Sunday, 12 August 2012

Symmetrel


Generic Name: amantadine (Oral route)

a-MAN-ta-deen

Commonly used brand name(s)

In the U.S.


  • Symmetrel

Available Dosage Forms:


  • Capsule, Liquid Filled

  • Solution

  • Tablet

  • Capsule

  • Syrup

Therapeutic Class: Antiparkinsonian


Pharmacologic Class: Anticholinergic


Chemical Class: Adamantane


Uses For Symmetrel


Amantadine is an antiviral medicine. It is used to prevent or treat certain influenza (flu) infections (type A). It may be given alone or along with flu shots. Amantadine will not work for colds, other types of flu, or other virus infections.


Amantadine is also an antidyskinetic medicine. It is used to treat Parkinson's disease, which is sometimes called paralysis agitans or shaking palsy. It may be given alone or with other medicines for Parkinson's disease. By improving muscle control and reducing stiffness, this medicine allows more normal movements of the body as the disease symptoms are reduced. Amantadine is also used to treat stiffness and shaking caused by certain medicines that are used to treat nervous, mental, and emotional conditions.


Amantadine 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, amantadine is used in certain patients with the following medical condition:


  • Unusual tiredness or weakness associated with multiple sclerosis

Before Using Symmetrel


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


Appropriate studies performed to date have not demonstrated pediatric-specific problems that would limit the usefulness of amantadine in children. Safety and efficacy have not been established in children younger than 1 year of age.


Geriatric


Appropriate studies performed to date have not demonstrated geriatric-specific problems that would limit the usefulness of amantadine in the elderly. However, elderly patients are more likely to have age-related kidney, liver, or heart disease which may require an adjustment in the dose for patients receiving amantadine.


Pregnancy








Pregnancy CategoryExplanation
All TrimestersCAnimal studies have shown an adverse effect and there are no adequate studies in pregnant women OR no animal studies have been conducted and there are no adequate studies in pregnant women.

Breast Feeding


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


Interactions with Medicines


Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. When you are taking this medicine, it is especially important that your healthcare professional know if you are taking any of the medicines listed below. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive.


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


  • Potassium

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.


  • Betel Nut

  • Bromperidol

  • Bupropion

  • Triamterene

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:


  • Congestive heart failure or

  • Eczema, recurrent, history of or

  • Epilepsy or seizures, history of or

  • Liver disease or

  • Low blood pressure (hypotension) or

  • Neuroleptic malignant syndrome (NMS), history of or

  • Peripheral edema (swelling of the hands, ankles, or feet) or

  • Psychosis (a mental disease), history of—Use with caution. May make these conditions worse.

  • Glaucoma, angle-closure, untreated (narrow-angle glaucoma)—Should not be used in patients with this condition.

  • Kidney disease—Use with caution. The effects of this medicine may be increased because of slower removal from the body.

Proper Use of Symmetrel


For patients taking amantadine to prevent or treat flu infections:


  • Talk to your doctor about the possibility of getting a flu shot if you have not had one yet.

  • This medicine is best taken before exposure, or as soon as possible after exposure, to people who have the flu.

  • To help keep yourself from getting the flu, keep taking this medicine for the full time of treatment. Or if you already have the flu, continue taking this medicine for the full time of treatment even if you begin to feel better after a few days. This will help to clear up your infection completely. If you stop taking this medicine too soon, your symptoms may return. This medicine should be taken for at least 2 days after all your flu symptoms have disappeared.

  • This medicine works best when there is a constant amount in the blood. To help keep the amount constant, do not miss any doses. Also, it is best to take the doses at evenly spaced times day and night. For example, if you are to take two doses a day, the doses should be spaced about 12 hours apart. If this interferes with your sleep or other daily activities, or if you need help in planning the best times to take your medicine, check with your doctor.

  • If you are using the oral liquid form of amantadine, use a specially marked measuring spoon or other device to measure each dose accurately. The average household teaspoon may not hold the right amount of liquid.

For patients taking amantadine for Parkinson's disease or movement problems caused by certain medicines used to treat nervous, mental, and emotional conditions:


  • Take this medicine exactly as directed by your doctor. Do not miss any doses and do not take more medicine than your doctor ordered.

  • Improvement in the symptoms of Parkinson's disease usually occurs in about 2 days. However, in some patients this medicine must be taken for up to 2 weeks before full benefit is seen.

The nasal flu vaccine (e.g., live attenuated influenza vaccine, Flumist®) should not be given in the 2 weeks before or 48 hours after taking this medicine.


Dosing


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


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


  • For oral dosage forms (capsules, syrup, and tablets):
    • For the treatment or prevention of flu:
      • Adults and teenagers—200 milligrams (mg) or four teaspoonfuls once a day as a single dose.

      • Older adults—100 milligrams (mg) once a day as a single dose.

      • Children 9 to 12 years of age—100 milligrams (mg) or two teaspoonfuls two times a day.

      • Children 1 to 9 years of age—Dose is based on body weight and must be determined by the doctor. The usual dose is 4.4 to 8.8 milligrams (mg) per kilogram (kg) of body weight per day. The dose is divided evenly and given two times a day. However, the dose is usually not more than 150 mg per day.

      • Children up to 1 year of age—Use and dose must be determined by your doctor.


    • For the treatment of Parkinson's disease or movement problems:
      • Adults—100 milligrams (mg) two times a day. Your doctor may adjust your dose if needed.

      • Older adults—At first, 100 milligrams (mg) once a day as a single dose. Your doctor may adjust your dose if needed.

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



Missed Dose


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


Storage


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


Keep out of the reach of children.


Do not keep outdated medicine or medicine no longer needed.


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


Precautions While Using Symmetrel


It is important that your doctor check your progress at regular visits to allow changes in your dose and to check for any unwanted effects.


Amantadine 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, your child, or your caregiver notice any of these adverse effects, tell your doctor or your child's doctor right away.


Some people who have used this medicine had unusual changes in their behavior. Talk with your doctor right away if you start having problems with gambling or an increased interest in sex while using this medicine.


Drinking alcoholic beverages while taking this medicine may cause increased side effects, such as circulation problems, dizziness, lightheadedness, fainting, or confusion. Do not drink alcoholic beverages while you are taking this medicine.


This medicine may cause some people to become dizzy, confused, or lightheaded, or to have blurred vision or trouble concentrating. Make sure you know how you react to this medicine before you drive, use machines, or do anything else that could be dangerous if you are dizzy or are not alert or able to see well. If these reactions are especially bothersome, check with your doctor.


Dizziness, lightheadedness, or fainting may occur with this medicine, especially when you get up from a lying or sitting position suddenly. These symptoms are more likely to occur when you begin taking this medicine, or when the dose is increased. Getting up slowly may help. If this problem continues or gets worse, check with your doctor.


Patients with Parkinson's disease must be careful not to overdo physical activities when their condition improves and body movements become easier since injuries resulting from falls may occur. Such activities must be gradually increased to give your body time to adjust to a change in balance, circulation, and coordination.


Amantadine may cause dryness of the mouth, nose, and throat. For temporary relief of mouth dryness, use sugarless candy or gum, 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 doctor or dentist. Continuing dryness of the mouth may increase the chance of dental disease, including tooth decay, gum disease, and fungus infections.


This medicine may cause purplish red, net-like, blotchy spots on the skin. This problem occurs more often in females and usually occurs on the legs and/or feet after this medicine has been taken regularly for a month or more. Although the blotchy spots may remain as long as you are taking this medicine, they usually go away gradually within 2 to 12 weeks after you stop taking the medicine. If you have any questions about this, check with your doctor.


Check with your doctor right away if you are having convulsions (seizures); difficulty with breathing; a fast heartbeat; a high fever; high or low blood pressure; increased sweating; loss of bladder control; severe muscle stiffness; unusually pale skin; or tiredness. These could be symptoms of a serious condition called neuroleptic malignant syndrome (NMS).


If you are using this medicine for Parkinson's disease, do not stop taking this medicine suddenly without first checking with your doctor. Your doctor may want you to gradually reduce the amount you are using before stopping it completely.


If you are using this medicine for Parkinson's disease, it is important that your doctor check your skin regularly for signs of a skin cancer called melanoma. If you notice any unusual red, brown, or black spots on your skin, talk to your doctor right away.


If your Parkinson's symptoms do not improve within a few days, if they become worse, or if this medicine appears less effective after a few weeks, check with your doctor.


Symmetrel 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
  • Blurred vision

  • confusion

  • difficult urination

  • dizziness or lightheadedness

  • fainting

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

  • swelling of the hands, feet, or lower legs

Rare
  • Convulsions (seizures)

  • decreased vision or any change in vision

  • difficulty in coordination

  • fever, chills, or sore throat

  • increased blood pressure

  • increase in body movements

  • irritation and swelling of the eye

  • loss of memory

  • mental depression

  • severe mood or mental changes

  • skin rash

  • slurred speech

  • thoughts of suicide or attempts at suicide

  • unexplained shortness of breath

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
  • Agitation, anxiety, or nervousness

  • difficulty concentrating

  • headache

  • irritability

  • loss of appetite

  • nausea

  • purplish red, net-like, or blotchy spots on the skin

  • trouble in sleeping or nightmares

Less common or rare
  • Constipation

  • decrease in sexual desire

  • diarrhea

  • drowsiness

  • dryness of the mouth, nose, and throat

  • false sense of well-being

  • vomiting

  • unusual tiredness or weakness

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: Symmetrel 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 Symmetrel resources


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


  • Symmetrel Prescribing Information (FDA)

  • Symmetrel Concise Consumer Information (Cerner Multum)

  • Symmetrel Monograph (AHFS DI)

  • Amantadine Prescribing Information (FDA)

  • Amantadine MedFacts Consumer Leaflet (Wolters Kluwer)



Compare Symmetrel with other medications


  • Extrapyramidal Reaction
  • Influenza
  • Influenza Prophylaxis
  • Parkinson's Disease

Thursday, 9 August 2012

Morphine Immediate-Release Tablets



Pronunciation: MORE-feen
Generic Name: Morphine
Brand Name: Generics only. No brands available.


Morphine Immediate-Release Tablets are used for:

Treating moderate to severe pain.


Morphine Immediate-Release Tablets are a narcotic pain reliever. It works in the brain and nervous system to decrease pain.


Do NOT use Morphine Immediate-Release Tablets if:


  • you are allergic to any ingredient in Morphine Immediate-Release Tablets

  • you have known or suspected bowel blockage (eg, paralytic ileus)

  • you have severe or persistent diarrhea associated with antibiotic use (pseudomembranous colitis)

  • you have slow or difficult breathing, severe asthma, severe hypercarbia or hypercapnia (high blood levels of carbon dioxide), or you are having an asthma attack

  • you are taking sodium oxybate (GHB) or you drink alcohol

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

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



Before using Morphine Immediate-Release Tablets:


Some medical conditions may interact with Morphine Immediate-Release Tablets. 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, especially other narcotic pain relievers (eg, codeine, hydromorphone); foods; or other substances

  • if you asthma, chronic obstructive pulmonary disease (COPD), or other lung or breathing problems

  • if you have increased pressure in the head, recent head injury, or growths in the brain (eg, tumors, lesions)

  • if you have a history of heart problems (eg, cor pulmonale), liver or kidney problems, thyroid problems, stomach or bowel problems (eg, constipation, blockage, inflammation), gallbladder or pancreas problems, prostate problems, trouble urinating, adrenal gland problems (eg, Addison disease), hypoxia (not enough oxygen in your body), hypercapnia or hypercarbia, curvature of the spine, or seizures

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

  • if you will be having surgery or you are currently having alcohol withdrawal

  • if you have severe drowsiness; low blood volume; stomach pain; very poor health; have had stomach or intestinal surgery; or you are in shock caused by heart problems, blood vessel problems, or severe bleeding

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


  • Mixed narcotic agonists/antagonists (eg, buprenorphine, butorphanol, pentazocine) or naltrexone because they may decrease Morphine Immediate-Release Tablets's effectiveness and withdrawal symptoms may occur

  • Fluoxetine, rifamycins (eg, rifampin), or risperidone because they may decrease Morphine Immediate-Release Tablets's effectiveness

  • Cimetidine, ketorolac, or tricyclic antidepressants (eg, amitriptyline) because the risk of side effects, such as severe drowsiness, slow or difficulty breathing, confusion, and seizures, may be increased

  • Anticholinergics (eg, scopolamine, oxybutynin), antihistamines (eg, diphenhydramine), antinausea medicines (eg, ondansetron), benzodiazepines (eg, lorazepam), MAOIs (eg, phenelzine), other narcotic pain medicines (eg, hydrocodone), phenothiazines (eg, chlorpromazine), quinidine, sleep medicines (eg, zolpidem), sodium oxybate (GHB) because they may increase the risk of Morphine Immediate-Release Tablets's side effects

  • Skeletal muscle relaxants (eg, cyclobenzaprine) because the risk of their side effects may be increased

  • Mexiletine or trovafloxacin because their effectiveness may be decreased by Morphine Immediate-Release Tablets

This may not be a complete list of all interactions that may occur. Ask your health care provider if Morphine Immediate-Release Tablets 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 Immediate-Release Tablets:


Use Morphine Immediate-Release Tablets as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • Take Morphine Immediate-Release Tablets by mouth with or without food.

  • If Morphine Immediate-Release Tablets are no longer needed, dispose of it as soon as possible. Ask your doctor or pharmacist how to dispose of Morphine Immediate-Release Tablets properly.

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

Ask your health care provider any questions you may have about how to use Morphine Immediate-Release Tablets.



Important safety information:


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

  • Do not drink alcohol while you are taking Morphine Immediate-Release Tablets.

  • Check with your doctor before you take medicines that may cause drowsiness (eg, sleep aids, muscle relaxers) while you are taking Morphine Immediate-Release Tablets; it may add to their effects. Ask your pharmacist if you have questions about which medicines may cause drowsiness.

  • Morphine Immediate-Release Tablets 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.

  • Morphine Immediate-Release Tablets may cause constipation. To prevent constipation, maintain a diet adequate in fiber, drink plenty of water, and exercise. Talk to your doctor about using fiber laxatives or stool softeners to prevent or treat constipation while you take Morphine Immediate-Release Tablets.

  • The risk of Morphine Immediate-Release Tablets becoming habit-forming may be greater if you take it in high doses or for a long time. Do NOT take more than the recommended dose or use for longer than prescribed without checking with your doctor. Do NOT change your dose or use more often than prescribed without checking with your doctor.

  • Do NOT suddenly stop taking Morphine Immediate-Release Tablets without checking with your doctor. If you have been taking Morphine Immediate-Release Tablets for more than a few weeks and your doctor tells you to stop taking it, your dose may need to be gradually lowered as directed by your doctor to avoid side effects.

  • Tell your doctor or dentist that you take Morphine Immediate-Release Tablets before you receive any medical or dental care, emergency care, or surgery.

  • Lab tests, including liver, kidney, or lung function, and complete blood cell counts, may be performed while you use Morphine Immediate-Release Tablets. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

  • Use Morphine Immediate-Release Tablets with caution in the ELDERLY; they may be more sensitive to its effects, especially severe drowsiness, or slow or shallow breathing.

  • Morphine Immediate-Release Tablets should be used with extreme caution in CHILDREN; safety and effectiveness in children have not been confirmed.

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

When used for long periods of time or at high doses, Morphine Immediate-Release Tablets 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 Immediate-Release Tablets stops working well. Do not take more than prescribed.


Some people who use Morphine Immediate-Release Tablets 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 Immediate-Release Tablets 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 Immediate-Release Tablets:


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; headache; lightheadedness; nausea; restless mood; sweating; 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, throat, or tongue); confusion; disorientation; fainting; fast, slow, or irregular heartbeat; hallucinations; mental or mood changes (eg, agitation, exaggerated sense of well-being); seizures; severe or persistent constipation or stomach pain; severe or persistent dizziness, drowsiness, or headache; shortness of breath; slow or shallow breathing; sudden chest pain; swelling of the hands, ankles, or feet; trouble urinating; unusual bruising or bleeding; unusual tiredness or weakness; vision problems (eg, blurred vision).



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



If OVERDOSE is suspected:


Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include bluish skin or nails; cold and clammy skin; coma; confusion; decreased muscle tone; decreased pupil size; loss of consciousness; low body temperature; seizures; severe drowsiness, dizziness, or lightheadedness; severe muscle pain or weakness; shortness of breath; slow heartbeat; slow or shallow breathing.


Proper storage of Morphine Immediate-Release Tablets:

Store Morphine Immediate-Release Tablets between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Morphine Immediate-Release Tablets out of the reach of children and away from pets.


General information:


  • If you have any questions about Morphine Immediate-Release Tablets, please talk with your doctor, pharmacist, or other health care provider.

  • Morphine Immediate-Release Tablets 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 Immediate-Release Tablets. 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 resources


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


Compare Morphine with other medications


  • Pain

Tuesday, 7 August 2012

Boots Antiseptic Gel






Boots Antiseptic Gel


(Cetylpyridinium Chloride)


  • Prevents Infection

  • Helps Healing Process

  • Effective Cleansing Action

e 30 g


Read all of this carton for full instructions.




What this medicine is for


This medicine contains Cetylpyridinium Chloride which belongs to a group of medicines called antiseptics, which act to prevent infection.


It can be used on cuts, grazes, insect bites, minor wounds, spots, minor burns and scalds.




Before you use this medicine



Do not use:



  • If you are allergic to any of the ingredients


  • On weeping or badly inflamed skin


  • Frequently or for long periods of time (you may become sensitive to the medicine)

You can use this medicine if you are pregnant or breastfeeding.




How to use this medicine


Check the seal is not broken before first use. If it is, do not use the gel.


Apply to the skin only.


Avoid contact with the eyes.



Children and adults:


Apply to the affected area of skin 2 or 3 times a day.


Do not use more than the amount recommended above.


If the skin does not appear to heal talk to your doctor.




If anyone accidentally swallows some:


Talk to a doctor straight away.





Possible side effects


Most people will not have problems, but some may get some.



If you get any of these side effects, stop using the gel and see a doctor:


  • Allergic reaction (e.g. skin rash, red or itchy skin)


These other effects are less serious. If they bother you talk to a pharmacist:


  • Skin irritation


If any side effect becomes severe, or you notice any side effect not listed here, please tell your pharmacist or doctor.



Keep all medicines out of the sight and reach of children.


Use by the date on the end flap of the carton.




Active ingredient


This gel contains Cetylpyridinium Chloride 0.025% w/w.


Also contains: purified water, glycerol, hypromellose, sodium citrate, citric acid.


PL 00014/0556


Text prepared 3/07




Manufactured by the Marketing Authorisation holder



The Boots Company PLC

Nottingham

NG2 3AA



If you need more advice ask your pharmacist.


BTC14517 vD 12-12-07





Monday, 6 August 2012

Vagisil Feminine Cream


Generic Name: benzocaine topical (BENZ oh kane TOP ik al)

Brand Names: Americaine, Americaine Hemorrhoidal, Anacaine, Anbesol Gel, Anbesol Liquid, Babee Teething Lotion, Benzo-O-Stetic, Boil Ease Pain Relieving, Cepacol Extra Strength, Cepacol Fizzlers, Dent-O-Kain, Dermoplast, Detane, Hurricaine, Lanacane, Maintain, Medicone Maximum Strength, Num-Zit, Numzident, Orabase, Orabase Gel-B, Orajel, Orajel Denture, Oral Pain Relief, OraMagic Plus, Outgro Pain Relief, Retre-Gel, Rid-A-Pain, Skeeter Stik, Solarcaine Aerosol, Sting-Kill, Topex, Trocaine, Vagisil Feminine Cream, zilactin-B


What is Vagisil Feminine Cream (benzocaine topical)?

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


Benzocaine topical is used to reduce pain or discomfort caused by minor skin irritations, sore throat, sunburn, teething pain, vaginal or rectal irritation, ingrown toenails, hemorrhoids, and many other sources of minor pain on a surface of the body. Benzocaine is also used to numb the skin or surfaces inside the mouth, nose, throat, vagina, or rectum to lessen the pain of inserting a medical instrument such as a tube or speculum.


There are many brands and forms of benzocaine topical available and not all brands are listed on this leaflet.


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


What is the most important information I should know about Vagisil Feminine Cream (benzocaine topical)?


There are many brands and forms of benzocaine topical available and not all brands are listed on this leaflet.


Benzocaine topical used in the mouth or throat may cause a life-threatening condition in which the amount of oxygen in your blood stream becomes dangerously low. This condition is called methemoglobinemia (met-HEEM-oh glo-bin-EE-mee-a) and it may occur after only one use of benzocaine or after several uses.

Signs and symptoms of methemoglobinemia may occur within minutes or up to 2 hours after using benzocaine topical in the mouth or throat. GET EMERGENCY MEDICAL HELP IF YOU HAVE ANY OF THESE SYMPTOMS: headache, tired feeling, confusion, fast heart rate, and feeling light-headed or short of breath, with a pale, blue, or gray appearance of your skin, lips, or fingernails.


Do not use benzocaine topical if you have ever had methemoglobinemia in the past. Do not use this medicine on a child younger than 2 years old without medical advice. An overdose of numbing medications can cause fatal side effects if too much of the medicine is absorbed through your skin and into your blood. This is more likely to occur when using a numbing medicine without the advice of a medical doctor (such as during a cosmetic procedure like laser hair removal). Overdose symptoms may include uneven heartbeats, seizure (convulsions), coma, slowed breathing, or respiratory failure (breathing stops).

Use the smallest amount of this medication needed to numb the skin or relieve pain. Do not use large amounts of benzocaine topical, or cover treated skin areas with a bandage or plastic wrap without medical advice. Be aware that many cosmetic procedures are performed without a medical doctor present.


Your body may absorb more of this medication if you use too much, if you apply it over large skin areas, or if you apply heat, bandages, or plastic wrap to treated skin areas. Skin that is cut or irritated may also absorb more topical medication than healthy skin.

Before using benzocaine topical, tell your doctor if you have any type of inherited enzyme deficiency, heart disease, a breathing disorder such as asthma, bronchitis, or emphysema, or if you smoke.


If you are treating a sore throat, call your doctor if the pain is severe or lasts longer than 2 days, especially if you also develop a fever, headache, skin rash, swelling, nausea, vomiting, cough, or breathing problems.


What should I discuss with my health care provider before using Vagisil Feminine Cream (benzocaine topical)?


Do not use benzocaine topical if you have ever had methemoglobinemia in the past. An overdose of numbing medications can cause fatal side effects if too much of the medicine is absorbed through your skin and into your blood. This is more likely to occur when using a numbing medicine without the advice of a medical doctor (such as during a cosmetic procedure like laser hair removal). Overdose symptoms may include uneven heartbeats, seizure (convulsions), coma, slowed breathing, or respiratory failure (breathing stops).

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



  • asthma, bronchitis, emphysema, or other breathing disorder;




  • heart disease;




  • a personal or family history of methemoglobinemia, or any genetic (inherited) enzyme deficiency; or




  • if you smoke.




FDA pregnancy category C. It is not known whether benzocaine topical will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medication.. It is not known whether benzocaine topical 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. Do not use this medicine on a child younger than 2 years old without medical advice.

How should I use Vagisil Feminine Cream (benzocaine topical)?


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


Your body may absorb more of this medication if you use too much, if you apply it over large skin areas, or if you apply heat, bandages, or plastic wrap to treated skin areas. Skin that is cut or irritated may also absorb more topical medication than healthy skin.

Use the smallest amount of medicine needed to numb the skin or relieve pain. Do not use large amounts of benzocaine topical, or cover treated skin areas with a bandage or plastic wrap without medical advice. Be aware that many cosmetic procedures are performed without a medical doctor present.


This medication comes with instructions for safe and effective application. Follow these directions carefully. Ask your doctor or pharmacist if you have any questions.


To treat minor skin conditions, apply a thin layer of benzocaine topical to the affected area up to 4 times per day. If using the spray, hold the container 6 to 12 inches away from the skin. Do not spray this medication onto your face. Spray it instead on your hands and then rub it onto the face, avoiding contact with your eyes.


To treat hemorrhoids, clean the area with soap and water before applying benzocaine topical. Apply the medication up to 6 times per day. If you are using the rectal suppository, try to empty your bowel and bladder before inserting the suppository. Remove the outer wrapper from the suppository before inserting it. Avoid handling the suppository too long or it will melt in your hands.


Do not use benzocaine topical to treat large skin areas or deep puncture wounds. Avoid using the medicine on skin that is raw or blistered, such as a severe burn or abrasion.

Call your doctor if your symptoms do not improve or if they get worse within the first 7 days of using benzocaine topical. Also call your doctor if your symptoms had cleared up but then came back.


If you are treating a sore throat, call your doctor if the pain is severe or lasts longer than 2 days, especially if you also develop a fever, headache, skin rash, swelling, nausea, vomiting, cough, or breathing problems.


Store at room temperature away from moisture and heat. Do not freeze.

What happens if I miss a dose?


Since benzocaine topical is used as needed, you may not be on a dosing schedule. If you are using the medication regularly, use the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not use extra medicine to make up the missed dose.


What happens if I overdose?


Seek emergency medical attention or call the Poison Help line at 1-800-222-1222. An overdose of benzocaine topical applied to the skin can cause life-threatening side effects such as uneven heartbeats, seizure (convulsions), coma, slowed breathing, or respiratory failure (breathing stops).

What should I avoid while taking Vagisil Feminine Cream (benzocaine topical)?


Avoid eating within 1 hour after using benzocaine topical on your gums or inside your mouth.


Benzocaine topical is for use only on the surface of your body, or just inside the mouth, vagina, or rectum. Avoid getting this medication in your eyes. Avoid swallowing the gel, liquid, or ointment while applying it to your gums or the inside of your mouth. The throat spray or oral lozenge may be swallowed gradually during use.

Do not apply other medications to the same affected areas you treat with benzocaine topical, unless your doctor has told you otherwise.


Vagisil Feminine Cream (benzocaine topical) side effects


Benzocaine topical used in the mouth or throat may cause a life-threatening condition in which the amount of oxygen in your blood stream becomes dangerously low. This condition is called methemoglobinemia (met-HEEM-oh glo-bin-EE-mee-a) and it may occur after only one use of benzocaine or after several uses.

Signs and symptoms may occur within minutes or up to 2 hours after using benzocaine topical in the mouth or throat. GET EMERGENCY MEDICAL HELP IF YOU HAVE:



  • headache, tired feeling, confusion;




  • fast heart rate;




  • feeling light-headed or short of breath; and




  • pale, blue, or gray appearance of your skin, lips, or fingernails.




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 benzocaine topical and call your doctor at once if you have any of these other serious side effects:

  • headache, weakness, dizziness, breathing problems, fast heart rate, and gray or bluish colored skin (rare but serious side effects of benzocaine);




  • severe burning, stinging, or sensitivity where the medicine is applied;




  • swelling, warmth, or redness; or




  • oozing, blistering, or any signs of infection.



Less serious side effects may include:



  • mild stinging, burning, or itching where the medicine is applied;




  • skin tenderness or redness; or




  • dry white flakes where the medicine was 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 Vagisil Feminine Cream (benzocaine topical)?


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



More Vagisil Feminine Cream resources


  • Vagisil Feminine Cream Side Effects (in more detail)
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Compare Vagisil Feminine Cream with other medications


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Where can I get more information?


  • Your pharmacist can provide more information about benzocaine topical.

See also: Vagisil Feminine side effects (in more detail)


Saturday, 4 August 2012

Cleocin T Solution


Pronunciation: KLIN-da-MYE-sin
Generic Name: Clindamycin
Brand Name: Cleocin T


Cleocin T Solution is used for:

Treating severe acne. It may also be used for other conditions as determined by your doctor.


Cleocin T Solution is a topical lincomycin antibiotic. It works by killing sensitive bacteria that cause acne and reducing the amount of free fatty acids that irritate the skin surface.


Do NOT use Cleocin T Solution if:


  • you are allergic to any ingredient in Cleocin T Solution or to lincomycin

  • you have Crohn disease, antibiotic-associated colitis, or ulcerative colitis

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



Before using Cleocin T Solution:


Some medical conditions may interact with Cleocin T Solution. 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 gastrointestinal (bowel) disease or diarrhea

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


  • Nondepolarizing muscle relaxants (eg, vecuronium) or succinylcholine because their actions and the risk of their side effects may be increased by Cleocin T Solution

  • Erythromycin because it may decrease Cleocin T Solution's effectiveness

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


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


  • Cleocin T Solution is for topical use on the skin only.

  • The medicine comes in a bottle with an applicator tip. Clean and dry the affected area. Use the applicator with a dabbing motion. Tilt the bottle and press the tip firmly against your skin. If the applicator tip is dry, turn the bottle upside down and press the tip several times to moisten it.

  • Cleocin T Solution works best if it is used at the same time each day.

  • Continue to use Cleocin T Solution even if your condition improves. Do not miss any doses.

  • If you miss a dose of Cleocin T Solution, 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 Cleocin T Solution.



Important safety information:


  • Cleocin T Solution is for external use only. Avoid contact with the eyes as burning or irritation can occur. If contact occurs with the eyes or sensitive surfaces (eg, mucous membranes, scraped skin), wash the area with cool tap water.

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

  • Cleocin T Solution has an unpleasant taste. Use caution when applying Cleocin T Solution around the mouth.

  • Several weeks may pass before you see improvement in your acne. Continue using Cleocin T Solution for the full time recommended by your doctor. If your acne does not improve or gets worse, check with your doctor.

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

  • If severe diarrhea, stomach pain or cramping, or bloody stools develop during treatment or within several months after treatment with Cleocin T Solution, check with your doctor or pharmacist right away. Do not treat it without first checking with your doctor.

  • Cleocin T Solution should not be used in CHILDREN younger than 12 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 Cleocin T Solution while you are pregnant. It is not known if Cleocin T Solution is found in breast milk. Do not breast-feed while taking Cleocin T Solution.


Possible side effects of Cleocin T Solution:


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:



Dryness; itching; mild stinging after applying; oiliness.



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

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); bloody stools; diarrhea; stomach cramps or pain; swelling, redness, burning, or peeling of the skin.



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: Cleocin T 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. Cleocin T Solution may be harmful if swallowed.


Proper storage of Cleocin T Solution:

Store Cleocin T Solution at room temperature, between 68 to 77 degrees F (20 to 25 degrees C), in a tightly closed container. Store away from heat, moisture, and light. Do not store in the bathroom. Protect from freezing. Keep Cleocin T Solution out of the reach of children and away from pets.


General information:


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

  • Cleocin T Solution 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 Cleocin T Solution. 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 Cleocin T resources


  • Cleocin T Side Effects (in more detail)
  • Cleocin T Use in Pregnancy & Breastfeeding
  • Cleocin T Drug Interactions
  • Cleocin T Support Group
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Friday, 3 August 2012

Boots Easy Breathing Pastilles





1. Name Of The Medicinal Product



Boots Easy Breathing Pastilles


2. Qualitative And Quantitative Composition










Sylvestris Pine Oil




0.3% V/W




Abietis Oil BPC 1949




0.3% V/W




Menthol BP




0.6% W/W



For full list of excipients, see section 6.1



3. Pharmaceutical Form



Pastille



4. Clinical Particulars



4.1 Therapeutic Indications



For the relief of catarrhal symptoms and coughs



4.2 Posology And Method Of Administration



One pastille to be dissolved slowly in the mouth as required.



ADULTS, THE ELDERLY AND CHILDREN OF 12 YEARS AND OVER:



Do not take more than 18 pastilles in 24 hours.



CHILDREN 6 – 12 YEARS:



Do not take more than 12 pastilles in 24 hours.



Not recommended for children under 6 years old.



4.3 Contraindications



Hypersensitivity to any of the ingredients



4.4 Special Warnings And Precautions For Use



Keep out of reach and sight of children. If symptoms persist consult your doctor.



Contains a total of 1.3g of sucrose and glucose per pastille. Patients with rare hereditary problems of fructose intolerance, glucose-galactose malabsorption or sucrase-isomaltase insufficiency should not take this medicine.



4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction



None reported



4.6 Pregnancy And Lactation



The use of Catarrh Pastilles during pregnancy and lactation is not restricted.



4.7 Effects On Ability To Drive And Use Machines



None



4.8 Undesirable Effects



Isolated cases of hypersensitivity reactions including anaphylaxis, angioedema, bronchospasm, rash, urticaria and flushing have been reported with menthol-containing preparations.



4.9 Overdose



No example of overdose has been reported.



5. Pharmacological Properties



5.1 Pharmacodynamic Properties



All the actives have decongestant properties.



5.2 Pharmacokinetic Properties



Not applicable



5.3 Preclinical Safety Data



There is no preclinical data available specific to the product.



6. Pharmaceutical Particulars



6.1 List Of Excipients



Granulated sugar



Modified starch



Liquid Glucose BPC



Peppermint oil



Eucalyptus oil



Water



6.2 Incompatibilities



None known



6.3 Shelf Life



60 months for the unopened pack.



3 months after opening the 45g pack.



6 months after opening the 500g pack.



6.4 Special Precautions For Storage



None



6.5 Nature And Contents Of Container



Tied polythene bag, 500 g



Securitainer, 500 g



Heat-sealed laminated sachet integral with carton, 45 g



6.6 Special Precautions For Disposal And Other Handling



None specific to the packs.



7. Marketing Authorisation Holder



Ernest Jackson & Co Ltd



High Street



Crediton



Devon, EX17 3AP, UK



8. Marketing Authorisation Number(S)



PL 0094/5014R



9. Date Of First Authorisation/Renewal Of The Authorisation



First granted 23 April 1987 / Renewed June 2004



10. Date Of Revision Of The Text



July 2011




Monday, 30 July 2012

Lysteda


Pronunciation: TRAN-ex-AM-ik AS-id
Generic Name: Tranexamic Acid
Brand Name: Lysteda


Lysteda is used for:

Treating heavy menstrual bleeding.


Lysteda is an antifibrinolytic. It works by preventing blood clots from breaking down too quickly. This helps to reduce excessive bleeding.


Do NOT use Lysteda if:


  • you are allergic to any ingredient in Lysteda

  • you have blood clots (eg, in the leg, lung, eye, brain), a history of blood clots, or conditions that may increase your risk of blood clots (eg, certain heart valve problems, certain types of irregular heartbeat, certain blood clotting problems)

  • you have bleeding in the brain, blood in the urine, or bleeding related to kidney problems

  • you have a disturbance of color vision

  • you have irregular menstrual bleeding of unknown cause

  • you are using medicine to help your blood clot (eg, factor IX complex concentrates or anti-inhibitor coagulant concentrates)

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



Before using Lysteda:


Some medical conditions may interact with Lysteda. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:


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

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

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

  • if you have a history of kidney problems, bleeding or blood clotting problems, a certain blood problem called disseminated intravascular coagulation (DIC), eye or vision problems, or bleeding in the brain

  • if the time between the start of your periods is less than 21 days or more than 35 days

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


  • Hormonal birth control (eg, birth control pills), medicines to help your blood clot (eg, anti-inhibitor coagulant concentrates, factor IX complex concentrates), or tretinoin (all-trans retinoic acid) because the risk of blood clots may be increased

  • Anticoagulants (eg, warfarin) because they may decrease Lysteda's effectiveness

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


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


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

  • Take Lysteda by mouth with or without food.

  • Swallow Lysteda whole with plenty of liquids. Do not break, crush, or chew before swallowing.

  • Only take Lysteda after your period has started. Do not take more than 3 doses within 24 hours. Do not take Lysteda for more than 5 days within any menstrual cycle. Discuss any questions with your doctor.

  • If you miss a dose of Lysteda, take it as soon as you remember, then take your next dose at least 6 hours later. Do not take 2 doses at once.

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



Important safety information:


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

  • If your symptoms do not get better after 2 menstrual cycles, if they get worse, or if Lysteda seems to stop working, check with your doctor.

  • If you notice an unusual change in your bleeding pattern, check with your doctor.

  • The risk of a stroke, a heart attack, or other blood clots may be increased when Lysteda is used with hormonal birth control (eg, birth control pills). The risk may be greater if you are very overweight or if you smoke cigarettes, especially if you are older than 35 years. Discuss any questions or concerns with your doctor.

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

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

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

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

  • Lysteda is not indicated in women who have been through menopause or in children who have not had their first menstrual period. Discuss any questions or concerns with your doctor.

  • PREGNANCY and BREAST-FEEDING: Lysteda is not approved for use in pregnant women. If you become pregnant while taking Lysteda, contact your doctor. Lysteda is found in breast milk. If you are or will be breast-feeding while you take Lysteda, check with your doctor or pharmacist. Discuss any possible risks to your baby.


Possible side effects of Lysteda:


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



Back pain; headache; joint pain; muscle pain, spasms, or cramps; nasal or sinus congestion; stomach pain; tiredness.



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 or throat; swelling of the mouth, face, lips, or tongue; flushing of the face); calf or leg pain, swelling, or tenderness; chest pain; confusion; coughing up blood; decreased urination or difficulty urinating; eye problems; fainting; numbness of an arm or leg; one-sided weakness; seizures; severe or persistent dizziness or light-headedness; shortness of breath; slurred speech; sudden, severe headache or vomiting; vision changes or problems (eg, disturbance of color vision, sharpness, or field of vision).



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


See also: Lysteda 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 dizziness when you stand up; fainting; light-headedness; mental or mood changes; muscle twitching; rash; seizures; severe diarrhea, nausea, or vomiting; vision problems.


Proper storage of Lysteda:

Store Lysteda at 77 degrees F (25 degrees C). Brief storage at room temperature 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 Lysteda out of the reach of children and away from pets.


General information:


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

  • Lysteda 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 Lysteda. 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 Lysteda resources


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


  • Lysteda Prescribing Information (FDA)

  • Lysteda Consumer Overview

  • Lysteda Advanced Consumer (Micromedex) - Includes Dosage Information

  • Tranexamic Acid Professional Patient Advice (Wolters Kluwer)

  • Cyklokapron Advanced Consumer (Micromedex) - Includes Dosage Information

  • Cyklokapron Prescribing Information (FDA)



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