Monday, October 24, 2016

urokinase


Generic Name: urokinase (URE oh KYE nase)

Brand names: Abbokinase, Kinlytic, Abbokinase Open-Cath


What is urokinase?

Urokinase is a man-made product developed using a protein that occurs naturally in the kidneys. Urokinase is a thrombolytic agent that works by dissolving blood clots.


Urokinase is used to treat blood clots in the lungs.


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


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


You should not use this medication if you are allergic to urokinase, or if you have internal bleeding, a brain tumor or aneurysm, hemophilia or other bleeding disorder, arterial hypertension, or if you have had a recent stroke, surgery, organ transplant, or medical emergency .

Before you receive urokinase, tell your doctor if you have liver or kidney disease, diabetes, heart problems, if you are pregnant or recently gave birth, a history of stroke or stomach bleeding.


Tell your caregivers at once if you have a serious side effect such as easy bruising or bleeding, blood in your stools, coughing up blood, chest pain, sudden problems with vision or speech, swelling, discoloration of your fingers or toes, severe stomach pain, weak or shallow breathing, fever, chills, or flu symptoms.

Before you receive urokinase, tell your doctor if you are using a blood thinner such as warfarin (Coumadin), aspirin or an NSAID (non-steroidal anti-inflammatory drug) such as ibuprofen (Motrin, Advil), naproxen (Aleve, Naprosyn), and others, or any medication used to prevent blood clots such as Kabikinase, Plavix, Ticlid, Persantine, Streptase, and others.


What should I discuss with my health care provider before I receive urokinase?


You should not use this medication if you are allergic to urokinase, or if you have:

  • internal bleeding;




  • a brain tumor;




  • a brain aneurysm (dilated blood vessel);




  • a bleeding or blood clotting disorder (such as hemophilia);




  • a condition called arterial hypertension;




  • if you have had a recent medical emergency requiring CPR (cardiopulmonary resuscitation);




  • if you have had a stroke, brain surgery, or spinal surgery within in the past 2 months.



If you have certain conditions, you may need a dose adjustment or special tests to safely use this medication. Before you receive urokinase, tell your doctor if you have:



  • a history of stroke;




  • severe liver or kidney disease;




  • eye problems caused by diabetes;




  • an infection of the lining of your heart (also called bacterial endocarditis);




  • a blood clot of your heart;




  • a recent history of stomach or intestinal bleeding;




  • if you are pregnant or have had a baby within the past 10 days; or




  • if you have had surgery or an organ transplant within the past 10 days.




FDA pregnancy category B. Urokinase is not expected to be harmful to an unborn baby. However, your doctor should know if you are pregnant before you receive this medication. It is not known whether urokinase 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.

Urokinase is made from human kidney cells and albumin (part of the blood) and it may contain viruses and other infectious agents that can cause disease. Although donated human blood is screened, tested, and treated to reduce the risk of it containing anything that could cause disease, there is still a small possibility it could transmit disease. Talk with your doctor about the risks and benefits of using this medication.


How is urokinase given?


Urokinase is given as an injection through a needle placed into a vein. You will receive this injection in a clinic or hospital setting.


Urokinase is given slowly, usually over a period of 12 hours, using a continuous infusion pump.


Your breathing, blood pressure, oxygen levels, and other vital signs will be watched closely while you are receiving urokinase.

What happens if I miss a dose?


Since urokinase is given by a healthcare professional in a clinical setting, you are not likely to miss a dose.


What happens if I overdose?


Because urokinase is given in a controlled clinical setting, an overdose is not expected to occur.


What should I avoid while receiving urokinase?


Avoid taking aspirin or ibuprofen (Motrin, Advil) to treat a fever shortly after you have received urokinase. These medications can increase your risk of bleeding. Ask your doctor about other methods of treating a fever.


Urokinase 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. Tell your caregivers at once if you have a serious side effect such as:

  • easy bruising or bleeding (nosebleeds, bleeding gums, bleeding from a wound, incision, catheter, or needle injection );




  • bloody or tarry stools, coughing up blood or vomit that looks like coffee grounds;




  • chest pain or heavy feeling, pain spreading to the arm or shoulder, nausea, sweating, general ill feeling;




  • sudden headache or problems with speech, vision, or balance;




  • fever, chills, flu symptoms, nausea, vomiting, back pain, or stomach pain;




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




  • swelling, weight gain, feeling short of breath;




  • urinating less than usual or not at all;




  • red or purple discoloration of fingers or toes;




  • weak or shallow breathing, blue-colored lips or fingernails;




  • dangerously high blood pressure (severe headache, blurred vision, buzzing in your ears, anxiety, confusion, chest pain, shortness of breath, uneven heartbeats, seizure); or




  • pancreatitis (severe pain in your upper stomach spreading to your back, nausea and vomiting, fast heart rate).



This is not a complete list of side effects and others may occur. Tell your doctor about any unusual or bothersome side effect. You may report side effects to FDA at 1-800-FDA-1088.


Urokinase Dosing Information


Usual Adult Dose for Myocardial Infarction:

Lysis of coronary artery thrombi:
Prior to beginning urokinase, a bolus of heparin 2500 to 10,000 units IV once should be given. Prior heparin administration should be considered when calculating the heparin dose.

Systemic thrombolytic administration:
1 to 2 million intl units administered IV once over 15 to 30 minutes. The rate of infusion is limited by side effects (fever, chills, rigors), and may need to be decreased in some patients. Doses up to 3 million intl units have been used to treat acute myocardial infarction (AMI).

To determine the response to urokinase, the manufacturer recommends serial angiography every 15 minutes. Maximal coronary artery opening usually occurs 15 to 30 minutes after opening begins.

Direct intracoronary artery infusion:
Following the heparin bolus, urokinase may be infused into the occluded artery at a rate of 6000 intl units/min for up to 2 hours, with an average total dose of 500,000 intl units administered.

Alternatively, some studies have reported administering urokinase infusions at a rate of 20,000 to 25,000 intl units/min for 10 to 20 minutes up to a total dose of 250,000 to 500,000 intl units. It has not been established that intracoronary administration of urokinase during evolving transmural AMI results in salvage of myocardial tissue, nor that it reduces mortality.

Heparin therapy (without a loading dose) is recommended when the thrombin time has decreased to less than twice the normal control value.

Usual Adult Dose for Pulmonary Embolism:

Initial: 4400 intl units/kg ideal body weight (IBW) administered as an IV bolus over 10 minutes.

Maintenance: 4400 intl units/kg (IBW) /hour administered as a continuous IV infusion for 12 hours.

Heparin therapy (without a loading dose) is recommended when the thrombin time has decreased to less than twice the normal control value.

Usual Adult Dose for Deep Vein Thrombosis:

Initial: 4400 intl units/kg ideal body weight (IBW) administered as an IV bolus over 10 minutes.

Maintenance: 4400 intl units/kg (IBW) /hour administered as a continuous IV infusion for 72 hours. Treatment may be needed for as long as 10 to 14 days in selected patients.

Heparin therapy (without a loading dose) is recommended when the thrombin time has decreased to less than twice the normal control value.

Usual Adult Dose for Thrombotic/Thromboembolic Disorder:

IV catheter clearance:
When the following procedure is used for thrombolysis of a central venous catheter, the patient should be asked to hold his/her breath at end-exhalation any time the catheter is not connected to IV tubing, a heparin lock, or a syringe (to avoid air embolism).

Once a clot is suspected (after gentle aspiration of the affected catheter with a 10 mL syringe), 5000 intl units urokinase in a 1 mL tuberculin syringe may be slowly and gently injected, using only an amount equivalent to the volume of the catheter. A 5 or 10 mL syringe may be used to gently aspirate from the catheter every 5 minutes. If the catheter is not open within 30 minutes, the catheter may be capped allowing urokinase to dwell inside for 30 to 60 minutes before again attempting to aspirate. A second injection may be necessary in resistant cases.

Once patency is restored, aspiration and removal of 5 mL of blood is recommended to remove all drug and clot residual. Flushing the catheter with normal saline injection is then recommended.


What other drugs will affect urokinase?


The following drugs can interact with urokinase. Tell your doctor if you are using any of these:



  • a blood thinner such as warfarin (Coumadin);




  • aspirin or an NSAID (non-steroidal anti-inflammatory drug) such as ibuprofen (Motrin, Advil), naproxen (Aleve, Naprosyn), diclofenac (Cataflam, Voltaren), etodolac (Lodine), indomethacin (Indocin), ketoprofen (Orudis), and others; or




  • medication used to prevent blood clots, such as alteplase (Activase), anistreplase (Eminase), clopidogrel (Plavix), dipyridamole (Persantine), streptokinase (Kabikinase, Streptase), or ticlopidine (Ticlid).



This list is not complete and there may be other drugs that can interact with urokinase. Tell your doctor about all your prescription and over-the-counter medications, vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start a new medication without telling your doctor.



More urokinase resources


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


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

  • Urokinase Monograph (AHFS DI)

  • Kinlytic Prescribing Information (FDA)



Compare urokinase with other medications


  • Deep Vein Thrombosis
  • Heart Attack
  • Pulmonary Embolism
  • Thrombotic/Thromboembolic Disorder


Where can I get more information?


  • Your doctor or pharmacist can provide more information about urokinase.

See also: urokinase side effects (in more detail)


Urso


Pronunciation: ERR-so-DIE-ole
Generic Name: Ursodiol
Brand Name: Examples include Actigall and Urso


Urso is used for:

Treating and preventing gallstones. It may also be used for other conditions as determined by your doctor.


Urso is a bile acid naturally found in the body. It works by dissolving the cholesterol that makes gallstones and inhibiting production of cholesterol in the liver and absorption in the intestines, which helps to decrease the formation of gallstones. It can also reduce the amount of other bile acids that can be harmful to liver cells when levels are elevated.


Do NOT use Urso if:


  • you are allergic to any ingredient in Urso

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



Before using Urso:


Some medical conditions may interact with Urso. 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 obstruction or inflammation of the bile duct, inflammation of the gallbladder, inflammation of the pancreas, or bleeding from the veins in the esophagus

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


  • Estrogens (eg, premarin, oral contraceptives) because they may decrease Urso's effectiveness

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


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


  • Take Urso by mouth with food or milk.

  • Do not take an antacid that has aluminum in it or a bile acid sequestrant (eg, cholestyramine, colestipol) within 1 hour before or 2 hours after you take Urso.

  • If you miss a dose of Urso, 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 Urso.



Important safety information:


  • It may take several months for Urso to work. Do not stop taking Urso without checking with your doctor.

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

  • Urso should be used with extreme caution in CHILDREN; safety and effectiveness in 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 Urso while you are pregnant. It is not known if Urso is found in breast milk. If you are or will be breast-feeding while you use Urso, check with your doctor. Discuss any possible risks to your baby.


Possible side effects of Urso:


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; diarrhea; dry skin; gas; headache; indigestion; metallic taste; muscle or joint pain; nausea; skin rash; stomach pain; swelling; tiredness.



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

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue).



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: Urso 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 diarrhea.


Proper storage of Urso:

Store Urso at room temperature, between 68 and 77 degrees F (20 and 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 Urso out of the reach of children and away from pets.


General information:


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

  • Urso 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 Urso. 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 Urso resources


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


  • Urso Concise Consumer Information (Cerner Multum)

  • Urso Prescribing Information (FDA)

  • Urso Advanced Consumer (Micromedex) - Includes Dosage Information

  • Ursodiol Prescribing Information (FDA)

  • Ursodiol Professional Patient Advice (Wolters Kluwer)

  • Ursodiol Monograph (AHFS DI)

  • Actigall Prescribing Information (FDA)



Compare Urso with other medications


  • Biliary Cirrhosis
  • Gallbladder Disease
  • Nonalcoholic Fatty Liver Disease

Urised


Generic Name: atropine, hyoscyamine, methenamine, methylene blue, phenyl salicylate, and benzoic acid (Oral route)


AT-roe-peen SUL-fate, hye-oh-SYE-a-meen SUL-fate, meth-EN-a-meen, METH-i-leen BLOO, FEN-il sal-I-si-late, ben-ZOE-ik AS-id


Commonly used brand name(s)

In the U.S.


  • Prosed EC

  • Trac Tabs

  • Urised

Available Dosage Forms:


  • Tablet

  • Tablet, Enteric Coated

Therapeutic Class: Urinary Antispasmodic


Pharmacologic Class: Atropine


Chemical Class: Salicylate, Non-Aspirin


Uses For Urised


Atropine , hyoscyamine , methenamine , methylene blue, phenyl salicylate , and benzoic acid combination medicine is an anticholinergic, anti-infective, and analgesic. It is given by mouth to help relieve the discomfort caused by urinary tract infections; however, it will not cure the infection itself. This combination medicine may also be used for other conditions as determined by your doctor.


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


Before Using Urised


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


Unusual excitement, nervousness, restlessness or irritability, and unusual warmth, dryness, and flushing of skin are more likely to occur in children, who are usually more sensitive to the effects of atropine and hyoscyamine (contained in this combination medicine). Also, when atropine and hyoscyamine are given to children during hot weather, a rapid increase in body temperature may occur. In infants and children, especially those with spastic paralysis or brain damage, this medicine may be more likely to cause severe side effects.


Geriatric


Confusion or memory loss, constipation, difficult urination, excitement, agitation, drowsiness, or dryness of mouth may be more likely to occur in elderly patients, who are usually more sensitive than younger adults to the effects of atropine and hyoscyamine. Also, this combination medicine may cause eye pain in patients who have untreated glaucoma.


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


Benzoic Acid

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


Methylene BlueBenzyl BenzoateMethenamineAtropineHyoscyamine

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.


  • Ambenonium

  • Amitriptyline

  • Amoxapine

  • Bupropion

  • Citalopram

  • Clomipramine

  • Desipramine

  • Desvenlafaxine

  • Doxepin

  • Duloxetine

  • Escitalopram

  • Fluoxetine

  • Fluvoxamine

  • Imipramine

  • Isocarboxazid

  • Linezolid

  • Maprotiline

  • Mirtazapine

  • Nortriptyline

  • Paroxetine

  • Phenelzine

  • Potassium

  • Protriptyline

  • Selegiline

  • Sertraline

  • Tranylcypromine

  • Trimipramine

  • Venlafaxine

  • Vilazodone

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.


  • Buspirone

  • Nefazodone

  • Trazodone

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.


  • Arbutamine

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:


  • Bleeding problems (severe)—This combination medicine may increase heart rate, which would make bleeding problems worse

  • Brain damage (in children)—May increase the central nervous system (CNS) effects of this combination medicine

  • Colitis (severe) or

  • Dryness of mouth (severe or continuing) or

  • Enlarged prostate or

  • Fever or

  • Glaucoma or

  • Heart disease or

  • Hernia (hiatal) or

  • High blood pressure or

  • Intestinal blockage or other intestinal or stomach problems or

  • Lung disease or

  • Myasthenia gravis or

  • Toxemia of pregnancy or

  • Urinary tract blockage or difficult urination—This combination medicine may make these conditions worse

  • Dehydration or

  • Kidney disease or

  • Liver disease—Higher levels of medicine may result and increase the risk of side effects

  • Overactive thyroid—May increase the heart rate

Proper Use of atropine, hyoscyamine, methenamine, methylene blue, phenyl salicylate, and benzoic acid

This section provides information on the proper use of a number of products that contain atropine, hyoscyamine, methenamine, methylene blue, phenyl salicylate, and benzoic acid. It may not be specific to Urised. Please read with care.


While you are taking this combination medicine, it is important for your urine to be acidic. To do this, your doctor may recommend that you eat more protein and such foods as cranberries (especially cranberry juice with vitamin C added), plums, or prunes. You should avoid foods that make the urine more alkaline, such as most fruits (especially citrus fruits and juices), milk, and other dairy products.


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


Each dose should be taken with a full glass (8 ounces) of water or other liquid (except citrus juices and milk). Drink plenty of water or other liquids every day, unless otherwise directed by your doctor. Drinking enough liquids will help your kidneys work better and lessen your discomfort.


To help clear up your infection completely, keep taking this medicine for the full time of treatment even if you begin to feel better after a few days. Do not miss any doses.


In order for this medicine to work well, your urine must be acid (pH 5.5 or below). To make sure that your urine is acid:


  • Before you start taking this medicine, check your urine with phenaphthazine paper or another test to see if it is acid. If you have any questions about this, check with your health care professional.

  • You may need to change your diet; however, check with your doctor first if you are on a special diet (for example, for diabetes). To help make your urine more acid you should avoid most fruits (especially citrus fruits and juices), milk and other dairy products, and other foods which make the urine more alkaline. Eating more protein and foods such as cranberries (especially cranberry juice with vitamin C added), plums, or prunes may also help. If your urine is still not acid enough, check with your doctor.

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 relief of urinary tract symptoms:
      • Adults and children 12 years of age and older—1 to 2 tablets four times a day.

      • Children 6 to 12 years of age—Dose must be determined by the doctor.

      • Children up to 6 years of age—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.


Precautions While Using Urised


If your symptoms do not improve within a few days or if they become worse, check with your doctor.


These medicines may make you sweat less, causing your body temperature to increase. Use extra care not to become overheated during exercise or hot weather while you are taking this medicine, since overheating may result in heat stroke. Also, hot baths or saunas may make you dizzy or faint while you are taking this medicine.


This medicine may cause some people to have blurred vision. 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 able to see well. If your vision continues to be blurred, check with your doctor.


This medicine may cause dryness of the mouth. For temporary relief, use sugarless candy or gum, melt bits of ice in your mouth, or use a saliva substitute. However, if your mouth continues to feel dry for more than 2 weeks, check with your dentist. Continuing dryness of the mouth may increase the chance of dental disease, including tooth decay, gum disease, and fungus infections.


Do not take this medicine within 2 or 3 hours of taking antacids or medicine for diarrhea. Taking antacids or antidiarrhea medicines and this medicine too close together may prevent this medicine from working properly.


Urised 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:


Less common or rare
  • Blurred vision

  • eye pain

  • skin rash or hives

Symptoms of overdose
  • Blood in urine and/or stools

  • diarrhea

  • dizziness

  • drowsiness (severe)

  • fast heartbeat

  • flushing or redness of face

  • headache (severe or continuing)

  • lower back pain

  • pain or burning while urinating

  • ringing or buzzing in the ears

  • shortness of breath or troubled breathing

  • sweating

  • 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:


Less common
  • Difficult urination (more common with large doses taken over a prolonged period of time)

  • dryness of mouth, nose, or throat

  • nausea or vomiting

  • stomach upset or pain (more common with large doses taken over a prolonged period of time)

This medicine may cause your urine and/or stools to turn blue or blue-green. This is to be expected while you are taking this medicine.


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: Urised 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 Urised resources


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


  • Urised MedFacts Consumer Leaflet (Wolters Kluwer)

  • Darcalma Concise Consumer Information (Cerner Multum)

  • Darcalma Prescribing Information (FDA)

  • Darpaz Prescribing Information (FDA)

  • Phosenamine Prescribing Information (FDA)

  • Phosphasal Prescribing Information (FDA)

  • Prosed/DS MedFacts Consumer Leaflet (Wolters Kluwer)

  • Urelle Prescribing Information (FDA)

  • Uribel Prescribing Information (FDA)

  • Urimax Delayed-Release Tablets MedFacts Consumer Leaflet (Wolters Kluwer)

  • Uritact-EC Delayed-Release Tablets MedFacts Consumer Leaflet (Wolters Kluwer)

  • Ustell Prescribing Information (FDA)

  • Uta MedFacts Consumer Leaflet (Wolters Kluwer)



Compare Urised with other medications


  • Urinary Tract Infection

Urobiotic





Dosage Form: Capsules

Each capsule contains


Oxytetracycline hydrochloride equivalent to. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 250 mg

  oxytetracycline


Sulfamethizole . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 250 mg


Phenazopyridine hydrochloride . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50 mg


Inert ingredients in the formulation are: hard gelatin capsules (which may contain Green 3, Yellow 6, Yellow 10 and other inert ingredients); magnesium stearate; sodium lauryl sulfate; starch.



ACTIONS


Urobiotic-250 is a product designed for use specifically in urinary tract infections.


Terramycin® (oxytetracycline HCl) is a widely used antibiotic with clinically proved activity against gram-positive and gram-negative bacteria, rickettsiae, spirochetes, large viruses, and certain protozoa. Terramycin is well tolerated and well absorbed after oral administration. It diffuses readily through the placenta and is present in the fetal circulation. It diffuses into the pleural fluid, and under some circumstances, into the cerebrospinal fluid. Oxytetracycline HCl appears to be concentrated in the hepatic system and is excreted in the bile. It is excreted in the urine and in the feces, in high concentrations, in a biologically active form.


Sulfamethizole is a chemotherapeutic agent active against a number of important gram-positive and gram-negative bacteria. This sulfonamide is well absorbed, has a low degree of acetylation, and is extremely soluble. Because of these features and its rapid renal excretion, sulfamethizole has a low order of toxicity and provides prompt and high concentrations of the active drug in the urinary tract.


Phenazopyridine is an orally absorbed agent which produces prompt and effective local analgesia and relief of urinary symptoms by virtue of its rapid excretion in the urinary tract. These effects are confined to the genitourinary system and are not accompanied by generalized sedation or narcosis.



INDICATIONS


Based on a review of this drug by the National Academy of Sciences-National Research Council and/or other information, FDA has classified the indications as follows:


"Lacking substantial evidence of effectiveness as a fixed combination":


Urobiotic-250 is indicated in the therapy of a number of genitourinary infections caused by susceptible organisms. These infections include the following: pyelonephritis, pyelitis, ureteritis, cystitis, prostatitis, and urethritis.


Since both Terramycin and sulfamethizole provide effective levels in blood, tissue, and urine, Urobiotic-250 provides a multiple antimicrobial approach at the site of infection. Both antibacterial components are active against the most common urinary pathogens, including Escherichia coli, Pseudomonas aeruginosa, Aerobacter aerogenes, Streptococcus faecalis, Streptococcus hemolyticus, and Micrococcus pyogenes. Urobiotic-250 is particularly useful in the treatment of infections caused by bacteria more sensitive to the combination than to either component alone. The combination is also of value in those cases with mixed infections, and in those instances where the causative organism is unknown pending laboratory isolation.


Final classification of the less than effective indications requires further investigation. Clinical studies to substantiate the efficacy of Urobiotic 250 are ongoing. Completion of these ongoing studies will provide data for final classification of these indications.



Contraindications


This drug is contraindicated in individuals who have shown hypersensitivity to any of its components.


This drug, because of the sulfonamide component, should not be used in patients with a history of sulfonamide sensitivities, and in pregnant females at term.



Warnings


If renal impairment exists, even usual oral or parenteral doses may lead to excessive systemic accumulation of the drug and possible liver toxicity. Under such conditions, lower than usual doses are indicated and if therapy is prolonged, tetracycline serum level determinations may be advisable.


Oxytetracycline HCl, which is one of the ingredients of Urobiotic-250, may form a stable calcium complex in any bone-forming tissue with no serious harmful effects reported thus far in humans. However, use of oxytetracycline during tooth development (last trimester of pregnancy, neonatal period and early childhood) may cause discoloration of the teeth (yellow-grey-brownish). This effect occurs mostly during long term use of the drug but it also has been observed in usual short treatment courses.


Because of its sulfonamide content, this drug should be used only after critical appraisal in patients with liver damage, renal damage, urinary obstruction, or blood dyscrasias. Deaths have been reported from hypersensitivity reactions, agranulocytosis, aplastic anemia, and other blood dyscrasias associated with sulfonamide administration. When used intermittently, or for a prolonged period, blood counts and liver and kidney function tests should be performed.


Certain hypersensitive individuals may develop a photodynamic reaction precipitated by exposure to direct sunlight during the use of this drug. This reaction is usually of the photoallergic type which may also be produced by other tetracycline derivatives. Individuals with a history of photosensitivity reactions should be instructed to avoid exposure to direct sunlight while under treatment with this or other tetracycline drugs, and treatment should be discontinued at first evidence of skin discomfort.


NOTE: Reactions of a photoallergic nature are exceedingly rare with Terramycin (oxytetracycline HCl). Phototoxic reactions are not believed to occur with Terramycin.



Precautions


As with all antibiotic preparations, use of this drug may result in overgrowth of nonsusceptible organisms, including fungi. If superinfection occurs, the antibiotic should be discontinued and appropriate specific therapy should be instituted. This drug should be used with caution in persons having histories of significant allergies and/or asthma.



Adverse Reactions


Glossitis, stomatitis, proctitis, nausea, diarrhea, vaginitis, and dermatitis, as well as reactions of an allergic nature, may occur during oxytetracycline HCl therapy, but are rare. If adverse reactions, individual idiosyncrasy, or allergy occur, discontinue medication. Rare instances of esophagitis and esophageal ulcerations have been reported in patients receiving capsule forms of drugs in the tetracycline class. Most of these patients took medications immediately before going to bed. (See Dosage and Administration.)


With oxytetracycline therapy bulging fontanels in infants and benign intracranial hypertension in adults have been reported in individuals receiving full therapeutic dosages. These conditions disappeared rapidly when the drug was discontinued.


As in all sulfonamide therapy, the following reactions may occur: nausea, vomiting, diarrhea, hepatitis, pancreatitis, blood dyscrasias, neuropathy, drug fever, skin rash, injection of the conjunctiva and sclera, petechiae, purpura, hematuria and crystalluria. The dosage should be decreased or the drug withdrawn, depending upon the severity of the reaction.



Urobiotic Dosage and Administration


Urobiotic-250 is recommended in adults only. A dose of 1 capsule four times daily is suggested. In refractory cases 2 capsules four times a day may be used.


Therapy should be continued for a minimum of seven days or until bacteriologic cure in acute urinary tract infections.


Administration of adequate amounts of fluid along with capsule forms of drugs in the tetracycline class is recommended to wash down the drugs and reduce the risk of esophageal irritation and ulceration. (SeeAdverse Reactions.)


To aid absorption of the drug, it should be given at least one hour before or two hours after eating. Aluminum hydroxide gel given with antibiotics has been shown to decrease their absorption and is contraindicated.



SUPPLY


Urobiotic-250 capsules: bottles of 50 (NDC 0049-0920-50), and unit dose packages of 100 (10 × 10's) (NDC 0049-0920-41).



Rx only



70-1636-00-9

December 1986








Urobiotic 
oxytetracycline hydrochloride, sulfamethizole and phenazopyridine hydrochloride  capsule










Product Information
Product TypeHUMAN PRESCRIPTION DRUGNDC Product Code (Source)0049-0920
Route of AdministrationORALDEA Schedule    



































INGREDIENTS
Name (Active Moiety)TypeStrength
oxytetracycline hydrochloride (oxytetracycline)Active250 MILLIGRAM  In 1 CAPSULE
sulfamethizole (sulfamethizole)Active250 MILLIGRAM  In 1 CAPSULE
phenazopyridine hydrochloride (phenazopyridine)Active50 MILLIGRAM  In 1 CAPSULE
gelatinInactive 
Green 3Inactive 
Yellow 6Inactive 
Yellow 10Inactive 
magnesium stearateInactive 
sodium lauryl sulfateInactive 
starchInactive 






















Product Characteristics
ColorGREEN (Yellow) , YELLOW (Yellow)Scoreno score
ShapeCAPSULE (Capsule)Size22mm
FlavorImprint CodePfizer;092
Contains      
CoatingfalseSymbolfalse














Packaging
#NDCPackage DescriptionMultilevel Packaging
10049-0920-5050 CAPSULE In 1 BOTTLENone
20049-0920-41100 CAPSULE In 1 PACKAGENone

Revised: 12/2005Roerig

More Urobiotic resources


  • Urobiotic Drug Interactions
  • Urobiotic Support Group
  • 0 Reviews · Be the first to review/rate this drug

Urogesic Blue





Dosage Form: tablet
UROGESIC-BLUE™

Rx Only



Description


Each tablet contains:














Methenamine, USP81.6 mg
Monobasic Sodium Phosphate, USP40.8 mg
Methylene Blue, USP10.8 mg
Hyoscyamine Sulfate, USP0.12 mg

Inactive Ingredients include: microcrystalline cellulose, NF, mannitol, USP, croscarmellose sodium, NF, magnesium stearate, NF and lake blend blue.


HYOSCYAMINE SULFATE is an alkaloid of belladonna. Exists as a white crystalline powder. Affected by light. It is very soluble in water; freely soluble in alcohol; practically insoluble in ether.


METHENAMINE exists as colorless, lustrous crystals or white crystalline powder. Its solutions are alkaline to litmus. Freely soluble in water; soluble in alcohol and in chloroform.


METHYLENE BLUE exists as dark green crystals. It is soluble in water and in chloroform; sparingly soluble in alcohol.


MONOBASIC SODIUM PHOSPHATE exists as a white crystalline powder. Its solutions are acidic to litmus. It is freely soluble in water and practically insoluble in alcohol.



Urogesic Blue - Clinical Pharmacology


HYOSCYAMINE is a parasympatholytic which relaxes smooth muscles and thus produces an antispasmodic effect. It is well absorbed from the gastrointestinal tract and is rapidly distributed throughout body tissues. Most is excreted in the urine within 12 hours, 13% to 50% being unchanged. Its biotransformation is hepatic. Its protein binding is moderate.


METHENAMINE degrades in an acidic urine environment releasing formaldehyde which provides bactericidal or bacteriostatic action. It is well absorbed from the gastrointestinal tract. 70% to 90% reaches the urine unchanged at which point it is hydrolyzed if the urine is acidic. Within 24 hours it is almost completely (90%) excreted; of this amount at pH 5, approximately 20% is formaldehyde. Protein binding: some formaldehyde is bound to substances in the urine and surrounding tissues. Methenamine is freely distributed to body tissue and fluids but is not clinically significant as it does not hydrolyze at pH greater than 6.8.


METHYLENE BLUE possesses weak antiseptic properties. It is well absorbed in the gastrointestinal tract and is rapidly reduced to leukomethylene blue which is stabilized in some combination form in the urine. 75% is excreted unchanged.


MONOBASIC SODIUM PHOSPHATE helps to maintain an acid pH in the urine necessary for the degradation of methenamine.



Indications and Usage for Urogesic Blue


UROGESIC-BLUE™ is indicated for the treatment of symptoms of irritative voiding. Indicated for the relief of local symptoms, such as hypermotility which accompany lower urinary tract infections and as antispasmodic. Indicated for the relief of urinary tract symptoms caused by diagnostic procedures.



Contraindications


UROGESIC-BLUE™ is contraindicated in patients with a hypersensitivity to any of the ingredients. Risk-benefit should be considered when the following medical problems exist: Cardiac disease (especially cardiac arrythmias, congestive heart failure, coronary heart disease, mitral stenosis); gastrointestinal tract obstructive disease; glaucoma; myasthenia gravis; acute urinary retention may be precipitated in obstructive uropathy (such as bladder neck obstruction due to prostatic hypertrophy).



Warnings


Do not exceed recommended dosage. If rapid pulse, dizziness, or blurring of vision occurs discontinue use immediately.



Precautions



Cross sensitivity and/or related problems


patients intolerant of belladonna alkaloids may be intolerant of this medication also.



Pregnancy/Reproduction


Pregnancy Category C

hyoscyamine and methenamine cross the placenta. Studies have not been done in animals or humans. It is not known whether UROGESIC-BLUE™ tablets cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. UROGESIC-BLUE™ tablets should be given to a pregnant woman only if clearly needed.



Breast-feeding


problems in humans have not been documented; however, methenamine and traces of hyoscyamine are excreted in breast milk.



Prolonged use


there have been no studies to establish the safety of prolonged use in humans. No known long-term animal studies have been performed to evaluate carcinogenic potential.



Pediatric


infants and young children are especially susceptible to the toxic effect of the belladonna alkaloids.



Geriatric


use with caution in elderly patients as they may respond to usual doses of hyoscyamine with excitement, agitation, drowsiness, or confusion.



Drug Interactions


because of this product's effect on gastrointestinal motility and gastric emptying, it may decrease the absorption of other oral medications during concurrent use such as: urinary alkalizers; thiazide diuretics (may cause the urine to become alkaline reducing the effectiveness of methenamine by inhibiting its conversion to formaldehyde); antimuscarinics (concurrent use may intensify antimuscarinic effects of hyoscyamine because of secondary antimuscarinic activities of these medications); antacids/antidiarrheals (may reduce absorption of hyoscyamine, concurrent use with antacids may cause urine to become alkaline reducing effectiveness of methenamine by inhibiting its conversion to formaldehyde) doses of these medications should be spaced 1 hour apart from doses of hyoscyamine; antimyasthenics (concurrent use with hyoscyamine may further reduce intestinal motility); ketoconazole (patients should be advised to take this combination at least 2 hours after ketoconazole); monoamine oxidase (MAO) Inhibitors (concurrent use may intensify antimuscarinic side effects, opoid (narcotic) analgesics may result in increased risk of severe constipation); sulfonamides (these drugs may precipitate with formaldehyde in the urine, increasing the danger of crystalluria).


Patients should be advised that the urine may become blue to blue green and the feces may be discolored as a result of the excretion of methylene blue.



Adverse Reactions


Cardiovascular – rapid pulse, flushing


Central Nervous System – blurred vision, dizziness


Respiratory – shortness of breath or troubled breathing


Genitourinary – difficulty micturition, acute urinary retention


Gastrointestinal – dry mouth, nausea/vomiting



Drug Abuse and Dependence


A dependence on the use of UROGESIC-BLUE™ has not been reported and due to the nature of its ingredients, abuse of UROGESIC-BLUE™ is not expected.



Overdosage


Emesis or gastric lavage. Slow intravenous administration of physostigmine in doses of 1 mg to 4 mg (0.5 mg to 1 mg in children), repeated as needed in one to two hours to reverse severe antimuscarinic symptoms. Administration of small doses of diazepam to control excitement and seizures. Artificial respiration with oxygen if needed for respiratory depression. Adequate hydration. Symptomatic treatment as necessary.



Urogesic Blue Dosage and Administration



Adults


One tablet orally 4 times per day followed by liberal fluid intake.



Older Children


Dosage must be individualized by physician. Not recommended for use in children up to 6 years of age.



How is Urogesic Blue Supplied


UROGESIC-BLUE™ are light blue to blue, oval, biconvex tablets debossed with "ED UB" with scoreline on one side and plain on the other side. Supplied in bottles of 100 tablets (NDC 0485-0051-01).



CAUTION


RX ONLY



STORAGE


Store at 25° C (77° F); excursions permitted to 15° C to 30° C (59° F to 86° F) [See USP Controlled Room Temperature]. Keep container tightly closed.



Manufactured for:

Edwards Pharmaceutical, Inc.

111 W. Mulberry St. Ripley, Mississippi 38663


Manufactured by:

Belcher Pharmaceuticals, Inc.

Largo, FL 33777


January 2010                    R - 0110



PRINCIPAL DISPLAY PANEL - 100 count Tablet Bottle Label


NDC 0485-0051-01


UROGESIC-BLUE ™


URINARY ANTISEPTIC

ANTISPASMODIC


DESCRIPTION: Each tablet contains:










Methenamine, USP81.6 mg
Monobasic Sodium Phosphate, USP40.8 mg
Methylene Blue, USP10.8 mg
Hyoscyamine Sulfate, USP0.12 mg

CONTENTS: 100 TABLETS


RX ONLY


Manufactured for

EDWARDS

PHARMACEUTICAL, INC.

Ripley, MS 38663










Urogesic Blue 
methenamine, sodium phosphate, monobasic, methylene blue, and hyoscyamine sulfate  tablet










Product Information
Product TypeHUMAN PRESCRIPTION DRUGNDC Product Code (Source)0485-0051
Route of AdministrationORALDEA Schedule    

















Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
METHENAMINE (METHENAMINE)METHENAMINE81.6 mg
SODIUM PHOSPHATE, MONOBASIC (SODIUM CATION)SODIUM PHOSPHATE, MONOBASIC40.8 mg
METHYLENE BLUE (METHYLENE BLUE)METHYLENE BLUE10.8 mg
HYOSCYAMINE SULFATE (HYOSCYAMINE)HYOSCYAMINE SULFATE0.12 mg












Inactive Ingredients
Ingredient NameStrength
CELLULOSE, MICROCRYSTALLINE 
MANNITOL 
CROSCARMELLOSE SODIUM 
MAGNESIUM STEARATE 


















Product Characteristics
ColorBLUEScore2 pieces
ShapeOVAL (biconvex)Size13mm
FlavorImprint CodeED;UB
Contains      










Packaging
#NDCPackage DescriptionMultilevel Packaging
10485-0051-01100 TABLET In 1 BOTTLE, PLASTICNone










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Unapproved drug other04/30/2010


Labeler - EDWARDS PHARMACEUTICAL, INC. (195118880)









Establishment
NameAddressID/FEIOperations
BELCHER PHARMACEUTIALS, INC.175968069MANUFACTURE, ANALYSIS, PACK, LABEL
Revised: 04/2010EDWARDS PHARMACEUTICAL, INC.

More Urogesic Blue resources


  • Urogesic Blue Use in Pregnancy & Breastfeeding
  • Urogesic Blue Drug Interactions
  • Urogesic Blue Support Group
  • 16 Reviews for Urogesic Blue - Add your own review/rating


Compare Urogesic Blue with other medications


  • Urinary Tract Infection

urofollitropin Intramuscular, Subcutaneous, Injection


ure-oh-FOL-li-troe-pin


Commonly used brand name(s)

In the U.S.


  • Bravelle

  • Fertinex

In Canada


  • Fertinorm Hp

  • Metrodin

Available Dosage Forms:


  • Powder for Solution

Therapeutic Class: Female Reproductive Agent


Pharmacologic Class: Human Follicle Stimulating Hormone


Uses For urofollitropin


Urofollitropin is a fertility drug that is identical to the hormone called follicle-stimulating hormone (FSH) that is produced naturally by the pituitary gland.


FSH is primarily responsible for stimulating growth of the ovarian follicle, which includes the developing egg, the cells surrounding the egg that produce the hormones needed to support a pregnancy, and the fluid around the egg. As the ovarian follicle grows, an increasing amount of the hormone estrogen is produced by the cells in the follicle and released into the bloodstream. Estrogen causes the endometrium (lining of the uterus) to thicken before ovulation occurs. The higher blood levels of estrogen will also provide a cue to the hypothalamus and pituitary gland to slow the production and release of FSH.


Another pituitary hormone, luteinizing hormone (LH), also helps to increase the amount of estrogen produced by the follicle cells. However, the main function of LH is to cause ovulation. The sharp rise in the blood level of LH that triggers ovulation is sometimes called the LH surge. After ovulation, the group of hormone-producing follicle cells become what is called the corpus luteum and will produce estrogen and large amounts of another hormone, progesterone. Progesterone causes the endometrium to mature so that it can support the egg after it is fertilized. If implantation of a fertilized egg does not occur, the levels of estrogen and progesterone decrease, the endometrium sloughs off, and menstruation occurs.


Urofollitropin is usually given in combination with human chorionic gonadotropin (hCG). The actions of hCG are almost identical to those of LH. It is given to simulate the natural LH surge. This results in predictable ovulation.


Urofollitropin is often used in women who have low levels of FSH and too-high levels of LH. Women with polycystic ovary syndrome usually have hormone levels such as this and are treated with urofollitropin to make up for the low amounts of FSH. Many women being treated with urofollitropin have already tried clomiphene (e.g., Serophene) and have not been able to conceive yet. Urofollitropin may also be used to cause the ovary to produce several follicles, which can then be harvested for use in gamete intrafallopian transfer (GIFT) or in vitro fertilization (IVF).


Urofollitropin is to be given only by or under the supervision of your doctor.


Before Using urofollitropin


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 urofollitropin, the following should be considered:


Allergies


Tell your doctor if you have ever had any unusual or allergic reaction to urofollitropin 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.


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. Tell your healthcare professional if you are taking any other prescription or nonprescription (over-the-counter [OTC]) medicine.


Interactions with Food/Tobacco/Alcohol


Certain medicines should not be used at or around the time of eating food or eating certain types of food since interactions may occur. Using alcohol or tobacco with certain medicines may also cause interactions to occur. Discuss with your healthcare professional the use of your medicine with food, alcohol, or tobacco.


Other Medical Problems


The presence of other medical problems may affect the use of urofollitropin. Make sure you tell your doctor if you have any other medical problems, especially:


  • Cyst on ovary—Urofollitropin can cause further growth of cysts on the ovary

  • Unusual vaginal bleeding—Some irregular vaginal bleeding is a sign that the endometrium is growing too rapidly, possibly of endometrial cancer, or some hormone imbalances; the increases in estrogen production caused by urofollitropin can make these problems worse. If a hormonal imbalance is present, it should be treated before beginning menotropins therapy

Proper Use of urofollitropin


Dosing


The dose of urofollitropin 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 urofollitropin. 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 becoming pregnant while having a condition called polycystic ovary syndrome:
      • Adults—75 Units injected under the skin or into a muscle once a day for seven or more days. Usually, another medicine called chorionic gonadotropin (hCG) will be given the day after the last dose. If needed, your doctor may then increase your dose of urofollitropin to 150 Units a day for another seven or more days. Higher doses may be prescribed by your doctor.


    • For becoming pregnant while using other pregnancy-promoting methods (assisted reproductive technology [ART]):
      • Adults—150 Units injected under the skin or into a muscle once a day. Your treatment will probably begin on Day 2 or Day 3 after your menstrual period begins. Usually, another medicine called chorionic gonadotropin (hCG) will be given the day after the last dose.



Precautions While Using urofollitropin


It is very important that your doctor check your progress at regular visits to make sure that the medicine is working properly and to check for unwanted effects. Your doctor will likely want to monitor the development of the ovarian follicle(s) by measuring the amount of estrogen in your bloodstream and by checking the size of the follicle(s) with ultrasound examinations.


If your doctor has asked you to record your basal body temperature (BBT) daily, make sure that you do this every day. It is important that intercourse take place around the time of ovulation to give you the best chance of becoming pregnant.


urofollitropin 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
  • Abdominal or pelvic pain

  • bloating (mild)

  • redness, pain, or swelling at the injection site

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

  • bloating (moderate to severe)

  • decreased amount of urine

  • feeling of indigestion

  • fever and chills

  • nausea, vomiting, or diarrhea (continuing or severe)

  • pelvic pain (severe)

  • shortness of breath

  • skin rash or hives

  • swelling of lower legs

  • weight gain (rapid)

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:


Less common or rare
  • Breast tenderness

  • diarrhea (mild)

  • nausea

  • vomiting

After you stop using urofollitropin, it may still produce some side effects that need attention. During this period of time, check with your doctor immediately if you notice the following side effects:


  • Abdominal or stomach pain (severe)

  • bloating (moderate to severe)

  • decreased amount of urine

  • feeling of indigestion

  • nausea, vomiting, or diarrhea (continuing or severe)

  • pelvic pain (severe)

  • shortness of breath

  • swelling of lower legs

  • weight gain (rapid)

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: urofollitropin Intramuscular, Subcutaneous, Injection 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 urofollitropin Intramuscular, Subcutaneous, Injection resources


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


Compare urofollitropin Intramuscular, Subcutaneous, Injection with other medications


  • Female Infertility
  • Follicle Stimulation

Uritact-EC Delayed-Release Tablets


Pronunciation: A-troe-peen/ben-ZOE-ik AS-id/hye-oh-SYE-a-meen/meth-EN-a-meen/METH-i-leen/FEN-ill sa-LI-si-late
Generic Name: Atropine/Benzoic Acid/Hyoscyamine/Methenamine/Methylene Blue/Phenyl Salicylate
Brand Name: Prosed ED and Uritact-EC


Uritact-EC Delayed-Release Tablets are used for:

Treating painful and irritating symptoms of the urinary tract due to urinary tract infections or diagnostic procedures.


Uritact-EC Delayed-Release Tablets are a urinary antiseptic, urinary acidifier, analgesic, and anticholinergic combination. It works by helping to kill bacteria in the urine, decreasing pain and inflammation, and reducing muscle spasms in the urinary tract. These actions work together to help relieve discomfort while urinating.


Do NOT use Uritact-EC Delayed-Release Tablets if:


  • you are allergic to any ingredient in Uritact-EC Delayed-Release Tablets

  • you have had a severe allergic reaction (eg, severe rash, hives, difficulty breathing, dizziness) to aspirin, other salicylate medicines, or a nonsteroidal anti-inflammatory drug (NSAID) (eg, ibuprofen, naproxen, celecoxib)

  • you have angle-closure glaucoma, problems with your esophagus, bowel motility problems, a blockage of your bladder or bowel, severe intestinal problems (eg, ulcerative colitis), severe bleeding, flu or chickenpox, myasthenia gravis, severe kidney problems, or you are severely dehydrated

  • you are taking a sulfonamide (eg, sulfamethoxazole)

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



Before using Uritact-EC Delayed-Release Tablets:


Some medical conditions may interact with Uritact-EC Delayed-Release Tablets. 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 constipation, diarrhea, an infection of the stomach or bowel, a hiatal hernia, or stomach ulcers

  • if you have nervous system problems, glucose-6-phosphate dehydrogenase (G-6-PD) deficiency, gout, influenza, Kawasaki syndrome, rheumatic disease, open-angle glaucoma, risk factors for angle-closure glaucoma, kidney or liver problems, an enlarged prostate, bladder problems, or you are unable to urinate

  • if you have a history of stroke or brain blood vessel problems (eg, aneurysm), an irregular heartbeat, heart blood vessel problems, congestive heart failure, heart valve problems, or other heart problems

  • if you are on a low-salt diet

Some MEDICINES MAY INTERACT with Uritact-EC Delayed-Release Tablets. Tell your health care provider if you are taking any other medicines, especially any of the following:


  • Anticholinergics (eg, benztropine) because they may increase the risk of Uritact-EC Delayed-Release Tablets's side effects.

  • Ketoconazole because it may decrease Uritact-EC Delayed-Release Tablets's effectiveness.

  • Monoamine oxidase inhibitors (MAOIs)or narcotic pain medicine (eg, codeine) because the risk of serious side effects may be increased.

  • Medicine for myasthenia gravis (eg, ambenonium), phenothiazines (eg, chlorpromazine), sulfonamides (eg, sulfamethoxazole), thiazide diuretics (eg, hydrochlorothiazide), or urinary alkalinizers (eg, sodium bicarbonate) because their effectiveness may be decreased by Uritact-EC Delayed-Release Tablets.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Uritact-EC Delayed-Release Tablets 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 Uritact-EC Delayed-Release Tablets:


Use Uritact-EC Delayed-Release Tablets as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • Take Uritact-EC Delayed-Release Tablets by mouth with or without food.

  • Swallow Uritact-EC Delayed-Release Tablets whole. Do not break, crush, or chew before swallowing.

  • Do not take an antacid or antidiarrheal medicine (eg, loperamide) within 1 hour before or after you take Uritact-EC Delayed-Release Tablets.

  • Drinking extra fluids while you are taking Uritact-EC Delayed-Release Tablets are recommended. Check with your doctor for instructions.

  • If you miss a dose of Uritact-EC Delayed-Release Tablets, 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 Uritact-EC Delayed-Release Tablets.



Important safety information:


  • Uritact-EC Delayed-Release Tablets may cause dizziness. These effects may be worse if you take it with alcohol or certain medicines. Use Uritact-EC Delayed-Release Tablets with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.

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

  • Uritact-EC Delayed-Release Tablets may discolor the urine or stools a blue-green color. This is normal and not a cause for concern.

  • Uritact-EC Delayed-Release Tablets contains salicylate. Salicylates have been linked to a serious illness called Reye syndrome. Do not give Uritact-EC Delayed-Release Tablets to a child or teenager who has the flu, chickenpox, or a viral infection. Contact your doctor with any questions or concerns.

  • Use Uritact-EC Delayed-Release Tablets with caution in the ELDERLY; they may be more sensitive to its effects, especially excitement, agitation, drowsiness, and confusion.

  • Uritact-EC Delayed-Release Tablets should not be used in CHILDREN younger than 6 years old; safety and effectiveness in these children have not been confirmed.

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


Possible side effects of Uritact-EC Delayed-Release Tablets:


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:



Dry mouth; flushing; nausea; 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, or tongue); blurred vision; difficulty urinating; dizziness; fast or irregular heartbeat.



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: Uritact-EC side effects (in more detail)


If OVERDOSE is suspected:


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


Proper storage of Uritact-EC Delayed-Release Tablets:

Store Uritact-EC Delayed-Release Tablets between 68 and 77 degrees F (20 and 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 Uritact-EC Delayed-Release Tablets out of the reach of children and away from pets.


General information:


  • If you have any questions about Uritact-EC Delayed-Release Tablets, please talk with your doctor, pharmacist, or other health care provider.

  • Uritact-EC Delayed-Release Tablets are 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 Uritact-EC Delayed-Release Tablets. 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 Uritact-EC resources


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


Compare Uritact-EC with other medications


  • Urinary Tract Infection