Friday, September 16, 2016

Marezine


Generic Name: cyclizine (SYE kli zeen)

Brand Names: Marezine


What is Marezine (cyclizine)?

Cyclizine is used to relieve nausea, vomiting, and dizziness associated with motion sickness.


Cyclizine may also be used for purposes other than those listed in this medication guide.


What is the most important information I should know about Marezine (cyclizine)?


Use caution when driving, operating machinery, or performing other hazardous activities. Cyclizine may cause dizziness, drowsiness, or blurred vision. If you experience dizziness, drowsiness, or blurred vision, avoid these activities. Use alcohol cautiously. Alcohol may increase drowsiness and dizziness while you are taking cyclizine.

Who should not take Marezine (cyclizine)?


Before taking this medication, tell your doctor if you have



  • kidney or liver disease,




  • an enlarged prostate,




  • difficulty urinating,




  • bladder problems, or




  • glaucoma.



You may not be able to take cyclizine, or you may require a lower dose or special monitoring during treatment if you have any of the conditions listed above.


Cyclizine is in the FDA pregnancy category B. This means that it is unlikely to harm an unborn baby. Do not take cyclizine without first talking to your doctor if you are pregnant. It is not known whether cyclizine passes into breast milk. Do not take cyclizine without first talking to your doctor if you are breast-feeding a baby. Cyclizine is not recommended for use by children younger than 12 years of age.

How should I take Marezine (cyclizine)?


Take cyclizine exactly as directed by your doctor. If you do not understand these directions, ask your pharmacist, nurse, or doctor to explain them to you.


Take each dose with a full glass of water.

Cyclizine usually is taken approximately 30 minutes before travel and then every 4 to 6 hours as needed. Do not take more than 200 mg of this medication in 1 day.


Store cyclizine at room temperature away from moisture and heat.

What happens if I miss a dose?


Take the missed dose as soon as you remember. However, if it is almost time for your next dose, skip the missed dose and take only your next regularly scheduled dose. Do not take a double dose of this medication.


What happens if I overdose?


Seek emergency medical attention.

Symptoms of a cyclizine overdose include drowsiness, agitation, excitability, seizures or convulsions, hallucinations, and death.


What should I avoid while taking Marezine (cyclizine)?


Use caution when driving, operating machinery, or performing other hazardous activities. Cyclizine may cause dizziness, drowsiness, or blurred vision. If you experience dizziness, drowsiness, or blurred vision, avoid these activities. Use alcohol cautiously. Alcohol may increase drowsiness and dizziness while you are taking cyclizine.

Marezine (cyclizine) side effects


Stop taking cyclizine and seek emergency medical attention if you experience an allergic reaction (difficulty breathing; closing of your throat; swelling of your lips, tongue, or face; or hives).

Other, less serious side effects may be more likely to occur. Continue to take cyclizine and talk to your doctor if you experience



  • drowsiness;




  • restlessness, excitation, nervousness, or insomnia;




  • blurred vision;




  • dry mouth, nose, or throat;




  • decreased appetite, nausea, or vomiting;




  • difficulty urinating; or




  • an irregular or fast heartbeat.



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. You may report side effects to FDA at 1-800-FDA-1088.


What other drugs will affect Marezine (cyclizine)?


Cyclizine may increase the effects of other drugs that cause drowsiness, including antidepressants, alcohol, antihistamines, sedatives (used to treat insomnia), pain relievers, anxiety medicines, and muscle relaxants. Tell your doctor about all medicines that you are taking, and do not take any medicine unless your doctor approves.


Drugs other than those listed here may also interact with cyclizine. Talk to your doctor and pharmacist before taking any prescription or over-the-counter medicines.



More Marezine resources


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


  • Marezine MedFacts Consumer Leaflet (Wolters Kluwer)

  • Bonine for Kids MedFacts Consumer Leaflet (Wolters Kluwer)



Compare Marezine with other medications


  • Motion Sickness
  • Nausea/Vomiting


Where can I get more information?


  • Your pharmacist has more information about cyclizine written for health professionals that you may read.

See also: Marezine side effects (in more detail)


Menthol Cream


Pronunciation: MEN-thol
Generic Name: Menthol
Brand Name: Stopain


Menthol Cream is used for:

Relieving minor pain caused by conditions such as arthritis, bursitis, tendonitis, muscle strains or sprains, backache, bruising, and cramping. It may also be used for other conditions as determined by your doctor.


Menthol Cream is a topical analgesic. It works by temporarily relieving minor pain.


Do NOT use Menthol Cream if:


  • you are allergic to any ingredient in Menthol Cream

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



Before using Menthol Cream:


Some medical conditions may interact with Menthol Cream. 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 cut, scraped, irritated, or damaged skin at the application site

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


Ask your health care provider if Menthol Cream 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 Menthol Cream:


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


  • Wash your hands before and right after using Menthol Cream.

  • Apply Menthol Cream to the affected area as directed by your doctor or on the package label.

  • Do not wrap, bandage, or use a heating pad on the treated area.

  • Do not apply Menthol Cream more than 4 times daily.

  • If you miss a dose of Menthol Cream, use it as soon as you remember. Continue to use it as directed by your doctor or on the package label.

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



Important safety information:


  • Menthol Cream is for external use only. Do not get it in your eyes, on your lips, or in your nose, mouth, or genital area. If you get it in any of these areas, rinse right away with cool tap water.

  • Do NOT use more than the recommended dose or use for longer than 1 week without checking with your doctor.

  • If your symptoms do not improve within 7 days, if they get worse, or if they clear up and then come back again, contact your doctor.

  • Menthol Cream should not be used in CHILDREN younger than 12 years old without first checking with the child's doctor; 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 Menthol Cream while you are pregnant. It is not known if Menthol Cream is found in breast milk after topical use. If you are or will be breast-feeding while you use Menthol Cream, check with your doctor. Discuss any possible risks to your baby.


Possible side effects of Menthol Cream:


All medicines may cause side effects, but many people have no, or minor, side effects. No COMMON side effects have been reported with Menthol Cream. 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); redness or irritation at the application site.



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: Menthol 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. Menthol Cream may be harmful if swallowed.


Proper storage of Menthol Cream:

Store Menthol Cream at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat and light. Keep Menthol Cream out of the reach of children and away from pets.


General information:


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

  • Menthol Cream 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 Menthol Cream. 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 Menthol resources


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


Compare Menthol with other medications


  • Cough
  • Pain

mechlorethamine


Generic Name: mechlorethamine (mech klor EH tha meen)

Brand Names: Mustargen


What is mechlorethamine?

Mechlorethamine is a cancer (antineoplastic) medication. Mechlorethamine interferes with the growth of cancer cells and slows their growth and spread in the body.


Mechlorethamine is used to treat several types of cancer, such as Hodgkin's Disease, lymphosarcoma, chronic myelocytic or chronic lymphocytic leukemia, lung cancer and mycosis fungoides. Mechlorethamine is also used to treat certain other blood disorders (polycythemia vera) and is sometimes injected into body spaces, such as the chest, abdomen or the sack containing the heart, to stop the accumulation of fluids caused by cancer.


Mechlorethamine may also be used for purposes other than those listed in this medication guide.


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


Mechlorethamine should only be administered under the supervision of a qualified healthcare provider experienced in the use of cancer chemotherapeutic agents.


Serious side effects have been reported with the use of mechlorethamine including: allergic reactions (difficulty breathing; closing of the throat; swelling of the lips, tongue, or face; or hives); decreased bone marrow function and blood problems (extreme fatigue; easy bruising or bleeding; black, bloody or tarry stools; fever or chills; or signs of infection such as fever; chills, or sore throat); severe nausea, vomiting, diarrhea, and loss of appetite; and others. Talk to your doctor about the possible side effects from treatment with mechlorethamine.


Mechlorethamine is highly toxic and both the powder and solution must be handled with care. Inhalation of dust or vapors and contact with skin or mucous membranes (eyes, nose and mouth) must be avoided.


Who should not take mechlorethamine?


Before taking mechlorethamine, tell your doctor if you



  • have had recent vaccinations;




  • have any type of infection;




  • have bone marrow problems;




  • have had radiation or x-ray therapy; or




  • have been treated with other cancer (chemotherapy) medicines.



You may not be able to take mechlorethamine, or you may require a dosage adjustment or special monitoring during treatment if you have any of the conditions listed above.


Mechlorethamine is in the FDA pregnancy category D. This means that mechlorethamine is known to cause birth defects in an unborn baby. Do not take mechlorethamine without first talking to your doctor if you are pregnant or could become pregnant during treatment. Contraceptive measures are recommended during treatment with mechlorethamine. It is not known whether mechlorethamine passes into breast milk. Do not take mechlorethamine without first talking to your doctor if you are breast feeding a baby.

How should I take mechlorethamine?


Mechlorethamine should only be administered under the supervision of a qualified healthcare provider experienced in the use of cancer chemotherapeutic agents.


Your doctor will determine the correct amount and frequency of treatment with mechlorethamine depending upon the type of cancer being treated and other factors. Talk to your doctor if you have any questions or concerns regarding the treatment schedule.


Your doctor will probably want you to have regularly scheduled blood tests and other medical evaluations during treatment with mechlorethamine to monitor progress and side effects.


Mechlorethamine is highly toxic and both the powder and solution must be handled with care. Inhalation of dust or vapors and contact with skin or mucous membranes (eyes, nose and mouth) must be avoided. Should accidental contact occur, rinse the area with water and seek emergency medical attention.


Your healthcare provider will store mechlorethamine as directed by the manufacturer.


What happens if I miss a dose?


Contact your doctor if you miss a dose of mechlorethamine injection.


What happens if I overdose?


If for any reason an overdose of mechlorethamine is suspected, seek emergency medical attention or contact your healthcare provider immediately.

Symptoms of a mechlorethamine overdose tend to be similar to side effects caused by the medication, although often more severe.


What should I avoid while taking mechlorethamine?


Mechlorethamine can lower the activity of your immune system making you susceptible to infections. Avoid contact with people who have colds, the flu, or other contagious illnesses and do not receive vaccines that contain live strains of a virus (e.g., live oral polio vaccine) during treatment with mechlorethamine. In addition, avoid contact with individuals who have recently been vaccinated with a live vaccine. There is a chance that the virus can be passed on to you.


Mechlorethamine is highly toxic and both the powder and solution must be handled with care. Inhalation of dust or vapors and contact with skin or mucous membranes (eyes, nose and mouth) must be avoided.


Mechlorethamine side effects


If you experience any of the following serious side effects, seek emergency medical attention or contact your doctor immediately:

  • an allergic reaction (shortness of breath; closing of your throat; difficulty breathing; swelling of your lips, face, or tongue; or hives);




  • blood in the urine;




  • black or tarry stools;




  • signs of infection such as fever; chills, or sore throat;




  • joint pain and stiffness similar to gout (high levels of uric acid in the blood);




  • jaundice (yellowing of the skin or eyes);or




  • unusual bleeding or bruising.



Other less serious side effects may be more likely to occur. Talk to your doctor if you experience:



  • nausea, vomiting, or decreased appetite;




  • mouth sores;




  • a sensation of spinning or dizziness (vertigo);




  • diarrhea;




  • temporary hair loss;




  • rash;




  • a ringing in the ears or decreased ability to hear; or




  • weakness.



In some cases, second malignancies have been reported to occur during and following treatment with mechlorethamine. Talk to your doctor about the risks and benefits of this medication.


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. You may report side effects to FDA at 1-800-FDA-1088.


Mechlorethamine Dosing Information


Usual Adult Dose for Malignant Disease:

0.4 mg/kg IV once a month or
0.2 mg/kg IV once a day for 2 days or
0.1 mg/kg IV once a day for 4 days or
6 mg/m² IV on days 1 and 8 of a 28 day cycle, as part of the MOPP regimen for Hodgkin's disease or
0.4 mg/kg intracavity injection one time or
0.2 mg/kg intrapericardial injection one time.

Usual Adult Dose for Mycosis Fungoides:

0.01% topically once a day.

Usual Pediatric Dose for Malignant Disease:

Child: 0.4 mg/kg IV once a month or
0.2 mg/kg IV once a day for 2 days or
0.1 mg/kg IV once a day for 4 days or
6 mg/m² IV on days 1 and 8 of a 28 day cycle, as part of the MOPP regimen for Hodgkin's disease or
0.4 mg/kg intracavity injection one time or
0.2 mg/kg intrapericardial injection one time.


What other drugs will affect mechlorethamine?


Do not receive "live" vaccines during treatment with mechlorethamine. Administration of a live vaccine may be dangerous during treatment with mechlorethamine.

Other drugs may interact with mechlorethamine. Talk to your doctor and pharmacist before taking any other prescription or over-the-counter medicines, including herbal products, during treatment with mechlorethamine.



More mechlorethamine resources


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


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

  • Mechlorethamine MedFacts Consumer Leaflet (Wolters Kluwer)

  • Mustargen Prescribing Information (FDA)



Compare mechlorethamine with other medications


  • Cancer
  • Mycosis Fungoides


Where can I get more information?


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

See also: mechlorethamine side effects (in more detail)


measles and rubella virus vaccine live Intramuscular, Injection


MEE-zuls VYE-rus VAX-een, lyve, roo-BELL-a VYE-rus VAX-een, lyve


Commonly used brand name(s)

In Canada


  • Eolarix

Available Dosage Forms:


  • Injectable

  • Powder for Solution

Therapeutic Class: Vaccine


Uses For measles and rubella virus vaccine live


Measles and rubella virus vaccine live is an active immunizing agent used to prevent infection by the measles and rubella viruses. It works by causing your body to produce its own protection (antibodies) against the viruses.


Measles (also known as coughing measles, hard measles, morbilli, red measles, rubeola, and 10-day measles) is an infection that is easily spread from one person to another. Infection with measles can cause serious problems, such as pneumonia, ear infections, sinus problems, convulsions (seizures), brain damage, and possibly death. The risk of serious complications and death is greater for adults and infants than for children and teenagers.


Rubella (also known as German measles) is a serious infection that causes miscarriages, stillbirths, or birth defects in unborn babies when pregnant women get the disease.


While immunization against measles and rubella is recommended for all persons 12 months of age and older, it is especially important for women of childbearing age and persons traveling outside the U.S.


If measles and rubella vaccine is to be given to a child, the child should be at least 12 months of age. This is to make sure the measles vaccine is effective. In a younger child, antibodies from the mother may prevent the vaccine from working.


This vaccine should be administered only by or under the supervision of your doctor or other health care professional.


Before Using measles and rubella virus vaccine live


In deciding to use a vaccine, the risks of taking the vaccine must be weighed against the good it will do. This is a decision you and your doctor will make. For this vaccine, the following should be considered:


Allergies


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


Pediatric


Use of this vaccine is not recommended for infants younger than 12 months of age, unless the risk of measles infection is high. Waiting until children are at least 12 months of age is important because antibodies that infants receive from their mothers before birth may interfere with the effectiveness of the vaccine. In addition, there may be special reasons why children between 6 months and 12 months of age also may require measles vaccination.


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


Studies in women suggest that this medication poses minimal risk to the infant when used during 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 receiving this vaccine, 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.


Receiving this vaccine 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.


  • Aclarubicin

  • Adalimumab

  • Aldesleukin

  • Alemtuzumab

  • Altretamine

  • Amonafide

  • Amsacrine

  • Asparaginase

  • Azacitidine

  • Azathioprine

  • Bleomycin

  • Broxuridine

  • Busulfan

  • Capecitabine

  • Carboplatin

  • Carmustine

  • Certolizumab Pegol

  • Chlorambucil

  • Cisplatin

  • Cladribine

  • Cyclophosphamide

  • Cytarabine

  • Cytarabine Liposome

  • Dacarbazine

  • Dactinomycin

  • Daunorubicin

  • Daunorubicin Citrate Liposome

  • Decitabine

  • Docetaxel

  • Doxifluridine

  • Doxorubicin Hydrochloride

  • Doxorubicin Hydrochloride Liposome

  • Edatrexate

  • Eflornithine

  • Epirubicin

  • Estramustine

  • Etanercept

  • Etoposide

  • Everolimus

  • Fingolimod

  • Floxuridine

  • Fludarabine

  • Fluorouracil

  • Fotemustine

  • Gallium Nitrate

  • Gemcitabine

  • Golimumab

  • Hydroxyurea

  • Idarubicin

  • Ifosfamide

  • Irinotecan

  • Lomustine

  • Mechlorethamine

  • Melphalan

  • Meningococcal Vaccine

  • Mercaptopurine

  • Methotrexate

  • Mitolactol

  • Mitomycin

  • Mitotane

  • Mitoxantrone

  • Mycophenolic Acid

  • Oxaliplatin

  • Paclitaxel

  • Pegaspargase

  • Pentostatin

  • Pipobroman

  • Pirarubicin

  • Plicamycin

  • Procarbazine

  • Raltitrexed

  • Rilonacept

  • Rituximab

  • Sirolimus

  • Streptozocin

  • Tacrolimus

  • Teceleukin

  • Tegafur

  • Temsirolimus

  • Teniposide

  • Thioguanine

  • Thiotepa

  • Topotecan

  • Treosulfan

  • Trimetrexate

  • Trofosfamide

  • Uracil Mustard

  • Ustekinumab

  • Vinblastine

  • Vincristine

  • Vincristine Liposome

  • Vindesine

  • Vinorelbine

Receiving this vaccine 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.


  • Abatacept

  • Cytomegalovirus Immune Globulin, Human

  • Hepatitis B Immune Globulin

  • Immune Globulin

  • Leflunomide

  • Rabies Immune Globulin

  • Respiratory Syncytial Virus Immune Globulin, Human

  • Rho(D) Immune Globulin

  • Tetanus Immune Globulin

  • Vaccinia Immune Globulin, Human

  • Varicella-Zoster Immune Globulin

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


  • Immune deficiency condition (or family history of)—Condition may increase the chance and severity of side effects of the vaccine and/or may decrease the useful effects of the vaccine

  • Severe illness with fever—The symptoms of the condition may be confused with the possible side effects of the vaccine

Proper Use of measles and rubella virus vaccine live


Dosing


The dose of measles and rubella virus vaccine live 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 measles and rubella virus vaccine live. 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 injection dosage form:
    • For prevention of measles and rubella:
      • Adults and children 12 months of age and older—One dose injected under the skin.

      • Children up to 12 months of age—Use is not recommended.



Precautions While Using measles and rubella virus vaccine live


Do not become pregnant for 3 months after receiving measles and rubella vaccine without first checking with your doctor. There may be a chance that this vaccine can cause birth defects.


Tell your doctor that you have received this vaccine:


  • If you are to receive a tuberculin skin test within 4 to 6 weeks after receiving this vaccine. The results of the test may be affected by this vaccine.

  • If you are to receive blood products or immune globulins within 14 days of receiving this vaccine.

  • If you are to receive this vaccine within 3 to 11 months of receiving blood products or immune globulins

measles and rubella virus vaccine live 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:


Symptoms of allergic reaction - rare
  • Difficulty in breathing or swallowing

  • hives

  • itching, especially of feet or hands

  • reddening of skin, especially around ears

  • swelling of eyes, face, or inside of nose

  • unusual tiredness or weakness (sudden and severe)

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


More common
  • Fever over 103 °F (39.4 °C)

Less common
  • Pain or tenderness of eyes

Rare
  • Bruising or purple spots on skin

  • confusion

  • convulsions (seizures)

  • double vision

  • headache (severe or continuing)

  • irritability

  • pain, numbness, or tingling of hands, arms, legs, or feet

  • stiff neck

  • vomiting

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 or stinging at place of injection

  • fever between 100 and 103 °F (37.7 and 39.4 °C)

  • skin rash

  • swelling of glands in neck

Less common
  • Aches or pain in joints

  • headache (mild)

  • itching, swelling, redness, tenderness, or hard lump at place of injection

  • nausea

  • runny nose

  • sore throat

  • vague feeling of bodily discomfort

The above side effects (especially aches or pain in joints) are more likely to occur in adults, particularly women.


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


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



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


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

Maxidex eent


Generic Name: Dexamethasone eent
Class: Corticosteroids
ATC Class: S01CA01
VA Class: OP350
CAS Number: 50-02-2

Introduction

A synthetic fluorinated corticosteroid.a b d


Uses for Maxidex


Ophthalmic Inflammation


Symptomatic relief of corticosteroid-responsive inflammatory conditions of the palpebral and bulbar conjunctiva, cornea, and anterior segment of the globe (e.g., allergic conjunctivitis, acne rosacea, superficial punctate keratitis, herpes zoster keratitis, iritis, cyclitis, selected infective conjunctivitides).a c d e f g h


Treatment of chronic anterior uveitis.e g h


Treatment of corneal injury from chemical, radiation, or thermal burns or penetration of foreign bodies.a c d e f g h


Bacterial Ophthalmic Infections


Used for anti-inflammatory properties in conjunction with appropriate anti-infective therapy in some bacterial infections of the eye;e f g h used in fixed combination with neomycin and polymyxin B sulfates or tobramycin when such combination therapy is indicated.e f g h If an ophthalmic corticosteroid is used in combination with an ophthalmic anti-infective, weigh benefits against risks.d (See Infections under Cautions.)


Otic Inflammation


Symptomatic relief of corticosteroid-responsive inflammatory conditions of the ear canal (e.g., allergic otitis externa).b c i


Bacterial Otic Infections


Used for anti-inflammatory properties in conjunction with ciprofloxacin for treatment of acute otitis externa and in pediatric patients with tympanostomy tubes for acute otitis media.i


Used to reduce edema and inflammation in select cases of purulent and nonpurulent infective otitis externa.c


If a corticosteroid is used alone or in combination with an otic anti-infective, weigh benefits against risks.d (See Infections under Cautions.)


Maxidex Dosage and Administration


Administration


Apply topically to the eye or ear.a b c e f g h i


Ophthalmic Administration


Apply topically to the eye as an ophthalmic ointment, solution, or suspension.a b c e f g h


Not for injection.e f g h


Shake suspension well prior to each use.a g


Avoid contamination of preparation container.a b e f


Do not administer solutions or suspensions containing benzalkonium chloride while wearing soft contact lenses.a c g Wait ≥15 minutes after instilling drops before inserting contact lenses.c (See Advice to Patients.)


Otic Administration


Apply topically to the ear as an otic suspension or an ophthalmic solution.b c i


Not for injection.i Do not instill otic preparations into the eye.i


May use dexamethasone sodium phosphate ophthalmic solution in the ear.b c


Shake suspension well prior to each use.i


To avoid dizziness that may result from instilling a cold preparation into the ear, warm the preparation by holding the bottle in the hands for 1–2 minutes prior to administration.i


Clean and dry ear canal prior to administration;b c d pH of otic preparations should be neutral or acidic.b


Lie with the affected ear upward and instill drops.i For pediatric patients with otitis media and tympanostomy tubes, pump the tragus 5 times to ease penetration of drops into the middle ear.i For acute otitis externa, pull outer ear lobe upward and backward to facilitate entry of drug into ear canal.i


Keep affected ear upward for ≥60 seconds following drug administration.i If necessary, repeat procedure for the opposite ear.i


Use otic corticosteroids sparingly to prevent an accumulation of excess debris in the ear canal.b d


Dosage


Commercially available alone or in fixed combination with anti-infectives; available as dexamethasone or dexamethasone sodium phosphate.a c d e f g h i Solution available as dexamethasone sodium phosphate; dosage expressed in terms of dexamethasone phosphate.c


Pediatric Patients


Bacterial Ophthalmic Infections

Duration of therapy depends on the type and severity of the disease and response to therapy.g Do not discontinue prematurely.g


When discontinuing therapy, gradually taper dosing frequency to avoid exacerbation of the disease.b


Dexamethasone 0.1% and Tobramycin 0.3%

Ophthalmic Suspension

Children ≥2 years of age: Initial 24–48 hours, 1 or 2 drop(s) into the conjunctival sac of the affected eye(s) every 2 hours.g Thereafter, 1 or 2 drops every 4–6 hours.g Gradually reduce dosing frequency as infection improves.g


Ophthalmic Ointment

Children ≥2 years of age: Apply a 1.25-cm ribbon into the conjunctival sac of the affected eye(s) up to 3 or 4 times daily.h


Bacterial Otic Infections

Acute Otitis Externa

Otic Suspension (Dexamethasone 0.1% and Ciprofloxacin 0.3%)

Children ≥6 months of age: 4 drops into the affected ear(s) twice daily for 7 days.i


Acute Otitis Media

Otic Suspension (Dexamethasone 0.1% and Ciprofloxacin 0.3%)

Children ≥6 months of age with tympanostomy tubes: 4 drops into the affected ear(s) twice daily for 7 days.i


Adults


Ophthalmic Inflammation and Bacterial Infections

Duration of therapy depends on the type and severity of the disease and response to therapy.g Do not discontinue prematurely.g


When discontinuing therapy, gradually taper dosing frequency to avoid exacerbation of the disease.b


Dexamethasone 0.1%

Ophthalmic Suspension

For mild inflammation: 1 or 2 drops into the conjunctival sac of the affected eye(s) up to 4–6 times daily.a


For severe inflammation: 1 or 2 drops into the conjunctival sac of the affected eye(s) every hour.a Taper dosing frequency as inflammation subsides.a


Dexamethasone Sodium Phosphate 0.1%

Ophthalmic Solution

Initially, 1 or 2 drops into the conjunctival sac of the affected eye(s) every hour during the day and every 2 hours during the night.c When a favorable response is attained, decrease to 1 drop every 4 hours.c May decrease to 1 drop 3 or 4 times daily to control symptoms.c


Dexamethasone 0.1%, Neomycin 0.35%, and Polymyxin B Sulfates 10,000 units

Ophthalmic Suspension

For mild inflammation: 1 or 2 drop(s) into the conjunctival sac of the affected eye(s) up to 4–6 times daily.f


For severe inflammation: 1 or 2 drops into the conjunctival sac of the affected eye(s) hourly.f As inflammation subsides, gradually reduce dosing frequency to discontinue.f


Ophthalmic Ointment

Apply a 1.25-cm ribbon into the conjunctival sac of the affected eye(s) up to 3 or 4 times daily.e


Dexamethasone 0.1% and Tobramycin 0.3%

Ophthalmic Suspension

Initial 24–48 hours, 1 or 2 drops into the conjunctival sac of the affected eye(s) every 2 hours; thereafter, 1 or 2 drops every 4 to 6 hours.g Gradually reduce dosing frequency as infection improves.g


Ophthalmic Ointment

Apply a 1.25-cm ribbon into the conjunctival sac of the affected eye(s) up to 3 or 4 times daily.h


Otic Inflammation

Dexamethasone Sodium Phosphate 0.1% Ophthalmic Solution

Otic

Initially, 3 or 4 drops of the ophthalmic solution into the ear canal 2 or 3 times daily.b c May reduce dosing frequency as symptoms improve.b c Gradually taper the drug when it is discontinued.c


Alternatively, a cotton wick saturated with the ophthalmic solution may be packed into the ear canal; keep the wick moist with the ophthalmic solution; remove saturated wick from ear after 12 to 24 hours.b c Repeat as necessary.b c


Duration of treatment may range from a few days to several weeks.b


Bacterial Otic Infections: Acute Otitis Externa

Dexamethasone 0.1% and Ciprofloxacin 0.3%

Otic

4 drops into the affected ear(s) twice daily for 7 days.i


Special Populations


No special population dosage recommendations at this time.a c e f g h i


Cautions for Maxidex


Contraindications



  • Known hypersensitivity to dexamethasone or any ingredient in the formulation.a c e f g h i



  • Ophthalmic Preparations


  • Viral diseases of the cornea and conjunctiva (e.g., epithelial herpes simplex keratitis [dendritic keratitis], vaccinia, varicella).a c e f g h




  • Mycobacterial infection (e.g., ocular tuberculosis) of the eye.a c e f g h




  • Fungal disease of ocular structures.a c e f g h



  • Otic Preparations


  • Viral infections of the external ear canal (e.g., herpes simplex).i




  • Perforation of the ear drum.c




  • Fungal diseases of auricular structures.c



Warnings/Precautions


Warnings


Ocular Effects

Risk of glaucoma with possible damage to the optic nerve, defects in visual acuity and fields of vision, and posterior subcapsular cataract formation with prolonged use of corticosteroids.a c d e f g h Use with caution in patients with glaucoma because IOP may increase.a c d e f g h


If used for ≥10 days, monitor IOP routinely even though monitoring may be difficult in children and uncooperative patients.a c d e f g h


In conditions causing thinning of the cornea or sclera, perforations reported with use of topical corticosteroids.a c d e f g h


Use of high-dose corticosteroids may delay healing.c h Use after cataract surgery may delay healing and increase incidence of bleb formation.c


Infections

Prolonged use may suppress the host response and thus increase the risk of secondary ocular infections.a c e f g


In acute purulent conditions of the eye or ear, corticosteroids may mask infection or enhance existing infection.a c d e f g h (See Contraindications under Cautions.)


Herpes Simplex

Use of corticosteroids in the treatment of herpes simplex infections other than epithelial herpes simplex keratitis, in which corticosteroids are contraindicated, requires great caution; periodic slit-lamp microscopy is essential.a c e f


General Precautions


Evaluation of Ocular Condition

Initial prescription or renewal of medication order beyond 8 g of 0.1% ointment or 20 mL of 0.1% suspension should be provided only after examination of the patient with the aid of magnification (e.g., slit lamp biomicroscopy, fluorescein staining where appropriate).e f g h


Fungal Infections

Long-term local corticosteroid application associated with development of fungal infections of the cornea.a d e f g h Consider possibility of fungal infection in patients with persistent corneal ulceration who have been or are receiving corticosteroid therapy.a c d e f h


Corneal Reepithelialization

Use of ophthalmic ointments may decrease rate of corneal reepithelialization.h


Use of Fixed Combination

When used in fixed combination with ciprofloxacin, neomycin and polymyxin B sulfates, or tobramycin, consider the cautions, precautions, and contraindications associated with the concomitant agents.e f g h i


Specific Populations


Pregnancy

Category C.a c e f g h i


Lactation

Not known whether topical administration of corticosteroids could result in sufficient systemic absorption to produce detectable quantities in milk.a e f g h i


Caution if used in nursing women.a e f g h


Dexamethasone sodium phosphate ophthalmic solution and dexamethasone in fixed combination with ciprofloxacin otic suspension: Manufacturers recommend discontinuing nursing or the drug.c i


Pediatric Use

Safety and efficacy of ophthalmic dexamethasone suspension or dexamethasone sodium phosphate solution not established.a c


Safety and efficacy of ophthalmic dexamethasone in fixed combination with neomycin and polymyxin B sulfates not established.e f


Safety and efficacy of ophthalmic dexamethasone in fixed combination with tobramycin not established in children <2 years of age.g h


Safety and efficacy of otic dexamethasone suspension in fixed combination with ciprofloxacin not established in infants <6 months of age.i


Geriatric Use

No substantial differences in safety or efficacy relative to younger patients.a e h


Common Adverse Effects


Ophthalmic administration: Elevated IOP,a c e f g h posterior subcapsular cataract formation,a c e g h optic nerve damage,a c e f g h delayed wound healing.e f h


Otic administration: Ear discomfort, ear pain, ear pruritus.i


Maxidex Pharmacokinetics


Absorption


Bioavailability


Corticosteroids are absorbed through the aqueous humor; because only low doses are given, little if any systemic absorption occurs after ophthalmic administration.d


Distribution


Extent


Systemically absorbed corticosteroids are distributed into milk; not known whether topical corticosteroids could produce detectable levels in human milk.a e f g h i


Stability


Storage


Ophthalmic


Ointment

Neomycin and polymyxin B sulfates and dexamethasone: 2–25°C.e


Tobramycin and dexamethasone: 8–27°C.h


Solution

Dexamethasone sodium phosphate: 15–30°C.c


Suspension

Dexamethasone: Tight, light-resistant containersb at 8–27°C;a store upright.a


Neomycin and polymyxin B sulfates and dexamethasone: 8–27°C.f


Tobramycin and dexamethasone: Upright containers at 8–27°C.g


Otic


Suspension

Ciprofloxacin and dexamethasone: 15–30°C; protect from light.i Do not freeze.i


ActionsActions



  • Corticosteroids suppress the inflammatory response to mechanical, chemical, or immunologic agents.a c d e f g h




  • Corticosteroids inhibit edema, fibrin deposition, capillary dilation, leukocyte and phagocyte migration; in addition, the drugs reduce capillary proliferation, fibroblast proliferation, deposition of collagen, and scar formation associated with inflammation.d



Advice to Patients



  • Importance of removing soft contact lenses prior to administering preparations containing benzalkonium chloridea g h and of delaying reinsertion of the lenses for ≥15 minutes after administration.c Importance of not wearing contact lenses if signs or symptoms of an eye infection occur.e




  • Importance of learning and adhering to proper administration techniques to avoid contamination of the tip of the container.a e f i




  • Importance of advising patients not to touch tip of dropper to eye or surrounding tissue.a c f g h i




  • Importance of informing a clinician if another eye condition (e.g., trauma, surgery, infection) develops during ophthalmic therapy.c




  • Advise patients to warm the ear suspension by holding the bottle in the hands for 1–2 minutes prior to administration.i




  • Importance of informing clinicians of existing or contemplated concomitant therapy, including prescription and OTC drugs as well as any concomitant illnesses.a c e g h i




  • Importance of women informing clinicians if they are or plan to become pregnant or plan to breast-feed.a c e g h i




  • Importance of informing patients of other important precautionary information. (See Cautions.)



Preparations


Excipients in commercially available drug preparations may have clinically important effects in some individuals; consult specific product labeling for details.













Dexamethasone

Routes



Dosage Forms



Strengths



Brand Names



Manufacturer



Ophthalmic



Suspension



0.1%



Maxidex (with benzalkonium chloride; viscous)



Alcon













Ciprofloxacin and Dexamethasone

Routes



Dosage Forms



Strengths



Brand Names



Manufacturer



Otic



Suspension



Ciprofloxacin 0.3% and Dexamethasone 0.1% per mL



Ciprodex (with benzalkonium chloride)



Alcon


* available from one or more manufacturer, distributor, and/or repackager by generic (nonproprietary) name




























Neomycin and Polymyxin B Sulfates and Dexamethasone

Routes



Dosage Forms



Strengths



Brand Names



Manufacturer



Ophthalmic



Ointment



Neomycin Sulfate 0.35% (of neomycin), Polymyxin B Sulfate 10,000 units (of polymyxin B) and Dexamethasone 0.1% per g*



Maxitrol



Alcon



Neomycin and Polymyxin B Sulfates and Dexamethasone



Bausch & Lomb, Falcon, Fougera



Suspension



Neomycin Sulfate 0.35% (of neomycin), Polymyxin B Sulfate 10,000 units (of polymyxin B) and Dexamethasone 0.1% per mL*



Maxitrol (with benzalkonium chloride; viscous)



Alcon



Neomycin and Polymyxin B Sulfates and Dexamethasone



Bausch & Lomb, Falcon


















Tobramycin and Dexamethasone

Routes



Dosage Forms



Strengths



Brand Names



Manufacturer



Ophthalmic



Ointment



0.3% Tobramycin and Dexamethasone 0.1% per g



TobraDex (with chlorobutanol)



Alcon



Suspension



0.3% Tobramycin and Dexamethasone 0.1% per mL



TobraDex (with benzalkonium chloride)



Alcon


* available from one or more manufacturer, distributor, and/or repackager by generic (nonproprietary) name













Dexamethasone Sodium Phosphate

Routes



Dosage Forms



Strengths



Brand Names



Manufacturer



Ophthalmic



Solution



0.1% (of dexamethasone phosphate)*



Dexamethasone Sodium Phosphate (with benzalkonium chloride)



Falcon


Comparative Pricing


This pricing information is subject to change at the sole discretion of DS Pharmacy. This pricing information was updated 03/2011. Actual costs to patients will vary depending on the use of specific retail or mail-order locations and health insurance copays.


Ciprodex 0.3-0.1% Suspension (ALCON VISION): 7/$142.98 or 22/$407.95


Dexamethasone Sodium Phosphate 0.1% Solution (FALCON PHARMACEUTICALS): 5/$19.99 or 10/$30.97


Maxidex 0.1% Suspension (ALCON VISION): 5/$56.27 or 15/$154.48


TobraDex 0.3-0.1% Ointment (ALCON VISION): 3/$139.99 or 10/$400.95


TobraDex 0.3-0.1% Suspension (ALCON VISION): 5/$112.99 or 15/$320.96


TobraDex 0.3-0.1% Suspension (ALCON VISION): 2/$61.99 or 7/$159.97


Tobramycin-Dexamethasone 0.3-0.1% Suspension (FALCON PHARMACEUTICALS): 10/$129.98 or 30/$359.96


Tobramycin-Dexamethasone 0.3-0.1% Suspension (FALCON PHARMACEUTICALS): 5/$69.99 or 15/$179.98



Disclaimer

This report on medications is for your information only, and is not considered individual patient advice. Because of the changing nature of drug information, please consult your physician or pharmacist about specific clinical use.


The American Society of Health-System Pharmacists, Inc. and Drugs.com represent that the information provided hereunder was formulated with a reasonable standard of care, and in conformity with professional standards in the field. The American Society of Health-System Pharmacists, Inc. and Drugs.com make no representations or warranties, express or implied, including, but not limited to, any implied warranty of merchantability and/or fitness for a particular purpose, with respect to such information and specifically disclaims all such warranties. Users are advised that decisions regarding drug therapy are complex medical decisions requiring the independent, informed decision of an appropriate health care professional, and the information is provided for informational purposes only. The entire monograph for a drug should be reviewed for a thorough understanding of the drug's actions, uses and side effects. The American Society of Health-System Pharmacists, Inc. and Drugs.com do not endorse or recommend the use of any drug. The information is not a substitute for medical care.

AHFS Drug Information. © Copyright, 1959-2011, Selected Revisions April 2010. American Society of Health-System Pharmacists, Inc., 7272 Wisconsin Avenue, Bethesda, Maryland 20814.




References



a. Alcon Laboratories, Inc. Maxidex 0.1% (dexamethasone ophthalmic suspension) prescribing information. Fort Worth, TX; 2007 May.



b. AHFS drug information 2008. McEvoy GK, ed. Dexamethasone. Bethesda, MD: American Society of Health-System Pharmacists; 2008: 2874-5.



c. Falcon Pharmaceuticals. Dexamethasone sodium phosphate ophthalmic solution, USP prescribing information. Fort Worth, TX; 2007 Jul.



d. AHFS drug information 2008. McEvoy GK, ed. EENT corticosteroids general statement. Bethesda, MD: American Society of Health-System Pharmacists; 2008: 2867-9.



e. Alcon Laboratories, Inc. Maxitrol(neomycin and polymyxin B sulfates, and dexamethasone ophthalmic ointment) prescribing information. Fort Worth, TX; 2003 Oct.



f. Alcon Laboratories, Inc. Maxitrol (neomycin and polymyxin B sulfates, and dexamethasone ophthalmic suspension) prescribing information. Fort Worth, TX; 2003 Aug.



g. Alcon Laboratories, Inc. TobraDex (tobramycin and dexamethasone ophthalmic suspension) prescribing information. Fort Worth, TX; 2006 May.



h. Alcon Laboratories, Inc. TobraDex (tobramycin and dexamethasone ophthalmic ointment) prescribing information. Fort Worth, TX; 2003 Oct.



i. Alcon Laboratories, Inc. Ciprodex (ciprofloxacin 0.3% and dexamethasone 0.1% sterile otic suspension) prescribing information. Fort Worth, TX; 2003 Jul.


Maraviroc


Pronunciation: MAR-a-VIR-ok
Generic Name: Maraviroc
Brand Name: Selzentry

Liver problems have been reported in some patients taking Maraviroc. An allergic reaction may occur before liver problems develop. Contact your doctor right away if you develop a rash; hives; itching; trouble breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue; yellowing of the eyes or skin; dark urine; pale stools; loss of appetite; or severe stomach pain.





Maraviroc is used for:

Treating patients with a certain type of HIV infection (CCR5-tropic HIV-1). It is used along with other HIV medicines.


Maraviroc is a CCR5 coreceptor antagonist. It works by blocking the virus from entering cells.


Do NOT use Maraviroc if:


  • you are allergic to any ingredient in Maraviroc

  • you are taking St. John's wort

  • you have severe kidney problems or you are on dialysis and you take certain other medicines. Talk to your doctor before taking Maraviroc if you have kidney problems

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



Before using Maraviroc:


Some medical conditions may interact with Maraviroc. 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 liver problems, hepatitis B or C, heart or kidney problems, or if you are at risk of heart problems

  • if you are on dialysis

  • if you have a history of low blood pressure or dizziness when you stand up

  • if you are taking medicine to lower your blood pressure

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


  • Azole antifungals (eg, itraconazole, ketoconazole), delavirdine, ketolides (eg, telithromycin), macrolides (eg, clarithromycin), nefazodone, or protease inhibitors (eg, amprenavir, boceprevir, ritonavir) because they may increase the risk of Maraviroc's side effects

  • Barbiturates (eg, phenobarbital), carbamazepine, efavirenz, etravirine, hydantoins (eg, phenytoin), rifamycins (eg, rifampin), or St. John's wort because they may decrease Maraviroc's effectiveness

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


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


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

  • Take Maraviroc by mouth with or without food.

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

  • Taking Maraviroc at the same time each day will help you remember to take it.

  • Continue to take Maraviroc even if you feel well. Do not miss any doses.

  • If you miss a dose of Maraviroc, take it as soon as possible. If your next dose is less than 6 hours away, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

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



Important safety information:


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

  • Maraviroc may cause dizziness, light-headedness, or fainting; alcohol, hot weather, exercise, or fever may increase these effects. Your risk may be greater if you have severe kidney problems. To prevent them, sit up or stand slowly, especially in the morning. Sit or lie down at the first sign of any of these effects.

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

  • Certain other medicines for HIV (eg, HIV protease inhibitors, delavirdine, efavirenz) may increase the side effects of Maraviroc or decrease its effectiveness. Talk with your doctor about all of your HIV medicines. Do not start, stop, or change the dose of any HIV medicine unless your doctor tells you to.

  • Maraviroc may improve immune system function. This may reveal hidden infections in some patients. Tell your doctor right away if you notice symptoms of infection (eg, fever, sore throat, weakness, cough, shortness of breath) after you start Maraviroc.

  • Maraviroc may increase the risk of developing an infection. Avoid contact with people who have colds or infections. Tell your doctor if you notice signs of infection like fever, sore throat, rash, or chills. Discuss any questions or concerns with your doctor.

  • It is possible that Maraviroc may increase the risk of developing cancer. No increase in cancer cases has been seen in patients who take Maraviroc. Discuss any questions or concerns with your doctor.

  • Maraviroc is not a cure for HIV infection. Patients may still get illnesses and infections associated with HIV. Remain under the care of your doctor.

  • When your medicine supply is low, get more from your doctor or pharmacist as soon as you can. Do not stop taking Maraviroc, even for a short period of time. If you do, the virus may grow resistant to the medicine and become harder to treat.

  • Maraviroc does not stop the spread of HIV to others through blood or sexual contact. Use barrier methods of birth control (eg, condoms) if you have HIV infection. Do not share needles, injection supplies, or items like toothbrushes or razors.

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

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

  • Maraviroc should not be used in CHILDREN younger than 16 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 Maraviroc while you are pregnant. It is not known if Maraviroc is found in breast milk. Mothers infected with HIV should not breast-feed. There is a risk of passing the HIV infection or Maraviroc to the baby.


Possible side effects of Maraviroc:


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



Constipation; cough; diarrhea; dizziness; muscle or joint pain; runny nose; sinus inflammation; stomach pain; trouble sleeping.



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

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); bloody diarrhea; burning, numbness, or tingling; chest, jaw, or left arm pain; confusion; depression; difficult or painful urination; fainting; fever, chills, or sore throat; flu-like symptoms; numbness of an arm or leg; one-sided weakness; red, swollen, blistered, or peeling skin; seizures; severe muscle pain; severe or persistent dizziness; severe or persistent stomach pain; shortness of breath; slurred speech; sores or white patches in the mouth; sudden, severe headache or vomiting; symptoms of liver problems (eg, yellowing of the eyes or skin, dark urine, pale stools, loss of appetite, nausea, unusual tiredness, vomiting); unusual lumps, skin growths, or skin changes; vision changes.



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: Maraviroc 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 fainting; severe or persistent dizziness.


Proper storage of Maraviroc:

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


General information:


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

  • Maraviroc 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 Maraviroc. 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 Maraviroc resources


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


  • Maraviroc Professional Patient Advice (Wolters Kluwer)

  • Maraviroc Monograph (AHFS DI)

  • maraviroc Advanced Consumer (Micromedex) - Includes Dosage Information

  • Selzentry Prescribing Information (FDA)

  • Selzentry Consumer Overview



Compare Maraviroc with other medications


  • HIV Infection

Magnevist


Generic Name: gadopentetate dimeglumine (gad oh PEN te tate dye MEG loo meen)

Brand Names: Magnevist


What is gadopentetate dimeglumine?

Gadopentetate dimeglumine is a contrast agent that produces magnetic effects. It is used in combination with magnetic resonance imaging (MRI) to allow blood vessels, organs, and other non-bony tissues to be seen more clearly on the MRI.


Gadopentetate dimeglumine is used to help diagnose certain disorders of the heart, brain, blood vessels, and spinal tissues.


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


What is the most important information I should know about gadopentetate dimeglumine?


Gadopentetate dimeglumine can cause a life-threatening condition in people with advanced kidney disease. The symptoms of this condition include:

  • burning, itching, swelling, scaling, and tightening or hardening of your skin;




  • muscle weakness;




  • joint stiffness in your arms, hands, legs, or feet;




  • deep bone pain in your ribs or your hips;




  • trouble moving; or




  • skin redness or discoloration.




Before receiving this medication, tell your doctor if you have kidney disease or if you are on dialysis. You may not be able to receive gadopentetate dimeglumine. Your doctor or other healthcare provider may want to watch you for a short time after your test is over. This is to make sure you do not have any unwanted side effects or delayed reactions.

What should I discuss with my health care provider before receiving gadopentetate dimeglumine?


Gadopentetate dimeglumine can cause a life-threatening condition in people with advanced kidney disease. The symptoms of this condition include:

  • burning, itching, swelling, scaling, and tightening or hardening of your skin;




  • muscle weakness;




  • joint stiffness in your arms, hands, legs, or feet;




  • deep bone pain in your ribs or your hips;




  • trouble moving; or




  • skin redness or discoloration.




Before receiving this medication, tell your doctor if you have kidney disease or if you are on dialysis. You may not be able to receive gadopentetate dimeglumine.

To make sure you can safely receive this medication, tell your doctor if you have any of these other conditions:



  • diabetes;




  • high blood pressure;




  • liver disease (or liver transplant);




  • asthma, hay fever, or a history of food or drug allergies;




  • if you are over 60 years old;




  • if you have ever had any type of reaction to a contrast agent; or




  • if you have recently had an injury, surgery, or severe infection.




FDA pregnancy category C. It is not known whether gadopentetate dimeglumine will harm an unborn baby. Before you receive this medication, tell your doctor if you are pregnant. Gadopentetate dimeglumine can pass into breast milk and may harm a nursing baby. Do not receive this medication without telling your doctor if you are breast-feeding a baby.

How is gadopentetate dimeglumine used?


Gadopentetate dimeglumine is injected into a vein through an IV. You will receive this injection in a clinic or hospital setting during your MRI.


Your doctor or other healthcare provider may want to watch you for a short time after your test is over. This is to make sure you do not have any unwanted side effects or delayed reactions.

What happens if I miss a dose?


Since gadopentetate dimeglumine is used only during your MRI, you will not be on a dosing schedule.


What happens if I overdose?


Since this medication is given by a healthcare professional in a medical setting, an overdose is unlikely to occur.


What should I avoid after receiving gadopentetate dimeglumine?


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


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

  • urinating less than usual or not at all;




  • drowsiness, confusion, mood changes, increased thirst, loss of appetite;




  • swelling, weight gain, feeling short of breath; or




  • swelling, irritation, or skin changes where the injection was given.



Less serious side effects may include:



  • headache;




  • dizziness; or




  • nausea.



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 gadopentetate dimeglumine?


This medication can harm the kidneys in certain people, and this effect may be increased if you also use other medicines harmful to the kidneys. Before you receive gadopentetate dimeglumine, tell your doctor about all other medications you use. Many other drugs (including some over-the-counter medicines) can be harmful to the kidneys.


There may be other drugs that can affect gadopentetate dimeglumine. 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 Magnevist resources


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


  • Magnevist Prescribing Information (FDA)

  • Magnevist Advanced Consumer (Micromedex) - Includes Dosage Information

  • Magnevist MedFacts Consumer Leaflet (Wolters Kluwer)

  • Magnevist Consumer Overview



Compare Magnevist with other medications


  • CNS Magnetic Resonance Imaging
  • Vascular Magnetic Resonance Imaging


Where can I get more information?


  • Your doctor or pharmacist can provide more information about gadopentetate dimeglumine.

See also: Magnevist side effects (in more detail)


Macugen


Generic Name: pegaptanib ophthalmic injection (peg AP ta nib off THAL mik in JEK tion)

Brand Names: Macugen


What is pegaptanib ophthalmic?

Pegaptanib is made from a human antibody fragment. It works by keeping new blood vessels from forming under the retina (a sensory membrane that lines the inside of the eye). In people with a certain type of eye disease, new blood vessels grow under the retina where they leak blood and fluid. This is known as the "wet form" of macular degeneration.


Pegaptanib ophthalmic (for the eyes) is used to treat wet age-related macular degeneration.


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


What is the most important information I should know about pegaptanib ophthalmic?


You should not receive pegaptanib if you are allergic to it, or if you have cataracts or glaucoma, or any type of bacterial, fungal, or viral infection in or around your eyes. Call your doctor at once if you have eye pain or redness, swelling or puffiness around your eyes, or sudden vision problems at any time during treatment.

What should I discuss with my healthcare provider before taking pegaptanib ophthalmic?


You should not receive pegaptanib if you are allergic to it, or if you have any type of bacterial, fungal, or viral infection in or around your eyes. FDA pregnancy category B. Pegaptanib is not expected to harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant during treatment. It is not known whether pegaptanib 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 take pegaptanib ophthalmic?


Pegaptanib ophthalmic is given as an injection into your eye. Your doctor will use a medicine to numb your eye before giving you the injection. You will receive this injection in your doctor's office or other clinic setting.


For a short time after your injection, your eyes will be checked periodically to make sure the injection has not caused any side effects.


Pegaptanib is usually given once every 6 weeks. Follow your doctor's dosing instructions very carefully.


What happens if I miss a dose?


Call your doctor for instructions if you miss an appointment for your pegaptanib injection.


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 pegaptanib ophthalmic?


This medication may cause blurred vision. Be careful if you drive or do anything that requires you to be able to see clearly.

Pegaptanib ophthalmic 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:

  • eye pain or redness, swelling around your eyes;




  • sudden vision problems;




  • seeing flashes of light or "floaters" in your vision;




  • eyes being more sensitive to light;




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




  • sudden severe headache, confusion, problems with speech or balance.



Less serious side effects may include:



  • watery eyes;




  • blurred vision;




  • swelling of the eyelids; or




  • mild eye pain or discomfort after the injection.



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 pegaptanib ophthalmic?


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



More Macugen resources


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


  • Macugen Prescribing Information (FDA)

  • Macugen Monograph (AHFS DI)

  • Macugen Advanced Consumer (Micromedex) - Includes Dosage Information

  • Macugen MedFacts Consumer Leaflet (Wolters Kluwer)

  • Macugen Consumer Overview



Compare Macugen with other medications


  • Macular Degeneration


Where can I get more information?


  • Your pharmacist can provide more information about pegaptanib ophthalmic.

See also: Macugen side effects (in more detail)