Tuesday, October 25, 2016

Xeomin


Pronunciation: IN-koe-BOT-ue-LYE-num-TOX-in-AY
Generic Name: IncobotulinumtoxinA
Brand Name: Xeomin

Xeomin may spread from the injection site to other areas of the body, causing symptoms of a serious condition called botulism. These symptoms may occur hours to weeks after you receive Xeomin. Symptoms may include loss of strength; muscle weakness; double or blurred vision; drooping eyelids; hoarseness; change or loss of voice; loss of bladder control; or trouble speaking, breathing, or swallowing. The risk may be greater in children being treated for spasticity (muscle spasms), but these symptoms may also occur in adults. Contact your doctor immediately if these symptoms occur.


Severe and sometimes fatal breathing or swallowing problems have been reported. The risk may be greater in patients who already have breathing or swallowing problems. Tell your doctor if you have or are at risk of developing breathing or swallowing problems.





Xeomin is used for:

Reducing the severity of abnormal head position and neck pain associated with neck problems. It may be used to treat certain types of eyelid muscle spasms after you have been treated with another medicine (onabotulinumtoxinA). It may be used to temporarily improve the appearance of moderate to severe lines between the eyebrows in certain patients. It may also be used for other conditions as determined by your doctor.


Xeomin is a neurotoxin. It works by blocking nerve impulses to the muscles, temporarily paralyzing the muscle.


Do NOT use Xeomin if:


  • you are allergic to any ingredient in Xeomin, including botulinum neurotoxin type A, human albumin, sucrose, or to another botulinum toxin product

  • you have an infection at the injection site

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



Before using Xeomin:


Some medical conditions may interact with Xeomin. 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 nerve problems or disease (eg, amyotrophic lateral sclerosis, motor neuropathy), muscle problems or disease (eg, myasthenia gravis, Lambert-Eaton syndrome), bleeding problems, or severe weakness or wasting of the muscles at the injection site

  • if you have a history of swallowing problems or aspiration (inhaling food or fluids into your lungs), breathing problems (eg, asthma, emphysema), eye problems (eg, glaucoma, drooping eyelid), or eye surgery

  • if you have a skin infection, or inflammation, scarring, or other skin disorders at the injection site

  • if you plan to have surgery or if you have received Xeomin or any other botulinum toxin in the past, especially within the last 4 months

  • if you have weakness in your forehead muscles, any change in the way your face normally looks, you plan to have surgery, or you have had surgery on your face

  • if you are taking an allergy or cold medicine

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


  • Aminoglycoside antibiotics (eg, gentamicin), muscle relaxants (eg, cyclobenzaprine), or sleep medicines (eg, zolpidem) because they may increase the risk of Xeomin's side effects

  • Anticoagulants (eg, warfarin) because the risk of bleeding at the injection site may be increased

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


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


  • Xeomin comes with an extra patient information sheet called a Medication Guide. Read it carefully. Read it again each time you get Xeomin refilled.

  • Xeomin is usually given as an injection at your doctor's office, hospital, or clinic.

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

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



Important safety information:


  • Xeomin may cause dizziness, loss of strength, weakness, or blurred vision. These effects may be worse if you take it with alcohol or certain medicines. Use Xeomin with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.

  • Do NOT use more than the recommended dose or use for longer than prescribed without checking with your doctor.

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

  • Do not switch brands of Xeomin or switch it with other botulinum toxin products. Contact your doctor if you have any questions.

  • Xeomin contains albumin, which comes from human blood. There is a very rare risk of getting a viral disease or a central nervous system disease called Creutzfeldt-Jakob disease from products with albumin. No cases of these problems have been found in patients who have used Xeomin.

  • To prevent injury, resume normal activities gradually after using Xeomin.

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

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


Possible side effects of Xeomin:


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:



Decreased blinking; diarrhea; dry mouth; dry or irritated eyes; headache; increased cough; muscle or bone pain; muscle weakness or spasms; nausea; neck pain; pain, redness, swelling, or tenderness at the injection site; runny nose; tiredness.



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

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue; unusual hoarseness); bleeding at the injection site; difficulty swallowing or breathing; dizziness; double or blurred vision or other vision changes; drooping of the upper eyelid; eye or eyelid swelling; eye pain or irritation; fainting; fever, chills, or persistent sore throat; loss of bladder control; loss of strength; severe or persistent muscle weakness or spasms; shortness of breath; speech changes or problems; wheezing.



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: Xeomin 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 body weakness; difficulty breathing; paralysis. Xeomin may be harmful if swallowed.


Proper storage of Xeomin:

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


General information:


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

  • Xeomin 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 Xeomin. 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 Xeomin resources


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


  • Xeomin Prescribing Information (FDA)

  • Xeomin Advanced Consumer (Micromedex) - Includes Dosage Information

  • Xeomin Consumer Overview

  • IncobotulinumtoxinA Professional Patient Advice (Wolters Kluwer)



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X-Viate Lotion



urea

Dosage Form: lotion
X-VIATE™

Drug Facts



Active Ingredient


Urea 40%



Purpose


Keratolytic Agent



Warnings


For external use only.


Avoid contact with eyes, lips, or mucous membranes.


Do not use:


  • On areas of broken skin

  • If known hypersensitivity to any of the listed ingredients.


Precautions


  • Stop use and ask a doctor if redness or irritation develops.

  • Keep out of the reach of children.

  • If swallowed, get medical help or contact a Poison Control Center right away.


Pregnancy


  • If pregnant or breast feeding, ask a health professional before use.


Directions


  • Apply to the affected skin twice per day, or as directed by a physician.

  • Rub in until completely absorbed.


Other Information


  • Store at controlled room temperature 15°-30°C (59°-86°F)

  • Protect from freezing.


Inactive Ingredients


Carbopol, Cetyl Alcohol, Glyceryl Stearate, Methyl Paraben, Mineral Oil, Propyl Paraben, Propylene Glycol, Purified Water, Trolamine, White Petrolatum and Xanthan Gum.



Manufactured by:

Sonar Products, Inc.

Carlstadt, New Jersey 07072


Exclusively for:

Stratus Pharmaceuticals Inc

12379 Southwest 130th Street

Miami, FL 33186



PRINCIPAL DISPLAY PANEL - 8.0 fl. oz. Label


NDC 58980-623-80


X-VIATE™


40 %

LOTION


Softens and

Moisturizes

Severe

Dry

Skin


Rx only


UREA 40%

IN A LOTION BASE


Distributed by:

STRATUS

PHARMACEUTICALS INC


8.0 fl. oz. (237 mL)




PRINCIPAL DISPLAY PANEL - 8.0 fl. oz. Box


NDC 58980-623-80


X-VIATE™


40 %

LOTION


Softens and

Moisturizes

Severe

Dry

Skin


Rx only


UREA 40%

IN A LOTION BASE


Distributed by:

STRATUS

PHARMACEUTICALS INC


8.0 fl. oz. (237 mL)










X VIATE 
urea  lotion










Product Information
Product TypeHUMAN PRESCRIPTION DRUGNDC Product Code (Source)58980-623
Route of AdministrationTOPICALDEA Schedule    








Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Urea (Urea)Urea94.8 mg  in 237 mL





Inactive Ingredients
Ingredient NameStrength
No Inactive Ingredients Found


















Product Characteristics
ColorWHITEScore    
ShapeSize
FlavorImprint Code
Contains      














Packaging
#NDCPackage DescriptionMultilevel Packaging
158980-623-801 BOTTLE In 1 BOXcontains a BOTTLE
1237 mL In 1 BOTTLEThis package is contained within the BOX (58980-623-80)










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Unapproved other09/01/2009


Labeler - Stratus Pharamceuticals, Inc (789001641)









Establishment
NameAddressID/FEIOperations
Sonar Products, Inc104283945MANUFACTURE
Revised: 08/2009Stratus Pharamceuticals, Inc




More X-Viate Lotion resources


  • X-Viate Lotion Side Effects (in more detail)
  • X-Viate Lotion Use in Pregnancy & Breastfeeding
  • X-Viate Lotion Support Group
  • 2 Reviews for X-Viate - Add your own review/rating


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Clinagel




Clinagel may be available in the countries listed below.


In some countries, this medicine may only be approved for veterinary use.

Ingredient matches for Clinagel



Gentamicin

Gentamicin sulfate (a derivative of Gentamicin) is reported as an ingredient of Clinagel in the following countries:


  • United Kingdom

International Drug Name Search

Inistolin Pediatrico Antitusivo




Inistolin Pediatrico Antitusivo may be available in the countries listed below.


Ingredient matches for Inistolin Pediatrico Antitusivo



Dextromethorphan

Dextromethorphan hydrobromide (a derivative of Dextromethorphan) is reported as an ingredient of Inistolin Pediatrico Antitusivo in the following countries:


  • Spain

Pseudoephedrine

Pseudoephedrine hydrochloride (a derivative of Pseudoephedrine) is reported as an ingredient of Inistolin Pediatrico Antitusivo in the following countries:


  • Spain

International Drug Name Search

Monday, October 24, 2016

Xeloda



Generic Name: capecitabine (Oral route)

kap-e-SYE-ta-been

Oral route(Tablet)

Patients receiving concomitant capecitabine and oral coumarin-derivative anticoagulant therapy should have their anticoagulant response (INR or prothrombin time) monitored frequently in order to adjust the anticoagulant dose accordingly. Altered coagulation parameters and/or bleeding, including death, have been reported in patients taking capecitabine concomitantly with coumarin-derivative anticoagulants. These events occurred in patients with and without liver metastases. Age greater than 60 and a diagnosis of cancer independently predispose patients to an increased risk of coagulopathy .



Commonly used brand name(s)

In the U.S.


  • Xeloda

Available Dosage Forms:


  • Tablet

Therapeutic Class: Antineoplastic Agent


Pharmacologic Class: Antimetabolite


Uses For Xeloda


Capecitabine belongs to the group of medicines called antimetabolites. It is used to treat breast cancer and colorectal cancer.


Capecitabine interferes with the growth of cancer cells, which are eventually destroyed. Since the growth of normal cells may also be affected by the medicine, other effects will also occur. Some of these may be serious and must be reported to your doctor. Other effects may not be serious but may cause concern.


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


Once a medicine has been approved for marketing for a certain use, experience may show that it is also useful for other medical problems. Although these uses are not included in product labeling, capecitabine is used in certain patients with the following medical conditions:


  • Advanced or metastatic stomach cancer, first-line therapy.

  • Metastatic colorectal cancer (cancer of the colon or rectum that has spread to other areas of the body), first-line therapy, in combination with bevacizumab and oxaliplatin.

Before Using Xeloda


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


There is no specific information comparing use of capecitabine in children with use in other age groups.


Geriatric


Patients 80 years of age or older may be more sensitive to the effects of capecitabine. Severe diarrhea, nausea, or vomiting may be more likely to occur in these patients. Patients 60 years of age and older and/or who are also taking an anticoagulant (blood thinner), may be more likely to have blood clotting problems.


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


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.


  • Rotavirus Vaccine, Live

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.


  • Adenovirus Vaccine Type 4, Live

  • Adenovirus Vaccine Type 7, Live

  • Bacillus of Calmette and Guerin Vaccine, Live

  • Influenza Virus Vaccine, Live

  • Measles Virus Vaccine, Live

  • Mumps Virus Vaccine, Live

  • Rotavirus Vaccine, Live

  • Rubella Virus Vaccine, Live

  • Smallpox Vaccine

  • Typhoid Vaccine

  • Varicella Virus Vaccine

  • Warfarin

  • Yellow Fever Vaccine

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.


  • Leucovorin

  • Levoleucovorin

  • Phenytoin

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:


  • Allergy to capecitabine or to any ingredients in this medicine or

  • Allergy to 5-fluorouracil or

  • Shortage of an enzyme called dihydropyrimidine dehydrogenase that your body needs—Capecitabine should not be used.

  • Bone marrow depression or

  • Cancer—May increase risk of blood clotting problems.

  • Chickenpox (including recent exposure) or

  • Herpes zoster (shingles)—Risk of severe disease affecting other parts of the body.

  • Heart disease—The risk of a side effect that affects the heart may be increased.

  • Infection—Capecitabine decreases your body's ability to fight infection.

  • Kidney disease, moderate or severe—The risk of side effects that affect the kidneys may be increased. Capecitabine should not be used in patients with severe kidney disease.

  • Liver disease—The amount of capecitabine in the body may be increased in patients with liver disease. Also, the risk of a side effect that affects the liver may be increased.

Proper Use of Xeloda


Each dose of this medicine should be taken within 30 minutes after the end of a meal.


Swallow the tablets with water.


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 breast cancer:
      • Adults—The starting dose is usually 2500 milligrams (mg) per square meter of body surface area a day, divided into two doses and taken about twelve hours apart within 30 minutes after the end of a meal. However, the dose may have to be decreased if certain side effects occur.

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


    • In combination with docetaxel to treat breast cancer:
      • The starting dose of capecitabine is usually 2500 milligrams (mg) per square meter of body surface area a day, divided into two doses and taken about twelve hours apart within 30 minutes after the end of a meal combined with docetaxel at 75 mg per square meter of body surface area as a 1 hour infusion every 3 weeks.

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


    • For colorectal cancer:
      • Adults—The starting dose is usually 2500 milligrams (mg) per square meter of body surface area a day, divided into two doses and taken about twelve hours apart within 30 minutes after the end of a meal. However, the dose may have to be decreased if certain side effects occur.

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



Missed Dose


If you miss a dose of this medicine, 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 Xeloda


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


Your health care professional may request that you have a test to determine if your blood is clotting properly and may preform this test frequently, if you are also taking an anticoagulant (blood thinner).


Check with your doctor immediately if you develop a fever of 100.5 degrees F or higher, or if you notice any other signs of a possible infection. These signs include cough or hoarseness, lower back or side pain, painful or difficult urination, sneezing, sore throat, stuffy nose, and white spots inside the mouth or throat.


Stop taking this medicine and check with your doctor immediately if any of the following occur:


  • Diarrhea, moderately severe (four to six stools a day more than usual, or during the night).

  • Pain, blistering, peeling, redness, or swelling of the palms of your hands and/or the bottoms of your feet that is severe enough to interfere with your normal activities.

  • Nausea that is severe enough to cause you to eat less than usual.

  • Vomiting that occurs two times, or more, in a 24-hour period.

  • Pain and redness, swelling, or sores or ulcers in your mouth or on your lips that are severe enough to interfere with eating.

If vomiting occurs less often than mentioned above, or if nausea does not cause you to eat less than usual, it is not necessary for you to stop taking the medicine or to check with your doctor (unless these effects are particularly bothersome). Also, you do not need to stop taking the medicine if diarrhea occurs less often than mentioned above or if the other side effects listed are not severe enough to interfere with eating or other daily activities. However, check with your doctor as soon as possible if they occur.


While you are being treated with capecitabine, and after you stop treatment with it, do not have any immunizations (vaccinations) without your doctor's approval. Capecitabine may lower your body's resistance and there is a chance you might get the infection the immunization is meant to prevent. In addition, other persons living in your household should not take oral polio vaccine since there is a chance they could pass the polio virus on to you. Also, avoid persons who have taken oral polio vaccine within the last several months. Do not get close to them, and do not stay in the same room with them for very long. If you cannot take these precautions, you should consider wearing a protective face mask that covers the nose and mouth.


Capecitabine can temporarily lower the number of white blood cells in your blood, increasing the chance of getting an infection. It can also lower the number of platelets, which are necessary for proper blood clotting. If this occurs, there are certain precautions you can take, especially when your blood count is low, to reduce the risk of infection or bleeding:


  • If you can, avoid people with infections. Check with your doctor immediately if you think you are getting an infection or if you get a fever or chills, cough or hoarseness, lower back or side pain, or painful or difficult urination.

  • Check with your doctor immediately if you notice any unusual bleeding or bruising; black, tarry stools; blood in urine or stools; or pinpoint red spots on your skin.

  • Be careful when using a regular toothbrush, dental floss, or toothpick. Your medical doctor, dentist, or nurse may recommend other ways to clean your teeth and gums. Check with your medical doctor before having any dental work done.

  • Do not touch your eyes or the inside of your nose unless you have just washed your hands and have not touched anything else in the meantime.

  • Be careful not to cut yourself when you are using sharp objects such as a safety razor or fingernail or toenail cutters.

  • Avoid contact sports or other situations where bruising or injury could occur.

Xeloda 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.


Stop taking this medicine and get emergency help immediately if any of the following effects occur:


More common
  • Diarrhea (moderately severe [four to six stools a day more than usual, or at night])

  • pain, blistering, peeling, redness, or swelling of palms of hands and/or bottoms of feet (severe enough to interfere with normal activities)

  • pain, redness, swelling, sores, or ulcers in your mouth or on your lips (severe enough to interfere with eating)

Less common
  • Nausea (severe, accompanied by loss of appetite)

  • vomiting (severe [occurring two times or more in 24 hours])

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


Less common or rare
  • Abdominal or stomach cramping or pain (severe)

  • agitation

  • back pain

  • bleeding and bruising

  • bleeding gums

  • blood in urine or stools

  • bloody nose

  • bloody or black, tarry stools

  • blurred vision

  • burning, dry, or itching eyes

  • chest pain

  • chills

  • cold

  • collapse

  • coma

  • confusion

  • constipation (severe)

  • convulsions

  • cough or hoarseness (accompanied by fever or chills)

  • cough producing mucus

  • coughing or spitting up blood

  • decreased frequency/amount of urine

  • difficulty breathing

  • difficulty in swallowing or pain in back of throat or chest when swallowing

  • discharge from eye

  • drowsiness

  • dry mouth

  • excessive tearing

  • extra heartbeats

  • eye redness, irritation, or pain

  • fainting

  • fast or irregular heartbeat

  • fever or chills

  • flu-like symptoms

  • hallucinations

  • headache, sudden and severe

  • heavier menstrual periods

  • high fever

  • hot, red skin on feet or legs

  • inability to speak

  • increased blood pressure

  • increased menstrual flow or vaginal bleeding

  • increased thirst

  • irritability

  • itching in genital or other skin areas

  • large amount of triglycerides in the blood

  • lightheadedness

  • loss of consciousness

  • lower back or side pain (accompanied by fever or chills)

  • mood or mental changes

  • muscle aches or cramps

  • muscle spasms

  • nosebleeds

  • numbness or tingling in hands, feet, or lips

  • painful or difficult urination (accompanied by fever or chills)

  • painful, swollen feet or legs

  • pain, tenderness, and/or swelling in upper abdominal (stomach) area

  • pale skin

  • paralysis

  • pinpoint red spots on skin

  • prolonged bleeding from cuts

  • rapid, shallow breathing

  • red or dark brown urine

  • redness, pain, or swelling of eye, eyelid, or inner lining of eyelid

  • scaling

  • seizures

  • severe constipation

  • shortness of breath, troubled breathing, tightness in chest, and/or wheezing

  • slow or irregular heartbeat

  • slurred speech

  • sneezing, sore throat, and/or stuffy nose

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

  • stiff neck

  • stomach bloating, burning, cramping, or pain

  • swelling of lymph nodes

  • temporary blindness

  • tiredness or weakness (severe)

  • trouble in speaking

  • twitching seizures

  • unusual bleeding or bruising

  • unusual lump or swelling in the chest

  • vomiting blood or material that looks like coffee grounds

  • weakness in arm and/or leg on one side of the body, sudden and severe

  • weight gain or loss

  • wheezing

  • white patches in the mouth or throat or on the tongue

  • white patches with diaper rash

  • yellow eyes or skin

Incidence not known
  • Continuing vomiting

  • dark-colored urine

  • general feeling of tiredness or weakness

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


More common
  • Abdominal or stomach pain (mild or moderate)

  • blistering, peeling, redness, and/or swelling of palms of hands or bottoms of feet (not severe enough to interfere with daily activities)

  • diarrhea (mild [fewer than four stools a day more than usual])

  • numbness, pain, tingling, or other unusual sensations in palms of hands or bottoms of feet

  • pain, redness, swelling, sores, or ulcers in your mouth or on your lips (not severe enough to interfere with eating)

  • unusual tiredness or weakness (mild or moderate)

Less common or rare
  • Clumsiness or unsteadiness

  • dark urine

  • decrease or increase in blood pressure

  • light-colored stools

  • problems with coordination

  • skin rash or itching

  • swelling of face, fingers, feet, or lower legs

  • swollen glands

  • unexplained nosebleeds

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
  • Constipation (mild or moderate)

  • loss of appetite (not due to nausea)

  • nausea (not accompanied by loss of appetite)

  • vomiting (mild [once a day or less])

Less common
  • Burning, crawling, itching, numbness, prickling, “pins and needles”, or tingling feelings

  • changes or discoloration in fingernails or toenails

  • difficulty in moving

  • discouragement

  • dizziness

  • fatigue

  • headache

  • heartburn

  • increase in heart rate

  • increased sensitivity of skin to sunlight

  • muscle pain

  • pain

  • pain in joints

  • pain in limbs

  • pain and redness of skin at place of earlier radiation (x-ray) treatment

  • red, sore eyes

  • sunken eyes

  • thirst

  • trouble in sleeping

  • weakness

  • wrinkled skin

Rare
  • Bone pain

  • change in color of treated skin

  • difficulty in walking

  • discouragement

  • dryness or soreness or throat

  • feeling of constant movement of self or surroundings

  • feeling sad or empty

  • full feeling in abdomen

  • full or bloated feeling or pressure in the stomach

  • general feeling of discomfort or illness

  • hoarseness

  • hot flushes

  • impaired balance

  • increased weight

  • joint pain

  • lack of appetite

  • loss of interest or pleasure

  • muscle weakness

  • noisy breathing

  • pain in rectum

  • pain, swelling, or redness in joints

  • passing less gas

  • rough, scratchy sound to voice

  • runny nose

  • sensation of spinning

  • shakiness in legs, arms, hands, or feet

  • shivering

  • sleepiness

  • sores on the skin

  • sweating increased

  • swelling of abdominal or stomach area

  • tremor or shaking of hands or feet

  • trouble concentrating

  • voice changes

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: Xeloda 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 Xeloda resources


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


  • Xeloda Prescribing Information (FDA)

  • Xeloda Consumer Overview

  • Xeloda Monograph (AHFS DI)

  • Xeloda MedFacts Consumer Leaflet (Wolters Kluwer)

  • Capecitabine Professional Patient Advice (Wolters Kluwer)



Compare Xeloda with other medications


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  • Stomach Cancer

Xylocaine Jelly


Generic Name: lidocaine topical (LYE doe kane TOP i kal)

Brand Names: AneCream, AneCream with Tegaderm, Anestacon, Bactine, LidaMantle, Lidocream, Lidoderm, Lidosense5, LMX 4, LMX 4 with Tegaderm, LMX 5, Medi-Quik Spray, Senatec, Solarcaine Aloe Extra Burn Relief, Solarcaine Cool Aloe, Uro-Jet, Uro-Jet AC, Xylocaine Jelly, Xylocaine Topical


What is Xylocaine Jelly (lidocaine topical)?

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


Lidocaine topical (for use on the skin) is used to reduce pain or discomfort caused by skin irritations such as sunburn, insect bites, poison ivy, poison oak, poison sumac, and minor cuts, scratches, hemorrhoids, and burns.


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


What is the most important information I should know about Xylocaine Jelly (lidocaine topical)?


An overdose of numbing medications can cause fatal side effects if too much of the medicine is absorbed through your skin and into your blood. This is more likely to occur when using a numbing medicine without the advice of a medical doctor (such as during a cosmetic procedure like laser hair removal). However, overdose has also occurred in women treated with a numbing medicine before having a mammography. Overdose symptoms may include uneven heartbeats, seizure (convulsions), coma, slowed breathing, or respiratory failure (breathing stops). Your body may absorb more of this medication if you use too much, if you apply it over large skin areas, or if you apply heat, bandages, or plastic wrap to treated skin areas. Skin that is cut or irritated may also absorb more topical medication than healthy skin.

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


Keep both used and unused lidocaine skin patches out of the reach of children or pets. The amount of lidocaine in the skin patches could be harmful to a child or pet who accidentally sucks on or swallows the patch. Seek emergency medical attention if this happens.

What should I discuss with my healthcare provider before using Xylocaine Jelly (lidocaine topical)?


An overdose of numbing medications can cause fatal side effects if too much of the medicine is absorbed through your skin and into your blood.

Overdose is more likely to occur when using a numbing medicine without the advice of a medical doctor (such as during a cosmetic procedure like laser hair removal). However, overdose has also occurred in women treated with a numbing medicine before having a mammography. Symptoms may include uneven heartbeats, seizure (convulsions), coma, slowed breathing, or respiratory failure (breathing stops).


You should not use lidocaine topical if you are allergic to any other type of numbing medicine.

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



  • liver disease; or




  • broken, swollen, or damaged skin.




FDA pregnancy category B. This medication is not expected to be harmful to an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant during treatment. Lidocaine topical 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.

How should I use Xylocaine Jelly (lidocaine 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.


Lidocaine topical comes in many different forms for different uses. Lidocaine topical cream, lotion, spray, solution, film, and transdermal patch are generally for use on the skin only.


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


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

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


Lidocaine topical may be applied with your finger tips or a cotton swab. Follow your doctor's instructions.


Do not apply this medication to swollen skin areas or deep puncture wounds. Avoid using the medicine on skin that is raw or blistered, such as a severe burn or abrasion. Store at room temperature away from moisture and heat. Keep both used and unused lidocaine topical patches out of the reach of children or pets. The amount of lidocaine in the skin patches could be harmful to a child or pet who accidentally sucks on or swallows the patch. Seek emergency medical attention if this happens.

What happens if I miss a dose?


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


What happens if I overdose?


Seek emergency medical attention or call the Poison Help line at 1-800-222-1222. Lidocaine topical applied to the skin is not likely to cause an overdose unless you apply more than the recommended dose. Overdose may also occur if you apply heat, bandages, or plastic wrap to treated skin areas.

Improper use of lidocaine topical may result in death.


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


What should I avoid while using Xylocaine Jelly (lidocaine topical)?


Do not allow this medication to come into contact with your eyes. If it does, rinse with water. Avoid touching the sticky side of a lidocaine skin patch while applying it.

Avoid using other topical medications on the affected area unless your doctor has told you to.


Xylocaine Jelly (lidocaine 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 lidocaine topical and call your doctor at once if you have any of these serious side effects:

  • uneven heartbeats;




  • drowsiness, confusion;




  • tremors, seizure (convulsions); or




  • blurred vision.



Less serious side effects include:



  • mild irritation, redness, or swelling where the medication is applied; or




  • numbness in places where the medicine is accidentally applied.



This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.


What other drugs will affect Xylocaine Jelly (lidocaine topical)?


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



  • quinidine (Quin-G);




  • disopyramide (Norpace);




  • flecainide (Tambocor);




  • mexiletine (Mexitil);




  • procainamide (Procan, Pronestyl);




  • tocainide (Tonocard); or




  • propafenone (Rythmol).



This list is not complete and other drugs may interact with lidocaine. 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 Xylocaine Jelly resources


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


  • Xylocaine Jelly Prescribing Information (FDA)

  • Xylocaine Jelly Gel MedFacts Consumer Leaflet (Wolters Kluwer)

  • Anestacon Topical Advanced Consumer (Micromedex) - Includes Dosage Information

  • Bactine Liquid MedFacts Consumer Leaflet (Wolters Kluwer)

  • LMX 5 Cream MedFacts Consumer Leaflet (Wolters Kluwer)

  • LidaMantle Cream MedFacts Consumer Leaflet (Wolters Kluwer)

  • Lidoderm Consumer Overview

  • Lidoderm Patch MedFacts Consumer Leaflet (Wolters Kluwer)

  • Lidoderm Prescribing Information (FDA)

  • Solarcaine Aerosol Spray MedFacts Consumer Leaflet (Wolters Kluwer)

  • Solarcaine Advanced Consumer (Micromedex) - Includes Dosage Information

  • Xylocaine Viscous Solution MedFacts Consumer Leaflet (Wolters Kluwer)

  • Zingo Prescribing Information (FDA)

  • Zingo Consumer Overview

  • Zingo System MedFacts Consumer Leaflet (Wolters Kluwer)



Compare Xylocaine Jelly with other medications


  • Anal Itching
  • Anesthesia
  • Burns, External
  • Hemorrhoids
  • Pain
  • Pruritus


Where can I get more information?


  • Your pharmacist has information about lidocaine topical.

See also: Xylocaine side effects (in more detail)


Friday, October 21, 2016

Xgeva



Pronunciation: den-OH-sue-mab
Generic Name: Denosumab
Brand Name: Xgeva


Xgeva is used for:

Preventing certain bone-related events in patients who have a certain type of tumor that has spread to the bones (bone metastases).


Xgeva is a receptor activator of nuclear factor-kappa B (RANK) ligand inhibitor. It works by decreasing the formation, function, and survival of certain bone cells (osteoclasts) that are responsible for slowing bone loss. Decreased osteoclast activity helps to reduce the risk of bone-related events in patients with cancer that has spread to the bone.


Do NOT use Xgeva if:


  • you are allergic to any ingredient in Xgeva

  • you have multiple myeloma

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



Before using Xgeva:


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


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

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

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

  • if you have a history of kidney problems or you are on dialysis

  • if you have low blood calcium levels, cannot take daily calcium or vitamin D supplements, or plan to have dental surgery or teeth removed

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


Ask your health care provider if Xgeva 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 Xgeva:


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


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

  • Use the proper technique taught to you by your doctor. Inject deep under the skin, NOT into a vein or muscle.

  • Xgeva is a colorless to pale yellow solution that may contain a very small amount of clear to white particles. Do not use Xgeva if it contains many particles or any foreign matter. Do not use it if the solution is cloudy or discolored, or if the vial is cracked or damaged.

  • Do not vigorously shake Xgeva.

  • 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 Xgeva, contact your doctor right away.

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



Important safety information:


  • Talk to your doctor about taking a calcium or vitamin D supplement while you use Xgeva.

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

  • Xgeva may cause jaw bone problems in some patients. Your risk may be greater if you have had a tooth removed, or a history of poor dental hygiene or use of a dental appliance. Your risk may also be greater if you have had certain dental procedures. Talk to your doctor about having a dental exam before you start to use Xgeva. Ask your doctor any questions you may have about dental treatment while you use Xgeva.

  • Proper dental care is important while you are taking Xgeva. Brush and floss your teeth and visit the dentist regularly.

  • If you have dental surgery while you are using Xgeva, contact your doctor if you have persistent pain or slow healing of the mouth or jaw after the surgery.

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

  • Xgeva should be used with extreme caution in CHILDREN; safety and effectiveness in children have not been confirmed. Xgeva may affect bone growth and tooth development in children.

  • PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Xgeva while you are pregnant. It is not known if Xgeva is found in breast milk. Do not breast-feed while taking Xgeva.


Possible side effects of Xgeva:


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:



Diarrhea; headache; nausea; tiredness; 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); cough; pain, numbness, swelling, or drainage from the jaw, mouth, or teeth; shortness of breath; symptoms of low blood calcium levels (eg, muscle spasms, twitches, or cramps; burning, numbness, or tingling in your fingers, toes, or around your mouth); symptoms of low blood phosphate levels (eg, new or worsening loss of appetite, muscle weakness or pain, seizures); ulcers of the gums.



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: Xgeva side effects (in more detail)


If OVERDOSE is suspected:


Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately.


Proper storage of Xgeva:

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


General information:


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

  • Xgeva 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 Xgeva. 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 Xgeva resources


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


  • Xgeva Prescribing Information (FDA)

  • Xgeva Advanced Consumer (Micromedex) - Includes Dosage Information

  • Xgeva Consumer Overview

  • Denosumab Professional Patient Advice (Wolters Kluwer)

  • Denosumab Monograph (AHFS DI)

  • Prolia Consumer Overview

  • Prolia Prescribing Information (FDA)



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