Sunday, October 7, 2012

Sargramostim


Pronunciation: sar-GRA-moe-stim
Generic Name: Sargramostim
Brand Name: Leukine


Sargramostim is used for:

Reducing severe, life-threatening, or fatal infections after chemotherapy for acute myelogenous leukemia (AML). It is also used to help increase the success of autologous bone marrow transplant and to help increase survival in patients who have bone marrow transplant failure. It may also be used for other conditions as determined by your doctor.


Sargramostim is a hematopoietic agent. It works by stimulating production of white blood cells in bone marrow.


Do NOT use Sargramostim if:


  • you are allergic to any ingredient in Sargramostim or to yeast products

  • you have certain bone marrow disorders

  • you have received chemotherapy or radiation therapy within the last 24 hours or you will be receiving chemotherapy or radiation therapy within the next 24 hours

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



Before using Sargramostim:


Some medical conditions may interact with Sargramostim. 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 other types of cancer or unusual growths or tumors

  • if you have a history of fluid retention, irregular heartbeat, heart disease or congestive heart failure, a lung disorder or breathing problems, or liver or kidney problems

  • if you are undergoing radiation therapy or chemotherapy

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


  • Corticosteroids (eg, prednisone) or lithium because they may increase the risk of Sargramostim's side effects

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


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


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

  • Do not shake Sargramostim.

  • Do not use Sargramostim if it contains particles, is cloudy or discolored, or if the vial is cracked or damaged.

  • Continue using Sargramostim for the full course of treatment unless your doctor directs otherwise.

  • 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 Sargramostim, contact your doctor right away.

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



Important safety information:


  • The first dose of Sargramostim may cause difficulty breathing, flushing, fainting, or fast or irregular heartbeat. These signs usually resolve and usually do not occur again. Contact your doctor for more information.

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

  • Diabetes patients - Sargramostim may affect your blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.

  • Lab tests, including liver function, kidney function, blood counts, body weight, and fluid and electrolyte tests, may be performed while you use Sargramostim. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

  • Sargramostim may have benzyl alcohol in it. Do not use it in NEWBORNS or INFANTS. It may cause serious and sometimes fatal nervous system problems and other side effects.

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


Possible side effects of Sargramostim:


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:



Bone, muscle, or joint pain; diarrhea; fever; general feeling of discomfort; hair loss; headache; loss of appetite; mild sweating of the hands, ankles, legs, or feet; nausea; sore mouth; stomach pain; 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); anxiety; black or tarry stools; blood in urine; chest pain; emotional or mood changes; fainting; fast or irregular heartbeat; severe or persistent fever; severe stomach pain; severe swelling of the hands, ankles, legs, or feet; shortness of breath; unusual or excessive bleeding; unusual swelling; vomiting blood.



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: Sargramostim 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 (http://www.aapcc.org ), or emergency room immediately. Symptoms may include chills; fast or irregular heartbeat; rash; severe or persistent fever, discomfort, headache, or nausea; shortness of breath.


Proper storage of Sargramostim:

Sargramostim is usually handled and stored by a health care provider. If you are using Sargramostim at home, store Sargramostim as directed by your pharmacist or health care provider. Keep Sargramostim out of the reach of children and away from pets.


General information:


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

  • Sargramostim 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 Sargramostim. 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 Sargramostim resources


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


  • Sargramostim Professional Patient Advice (Wolters Kluwer)

  • Sargramostim Monograph (AHFS DI)

  • sargramostim Intravenous Advanced Consumer (Micromedex) - Includes Dosage Information

  • Leukine Prescribing Information (FDA)

  • Leukine Consumer Overview



Compare Sargramostim with other medications


  • Aplastic Anemia
  • Bone Marrow Transplantation
  • Bone Marrow Transplantation, Failure or Engraftment Delay
  • Bone Marrow Transplantation, Myeloid Reconstruction
  • Neutropenia Associated with Chemotherapy


Thursday, October 4, 2012

Novacort


Generic Name: hydrocortisone and pramoxine topical (HYE droe KOR ti sone and pra MOX een)

Brand Names: Analpram E, Analpram-HC, Epifoam, HC Pramoxine, Hydropram, Novacort, Pramosone, Proctofoam HC, Rectocort HC, ZyPram


What is Novacort (hydrocortisone and pramoxine topical)?

Pramoxine is an anesthetic. It works by interfering with pain signals sent from the nerves to the brain.


Hydrocortisone is a steroid. It reduces the actions of chemicals in the body that cause inflammation, redness, and swelling.


The combination of hydrocortisone and pramoxine topical is used to treat pain, itching, or inflammation of the skin caused by a number of conditions such as allergic reactions, eczema, psoriasis, insect bites, and minor burns or scrapes. This medication is also used on the rectal area to treat itching and inflammation caused by hemorrhoids, anal fissures, or other rectal irritation.


Hydrocortisone and pramoxine topical may also be used for other purposes not listed in this medication guide.


What is the most important information I should know about Novacort (hydrocortisone and pramoxine topical)?


You should not use this medication if you are allergic to hydrocortisone or pramoxine, or if you have chickenpox or measles.

Before using hydrocortisone and pramoxine topical, tell your doctor if you are allergic to any drugs or any other anesthetics or "numbing medicines."


Hydrocortisone and pramoxine topical will not treat a bacterial, fungal, or viral skin infection. If you have a skin infection, you should not use this medication until your infection is treated and clears up.


Avoid using this medication on your face, near your eyes, or on body areas where you have skin folds or thin skin.


Do not use this medication on a child without a doctor's advice. Children are more sensitive to the effects of topical hydrocortisone. Do not cover treated skin areas with a bandage or other covering unless your doctor has told you to. If you are treating the diaper area of a baby, do not use plastic pants or tight-fitting diapers. Covering the skin that is treated with hydrocortisone topical can increase the amount of the drug your skin absorbs, which may lead to unwanted side effects. Follow your doctor's instructions. Contact your doctor if your condition does not improve or if it gets worse after using this medication for several days.

Do not use hydrocortisone and pramoxine topical for any condition that has not been checked by a doctor.


What should I discuss with my health care provider before using Novacort (hydrocortisone and pramoxine topical)?


You should not use this medication if you are allergic to hydrocortisone or pramoxine, or if you have chickenpox or measles.

Before using hydrocortisone and pramoxine topical, tell your doctor if you are allergic to any drugs or any other anesthetics or "numbing medicines." Also tell your doctor if you have:



  • liver disease;




  • diabetes;




  • problems with your eyes;




  • a stomach or intestinal disorder;




  • a rectal sore or infection; or




  • if you use any drugs that weaken the immune system, including steroids.



Hydrocortisone and pramoxine topical will not treat a bacterial, fungal, or viral skin infection. If you have a skin infection, you should not use this medication until your infection is treated and clears up.


FDA pregnancy category C. It is not known whether this medication is harmful to an unborn baby. Before using hydrocortisone and pramoxine topical, tell your doctor if you are pregnant or plan to become pregnant during treatment. It is not known whether hydrocortisone and pramoxine topical passes into breast milk or if it could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby. Do not use this medication on a child without a doctor's advice. Children are more sensitive to the effects of topical hydrocortisone.

How should I use Novacort (hydrocortisone and pramoxine topical)?


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


Hydrocortisone and pramoxine topical is usually applied 3 or more times daily, depending on which form of this medication you use. Follow the label directions or your doctor's instructions about how much of this medication to use and how often. Do not use hydrocortisone and pramoxine topical for any condition that has not been checked by a doctor.


Wash your hands before and after applying this medication, unless you are using hydrocortisone and pramoxine topical to treat a hand condition.

When using this medication on the skin, apply just enough of the medication to cover the area to be treated. Rub in gently.


Avoid using this medication on your face, near your eyes or mouth, or on body areas where you have skin folds or thin skin.


Do not cover treated skin areas with a bandage or other covering unless your doctor has told you to. If you are treating the diaper area of a baby, do not use plastic pants or tight-fitting diapers. Covering the skin that is treated with hydrocortisone topical can increase the amount of the drug your skin absorbs, which may lead to unwanted side effects. Follow your doctor's instructions.

Before apply the rectal form of this medication (cream, lotion, or foam), clean the rectal area with mild soap and pat dry.


Use only a small amount of medicine when applying hydrocortisone and pramoxine around the outside of the rectum. You may first place the medicine onto a clean tissue and then wipe it gently onto your rectum.


When using this medication inside the rectum, insert only the applicator tip of the medicine tube or foam can into the anus, no deeper than 1 inch.


Shake the hydrocortisone and pramoxine rectal foam before each use. Contact your doctor if your condition does not improve or if it gets worse after using this medication for several days, or if your condition clears up and then comes back. Do not stop using hydrocortisone and pramoxine topical suddenly after long-term use, or you could have unpleasant withdrawal symptoms. Talk to your doctor about how to avoid withdrawal symptoms when you stop using the medication. Store this medication at room temperature away from moisture and heat. Keep the rectal foam canister away from open flame or high heat. The canister may explode if it gets too hot. Do not puncture or burn an empty canister.

What happens if I miss a dose?


Use the medication as soon as you remember. If it is almost time for the next dose, skip the missed dose and use the medicine at the next regularly scheduled time. Do not use extra medicine to make up the missed dose.


What happens if I overdose?


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

An overdose of hydrocortisone and pramoxine topical is not expected to produce life-threatening symptoms. However, long-term use of high steroid doses can lead to symptoms such as thinning skin, easy bruising, changes in the shape or location of body fat (especially in your face, neck, back, and waist), increased acne or facial hair, menstrual problems, impotence, or loss of interest in sex.


What should I avoid while using Novacort (hydrocortisone and pramoxine topical)?


Avoid using this medication on your face, near your eyes, or on body areas where you have skin folds or thin skin. If it does get into any of these areas, wash with water. Do not use hydrocortisone and pramoxine topical on deep skin wounds, blistered skin, severe burns, irritated skin, or large skin areas. Also avoid using this medication in open wounds.

Avoid applying other skin medications on the same treatment area with hydrocortisone and pramoxine topical, unless your doctor has told you to.


Using a steroid can lower the blood cells that help your body fight infections. This can make it easier for you to get sick from being around others who are ill. Call your doctor for preventive treatment if you are exposed to chicken pox or measles. These conditions can be serious or even fatal in people who are using steroid medicines.


Hydrocortisone pramoxine topical 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 any of these serious side effects:

  • blurred vision, or seeing halos around lights;




  • uneven heartbeats;




  • sleep problems (insomnia);




  • ongoing headache;




  • weight gain, puffiness in your face;




  • increased thirst or urination, weight loss, unusual weakness;




  • fever, sore throat, tired feeling;




  • severe pain, burning, or irritation of treated skin;




  • rectal bleeding;




  • any new redness or swelling where the medicine was applied; or




  • itching, oozing, or other signs of infection.



Less serious side effects may include:



  • mild skin redness, burning, itching, dryness, or peeling;




  • acne;




  • changes in the color of treated skin;




  • thinning of your skin;




  • blistering skin; or




  • stretch marks.



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 Novacort (hydrocortisone and pramoxine topical)?


It is not likely that other drugs you take orally or inject will have an effect on topically applied hydrocortisone and pramoxine. But many drugs can interact with each other. Tell your doctor about all your prescription and over-the-counter medications, vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start a new medication without telling your doctor.



More Novacort resources


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


  • Novacort MedFacts Consumer Leaflet (Wolters Kluwer)

  • Analpram-HC Cream MedFacts Consumer Leaflet (Wolters Kluwer)

  • Epifoam Prescribing Information (FDA)

  • Epifoam Foam MedFacts Consumer Leaflet (Wolters Kluwer)

  • Pramosone Prescribing Information (FDA)

  • Pramosone Lotion MedFacts Consumer Leaflet (Wolters Kluwer)

  • Proctocream HC Prescribing Information (FDA)

  • Proctofoam HC Prescribing Information (FDA)

  • Proctofoam HC Foam MedFacts Consumer Leaflet (Wolters Kluwer)



Compare Novacort with other medications


  • Dermatitis
  • Dermatological Disorders
  • Hemorrhoids
  • Psoriasis


Where can I get more information?


  • Your pharmacist can provide more information about hydrocortisone and pramoxine topical.

See also: Novacort side effects (in more detail)



Wednesday, October 3, 2012

SunVanish Cream




Generic Name: hydroquinone

Dosage Form: cream
Glytone skin Bleaching sunvanish



Dosage Apply SunVanish in the morning to the affected area or as directed by your physician.





Warnings Contains sodium Metabisulfite, a sulfite that may cause serious allergic type reactions (eg hives, itching, wheezing, anaphylaxis, severe asthma attack) in certain susceptible persons.


For external use only





Distributed by


Genesis Pharmaceuticals Inc


Parsippany, NJ  07054


Made in USA


18004598663


www.glytone.com





Keep out of reach of children





Contains Each gram of SunVanish contains 40 mg of hydroquinone USP, 75 mg of octinoxate and 50 mg of oxybenzone in a cream base of purified water, proplyene glycol, cetostearyl alcohol, glycerin, isopropyl palmitate, sodium metabisulfite, sodium lauryl sulfate, and sorbic acid






Glytone skin bleaching sunvanish with sunscreen


hydroquinone USP, 4%


RX only


Net wt 2 oz (56 g)









SUNVANISH 
hydroquinone  cream










Product Information
Product TypeHUMAN PRESCRIPTION DRUGNDC Product Code (Source)64760-201
Route of AdministrationTOPICALDEA Schedule    








Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Hydroquinone (Hydroquinone)Hydroquinone40 mg  in 1 g




















Inactive Ingredients
Ingredient NameStrength
WATER 
PROPYLENE GLYCOL 
CETOSTEARYL ALCOHOL 
GLYCERIN 
ISOPROPYL PALMITATE 
SODIUM METABISULFITE 
SODIUM LAURYL SULFATE 
SORBIC ACID 


















Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains      














Packaging
#NDCPackage DescriptionMultilevel Packaging
164760-201-011 TUBE In 1 BOXcontains a TUBE
156 g In 1 TUBEThis package is contained within the BOX (64760-201-01)










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart358A10/01/2009


Labeler - Glytone (117196928)
Revised: 01/2011Glytone




More SunVanish Cream resources


  • SunVanish Cream Side Effects (in more detail)
  • SunVanish Cream Use in Pregnancy & Breastfeeding
  • 0 Reviews for SunVanish - Add your own review/rating


Compare SunVanish Cream with other medications


  • Dermatological Disorders


Sentry SA Dritail





Dosage Form: FOR ANIMAL USE ONLY
Treatment for Diarrhea ("Wet Tail")

Indications and Usage for Sentry SA Dritail


SYMPTOMS:     

  • Diarrhea

  • Wet or matted tail

  • Dehydration

  • Obvious changes in appearance or behavior


Concentrated formula

Easily administered in water

Designed to appeal to small animals' tastes

Treats symptoms in hamsters, gerbils, mice, rats , and guinea pigs.

DOSAGE & ADMINISTRATION


Treat animal with full recommended dosage.  Discontinue feeding greens and roughage to animals that have diarrhea.  Treat for a minimum of 5 days.  Repeat the treatment if necessary.  If condition persists and no improvement is noted during treatment, consult your veterinarian.  Sick animals should be separated from healthy animals.  If more than one animal is caged together, all animals should be treated for a period of 5 days to prevent infection.


Oral Dropper Method (for hamsters and guinea pigs only):

Weigh your pet and use the weight chart to determine the amount of DriTail to use.  Young animals (six months old or less) should be given 1/2 the recommended adult dosage.  Allow the animal to lap medicine from the dropper; be careful not to force medicine into the mouth faster than your pet can lap it up.






















Common NameWeightAmount of DriTail
Siberian Hamster25-35g (1 oz)1/4 mL (8 drops) once daily
Chinese Hamster30-50g (1 1/2 oz)1/4 mL (8 drops) once daily
Golden Hamster
110-140g (4-5 oz)1/2 mL (16 drops) once daily
Guinea Pig800-1200g (2-2 1/2 lbs)3/4 mL (24 drops) once daily







Oral Drinking Water Method (gerbils, mice, rats, hamsters, guinea pigs):

Add 3 teaspoons (15 mL) of DriTail to 4 oz. (120 mL) of water.  The water should be changed daily and should be your pet's only source of water. 

Precautions


Do not use for nonrodents such as rabbits.  For pet animal use only.

KEEP OUT OF REACH OF CHILDREN





ACTIVE INGREDIENT


Neomycin sulfate equivalent to not less than 20 mg/mL of neomycin base.

How is Sentry SA Dritail Supplied


Net Contents:


1 fl. oz. (29.5 mL) Dropper


16 fl. oz. (473 mL)

PACKAGE LABEL PRINCIPLE DISPLAY PANEL


Distributed by:


Sergeant's Pet Care Products, Inc., Omaha NE 68130


Made in USA


www.sentrypetcare.com










Sentry SA Dritail 
neomycin sulfate  liquid










Product Information
Product TypeOTC ANIMAL DRUGNDC Product Code (Source)21091-932
Route of AdministrationORALDEA Schedule    








Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NEOMYCIN SULFATE (NEOMYCIN)NEOMYCIN SULFATE20 mg  in 1 mL





Inactive Ingredients
Ingredient NameStrength
No Inactive Ingredients Found


















Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains      


















Packaging
#NDCPackage DescriptionMultilevel Packaging
121091-932-011 BOTTLE In 1 BLISTER PACKcontains a BOTTLE, PLASTIC
129.5 mL In 1 BOTTLE, PLASTICThis package is contained within the BLISTER PACK (21091-932-01)
221091-932-16473 mL In 1 BOTTLE, PLASTICNone










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other12/08/2008


Labeler - Sergeant's Pet Care Products, Inc. (876995171)
Revised: 12/2009Sergeant's Pet Care Products, Inc.