece of the inhaler. Breathe out fully. Put the mouthpiece into your mouth and close your lips. Breathe in slowly while pushing down on the canister. Hold your breath for 10 seconds, then breathe out slowly.


  • If you use more than one inhalation at a time, wait at least 1 minute before using the second inhalation and shake the inhaler again.




  • Keep your inhaler clean and dry, and store it with the cap on the mouthpiece. Clean your inhaler once a week by removing the canister and placing the mouthpiece under warm running water for at least 30 seconds. Shake out the excess water and allow the parts to air dry completely before putting the inhaler back together.



To use the solution with a nebulizer:



  • Measure the correct amount of medicine using the dropper provided, or use the proper number of ampules. Place the liquid into the medication chamber of the nebulizer.




  • Attach the mouthpiece or face mask to the drug chamber. Then, attach the drug chamber to the compressor. Sit upright and place the mouthpiece into your mouth, or cover your nose and mouth with the face mask. Breathe slowly and evenly until you have inhaled all of the medicine (usually 5 to 15 minutes). The treatment is complete when the drug chamber is empty.




  • Clean the nebulizer after each use. Follow the cleaning directions that came with your nebulizer.



Call your doctor right away if you feel that this medicine is not working as well as usual, or if it makes your condition worse. If it seems like you need to use more of any of your medications in a 24-hour period, talk with your doctor.


It is important to keep this medication on hand at all times. Get your prescription refilled before you run out of medicine completely. Keep using all of your other medications as prescribed by your doctor.


Store this medication at room temperature away from moisture and heat. Extreme heat can cause the medicine canister to burst. Do not store it in your car on hot days. Do not throw an empty canister into open flame.

What happens if I miss a dose?


Use the medication as soon as you remember. If it is almost time for the next dose, skip the missed dose and use the medicine at the next regularly scheduled time. Do not use 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 albuterol can be fatal. Overdose symptoms may include nervousness, headache, tremor, dry mouth, chest pain or heavy feeling, rapid or uneven heart rate, pain spreading to the arm or shoulder, nausea, sweating, dizziness, seizure (convulsions), feeling light-headed or fainting.

What should I avoid while using Proventil HFA (albuterol inhalation)?


Avoid getting this medication in your eyes. If this does happen, rinse the eyes with water and seek medical attention.

Proventil HFA (albuterol inhalation) side effects


Stop using this medication and 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. Call your doctor at once if you have a serious side effect such as:

  • bronchospasm (wheezing, chest tightness, trouble breathing), especially after starting a new canister of this medicine;




  • chest pain and fast, pounding, or uneven heart beats;




  • tremor, nervousness;




  • low potassium (confusion, uneven heart rate, extreme thirst, increased urination, leg discomfort, muscle weakness or limp feeling); or




  • dangerously high blood pressure (severe headache, blurred vision, buzzing in your ears, anxiety, confusion, chest pain, shortness of breath, uneven heartbeats, seizure).



Less serious side effects may include:



  • headache, dizziness, nervousness;




  • sleep problems (insomnia);




  • cough, hoarseness, sore throat, runny or stuffy nose;




  • dry mouth and throat;




  • muscle pain; or




  • diarrhea.



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 Proventil HFA (albuterol inhalation)?


Before using this medication, tell your doctor if you are taking any of the following medicines:



  • a diuretic (water pill);



  • digoxin (digitalis, Lanoxin);

  • a beta-blocker such as atenolol (Tenormin), metoprolol (Lopressor), propranolol (Inderal), and others;


  • an antidepressant such as amitriptyline (Elavil, Etrafon), doxepin (Sinequan), imipramine (Janimine, Tofranil), nortriptyline (Pamelor), and others;




  • an MAO inhibitor such as isocarboxazid (Marplan), phenelzine (Nardil), rasagiline (Azilect), selegiline (Eldepryl, Emsam), or tranylcypromine (Parnate); or




  • other bronchodilators such as levalbuterol (Xopenex), bitolterol (Tornalate), pirbuterol (Maxair), terbutaline (Brethine, Bricanyl), salmeterol (Serevent), isoetherine (Bronkometer), metaproterenol (Alupent, Metaprel), or isoproterenol (Isuprel Mistometer).



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



More Proventil HFA resources


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


  • Proventil HFA Advanced Consumer (Micromedex) - Includes Dosage Information

  • Proventil HFA Aerosol MedFacts Consumer Leaflet (Wolters Kluwer)

  • Proventil HFA Prescribing Information (FDA)

  • Albuterol Prescribing Information (FDA)

  • albuterol Advanced Consumer (Micromedex) - Includes Dosage Information

  • Albuterol Monograph (AHFS DI)

  • Albuterol Professional Patient Advice (Wolters Kluwer)

  • Albuterol MedFacts Consumer Leaflet (Wolters Kluwer)

  • AccuNeb Solution MedFacts Consumer Leaflet (Wolters Kluwer)

  • Accuneb Prescribing Information (FDA)

  • Airet Solution MedFacts Consumer Leaflet (Wolters Kluwer)

  • ProAir HFA Prescribing Information (FDA)

  • ProAir HFA Aerosol MedFacts Consumer Leaflet (Wolters Kluwer)

  • Proventil Aerosol MedFacts Consumer Leaflet (Wolters Kluwer)

  • Proventil Consumer Overview

  • Proventil Repetabs Controlled-Release Tablets MedFacts Consumer Leaflet (Wolters Kluwer)

  • Ventolin Consumer Overview

  • Ventolin Prescribing Information (FDA)

  • Vospire ER Extended-Release Tablets MedFacts Consumer Leaflet (Wolters Kluwer)



Compare Proventil HFA with other medications


  • Asthma, acute
  • Asthma, Maintenance
  • Bronchospasm Prophylaxis
  • COPD, Acute
  • COPD, Maintenance


Where can I get more information?


  • Your pharmacist can provide more information about albuterol inhalation.

See also: Proventil HFA side effects (in more detail)


Wednesday, 25 July 2012

Allerest Headache Strength


Generic Name: acetaminophen, chlorpheniramine, and pseudoephedrine (a seet a MIN oh fen, klor fen IR a meen, soo doe e FED rin)

Brand Names: Alka-Seltzer Plus Cold Liquigel, Allerest Headache Strength, Allerest Sinus, Cold Medicine Plus, Comtrex Allergy Sinus, Comtrex Allergy Sinus Maximum Strength, Comtrex Allergy Sinus Night and Day, Kolephrin, Sinarest, Sinutab Ex-Strength, Theraflu Cold & Sore Throat (pseudoephedrine), Theraflu Flu & Sore Throat (pseudoephedrine), Theraflu Maximum Strength


What is Allerest Headache Strength (acetaminophen, chlorpheniramine, and pseudoephedrine)?

Acetaminophen is a pain reliever and fever reducer.


Chlorpheniramine is an antihistamine that reduces the natural chemical histamine in the body. Histamine can produce symptoms of sneezing, itching, watery eyes, and runny nose.


Pseudoephedrine is a decongestant that shrinks blood vessels in the nasal passages. Dilated blood vessels can cause nasal congestion (stuffy nose).


The combination of acetaminophen, chlorpheniramine, and pseudoephedrine is used to treat headache, fever, body aches, runny or stuffy nose, sneezing, itching, watery eyes, and sinus congestion caused by allergies, the common cold, or the flu.


Acetaminophen, chlorpheniramine, and pseudoephedrine may also be used for purposes not listed in this medication guide.


What is the most important information I should know about Allerest Headache Strength (acetaminophen, chlorpheniramine, and pseudoephedrine)?


Do not take more of this medication than is recommended. An overdose of acetaminophen can damage your liver or cause death. Do not take this medication without a doctor's advice if you have ever had alcoholic liver disease (cirrhosis) or if you drink more than 3 alcoholic beverages per day. You should not use this medicine if you have severe constipation, a blockage in your stomach or intestines, or if you are unable to urinate. Do not use this medicine if you have untreated or uncontrolled diseases such as glaucoma, asthma or COPD, high blood pressure, heart disease, coronary artery disease, or overactive thyroid. Avoid drinking alcohol. It may increase your risk of liver damage while taking acetaminophen and can increase certain side effects of chlorpheniramine. Do not use this medicine if you have used an MAO inhibitor such as furazolidone (Furoxone), isocarboxazid (Marplan), phenelzine (Nardil), rasagiline (Azilect), selegiline (Eldepryl, Emsam, Zelapar), or tranylcypromine (Parnate) in the last 14 days. A dangerous drug interaction could occur, leading to serious side effects. Ask a doctor or pharmacist before using any other cold, allergy, pain, or sleep medication. Acetaminophen (sometimes abbreviated as APAP) is contained in many combination medicines. Taking certain products together can cause you to get too much acetaminophen which can lead to a fatal overdose.

What should I discuss with my healthcare provider before taking Allerest Headache Strength (acetaminophen, chlorpheniramine, and pseudoephedrine)?


You should not use this medicine if you have severe constipation, a blockage in your stomach or intestines, or if you are unable to urinate. Do not take this medication without a doctor's advice if you have ever had alcoholic liver disease (cirrhosis) or if you drink more than 3 alcoholic beverages per day. You may not be able to take medicine that contains acetaminophen. Do not use this medicine if you have untreated or uncontrolled diseases such as glaucoma, asthma or COPD, high blood pressure, heart disease, coronary artery disease, or overactive thyroid. Do not use this medicine if you have used an MAO inhibitor such as furazolidone (Furoxone), isocarboxazid (Marplan), phenelzine (Nardil), rasagiline (Azilect), selegiline (Eldepryl, Emsam, Zelapar), or tranylcypromine (Parnate) in the last 14 days. A dangerous drug interaction could occur, leading to serious side effects.

Ask a doctor or pharmacist if it is safe for you to take this medicine if you have:



  • liver disease, cirrhosis, or a history of alcoholism;




  • a blockage in your digestive tract (stomach or intestines);




  • diabetes;




  • kidney disease;




  • epilepsy or other seizure disorder;




  • cough with mucus, or cough caused by smoking, emphysema, or chronic bronchitis;




  • enlarged prostate or urination problems;




  • low blood pressure;




  • pheochromocytoma (an adrenal gland tumor); or




  • if you take potassium (Cytra, Epiklor, K-Lyte, K-Phos, Kaon, Klor-Con, Polycitra, Urocit-K).




It is not known whether acetaminophen, chlorpheniramine, and pseudoephedrine will harm an unborn baby. Do not use this medicine without your doctor's advice if you are pregnant. This medication may pass into breast milk and may harm a nursing baby. Antihistamines and decongestants may also slow breast milk production. Do not use this medicine without your doctor's advice if you are breast-feeding a baby.

How should I take Allerest Headache Strength (acetaminophen, chlorpheniramine, and pseudoephedrine)?


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. This medicine is usually taken only for a short time until your symptoms clear up.


Do not take more of this medication than is recommended. An overdose of acetaminophen can damage your liver or cause death.

Dissolve one packet of the powder in at least 4 ounces of water. Stir this mixture and drink all of it right away.


Do not give this medication to a child younger than 4 years old. Always ask a doctor before giving a cough or cold medicine to a child. Death can occur from the misuse of cough and cold medicines in very young children.

Do not take for longer than 7 days in a row. Stop taking the medicine and call your doctor if you still have a fever after 3 days of use, you still have pain after 7 days (or 5 days if treating a child), if your symptoms get worse, or if you have a skin rash, ongoing headache, or any redness or swelling.


If you need surgery or medical tests, tell the surgeon or doctor ahead of time if you have taken this medicine within the past few days. Store at room temperature away from moisture and heat. Do not allow liquid medicine to freeze.

What happens if I miss a dose?


Since this medicine is taken when needed, you may not be on a dosing schedule. If you are taking the medication regularly, 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 or call the Poison Help line at 1 800 222 1222. An overdose of acetaminophen can be fatal.

The first signs of an acetaminophen overdose include loss of appetite, nausea, vomiting, stomach pain, sweating, and confusion or weakness. Later symptoms may include pain in your upper stomach, dark urine, and yellowing of your skin or the whites of your eyes.


Overdose symptoms may also include severe forms of some of the side effects listed in this medication guide.


What should I avoid while taking Allerest Headache Strength (acetaminophen, chlorpheniramine, and pseudoephedrine)?


Ask a doctor or pharmacist before using any other cold, allergy, pain, or sleep medication. Acetaminophen (sometimes abbreviated as APAP) is contained in many combination medicines. Taking certain products together can cause you to get too much acetaminophen which can lead to a fatal overdose. Check the label to see if a medicine contains acetaminophen or APAP. Avoid drinking alcohol. It may increase your risk of liver damage while taking acetaminophen, and can increase certain side effects of chlorpheniramine. This medicine may cause blurred vision or impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert and able to see clearly.

Allerest Headache Strength (acetaminophen, chlorpheniramine, and pseudoephedrine) side effects


Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Stop using this medication and call your doctor at once if you have a serious side effect such as:

  • chest pain, rapid pulse, fast or uneven heart rate;




  • confusion, hallucinations, severe nervousness;




  • tremor, seizure (convulsions);




  • easy bruising or bleeding, unusual weakness;




  • urinating less than usual or not at all;




  • nausea, pain in your upper stomach, itching, loss of appetite, dark urine, clay-colored stools, jaundice (yellowing of your skin or eyes); or




  • dangerously high blood pressure (severe headache, blurred vision, buzzing in your ears, anxiety, chest pain, shortness of breath, uneven heartbeats, seizure).



Less serious side effects may include:



  • dizziness, drowsiness;




  • mild headache;




  • dry mouth, nose, or throat;




  • constipation;




  • blurred vision;




  • feeling nervous; or




  • sleep problems (insomnia);



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 Allerest Headache Strength (acetaminophen, chlorpheniramine, and pseudoephedrine)?


Ask a doctor or pharmacist before using this medicine if you regularly use other medicines that make you sleepy (such as narcotic pain medication, sedatives, sleeping pills, muscle relaxers, and medicine for seizures, depression or anxiety). They can add to sleepiness caused by chlorpheniramine.

Tell your doctor about all other medicines you use, especially:



  • leflunomide (Arava);




  • topiramate (Topamax);




  • zonisamide (Zonegran);




  • an antibiotic, antifungal medicine, sulfa drug, or tuberculosis medicine;




  • an antidepressant;




  • birth control pills or hormone replacement therapy;




  • bladder or urinary medications;




  • blood pressure medication;




  • a bronchodilator;




  • cancer medicine;




  • cholesterol-lowering medications such as Lipitor, Niaspan, Zocor, Vytorin, and others;




  • gout or arthritis medications (including gold injections);




  • HIV/AIDS medication;




  • medication for nausea and vomiting, stomach ulcers, or irritable bowel syndrome;




  • medicines to treat psychiatric disorders;




  • an NSAID such as Advil, Aleve, Arthrotec, Cataflam, Celebrex, Indocin, Motrin, Naprosyn, Treximet, Voltaren, others; or




  • seizure medication.



This list is not complete and other drugs may interact with acetaminophen, chlorpheniramine, and pseudoephedrine. 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 Allerest Headache Strength resources


  • Allerest Headache Strength Use in Pregnancy & Breastfeeding
  • Allerest Headache Strength Drug Interactions
  • 0 Reviews for Allerest Headache Strength - Add your own review/rating


  • Children's Tylenol Cold Chewable Tablets MedFacts Consumer Leaflet (Wolters Kluwer)



Compare Allerest Headache Strength with other medications


  • Cold Symptoms
  • Hay Fever


Where can I get more information?


  • Your pharmacist can provide more information about acetaminophen, chlorpheniramine, and pseudoephedrine.


Tuesday, 24 July 2012

Xylocaine-MPF


Generic Name: lidocaine injection (LYE doe kane)

Brand Names: Anestacaine, UAD Caine, Xylocaine HCl, Xylocaine-MPF


What is Xylocaine-MPF (lidocaine injection)?

Lidocaine is a local anesthetic (numbing medication). It works by blocking nerve signals in your body.


Lidocaine injection is used to numb an area of your body to help reduce pain or discomfort caused by invasive medical procedures such as surgery, needle punctures, or insertion of a catheter or breathing tube.


Lidocaine injection is also given in an epidural (spinal block) to reduce the discomfort of contractions during labor.


Lidocaine injection is sometimes used to treat irregular heart rhythms that may signal a possible heart attack.


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


What is the most important information I should know about Xylocaine-MPF (lidocaine injection)?


You should not receive this medication if you are allergic to lidocaine or any other type of numbing medicine.

Before you receive lidocaine injection, tell your doctor if you have liver or kidney disease, heart disease, coronary artery disease, circulation problems, or a history of malignant hyperthermia.


To treat irregular heart rhythms, your doctor may prescribe a LidoPen auto-injector. This is a prefilled automatic injection device to be used in an emergency. Keep the device with you at all times.


Your doctor will describe the signs and symptoms to watch for when deciding when it's time to use lidocaine injection at home. Never use the LidoPen auto-injector without first calling your doctor.

With the LidoPen auto-injector you will also receive a CardioBeeper to transmit your heart rate and rhythm to your doctor over a telephone. Read all provided instructions and practice using the CardioBeeper.


Lidocaine can cause side effects that may impair your thinking or reactions. Unless absolutely necessary, do not drive after using this medication

What should I discuss with my healthcare provider before receiving Xylocaine-MPF (lidocaine injection)?


You should not receive this medication if you are allergic to lidocaine or any other type of numbing medicine.

If you have any of these other conditions, you may need a dose adjustment or special tests to safely use lidocaine injection:


  • liver disease;

  • kidney disease;


  • heart disease;




  • coronary artery disease, circulation problems; or




  • a history of malignant hyperthermia.




FDA pregnancy category B. This medication is not expected to be harmful to an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant during treatment. It is not known whether lidocaine injection 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 lidocaine injection given?


Lidocaine is given as an injection through a needle placed into a vein or directly into the body area to be numbed. Your doctor, nurse, or other healthcare provider will give you this injection.


Your breathing, blood pressure, oxygen levels, and other vital signs will be watched closely while you are receiving lidocaine injection in a hospital setting.

To treat irregular heart rhythms, you may be shown how to use your medicine at home. Do not self-inject this medicine if you do not fully understand how to give the injection and properly dispose of needles and other items used in giving the medicine.


The LidoPen auto-injector is a prefilled automatic injection device to be used in an emergency. Keep the device with you at all times. Your doctor will describe the signs and symptoms to watch for when deciding when it's time to use the injection.


Never use the LidoPen auto-injector without first calling your doctor.

Do not use the auto-injector in or near a vein or into your buttocks. Inject the medication only in your upper thigh or upper arm.


With the LidoPen auto-injector you will also receive a CardioBeeper. This device is used to transmit your heart rate and rhythm to your doctor over a telephone. Read all provided instructions and practice using the CardioBeeper so you will be able to quickly use it in an emergency.


Store the LidoPen auto-injector at room temperature away from moisture and extreme hot or cold.

What happens if I miss a dose?


Since lidocaine injection is used only when needed, you are not likely to be on a dosing schedule.


Never use the LidoPen auto-injector without first calling your doctor.


What happens if I overdose?


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

Overdose symptoms may include drowsiness, confusion, nervousness, ringing in your ears, blurred vision, feeling hot or cold, numbness, muscle twitches, uneven heartbeats, seizure (convulsions), slowed breathing, or respiratory failure (breathing stops).


What should I avoid while receiving Xylocaine-MPF (lidocaine injection)?


Lidocaine can cause side effects that may impair your thinking or reactions. Unless absolutely necessary, do not drive after using this medication

Avoid eating or chewing within 1 hour after lidocaine injection is used to numb your mouth or throat. You may have trouble swallowing which could lead to choking. You may also accidentally bite the inside of your mouth if you are still numb an hour after treatment with lidocaine injection.


Xylocaine-MPF (lidocaine injection) 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. Tell your caregivers at once if you have any of these serious side effects:

  • feeling anxious, shaky, dizzy, restless, or depressed;




  • drowsiness, vomiting, ringing in your ears, blurred vision;




  • confusion, twitching, seizure (convulsions);




  • fast heart rate, rapid breathing, feeling hot or cold;




  • weak or shallow breathing, slow heart rate, weak pulse; or




  • feeling like you might pass out.



Less serious side effects include:



  • mild bruising, redness, itching, or swelling where the medication was injected;




  • mild dizziness;




  • nausea;




  • numbness in places where the medicine is accidentally applied.



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 Xylocaine-MPF (lidocaine injection)?


There may be other drugs that can interact with lidocaine injection. Tell your doctor about all the prescription and over-the-counter medications you use. This includes vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start using a new medication without telling your doctor.



More Xylocaine-MPF resources


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


  • Lidocaine Aerosol MedFacts Consumer Leaflet (Wolters Kluwer)

  • lidocaine Intradermal Advanced Consumer (Micromedex) - Includes Dosage Information

  • Lidocaine Prescribing Information (FDA)

  • Lidocaine Hydrochloride Monograph (AHFS DI)

  • Lidocaine Hydrochloride (Local Anesthetic) Monograph (AHFS DI)



Compare Xylocaine-MPF with other medications


  • Anesthesia
  • Arrhythmia
  • Ventricular Fibrillation
  • Ventricular Tachycardia


Where can I get more information?


  • Your doctor or pharmacist can provide more information about lidocaine injection.

See also: Xylocaine-MPF side effects (in more detail)


Monday, 23 July 2012

Je-Vax Nakayama


Generic Name: Japanese encephalitis virus vaccine (Nakayama) (JAP a NEEZ en CEF a LYE tis NA ka YA ma)

Brand Names: Je-Vax


What is Japanese encephalitis virus vaccine (Nakayama)?

Japanese encephalitis is a serious disease caused by a virus. It is the leading cause of viral encephalitis (inflammation of the brain) in Asia. Encephalitis is an infection of the membrane around the brain and spinal cord. This infection often causes only mild symptoms, but prolonged swelling of the brain can cause permanent brain damage or death.


Japanese encephalitis virus is carried and spread by mosquitos.


The Japanese encephalitis Nakayama vaccine is used to help prevent this disease in adults and children who are at least 12 months old.


This vaccine works by exposing you to a small dose of the virus, which causes the body to develop immunity to the disease. This vaccine will not treat an active infection that has already developed in the body.


This vaccine is recommended for people who plan to spend 30 days or longer in areas where Japanese encephalitis is known to exist, or where an epidemic has recently occurred. The vaccine should also be given to people who will spend any amount of time in rural areas where Japanese encephalitis is endemic, or those who are otherwise at high risk of coming into contact with the virus.


You should receive this vaccine and all booster shots at least 10 days prior to your arrival in an area where you may be exposed to the virus.


Not everyone who travels to Asia needs to receive a Japanese encephalitis vaccine. Follow your doctor instructions or the recommendations of the Centers for Disease Control and Prevention (CDC).

This vaccine is also recommended for people who work in a research laboratory and may be exposed to Japanese encephalitis virus through needle-stick accidents or inhalation of viral droplets in the air.


Like any vaccine, the Japanese encephalitis Nakayama vaccine may not provide protection from disease in every person.


What is the most important information I should know about this vaccine?


The Japanese encephalitis Nakayama vaccine is given in a series of 3 shots. The booster shots are usually given 7 days and 2 weeks to 1 month after the first shot. Your individual booster schedule may be different from these guidelines. Follow your doctor's instructions or the schedule recommended by the health department of the state you live in.


Japanese encephalitis Nakayama vaccine is for use in adults and children who are at least 12 months old.


This vaccine is recommended for people who plan to spend 30 days or longer in areas where Japanese encephalitis is known to exist, or where an epidemic has recently occurred. The vaccine should also be given to people who will spend any amount of time in rural areas where Japanese encephalitis is endemic, or those who are otherwise at high risk of coming into contact with the virus.


You should receive the vaccine and all booster doses at least 10 days prior to your arrival in an area where you may be exposed to the virus.


Not everyone who travels to Asia needs to receive a Japanese encephalitis vaccine. Follow your doctor instructions or the recommendations of the Centers for Disease Control and Prevention (CDC).

This vaccine is also recommended for people who work in a research laboratory and may be exposed to Japanese encephalitis virus through needle-stick accidents or inhalation of viral droplets in the air.


Becoming infected with Japanese encephalitis is much more dangerous to your health than receiving the vaccine to protect against it. Like any medicine, this vaccine can cause side effects, but the risk of serious side effects is extremely low.


What should I discuss with my healthcare provider before receiving this vaccine?


You should not receive this vaccine if you have ever had a life-threatening allergic reaction to a Japanese encephalitis vaccine, or if you are allergic to mouse proteins or a preservative called thimerosal. You should also not receive this vaccine if you have received cancer chemotherapy or radiation treatment in the past 3 months.

Before receiving this vaccine, tell the doctor if you are allergic to any foods or drugs, or if you have:



  • an allergy to insect (such as bee or wasp) stings;




  • a history of seizures;




  • a neurologic disorder or disease affecting the brain (or if this was a reaction to a previous vaccine); or




  • a weak immune system caused by disease, bone marrow transplant, or by using certain medicines or receiving cancer treatments.



You can still receive a vaccine if you have a cold or fever. In the case of a more severe illness with a fever or any type of infection, wait until you get better before receiving this vaccine.


Vaccines may be harmful to an unborn baby and generally should not be given to a pregnant woman. However, not vaccinating the mother could be more harmful to the baby if the mother becomes infected with a disease that this vaccine could prevent. Your doctor will decide whether you should receive this vaccine, especially if you have a high risk of infection with the Japanese encephalitis virus. Do not receive this vaccine without telling your doctor if you are breast-feeding a baby.

How is this vaccine given?


This vaccine is given as an injection (shot) under the skin. You will receive this injection in a doctor's office or other clinic setting.


The Japanese encephalitis Nakayama vaccine is given in a series of 3 shots. The booster shots are usually given 7 days and 2 weeks to 1 month after the first shot. Your individual booster schedule may be different from these guidelines. Follow your doctor's instructions or the schedule recommended by the health department of the state you live in.


Your care providers may want to watch you for signs of allergic reaction for at least 30 minutes after you receive this vaccine.


In addition to receiving the Japanese encephalitis vaccine, use protective clothing, insect repellents, and mosquito netting around your bed to further prevent mosquito bites that could infect you with the Japanese encephalitis virus.


For at least 10 days after receiving a Japanese encephalitis vaccine, be sure to stay in an area where you have access to medical care in case of a delayed allergic reaction.

Your doctor may recommend treating fever and pain with an aspirin-free pain reliever such as acetaminophen (Tylenol) or ibuprofen (Motrin, Advil, and others) when the shot is given and for the next 24 hours. Follow the label directions or your doctor's instructions about how much of this medicine to take.


It is especially important to prevent fever from occurring if you have a seizure disorder such as epilepsy.


What happens if I miss a dose?


Contact your doctor if you will miss a booster dose or if you get behind schedule. The next dose should be given as soon as possible. There is no need to start over.


Be sure you receive all recommended doses of this vaccine. If you do not receive the full series of vaccines, you may not be fully protected against the disease.


What happens if I overdose?


An overdose of this vaccine is unlikely to occur.


What should I avoid before or after receiving this vaccine?


Avoid drinking large amounts of alcohol for at least 48 hours after you receive a Japanese encephalitis vaccine.

This vaccine side effects


You should not receive a booster vaccine if you had a life-threatening allergic reaction after the first shot. Keep track of any and all side effects you have after receiving this vaccine. When you receive a booster dose, you will need to tell the doctor if the previous shots caused any side effects.

Becoming infected with Japanese encephalitis is much more dangerous to your health than receiving the vaccine to protect against it. Like any medicine, this vaccine can cause side effects, but the risk of serious side effects is extremely low.


Get emergency medical help if you have any of these signs of an allergic reaction (which may occur up to 17 days after you receive the shot): hives; difficulty breathing; swelling of your face, lips, tongue, or throat.

Call your doctor at once if you have any of these serious side effects:



  • feeling light-headed, fainting;




  • high fever;




  • behavior changes; or




  • seizures (black-out or convulsions).



Less serious side include:



  • redness, pain, or swelling where the shot was given;




  • low fever, chills, flu symptoms;




  • headache, tired feeling;




  • muscle pain;




  • nausea, vomiting, stomach pain; or




  • mild itching or skin rash.



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 Japanese encephalitis virus vaccine (Nakayama)?


Before receiving this vaccine, tell the doctor about all other vaccines you have recently received.

Also tell the doctor if you have recently received drugs or treatments that can weaken the immune system, including:



  • an oral, nasal, inhaled, or injectable steroid medicine;




  • medications to treat psoriasis, rheumatoid arthritis, or other autoimmune disorders, such as azathioprine (Imuran), efalizumab (Raptiva), etanercept (Enbrel), leflunomide (Arava), and others; or




  • medicines to treat or prevent organ transplant rejection, such as basiliximab (Simulect), cyclosporine (Sandimmune, Neoral, Gengraf), muromonab-CD3 (Orthoclone), mycophenolate mofetil (CellCept), sirolimus (Rapamune), or tacrolimus (Prograf).



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



More Je-Vax resources


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


Compare Je-Vax with other medications


  • Japanese Encephalitis Virus Prophylaxis


Where can I get more information?


  • Your doctor or pharmacist may have information about this vaccine written for health professionals that you may read. You may also find additional information from your local health department or the Centers for Disease Control and Prevention.

See also: Je-Vax side effects (in more detail)


pitavastatin


pi-tav-a-STAT-in


Commonly used brand name(s)

In the U.S.


  • Livalo

Available Dosage Forms:


  • Tablet

Pharmacologic Class: HMG-COA Reductase Inhibitor


Uses For pitavastatin


Pitavastatin is used together with a proper diet to treat high cholesterol levels and triglyceride (fats) levels in the blood. pitavastatin may help prevent medical problems caused by clogged blood vessels such as heart attacks and strokes.


Pitavastatin belongs to the group of medicines called HMG-CoA reductase inhibitors or "statins". It works to reduce the amount of cholesterol in the blood by blocking an enzyme that is needed to make cholesterol.


pitavastatin is available only with your doctor's prescription.


Before Using pitavastatin


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 pitavastatin, the following should be considered:


Allergies


Tell your doctor if you have ever had any unusual or allergic reaction to pitavastatin 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 pitavastatin 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 pitavastatin in the elderly. However, elderly patients are more likely to have kidney problems, which may require an adjustment in the dose for patients receiving pitavastatin.


Pregnancy








Pregnancy CategoryExplanation
All TrimestersXStudies in animals or pregnant women have demonstrated positive evidence of fetal abnormalities. This drug should not be used in women who are or may become pregnant because the risk clearly outweighs any possible benefit.

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 pitavastatin, 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 pitavastatin 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.


  • Cyclosporine

Using pitavastatin 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.


  • Erythromycin

  • Fenofibrate

  • Gemfibrozil

  • Niacin

  • Ritonavir

Using pitavastatin 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.


  • Rifampin

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


  • Alcohol abuse, or history of or

  • Dehydration or

  • Hypotension (low blood pressure) or

  • Hypothyroidism (underactive thyroid), not adequately treated or

  • Seizures, uncontrolled or

  • Sepsis (severe infection in the blood) or

  • Surgery, major and recent or

  • Trauma (injury), major and recent—Use with caution. May increase risks for more serious side effects.

  • Kidney disease, severe (including dialysis)—Use with caution. The effects may be increased because of slower removal of the medicine from the body.

  • Liver disease, active (including elevated liver enzymes)—Should not be used in patients with these conditions.

  • Muscle pain or tenderness, history of or

  • Muscle weakness, history of—Use with caution. May make these conditions worse.

Proper Use of pitavastatin


Take pitavastatin only as directed by your doctor. Do not use more of it, do not use it more often, and do not use it for a longer time than your doctor ordered.


Before prescribing medicine for your high cholesterol, your doctor will probably try to control it by changing your diet. The diet may be low in fats, sugars, or cholesterol. Carefully follow the diet your doctor gave you. The medicine will work better when it is used together with a modified diet and exercise.


Remember that pitavastatin will not cure your high cholesterol, but it does help control it. You must continue to take it as directed if you want to keep your cholesterol levels low.


You may take pitavastatin with or without food.


Dosing


The dose of pitavastatin 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 pitavastatin. 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 high cholesterol:
      • Adults—At first, 2 milligrams (mg) once a day. Your doctor may adjust your dose as needed. However, the dose is usually not more than 4 mg a day.

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



Missed Dose


If you miss a dose of pitavastatin, 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 pitavastatin


It is very important that your doctor check your progress at regular visits to make sure that pitavastatin is working properly. Blood tests may be needed to check for unwanted effects.


Using pitavastatin while you are pregnant 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.


Do not use cyclosporine (Gengraf®, Neoral®, Sandimmune®) while you are taking pitavastatin. Using these medicines together may cause serious side effects.


Stop using pitavastatin and call your doctor right away if you have unexplained muscle pain, tenderness, or weakness, especially if you also have unusual tiredness or a fever. These could be symptoms of a serious muscle problem called myopathy.


Stop using pitavastatin and check with your doctor right away if you have dark-colored urine, diarrhea, a fever, muscle cramps or spasms, muscle pain or stiffness, or feel very tired or weak. These could be symptoms of a serious muscle problem called rhabdomyolysis, which can cause kidney problems.


Do not use excessive amounts of alcohol while taking pitavastatin. This could cause side effects in the liver.


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.


pitavastatin Side Effects


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


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


Less common
  • Difficulty with moving

  • joint pain

  • muscle aching or cramping

  • muscle pains or stiffness

  • pain in the arms and legs

  • swollen joints

Incidence not known
  • Chills

  • cough

  • diarrhea

  • fever

  • general feeling of discomfort or illness

  • headache

  • loss of appetite

  • nausea

  • runny nose

  • shivering

  • sore throat

  • sweating

  • trouble with sleeping

  • unusual tiredness or weakness

  • 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:


Less common
  • Back pain

  • difficulty having a bowel movement (stool)

Incidence not known
  • Hives or welts

  • itching skin

  • rash

  • redness of the skin

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: pitavastatin 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 pitavastatin resources


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


  • Pitavastatin Professional Patient Advice (Wolters Kluwer)

  • Pitavastatin MedFacts Consumer Leaflet (Wolters Kluwer)

  • Livalo Prescribing Information (FDA)

  • Livalo Monograph (AHFS DI)

  • Livalo Consumer Overview



Compare pitavastatin with other medications


  • High Cholesterol

Friday, 20 July 2012

Qutenza Patch


Pronunciation: kap-SAY-sin
Generic Name: Capsaicin
Brand Name: Qutenza


Qutenza Patch is used for:

Treating a certain type of nerve pain caused by the shingles (postherpetic neuralgia). It may also be used for other conditions as determined by your doctor.


Qutenza Patch is a TRVP1 channel agonist. It works by decreasing certain pain receptors on some nerve endings.


Do NOT use Qutenza Patch if:


  • you are allergic to any ingredient in Qutenza Patch

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



Before using Qutenza Patch:


Some medical conditions may interact with Qutenza Patch. 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 broken or damaged skin at the application site

  • if you have a history of high blood pressure, other heart problems, or recent heart attack or stroke

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


Ask your health care provider if Qutenza Patch 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 Qutenza Patch:


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


  • Qutenza Patch is usually applied at your doctor's office, hospital, or clinic. If you will be using Qutenza Patch at home, a health care provider will teach you how to use it. Be sure you understand how to use Qutenza Patch. Follow the procedures you are taught when you use it. Contact your health care provider if you have any questions.

  • Do not remove the patch from the sealed pouch until right before use.

  • You may receive other medicine to treat pain that occurs during and after your treatment with Qutenza Patch. Discuss any questions or concerns with your doctor.

  • Do not touch the patch while it is on your skin. Burning or stinging may occur.

  • If you miss a dose of Qutenza Patch, contact your doctor right away.

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



Important safety information:


  • Do not use Qutenza Patch on the face or scalp. Do not get it in the eyes, nose, mouth, or genital area. If you get Qutenza Patch in any of these areas, rinse right away with cool water.

  • Do not inhale any of Qutenza Patch. It may cause shortness of breath, coughing, or sneezing. Tell your health care provider if any of these symptoms occur.

  • Do not get Qutenza Patch on skin that is not being treated. Tell your health care provider if Qutenza Patch comes into contact with skin that is not being treated.

  • The treated area may be sensitive to heat (eg, hot showers or baths, direct sunlight, strong exercise) for a few days after Qutenza Patch is applied.

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

  • Qutenza Patch should be used with extreme caution in CHILDREN younger than 18 years old; safety and effectiveness in these children have not been confirmed.

  • PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Qutenza Patch while you are pregnant. It is not known if Qutenza Patch is found in breast milk. Do not breast-feed on the day of treatment after you have received your treatment with Qutenza Patch.


Possible side effects of Qutenza Patch:


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 pain, redness, burning, or itching at the application site; mild sore throat; nausea.



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); blisters or swelling at the application site; severe or persistent dizziness or headache; severe or persistent pain, redness, burning, or itching at the application site; shortness of breath, coughing, or sneezing.



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: Qutenza 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 Qutenza Patch:

Store Qutenza Patch between 68 and 77 degrees F (20 and 25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Qutenza Patch out of the reach of children and away from pets.


General information:


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

  • Qutenza Patch 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 Qutenza Patch. 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 Qutenza resources


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


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Thursday, 19 July 2012

Morphine/Naltrexone Extended-Release Capsules


Pronunciation: MORE-feen/nal-TREX-ohn
Generic Name: Morphine/Naltrexone
Brand Name: Embeda

Morphine/Naltrexone Extended-Release Capsules are a narcotic pain reliever used for around-the-clock treatment of moderate or severe pain. It should not be used to treat occasional pain.


Morphine/Naltrexone Extended-Release Capsules should only be used by patients who have already been taking narcotic pain medicine and are tolerant to its effect. The use of Morphine/Naltrexone Extended-Release Capsules by people who are not used to taking narcotic pain medicine may cause severe and sometimes fatal breathing problems.


Swallow Morphine/Naltrexone Extended-Release Capsules whole. Do NOT crush, chew, or dissolve Morphine/Naltrexone Extended-Release Capsules; it may cause the release of too much medicine into the bloodstream, which could be fatal. Doing this may also release the naltrexone in Morphine/Naltrexone Extended-Release Capsules, which may cause withdrawal symptoms.


If you have trouble swallowing Morphine/Naltrexone Extended-Release Capsules whole, you may sprinkle the contents of the capsule on a small amount of applesauce and then swallow the mixture. Do NOT chew, crush, or dissolve the contents of the capsule before swallowing.


Do not drink alcoholic beverages or take any prescription or nonprescription medicines that contain alcohol at any time while you are taking Morphine/Naltrexone Extended-Release Capsules. Doing this may cause too much medicine to be absorbed too quickly and may cause severe or possibly fatal side effects.





Morphine/Naltrexone Extended-Release Capsules are used for:

Managing moderate to severe pain that continues around-the-clock and is expected to last for a long period of time. Morphine/Naltrexone Extended-Release Capsules are used in patients who have already been taking narcotic pain medicine and are tolerant to its effects.


Morphine/Naltrexone Extended-Release Capsules are a narcotic pain reliever. It works in the brain to dull pain. Morphine/Naltrexone Extended-Release Capsules also contains naltrexone, an opioid receptor antagonist, inside a special coating. If Morphine/Naltrexone Extended-Release Capsules are crushed or chewed, the naltrexone will be released and may cause withdrawal symptoms.


Do NOT use Morphine/Naltrexone Extended-Release Capsules if:


  • you are allergic to any ingredient in Morphine/Naltrexone Extended-Release Capsules

  • you have paralysis of the stomach or intestines

  • you have very slow or shallow breathing, severe asthma, hypercapnia (high levels of carbon dioxide in your blood), or you are having an asthma attack

  • you are taking sodium oxybate (GHB)

  • you are taking or have taken a monoamine oxidase inhibitor (MAOI) (eg, phenelzine) within the past 14 days

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



Before using Morphine/Naltrexone Extended-Release Capsules:


Some medical conditions may interact with Morphine/Naltrexone Extended-Release Capsules. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:


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

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

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

  • if you are allergic to other narcotic pain medicines (eg, codeine)

  • if you have diarrhea or constipation, are dehydrated, have low blood volume, or are in shock

  • if you have severe drowsiness or are very weak, very overweight, or in very poor health

  • if you have increased pressure in the head, a recent head injury, or an abnormal growth in the brain

  • if you have gallbladder problems, pancreas problems (eg, inflammation), bladder blockage or trouble urinating, enlarged prostate, stomach or bowel problems (eg, blockage, inflammation, severe diarrhea caused by antibiotic use), or have had recent stomach or bowel surgery

  • if you have a history of liver or kidney problems, heart problems (eg, cor pulmonale), low blood pressure, lung or breathing problems (eg, asthma, chronic obstructive pulmonary disease [COPD]), sleep apnea (trouble breathing when you sleep), thyroid problems (eg, underactive thyroid), adrenal gland problems (eg, Addison disease), or curvature of the spine (eg, scoliosis)

  • if you have a history of seizures, mental or mood problems (eg, hallucinations), suicidal thoughts or actions, alcohol or other substance abuse or dependence, or if you are currently experiencing alcohol withdrawal

  • if you are taking another medicine that contains naltrexone

  • if you will be having surgery, or if you have a gastric or nasogastric tube

Some MEDICINES MAY INTERACT with Morphine/Naltrexone Extended-Release Capsules. Tell your health care provider if you are taking any other medicines, especially any of the following:


  • Cimetidine, MAOIs (eg, phenelzine ), muscle relaxants (eg, cyclobenzaprine), other narcotic pain medicines (eg, oxycodone), phenothiazines (eg, chlorpromazine), or quinidine because the risk of severe side effects (eg, severe drowsiness, very slow or shallow breathing, confusion, seizures) may be increased

  • Anticholinergics (eg, scopolamine) because the risk of trouble urinating and severe constipation may be increased

  • Narcotic agonists/antagonists (eg, pentazocine) or rifampin because they may decrease Morphine/Naltrexone Extended-Release Capsules's effectiveness

  • Sodium oxybate (GHB) because the risk of its side effects may be increased by Morphine/Naltrexone Extended-Release Capsules

  • Diuretics (eg, furosemide, hydrochlorothiazide) or trovafloxacin because their effectiveness may be decreased by Morphine/Naltrexone Extended-Release Capsules

This may not be a complete list of all interactions that may occur. Ask your health care provider if Morphine/Naltrexone Extended-Release Capsules may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.


How to use Morphine/Naltrexone Extended-Release Capsules:


Use Morphine/Naltrexone Extended-Release Capsules as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • Morphine/Naltrexone Extended-Release Capsules comes with an extra patient information sheet called a Medication Guide. Read it carefully. Read it again each time you get Morphine/Naltrexone Extended-Release Capsules refilled.

  • Take Morphine/Naltrexone Extended-Release Capsules by mouth with or without food.

  • Swallow Morphine/Naltrexone Extended-Release Capsules whole. Do not dissolve, crush, or chew before swallowing.

  • If you cannot swallow the capsule whole, contact your doctor. You may be able to open the capsule and sprinkle the pellets over a tablespoonful of applesauce. If you do this, swallow the applesauce and pellet mixture right away, followed by a glass of water. Do not crush or chew the medicine before swallowing. Do not store the mixture for future use. Dispose of the empty capsule as directed by your doctor or pharmacist.

  • Take Morphine/Naltrexone Extended-Release Capsules on a regular schedule to get the most benefit from it.

  • Taking Morphine/Naltrexone Extended-Release Capsules at the same time each day will help you remember to take it.

  • Morphine/Naltrexone Extended-Release Capsules should not be used more often than every 12 hours.

  • Do not suddenly stop taking Morphine/Naltrexone Extended-Release Capsules. If you need to stop taking Morphine/Naltrexone Extended-Release Capsules, your dose may need to be slowly lowered in order to avoid withdrawal symptoms. Discuss any questions or concerns with your doctor.

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

Ask your health care provider any questions you may have about how to use Morphine/Naltrexone Extended-Release Capsules.



Important safety information:


  • Morphine/Naltrexone Extended-Release Capsules may cause dizziness or drowsiness. These effects may be worse if you take it with alcohol or certain medicines. Use Morphine/Naltrexone Extended-Release Capsules with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.

  • Check with your doctor before you use medicines that may cause drowsiness (eg, sleep aids, muscle relaxers) while you are using Morphine/Naltrexone Extended-Release Capsules; it may add to their effects. Ask your pharmacist if you have questions about which medicines may cause drowsiness.

  • Do not drink alcohol or take any prescription or nonprescription medicines that have alcohol in them while you are taking Morphine/Naltrexone Extended-Release Capsules. Ask your pharmacist if you have questions about whether any of your medicines have alcohol in them.

  • Morphine/Naltrexone Extended-Release Capsules may cause dizziness, lightheadedness, or fainting; alcohol, hot weather, exercise, or fever may increase these effects. To prevent them, sit up or stand slowly, especially in the morning. Sit or lie down at the first sign of any of these effects.

  • Constipation is a common side effect of Morphine/Naltrexone Extended-Release Capsules. Talk to your doctor about using laxatives or stool softeners to prevent or treat constipation while you use Morphine/Naltrexone Extended-Release Capsules.

  • Do not take more than the recommended dose or use more often than prescribed without checking with your doctor. If Morphine/Naltrexone Extended-Release Capsules stops working well, contact your doctor.

  • Tell your doctor or dentist that you take Morphine/Naltrexone Extended-Release Capsules before you receive any medical or dental care, emergency care, or surgery.

  • If you no longer need Morphine/Naltrexone Extended-Release Capsules, check with your doctor or pharmacist about how to properly dispose of unused capsules.

  • Use Morphine/Naltrexone Extended-Release Capsules with caution in the ELDERLY; they may be more sensitive to its effects.

  • Morphine/Naltrexone Extended-Release Capsules should be used with extreme caution in CHILDREN younger than 18 years old; safety and effectiveness in children have not been confirmed.

  • PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Morphine/Naltrexone Extended-Release Capsules while you are pregnant. Morphine/Naltrexone Extended-Release Capsules are found in breast milk. Do not breast-feed while taking Morphine/Naltrexone Extended-Release Capsules.

When used for long periods of time or at high doses, Morphine/Naltrexone Extended-Release Capsules may not work as well and may require higher doses to obtain the same effect as when originally taken. This is known as TOLERANCE. Talk with your doctor if Morphine/Naltrexone Extended-Release Capsules stops working well. Do not take more than prescribed.


Some people who use Morphine/Naltrexone Extended-Release Capsules for a long time may develop a need to continue taking it. People who take high doses are also at risk. This is known as DEPENDENCE or addiction. If you stop taking Morphine/Naltrexone Extended-Release Capsules suddenly, you may have WITHDRAWAL symptoms. These may include anxiety; diarrhea; fever, runny nose, or sneezing; goose bumps and abnormal skin sensations; nausea; vomiting; pain; rigid muscles; rapid heartbeat; seeing, hearing, or feeling things that are not there; shivering or tremors; sweating; and trouble sleeping.



Possible side effects of Morphine/Naltrexone Extended-Release Capsules:


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



Constipation; dizziness; drowsiness; dry mouth; headache; increased sweating; lightheadedness; mild itching; nausea; tiredness; 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); chest pain; confusion; fainting; hallucinations; mental or mood changes; numbness of an arm or leg; pounding in the chest; seizures; severe dizziness or drowsiness; shortness of breath; slow, shallow breathing; sudden, severe nausea, vomiting, or headache.



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: Morphine/Naltrexone side effects (in more detail)


If OVERDOSE is suspected:


Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include cold and clammy skin; convulsions; deep sleep; lightheadedness; limp muscles; loss of consciousness; low body temperature; pinpoint pupils; severe dizziness or drowsiness; shortness of breath; slow, shallow breathing; slowed heartbeat; wide pupils.


Proper storage of Morphine/Naltrexone Extended-Release Capsules:

Store Morphine/Naltrexone Extended-Release Capsules at 77 degrees F (25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Morphine/Naltrexone Extended-Release Capsules out of the reach of children and away from pets


General information:


  • If you have any questions about Morphine/Naltrexone Extended-Release Capsules, please talk with your doctor, pharmacist, or other health care provider.

  • Morphine/Naltrexone Extended-Release Capsules are to be used only by the patient for whom it is prescribed. Do not share it with other people.

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

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

This information is a summary only. It does not contain all information about Morphine/Naltrexone Extended-Release Capsules. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.



Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Morphine/Naltrexone resources


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


Compare Morphine/Naltrexone with other medications


  • Pain