Monday, October 8, 2012

Topisulf


Generic Name: sulfacetamide sodium and sulfur topical (SUL fa SEET a mide SOE dee um and SUL fur TOP i kal)

Brand Names: Avar Cleanser, Avar Gel, Avar LS Cleanser, Avar-E, Avar-E Emollient, Avar-E Green, Avar-e LS, BP 10-Wash, Clarifoam EF, Clenia Emollient Cream, Clenia Foaming Wash, Plexion , Plexion Cleanser, Plexion Cleansing Cloths, Plexion SCT, Prascion, Prascion Cleanser, Prascion FC Cloths, Prascion RA, Rosac, Rosac Wash, Rosaderm Cleanser, Rosanil Cleanser, Rosula, SE 10-5 SS, Sulfacet-R, Sulfatol C, Sulfatol SS, SulZee Wash, Sumaxin, Sumaxin TS, Sumaxin Wash, Suphera, Topisulf, Zencia Wash, Zetacet


What is Topisulf (sulfacetamide sodium and sulfur topical)?

Sulfacetamide sodium and sulfur are antibiotic that fight bacteria.


The combination of sulfacetamide sodium and sulfur topical (for the skin) is used to treat acne, rosacea, and seborrheic dermatitis (a red, flaking skin rash).


Sulfacetamide sodium and sulfur topical may also be used for purposes not listed in this medication guide.


What is the most important information I should know about Topisulf (sulfacetamide sodium and sulfur topical)?


You should not use this medication if you are allergy to sulfa drugs or if you have kidney disease. Avoid getting this medication in your eyes, nose, or mouth. If this does happen, rinse with water.

Do not cover the treated skin area unless your doctor has told you to.


Avoid using other medications on the areas you treat with sulfacetamide sodium and sulfur topical unless you doctor tells you to.

What should I discuss with my healthcare provider before using Topisulf (sulfacetamide sodium and sulfur topical)?


You should not use this medication if you are allergy to sulfa drugs or if you have kidney disease.

To make sure you can safely use this medication, tell your doctor about all of your medical conditions.


FDA pregnancy category C. It is not known whether sulfacetamide sodium and sulfur 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 sulfacetamide sodium and sulfur 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.

How should I use Topisulf (sulfacetamide sodium and sulfur topical)?


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.


Wash your hands before and after applying this medication.

Do not cover the treated skin area unless your doctor has told you to.


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


Store at room temperature away from moisture and heat.

What happens if I miss a dose?


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.


What should I avoid while using Topisulf (sulfacetamide sodium and sulfur topical)?


Avoid getting this medication in your eyes, nose, or mouth. If this does happen, rinse with water. Do not use sulfacetamide sodium and sulfur topical on sunburned, windburned, dry, chapped, irritated, or broken skin.

Avoid using other medications on the areas you treat with sulfacetamide sodium and sulfur topical unless you doctor tells you to.


Topisulf (sulfacetamide sodium and sulfur topical) 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 this medication and call your doctor at once if you have a serious side effect such as:

  • new or worsening skin rash;




  • joint pain;




  • fever; or




  • mouth sores.



Less serious side effects may include redness, warmth, swelling, itching, stinging, burning, or irritation of treated skin.


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 Topisulf (sulfacetamide sodium and sulfur topical)?


It is not likely that other drugs you take orally or inject will have an effect on topically applied sulfacetamide sodium and sulfur. 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 Topisulf resources


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


  • Avar LS Cleanser MedFacts Consumer Leaflet (Wolters Kluwer)

  • Clarifoam EF Foam MedFacts Consumer Leaflet (Wolters Kluwer)

  • Clarifoam EF Prescribing Information (FDA)

  • Plexion Prescribing Information (FDA)

  • Plexion Cleansing Cloths MedFacts Consumer Leaflet (Wolters Kluwer)

  • Plexion SCT Cream MedFacts Consumer Leaflet (Wolters Kluwer)

  • Plexion TS Emulsion MedFacts Consumer Leaflet (Wolters Kluwer)

  • Prascion Cleanser Prescribing Information (FDA)

  • Rosac Cream MedFacts Consumer Leaflet (Wolters Kluwer)

  • Rosaderm Cleanser Prescribing Information (FDA)

  • Rosanil Cleanser Prescribing Information (FDA)

  • Rosula Foam MedFacts Consumer Leaflet (Wolters Kluwer)

  • Rosula Prescribing Information (FDA)

  • Rosula Cleanser Emulsion MedFacts Consumer Leaflet (Wolters Kluwer)

  • Sumadan MedFacts Consumer Leaflet (Wolters Kluwer)

  • Sumadan Wash Prescribing Information (FDA)

  • Sumaxin Wash MedFacts Consumer Leaflet (Wolters Kluwer)

  • Sumaxin Wash Prescribing Information (FDA)

  • Zencia Wash Prescribing Information (FDA)



Compare Topisulf with other medications


  • Acne
  • Rosacea
  • Seborrheic Dermatitis


Where can I get more information?


  • Your pharmacist can provide more information about sulfacetamide sodium and sulfur topical.

See also: Topisulf side effects (in more detail)



Sunday, October 7, 2012

Spectinomycin


Generic Name: spectinomycin (speck TIH no my sin)

Brand Names: Trobicin


What is spectinomycin?

Spectinomycin is an antibiotic. It fights bacteria in the body.


Spectinomycin is used in the treatment of gonorrhea.


Spectinomycin may also be used for purposes other than those listed here.


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


Do not take spectinomycin without first talking to your doctor if you have had an allergic reaction to it in the past.

What should I discuss with my health care provider before taking spectinomycin?


Do not take spectinomycin without first talking to your doctor if you have had an allergic reaction to it in the past.

Before taking spectinomycin, talk to your doctor if you have liver or kidney disease or other serious medical problems. You may not be able to use spectinomycin, or you may require a dosage adjustment or special monitoring during treatment.


Spectinomycin is in the FDA pregnancy category B. This means that it is not expected to be harmful to an unborn baby. Do not use spectinomycin without first talking to your doctor if you are pregnant or could become pregnant during treatment. It is not known whether spectinomycin passes into breast milk. Do not take spectinomycin without first talking to your doctor if you are breast-feeding a baby.

How should I take spectinomycin?


Spectinomycin will be administered as an injection by a healthcare provider.


What happens if I miss a dose?


Since spectinomycin is usually administered as a single injection, missing dose is not likely to occur.


What happens if I overdose?


Seek emergency medical attention if an overdose of spectinomycin is suspected.

Symptoms of a spectinomycin overdose are not known.


What should I avoid while taking spectinomycin?


There are no restrictions on food, beverages, or activities during treatment with spectinomycin unless otherwise directed by your doctor.


Spectinomycin side effects


If you experience a rare but serious allergic reaction (difficulty breathing; closing of the throat; swelling of the lips, tongue, or face; or hives), stop taking spectinomycin and seek emergency medical attention.

Other less serious side effects may be more likely to occur. Continue to use spectinomycin and talk to your doctor if you experience:



  • nausea;




  • dizziness;




  • soreness at the injection site; or




  • fever.



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


What other drugs will affect spectinomycin?


Talk to your doctor and pharmacist before taking spectinomycin if you are taking any other prescription or over-the-counter medicines, including vitamins, minerals, and herbal products.



More spectinomycin resources


  • Spectinomycin Drug Interactions
  • Spectinomycin Support Group
  • 0 Reviews for Spectinomycin - Add your own review/rating


  • spectinomycin Intramuscular Advanced Consumer (Micromedex) - Includes Dosage Information

  • Spectinomycin Professional Patient Advice (Wolters Kluwer)

  • Spectinomycin Hydrochloride Monograph (AHFS DI)

  • Trobicin Prescribing Information (FDA)



Compare spectinomycin with other medications


  • Gonococcal Infection
  • Gonococcal Infection, Disseminated
  • Gonococcal Infection, Uncomplicated


Where can I get more information?


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

What does my medication look like?


Spectinomycin is available with a prescription under then brand name Trobicin. Other brand or generic formulations may also be available. Ask your pharmacist any questions you have about this medication, especially if it is new to you.




Friday, October 5, 2012

Suclor


Generic Name: chlorpheniramine and pseudoephedrine (klor fen EER a meen and soo doe e FED rin)

Brand Names: AccuHist Drops, Allerest Maximum Strength, Brexin L.A., Colfed-A, D-Amine-SR, Dayquil Allergy, Deconamine, Dicel, Dicel Chewables, Dura-Tap/PD, Durafed, Duratuss DA, Dynahist-ER Pediatric, Genaphed Plus, Histade, Histex, Kronofed-A, Kronofed-A-Jr, LoHist-D, Mintex, Neutrahist Drops, Re2+30, Rescon-Ed, Suclor, SudaHist, Sudal-12 Chewable, Sudal-12 Tannate, Sudogest Cold & Allergy, SudoGest Sinus & Allergy, Tavist-DA, Triaminic Cold and Allergy, Triaminic Softchew Cold and Allergy, Triaminic Softchews Allergy Runny Nose and Congestion


What is Suclor (chlorpheniramine and pseudoephedrine)?

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


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


The combination of chlorpheniramine and pseudoephedrine is used to treat symptoms of the common cold or seasonal allergies, including sneezing, runny or stuffy nose, and itchy, watery eyes.


Chlorpheniramine and pseudoephedrine may also be used for other purposes not listed in this medication guide.


What is the most important information I should know about Suclor (chlorpheniramine and pseudoephedrine)?


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


Do not use chlorpheniramine and pseudoephedrine 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. You should not use this medication if you are allergic to chlorpheniramine or pseudoephedrine, or if you have severe high blood pressure or coronary artery disease, narrow-angle glaucoma, a stomach ulcer, or if you are unable to urinate.

Do not use this medication during an asthma attack.


This medication may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert. Drinking alcohol can increase certain side effects of chlorpheniramine and pseudoephedrine. Older adults may be more likely to have side effects from this medicine. Do not give this medication to a child younger than 4 years old. Always ask a doctor before giving a cough or cold medicine to a child. Death can occur from the misuse of cough and cold medicines in very young children.

Talk with your doctor if your symptoms do not improve after 7 days of treatment, or if you have a fever with a headache, cough, or skin rash.


What should I discuss with my healthcare provider before taking Suclor (chlorpheniramine and pseudoephedrine)?


Do not use chlorpheniramine and pseudoephedrine 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. You should not use this medication if you are allergic to chlorpheniramine or pseudoephedrine, or if you have:

  • severe or uncontrolled high blood pressure;




  • severe coronary artery disease;




  • narrow angle glaucoma;




  • a stomach ulcer;




  • if you are unable to urinate; or




  • if you are having an asthma attack.



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


  • kidney disease;

  • liver disease;


  • diabetes;




  • glaucoma;




  • circulation problems;




  • heart disease or high blood pressure;




  • overactive thyroid;




  • a seizure disorder such as epilepsy;




  • asthma, emphysema or chronic bronchitis; or




  • urination problems or an enlarged prostate.




FDA pregnancy category C. It is not known whether chlorpheniramine and pseudoephedrine 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 chlorpheniramine and pseudoephedrine 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. Older adults may be more likely to have side effects from this medicine.

Artificially sweetened liquid cold medicine may contain phenylalanine. If you have phenylketonuria (PKU), check the medication label to see if the product contains phenylalanine.


How should I take Suclor (chlorpheniramine and pseudoephedrine)?


Use exactly as directed on the label, or as prescribed by your doctor. Do not use in larger or smaller amounts or for longer than recommended. Cold medicine is usually taken only for a short time until your symptoms clear up.


Do not give this medication to a child younger than 4 years old. Always ask a doctor before giving a cough or cold medicine to a child. Death can occur from the misuse of cough and cold medicines in very young children. Do not crush, chew, break, or open an extended-release tablet or capsule. Swallow it whole. Breaking or opening the pill may cause too much of the drug to be released at one time.

The chewable tablet must be chewed before swallowing.


Measure liquid medicine with a special dose-measuring spoon or medicine cup, not with a regular table spoon. If you do not have a dose-measuring device, ask your pharmacist for one.


Talk with your doctor if your symptoms do not improve after 7 days of treatment, or if you have a fever with a headache, cough, or skin rash.


This medication can cause unusual results with allergy skin tests. Tell any doctor who treats you that you are taking an antihistamine.


If you need surgery, tell the surgeon ahead of time if you have taken a cold medicine within the past few days.


Store at room temperature away from moisture and heat.

What happens if I miss a dose?


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


What happens if I overdose?


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

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


What should I avoid while taking Suclor (chlorpheniramine and pseudoephedrine)?


This medication may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert. Drinking alcohol can increase certain side effects of chlorpheniramine and pseudoephedrine. Ask a doctor or pharmacist before using any other cold, allergy, or sleep medicine. Chlorpheniramine and pseudoephedrine are contained in many combination medicines. Taking certain products together can cause you to get too much of a certain drug. Check the label to see if a medicine contains an antihistamine or decongestant.

Avoid taking this medication if you also take diet pills, caffeine pills, or other stimulants (such as ADHD medications). Taking a stimulant together with a decongestant can increase your risk of unpleasant side effects.


Suclor (chlorpheniramine and pseudoephedrine) side effects


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

  • fast or pounding heartbeats;




  • confusion, hallucinations, unusual thoughts or behavior;




  • severe dizziness, anxiety, restless feeling, nervousness;




  • urinating less than usual or not at all;




  • easy bruising or bleeding, unusual weakness; or




  • seizure (black-out or convulsions).



Less serious side effects may include:



  • blurred vision;




  • dry nose or mouth;




  • nausea, stomach pain, constipation, loss of appetite;




  • dizziness, drowsiness;




  • problems with memory or concentration;




  • ringing in your ears; or




  • feeling restless or excited (especially in children).



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 Suclor (chlorpheniramine and pseudoephedrine)?


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

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



  • mecamylamine (Inversine);




  • methyldopa (Aldomet);




  • reserpine;




  • a beta-blocker such as atenolol (Tenormin, Tenoretic), carvedilol (Coreg), labetalol (Normodyne, Trandate), metoprolol (Lopressor, Toprol), nadolol (Corgard), propranolol (Inderal, InnoPran), sotalol (Betapace), and others;




  • a barbiturate such as butabarbital (Butisol), secobarbital (Seconal), pentobarbital (Nembutal), or phenobarbital (Solfoton); or




  • an antidepressant such as amitriptyline (Elavil, Vanatrip), doxepin (Sinequan), nortriptyline (Pamelor), and others.



This list is not complete and other drugs may interact with chlorpheniramine and pseudoephedrine. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor.



More Suclor resources


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


  • AccuHist Drops Prescribing Information (FDA)

  • Biohist LA Sustained-Release Tablets MedFacts Consumer Leaflet (Wolters Kluwer)

  • Deconamine MedFacts Consumer Leaflet (Wolters Kluwer)

  • Deconamine SR Controlled-Release Capsules MedFacts Consumer Leaflet (Wolters Kluwer)

  • Duotan Suspension MedFacts Consumer Leaflet (Wolters Kluwer)

  • QDALL 24-Hour Sustained-Release Capsules MedFacts Consumer Leaflet (Wolters Kluwer)



Compare Suclor with other medications


  • Hay Fever
  • Sinusitis


Where can I get more information?


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



Sorilux Topical


Generic Name: calcipotriene (Topical route)

kal-si-poe-TRYE-een

Commonly used brand name(s)

In the U.S.


  • Calcitrene

  • Dovonex

  • Sorilux

Available Dosage Forms:


  • Cream

  • Foam

  • Ointment

  • Solution

Therapeutic Class: Antipsoriatic


Pharmacologic Class: Vitamin D3, Synthetic


Uses For Sorilux


Calcipotriene is used on the skin and scalp to treat plaque psoriasis. It is a form of vitamin D that works by changing how the skin cells are made in the areas affected by psoriasis.


This medicine is available only with your doctor's prescription.


Before Using Sorilux


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 have not been performed on the relationship of age to the effects of calcipotriene in the pediatric population. Safety and efficacy have not been established.


Geriatric


Appropriate studies performed to date have not demonstrated geriatric-specific problems that would limit the usefulness of calcipotriene in the elderly.


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


  • Hypercalcemia (high calcium in the blood)—Should not be used in patients with this condition.

  • Skin irritation in psoriasis areas—May make this condition worse.

Proper Use of calcipotriene

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


It is very important that you use this medicine only as directed by your doctor. Do not use more of it, do not use it more often, and do not use it for a longer time than your doctor ordered. To do so may cause unwanted side effects or skin irritation.


This medicine should only be used on the skin. Do not get it in your eyes, nose, mouth, or vagina. Do not use it on skin areas that have cuts, scrapes, or burns. If it does get on these areas, rinse it off right away with water.


To help clear up your skin problem completely, it is very important that you keep using calcipotriene for the full time of treatment. Do not miss any doses.


This medicine should only be used for skin conditions that your doctor is treating. Check with your doctor before using it for other skin conditions, especially if you think that a skin infection may be present. This medicine should not be used to treat certain kinds of skin infections or conditions, such as severe burns.


To use the cream or ointment:


  • Wash your hands with soap and water before and after using this medicine. If the skin on your hands is being treated with the medicine, only wash the skin that is not affected.

  • Apply a thin layer to the affected area of the skin. Rub it in gently until it disappears into the skin.

  • Do not get any medicine on your face or in your eyes.

To use the scalp solution:


  • Wash your hands with soap and water before and after using this medicine.

  • Before using the medicine, comb your dry hair to remove any skin flakes. Part your hair so you can see the scalp lesions.

  • Apply the solution only to the scalp lesions. Rub it in gently until it disappears into the scalp.

  • Do not get any medicine on your forehead or in your eyes.

  • Do not use this medicine near heat, an open flame, or while smoking.

To use the foam:


  • This medicine comes with a patient information insert. Read and follow the instructions carefully.

  • Wash your hands with soap and water before and after using this medicine. If the skin on your hands is being treated with the medicine, only wash the skin that is not affected.

  • Break the tiny plastic piece on the nozzle of the foam can.

  • Shake the can before each use.

  • Turn the can upside down and place a small amount into the palm of your hand.

  • Apply a thin layer to the affected area of the skin. Rub it in gently until it disappears into the skin.

  • Do not use the medicine in or near your eyes, mouth, or vagina. If the foam does get in your eyes, wash them right away with water.

  • Do not use this medicine near heat, an open flame, or while smoking.

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 topical dosage form (cream, foam, ointment, scalp solution):
    • For plaque psoriasis:
      • Adults—Apply to the affected area of the skin or scalp once per day or two times per day as directed by your doctor.

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



Missed Dose


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


Storage


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.


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


The scalp solution and foam are flammable. Keep them away from an open flame or heat. Do not smoke when you are applying the medicine. Do not poke holes in the foam canister or throw it into a fire, even if the canister is empty. Do not keep the foam inside a car where it could be exposed to extreme heat.


Precautions While Using Sorilux


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


Stop using this medicine and check with your doctor right away if you have a skin rash, burning, stinging, redness, swelling, or irritation on the skin.


If your psoriasis does not improve within a few weeks or becomes worse, check with your doctor.


Calcipotriene may make your skin more sensitive to sunlight. Use a sunscreen and wear protective clothing, including a hat, when you are outdoors. Avoid sunlamps and tanning beds.


Do not use cosmetics or other skin care products on the treated areas unless directed to do so by your doctor.


Sorilux Side Effects


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


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


More common
  • Skin redness, swelling, or itching

  • skin rash

  • worsening of psoriasis

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, dryness, irritation, peeling, or redness of the skin

Less common or rare
  • Darker color in treated areas of the skin

  • pus in the hair follicles

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: Sorilux Topical side effects (in more detail)



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More Sorilux Topical resources


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


Compare Sorilux Topical with other medications


  • Psoriasis


Sunday, September 30, 2012

Klaron





Dosage Form: lotion
Klaron® (sodium sulfacetamide lotion) Lotion, 10%

Klaron Description


Each mL of Klaron® (sodium sulfacetamide lotion) Lotion, 10% contains 100 mg of sodium sulfacetamide in a vehicle consisting of purified water; propylene glycol; lauramide DEA (and) diethanolamine; polyethylene glycol 400, monolaurate; hydroxyethyl cellulose; sodium chloride; sodium metabisulfite; methylparaben; xanthan gum; EDTA and simethicone.


Sodium sulfacetamide is a sulfonamide with antibacterial activity. Chemically, sodium sulfacetamide is N'-[(4-aminophenyl)sulfonyl]-acetamide, monosodium salt, monohydrate. The structural formula is:




Klaron - Clinical Pharmacology


The most widely accepted mechanism of action of sulfonamides is the Woods-Fildes theory, based on sulfonamides acting as a competitive inhibitor of para-aminobenzoic acid (PABA) utilization, an essential component for bacterial growth. While absorption through intact skin in humans has not been determined, in vitro studies with human cadaver skin indicated a percutaneous absorption of about 4%. Sodium sulfacetamide is readily absorbed from the gastrointestinal tract when taken orally and excreted in the urine largely unchanged. The biological half-life has been reported to be between 7 to 13 hours.



The pharmacokinetics of sulfacetamide and its major metabolite sulfaniliamide in Klaron Lotion was evaluated in adult subjects (N=14) with acne vulgaris. The subjects applied Klaron Lotion to their face, back, chest and shoulders every 12 hours for 28 days. The percentage of the applied dose of Klaron Lotion excreted in the urine as sulfacetamide plus sulfanilamide, ranged from 0.08 to 0.33%.



INDICATIONS


Klaron Lotion is indicated in the topical treatment of acne vulgaris.



Contraindications


Klaron Lotion is contraindicated for use by patients having known hypersensitivity to sulfonamides or any other component of this preparation (see WARNINGS section).



Warnings


Fatalities have occurred, although rarely, due to severe reactions to sulfonamides including Stevens-Johnson syndrome, toxic epidermal necrolysis, fulminant hepatic necrosis, agranulocytosis, aplastic anemia, and other blood dyscrasias. Hypersensitivity reactions may occur when a sulfonamide is readministered, irrespective of the route of administration. Sensitivity reactions have been reported in individuals with no prior history of sulfonamide hypersensitivity. At the first sign of hypersensitivity, skin rash or other reactions, discontinue use of this preparation (see ADVERSE REACTIONS section).


Klaron Lotion contains sodium metabisulfite, a sulfite that may cause allergic-type reactions including anaphylactic symptoms and life-threatening or less severe asthmatic episodes in certain susceptible people. The overall prevalence of sulfite sensitivity in the general population is unknown and probably low. Sulfite sensitivity is seen more frequently in asthmatic than in non-asthmatic people (see CONTRAINDICATIONS section).



Precautions



General


For external use only. Keep away from eyes. If irritation develops, use of the product should be discontinued and appropriate therapy instituted. Patients should be carefully observed for possible local irritation or sensitization during long-term therapy. Hypersensitivity reactions may occur when a sulfonamide is readministered irrespective of the route of administration, and cross-sensitivity between different sulfonamides may occur. Sodium sulfacetamide can cause reddening and scaling of the skin. Particular caution should be employed if areas of involved skin to be treated are denuded or abraded.


Keep out of the reach of children.



Carcinogenesis, Mutagenesis and Impairment of Fertility


Long-term studies in animals have not been performed to evaluate carcinogenic potential.



Pregnancy – Category C


Animal reproduction studies have not been conducted with Klaron® Lotion. It is also not known whether Klaron Lotion can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Klaron Lotion should be given to a pregnant woman only if clearly needed.


Kernicterus may occur in the newborn as a result of treatment of a pregnant woman at term with orally administered sulfonamide. There are no adequate and well controlled studies of Klaron Lotion in pregnant women, and it is not known whether topically applied sulfonamides can cause fetal harm when administered to a pregnant woman.



Nursing Mothers


It is not known whether sodium sulfacetamide is excreted in the human milk following topical use of Klaron Lotion. Systemically administered sulfonamides are capable of producing kernicterus in the infants of lactating women. Small amounts of orally administered sulfonamides have been reported to be eliminated in human milk. Because many drugs are excreted in human milk, caution should be exercised in prescribing for nursing women.



Pediatric Use


Safety and effectiveness in pediatric patients under the age of 12 have not been established.



Adverse Reactions


In controlled clinical trials for the management of acne vulgaris, the occurrence of adverse reactions associated with the use of Klaron Lotion was infrequent and restricted to local events. The total incidence of adverse reactions reported in these studies was less than 2%. Only one of 105 patients treated with Klaron Lotion had adverse reactions of erythema, itching and edema. It has been reported that sodium sulfacetamide may cause local irritation, stinging and burning. While the irritation may be transient, occasionally, the use of medication has to be discontinued.



Klaron Dosage and Administration


Apply a thin film to affected areas twice daily.



How is Klaron Supplied


4 FL OZ (118mL) bottles (NDC 0066-7500-04).


Store at Controlled Room Temperature 20 to 25°C (68 to 77°F) [see USP].

Shake well before using. Keep tightly closed.



Prescribing information as of July 2010.

Dermik Laboratories

a business of sanofi-aventis U.S. LLC

Bridgewater, NJ 08807



PRINCIPAL DISPLAY PANEL - 118mL Bottle Carton


NDC 0066-7500-04


Klaron®


sodium

sulfacetamide

lotion


Lotion, 10%


FOR TOPICAL USE ONLY


One 4 fl oz (118mL) Bottle


DERMIK®


sanofi aventis










Klaron 
sulfacetamide sodium  lotion










Product Information
Product TypeHUMAN PRESCRIPTION DRUGNDC Product Code (Source)0066-7500
Route of AdministrationTOPICALDEA Schedule    








Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
sulfacetamide sodium (sulfacetamide)sulfacetamide sodium10 mg  in 1 mL
























Inactive Ingredients
Ingredient NameStrength
water 
propylene glycol 
Lauric Diethanolamide 
diethanolamine 
polyethylene glycol 400 
sodium chloride 
sodium metabisulfite 
methylparaben 
xanthan gum 
EDETIC ACID 


















Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains      










Packaging
#NDCPackage DescriptionMultilevel Packaging
10066-7500-04118 mL In 1 BOTTLE, PLASTICNone










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA01993112/23/1996


Labeler - Dermik Laboratories (824676584)









Establishment
NameAddressID/FEIOperations
sanofi-aventis Canada Inc.251046934MANUFACTURE
Revised: 12/2011Dermik Laboratories

Friday, September 28, 2012

Tradjenta


Generic Name: linagliptin (Oral route)

lin-a-GLIP-tin

Commonly used brand name(s)

In the U.S.


  • Tradjenta

Available Dosage Forms:


  • Tablet

Pharmacologic Class: Dipeptidyl Peptidase IV Inhibitor


Uses For Tradjenta


Linagliptin is used together with proper diet and exercise to treat high blood sugar levels caused by type 2 diabetes. Normally, after you eat, your pancreas releases insulin to help your body store excess sugar for later use. This process occurs during normal digestion of food. In type 2 diabetes, your body does not work properly to store excess sugar and the sugar remains in your blood. Chronic high blood sugar can lead to serious health problems in the future.


Proper diet is the first step in managing type 2 diabetes, but often medicines are needed to help your body. Linagliptin helps to control blood sugar levels by increasing substances in the body that make the pancreas release more insulin. It also signals the liver to stop producing sugar (glucose) when there is too much sugar in the blood.


Linagliptin does not help patients who have insulin-dependent or type 1 diabetes, because they do not produce insulin from the pancreas. The high blood sugar is best controlled with insulin injections in these patients.


This medicine is available only with your doctor's prescription.


Before Using Tradjenta


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 have not been performed on the relationship of age to the effects of linagliptin in the pediatric population. Safety and efficacy have not been established.


Geriatric


Appropriate studies performed to date have not demonstrated geriatric-specific problems that would limit the usefulness of linagliptin in the elderly.


Pregnancy








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

Breast Feeding


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


Interactions with Medicines


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


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


  • Carbamazepine

  • Phenobarbital

  • Phenytoin

  • Rifabutin

  • Rifampin

  • St John's Wort

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:


  • Diabetic ketoacidosis (high ketones and acid in the blood) or

  • Type 1 diabetes—Should not be used in patients with these conditions.

  • Fever or

  • Infection or

  • Surgery or

  • Trauma—These conditions may cause temporary problems with blood sugar control. Your doctor may need to change your dose of linagliptin.

Proper Use of Tradjenta


Take this medicine exactly as directed by your doctor. Do not take more of it, do not take it more often, and do not take it for a longer time than your doctor ordered. To do so may increase the chance of side effects.


Carefully follow the special meal plan your doctor gave you. This is the most important part of controlling your diabetes, and is necessary if the medicine is to work properly. Exercise regularly and test for sugar in your blood or urine as directed.


This medicine comes with a patient information insert. It is very important that you read and understand this information. Be sure to ask your doctor about anything you do not understand.


Linagliptin may be taken with or without food.


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 form (tablets):
    • For type 2 diabetes:
      • Adults—5 milligrams (mg) once a day.

      • 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 Tradjenta


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


This medicine may cause hypoglycemia (low blood sugar). Low blood sugar can also occur if you delay or miss a meal or snack, exercise more than usual, drink alcohol, cannot eat because of nausea or vomiting, take certain medicines, or take linagliptin with other diabetes medicine (e.g., glimepiride, glipizide, or glyburide). Symptoms of low blood sugar must be treated before they cause you to pass out (unconsciousness). People feel different symptoms with low blood sugar. It is important that you learn which symptoms you usually have so you can treat it quickly.


The symptoms of low blood sugar include anxiety; behavior changes similar to being drunk; blurred vision; cold sweats; confusion; cool, pale skin; difficulty with thinking; drowsiness; excessive hunger; a fast heartbeat; headaches that continue; nausea; nervousness; nightmares; restless sleep; shakiness; slurred speech; or unusual tiredness or weakness.


If symptoms of low blood sugar occur, check your blood sugar level. If you have low blood sugar, eat glucose tablets or gel, corn syrup, honey, or sugar cubes; or drink fruit juice, non-diet soft drinks, or sugar dissolved in water. Glucagon is a medicine that is used in emergency situations when severe symptoms, such as seizures (convulsions) or unconsciousness occur. Have a glucagon kit available, along with a syringe and needle, and know how to use it. The members of your family should also know how to use glucagon.


Hyperglycemia (high blood sugar) may occur if you do not take enough or skip a dose of your medicine, overeat or do not follow your diet plan, have a fever or infection, or do not exercise as much as usual.


The symptoms of high blood sugar include blurred vision; drowsiness; dry mouth; flushed, dry skin; fruit-like breath odor; increased urination (frequency and amount); loss of appetite; sleepiness; stomachache, nausea, or vomiting; tiredness; troubled breathing (rapid and deep); unconsciousness (passed out); or unusual thirst.


If symptoms of high blood sugar occur, check your blood sugar level and call your doctor for instructions.


There may be a time when you need emergency help for a problem caused by your diabetes. You need to be prepared for these emergencies. It is a good idea to wear a medical identification (ID) bracelet or neck chain at all times. Also, carry an ID card in your wallet or purse that says you have diabetes with a list of all your medicines.


Do not take other medicines unless they have been discussed with your doctor. This includes prescription or nonprescription (over-the-counter [OTC]) medicines and herbal or vitamin supplements.


Tradjenta Side Effects


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


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


More common
  • Anxiety

  • blurred vision

  • chills

  • cold sweats

  • coma

  • confusion

  • cool, pale skin

  • depression

  • dizziness

  • fast heartbeat

  • headache

  • increased hunger

  • nausea

  • nervousness

  • nightmares

  • seizures

  • shakiness

  • slurred speech

  • unusual tiredness or weakness

Rare
  • Bloating

  • constipation

  • darkened urine

  • fever

  • indigestion

  • loss of appetite

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

  • vomiting

  • yellow eyes or skin

Incidence not known
  • Flaking and falling off of the skin

  • hives or welts

  • itching

  • large, hive-like swelling on the face, eyelids, lips, tongue, throat, hands, legs, feet, or sex organs

  • redness of the skin

  • skin rash

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
  • Back pain

  • difficulty with moving

  • muscle aches

  • muscle pain or stiffness

  • pain in the joints

  • sore throat

  • stuffy or runny nose

Less common
  • Cough

  • weight gain

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: Tradjenta 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 Tradjenta resources


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


  • Tradjenta Prescribing Information (FDA)

  • Tradjenta MedFacts Consumer Leaflet (Wolters Kluwer)

  • Tradjenta Consumer Overview

  • Linagliptin Professional Patient Advice (Wolters Kluwer)



Compare Tradjenta with other medications


  • Diabetes, Type 2


Thursday, September 27, 2012

Soliris


Generic Name: eculizumab (E kue LIZ oo mab)

Brand Names: Soliris


What is eculizumab?

Eculizumab is a monoclonal antibody that binds to proteins in the blood that can destroy red blood cells in people with a genetic condition that affects the natural defenses of red blood cells.


Eculizumab is used to prevent the breakdown of red blood cells in people with paroxysmal nocturnal hemoglobinemia (PNH).


Eculizumab is also used to treat a rare chronic blood disease called atypical hemolytic (HEEM-oh-LIT-ik yoo-REEM-ik) uremic syndrome.


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


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


Do not shake the eculizumab vial (bottle) or you may ruin the medicine. Eculizumab affects your immune system, and using this medication may increase your risk of serious infection such as meningitis. You must be vaccinated against meningococcal infection at least 2 weeks before you start treatment with eculizumab. If you have been vaccinated in the past, you may need a booster dose. Call your doctor at once if you have a serious side effect such as severe headache, high fever, chills, stiffness in your neck or back, confusion, sensitivity to bright light, purple spots on the skin, nausea or vomiting, and/or seizure (convulsions). With your medication you will receive a Patient Safety Card listing the symptoms of meningococcal infection. Carry this card with you at all times. Seek emergency medical attention or call your doctor right away if you notice any of these symptoms. You should not use this medication if you are allergic to eculizumab, if you have bacterial meningitis, or if you have not been vaccinated against meningitis.

Before using eculizumab, tell your doctor if you have a fever or any type of infection.


Do not stop using eculizumab without first talking to your doctor. Stopping or interrupting your treatment could cause sudden and serious effects on your red blood cells. This may result in symptoms such as pale skin, easy bruising, confusion, chest pain, blood clots, or kidney problems.

Eculizumab is available only under a special program called Soliris REMS. You must be registered in the program and sign documents stating that you understand the risks and benefits of taking this medication.


What should I discuss with my health care provider before taking eculizumab?


Eculizumab affects your immune system, and using this medication may increase your risk of serious infection such as meningitis. Get emergency medical help if you have any signs of meningitis, such as severe headache with fever, confusion, purple spots on the skin, and nausea or vomiting, stiffness in your neck or back, sensitivity to bright light, or a high fever (103 degrees or higher), chills, body aches, and other flu-like symptoms. You must be vaccinated against meningococcal infection at least 2 weeks before you start treatment with eculizumab. If you have been vaccinated in the past, you may need a booster dose. It is best to stay current on all of your vaccinations while you are using eculizumab, and your doctor may recommend other vaccines before or during treatment. You should not use this medication if you are allergic to eculizumab, if you have bacterial meningitis, or if you have not been vaccinated against meningitis.

With your medication you will receive a Patient Safety Card listing the symptoms of meningococcal infection. Carry this card with you at all times. Seek emergency medical attention or call your doctor right away if you notice any of these symptoms.


Eculizumab is available only under a special program called Soliris REMS. You must be registered in the program and sign documents stating that you understand the risks and benefits of taking this medication.


To make sure you can safely use eculizumab, tell your doctor if you have a fever or any type of infection.


FDA pregnancy category C. It is not known whether eculizumab 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 eculizumab passes into breast milk or if it could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.

How is eculizumab given?


Eculizumab is injected into a vein through an IV. You may be shown how to use an IV 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, IV tubing, and other items used to inject the medicine.


Eculizumab is usually given every 7 days for 5 weeks, and then once every 2 weeks thereafter. Follow your doctor's instructions. The medicine must be given slowly through an IV infusion, and can take up to 2 hours to complete.


You may have a reaction to the infusion (when the medicine is injected into the vein). If this happens, you may need to slow down the speed of your IV infusion, and the infusion should not take more than 2 hours to complete. A caregiver or family member should then watch you for at least 1 hour after your injection to make sure you have no further side effects.

Eculizumab must be mixed in an IV bag with a liquid (diluent) before injecting it. If you are using the injections at home, be sure you understand how to properly mix and store the medication.


Do not shake the medication vial (bottle) or you may ruin the medicine. Prepare your dose in a syringe only when you are ready to give yourself an injection. Do not use the medication if it has changed colors or has particles in it. Call your doctor for a new prescription. To reduce discomfort from your injection, allow the mixed medicine to reach room temperature before using, but never warm the medicine in hot water or a microwave. You may store the mixture at room temperature but you must use it within 24 hours or throw the mixture away.

Use a disposable needle only once. Throw away used needles in a puncture-proof container (ask your pharmacist where you can get one and how to dispose of it). Keep this container out of the reach of children and pets.


Do not stop using eculizumab without first talking to your doctor. Stopping or interrupting your treatment could cause sudden and serious effects on your red blood cells. This may result in symptoms such as pale skin, easy bruising, confusion, chest pain, blood clots, or kidney problems.

If you stop using eculizumab for any reason, your blood may need to be tested on a regular basis for 8 to 12 weeks. Do not miss any scheduled visits to your doctor during this follow-up period.


Store in the refrigerator. Protect from light and do not freeze. Keep unopened eculizumab vials in their original carton. Throw away any unused vials after the expiration date on the label has passed.

What happens if I miss a dose?


Call your doctor for instructions if you miss a dose of this medication.


What happens if I overdose?


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

What should I avoid while taking eculizumab?


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


Eculizumab 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. Call your doctor at once if you have a serious side effect such as:

  • severe headache with fever, confusion, purple spots on the skin, nausea or vomiting, and/or seizure (convulsions);




  • stiffness in your neck or back;




  • sensitivity to bright light;




  • high fever (103 degrees or higher), chills, body aches, flu symptoms;




  • pain or burning when you urinate;




  • any signs of a new illness or infection; or




  • signs that the medication is not working (pale skin, easy bruising, weakness, dark urine, feeling short of breath, or sudden numbness, severe headache, deep leg pain, or problems with vision, speech, or balance).



Less serious side effects may include:



  • nausea;




  • diarrhea;




  • mild headache;




  • runny nose, sore throat; or




  • back pain.



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 eculizumab?


There may be other drugs that can interact with eculizumab. 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 Soliris resources


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


  • Soliris Prescribing Information (FDA)

  • Soliris Monograph (AHFS DI)

  • Soliris Advanced Consumer (Micromedex) - Includes Dosage Information

  • Soliris Consumer Overview

  • Soliris MedFacts Consumer Leaflet (Wolters Kluwer)

  • Eculizumab Professional Patient Advice (Wolters Kluwer)



Compare Soliris with other medications


  • Hemolytic Uremic Syndrome
  • Myasthenia Gravis
  • Paroxysmal Nocturnal Hemoglobinuria


Where can I get more information?


  • Your pharmacist can provide more information about eculizumab.

See also: Soliris side effects (in more detail)