понедельник, 30 апреля 2012 г.

Cresyl Acetate Drops


Pronunciation: KREE-sil AS-e-tate
Generic Name: Cresyl Acetate
Brand Name: Cresylate


Cresyl Acetate Drops are used for:

Treating bacterial and fungal infections of the outer ear.


Cresyl Acetate Drops are an antibacterial agent. It works by killing sensitive bacteria and fungi.


Do NOT use Cresyl Acetate Drops if:


  • you are allergic to any ingredient in Cresyl Acetate Drops

  • you have a perforated eardrum

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



Before using Cresyl Acetate Drops:


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


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

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

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

Some MEDICINES MAY INTERACT with Cresyl Acetate Drops. Because little, if any, of Cresyl Acetate Drops are absorbed into the blood, the risk of it interacting with another medicine is low.


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


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


  • Do not allow Cresyl Acetate Drops to come into contact with hearing aids.

  • To use ear drops, lie down or tilt your head so that the affected ear faces up. For adults, gently pull the earlobe up and back to straighten the ear canal. For children, gently pull the earlobe down and back to straighten the ear canal. Drop the medicine into the ear canal. Keep the ear facing up for several minutes so the medicine can run to the bottom of the ear canal. A clean cotton plug may be gently inserted into the ear canal to prevent medicine from leaking out.

  • To prevent germs from contaminating your medicine, do not touch the applicator to any surface, including the ear. Keep the container tightly closed.

  • Do not use Cresyl Acetate Drops if it is brown in color.

  • If you miss a dose of Cresyl Acetate Drops, use it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Cresyl Acetate Drops.



Important safety information:


  • Cresyl Acetate Drops are for use in the ear only. Do not get Cresyl Acetate Drops in your eyes, nose, or mouth. If you get Cresyl Acetate Drops in your eyes, rinse immediately with cool water.

  • If your symptoms do not improve within 2 weeks or if they become worse, contact your doctor.

  • PREGNANCY and BREAST-FEEDING: If you become pregnant while taking Cresyl Acetate Drops, discuss with your doctor the benefits and risks of using Cresyl Acetate Drops during pregnancy. It is unknown if Cresyl Acetate Drops are excreted in breast milk after topical use. If you are or will be breast-feeding while you are using Cresyl Acetate Drops, check with your doctor or pharmacist to discuss the risks to your baby.


Possible side effects of Cresyl Acetate Drops:


All medicines may cause side effects, but many people have no, or minor, side effects. No COMMON side effects have been reported with Cresyl Acetate Drops. 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); irritation, itching, or redness of the ear.



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



If OVERDOSE is suspected:


Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Cresyl Acetate Drops may be harmful if swallowed.


Proper storage of Cresyl Acetate Drops:

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


General information:


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

  • If your symptoms do not improve or if they become worse, check with your doctor.

  • Cresyl Acetate Drops are to be used only by the patient for whom it is prescribed. Do not share it with other people.

  • Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Cresyl Acetate Drops. 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 Cresyl Acetate resources


  • Cresyl Acetate Use in Pregnancy & Breastfeeding
  • Cresyl Acetate Support Group
  • 0 Reviews for Cresyl Acetate - Add your own review/rating


Compare Cresyl Acetate with other medications


  • Bacterial Infection

суббота, 28 апреля 2012 г.

Curosurf


Generic Name: Poractant Alfa
Class: Pulmonary Surfactants
VA Class: RE900
CAS Number: 129069-19-8

Introduction

Exogenous natural pulmonary surfactant preparation; porcine lung extract containing mostly phospholipids.1 3


Uses for Curosurf


Respiratory Distress Syndrome (RDS)


Treatment (rescue) of RDS (hyaline membrane disease) in premature neonates (designated an orphan drug by FDA for this use).1 2 6 8


Prevention of RDS in infants at high risk for RDS.3 7 8


Curosurf Dosage and Administration


General



  • Observe clinical status and monitor systemic oxygenation frequently; decrease inspired oxygen concentrations and ventilator pressures gradually to prevent hyperoxia.1 2




  • Following completion of dosing procedure, resume usual ventilator management and clinical care.1 Do not suction airways for 1 hour after dosing unless substantial obstruction occurs.1 (See Experience of Supervising Clinician under Cautions.)



Administration


Intratracheal Administration


Administer only by intratracheal instillation using specialized techniques.1 Consult manufacturer’s labeling or specialized references for guidelines on administration techniques.1 2


Allow drug to reach room temperature before administration.1 Gently invert vial to obtain a uniform suspension; do not shake.1


Contains no preservatives; discard unused portion.1


Dosage


Available as poractant alfa; dosage expressed in terms of phospholipids.1 4 5


Each mL of the commercially available formulation contains 80 mg of phospholipids (including 54 mg of phosphatidylcholine, of which 30.5 mg is dipalmitoyl phosphatidylcholine) and 1 mg of surfactant proteins (SP-B, SP-C).1 2 8


Pediatric Patients


Treatment of RDS

Intratracheal

Premature neonates: 2.5 mL/kg (200 mg/kg) of birthweight.1


Administer up to 2 repeat doses (1.25 mL/kg of birth weight), given at 12-hour intervals, if neonate remains intubated and respiratory manifestations of RDS persist or worsen.1


Prevention of RDS

Intratracheal

100 or 200 mg/kg, given as a single dose within 10 minutes of birth.3 7


Prescribing Limits


Pediatric Patients


Treatment of RDS

Intratracheal

Premature neonates: Total dosage (initial and repeat doses) should not exceed 5 mL/kg.1 Safety and efficacy not established for administration of >3 doses (1 initial and 2 repeat doses), administration more frequently than every 12 hours, and initiation of therapy >15 hours after diagnosis of RDS.1


Cautions for Curosurf


Contraindications



  • No known contraindications.1



Warnings/Precautions


Warnings


Experience of Supervising Clinician

Use only by clinicians experienced in resuscitation, stabilization, and general care of premature neonates.1


Respiratory Effects

Therapy can rapidly affect oxygenation and lung compliance.1 Perform frequent clinical and laboratory assessments; modify oxygen and ventilatory support in response to respiratory changes.1 2


Transient episodes of decreased oxygen saturation reported.1 If this occurs, discontinue administration and initiate appropriate measures to alleviate the condition; following stabilization, resume therapy and monitor appropriately.1


Cardiovascular Effects

Transient episodes of bradycardia and hypotension reported.1 If these occur, discontinue administration and initiate appropriate measures to alleviate the condition; following stabilization, resume therapy and monitor appropriately.1


Endotracheal Tube Complications

Transient endotracheal tube blockage, reflux of surfactant into endotracheal tube, and airway obstruction reported.1 If these occur, discontinue administration and initiate appropriate measures to alleviate the condition; following stabilization, resume therapy and monitor appropriately.1


General Precautions


Concurrent Illness

Correction of acidosis, hypotension, anemia, hypoglycemia, and hypothermia recommended prior to administration.1


Complications of Prematurity

Therapy expected to reduce severity of RDS but will not eliminate morbidity and mortality associated with other complications of prematurity (e.g., pneumonia, septicemia, intracranial hemorrhage, patent ductus arteriosus).1


Use with Investigational Treatments for RDS

Safety and efficacy in conjunction with investigational therapies for RDS (e.g., high-frequency ventilation) not established.1


Specific Populations


Pregnancy

Not intended for use in adults.1


Lactation

Not intended for use in adults.1


Common Adverse Effects


Transient bradycardia, hypotension, endotracheal tube blockage, decreased oxygen saturation.1


Interactions for Curosurf


No drug interactions reported.1


Curosurf Pharmacokinetics


No pharmacokinetic studies in humans.1


Absorption


Onset


Marked improvements in oxygenation occur within minutes of administration.1


Stability


Storage


Intratracheal


Suspension

2–8° C.1 Protect from light.1


Prior to use, warm to room temperature for up to 24 hours.1


May return unopened, unused vials to refrigerator within 24 hours of warming.1 Do not warm and return to refrigeration more than once.1


ActionsActions



  • Natural porcine lung extract containing mostly phospholipids and small amounts of neutral lipids, fatty acids, and surfactant-associated proteins (SP-B, SP-C).1 3




  • Endogenous pulmonary surfactant reduces alveolar surface tension and increases alveolar stability.1




  • Poractant compensates for surfactant deficiency in premature neonates.1 Increases alveolar stability and pulmonary compliance, decreases pulmonary edema and work required for breathing, and facilitates uniform alveolar recruitment on inspiration.1 3



Advice to Patients



  • Advise patient’s parent(s) or guardian that other complications of prematurity (e.g., pneumonia, septicemia, intracranial hemorrhage, patent ductus arteriosus) will not be eliminated by poractant therapy.1




  • Importance of informing parent(s) or guardian of other important precautionary information. (See Cautions.)1



Preparations


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


















Poractant Alfa

Routes



Dosage Forms



Strengths



Brand Names



Manufacturer



Intratracheal



Suspension



1.5 mL (120 mg phospholipids)



Curosurf



Dey



3 mL (240 mg phospholipids)



Curosurf



Dey



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 September 2005. American Society of Health-System Pharmacists, Inc., 7272 Wisconsin Avenue, Bethesda, Maryland 20814.


† Use is not currently included in the labeling approved by the US Food and Drug Administration.




References



1. Dey. Curosurf (poractant alfa) intratracheal suspension prescribing information. Napa, CA; 2000 Feb.



2. Anon. Med Lett Drugs Ther. 42; 2000;27-8.



3. Wiseman LR, Bryson HM. Porcine-derived lung surfactant: a review of the therapeutic efficacy and clinical tolerability of a natural surfactant preparation (Curosurf) in neonatal respiratory distress syndrome. Drugs. 1994; 48:386-403. [PubMed 7527760]



4. Collaborative European Multicenter Study Group. Surfactant replacement therapy for severe neonatal respiratory distress syndrome: an international randomized clinical trial. Pediatrics. 1988; 82:683-91. [IDIS 247745] [PubMed 2903480]



5. Speer CP, Robertson B, Curstedt T et al. Randomized European multicenter trial of surfactant replacement therapy for severe neonatal respiratory distress syndrome: single versus multiple doses of Curosurf. Pediatrics. 1992; 89:13-20. [IDIS 290105] [PubMed 1727997]



6. Food and Drug Administration. Orphan designations pursuant to Section 526 of the Federal Food and Cosmetic Act as amended by the Orphan Drug Act (P.L. 97-414). Rockville, MD; [December 18, 2000]. From FDA web site ().



7. Egberts J, Brand R, Walti H et al. Mortality, severe respiratory distress syndrome, and chronic lung disease of the newborn are reduced more after prophylactic than after therapeutic administration of the surfactant Curosurf. Pediatrics. 1997; 100: E4. [IDIS 427502] [PubMed 9200378]



8. Dey, Napa, CA: Personal communication.



More Curosurf resources


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


  • Curosurf Prescribing Information (FDA)



Compare Curosurf with other medications


  • Respiratory Distress Syndrome

пятница, 27 апреля 2012 г.

Crinone


Generic Name: progestin (Oral route, Parenteral route, Vaginal route)


Commonly used brand name(s)

In the U.S.


  • Aygestin

  • Camila

  • Crinone

  • Errin

  • First-Progesterone VGS

  • Jolivette

  • Megace

  • Megace ES

  • Next Choice

  • Ovrette

  • Plan B

  • Prochieve

  • Prometrium

In Canada


  • Alti-Mpa

  • Megace Os

Available Dosage Forms:


  • Tablet

  • Suspension

  • Capsule, Liquid Filled

  • Gel/Jelly

  • Cream

  • Kit

  • Suppository

Uses For Crinone


Progestins are hormones. They are used by both men and women for different purposes.


Progestins are prescribed for several reasons:


  • To properly regulate the menstrual cycle and treat unusual stopping of the menstrual periods (amenorrhea). Progestins work by causing changes in the uterus. After the amount of progestins in the blood drops, the lining of the uterus begins to come off and vaginal bleeding occurs (menstrual period). Progestins help other hormones start and stop the menstrual cycle. .

  • To help a pregnancy occur during egg donor or infertility procedures in women who do not produce enough progesterone. Also, progesterone is given to help maintain a pregnancy when not enough of it is made by the body.

  • To prevent estrogen from thickening the lining of the uterus (endometrial hyperplasia) in women around menopause who are being treated with estrogen for ovarian hormone therapy (OHT). OHT is also called hormone replacement therapy (HRT) and estrogen replacement therapy (ERT).

  • To treat pain that is related to endometriosis, a condition where the endometrial tissue which lines the uterus becomes displaced in other female organs.

  • To treat a condition called endometriosis, to help prevent endometrial hyperplasia, or to treat unusual and heavy bleeding of the uterus (dysfunctional uterine bleeding) by starting or stopping the menstrual cycle.

  • To help treat cancer of the breast, kidney, or uterus. Progestins help change the cancer cell's ability to react to other hormones and proteins that cause tumor growth. In this way, progestins can stop the growth of a tumor.

  • To test the body's production of certain hormones such as estrogen.

  • To treat loss of appetite and severe weight or muscle loss in patients with acquired immunodeficiency syndrome (AIDS) or cancer by causing certain proteins to be produced that cause increased appetite and weight gain.

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


Depending on how much and which progestin you use or take, a progestin can have different effects. For instance, high doses of progesterone are necessary for some women to continue a pregnancy while other progestins in low doses can prevent a pregnancy from occurring. Other effects include causing weight gain, increasing body temperature, developing the milk-producing glands for breast-feeding, and relaxing the uterus to maintain a pregnancy.


Progestins can help other hormones work properly. Progestins may help to prevent anemia (low iron in blood), too much menstrual blood loss, and cancer of the uterus.


Progestins are 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, progestins are used in certain patients with the following medical conditions:


  • Carcinoma of the prostate

  • Corpus luteum insufficiency

  • Hot flashes

  • Polycystic ovary syndrome

  • Precocious puberty

Before Using Crinone


Allergies


Tell your doctor if you have ever had any unusual or allergic reaction to medicines in this group 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


Although there is no specific information comparing use of progestins in children or teenagers with use in other age groups, this medicine is not expected to cause different side effects or problems in children or teenagers than it does in adults.


Geriatric


This medicine has been tested and has not been shown to cause different side effects or problems in older people than it does in younger adults.


Pregnancy


Progesterone, a natural hormone that the body makes during pregnancy, has not caused problems. In fact, it is sometimes used in women to treat a certain type of infertility and to aid in egg donor or infertility procedures.


Other progestins have not been studied in pregnant women. Be sure to tell your doctor if you become pregnant while using any of the progestins. It is best to use some kind of birth control method while you are receiving progestins in high doses. High doses of progestins are not recommended for use during pregnancy since there have been some reports that they may cause birth defects in the genitals (sex organs) of a male fetus. Also, some of these progestins may cause male-like changes in a female fetus and female-like changes in a male fetus, but these problems usually can be reversed. Low doses of progestins, such as those doses used for contraception, have not caused major problems when used accidentally during pregnancy.


Breast Feeding


Although progestins pass into the breast milk, they have not been shown to cause problems in nursing babies. However, progestins may change the quality or amount (increase or decrease) of the mother's breast milk. It may be necessary for you to take another medicine or to stop breast-feeding during treatment. Be sure you have discussed the risks and benefits of the medicine with your doctor.


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 any of these medicines, 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 medicines in this class with any of the following medicines is not recommended. Your doctor may decide not to treat you with a medication in this class or change some of the other medicines you take.


  • Boceprevir

  • Dofetilide

Using medicines in this class 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.


  • Felbamate

  • Isotretinoin

  • Theophylline

  • Tizanidine

  • Tranexamic Acid

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


  • Asthma or

  • Epilepsy (or history of) or

  • Heart or circulation problems or

  • Kidney disease (severe) or

  • Migraine headaches—Progestins may cause fluid retention which may cause these conditions to become worse.

  • Bleeding problems, undiagnosed, such as blood in the urine or changes in vaginal bleeding—May make diagnosis of these problems more difficult.

  • Blood clots, or history of or

  • Breast cancer, or history of or

  • Deep vein thrombosis (blood clot in the leg), active or history of or

  • Heart attack, active or history of or

  • Liver disease, including jaundice, or history of or

  • Pulmonary embolism (clot in the lung), active or history of or

  • Stroke , active or history of or

  • Venous thromboembolism (clot in the veins), or history of—Progestins should not be used in patients with these conditions.

  • Breast disease (such as breast lumps or cysts), history of—May make this condition worse for diseases that do not react in a positive way to progestins.

  • Diabetes mellitus—May cause an increase in your blood sugar and a change in the amount of medicine you take for diabetes; progestins in high doses are more likely to cause this problem.

  • Memory loss (dementia)—May make this condition worse.

  • Vision changes—This medicine may cause changes in vision; your medicine may need to be stopped if these conditions become worse.

Proper Use of progestin

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


To make the use of a progestin as safe and reliable as possible, you should understand how and when to take it and what effects may be expected. Progestins usually come with patient directions. Read them carefully before taking or using this medicine.


Take this medicine only as directed by your doctor. Do not take more of it and do not take it for a longer time than your doctor ordered. To do so may increase the chance of side effects. Try to take the medicine at the same time each day to reduce the possibility of side effects and to allow it to work better.


Progestins are often given together with certain medicines. If you are using a combination of medicines, make sure that you take each one at the proper time and do not mix them. Ask your health care professional to help you plan a way to remember to take your medicines at the right times.


Dosing


The dose medicines in this class 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 these medicines. 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 medroxyprogesterone

  • For oral dosage form (tablets):
    • For controlling unusual and heavy bleeding of the uterus (dysfunctional uterine bleeding) or treating unusual stopping of menstrual periods (amenorrhea):
      • Adults and teenagers—5 to 10 milligrams (mg) per day for five to ten days as directed by your doctor.


    • For preparing the uterus for the menstrual period:
      • Adults and teenagers—10 milligrams (mg) per day for five or ten days as directed by your doctor.


    • For preventing estrogen from thickening the lining of the uterus (endometrial hyperplasia) when taking estrogen for ovarian hormone therapy in postmenopausal women:
      • Adults—When taking estrogen each day on Days 1 through 25: Oral, 5 to 10 milligrams (mg) of medroxyprogesterone per day for ten to fourteen or more days each month as directed by your doctor. Or, your doctor may want you to take 2.5 or 5 mg per day without stopping. Your doctor will help decide the number of tablets that is best for you and when to take them.



  • For intramuscular injection dosage form:
    • For treating cancer of the kidneys or uterus:
      • Adults and teenagers—At first, 400 to 1000 milligrams (mg) injected into a muscle as a single dose once a week. Then, your doctor may lower your dose to 400 mg or more once a month.



  • For subcutaneous injection dosage form:
    • For treating pain related to endometriosis:
      • Adults and teenagers—104 milligrams (mg) injected under the skin of the anterior thigh or abdomen every three months (12 to 14 weeks) for not more than 2 years.



  • For megestrol

  • For oral dosage form (suspension):
    • For treating loss of appetite (anorexia), muscles (cachexia), or weight caused by acquired immunodeficiency syndrome (AIDS):
      • Adults and teenagers—800 milligrams (mg) a day for the first month. Then your doctor may want you to take 400 or 800 mg a day for three more months.



  • For oral dosage form (tablets):
    • For treating cancer of the breast:
      • Adults and teenagers—160 milligrams (mg) a day as a single dose or in divided doses for two or more months.


    • For treating cancer of the uterus:
      • Adults and teenagers—40 to 320 milligrams (mg) a day for two or more months.


    • For treating loss of appetite (anorexia), muscles (cachexia), or weight caused by cancer:
      • Adults and teenagers—400 to 800 milligrams (mg) a day.



  • For norethindrone

  • For oral dosage form (tablets):
    • For controlling unusual and heavy bleeding of the uterus (dysfunctional uterine bleeding) or treating unusual stopping of menstrual periods (amenorrhea):
      • Adults and teenagers—2.5 to 10 milligrams (mg) a day from Day 5 through Day 25 (counting from the first day of the last menstrual cycle). Or, your doctor may want you to take the medicine only for five to ten days as directed.


    • For treating endometriosis:
      • Adults and teenagers—At first, 5 milligrams (mg) a day for two weeks. Then, your doctor may increase your dose slowly up to 15 mg a day for six to nine months. Let your doctor know if your menstrual period starts. Your doctor may want you to take more of the medicine or may want you to stop taking the medicine for a short period of time.



  • For progesterone

  • For oral dosage form (capsules):
    • For preventing estrogen from thickening the lining of the uterus (endometrial hyperplasia) when taking estrogen for ovarian hormone therapy in postmenopausal women:
      • Adults—200 milligrams (mg) per day at bedtime for 12 continuous days per 28-day cycle of estrogen treatment each month.


    • For treating unusual stopping of menstrual periods (amenorrhea):
      • Adults—400 milligrams (mg) per day at bedtime for ten days.



  • For vaginal dosage form (gel):
    • For treating unusual stopping of menstrual periods (amenorrhea):
      • Adults and teenagers—45 milligrams (mg) (one applicatorful of 4% gel) once every other day for up to six doses. Dose may be increased to 90 mg (one applicatorful of 8% gel) once every other day for up to six doses if needed.


    • For use with infertility procedures:
      • Adults and teenagers—90 milligrams (mg) (one applicatorful of 8% gel) one or two times a day. If pregnancy occurs, treatment can continue for up to ten to twelve weeks.



  • For injection dosage form:
    • For controlling unusual and heavy bleeding of the uterus (dysfunctional uterine bleeding) or treating unusual stopping of menstrual periods (amenorrhea):
      • Adults and teenagers—5 to 10 milligrams (mg) a day injected into a muscle for six to ten days. Or, your doctor may want you to receive 100 or 150 mg injected into a muscle as a single dose. Sometimes your doctor may want you first to take another hormone called estrogen. If your menstrual period starts, your doctor will want you to stop taking the medicine.



  • For vaginal dosage form (suppositories):
    • For maintaining a pregnancy (at ovulation and at the beginning of pregnancy):
      • Adults and teenagers—25 mg to 100 milligrams (mg) (one suppository) inserted into the vagina one or two times a day beginning near the time of ovulation. Your doctor may want you to receive the medicine for up to eleven weeks.



Missed Dose


If you miss a dose of this medicine, take it as soon as possible. However, if it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not double doses.


For all progestins, except for progesterone capsules for postmenopausal women: If you miss a dose of this medicine, take the missed dose as soon as possible. However, if it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not double doses.


For progesterone capsules for postmenopausal women: If you miss a dose of 200 mg of progesterone capsules at bedtime, take 100 mg in the morning then go back to your regular dosing schedule. If you take 300 mg of progesterone a day and you miss your morning and evening doses, you should not take the missed dose. Return to your regular dosing schedule.


Storage


Keep out of the reach of children.


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


Do not keep outdated medicine or medicine no longer needed.


Precautions While Using Crinone


It is very important that your doctor check your progress at regular visits. This will allow for your dosage to be adjusted and for any unwanted effects to be detected. These visits will usually be every 6 to 12 months, but some doctors require them more often.


The Prometrium® capsules contain peanut oil. If you have an allergy to peanuts, make sure your doctor knows this before you take this brand of progestin.


Progestins may cause some people to become dizzy. For oral or vaginal progesterone, dizziness or drowsiness may occur 1 to 4 hours after taking or using it. Make sure you know how you react to this medicine before you drive, use machines, or do anything else that could be dangerous if you are not alert.


Unusual or unexpected vaginal bleeding of various amounts may occur between your regular menstrual periods during the first 3 months of use. This is sometimes called spotting when slight, or breakthrough menstrual bleeding when heavier. If this should occur, continue on your regular dosing schedule. Check with your doctor:


  • If unusual or unexpected vaginal bleeding continues for an unusually long time.

  • If your menstrual period has not started within 45 days of your last period.

Missed menstrual periods may occur. If you suspect a pregnancy, you should stop taking this medicine immediately and call your doctor. Your doctor will let you know if you should continue taking the progestin.


If you are scheduled for any laboratory tests, tell your health care professional that you are taking a progestin. Progestins can change certain test results.


In some patients, tenderness, swelling, or bleeding of the gums may occur. Brushing and flossing your teeth carefully and regularly and massaging your gums may help prevent this. See your dentist regularly to have your teeth cleaned. Check with your medical doctor or dentist if you have any questions about how to take care of your teeth and gums, or if you notice any tenderness, swelling, or bleeding of your gums.


You will need to use a birth control method while taking progestins for noncontraceptive use if you are fertile and sexually active.


If you are using vaginal progesterone, avoid using other vaginal products for 6 hours before and for 6 hours after inserting the vaginal dose of progesterone.


Since it is possible that certain doses of progestins may cause temporary thinning of the bones by changing your hormone balance, it is important that your doctor know if you have an increased risk of osteoporosis. Some things that can increase your risk for having osteoporosis include cigarette smoking, abusing alcohol, taking or drinking large amounts of caffeine, and having a family history of osteoporosis or easily broken bones. Some medicines, such as glucocorticoids (cortisone-like medicines) or anticonvulsants (seizure medicine), can also cause thinning of the bones. However, it is thought that progestins can help protect against osteoporosis in postmenopausal women.


Crinone Side Effects


Along with their needed effects, progestins used in high doses sometimes cause some unwanted effects such as blood clots, heart attacks, and strokes, or problems of the liver and eyes. Although these effects are rare, some of them can be very serious and cause death. It is not clear if these problems are due to the progestin. They may be caused by the disease or condition for which progestins are being used.


The following side effects may be caused by blood clots. Although not all of these side effects may occur, if they do occur they need immediate medical attention.


Get emergency help immediately if any of the following side effects occur:


Rare
  • Symptoms of blood clotting problems, usually severe or sudden, such as:

  • headache or migraine

  • loss of or change in speech, coordination, or vision

  • numbness of or pain in chest, arm, or leg

  • unexplained shortness of breath

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


More common
  • Changes in vaginal bleeding (increased amounts of menstrual bleeding occurring at regular monthly periods, lighter vaginal bleeding between menstrual periods, heavier vaginal bleeding between regular monthly periods, or stopping of menstrual periods)

  • symptoms of blood sugar problems (dry mouth, frequent urination, loss of appetite, or unusual thirst)

Less common
  • Mental depression

  • skin rash

  • unexpected or increased flow of breast milk

RareFor megestrol—During chronic treatment
  • Backache

  • dizziness

  • filling or rounding out of the face

  • irritability

  • mental depression

  • nausea or vomiting

  • unusual decrease in sexual desire or ability in men

  • unusual tiredness or weakness

Some side effects may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:


More common
  • Abdominal pain or cramping

  • bloating or swelling of ankles or feet

  • blood pressure increase (mild)

  • dizziness

  • drowsiness (progesterone only)

  • headache (mild)

  • mood changes

  • nervousness

  • pain or irritation at place of injection site

  • swelling of face, ankles, or feet

  • unusual or rapid weight gain

Less common
  • Acne

  • breast pain or tenderness

  • brown spots on exposed skin, possibly long-lasting

  • hot flashes

  • loss or gain of body, facial, or scalp hair

  • loss of sexual desire

  • trouble in sleeping

Not all of the side effects listed above have been reported for each of these medicines, but they have been reported for at least one of them. All of the progestins are similar, so any of the above side effects may occur with any of these medicines.


After you stop using this medicine, your body may need time to adjust. The length of time this takes depends on the amount of medicine you were using and how long you used it. During this period of time check with your doctor if you notice the following side effect:


For megestrol
  • Dizziness

  • nausea or vomiting

  • unusual tiredness or weakness

  • Delayed return to fertility

  • stopping of menstrual periods

  • unusual menstrual bleeding (continuing)

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.

суббота, 21 апреля 2012 г.

Cuprimine


Generic Name: penicillamine (Oral route)

pen-i-SIL-a-meen

Oral route(Capsule;Tablet)

Physicians planning to use penicillamine should thoroughly familiarize themselves with its toxicity, special dosage considerations, and therapeutic benefits. Patients should be warned to report promptly any symptoms suggesting toxicity .



Commonly used brand name(s)

In the U.S.


  • Cuprimine

  • Depen

Available Dosage Forms:


  • Capsule

  • Tablet

Therapeutic Class: Antirheumatic


Uses For Cuprimine


Penicillamine is used in the treatment of medical problems such as Wilson's disease (too much copper in the body) and rheumatoid arthritis. Also, it is used to prevent kidney stones. Penicillamine may also be used for other conditions as determined by your doctor.


In addition to the helpful effects of this medicine, it has side effects that can be very serious. Before you take penicillamine, be sure that you have discussed the use of it with your doctor.


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


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


  • Felty's syndrome

  • Heavy metal toxicity

  • Rheumatoid vasculitis

Before Using Cuprimine


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


Although there is no specific information about the use of penicillamine in children, it is not expected to cause different side effects or problems in children than it does in adults.


Geriatric


This medicine has been tested in a limited number of patients 65 years of age or older. In clinical trials, elderly people may have an increased chance for getting a skin rash.


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.


  • Aurothioglucose

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.


  • Auranofin

  • Gold Sodium Thiomalate

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.


  • Iron

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. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive.


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:


  • Blood disease caused by penicillamine treatment, history of or

  • Kidney disease or history of (only for patients with rheumatoid arthritis)—The chance of side effects may be increased

Proper Use of penicillamine

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


Since penicillamine is taken in different ways for different medical problems, it is very important that you understand exactly why you are taking this medicine and how to take it. See below for information on specific medical problems. If you have any questions about this, check with your doctor.


For patients taking this medicine to prevent kidney stones:


  • Take this medicine on an empty stomach (at least 1 hour before meals or 2 hours after meals) and at least 1 hour before or after any other food, milk, or medicine.

  • You should drink 2 full glasses (8 ounces each) of water at bedtime and another 2 full glasses (8 ounces each) during the night.

  • It is very important that you follow any special instructions from your doctor, such as following a low-methionine diet. If you have any questions about this, check with your doctor.

For patients taking this medicine for rheumatoid arthritis :


  • Take this medicine on an empty stomach (at least 1 hour before meals or 2 hours after meals) and at least 1 hour before or after any other food, milk, or medicine.

  • After you begin taking this medicine, 2 to 3 months may pass before you feel its effects. It is very important that you keep taking the medicine, even if you do not feel better, in order to give it time to work.

For patients taking this medicine for Wilson's disease :


  • Take this medicine on an empty stomach (at least 1 hour before meals or 2 hours after meals).

  • It is very important that you follow any special instructions from your doctor, such as following a low-copper diet. If you have any questions about this, check with your doctor.

  • After you begin taking this medicine, 1 to 3 months may pass before you notice any improvement in your condition.

For patients taking this medicine for lead poisoning :


  • Take this medicine on an empty stomach (2 hours before meals or at least 3 hours after meals).

For all patients:


  • Take this medicine regularly as directed. Do not stop taking it without first checking with your doctor, since stopping the medicine and then restarting it may increase the possibility of side effects.

Dosing


The dose of this medicine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so.


The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.


  • For oral dosage forms (capsules or tablets):
    • For Wilson's disease (too much copper in the body):
      • Adults and teenagers—At first, 250 milligrams (mg) four times a day. After a while your doctor may need to increase the dose, depending on the amount of copper in your urine. Most people do not need more than 2000 mg a day (two 250-mg capsules or tablets four times a day).

      • Children (older than 6 months of age)—At first, 250 mg a day. After a while your doctor may need to increase the dose, depending on the amount of copper in your urine. Older children may need the same dose as adults.


    • For rheumatoid arthritis:
      • Adults—At first, 125 or 250 mg once a day. Your doctor may increase the dose after a few months, depending on how well the medicine is working and whether it causes any side effects. The largest dose is not more than 1500 mg a day (two 250-mg capsules or tablets three times a day).

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


    • For preventing kidney stones:
      • Adults—At first, 500 mg (two 250-mg capsules or tablets) four times a day. After a while your doctor may need to change the dose, depending on the results of your urine tests. Some people may need as much as 4000 mg a day (four 250-mg capsules or tablets four times a day).

      • Children—The dose is based on body weight and must be determined by your doctor. At first, 7.5 mg per kilogram (kg) (about 3.5 mg per pound) of body weight four times a day. After a while your doctor may need to change the dose, depending on the results of your urine tests.



Missed Dose


If you miss a dose of this medicine, take it as soon as possible. However, if it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not double doses.


Storage


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


Keep out of the reach of children.


Do not keep outdated medicine or medicine no longer needed.


Precautions While Using Cuprimine


Your doctor should check your progress at regular visits to make sure that this medicine does not cause unwanted effects.


Before having any kind of surgery (including dental surgery), tell the medical doctor or dentist in charge that you are taking this medicine.


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 take iron preparations or vitamin preparations containing iron without checking with your healthcare provider. If your doctor tells you to take iron preparations, or vitamin preparations containing iron, do not take them within 2 hours of the time you take this medicine. Taking the two medicines too close together may keep the penicillamine from working properly.


Tell your doctor right away if you get a fever, sore throat, chills, bruising, or bleeding. These may be symptoms of a serious blood problem.


Tell your doctor right away if you have trouble breathing, noisy breathing, or an unexplained cough. These may be symptoms of a serious lung problem.


Cuprimine Side Effects


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


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


More common
  • Fever

  • joint pain

  • lesions on the face, neck, scalp, and/or trunk

  • skin rash, hives, or itching

  • swollen and/or painful glands

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

Less common
  • Bloody or cloudy urine

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

  • sore throat and fever with or without chills

  • swelling of face, feet, or lower legs

  • unusual bleeding or bruising

  • unusual tiredness or weakness

  • weight gain

Rare
  • Abdominal or stomach pain (severe)

  • blisters on skin

  • bloody or black, tarry stools

  • chest pain

  • coughing or hoarseness

  • dark urine

  • difficulty in breathing, chewing, talking, or swallowing

  • eye pain, blurred or double vision, or any change in vision

  • general feeling of discomfort or illness or weakness

  • lower back or side pain

  • muscle weakness

  • painful or difficult urination

  • pale stools

  • pinpoint red spots on skin

  • redness, tenderness, itching, burning, or peeling of skin

  • red or irritated eyes

  • red, thick, or scaly skin

  • ringing or buzzing in the ears

  • spitting blood

  • yellow eyes or skin

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
  • Diarrhea

  • lessening or loss of sense of taste

  • loss of appetite

  • nausea or vomiting

  • stomach pain (mild)

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: Cuprimine 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 Cuprimine resources


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


  • Cuprimine Prescribing Information (FDA)

  • Cuprimine MedFacts Consumer Leaflet (Wolters Kluwer)

  • Cuprimine Concise Consumer Information (Cerner Multum)

  • Penicillamine Professional Patient Advice (Wolters Kluwer)

  • Penicillamine Monograph (AHFS DI)

  • Depen Prescribing Information (FDA)



Compare Cuprimine with other medications


  • Cystinuria
  • Rheumatoid Arthritis
  • Wilson's Disease

Clarinex Syrup


Pronunciation: DES-lor-A-ta-deen
Generic Name: Desloratadine
Brand Name: Clarinex


Clarinex Syrup is used for:

Treating allergy symptoms and chronic hives. It may also be used for other conditions as determined by your doctor.


Clarinex Syrup is an antihistamine. It works by blocking the action of histamine to relieve allergy symptoms, such as sneezing, runny nose, and itchy or watery eyes, and to relieve itching and rash due to chronic hives.


Do NOT use Clarinex Syrup if:


  • you are allergic to any ingredient in Clarinex Syrup or to loratadine

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



Before using Clarinex Syrup:


Some medical conditions may interact with Clarinex Syrup. 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 kidney or liver problems

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


  • Amiodarone because the risk of fast or irregular heartbeat may be increased

  • Other antihistamines (eg, diphenhydramine), azithromycin, cimetidine, erythromycin, fluoxetine, or ketoconazole because they may increase the risk of Clarinex Syrup's side effects

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


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


  • An extra patient leaflet is available with Clarinex Syrup. Talk to your pharmacist if you have questions about this information.

  • Take Clarinex Syrup by mouth with or without food.

  • Use a measuring device marked for medicine dosing. Ask your pharmacist for help if you are unsure of how to measure your dose.

  • If you miss a dose of Clarinex Syrup and you are taking it regularly, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

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



Important safety information:


  • Clarinex Syrup may cause drowsiness or dizziness. These effects may be worse if you take it with alcohol or certain medicines. Use Clarinex Syrup with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.

  • Do not change your dose or take Clarinex Syrup more often than prescribed without checking with your doctor. Drowsiness may occur if you take more of Clarinex Syrup than prescribed.

  • Clarinex Syrup may interfere with skin allergy tests. If you are scheduled for a skin test, talk to your doctor. You may need to stop taking Clarinex Syrup for a few days before the tests.

  • Clarinex Syrup should be used with extreme caution in CHILDREN younger than 6 months 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 Clarinex Syrup while you are pregnant. Clarinex Syrup is found in breast milk. Do not breast-feed while taking Clarinex Syrup.


Possible side effects of Clarinex Syrup:


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:



Cough; diarrhea; dizziness; drowsiness; increased or decreased appetite; nausea; nosebleed; sore throat; trouble sleeping; vomiting.



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, throat, or tongue); dark urine; ear pain or discharge; fast or irregular heartbeat; fever, chills, or sore throat; mental or mood changes; pale stools; seizures; severe or persistent cough; severe or persistent nosebleed; yellowing of the skin or eyes.



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: Clarinex 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 drowsiness; fast or irregular heartbeat.


Proper storage of Clarinex Syrup:

Store Clarinex Syrup at 77 degrees F (25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Clarinex Syrup out of the reach of children and away from pets.


General information:


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

  • Clarinex Syrup 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 Clarinex Syrup. 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 Clarinex resources


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


Compare Clarinex with other medications


  • Hay Fever
  • Urticaria

Corid Granules





Dosage Form: FOR ANIMAL USE ONLY
CORID®

(amprolium)

Type A Medicated Article 25%

INDICATIONS


An aid in the prevention and treatment of coccidiosis caused by Eimeria bovis and E. zurnii in calves.



Warning


Keep this and all drugs out of the reach of children. NOT FOR HUMAN USE.


The Material Safety Data Sheet (MSDS) contains more detailed occupational safety information. To report adverse effects, obtain an MSDS or for assistance, contact Merial at 1-888-637-4251, Option 3.



Withdraw 24 hours before slaughter. A withdrawal period has not been established for this product in pre-ruminating calves. Do not use in calves to be processed for veal.



CAUTION


For satisfactory diagnosis, a microscopic examination of the feces should be done by a veterinarian or diagnostic laboratory before treatment. When treating outbreaks, drug should be administered promptly after diagnosis is determined.


Do not use in feeds containing bentonite.

Use as the sole source of amprolium.

Restricted Drug – Use only as directed (California).



MIXING DIRECTIONS


CORID 25% should be thoroughly and evenly mixed in the feed. CORID 25% may be used to manufacture a Type B medicated feed with a concentration of 2.5% amprolium or a Type C medicated feed in the concentration range of 0.0125% to 1.25% amprolium.


  • Use 200 pounds of CORID 25% per ton of feed to produce Type B medicated feed containing 2.5% amprolium.

  • Use 1 pound of CORID 25% per ton of feed to produce Type C medicated feed containing 0.0125% amprolium.1

  • Use 100 pounds of CORID 25% per ton of feed to produce Type C medicated feed containing 1.25% amprolium.

  • Use 10 pounds of 2.5% Type B per ton of feed to produce Type C medicated feed containing 0.0125% amprolium.

  • Use 1000 pounds of 2.5% Type B per ton of feed to produce Type C medicated feed containing 1.25% amprolium.


1

To aid in even distribution of CORID 25% in the finished feed, prepare a mixture of CORID 25% in a portion of complete feed ingredient before mixing into the finished ration. Blend the mixture with the remainder of the finished feed and mix thoroughly.


AMOUNT AND DIRECTIONS FOR USE



Prevention


227 mg amprolium/100 lb (5 mg/kg) body weight per day for 21 days during periods of exposure of when experience indicates that coccidiosis is likely to be a hazard.



Treatment


454 mg amprolium/100 lb (10 mg/kg) body weight per day for 5 days. Use on a herd basis only; when one or more calves show signs of coccidiosis, it is likely that the rest of the group has been exposed and all calves in the group should be treated.


The proper amount of amprolium supplement is mixed with the amount of ration usually consumed in one day. The tables below give suggested examples for using Type C medicated feed.











































21 DAY PREVENTIVE PROGRAM
DMI (as % Body Weight)432
Body Weight

(lb)
Amprolium per Day (mg)0.0125%

Amprolium
0.0167%

Amprolium
0.025%

Amprolium
Amount of Feed per Day in Pounds
100227432
200454864
3006811296
40090816128
5001134201510
6001361241812









































5 DAY TREATMENT PROGRAM
DMI (as % Body Weight)432
Body Weight

(lb)
Amprolium per Day (mg)0.025%

Amprolium
0.033%

Amprolium
0.05%

Amprolium
Amount of Feed per Day in Pounds
100454432
200908864
30013621296
400181616128
5002268201510
6002722241812


www.corid.com


Merial Limited, a company limited by shares registered in England and Wales (registered number 3332751) with a registered office at PO Box 327, Sandringham House, Sandringham Avenue, Harlow Business Park, Harlow, Essex CM19 5QA, England, and domesticated in Delaware, USA as Merial LLC.


1075-1735-01

Rev. 05-2006



PRINCIPAL DISPLAY PANEL - 22.68 kg Bottle Label


CORID®

(amprolium)


Type A Medicated Article 25%

Coccidiostat


To be used in the preparation of medicated feed to aid

in the prevention and treatment of coccidiosis in calves.


ACTIVE DRUG INGREDIENT:    Amprolium . . . . . . . . . . . . . . . . . . . . 25%


INGREDIENTS: Corn Gluten Feed and Soybean Oil


SEE DIRECTIONS ON BACK PANEL


NADA 12-350

Approved by the FDA


www.corid.com


® CORID and the CATTLE HEAD logo are registered trademarks of Merial Limited.

Copyright © 2006 Merial Limited. All rights reserved.


Net Wt.:    50 lb (22.68 kg)


Product 970450


Merial Limited

3239 Satellite Blvd.

Duluth, Georgia

30096-4640, U.S.A.


MERIAL










CORID 
amprolium  granule










Product Information
Product TypeOTC TYPE A MEDICATED ARTICLE ANIMAL DRUGNDC Product Code (Source)50604-9704
Route of AdministrationORALDEA Schedule    








Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
amprolium (amprolium)amprolium250 mg  in 0.001 kg





Inactive Ingredients
Ingredient NameStrength
No Inactive Ingredients Found


















Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains      










Packaging
#NDCPackage DescriptionMultilevel Packaging
150604-9704-122.68 kg In 1 BAGNone










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NADANADA01235001/01/1961


Labeler - Merial Limited (034393582)
Revised: 08/2010Merial Limited



четверг, 19 апреля 2012 г.

Covaryx


Generic Name: esterified estrogens and methyltestosterone (Oral route)


es-TER-i-fide ES-troe-jenz, meth-il-tes-TOS-ter-one


Oral route(Tablet)

Estrogens increase the risk of endometrial cancer; monitor for abnormal vaginal bleeding. Estrogens with or without progestins should not be used for the prevention of cardiovascular disease or dementia. Increased risks of myocardial infarction, stroke, invasive breast cancer, pulmonary emboli, and deep vein thrombosis in postmenopausal women (50 to 79 years of age) have been reported. An increased risk of developing probable dementia in postmenopausal women 65 years of age or older has also been reported. This product contains an estrogen and androgen, not a progestin. This combination should not be used during a known or suspected pregnancy.



Commonly used brand name(s)

In the U.S.


  • Covaryx

  • Covaryx HS

  • Essian

  • Estratest

  • Menogen

  • Syntest D.S.

  • Syntest H.S.

Available Dosage Forms:


  • Tablet

Therapeutic Class: Estrogen/Androgen Combination


Pharmacologic Class: Estrogen


Uses For Covaryx


Esterified estrogens and methyltestosterone combination is used to treat the symptoms of menopause in patients who did not get relief after being treated with estrogens alone. These symptoms may include a feeling of heat, sweating, and warmth in the face, neck, or chest ("hot flashes"); and dryness, burning, and itching in the vagina.


Esterified estrogens are a man-made mixture of estrogens. Estrogen is a hormone that is produced by the body in greater amounts in females. It is necessary for normal sexual development of the female and for regulation of the menstrual cycle during the childbearing years. Methyltestosterone is a man-made form of testosterone, a hormone that is produced by the body in greater amounts in males and small amounts in females. Menopause symptoms occur when the hormone balance changes in the female body. This combination of hormones will relieve the symptoms of menopause by adding more hormones to the body.


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


Before Using Covaryx


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


The use of esterified estrogens and methyltestosterone combination is not recommended in children.


Geriatric


Appropriate studies performed to date have not demonstrated geriatric-specific problems that would limit the usefulness of esterified estrogens and methyltestosterone combination in the elderly. However, elderly patients are more likely to develop dementia and age-related kidney, liver, or heart problems, which may require caution and an adjustment in the dose for patients receiving this medicine.


Pregnancy








Pregnancy CategoryExplanation
All TrimestersXStudies in animals or pregnant women have demonstrated positive evidence of fetal abnormalities. This drug should not be used in women who are or may become pregnant because the risk clearly outweighs any possible benefit.

Breast Feeding


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


Interactions with Medicines


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


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


  • Anisindione

  • Bupropion

  • Dicumarol

  • Phenprocoumon

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.


  • Clarithromycin

  • Ginseng

  • Itraconazole

  • Ketoconazole

  • Levothyroxine

  • Licorice

  • Tipranavir

  • Warfarin

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. 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 may cause an increased risk of certain side effects but may be unavoidable in some cases. If used together, your doctor may change the dose or how often you use this medicine, or give you special instructions about the use of food, alcohol, or tobacco.


  • Grapefruit Juice

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:


  • Abnormal vaginal bleeding, undiagnosed or

  • Blood clotting problems (e.g., deep vein thrombosis, pulmonary embolism), history of or

  • Breast cancer, or history of or

  • Heart attack, recent or history of or

  • Liver disease, severe or

  • Stroke, recent or history of—Should not be used in patients with these conditions.

  • Asthma or

  • Cancer (e.g., breast, cervix, liver, vagina) or

  • Depression, history of or

  • Diabetes or

  • Edema (fluid retention) or

  • Endometriosis (problem with the lining of the uterus) or

  • Epilepsy or

  • Eye or vision problems (e.g., retinal vascular thrombosis) or

  • Gallbladder disease or

  • Hepatitis (including cholestatic jaundice), history of or

  • Hypercalcemia (high calcium in the blood) or

  • Hypocalcemia (high calcium in the blood) or

  • Hypothyroidism (underactive thyroid) or

  • Migraine headaches, history of or

  • Porphyria (enzyme problem) or

  • Systemic lupus erythematosus—Use with caution. May make these conditions worse.

  • Heart or blood vessel disease or

  • Hypercholesterolemia (high cholesterol in the blood) or

  • Hypertension (high blood pressure) or

  • Hypertriglyceridemia (high triglycerides or fat in the blood) or

  • Venous thromboembolism (clot in the veins), history of—May increase risk for more serious side effects.

Proper Use of esterified estrogens and methyltestosterone

This section provides information on the proper use of a number of products that contain esterified estrogens and methyltestosterone. It may not be specific to Covaryx. Please read with care.


Take this medicine only as directed by your doctor. Do not take more of it, do not take it more often, and do not take it for a longer time than your doctor ordered.


This medicine comes with a patient information insert. Read and follow the instructions in the insert carefully. Ask your doctor if you have any questions.


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 treatment of menopause symptoms:
      • Adults—One to two tablets once a day.

      • Children—Use is not recommended.



Missed Dose


If you miss a dose of this medicine, take it as soon as possible. However, if it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not double doses.


Storage


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


Keep out of the reach of children.


Do not keep outdated medicine or medicine no longer needed.


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


Precautions While Using Covaryx


It is very important that your doctor check your progress at regular visits to make sure the medicine is working properly and to decide if you should continue to take it. These visits should be every 6 to 12 months or as otherwise directed by your doctor.


It is unlikely that a postmenopausal woman may become pregnant. But, you should know that using this medicine while you are pregnant could harm your unborn baby. If you think you have become pregnant while using the medicine, tell your doctor right away.


Very rarely, this medicine can cause serious side effects such as a heart attack or stroke. You are much more likely to have these side effects if you smoke cigarettes or are overweight, or if you have diabetes, high blood pressure, or a high blood cholesterol. Talk with your doctor if you think you might be at risk.


Using large doses of estrogen alone over a long period of time may increase the risk of some kinds of cancer (e.g., endometrial cancer). Talk with your doctor about this risk. If you have vaginal bleeding with this medicine, call your doctor right away.


This medicine may increase the risk of getting breast cancer. It is very important that you check your breasts on a regular basis for any unusual lumps or discharge, and that you have breast x-rays every year as directed by your doctor. These exams are very important if you have a family member with a history of breast cancer. Talk with your doctor about this risk.


This medicine may increase the risk of getting dementia in elderly women (above 65 years of age). Talk with your doctor if this concerns you.


Check with your doctor right away if blurred vision, difficulty with reading, or any other change in vision occurs during or after treatment. Your doctor may want you to have your eyes checked by an ophthalmologist (eye doctor).


Using large doses of methyltestosterone over a long period of time may increase the risk of serious liver problems (e.g., peliosis hepatis or liver cancer). Talk with your doctor about this risk.


Before you have any medical tests, tell the medical doctor in charge that you are taking this medicine. The results of some tests may be affected by this medicine. Also, you may need to stop using this medicine for a few weeks before and after having surgery, or if you are inactive for a long period of time.


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


Covaryx Side Effects


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


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


More common
  • Absent, missed, or irregular menstrual periods

  • acne or oily skin

  • decreased breast size

  • enlarging clitoris

  • hoarseness or deepening of the voice

  • menstrual changes

  • stopping of menstrual bleeding

  • unnatural hair growth or loss

Rare
  • Continuing nausea

  • cough

  • dark-colored urine

  • difficulty with swallowing

  • dizziness

  • fast heartbeat

  • fever

  • hives

  • itching

  • light-colored stools

  • loss of appetite

  • puffiness or swelling of the eyelids or around the eyes, face, lips, or tongue

  • purple or red-colored spots on the body or inside the mouth or nose

  • shortness of breath

  • skin rash

  • sore throat

  • tightness in the chest

  • unusual tiredness or weakness

  • vomiting

  • wheezing

Incidence not known
  • Abdominal or stomach bloating, cramps, or pain

  • anxiety

  • bleeding from gums or nose

  • blistering, peeling, or loosening of the skin

  • bloating

  • bloody or cloudy urine

  • burning, crawling, itching, numbness, prickling, "pins and needles", or tingling feelings

  • change in vaginal discharge

  • changes in skin color, pain, or tenderness

  • chest pain or discomfort

  • chills

  • clay-colored stools

  • clear or bloody discharge from nipple

  • confusion

  • constipation

  • convulsions

  • darkening of urine

  • decrease in amount of urine

  • diarrhea

  • difficult, burning, or painful urination

  • difficulty with breathing

  • difficulty with moving

  • difficulty with speaking

  • dimpling of the breast skin

  • dizziness or lightheadedness

  • double vision

  • eye pain

  • fainting

  • fever

  • fluid-filled skin blisters

  • frequent urge to urinate

  • headache

  • heavy bleeding

  • inability to move the arms, legs, or facial muscles

  • inability to speak

  • indigestion

  • inverted nipple

  • irregular heartbeats

  • itching of the vagina or genital area

  • joint or muscle pain

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

  • light-colored stools

  • loss of appetite

  • lump in the breast or under the arm

  • mood or mental changes

  • muscle cramps in the hands, arms, feet, legs, or face

  • muscle pain or stiffness

  • nausea

  • noisy, rattling breathing

  • numbness and tingling around the mouth, fingertips, or feet

  • pain

  • pain during sexual intercourse

  • pain in the ankles or knees

  • pain or discomfort in the arms, jaw, back, or neck

  • pain or feeling of pressure in pelvis

  • painful, red lumps under the skin, mostly on the legs

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

  • pelvic pain

  • persistent crusting or scaling of the nipple

  • pinpoint red or purple spots on the skin

  • poor insight and judgment problems with memory or speech

  • red, irritated eyes

  • redness or swelling of the breast

  • ringing in the ears

  • sensitivity to the sun

  • shortness of breath

  • skin thinness

  • slow speech

  • sore on the skin of the breast that does not heal

  • sore throat

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

  • stomach pain

  • sudden shortness of breath or troubled breathing

  • sweating

  • swelling

  • swelling of the fingers, hands, feet, or lower legs

  • tenderness of the breast

  • thick, white curd-like vaginal discharge without odor or with mild odor

  • tiredness

  • tremor

  • trouble recognizing objects

  • trouble thinking and planning

  • trouble walking

  • troubled breathing at rest

  • unexpected or excess milk flow from breasts

  • unpleasant breath odor

  • vaginal bleeding

  • vision changes

  • vomiting of blood

  • weakness

  • weight gain

  • yellow eyes or skin

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:


Incidence not known
  • Blemishes on the skin

  • brown, blotchy spots on the exposed skin

  • decreased interest in sexual intercourse

  • depression

  • headache, severe and throbbing

  • inability to have or keep an erection

  • increase or decrease in weight

  • increased hair growth, especially on the face

  • increased in sexual ability, desire, drive, or performance

  • increased interest in sexual intercourse

  • irritability

  • leg cramps

  • loss in sexual ability, desire, drive, or performance

  • loss of hair

  • mental depression

  • pimples

  • redness of the skin

  • swelling or inflammation of the mouth

  • twitching, uncontrolled movements of the tongue, lips, face, arms, or legs

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: Covaryx side effects (in more detail)



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More Covaryx resources


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


  • Covaryx Concise Consumer Information (Cerner Multum)

  • Estratest MedFacts Consumer Leaflet (Wolters Kluwer)



Compare Covaryx with other medications


  • Hot Flashes
  • Menopausal Disorders
  • Postmenopausal Symptoms