Thursday, October 27, 2016

Aquavite-E


Generic Name: vitamin E (VYE ta min E)

Brand Names: Amino-Opti-E, Aqua-E, Aquasol E, Aquavite-E, Aqueous Vitamin E, E Pherol, E-400 Clear, Vita-Plus E Natural


What is Aquavite-E (vitamin E)?

Vitamin E is an antioxidant that occurs naturally in foods such as nuts, seeds, and leafy green vegetables. Vitamin E is important for many processes in the body.


Vitamin E is used to prevent and to treat a deficiency vitamin E. People with certain diseases may need extra vitamin E.


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


What is the most important information I should know about Aquavite-E (vitamin E)?


Before using vitamin E, tell your healthcare provider if you have liver disease, diabetes, active bleeding, a vitamin K deficiency, retinitis pigmentosa, chronic diarrhea, if you are being treated for cancer, or if you have a history of heart attack, stroke, blood clot, or recent surgery.


Do not use this product without a doctor's advice your doctor if you are pregnant or breast-feeding. Your dose needs may be different during pregnancy or while you are nursing a baby. Do not take vitamin E without a doctor's advice if you are using any type of medication to treat or prevent blood clots.

There are many other drugs that can interact with or be made less effective by vitamin E. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor. Keep a list of all your medicines and show it to any healthcare provider who treats you.


Stop taking vitamin E and call your doctor at once if you have any unusual bleeding or bruising, or if you feel like you might pass out.

What should I discuss with my healthcare provider before taking Aquavite-E (vitamin E)?


Before using vitamin E, talk to your doctor, pharmacist, herbalist, or other healthcare provider. You may not be able to take vitamin E if you have certain medical conditions.


You may need a dose adjustment or special tests if you have:

  • liver disease;




  • diabetes;




  • active or uncontrolled bleeding;




  • a vitamin K deficiency;




  • retinitis pigmentosa;




  • short bowel syndrome;




  • chronic diarrhea;




  • a history of heart attack, stroke, or blood clot;




  • if you have recently had surgery; or




  • if you are receiving cancer treatment (chemotherapy or radiation).




It is not known whether vitamin E is harmful to an unborn baby. Your dose needs may be different during pregnancy. Do not use this product without a doctor's advice if you are pregnant or plan to become pregnant while using vitamin E. It is not known whether vitamin E passes into breast milk or if it could harm a nursing baby. Your dose needs may be different while you are nursing. Do not use this product without a doctor's advice if you are breast-feeding a baby.

How should I take Aquavite-E (vitamin E)?


Take exactly as directed on the label, or as prescribed by your doctor. Do not take in larger or smaller amounts or for longer than recommended.


Take vitamin E with a full glass of water.

The chewable tablet must be chewed completely before you swallow it.


Measure liquid medicine with a special dose-measuring spoon or medicine cup, not with a regular table spoon. If you do not have a dose-measuring device, ask your pharmacist for one.


You may take vitamin E with or without food. You do not need to eat extra fat to help your body absorb vitamin E.


The recommended dietary allowance of vitamin E increases with age. Follow your healthcare provider's instructions. You may also consult the National Academy of Sciences "Dietary Reference Intake" or the U.S. Department of Agriculture's "Dietary Reference Intake" (formerly "Recommended Daily Allowances" or RDA) listings for more information.


Store at room temperature away from moisture and heat.

What happens if I miss a dose?


Skip the missed dose if it is almost time for your next scheduled dose. Do not use extra medicine to make up the missed dose.


What happens if I overdose?


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

Overdose symptoms may include unusual bleeding or bruising.


What should I avoid while taking Aquavite-E (vitamin E)?


Avoid taking other vitamins, mineral supplements, or nutritional products without your doctor's advice.


Aquavite-E (vitamin E) side effects


Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficult breathing; swelling of your face, lips, tongue, or throat. Stop taking vitamin E and call your doctor at once if you have a serious side effect such as:

  • feeling like you might pass out;




  • easy bruising; or




  • unusual bleeding (nose, mouth, vagina, or rectum).



Less serious side effects may include:



  • nausea, diarrhea, stomach cramps;




  • tired feeling;




  • headache;




  • blurred vision; or




  • mild rash.



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


What other drugs will affect Aquavite-E (vitamin E)?


Do not take vitamin E without a doctor's advice if you are using any type of medication to treat or prevent blood clots, such as:

  • heparin, warfarin (Coumadin);




  • alteplase (Activase), tenecteplase (TNKase), urokinase (Abbokinase);




  • argatroban (Acova), bivalirudin (Angiomax), lepirudin (Refludan);




  • dalteparin (Fragmin), enoxaparin (Lovenox), fondaparinux (Arixtra); or




  • abciximab (ReoPro), anagrelide (Agrylin), cilostazol (Pletal), clopidogrel (Plavix), dipyridamole (Persantine, Aggrenox), eptifibatide (Integrelin), prasugrel (Effient), ticlopidine (Ticlid), tirofiban (Aggrastat).



The following drugs can interact with or be made less effective by vitamin E. Tell your doctor if you are using any of these:



  • cyclosporine (Gengraf, Neoral, Sandimmune);




  • diazepam (Valium) and other sedatives;




  • fluoxetine (Prozac) and other antidepressants;




  • mineral oil, orlistat (alli, Xenical);




  • an antibiotic such as clarithromycin (Biaxin), doxycycline (Doryx, Vibramycin), trimethoprim (Bactrim, Septra, SMX-TMP), and others;




  • antifungal medication such as itraconazole (Sporanox) or ketoconazole (Extina, Ketozole, Nizoral, Xolegal);




  • cholesterol-lowering medicines such as atorvastatin (Lipitor), cholestyramine (Questran), colestipol (Colestid), simvastatin (Zocor, Simcor), lovastatin (Mevacor, Advicor), pravastatin (Pravachol), niacin (Niaspan, Slo-Niacin), and others;




  • heart or blood pressure medications such as diltiazem (Cartia, Cardizem), losartan (Cozaar), propranolol (Inderal), verapamil (Calan, Covera, Isoptin), and others;




  • HIV medicines such as fosamprenavir (Lexiva), ritonavir (Norvir, Kaletra), and others;




  • narcotic medication such as fentanyl (Actiq, Duragesic, Fentora);




  • seizure medication such as carbamazepine (Carbatrol, Tegretol), phenobarbital (Solfoton), phenytoin (Dilantin), and others; or




  • stomach acid reducers such as cimetidine (Tagamet), omeprazole (Prilosec), lansoprazole (Prevacid), and others.



This list is not complete and there are many other drugs that can interact with vitamin E. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor. Keep a list of all your medicines and show it to any healthcare provider who treats you.



More Aquavite-E resources


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


  • Aquasol E Advanced Consumer (Micromedex) - Includes Dosage Information

  • Aquasol E Monograph (AHFS DI)

  • Vitamin E Natural MedFacts for Professionals (Wolters Kluwer)

  • Vitamin E Natural MedFacts for Consumers (Wolters Kluwer)



Compare Aquavite-E with other medications


  • Alzheimer's Disease
  • Anemia, Sickle Cell
  • Cystic Fibrosis
  • Dietary Supplementation
  • Nocturnal Leg Cramps
  • Retinopathy Prophylaxis
  • Tardive Dyskinesia
  • Vitamin E Deficiency


Where can I get more information?


  • Your pharmacist can provide more information about vitamin E.

See also: Aquavite-E side effects (in more detail)



Wednesday, October 26, 2016

Aminofen


Generic Name: acetaminophen (Oral route, Rectal route)

a-seet-a-MIN-oh-fen

Commonly used brand name(s)

In the U.S.


  • Actamin Maximum Strength

  • Altenol

  • Aminofen

  • Anacin Aspirin Free

  • Apra

  • Cetafen

  • Children's Nortemp

  • Comtrex Sore Throat Relief

  • Dolono

  • Feverall

  • Genapap

  • Tylenol

In Canada


  • Abenol

  • Acetaminophen

  • Actimol Children's

  • Actimol Infant

  • Atasol

  • Children's Acetaminophen

  • Children's Acetaminophen Bubble Gum Flavor

  • Children's Acetaminophen Cherry Flavor

  • Children's Acetaminophen Grape Flavor

  • Children's Acetaminophen Suspension Bubble Gum Flavor - Ages 2 To 11

  • Children's Acetaminophen Suspension Cherry Flavor

  • Children's Acetaminophen Suspension Grape Flavor - Ages 2 To 11

Available Dosage Forms:


  • Solution

  • Tablet, Disintegrating

  • Suppository

  • Powder

  • Syrup

  • Tablet

  • Tablet, Chewable

  • Capsule

  • Powder for Solution

  • Suspension

  • Elixir

  • Tablet, Extended Release

  • Capsule, Liquid Filled

  • Liquid

  • Tablet, Effervescent

Therapeutic Class: Analgesic


Uses For Aminofen


Acetaminophen is used to relieve minor aches and pain and reduce fever. Unlike aspirin, it does not relieve the redness, stiffness, or swelling caused by rheumatoid arthritis. However, it may relieve the pain caused by mild forms of arthritis.


This medicine is available without a prescription.


Before Using Aminofen


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


Appropriate studies performed to date have not demonstrated pediatric-specific problems that would limit the usefulness of acetaminophen in children. However, do not administer the over-the-counter products to children under 2 years old unless your doctor has instructed you to do so.


Geriatric


Appropriate studies performed to date have not demonstrated geriatric-specific problems that would limit the usefulness of acetaminophen in the elderly.


Pregnancy








Pregnancy CategoryExplanation
All TrimestersCAnimal studies have shown an adverse effect and there are no adequate studies in pregnant women OR no animal studies have been conducted and there are no adequate studies in pregnant women.

Breast Feeding


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


Interactions with Medicines


Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. When you are 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 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.


  • Acenocoumarol

  • Carbamazepine

  • Isoniazid

  • Phenytoin

  • Warfarin

  • Zidovudine

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 is usually not recommended, 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.


  • Ethanol

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.


  • Cabbage

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:


  • Alcohol abuse, or history of or

  • Kidney disease, severe or

  • Liver disease (including hepatitis)—The chance of serious side effects may be increased.

  • Phenylketonuria (PKU)—Some brands of acetaminophen contain aspartame, which can make your condition worse.

Proper Use of acetaminophen

This section provides information on the proper use of a number of products that contain acetaminophen. It may not be specific to Aminofen. 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. If too much of this medicine is taken for a long time, it may cause an overdosage. Liver damage can occur if large amounts of acetaminophen are taken for a long time.


Carefully check the labels of all other medicines you are using, because they may also contain acetaminophen. It is not safe to use more than 4 grams (4,000 milligrams) of acetaminophen in one day (24 hours).


You may take this medicine with or without food.


If you are taking this medicine without the advice of your doctor, carefully read and follow the drug facts label and dosing instructions on the medicine package. This is to avoid confusion and dosing errors. Ask your doctor if you have any questions.


For patients using the oral liquid with syringe (e.g. Little Fevers®):


  • Shake the bottle well before each use.

  • Measure the dose with the provided dose syringe (e.g., AccuSafe™) that comes with the package. Do not use any other syringe, dropper, spoon, or dosing device when giving this medicine to your child.

  • Remove the cap, attach the syringe to the flow restrictor, and invert the bottle.

  • Pull back the syringe until filled with the dose prescribed by your doctor.

  • Slowly give the medicine into your child's mouth (towards the inner cheek).

  • Replace the cap back tightly.

For patients using the oral liquid with dropper:


  • Shake the bottle well before each use.

  • Measure the dose with the provided dropper. Do not use any other syringe, dropper, spoon, or dosing device when giving this medicine to your child.

  • Remove the cap, insert the dropper and withdraw the dose prescribed by your doctor.

  • Slowly give the medicine into your child's mouth (towards the inner cheek).

  • Replace the cap back tightly.

For patients using acetaminophen oral granules (e.g., Snaplets-FR):


  • Just before the medicine is to be taken, open the number of packets needed for one dose.

  • Mix the granules inside of the packets with a small amount of soft food, such as applesauce, ice cream, or jam.

  • Eat the acetaminophen granules along with the food.

For patients using acetaminophen oral powders (e.g., Feverall® Sprinkle Caps [Children's or Junior Strength]):


  • These capsules are not intended to be swallowed whole. Instead, just before the medicine is to be taken, open the number of capsules needed for one dose.

  • Empty the powder from each capsule into 1 teaspoonful (5 mL) of water or other liquid.

  • Drink the medicine along with the liquid. You may drink more liquid after taking the medicine.

  • You may also mix the powder with a small amount of soft food, such as applesauce, ice cream, or jam. Eat the acetaminophen powder along with the food.

For patients using acetaminophen suppositories:


  • If the suppository is too soft to insert, chill it in the refrigerator for 30 minutes or run cold water over it before removing the foil wrapper.

  • To insert the suppository:
    • First remove the foil wrapper and moisten the suppository with cold water.

    • Lie down on your side and use your finger to push the suppository well up into the rectum.


Use only the brand of this medicine that your doctor prescribed. Different brands may not work the same way.


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 pain or fever:
    • For oral dosage forms (capsules, granules, powders, solution, suspension, or tablets) and rectal dosage forms (suppositories):
      • Adults and teenagers—325 or 500 milligrams (mg) every 3 or 4 hours, 650 mg every 4 to 6 hours, or 1000 mg every 6 hours as needed. The total dose should not be more than 4000 mg (for example, eight 500–mg tablets) a day.

      • Children—Dose is based on the child's age, do not administer the over-the-counter products to children under the age of 2 unless directed to do so by your doctor:
        • Children 11 to 12 years of age: 320 to 480 mg every 4 hours as needed.

        • Children 9 to 11 years of age: 320 to 400 mg every 4 hours as needed.

        • Children 6 to 9 years of age: 320 mg every 4 hours as needed.

        • Children 4 to 6 years of age: 240 mg every 4 hours as needed.

        • Children 2 to 4 years of age: 160 mg every 4 hours as needed.

        • Children 1 to 2 years of age: 120 mg every 4 hours as needed.

        • Infants 4 to 12 months of age: 80 mg every 4 hours as needed.

        • Infants up to 3 months of age: 40 mg every 4 hours as needed.




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 the bottle closed when you are not using it. Store it at room temperature, away from light and heat. Do not freeze.


You may store the suppositories in the refrigerator, but do not freeze them.


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 Aminofen


It is very important that your doctor check the progress of you or your child while you are using this medicine. This will allow your doctor to see if the medicine is working properly and to decide if you or your child should continue to take it.


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


Stop using this medicine and check with your doctor or dentist right away:


  • If you are taking this medicine to relieve pain, including arthritis pain, and the pain lasts for more than 10 days for adults or 5 days for children or if the pain gets worse, new symptoms occur, or the painful area is red or swollen. These could be signs of a serious condition that needs medical or dental treatment.

  • If you are taking this medicine to bring down a fever, and the fever lasts for more than 3 days or returns, the fever gets worse, new symptoms occur, or redness or swelling is present. These could be signs of a serious condition that needs treatment.

  • If you are taking this medicine for a sore throat, and the sore throat is very painful, lasts for more than 2 days, or occurs together with or is followed by fever, headache, skin rash, nausea, or vomiting.

Many combination medicines contain acetaminophen, including products with brand names such as Alka-Seltzer Plus®, Comtrex®, Drixoral®, Excedrin Migraine®, Midol®, Sinutab®, Sudafed®, Theraflu®, and Vanquish®. Adding these medicines to the medicine that you are already taking may cause you to get more than a safe amount of acetaminophen. Talk to your doctor before taking more than one medicine that contains acetaminophen.


Check with your doctor right away if you or your child have pain or tenderness in the upper stomach; pale stools; dark urine; loss of appetite; nausea; unusual tiredness or weakness; or yellow eyes or skin. These could be symptoms of a serious liver problem.


If you will be taking more than an occasional 1 or 2 doses of acetaminophen, do not drink alcoholic beverages. To do so may increase the chance of liver damage, especially if you drink large amounts of alcoholic beverages regularly, if you take more acetaminophen than is recommended on the package label, or if you take it regularly for a long time.


Taking certain other medicines together with acetaminophen may increase the chance of unwanted effects. The risk will depend on how much of each medicine you take every day, and on how long you take the medicines together. If your doctor or dentist directs you to take these medicines together on a regular basis, follow his or her directions carefully. However, do not take any of the following medicines together with acetaminophen for more than a few days unless your doctor has directed you to do so and is following your progress:


  • Aspirin or other salicylates

  • Diclofenac (e.g., Voltaren®)

  • Diflunisal (e.g., Dolobid®)

  • Etodolac (e.g., Lodine®)

  • Fenoprofen (e.g., Nalfon®)

  • Floctafenine (e.g., Idarac®)

  • Flurbiprofen, oral (e.g., Ansaid®)

  • Ibuprofen (e.g., Motrin®)

  • Indomethacin (e.g., Indocin®)

  • Ketoprofen (e.g., Orudis®)

  • Ketorolac (e.g., Toradol®)

  • Meclofenamate (e.g., Meclomen®)

  • Mefenamic acid (e.g., Ponstel®)

  • Nabumetone (e.g., Relafen®)

  • Naproxen (e.g., Naprosyn®)

  • Oxaprozin (e.g., Daypro®)

  • Phenylbutazone (e.g., Butazolidin®)

  • Piroxicam (e.g., Feldene®)

  • Sulindac (e.g., Clinoril®)

  • Tenoxicam (e.g., Apo-Tenoxicam®)

  • Tiaprofenic acid (e.g., Surgam®)

  • Tolmetin (e.g., Tolectin®).

Acetaminophen may interfere with the results of some medical tests. Before you have any medical tests, tell the person in charge if you have taken acetaminophen within the past 3 or 4 days. If possible, it is best to call the laboratory where the test will be done about 4 days ahead of time, to find out whether this medicine may be taken during the 3 or 4 days before the test.


For diabetic patients:


  • Acetaminophen may cause false results with some blood glucose (sugar) tests. If you notice any change in your test results, or if you have any questions about this possible problem, check with your doctor. This is especially important if your diabetes is not well-controlled.

For patients taking one of the products that contain caffeine in addition to acetaminophen:


  • Caffeine may interfere with the results of a test that uses adenosine (e.g., Adenocard®) or dipyridamole (e.g., Persantine®) to help find out how well your blood is flowing through certain blood vessels. Therefore, you should not have any caffeine for 8 to 12 hours before the test.

If you think that you or anyone else may have taken an overdose of acetaminophen, get emergency help at once, even if there are no signs of poisoning. Signs of severe poisoning may not appear for 2 to 4 days after the overdose is taken, but treatment to prevent liver damage or death must be started as soon as possible. Treatment started more than 24 hours after the overdose is taken may not be effective.


Aminofen 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:


Rare
  • Bloody or black, tarry stools

  • bloody or cloudy urine

  • fever with or without chills (not present before treatment and not caused by the condition being treated)

  • pain in the lower back and/or side (severe and/or sharp)

  • pinpoint red spots on the skin

  • skin rash, hives, or itching

  • sore throat (not present before treatment and not caused by the condition being treated)

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

  • sudden decrease in the amount of urine

  • unusual bleeding or bruising

  • unusual tiredness or weakness

  • yellow eyes or skin

Get emergency help immediately if any of the following symptoms of overdose occur:


Symptoms of overdose
  • Diarrhea

  • increased sweating

  • loss of appetite

  • nausea or vomiting

  • stomach cramps or pain

  • swelling, pain, or tenderness in the upper abdomen or stomach area

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: Aminofen 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 Aminofen resources


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


Compare Aminofen with other medications


  • Fever
  • Muscle Pain
  • Pain
  • Sciatica


Acular LS


Generic Name: ketorolac ophthalmic (KEE toe ROLE ak)

Brand Names: Acular, Acular LS, Acular PF, Acuvail


What is Acular LS (ketorolac ophthalmic)?

Ketorolac is in a group of drugs called nonsteroidal anti-inflammatory drugs (NSAIDs). Ketorolac works by reducing hormones that cause inflammation and pain in the body.


Ketorolac ophthalmic (for the eye) is used to relieve eye itching caused by seasonal allergies.

Ketorolac ophthalmic is also used to reduce swelling, pain, and burning or stinging after cataract surgery or corneal refractive surgery.


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


What is the most important information I should know about Acular LS (ketorolac ophthalmic)?


You should not use this medication if you are allergic to ketorolac or other NSAIDs (nonsteroidal anti-inflammatory drugs).

Before using ketorolac ophthalmic, tell your doctor if you are allergic to any medications, or if you have a bleeding or blood-clotting disorder, diabetes, arthritis, glaucoma, dry eye syndrome, or if you have had other recent eye surgeries.


Tell your doctor about all other medications you use, especially a blood thinner such as warfarin (Coumadin).


Use this medication exactly as prescribed by your doctor. Do not use it in larger amounts or for longer than recommended. Follow the directions on your prescription label. Using the medication for longer than prescribed may increase the risk of serious side effects on your eyes.


While you are using this medication, do not wear any contact lens that has not been approved by your doctor. Do not use any other eye medications unless your doctor has prescribed them.

What should I discuss with my healthcare provider before I use Acular LS (ketorolac ophthalmic)?


You should not use this medication if you are allergic to ketorolac or other NSAIDs.

If you have any of these other conditions, you may need a dose adjustment or special tests to safely use this medication:



  • a bleeding or blood-clotting disorder;




  • diabetes;




  • arthritis;




  • glaucoma;




  • dry eye syndrome; or




  • if you have had other recent eye surgeries.




FDA pregnancy category C. It is not known whether ketorolac ophthalmic is harmful to an unborn baby. Before taking this medication, tell your doctor if you are pregnant or plan to become pregnant during treatment. It is not known whether ketorolac ophthalmic passes into breast milk or if it could harm a nursing baby. Do not use ketorolac ophthalmic without telling your doctor if you are breast-feeding a baby.

How should I use Acular LS (ketorolac ophthalmic)?


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


Ketorolac ophthalmic is usually given 24 hours before cataract surgery, and continued for up to 14 days after surgery. Using the medication for longer than prescribed may increase the risk of serious side effects on your eyes.


Wash your hands before using the eye drops.

To apply the eye drops:



  • Tilt your head back slightly and pull down your lower eyelid to create a small pocket. Hold the dropper above the eye with the dropper tip down. Look up and away from the dropper as you squeeze out a drop, then close your eye.




  • Gently press your finger to the inside corner of the eye (near your nose) for about 1 minute to keep the liquid from draining into your tear duct.




  • Use the eye drops only in the eye you are having surgery on.




  • Do not allow the dropper tip to touch any surface, including the eyes or hands. If the dropper becomes contaminated it could cause an infection in your eye, which can lead to vision loss or serious damage to the eye.



Do not use the eye drops if the liquid has changed colors or has particles in it. Call your doctor for a new prescription.


Store the drops at room temperature away from heat and moisture. Keep the bottle tightly closed when not in use.

What happens if I miss a dose?


Use the missed dose as soon as you remember. If it is almost time for your next dose, wait until then to use the medicine and skip the missed dose. Do not use extra medicine to make up the missed dose.


What happens if I overdose?


Seek emergency medical attention if you think you have used too much of this medicine.

An overdose of ketorolac is not likely to cause life-threatening symptoms.


What should I avoid while using Acular LS (ketorolac ophthalmic)?


While using this medication, do not wear any contact lens that has not been approved by your doctor.

Do not use any other eye medications unless your doctor has prescribed them.


Acular LS (ketorolac ophthalmic) side effects


Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Call your doctor at once if you have a serious side effect such as:

  • severe burning, stinging, or itching of your eyes;




  • eye pain, redness, or watering;




  • vision changes, increased sensitivity to light;




  • white patches on your eyes; or




  • crusting or drainage from your eyes.



Less serious side effects may include:



  • mild burning, stinging, or itching of your eyes;




  • swollen or puffy eyelids; or




  • headache.



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


What other drugs will affect Acular LS (ketorolac ophthalmic)?


Tell your doctor about all other medications you use, especially a blood thinner such as warfarin (Coumadin).


This list is not complete and there may be other drugs that can interact with ketorolac ophthalmic. 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 Acular LS resources


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


  • Acular LS Prescribing Information (FDA)

  • Acular LS Drops MedFacts Consumer Leaflet (Wolters Kluwer)

  • Acular LS Advanced Consumer (Micromedex) - Includes Dosage Information

  • Acular Drops MedFacts Consumer Leaflet (Wolters Kluwer)

  • Acular Prescribing Information (FDA)

  • Acular eent Monograph (AHFS DI)

  • Acular PF Prescribing Information (FDA)

  • Acular PF Drops MedFacts Consumer Leaflet (Wolters Kluwer)

  • Acuvail Prescribing Information (FDA)

  • Acuvail Drops MedFacts Consumer Leaflet (Wolters Kluwer)

  • Acuvail Consumer Overview



Compare Acular LS with other medications


  • Corneal Refractive Surgery
  • Postoperative Ocular Inflammation
  • Seasonal Allergic Conjunctivitis


Where can I get more information?


  • Your doctor or pharmacist can provide more information about ketorolac ophthalmic.

See also: Acular LS side effects (in more detail)



Up and Up Childrens All Day Allergy Relief





Dosage Form: liquid
Target Corp. Children's All Day Allergy Relief Drug Facts

Active ingredient (in each 5 mL teaspoonful)


Cetirizine HCl 5 mg



Purpose


Antihistamine



Uses


temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:


  • runny nose

  • sneezing

  • itchy, watery eyes

  • itching of the nose or throat


Warnings



Do not use


if you have ever had an allergic reaction to this product or any of its ingredients or to an antihistamine containing hydroxyzine.



Ask a doctor before use if you have


liver or kidney disease. Your doctor should determine if you need a different dose.



Ask a doctor or pharmacist before use if you are


taking tranquilizers or sedatives.



When using this product


  • drowsiness may occur avoid alcoholic drinks

  • alcohol, sedatives, and tranquilizers may increase drowsiness

  • be careful when driving a motor vehicle or operating machinery


Stop use and ask a doctor if


an allergic reaction to this product occurs. Seek medical help right away.



If pregnant or breast-feeding:


  • if breast-feeding: not recommended

  • if pregnant: ask a health professional before use.


Keep out of reach of children.


In case of overdose, get medical help or contact a Poison Control Center right away.



Directions


  • use only with enclosed dosing cup












adults and children 6 years and over1 teaspoonful (5 mL) or 2 teaspoonfuls (10 mL) once daily depending upon severity of symptoms; do not take more than 2 teaspoonfuls (10 mL) in 24 hours.
adults 65 years and over1 teaspoonful (5 mL) once daily; do not take more than 1 teaspoonful (5 mL) in 24 hours.
children 2 to under 6 years of age1/2 teaspoonful (2.5 mL) once daily. If needed, dose can be increased to a maximum of 1 teaspoonful (5 mL) once daily or 1/2 teaspoonful (2.5 mL) every 12 hours. Do not give more than 1 teaspoonful (5 mL) in 24 hours.
children under 2 years of ageask a doctor
consumers with liver or kidney diseaseask a doctor

Other information


  • do not use if carton is opened, or if printed neckband is broken or missing

  • store between 20° to 25°C (68° to 77°F)


Inactive ingredients


acetic acid, artificial grape flavor, glycerin, methylparaben, natural banana flavor, propylene glycol, propylparaben, sodium acetate, sucrose, water



Questions or comments?


Call 1-800-910-6874



Principal Display Panel


Children's All Day Allergy Relief


Cetirizine Hydrochloride Oral Solution 1 mg/mL


Antihistamine


Compare to active ingredient in Children's Zyrtec®


Original Prescription Strength


Indoor and Outdoor Allergies


24 Hour Relief of:


Sneezing/Runny Nose/Itchy, Watery Eyes/Itchy Throat or Nose


Dosing Cup Included


24 Hour Relief


Grape Flavor


Age 2+ Years


Children's All Day Allergy Relief Carton










Up and Up Childrens All Day Allergy Relief 
cetirizine hydrochloride  liquid










Product Information
Product TypeHUMAN OTC DRUGNDC Product Code (Source)11673-974
Route of AdministrationORALDEA Schedule    








Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CETIRIZINE HYDROCHLORIDE (CETIRIZINE)CETIRIZINE HYDROCHLORIDE5 mg  in 5 mL





Inactive Ingredients
Ingredient NameStrength
No Inactive Ingredients Found


















Product Characteristics
ColorYELLOW (Pale Yellow)Score    
ShapeSize
FlavorGRAPEImprint Code
Contains      














Packaging
#NDCPackage DescriptionMultilevel Packaging
111673-974-261 BOTTLE In 1 CARTONcontains a BOTTLE
1118 mL In 1 BOTTLEThis package is contained within the CARTON (11673-974-26)










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA09025406/12/2009


Labeler - Target Corporation (006961700)
Revised: 05/2009Target Corporation




More Up and Up Childrens All Day Allergy Relief resources


  • Up and Up Childrens All Day Allergy Relief Side Effects (in more detail)
  • Up and Up Childrens All Day Allergy Relief Use in Pregnancy & Breastfeeding
  • Drug Images
  • Up and Up Childrens All Day Allergy Relief Drug Interactions
  • Up and Up Childrens All Day Allergy Relief Support Group
  • 73 Reviews for Up and Up Childrens All Day Allergy Relief - Add your own review/rating


Compare Up and Up Childrens All Day Allergy Relief with other medications


  • Hay Fever
  • Urticaria


Atelvia Delayed-Release Tablets


Pronunciation: RIS-e-DROE-nate
Generic Name: Risedronate
Brand Name: Atelvia


Atelvia Delayed-Release Tablets are used for:

Treating osteoporosis (weak bones) in women who have gone through menopause. It may also be used for other conditions as determined by your doctor.


Atelvia Delayed-Release Tablets are a bisphosphonate. It works by slowing bone loss.


Do NOT use Atelvia Delayed-Release Tablets if:


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

  • you have certain esophagus problems (eg, narrowing, blockage)

  • you are unable to stand or sit upright for at least 30 minutes

  • you are unable to swallow Atelvia Delayed-Release Tablets whole

  • you have low blood calcium levels or severe kidney problems

  • you are taking another medicine that contains risedronate

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



Before using Atelvia Delayed-Release Tablets:


Some medical conditions may interact with Atelvia 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 a history of stomach or bowel problems (eg, inflammation, ulcer), esophagus problems (eg, narrowing, blockage, heartburn, reflux disease, severe irritation), kidney problems, or if you have difficult or painful swallowing

  • if you have low blood vitamin D levels, cancer, anemia, blood clotting problems, an infection, calcium metabolism problems, nutrient absorption problems (eg, malabsorption syndrome), or are unable to take calcium or vitamin D supplements

  • if you have poor dental hygiene or other dental problems, or if you will be having a dental procedure (eg, tooth extraction)

  • if you smoke or drink alcohol

  • if you have had or will be having chemotherapy or radiation treatment

  • if you have a mental disorder or other condition that may decrease your ability to follow the dosing instructions for Atelvia Delayed-Release Tablets

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


  • Aspirin or nonsteroidal anti-inflammatory drugs (NSAIDs) (eg, ibuprofen, naproxen) because the risk of stomach or bowel problems may be increased

  • H2 blockers (eg, ranitidine) or proton pump inhibitors (PPIs) (eg, omeprazole) because they may decrease Atelvia Delayed-Release Tablets's effectiveness

  • Corticosteroids (eg, prednisone) because the risk of jawbone problems may be increased

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


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


  • Atelvia Delayed-Release Tablets comes with an extra patient information sheet called a Medication Guide. Read it carefully. Read it again each time you get Atelvia Delayed-Release Tablets refilled.

  • Take Atelvia Delayed-Release Tablets by mouth in the morning immediately after breakfast. Do NOT take Atelvia Delayed-Release Tablets before breakfast.

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

  • Take Atelvia Delayed-Release Tablets while you are sitting up or standing. Do not lie down or take other medicines for 30 minutes after taking Atelvia Delayed-Release Tablets.

  • Take Atelvia Delayed-Release Tablets with at least 4 oz (120 mL) of plain water. Do not take Atelvia Delayed-Release Tablets with mineral water, coffee, tea, milk, or juice.

  • Do not take antacids, calcium, certain vitamin products, iron, or products that contain magnesium (eg, certain laxatives) at the same time of day that you take Atelvia Delayed-Release Tablets. Ask your pharmacist if you have questions about how to take any of these products with Atelvia Delayed-Release Tablets.

  • If you take H2 blockers (eg, ranitidine) or PPIs (eg, omeprazole), ask your doctor or pharmacist how to take them with Atelvia Delayed-Release Tablets.

  • Atelvia Delayed-Release Tablets are usually taken 1 time each week. Be sure you understand how to take Atelvia Delayed-Release Tablets. Contact your doctor or pharmacist if you have any questions.

  • Continue to take Atelvia Delayed-Release Tablets even if you feel well. Do not miss any doses.

  • If you miss a dose of Atelvia Delayed-Release Tablets, take 1 tablet on the morning after you remember, then go back to taking Atelvia Delayed-Release Tablets on your regularly scheduled day. Do not take 2 doses on the same day.

Ask your health care provider any questions you may have about how to use Atelvia Delayed-Release Tablets.



Important safety information:


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

  • Talk to your doctor before you drink alcohol, smoke, or use other tobacco products while taking Atelvia Delayed-Release Tablets.

  • Follow the diet and exercise program given to you by your health care provider. Talk to your doctor about whether you should take a calcium and vitamin D supplement while you take Atelvia Delayed-Release Tablets.

  • Talk to your doctor about the use of weight-bearing exercises to help prevent weak bones.

  • Certain fractures of the thigh bone (femur) have been reported in patients using bisphosphonates. It is not known if bisphosphonates contributed to the fractures. Contact your doctor right away if you experience hip, thigh, or groin pain. Discuss any questions or concerns with your doctor.

  • Atelvia Delayed-Release Tablets may cause jawbone problems in some patients. Your risk may be greater if you have cancer, poor dental hygiene, ill-fitting dentures, or certain other conditions (eg, anemia, blood clotting problems, infections, dental problems). Your risk may also be greater if you have certain dental procedures or you use certain medicines or therapies (eg, chemotherapy, corticosteroids, radiation). Talk to your doctor about having a dental exam before you start to use Atelvia Delayed-Release Tablets. Ask your doctor any questions you may have about dental treatment while you use Atelvia Delayed-Release Tablets.

  • Proper dental care is important while you are taking Atelvia Delayed-Release Tablets. Brush and floss your teeth and visit the dentist regularly.

  • Certain dental procedures should be avoided if possible while you are taking Atelvia Delayed-Release Tablets. Tell your doctor or dentist that you take Atelvia Delayed-Release Tablets before you receive any medical or dental care, emergency care, or surgery.

  • Atelvia Delayed-Release Tablets may interfere with certain lab tests. Be sure your doctor and lab personnel know you are taking Atelvia Delayed-Release Tablets.

  • Lab tests, including bone density and blood calcium levels, may be performed while you take Atelvia Delayed-Release Tablets. These tests may be used to monitor your condition or check for side effects. Your doctor may also want to evaluate you periodically while you take Atelvia Delayed-Release Tablets to assess the need to continue treatment. Be sure to keep all doctor and lab appointments.

  • Atelvia Delayed-Release Tablets should not be used in CHILDREN; safety and effectiveness in children have not been confirmed. Atelvia Delayed-Release Tablets are not approved for use in children.

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


Possible side effects of Atelvia 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:



Constipation; diarrhea; dizziness; mild flu-like symptoms (eg, fever, headache, muscle aches, tiredness); mild joint, back, or muscle pain; mild stomach pain or upset; 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, throat, or tongue; unusual hoarseness); black, tarry, or bloody stools; chest pain; coughing or vomiting blood; difficult or painful swallowing; mouth sores; new, worsening, or persistent heartburn; severe bone, muscle, or joint pain (especially in the groin, hip, or thigh); severe headache, dizziness, or blurred vision; severe or persistent sore throat or stomach pain; swelling or pain in your jaw; symptoms of low blood calcium (eg, spasms, twitches, or cramps in your muscles; numbness or tingling in your fingers or toes, or around your mouth); unusual eye pain, swelling, redness, or sensitivity to light.



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: Atelvia 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. Do not lie down or try to vomit. Symptoms of overdose may include muscle weakness, spasms, twitching, or cramps; numbness or tingling in the fingers or toes, or around the mouth; seizures; severe heartburn; stomach pain or upset.


Proper storage of Atelvia Delayed-Release Tablets:

Store Atelvia Delayed-Release Tablets at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Atelvia Delayed-Release Tablets out of the reach of children and away from pets.


General information:


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

  • Atelvia 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 Atelvia 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 Atelvia resources


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


Compare Atelvia with other medications


  • Osteoporosis


Tuesday, October 25, 2016

Activase


Pronunciation: AL-teh-PLACE
Generic Name: Alteplase
Brand Name: Activase


Activase is used for:

Treating blood clots in the lungs and improving heart function and survival following a heart attack. Activase may also be used to improve recovery and reduce disability in certain patients who have had a stroke. It may also be used for other conditions as determined by your doctor.


Activase is a tissue plasminogen activator (tPA). It works by helping to break down unwanted blood clots.


Do NOT use Activase if:


  • you are allergic to any ingredient in Activase

  • you have active internal bleeding, history of stroke, recent brain or spinal surgery (within 3 months), a growth in the brain, abnormal formation of blood vessels, or a certain type of bulging blood vessel (aneurysm)

  • you have a heart attack or blood clot in the lung and you also have had recent brain or spinal injury, a history of bleeding problems, or severe uncontrolled high blood pressure

  • you have a stroke and you also have known or suspected bleeding in the head or brain, a history of bleeding in the brain, a recent serious head injury, uncontrolled high blood pressure, low platelet count, high international normalized ratio (INR) or prothrombin time (PT), or a history of bleeding problems, or if you had a seizure at the onset of the stroke

  • you have a stroke and you are taking warfarin, or you have used heparin within the past 48 hours and you currently have a high activated partial thromboplastin time (aPTT)

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



Before using Activase:


Tell your health care provider 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 had recent major surgery or have recently undergone childbirth

  • if you have a disease of the blood vessels in your brain; recent bleeding of the stomach, bowel, genitals, or urinary tract; a recent injury; high blood pressure; inflammation around the heart; inflammation inside the heart due to an infection; blood problems (including blood clotting problems); moderate to severe liver disease; severe kidney disease; bleeding in the eye due to diabetes or other problems; a serious infection; or blood vessel inflammation

  • if you have an increased risk of a blood clot in your heart

  • if you are older than 75 years of age

Some MEDICINES MAY INTERACT with Activase. Tell your health care provider if you are taking any of the following medicines.


  • Abciximab, anticoagulants (eg, warfarin, heparin), aspirin, or dipyridamole because the risk of serious side effects, such as bleeding, may be increased

  • Angiotensin-converting enzyme (ACE) inhibitors (eg, lisinopril) because the risk of serious side effects, such as severe swelling or trouble breathing, may be increased

  • Nitrates (eg, nitroglycerin, isosorbide dinitrate) because the effectiveness of Activase may be decreased

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


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


  • Activase is usually administered as an injection at your doctor's office, hospital, or clinic. If you are using Activase at home, carefully follow the injection procedures taught to you by your health care provider.

  • If Activase contains particles or is discolored, or if the vial is cracked or damaged in any way, do not use it.

  • Mix Activase by swirling gently. Do not shake.

  • Throw away any unused medicine left in the vial.

  • Do not reuse needles, syringes, or other materials. Dispose of properly after use. Ask your doctor or pharmacist to explain local regulations for selecting an appropriate container and properly disposing of the container when full.

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

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



Important safety information:


  • Do not drive, operate machinery, or do anything else that could be dangerous until you know how you react to Activase. Using Activase alone, with certain other medicines, or with alcohol may lessen your ability to drive or to perform other potentially dangerous tasks.

  • Activase may reduce the number of cells in your blood that help your blood clot (platelets). To prevent bleeding, avoid situations in which bruising or injury may occur. Report any unusual bleeding, bruising, blood in stools, or dark, tarry stools to your doctor.

  • If serious bleeding occurs while you are using Activase, contact your doctor immediately.

  • LAB TESTS, including electrocardiogram (ECG), blood coagulation, and blood pressure, may be performed to monitor your progress or to check for side effects. Be sure to keep all doctor and lab appointments.

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

  • Use Activase with extreme caution in CHILDREN. Safety and effectiveness in this age group have not been confirmed.

  • PREGNANCY AND BREAST-FEEDING: If you plan on becoming pregnant, discuss with your doctor the benefits and risks of using this product during pregnancy. It is unknown if Activase is excreted in breast milk. If you are or will be breast-feeding while you are using Activase, check with your doctor or pharmacist to discuss the risks to your baby.


Possible side effects of Activase:


All medicines may cause side effects, but many people have no, or minor, side effects. When used in small doses, no COMMON side effects have been reported with this product. Seek medical attention right away if any of these SEVERE side effects occur:



Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); black or bloody stools; bloody vomit; change in color of your fingers or toes; changes in vision; chills; coughing up blood; decreased amount of urine produced; difficulty breathing or sudden shortness of breath; difficulty swallowing; fast, slow, or irregular heartbeat; fever; hoarseness; numbness in arm or leg; one-sided weakness; pain, redness, or swelling at the injection site; purple skin color; rectal bleeding; seizures; severe bleeding; severe muscle aches or pain; severe stomach pain; sharp or crushing chest pain; speech problems or changes; sudden arm or leg pain; sudden dizziness, fainting, severe headache, or vomiting; unusual or easy bleeding or bruising.



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: Activase 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 severe bleeding.


Proper storage of Activase:

Store Activase at room temperature, below 86 degrees F (30 degrees C), or under refrigeration, between 36 and 46 degrees F (2 and 8 degrees C). Store away from heat, moisture, and light. Keep Activase, as well as syringes and needles, out of the reach of children and away from pets.


General information:


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

  • Activase 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 Activase. 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 Activase resources


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


  • Activase Advanced Consumer (Micromedex) - Includes Dosage Information

  • Alteplase Monograph (AHFS DI)



Compare Activase with other medications


  • Heart Attack
  • Ischemic Stroke
  • Pulmonary Embolism
  • Thrombotic/Thromboembolic Disorder


Anesthetic, local Rectal


Class Name: anesthetic, local (Rectal route)


Commonly used brand name(s)

In the U.S.


  • AnaMantle HC

  • Proctofoam-NS

In Canada


  • Tronothane

Available Dosage Forms:


  • Suppository

  • Foam

Uses For This Medicine


Rectal anesthetics are used to relieve the pain and itching of hemorrhoids (piles) and other problems in the rectal area. However, if you have hemorrhoids that bleed, especially after a bowel movement, check with your doctor before using this medicine. Bleeding may mean that you have a condition that needs other treatment.


These medicines are available without a prescription; however, your doctor may have special instructions on the proper use and dose for your medical problem.


Before Using This Medicine


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


Children may be especially sensitive to the effects of local anesthetics. This may increase the chance of side effects during treatment.


Geriatric


Elderly people are especially sensitive to the effects of local anesthetics. This may increase the chance of side effects during treatment.


Pregnancy


Rectal anesthetics have not been reported to cause birth defects or other problems in humans.


Breast Feeding


Rectal anesthetics have not been reported to cause problems in nursing babies.


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


  • Infection at or near place of treatment or

  • Large sores, broken skin, or severe injury at or near place of treatment—The chance of unwanted effects may be increased.

Proper Use of This Medicine


For safe and effective use of this medicine:


  • Rectal anesthetics usually come with patient directions. Read them carefully before using the medicine, even if it was prescribed by your doctor. Check with your pharmacist if you have any questions about how to use the product.

  • Follow your doctor's instructions if this medicine was prescribed.

  • Follow the manufacturer's package directions if you are treating yourself.

  • Do not use more of this medicine, do not use it more often, and do not use it for a longer time than directed. To do so may increase the chance of absorption into the body and the chance of unwanted effects.

This medicine should be used only for conditions being treated by your doctor or for problems listed on the package label. Do not use it for other problems without first checking with your doctor. This medicine should not be used if certain kinds of infections are present.


For applying a rectal anesthetic to the area around the rectum:


  • First, clean the area, using mild soap and water or a cleansing wipe. Rinse the area carefully and dry it gently with a soft towel or toilet paper.

  • Apply a small amount of medicine to the sore area, using a piece of gauze, a tissue, or a "finger cot."

For inserting a rectal cream or ointment inside the rectum:


  • Use only products that come packaged in pre-filled applicators or that come packaged with a special inserter called a rectal tube.

  • If you are using a product that has an inserter (rectal tube) packaged separately from the tube of cream or ointment:
    • Remove the cap from the tube of cream or ointment. Attach the inserter to the top of the tube. Squeeze the tube until a little cream or ointment comes out on the inserter. Then spread the cream or ointment over the inserter.

    • Place the inserter into your rectum and squeeze the tube until a small amount of medicine comes out. Then remove the inserter from your body.

    • Remove the inserter from the tube and replace the cap. Then wash the applicator carefully.


  • If you are using the product that comes in pre-filled applicators:
    • Follow the manufacturer's directions for using the applicator and inserting the medicine. Each applicator is meant to be used only once. Throw the applicator away after using it.


For inserting the rectal aerosol foam (e.g., Proctofoam/nonsteroid) into the rectum:


  • Do not insert the container itself into your rectum. Use the applicator provided.

  • To fill the container—First, shake the container hard for several seconds. Then, holding the container upright, insert it into the applicator. Press the cap of the container until the foam reaches the fill line of the applicator. Remove the applicator from the container.

  • To use the medicine—Place a small amount of foam on the tip of the applicator. Insert the applicator into your rectum, then push the plunger as far as possible. Remove the applicator. Then take it apart and wash it carefully.

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 benzocaine

  • For pain and itching of hemorrhoids or other problems in the rectal area:
    • For rectal ointment dosage form:
      • Adults—Apply a small amount of ointment to the area around the rectum up to six times a day.

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



  • For dibucaine

  • For pain and itching of hemorrhoids or other problems in the rectal area:
    • For rectal ointment dosage form:
      • Adults—Insert a small amount of ointment into the rectum three or four times a day, in the morning, in the evening, and after bowel movements. Or, apply a small amount of ointment to the area around the rectum three or four times a day.

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



  • For pramoxine

  • For pain and itching of hemorrhoids or other problems in the rectal area:
    • For rectal cream dosage form:
      • Adults—Apply a small amount to the area around the rectum up to five times a day, in the morning, in the evening, and after bowel movements.

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


    • For rectal ointment dosage form:
      • Adults—Insert a small amount of ointment into the rectum up to five times a day, in the morning, in the evening, and after bowel movements. Or, apply a small amount to the area around the rectum up to five times a day, in the morning, in the evening, and after bowel movements.


    • For the rectal aerosol foam dosage form:
      • Adults—Insert 1 applicatorful into the rectum two or three times a day. Or, apply a small amount to the area around the rectum two or three times a day.

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



  • For tetracaine and for tetracaine and menthol

  • For pain and itching of hemorrhoids or other problems in the rectal area:
    • For the rectal cream or rectal ointment dosage form:
      • Adults—Insert a small amount into the rectum up to six times a day. Or, apply a small amount to the area around the rectum up to six times a day.

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



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


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.


Store the canister at room temperature, away from heat and direct light. Do not freeze. Do not keep this medicine inside a car where it could be exposed to extreme heat or cold. Do not poke holes in the canister or throw it into a fire, even if the canister is empty.


Do not keep outdated medicine or medicine no longer needed.


Precautions While Using This Medicine


Check with your doctor:


  • If your condition does not improve after you have been using this medicine regularly for 7 days, or if it becomes worse.

  • If any bleeding from the rectum occurs.

  • If you notice any rash, redness, or irritation that was not present before you started using this medicine.

False test results may occur if benzocaine or tetracaine is present in your body when a certain laboratory test is done. This test uses a medicine called bentiromide (e.g., Chymex) to show how well your pancreas is working. You should not use any products containing benzocaine or tetracaine for about 72 hours (3 days) before this test is done.


Side Effects of This Medicine


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


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


Signs and symptoms of too much medicine being absorbed by the body
  • Blurred or double vision

  • confusion

  • convulsions (seizures)

  • dizziness or lightheadedness

  • drowsiness

  • feeling hot, cold, or numb

  • increased sweating

  • ringing or buzzing in ears

  • shivering or trembling

  • slow or irregular heartbeat

  • unusual anxiety, excitement, nervousness, or restlessness

  • unusual paleness

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


Less common
  • Burning, stinging, swelling, or tenderness not present before treatment

  • skin rash, redness, itching, or hives at or near place of application

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.



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