Saturday, June 30, 2012

Sumatriptan injection



Generic Name: sumatriptan (injection) (soo ma TRIP tan)

Brand Names: Alsuma, Imitrex, Imitrex Statdose, Imitrex Statdose Refill, Sumavel DosePro


What is sumatriptan injection?

Sumatriptan is a headache medicine that narrows blood vessels around the brain. Sumatriptan also reduces substances in the body that can trigger headache pain, nausea, sensitivity to light and sound, and other migraine symptoms.


Sumatriptan is used to treat migraine headaches and cluster headaches. Sumatriptan will only treat a headache that has already begun. It will not prevent headaches or reduce the number of attacks.


Sumatriptan should not be used to treat a common tension headache, a headache that causes loss of movement on one side of your body, or any headache that seems to be different from your usual migraine headaches. Use this medication only if your condition has been confirmed by a doctor as migraine headaches.

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


What is the most important information I should know about sumatriptan injection?


You should not use this medication if you are allergic to sumatriptan, if you have any history of heart disease, or if you have coronary heart disease, angina, blood circulation problems, lack of blood supply to the heart, uncontrolled high blood pressure, severe liver disease, ischemic bowel disease, a history of a heart attack or stroke, or if your headache seems to be different from your usual migraine headaches. Do not use sumatriptan within 24 hours before or after using another migraine headache medicine, including sumatriptan tablets or nasal spray, almotriptan (Axert), eletriptan (Relpax), frovatriptan (Frova), rizatriptan (Maxalt), naratriptan (Amerge), zolmitriptan (Zomig), or ergot medicine such as dihydroergotamine (D.H.E. 45, Migranal), ergotamine (Ergomar, Cafergot, Migergot), dihydroergotamine (D.H.E. 45, Migranal), or methylergonovine (Methergine). Do not use sumatriptan 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.

Before using sumatriptan, tell your doctor if you have liver or kidney disease, seizures, high blood pressure, a heart rhythm disorder, or coronary heart disease (or risk factors such as diabetes, menopause, smoking, being overweight, having high cholesterol, having a family history of coronary artery disease, being older than 40 and a man, or being a woman who has had a hysterectomy).


Also tell your doctor if you are taking an antidepressant such as citalopram (Celexa), desvenlafaxine (Pristiq), duloxetine (Cymbalta), escitalopram (Lexapro), fluoxetine (Prozac, Sarafem), fluvoxamine (Luvox), paroxetine (Paxil), sertraline (Zoloft), or venlafaxine (Effexor).


Sumatriptan will only treat a headache that has already begun. It will not prevent headaches or reduce the number of attacks.


After using a sumatriptan injection, you must wait one (1) hour before using a second injection. Do not use more than two injections in 24 hours.


What should I discuss with my health care provider before using sumatriptan injection?


You should not use this medication if you are allergic to sumatriptan, or if you have:

  • coronary heart disease, angina (chest pain), blood circulation problems, lack of blood supply to the heart;




  • a history of heart disease, heart attack, or stroke, including "mini-stroke";




  • severe or uncontrolled high blood pressure;



  • severe liver disease;


  • ischemic bowel disease; or




  • a headache that seems different from your usual migraine headaches.




Do not use sumatriptan 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.

To make sure you can safely use sumatriptan, tell your doctor if you have any of these other conditions:


  • liver disease;

  • kidney disease;


  • epilepsy or other seizure disorder;




  • high blood pressure, a heart rhythm disorder; or




  • coronary heart disease (or risk factors such as diabetes, menopause, smoking, being overweight, having high cholesterol, having a family history of coronary artery disease, being older than 40 and a man, or being a woman who has had a hysterectomy).




FDA pregnancy category C. It is not known whether sumatriptan will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medication.

Your name may need to be listed on a sumatriptan pregnancy registry when you start using this medication.


Sumatriptan can pass into breast milk and may harm a nursing baby. Do not breast-feed within 12 hours after using a sumatriptan injection. If you use a breast pump during this time, throw out any milk you collect. Do not feed it to your baby. This medicine should not be given to anyone under 18 or over 65 years of age.

How should I use sumatriptan injection?


Use exactly as prescribed by your doctor. Do not use in larger or smaller amounts or for longer than recommended. Follow the directions on your prescription label. Overuse of migraine headache medicine can actually make your headaches worse.


Sumatriptan is injected under the skin. You may be shown how to use injections at home. Do not self inject this medicine if you do not fully understand how to give the injection and properly dispose of used needles and syringes.


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


Use sumatriptan as soon as you notice headache symptoms, or after an attack has already begun.


Your doctor may want to give your first dose of this medicine in a hospital or clinic setting to see if you have any serious side effects.


Sumatriptan injection comes in a vial (bottle), in a prefilled cartridge to be loaded into an auto-injector syringe (Imitrex Statdose), or in a needle-free injector device (Sumavel DosePro). Each vial, cartridge, or needle-free device is for one use only.


After using an injection: If your headache does not completely go away after the injection, call your doctor before using a second sumatriptan injection. If your headache goes away and then comes back, you may use a second injection if it has been at least one hour since your first injection. Do not use more than two (2) injections in 24 hours. If your symptoms do not improve, contact your doctor before using any more injections.


Store at room temperature away from moisture, heat, and light. Throw away any unused medicine after the expiration date on the label has passed.

What happens if I miss a dose?


Since sumatriptan is used as needed, it does not have a daily dosing schedule. Call your doctor promptly if your symptoms do not improve after using sumatriptan.


After using a sumatriptan injection, you must wait one (1) hour before using a second injection. Do not use more than two (2) injections in 24 hours.


What happens if I overdose?


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

Overdose symptoms may include tremors or shaking, skin redness, breathing problems, blue-colored lips or fingernails, vision problems, watery eyes or mouth, weakness, lack of coordination, or seizure (convulsions).


What should I avoid while using sumatriptan injection?


Do not use sumatriptan within 24 hours before or after using another migraine headache medicine, including:

  • sumatriptan tablets or nasal spray, almotriptan (Axert), eletriptan (Relpax), frovatriptan (Frova), naratriptan (Amerge), rizatriptan (Maxalt, Maxalt-MLT), or zolmitriptan (Zomig); or




  • ergot medicine such as dihydroergotamine (D.H.E. 45, Migranal), ergotamine (Ergomar, Cafergot, Migergot), dihydroergotamine (D.H.E. 45, Migranal), or methylergonovine (Methergine).




Sumatriptan may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert.

Sumatriptan 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. Stop using sumatriptan and call your doctor if you have a serious side effect such as:

  • feeling of pain or tightness in your jaw, neck, or throat;




  • chest pain or heavy feeling, pain spreading to the arm or shoulder, nausea, sweating, general ill feeling;




  • sudden numbness or weakness, especially on one side of the body;




  • sudden severe headache, confusion, problems with vision, speech, or balance;




  • sudden and severe stomach pain and bloody diarrhea;




  • seizure (convulsions);




  • numbness or tingling and a pale or blue-colored appearance in your fingers or toes; or




  • (if you are also taking an antidepressant) -- agitation, hallucinations, fever, fast heart rate, overactive reflexes, nausea, vomiting, diarrhea, loss of coordination, fainting.



Less serious side effects may include:



  • mild headache (not a migraine);




  • pressure or heavy feeling in any part of your body;




  • discomfort in your nose or throat;




  • dizziness, spinning sensation;




  • muscle pain, neck pain or stiffness;




  • warmth, redness, or mild tingling under your skin; or




  • pain, redness, bleeding, swelling, or bruising where you injected the medicine.



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.


Sumatriptan Dosing Information


Usual Adult Dose for Cluster Headache:

Initial dosage when symptoms of headache appear:

Subcutaneously: 4 to 6 mg; may repeat if needed at least 1 hour after initial dose; maximum: 12 mg/day.

ORAL: Initial single dose: 25 mg given with fluids as soon as possible after the onset of a migraine; range: 25 to 100 mg/dose; maximum single dose: 100 mg; may repeat after 2 hours; maximum: 200 mg/day taken. The maximum single oral dose recommended is 100 mg. Do not split tablets.

NASAL SPRAY: Initial single dose: 5 mg, 10 mg, or 20 mg administered in one nostril, given as soon as possible after the onset of migraine; 10 mg dose may be administered as 5 mg in each nostril; may repeat after 2 hours; maximum: 40 mg/day.

Usual Adult Dose for Migraine:

Initial dosage when symptoms of headache appear:

Subcutaneously: 4 to 6 mg; may repeat if needed at least 1 hour after initial dose; maximum: 12 mg/day.

ORAL: Initial single dose: 25 mg given with fluids as soon as possible after the onset of a migraine; range: 25 to 100 mg/dose; maximum single dose: 100 mg; may repeat after 2 hours; maximum: 200 mg/day taken. The maximum single oral dose recommended is 100 mg. Do not split tablets.

NASAL SPRAY: Initial single dose: 5 mg, 10 mg, or 20 mg administered in one nostril, given as soon as possible after the onset of migraine; 10 mg dose may be administered as 5 mg in each nostril; may repeat after 2 hours; maximum: 40 mg/day.

Usual Pediatric Dose for Migraine:

Use in children and adolescents less than 18 years of age not recommended by manufacturer. Results of clinical studies are mixed with regards to efficacy, particularly with oral and injectable sumatriptan.

Intranasal:
Children 5 to 12 years: 5 mg, 10 mg, or 20 mg administered in one nostril as a single dose. A double-blind, placebo controlled study of 129 patients (8 to 17 years) used a weight-based dosing regimen: 20 to 39 kg: 10 mg; 40 kg or more: 20 mg. A small retrospective review of 10 children (5 to 12 years; mean: 9.9 years), used intranasal doses of 5 mg (n=2) or 20 mg (n=8).
Adolescents 12 years or older: 5 mg, 10 mg, or 20 mg administered in one nostril as a single dose.

Subcutaneously: Children and Adolescents 6 to 18 years: 3 to 6 mg single dose. An open labeled prospective trial of 17 children 6 to 16 years with juvenile migraine used subcutaneous doses of 6 mg in 15 children (30 to 70 kg), and 3 mg/dose in two children (22 kg and 30 kg). Another open-label prospective trial in 50 consecutive children (ages 6 to 18 years) with severe migraine used subcutaneous doses of 0.06 mg/kg/dose. Relief was reported as good/excellent in 84% of the patients; 16% reported fair to poor relief; additional studies are needed.


What other drugs will affect sumatriptan injection?


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



  • an antidepressant such as citalopram (Celexa), desvenlafaxine (Pristiq), duloxetine (Cymbalta), escitalopram (Lexapro), fluoxetine (Prozac, Sarafem), fluvoxamine (Luvox), paroxetine (Paxil), sertraline (Zoloft), or venlafaxine (Effexor).



This list is not complete and other drugs may interact with sumatriptan. 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 sumatriptan resources


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


Compare sumatriptan with other medications


  • Cluster Headaches
  • Cyclic Vomiting Syndrome
  • Migraine
  • New Daily Persistent Headache


Where can I get more information?


  • Your pharmacist can provide more information about sumatriptan.

See also: sumatriptan side effects (in more detail)



Friday, June 29, 2012

Silver sulfadiazine Topical


SIL-ver sul-fa-DYE-a-zeen


Commonly used brand name(s)

In the U.S.


  • Silvadene

  • SSD

  • SSD AF

  • Thermazene

In Canada


  • Flamazine

  • Ssd

Available Dosage Forms:


  • Cream

Therapeutic Class: Antibacterial


Chemical Class: Sulfonamide


Uses For silver sulfadiazine


Silver sulfadiazine , a sulfa medicine, is used to prevent and treat bacterial or fungus infections. It works by killing the fungus or bacteria.


Silver sulfadiazine cream is applied to the skin and/or burned area(s) to prevent and treat bacterial or fungus infections that may occur in burns. silver sulfadiazine may also be used for other problems as determined by your doctor.


Other medicines are used along with silver sulfadiazine for burns. Patients with severe burns or burns over a large area of the body must be treated in a hospital.


Silver sulfadiazine is available only with your doctor's prescription.


Before Using silver sulfadiazine


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 silver sulfadiazine, the following should be considered:


Allergies


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


Pediatric


Use is not recommended in premature or newborn infants up to 2 months of age. Sulfa medicines may cause liver problems in these infants. Although there is no specific information comparing use of silver sulfadiazine in older infants and children with use in other age groups, silver sulfadiazine is not expected to cause different side effects or problems in older infants and children than it does in adults.


Geriatric


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


Pregnancy








Pregnancy CategoryExplanation
All TrimestersBAnimal studies have revealed no evidence of harm to the fetus, however, there are no adequate studies in pregnant women OR animal studies have shown an adverse effect, but adequate studies in pregnant women have failed to demonstrate a risk to the fetus.

Breast Feeding


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


Interactions with Medicines


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


Interactions with Food/Tobacco/Alcohol


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


Other Medical Problems


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


  • Blood problems or

  • Glucose-6-phosphate dehydrogenase deficiency (lack of G6PD enzyme)—Use of silver sulfadiazine may cause blood problems or make them worse

  • Kidney disease or

  • Liver disease—In persons with these conditions, use may result in higher blood levels of silver sulfadiazine; a smaller dose may be needed

  • Porphyria—Use of silver sulfadiazine may result in a severe attack of porphyria

Proper Use of silver sulfadiazine


silver sulfadiazine should not be used on premature or newborn infants up to 2 months of age, unless otherwise directed by your doctor. It may cause liver problems in these infants.


To use:


  • Before applying silver sulfadiazine, cleanse the affected area(s). Remove dead or burned skin and other debris.

  • Wear a sterile glove to apply silver sulfadiazine. Apply a thin layer (about 1/16 inch) of silver sulfadiazine to the affected area(s). Keep the affected area(s) covered with the medicine at all times.

  • If silver sulfadiazine is rubbed off the affected area(s) by moving around or if it is washed off during bathing, showering, or the use of a whirlpool bath, reapply the medicine.

  • After silver sulfadiazine has been applied, the treated area(s) may be covered with a dressing or left uncovered as desired.

To help clear up your skin and/or burn infection completely, keep using silver sulfadiazine for the full time of treatment. You should keep using silver sulfadiazine until the burned area has healed or is ready for skin grafting. Do not miss any doses.


Dosing


The dose of silver sulfadiazine 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 silver sulfadiazine. 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 topical dosage form (cream):
    • For burn wound infections:
      • Adults and children 2 months of age and older—Use one or two times a day.

      • Premature and newborn infants up to 2 months of age—Use and dose must be determined by the doctor.



Missed Dose


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


Storage


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


Keep out of the reach of children.


Do not keep outdated medicine or medicine no longer needed.


Precautions While Using silver sulfadiazine


It is important that your doctor check your progress at regular visits.


If your skin infection or burn does not improve within a few days or weeks (for more serious burns or burns over larger areas), or if it becomes worse, check with your doctor.


silver sulfadiazine may rarely stain skin brownish gray.


silver sulfadiazine Side Effects


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


Check with your doctor as soon as possible if any of the following side effects occur:


Rare
  • Blistering, peeling or loosening of skin

  • bloody or cloudy urine

  • chills or fever

  • cough

  • decreased amount of urine or less frequent urination

  • increased sensitivity of skin to sunlight, especially in patients with burns on large areas

  • intense itching of burn wounds

  • pain at site of application

  • painful or difficult urination

  • red skin lesions, often with a purple center

  • shortness of breath

  • sore throat

  • sores, ulcers or white spots on lips or in mouth

  • swollen glands

  • unusual bleeding or bruising

  • unusual tiredness or weakness

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
  • Burning feeling on treated area(s)

Less common or rare
  • Brownish-gray skin discoloration

  • itching or skin rash

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: silver sulfadiazine Topical 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 silver sulfadiazine Topical resources


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


  • Silvadene Prescribing Information (FDA)

  • Silvadene MedFacts Consumer Leaflet (Wolters Kluwer)

  • Thermazene Prescribing Information (FDA)

  • silver sulfadiazine topical Concise Consumer Information (Cerner Multum)



Compare silver sulfadiazine Topical with other medications


  • Burns, External


Nicotrol Oral, Transdermal


Generic Name: nicotine (Oral route, Transdermal route)

NIK-oh-teen

Commonly used brand name(s)

In the U.S.


  • Habitrol

  • Nicoderm CQ

  • Nicotrol

In Canada


  • Nicoderm

Available Dosage Forms:


  • Patch, Extended Release

Therapeutic Class: Smoking Cessation Agent


Pharmacologic Class: Cholinergic


Uses For Nicotrol


Nicotine, in a flavored chewing gum, a lozenge, or a skin patch, is used to help you stop smoking. It is used for up to 12 weeks as part of a stop-smoking program. This program may include education, counseling, and psychological support.


As you chew nicotine gum or suck on the nicotine lozenge, nicotine passes through the lining of your mouth and into your blood stream. When you wear a nicotine patch, nicotine passes through your skin into your blood stream. This nicotine takes the place of nicotine that you would otherwise get from smoking. In this way, the withdrawal effects of not smoking are less severe. Then, as your body adjusts to not smoking, the use of the nicotine gum is decreased gradually until use is stopped altogether. For most brands of patches, the strength of the patch you use will be decreased over a few weeks until use is stopped. If you are using the brand of patch that is available in only one strength, use is stopped after the treatment period indicated on the label.


Children, pregnant women, and nonsmokers should not use nicotine gum or patches because of harmful effects.


Nicotine transdermal patches, gum, and lozenges are available without a prescription.


Before Using Nicotrol


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


Small amounts of nicotine can cause serious harm in children. Even nicotine patches that have been used still contain enough nicotine to cause problems in children. Although there is no specific information comparing use of nicotine in teenagers with use in other age groups, this medicine is not expected to cause different side effects or problems in nicotine-dependent teenagers than it does in adults.


Geriatric


Nicotine gum, lozenges, and patches have been used in a limited number of patients 60 years of age or older, and have not been shown to cause different side effects or problems in older people than in younger adults.


Pregnancy








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

Breast Feeding


Studies in women breastfeeding have demonstrated harmful infant effects. An alternative to this medication should be prescribed or you should stop breastfeeding while using this medicine.


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 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.


  • Clozapine

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:


  • Dental problems (with gum only) or

  • Diabetes, type 1 (sugar diabetes) or

  • Heart or blood vessel disease or

  • High blood pressure or

  • Inflammation of mouth or throat (with gum only) or

  • Irritated skin (with patches only) or

  • Overactive thyroid or

  • Pheochromocytoma (PCC) or

  • Stomach ulcer or

  • Stroke, recent or

  • Temporomandibular (jaw) joint disorder (TMJ) (with gum only)—Nicotine may make the condition worse.

Proper Use of nicotine

This section provides information on the proper use of a number of products that contain nicotine. It may not be specific to Nicotrol. Please read with care.


For patients using the chewing gum:


  • Nicotine gum usually comes with patient directions. Read the directions carefully before using this medicine.

  • Use nicotine gum exactly as directed on the label. Remember that it is also important to participate in a stop-smoking program during treatment. This may make it easier for you to stop smoking.

  • When you feel the urge to smoke, chew one piece of gum very slowly until you taste it or feel a slight tingling in your mouth. Stop chewing, and place (“park”) the chewing gum between your cheek and gum until the taste or tingling is almost gone. Then chew slowly until you taste it again. Continue chewing and stopping (“parking”) in this way for about 30 minutes in order to get the full dose of nicotine.

  • Do not chew too fast, do not chew more than one piece at a time, and do not chew more than one piece of gum within an hour. To do so may cause unpleasant side effects or an overdose. Also, slower chewing will reduce the possibility of belching.

  • You should not drink acidic beverages, such as citrus fruit juices, coffee, soft drinks, or tea within 15 minutes before or while chewing a piece of gum. The acid will prevent the nicotine from being released from the gum.

  • As your urge to smoke becomes less frequent, gradually reduce the number of pieces of gum you chew each day until you are chewing three to six pieces a day. This may be possible within 2 to 3 months.

  • Remember to carry nicotine gum with you at all times in case you feel the sudden urge to smoke. One cigarette may be enough to start you on the smoking habit again.

  • Using hard sugarless candy between doses of gum may help to relieve any nicotine cravings you may have between doses of gum.

For patients using the lozenge:


  • Nicotine lozenges usually come with patient directions. Read the directions carefully before using this medicine.

  • Use nicotine lozenges exactly as directed on the label. Remember that it is also important to participate in a stop-smoking program during treatment. This may make it easier for you to stop smoking.

  • Do not eat or drink for 15 minutes before using a nicotine lozenge.

  • When you feel the urge to smoke, suck one lozenge slowly until it dissolves. Do not bite or chew the lozenge like a hard candy. Do not swallow the lozenge.

  • As your urge to smoke becomes less frequent, gradually reduce the number of lozenges you use each day until you are using three to six lozenges a day. This should be possible within 12 weeks.

  • Remember to carry nicotine lozenges with you at all times in case you feel the sudden urge to smoke. One cigarette may be enough to start you on the smoking habit again.

For patients using the transdermal system (skin patch):


  • Nicotine patches usually come with patient instructions. Read them carefully before using this medicine. Nicotine patches will work only if applied correctly.

  • Remember that it is also important to participate in a stop-smoking program during treatment. This may make it easier for you to stop smoking.

  • Do not remove the patch from its sealed pouch until you are ready to put it on your skin. The patch may not work as well if it is unwrapped too soon.

  • Do not try to trim or cut the adhesive patch to adjust the dosage. Check with your doctor if you think the medicine is not working as it should.

  • Apply the patch to a clean, dry area of skin on your upper arm, chest, or back. Choose an area that is not very oily, has little or no hair, and is free of scars, cuts, burns, or any other skin irritations.

  • Press the patch firmly in place with the palm of your hand for about 10 seconds. Make sure there is good contact with your skin, especially around the edges of the patch.

  • The patch should stay in place even when you are showering, bathing, or swimming. Apply a new patch if one falls off.

  • Rinse your hands with plain water after you have finished applying the patch to your skin. Nicotine on your hands could get into your eyes and nose and cause stinging, redness, or more serious problems. Using soap to wash your hands will increase the amount of nicotine that passes through your skin.

  • After 16 or 24 hours, depending on which product you are using, remove the patch. Choose a different place on your skin to apply the next patch. Do not put a new patch in the same place for at least 1 week. Do not leave the patch on for more than 24 hours. It will not work as well after that time and it may irritate your skin.

  • After removing a used patch, fold the patch in half with the sticky sides together. Place the folded, used patch in its protective pouch or in aluminum foil. Make sure to dispose of it out of the reach of children and pets.

  • Try to change the patch at the same time each day. If you want to change the time when you put on your patch, just remove the patch you are wearing and put on a new patch. After that, apply a fresh patch at the new time each day.

  • Nicotine patches should be removed from the skin during strenuous exercise. If a patch is left on, too much nicotine may pass through your skin into your blood stream.

  • If you are using a 24-hour patch and begin having unusual dreams or disturbed sleep, you may take the patch off before going to bed and put a new one on after you wake up the next morning.

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 the oral dosage form (chewing gum):
    • To help you stop smoking:
      • Adults and teenagers—The usual dose is one piece of chewing gum every one to two hours for six weeks, one piece of chewing gum every two to four hours for three weeks, then one piece of chewing gum every four to eight hours for three weeks. You should not chew more than 24 pieces of gum a day.

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



  • For the oral dosage form (lozenge):
    • To help you stop smoking:
      • Adults and teenagers—The usual dose is suck slowly one lozenge until it dissolves every one to two hours for six weeks, suck one lozenge every two to four hours for three weeks, then suck one lozenge every four to eight hours for three weeks. You should not use more than 20 lozenges a day.

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



  • For the transdermal (stick-on) skin patch:
    • To help you stop smoking:
      • Adults and teenagers—The dose you receive will be based on your body weight, how often you have the urge to smoke, and the brand and strength of the patch you use. This dose will be provided on the package label.

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



Storage


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


Keep out of the reach of children.


Do not keep outdated medicine or medicine no longer needed.


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


Precautions While Using Nicotrol


Do not smoke during treatment with nicotine gum, lozenges, or patches because of the risk of nicotine overdose.


Nicotine should not be used in pregnancy. If there is a possibility you might become pregnant, you may want to use some type of birth control. If you think you may have become pregnant, stop using this medicine immediately and check with your doctor.


Nicotine products must be kept out of the reach of children and pets. Even nicotine patches that have been used still contain enough nicotine to cause problems in children. If a child chews or swallows one or more pieces of nicotine gum or lozenges, contact your doctor or poison control center at once. If a child puts on a nicotine patch or plays with a patch that is out of the sealed pouch, take it away from the child and contact your doctor or poison control center at once.


For patients using the chewing gum:


  • Do not chew more than 24 pieces of gum a day. Chewing too many pieces may be harmful because of the risk of overdose.

  • Do not use nicotine gum for longer than 12 weeks. To do so may result in physical dependence on the nicotine. If you feel the need to continue using the gum after 12 weeks, contact your doctor.

  • If the gum sticks to your dental work, stop using it and check with your medical doctor or dentist. Dentures or other dental work may be damaged because nicotine gum is stickier and harder to chew than ordinary gum.

For patients using the lozenges:


  • Do not use more than 20 lozenges a day. Sucking too many pieces may be harmful because of the risk of overdose.

  • Do not use nicotine lozenges for longer than 12 weeks. If you feel the need to continue using the lozenges after 12 weeks, contact your doctor.

For patients using the transdermal system (skin patch) :


  • Mild itching, burning, or tingling may occur when the patch is first applied, and should go away within 24 hours. After a patch is removed, the skin underneath it may be red. It should not remain red for more than a day. If you get a skin rash from the patch, or if the skin becomes swollen or very red, call your doctor. Do not put on a new patch. If you become allergic to the nicotine in the patch, you could get sick from using cigarettes or other products that contain nicotine.

  • Do not use nicotine patches for longer than 12 weeks if you have stopped smoking. If you feel the need to continue using nicotine patches after 12 weeks, contact your doctor.

  • The patch may cause skin burns when used during a procedure called magnetic resonance imaging (MRI). To prevent skin burns, make sure the patch is removed before having an MRI .

Nicotrol Side Effects


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


Check with your doctor as soon as possible if any of the following side effects occur:


More common
  • Injury or irritation to mouth, teeth, or dental work—with chewing gum only

Less common
  • High blood pressure

Rare
  • Fast or irregular heartbeat

  • hives, itching, rash, redness, or swelling of skin

Symptoms of overdose (may occur in the following order)
  • Nausea and/or vomiting

  • increased watering of mouth (severe)

  • abdominal or stomach pain (severe)

  • diarrhea (severe)

  • pale skin

  • cold sweat

  • headache (severe)

  • dizziness (severe)

  • disturbed hearing and vision

  • tremor

  • confusion

  • weakness (severe)

  • extreme exhaustion

  • fainting

  • low blood pressure

  • difficulty in breathing (severe)

  • fast, weak, or irregular heartbeat

  • convulsions (seizures)

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
  • Belching—with chewing gum and lozenges

  • headache (mild)

  • increased appetite

  • increased watering of mouth (mild)—with chewing gum only

  • jaw muscle ache—with chewing gum only

  • redness, itching, and/or burning at site of application of patch—usually stops within 24 hours

  • sore mouth or throat—with chewing gum only

Less common or rare
  • Abdominal or stomach pain (mild)

  • change in sense of taste

  • constipation

  • coughing (increased)

  • diarrhea

  • dizziness or lightheadedness (mild)

  • drowsiness

  • dryness of mouth

  • hiccups—with chewing gum and lozenges

  • hoarseness—with chewing gum only

  • indigestion (mild)

  • loss of appetite

  • menstrual pain

  • muscle or joint pain

  • nausea or vomiting (mild)

  • passing of gas

  • sweating (increased)

  • trouble in sleeping or unusual dreams

  • unusual irritability or nervousness

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: Nicotrol Oral, Transdermal 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 Nicotrol Oral, Transdermal resources


  • Nicotrol Oral, Transdermal Side Effects (in more detail)
  • Nicotrol Oral, Transdermal Use in Pregnancy & Breastfeeding
  • Nicotrol Oral, Transdermal Drug Interactions
  • Nicotrol Oral, Transdermal Support Group
  • 15 Reviews for Nicotrol Oral, Transdermal - Add your own review/rating


Compare Nicotrol Oral, Transdermal with other medications


  • Smoking Cessation


Thursday, June 28, 2012

Terumo



Pronunciation: IN-su-lin
Generic Name: Insulin
Brand Name: Examples include Terumo and BD


Terumo is used for:

Drawing and injecting insulin (and other solutions as determined by your doctor) into a preselected site of the body.


Do NOT use Terumo if:


  • you are allergic to any ingredient in Terumo

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



Before using Terumo:


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


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

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

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

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


Ask your health care provider if Terumo 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 Terumo:


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


  • To prepare your dose of insulin, pull the syringe plunger back to draw air into the syringe. The amount of air in the syringe should be equal to the number of units of insulin that you will be injecting. Insert the needle through the rubber cap of the insulin bottle and inject the air into the bottle. Invert the bottle and syringe. Pull back on the plunger to draw insulin into the syringe and measure the correct number of units of insulin. Check for any bubbles in the syringe. Eliminate any air bubbles found by tapping gently on the syringe.

  • Insulin can be injected into the abdomen, buttocks, thighs, and arms. First clean the skin at the injection site with an alcohol pad or rubbing alcohol. Pinch a fold of skin at the injection site with your fingers. The pinch should include at least 3 inches of skin. Insert the needle at a 45 to 90 degree angle. Then, inject the insulin, withdraw the needle, and press lightly on the skin.

  • Keep this product, as well as syringes and needles, out of the reach of children and pets. Do not reuse needles, syringes, or other materials. Ask your health care provider how to dispose of these materials after use. Follow all local rules for disposal.

  • If you miss a dose of your medicine, follow the missed dose instructions that came with your medicine. Contact your doctor if you are unsure what to do if you miss a dose of insulin.

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



Important safety information:


  • Do not reuse needles, syringes, or other materials.

  • Use a different site for each injection; about 1 inch away from previous injection sites, but in the same general area. Use all available sites in the same general area before switching to a different area. Do not use the same injection site more often than once every month or two.

  • If you have trouble seeing the small markings on the syringe, have someone help you. Also, let your doctor or pharmacist know about this problem. They can provide tools that are easier to read, special tools to help you fill the syringe, or prefilled syringes.


Possible side effects of Terumo:


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:



Redness, swelling, or itching at injection sites.



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).



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.


Proper storage of Terumo:

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


General information:


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

  • Terumo 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 Terumo. 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 Terumo resources


  • Terumo Use in Pregnancy & Breastfeeding
  • Terumo Drug Interactions
  • Terumo Support Group
  • 0 Reviews · Be the first to review/rate this drug


Tur-Bi-Cal



Generic Name: phenylephrine (Nasal route)

fen-il-EF-rin

Commonly used brand name(s)

In the U.S.


  • Neo-Synephrine

  • Nostril

  • Pretz-D

  • Rhinall

  • Tur-Bi-Cal

  • Vicks Sinex

Available Dosage Forms:


  • Solution

  • Gel/Jelly

  • Spray

Therapeutic Class: Decongestant


Pharmacologic Class: Sympathomimetic


Chemical Class: Alkylarylamine


Uses For Tur-Bi-Cal


Phenylephrine is used for the temporary relief of congestion or stuffiness in the nose caused by hay fever or other allergies, colds, or sinus trouble. It may also be used in ear infections to relieve congestion.


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


This medicine is available without a prescription.


Do not give any over-the-counter (OTC) cough and cold medicine to a baby or child under 4 years of age. Using these medicines in very young children might cause serious or possibly life-threatening side effects .


Before Using Tur-Bi-Cal


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


Children may be especially sensitive to the effects of nasal phenylephrine. This may increase the chance of side effects during treatment.


Do not give any over-the-counter (OTC) cough and cold medicine to a baby or child under 4 years of age. Using these medicines in very young children might cause serious or possibly life-threatening side effects .


Geriatric


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


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.


  • Rasagiline

  • Selegiline

Using this medicine with any of the following medicines is usually not recommended, but may be required in some cases. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines.


  • Amitriptyline

  • Amoxapine

  • Clomipramine

  • Desipramine

  • Dothiepin

  • Doxepin

  • Imipramine

  • Lofepramine

  • Nortriptyline

  • Opipramol

  • Protriptyline

  • Trimipramine

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:


  • Type 2 diabetes mellitus or

  • Heart or blood vessel disease or

  • High blood pressure or

  • Overactive thyroid—Nasal phenylephrine may make the condition worse

Proper Use of phenylephrine

This section provides information on the proper use of a number of products that contain phenylephrine. It may not be specific to Tur-Bi-Cal. Please read with care.


To use the nose drops:


  • Blow your nose gently. Tilt the head back while standing or sitting up, or lie down on a bed and hang head over the side. Place the drops into each nostril and keep the head tilted back for a few minutes to allow the medicine to spread throughout the nose.

  • Rinse the dropper with hot water and dry with a clean tissue. Replace the cap right after use.

  • To avoid spreading the infection, do not use the container for more than one person.

To use the nose spray:


  • Blow your nose gently. With the head upright, spray the medicine into each nostril. Sniff briskly while squeezing the bottle quickly and firmly. For best results, spray once or twice into each nostril and wait 3 to 5 minutes to allow the medicine to work. Then, blow your nose gently and thoroughly. Repeat until the complete dose is used.

  • Rinse the tip of the spray bottle with hot water, taking care not to suck water into the bottle, and dry with a clean tissue. Replace the cap right after use.

  • To avoid spreading the infection, do not use the container for more than one person.

To use the nose jelly:


  • Blow your nose gently. Wash your hands before applying the medicine. With your finger, place a small amount of jelly (about the size of a pea) up each nostril. Sniff it well back into the nose.

  • Wipe the tip of the tube with a clean, damp tissue and replace the cap right after use.

Use this medicine only as directed. Do not use more of it, do not use it more often, and do not use it for longer than 3 days without first checking with your doctor. To do so may make your runny or stuffy nose worse and may also increase the chance of side effects.


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 stuffy nose:
    • For nose jelly dosage form:
      • Adults—Use a small amount in the nose every three or four hours as needed.

      • Children—Use is not recommended.


    • For nose drops dosage form:
      • Adults and children 12 years of age and older—Use two or three drops of a 0.25 to 0.5% solution in the nose every four hours as needed.

      • Children 6 to 12 years of age—Use two or three drops of a 0.25% solution in the nose every four hours as needed.

      • Children 4 to 6 years of age—Use two or three drops of a 0.125 or 0.16% solution in the nose every four hours as needed.

      • Children and infants up to 4 years of age—Use is not recommended .


    • For nose spray dosage form:
      • Adults and children 12 years of age and older—Use two or three sprays of a 0.25 to 0.5% solution in the nose every four hours as needed.

      • Children 6 to 12 years of age—Use two or three sprays of a 0.25% solution in the nose every four hours as needed.

      • Children 4 to 6 years of age—Use and dose must be determined by your doctor.

      • Children and infants up to 4 years of age—Use is not recommended .



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.


Tur-Bi-Cal Side Effects


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


Check with your doctor as soon as possible if any of the following side effects occur:


Symptoms of too much medicine being absorbed into the body

Note: The above side effects are more likely to occur in children because there is a greater chance that too much of this medicine may be absorbed into the body.


  • Fast, irregular, or pounding heartbeat

  • headache or dizziness

  • increased sweating

  • nervousness

  • paleness

  • trembling

  • trouble in sleeping

  • Increase in runny or stuffy nose

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:


  • Burning, dryness, or stinging of inside of nose

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


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



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


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


More Tur-Bi-Cal resources


  • Tur-Bi-Cal Use in Pregnancy & Breastfeeding
  • Tur-Bi-Cal Drug Interactions
  • Tur-Bi-Cal Support Group
  • 4 Reviews for Tur-Bi-Cal - Add your own review/rating


Compare Tur-Bi-Cal with other medications


  • Nasal Congestion


Wednesday, June 27, 2012

Salicylic Acid Film-Forming Liquid


Pronunciation: SAL-i-SIL-ik AS-id
Generic Name: Salicylic Acid
Brand Name: Virasal


Salicylic Acid Film-Forming Liquid is used for:

Treating and removing common warts and plantar warts. It may also be used for other conditions as determined by your doctor.


Salicylic Acid Film-Forming Liquid is a topical salicylate. It works by causing the skin to swell, soften, and then slough or peel in areas where it is applied.


Do NOT use Salicylic Acid Film-Forming Liquid if:


  • you are allergic to any ingredient in Salicylic Acid Film-Forming Liquid

  • you have diabetes or poor blood circulation

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



Before using Salicylic Acid Film-Forming Liquid:


Some medical conditions may interact with Salicylic Acid Film-Forming Liquid. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:


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

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

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

  • if you have had a severe allergic reaction (eg, severe rash, hives, difficulty breathing, dizziness) to aspirin or a nonsteroidal anti-inflammatory drug (NSAID) (eg, ibuprofen, naproxen, celecoxib)

  • if you have liver or kidney problems, a skin infection, or skin irritation

Some MEDICINES MAY INTERACT with Salicylic Acid Film-Forming Liquid. Tell your health care provider if you are taking any other medicines, especially any of the following:


  • Anticoagulants, (eg, heparin, warfarin), aspirin, methotrexate, or sulfonylureas (eg, glipizide) because the risk of side effects may be increased by Salicylic Acid Film-Forming Liquid

This may not be a complete list of all interactions that may occur. Ask your health care provider if Salicylic Acid Film-Forming Liquid 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 Salicylic Acid Film-Forming Liquid:


Use Salicylic Acid Film-Forming Liquid as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • Soak the affected area in warm water for about 5 minutes. Remove any loosened skin by gently rubbing with a brush, washcloth, or emery board. Dry thoroughly. Using the brush applicator supplied with Salicylic Acid Film-Forming Liquid, apply Salicylic Acid Film-Forming Liquid to the entire wart surface. Be careful not to apply Salicylic Acid Film-Forming Liquid to the surrounding skin. If your doctor directs you to apply Salicylic Acid Film-Forming Liquid 2 times to the affected area, allow the first application to dry before applying the second application.

  • Unless your hands are being treated, be sure to wash your hands after each application.

  • If you miss a dose of Salicylic Acid Film-Forming Liquid, 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 Salicylic Acid Film-Forming Liquid.



Important safety information:


  • Salicylic Acid Film-Forming Liquid is for external use only. Avoid getting Salicylic Acid Film-Forming Liquid in your eyes, nose, or mouth, or on the genitals. If contact with your eyes occurs, flush with water for 15 minutes. Do not inhale the vapors of Salicylic Acid Film-Forming Liquid.

  • Do NOT use Salicylic Acid Film-Forming Liquid longer or more often than recommended by your doctor.

  • Visible improvement will normally occur during the first or second week of treatment with Salicylic Acid Film-Forming Liquid. It may take 4 to 6 weeks before the wart is completely removed. Discuss any questions or concerns with your doctor.

  • Be sure to apply Salicylic Acid Film-Forming Liquid only to the affected area and not to normal, healthy skin.

  • Do not use Salicylic Acid Film-Forming Liquid on skin that is irritated, infected, or reddened.

  • Do not use Salicylic Acid Film-Forming Liquid on open skin wounds, moles, birthmarks, genital warts, warts on the face, or warts growing hair.

  • Do not use any other medicines or drying products on your skin unless your doctor instructs you otherwise.

  • Salicylic Acid Film-Forming Liquid may interfere with certain lab test results. Make sure your doctor and lab personnel know you are using Salicylic Acid Film-Forming Liquid.

  • Salicylic Acid Film-Forming Liquid is extremely flammable. Do not store or use Salicylic Acid Film-Forming Liquid near a fire or other open flame.

  • Salicylic Acid Film-Forming Liquid may be harmful if swallowed. If you may have taken Salicylic Acid Film-Forming Liquid by mouth, contact your local poison control center or emergency room immediately.

  • Salicylic Acid Film-Forming Liquid contains a salicylate, which has been linked to Reye syndrome. Do not use Salicylic Acid Film-Forming Liquid on children or teenagers during or after chickenpox, flu, or other viral infections without checking with your doctor or pharmacist.

  • Caution is advised when using Salicylic Acid Film-Forming Liquid in CHILDREN; they may be more sensitive to its effects.

  • PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Salicylic Acid Film-Forming Liquid while you are pregnant. It is not known if Salicylic Acid Film-Forming Liquid is found in breast milk. If you are or will be breast-feeding while you are using Salicylic Acid Film-Forming Liquid, check with your doctor or pharmacist to discuss the risks to your baby.


Possible side effects of Salicylic Acid Film-Forming Liquid:


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:



Dry, peeling, red, or scaling skin.



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

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); severe skin irritation.



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


See also: Salicylic Acid 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 agitation; diarrhea; dizziness; loss of appetite; loss of hearing; mental disturbances; nausea; rapid or difficult breathing; ringing in the ears; seizures; sluggishness; vomiting; yellowing of the skin or eyes.


Proper storage of Salicylic Acid Film-Forming Liquid:

Store Salicylic Acid Film-Forming Liquid at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Keep the bottle tightly capped when not in use. Store away from heat, moisture, and light. Do not freeze. Do not store in the bathroom. Keep Salicylic Acid Film-Forming Liquid out of the reach of children and away from pets.


General information:


  • If you have any questions about Salicylic Acid Film-Forming Liquid, please talk with your doctor, pharmacist, or other health care provider.

  • Salicylic Acid Film-Forming Liquid 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 Salicylic Acid Film-Forming Liquid. 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 Salicylic Acid resources


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


Compare Salicylic Acid with other medications


  • Acne
  • Dermatological Disorders
  • Warts


Monday, June 25, 2012

Tenuate Dospan


Generic Name: diethylpropion (dye eth ill PROE pee on)

Brand Names: Tenuate


What is Tenuate Dospan (diethylpropion)?

Diethylpropion is an appetite suppressant similar to an amphetamine. Diethylpropion stimulates your central nervous system (nerves and brain), which increases your heart rate and blood pressure and decreases your appetite.


Diethylpropion is used as together with diet and exercise to treat of obesity.


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


What is the most important information I should know about Tenuate Dospan (diethylpropion)?


Taking diethylpropion in combination with other diet pills or appetite suppressants can cause serious or life threatening medical problems. Do not use any other diet medications while taking diethylpropion, unless your doctor tells you to. You should not take this medication if you are allergic to diethylpropion or if you have pulmonary hypertension, severe coronary artery disease, glaucoma, overactive thyroid, uncontrolled high blood pressure, a history of drug or alcohol addiction, if you are agitated, or if you are taking any other diet pills. Do not use diethylpropion 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.

Before you take diethylpropion, tell your doctor if you have a heart murmur, heart valve disorder, heart rhythm disorder, epilepsy, or if you have taken other diet pills within the past 12 months.


This medication may cause blurred vision and may impair your thinking or reactions. Diethylpropion may also cause restless feelings that can hide the symptoms of extreme tiredness. Be careful if you drive or do anything that requires you to be alert and able to see clearly. Diethylpropion may be habit-forming and should be used only by the person it was prescribed for. Keep the medication in a secure place where others cannot get to it. Do not stop using diethylpropion suddenly after long-term use, or you could have unpleasant withdrawal symptoms. Ask your doctor how to avoid withdrawal symptoms when you stop using diethylpropion.

What should I discuss with my healthcare provider before taking Tenuate Dospan (diethylpropion)?


Taking diethylpropion in combination with other diet pills or appetite suppressants can cause serious or life threatening medical problems. Do not use any other diet medications while taking diethylpropion, unless your doctor tells you to. You should not take this medication if you are allergic to diethylpropion or similar medicines (stimulants, diet pills, cold or allergy medicines), or if you have:

  • pulmonary hypertension;




  • severe coronary artery disease (hardened arteries);




  • glaucoma;




  • overactive thyroid;




  • severe or uncontrolled high blood pressure;




  • a history of drug or alcohol addiction;




  • if you are in an agitated state; or




  • if you are taking any other appetite suppressants or diet pills.




Do not use diethylpropion 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.

To make sure you can safely take diethylpropion, tell your doctor if you have any of these other conditions:



  • a heart murmur, heart valve disorder, or heart rhythm disorder;




  • epilepsy or other seizure disorder; or




  • if you have taken other diet pills within the past 12 months.




Diethylpropion may be habit forming and should be used only by the person it was prescribed for. Never share diethylpropion with another person, especially someone with a history of drug abuse or addiction. Keep the medication in a place where others cannot get to it. FDA pregnancy category B. Diethylpropion is not expected to harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant during treatment. Diethylpropion can pass into breast milk and may harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby. Do not give this medicine to a child younger than 16 years old.

How should I take Tenuate Dospan (diethylpropion)?


Take exactly as prescribed. Never take diethylpropion in larger amounts, or for longer than recommended by your doctor. Follow the directions on your prescription label. Tell your doctor if the medicine seems to stop working as well in relieving your hunger.


Tell your doctor if you do not lose at least 4 pounds after taking the medication for 4 weeks along with a low calorie diet.

Diethylpropion is usually taken once a day in the midmorning.


Do not crush, chew, or break a controlled release tablet. Swallow it whole. Breaking or opening the pill may cause too much of the drug to be released at one time. Store at room temperature away from moisture and heat.

Keep track of the amount of medicine used from each new bottle. Diethylpropion is a drug of abuse and you should be aware if anyone is using your medicine improperly or without a prescription.


What happens if I miss a dose?


Take the missed dose as soon as you remember. Skip the missed dose if it is already evening. Wait until the next morning to take 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.

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


What should I avoid while taking Tenuate Dospan (diethylpropion)?


This medication may cause blurred vision and may impair your thinking or reactions. Diethylpropion may also cause restless feelings that can hide the symptoms of extreme tiredness. Be careful if you drive or do anything that requires you to be alert and able to see clearly. Drinking alcohol can increase certain side effects of diethylpropion.

Tenuate Dospan (diethylpropion) side effects


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

  • fast, pounding, or uneven heartbeats;




  • chest pain, feeling short of breath (even with mild exertion);




  • feeling like you might pass out;




  • swelling in your ankles or feet;




  • confusion, hallucinations, unusual thoughts or behavior;




  • seizure (convulsions);




  • muscle movements you cannot control; or




  • sudden numbness or weakness, especially on one side of the body.



Less serious side effects may include:



  • nausea, vomiting, diarrhea, upset stomach;




  • headache, blurred vision;




  • feeling nervous, anxious, or jittery;




  • sleep problems (insomnia);




  • dizziness, drowsiness, tired feeling;




  • depressed mood;




  • dry mouth, unpleasant taste in your mouth;




  • decreased sex drive; or




  • mild itching or 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 Tenuate Dospan (diethylpropion)?


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



  • insulin or oral diabetes medication;




  • blood pressure medication; or




  • stimulants, cold or allergy medicines, ADHD (attention deficit hyperactivity disorder) medicine such as Adderall or Ritalin.



This list is not complete and other drugs may interact with diethylpropion. 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 Tenuate Dospan resources


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


  • Tenuate Dospan Advanced Consumer (Micromedex) - Includes Dosage Information

  • Tenuate Dospan Controlled-Release Tablets MedFacts Consumer Leaflet (Wolters Kluwer)

  • Diethylpropion Prescribing Information (FDA)

  • Diethylpropion MedFacts Consumer Leaflet (Wolters Kluwer)

  • Diethylpropion Hydrochloride Monograph (AHFS DI)

  • Tenuate Consumer Overview



Compare Tenuate Dospan with other medications


  • Obesity


Where can I get more information?


  • Your pharmacist can provide more information about diethylpropion.

See also: Tenuate Dospan side effects (in more detail)



Tuesday, June 19, 2012

Sensipar



Pronunciation: SIN-a-KAL-set
Generic Name: Cinacalcet
Brand Name: Sensipar


Sensipar is used for:

Treating an overactive parathyroid gland in dialysis patients with chronic kidney disease. It is also used to treat high blood calcium levels in patients with parathyroid cancer. It is also used to treat severe high blood calcium levels in patients with an overactive parathyroid gland who are unable to undergo surgery to remove the parathyroid gland. It may also be used for other conditions as determined by your doctor.


Sensipar is a calcimimetic agent. It works by causing the parathyroid to produce less parathyroid hormone (PTH), which helps to lower blood calcium levels.


Do NOT use Sensipar if:


  • you are allergic to any ingredient in Sensipar

  • you have low blood calcium levels

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



Before using Sensipar:


Some medical conditions may interact with Sensipar. 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 liver problems

  • if you have a history of low blood pressure; fast, slow, or irregular heartbeat; heart problems (eg, heart failure); bone problems; low blood calcium levels; or seizures

  • if you are taking medicine to prevent seizures

Some MEDICINES MAY INTERACT with Sensipar.


  • Azole antifungals (eg, itraconazole, ketoconazole) or erythromycin because they may increase the risk of Sensipar's side effects

  • Carvedilol, flecainide, metoprolol, thioridazine, tricyclic antidepressants (eg, amitriptyline), or vinblastine because the risk of their side effects may be increased by Sensipar

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


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


  • Take Sensipar by mouth with food or shortly after a meal.

  • Swallow Sensipar whole. Do not break, crush, or chew before swallowing.

  • If you miss a dose of Sensipar, 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 Sensipar.



Important safety information:


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

  • Lab tests, including calcium, phosphorous, and parathyroid hormone blood levels, may be performed while you take Sensipar. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

  • Sensipar 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 Sensipar while you are pregnant. It is not known if Sensipar is found in breast milk. Do not breast-feed while taking Sensipar.


Possible side effects of Sensipar:


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



Constipation; diarrhea; dizziness; headache; loss of appetite; nausea; tiredness; vomiting; weakness.



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

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue; unusual hoarseness); burning, numbness, or tingling of the skin; chest pain; confusion; decreased urination; depression; fainting; fast, slow, or irregular heartbeat; joint pain; muscle aches, cramps, pain, spasms, or weakness; seizures; severe or persistent dizziness or headache; severe or persistent nausea or vomiting; shortness of breath; swelling of the hands or feet; tremors; unusual bone pain; unusual thirst; unusual tiredness or weakness; very dry mouth.



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: Sensipar 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 burning, numbness, or tingling of the skin; muscle aches, cramps, pain, spasms, or weakness; seizures.


Proper storage of Sensipar:

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


General information:


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

  • Sensipar 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 Sensipar. 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 Sensipar resources


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


  • Sensipar Prescribing Information (FDA)

  • Sensipar Monograph (AHFS DI)

  • Sensipar Advanced Consumer (Micromedex) - Includes Dosage Information

  • Sensipar Consumer Overview



Compare Sensipar with other medications


  • Hypercalcemia of Malignancy
  • Secondary Hyperparathyroidism