Tuesday, July 3, 2012

Tums


Generic Name: calcium carbonate (KAL see um KAR boe nate)

Brand Names: Alka-Mints, Cal-Gest, Calcarb, Calci Mix, Calci-Chew, Calci-Mix, Calcium Concentrate, Calcium Liquid Softgel, Calcium Oyster Shell, Caltrate, Chooz, Extra Strength Mylanta Calci Tabs, Icar Prenatal Chewable Calcium, Maalox Antacid Barrier, Maalox Childrens', Maalox Quick Dissolve, Maalox Quick Dissolve Maximum Strength, Maalox Regular Strength, Mylanta Child, Nephro Calci, Os-Cal 500, Oysco 500, Oyst Cal 500, Oyster Cal, Oyster Calcium, Oyster Shell, Pepto Children's, Rolaids Sodium Free, Rolaids Soft Chew, Titralac, Tums, Tums 500, Tums E-X, Tums Kids, Tums QuikPak, Tums Ultra


What is Tums (calcium carbonate)?

Calcium is a mineral that is found naturally in foods. Calcium is necessary for many normal functions of the body, especially bone formation and maintenance. Calcium can also bind to other minerals (such as phosphate) and aid in their removal from the body.


Calcium carbonate is used to prevent and to treat calcium deficiencies.


Calcium carbonate may also be used for purposes not listed in this medication guide.


What is the most important information I should know about Tums (calcium carbonate)?


Do not take calcium carbonate or antacids that contain calcium without first asking your doctor if you also take other medicines. Calcium can make it harder for your body to absorb certain medicines. Calcium carbonate works best if you take it with food.

What should I discuss with my healthcare provider before taking Tums (calcium carbonate)?


To make sure you can safely take calcium carbonate, tell your doctor if you have any of these other conditions:



  • a history of kidney stones; or




  • a parathyroid gland disorder.




Talk to your doctor before taking calcium carbonate if you are pregnant. Talk to your doctor before taking calcium carbonate if you are breast-feeding a baby.

How should I take Tums (calcium carbonate)?


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


Calcium carbonate works best if you take it with food. Swallow the calcium carbonate tablet or capsule with a full glass of water.

The chewable tablet should be chewed before you swallow it.


Use the calcium carbonate powder as directed. Allow the powder to dissolve completely, then consume the mixture.


Shake the oral suspension (liquid) well just before you measure a dose. Measure the liquid 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. Store at room temperature away from moisture and heat.

What happens if I miss a dose?


Take the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not take 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 nausea, vomiting, decreased appetite, constipation, confusion, delirium, stupor, and coma.


What should I avoid while taking Tums (calcium carbonate)?


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


Tums (calcium carbonate) 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.

Less serious side effects may include:



  • nausea or vomiting;




  • decreased appetite;




  • constipation;




  • dry mouth or increased thirst; or




  • urinating more than usual.



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 can affect Tums (calcium carbonate)?


Calcium carbonate can make it harder for your body to absorb other medications you take by mouth. Tell your doctor if you are taking:



  • digoxin (Lanoxin, Lanoxicaps);




  • antacids or other calcium supplements;




  • calcitriol (Rocaltrol) or vitamin D supplements; or




  • doxycycline (Adoxa, Doryx, Oracea, Vibramycin), minocycline (Dynacin, Minocin, Solodyn, Vectrin), or tetracycline (Brodspec, Panmycin, Sumycin, Tetracap).



This list is not complete and other drugs may interact with calcium carbonate. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor.



More Tums resources


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


  • Tums Chewable Tablets MedFacts Consumer Leaflet (Wolters Kluwer)

  • Calcium Carbonate MedFacts Consumer Leaflet (Wolters Kluwer)

  • Titralac Consumer Overview

  • Titralac MedFacts Consumer Leaflet (Wolters Kluwer)



Compare Tums with other medications


  • Duodenal Ulcer
  • Erosive Esophagitis
  • GERD
  • Indigestion
  • Stomach Ulcer


Where can I get more information?


  • Your doctor or pharmacist can provide more information about calcium carbonate.

See also: Tums side effects (in more detail)



Topcare Complete Acid Reducer plus Antacid





Dosage Form: tablet, chewable
Topco Complete Acid Reducer plus Antacid Drug Facts

Active ingredient (in each chewable tablet)


Famotidine 10 mg


Calcium carbonate 800 mg


Magnesium hydroxide 165 mg



Purpose


Acid reducer


Antacid



Uses


relieves heartburn associated with acid indigestion and sour stomach



Warnings


Allergy alert: Do not use if you are allergic to famotidine or other acid reducers



Do not use


  • if you have trouble or pain swallowing food, vomiting with blood, or bloody or black stools. These may be signs of a serious condition. See your doctor.

  • with other acid reducers


Ask a doctor before use if you have


  • had heartburn over 3 months. This may be a sign of a more serious condition.

  • heartburn with lightheadedness, sweating, or dizziness

  • chest pain or shoulder pain with shortness of breath; sweating; pain spreading to arms, neck or shoulders; or lightheadedness

  • frequent chest pain

  • frequent wheezing, particularly with heartburn

  • unexplained weight loss

  • nausea or vomiting

  • stomach pain


Ask a doctor or pharmacist before use if you are


presently taking a prescription drug. Antacids may interact with certain prescription drugs.



Stop use and ask a doctor if


  • your heartburn continues or worsens

  • you need to take this product for more than 14 days


If pregnant or breast-feeding,


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


  • adults and children 12 years and over:

  • do not swallow tablet whole: chew completely

  • to relieve symptoms, chew 1 tablet before swallowing

  • do not use more than 2 chewable tablets in 24 hours

  • children under 12 years: ask a doctor


Other information


  • each tablet contains: calcium 320 mg; magnesium 65 mg

  • Phenylketonurics: Contains Phenylalanine 2.2 mg per tablet

  • read the directions and warnings before use

  • read the bottle label. It contains important information.

  • store at 20°-25°C (68°-77°F)

  • protect from moisture


Inactive ingredients


aspartame, D&C red no. 7 calcium, dextrates, FD&C blue no. 1 lake, FD&C red no. 40 lake, flavor, glyceryl monostearate, lactose anhydrous, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyacrylate dispersion, polysorbate 80, povidone, pregelatinized starch, sodium starch glycolate, talc



Questions or comments?


1-888-423-0139



Principal Display Panel


Dual Action


Complete


Famotidine 10 mg/Calcium Carbonate 800 mg/Magnesium Hydroxide 165 mg Tablets


Acid Reducer plus Antacid


Just One Tablet


Relieves Heartburn Due to Acid Indigestion


Berry Flavor


Actual Size


Compare to Pepcid® Complete active ingredients


Complete Acid Reducer plus Antacid Label










TOPCARE COMPLETE 
famotidine, calcium carbonate and magnesium hydroxide  tablet, chewable










Product Information
Product TypeHUMAN OTC DRUGNDC Product Code (Source)36800-321
Route of AdministrationORALDEA Schedule    














Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
FAMOTIDINE (FAMOTIDINE)FAMOTIDINE10 mg
MAGNESIUM HYDROXIDE (MAGNESIUM HYDROXIDE)MAGNESIUM HYDROXIDE165 mg
CALCIUM CARBONATE (CARBONATE ION)CALCIUM CARBONATE800 mg





Inactive Ingredients
Ingredient NameStrength
No Inactive Ingredients Found


















Product Characteristics
ColorPINK (mottled)Scoreno score
ShapeROUND (bi-layered)Size17mm
FlavorBERRYImprint CodeL321
Contains      


















Packaging
#NDCPackage DescriptionMultilevel Packaging
136800-321-6325 TABLET In 1 BOTTLENone
236800-321-7150 TABLET In 1 BOTTLENone
336800-321-0965 TABLET In 1 BOTTLENone










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07735508/05/2008


Labeler - Topco Associates LLC (006935977)
Revised: 05/2009Topco Associates LLC




More Topcare Complete Acid Reducer plus Antacid resources


  • Topcare Complete Acid Reducer plus Antacid Use in Pregnancy & Breastfeeding
  • Topcare Complete Acid Reducer plus Antacid Drug Interactions
  • Topcare Complete Acid Reducer plus Antacid Support Group
  • 0 Reviews for Topcare Complete Acid Reducer plus Antacid - Add your own review/rating


Compare Topcare Complete Acid Reducer plus Antacid with other medications


  • GERD


Friday, June 29, 2012

Somavert


Pronunciation: peg-VI-soe-mant
Generic Name: Pegvisomant
Brand Name: Somavert


Somavert is used for:

Treating acromegaly in patients who have not responded to surgery, radiation therapy, or other medical procedures, or who are not candidates for those treatments.


Somavert is a growth hormone receptor antagonist. It works by blocking the site of action for growth hormone, which helps to block the effects of growth hormone.


Do NOT use Somavert if:


  • you are allergic to any ingredient in Somavert, including polyethylene glycol

  • you are allergic to latex

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



Before using Somavert:


Some medical conditions may interact with Somavert. 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 diabetes, a tumor or other growths, liver problems, or a history of alcohol abuse

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


  • Narcotic pain medicine (eg, codeine) because it may decrease Somavert's effectiveness

  • Insulin or oral hypoglycemic agents because the risk of their side effects may be increased by Somavert

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


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


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

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

  • Do not use Somavert if it contains particles, is cloudy or discolored, or if the vial is cracked or damaged.

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

  • Somavert must be mixed before you use it. Follow your doctor's instructions on how to mix Somavert.

  • Do not shake Somavert after mixing it. Hold the vial between the palms of both hands and gently roll it to dissolve the powder.

  • Use Somavert within 6 hours after mixing it. Throw away any unused medicine left in the vial after your dose. If you do not use Somavert within 6 hours after you mix it, throw it away.

  • Choose a different injection site each day (eg, upper arm, upper thigh, stomach area, buttocks) to help prevent lumps at the injection sites.

  • Keep this product, as well as syringes and needles, out of the reach of children and pets. Do not reuse needles, syringes, or other materials. Ask your health care provider how to dispose of these materials after use. Follow all local rules for disposal.

  • If you miss a dose of Somavert skip the missed dose and go back to your regular dosing schedule. Do not use 2 doses at once.

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



Important safety information:


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

  • Diabetes patients - Somavert may affect your blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.

  • Somavert may interfere with certain lab tests, including some growth hormone level tests. Be sure your doctor and lab personnel know you are taking Somavert.

  • Lab tests, including growth hormone blood levels, insulin-like growth factor blood levels, and liver function, may be performed while you use Somavert. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

  • Somavert 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 Somavert while you are pregnant. It is not known if Somavert is found in breast milk. If you are or will be breast-feeding while you use Somavert, check with your doctor. Discuss any possible risks to your baby.


Possible side effects of Somavert:


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:



Back pain; diarrhea; dizziness; flu-like symptoms (eg, mild fever or chills, muscle aches, weakness); nausea; pain, redness, or itching at the injection site; sinus inflammation.



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); chest pain; swelling of the legs and feet; symptoms of liver problems (eg, yellowing of the skin or eyes, dark urine, pale stools, unusual tiredness, severe or persistent nausea or stomach pain, loss of appetite); thickening of the skin or lumps at the injection site; unusual weight gain.



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: Somavert 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 increased fatigue.


Proper storage of Somavert:

Before mixing, store Somavert in the refrigerator between 36 and 46 degrees F (2 and 8 degrees C). Do not freeze. After mixing, Somavert may be kept at room temperature for up to 6 hours. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Somavert out of the reach of children and away from pets.


General information:


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

  • Somavert 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 Somavert. 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 Somavert resources


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


  • Somavert Prescribing Information (FDA)

  • Somavert Consumer Overview

  • Somavert Monograph (AHFS DI)

  • Somavert Advanced Consumer (Micromedex) - Includes Dosage Information

  • Pegvisomant Professional Patient Advice (Wolters Kluwer)



Compare Somavert with other medications


  • Acromegaly


Thursday, June 28, 2012

Keppra Tablets


Pronunciation: LEE-va-tye-RA-se-tam
Generic Name: Levetiracetam
Brand Name: Keppra


Keppra is used for:

Treating partial-onset, myoclonic, or generalized tonic-clonic seizures in patients with epilepsy. It is used in combination with other medicines. It may also be used for other conditions as determined by your doctor.


Keppra is an anticonvulsant. Exactly how it works is not known, but it may work by slowing abnormal nerve impulses in the brain.


Do NOT use Keppra if:


  • you are allergic to any ingredient in Keppra

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



Before using Keppra:


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 kidney problems or you are on dialysis

  • if you have a history of mental or mood problems (eg, depression), or suicidal thoughts or actions

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


Ask your health care provider if Keppra 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 Keppra:


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


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

  • Take Keppra by mouth with or without food.

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

  • Keppra works best if it is taken at the same time(s) each day.

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

  • If you miss a dose of Keppra, 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 Keppra.



Important safety information:


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

  • Do not suddenly stop taking Keppra or your other seizure medicines. You may have an increased risk of side effects (eg, seizures). If you need to stop Keppra or add a new medicine, your doctor will gradually lower your dose.

  • Contact your health care provider if your seizures become worse or if you have a new type of seizure.

  • Patients who take Keppra may be at increased risk for suicidal thoughts or actions. The risk may be greater in patients who have had suicidal thoughts or actions in the past. Watch patients who take Keppra closely. Contact the doctor at once if new, worsened, or sudden symptoms such as depressed mood; anxious, restless, or irritable behavior; panic attacks; or any unusual changes in mood or behavior occur. Contact the doctor right away if any signs of suicidal thoughts or actions occur.

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

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

  • Keppra should be used with extreme caution in CHILDREN younger than 4 years old; safety and effectiveness in these children have not been confirmed.

  • Caution is advised when using Keppra in CHILDREN; they may be more sensitive to its effects, especially weakness and mood or behavior changes.

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


Possible side effects of Keppra:


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:



Dizziness; drowsiness; irritability; runny nose; sore throat; tiredness; vomiting; weakness.



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

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); abnormal thoughts; dark urine; decreased coordination; extreme drowsiness, dizziness, tiredness, or weakness; fever, chills, or persistent sore throat; hallucinations; memory loss; mouth sores; new or worsening mental, mood, or behavior changes (eg, aggression, agitation, anger, anxiety, apathy, depression, hostility, irritability, panic attacks, restlessness); new or worsening seizures; suicidal thoughts or attempts; trouble sleeping; unusual bruising or bleeding; vision changes; yellowing of the skin or eyes.



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


See also: Keppra 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 aggression; agitation; difficult or slow breathing; loss of consciousness; severe drowsiness.


Proper storage of Keppra:

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


General information:


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

  • Keppra 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 Keppra. 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 Keppra resources


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


Compare Keppra with other medications


  • Bipolar Disorder
  • Epilepsy
  • Hyperekplexia
  • Neuralgia
  • New Daily Persistent Headache
  • Seizures


Tuesday, June 26, 2012

Tygacil


Generic Name: tigecycline (Intravenous route)

tye-ge-SYE-kleen

Commonly used brand name(s)

In the U.S.


  • Tygacil

Available Dosage Forms:


  • Powder for Solution

Therapeutic Class: Antibiotic


Chemical Class: Glycylcycline


Uses For Tygacil


Tigecycline is an antibiotic. It is used to treat bacterial infections in many different parts of the body (e.g., infections on the skin, stomach, or lungs). It works by killing bacteria or preventing their growth. However, this medicine will not work for colds, flu, or other virus infections.


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


Before Using Tygacil


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 have not been performed on the relationship of age to the effects of tigecycline in the pediatric population. Safety and efficacy have not been established.


Geriatric


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


Pregnancy








Pregnancy CategoryExplanation
All TrimestersDStudies in pregnant women have demonstrated a risk to the fetus. However, the benefits of therapy in a life threatening situation or a serious disease, may outweigh the potential risk.

Breast Feeding


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


Interactions with Medicines


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


  • Warfarin

Interactions with Food/Tobacco/Alcohol


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


Other Medical Problems


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


  • Diarrhea from an antibiotic or

  • Liver disease or

  • Pancreatitis (inflammation of the pancreas)—Use with caution. May make these conditions worse.

  • Liver disease, severe—Use with caution. The effects may be increased because of slower removal from the body.

Proper Use of Tygacil


A nurse or other trained health professional will give you this medicine. This medicine is given through a needle placed in one of your veins. This medicine is given slowly, so the needle will remain in place for about 30 to 60 minutes.


Precautions While Using Tygacil


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


Using this medicine while you are pregnant can harm your unborn baby. Use an effective form of birth control to keep from getting pregnant. If you think you have become pregnant while using the medicine, tell your doctor right away.


Birth control pills may not work while you are using tigecycline. To keep from getting pregnant, use another form of birth control along with your birth control pills. Other forms include condoms, a diaphragm, or a contraceptive foam or jelly.


This medicine may cause serious allergic reactions, including anaphylaxis, which can be life-threatening and require immediate medical attention. Call your doctor right away if you have itching; hives; hoarseness; shortness of breath; trouble breathing; trouble swallowing; or any swelling of your hands, face, or mouth after you receive this medicine.


Tigecycline may cause diarrhea, and in some cases it can be severe. Do not take any medicine to treat diarrhea without first checking with your doctor. Diarrhea medicines may make the diarrhea worse or make it last longer. If you have any questions about this or if mild diarrhea continues or gets worse, check with your doctor.


Tigecycline may cause your skin to be more sensitive to sunlight than it is normally. Exposure to sunlight, even for brief periods of time, may cause a skin rash, itching, redness or other discoloration of the skin, or a severe sunburn. Use a sunscreen when you are outdoors. Wear protective clothing (including a hat) and sunglasses. Avoid sunlamps and tanning beds or booths.


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


Tygacil 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 or nurse immediately if any of the following side effects occur:


More common
  • Cough or hoarseness

  • dizziness

  • fever or chills

  • headache

  • lower back or side pain

  • pain, warmth, or burning in the fingers, toes, and legs

  • painful or difficult urination

  • problems with vision or hearing

Less common
  • Abdominal or stomach pain

  • accumulation of pus

  • bloating or swelling of the face, arms, hands, lower legs, or feet

  • bluish color

  • blurred vision

  • changes in skin color

  • confusion

  • convulsions

  • decreased urine

  • diarrhea

  • difficult or labored breathing

  • dizziness, faintness, or lightheadedness when getting up from a lying or sitting position suddenly

  • dry mouth

  • eye pain

  • fat in the stool

  • flushed, dry skin

  • fruit-like breath odor

  • general feeling of illness

  • increased hunger

  • increased thirst

  • increased urination

  • irregular heartbeat

  • loss of appetite

  • mood changes

  • muscle pain or cramps

  • nausea or vomiting

  • nervousness

  • numbness or tingling in the hands, feet, or lips

  • pain

  • pale skin

  • pounding in the ears

  • rapid weight gain

  • shortness of breath

  • slow or fast heartbeat

  • sore throat

  • sweating

  • swollen, red, tender area of infection

  • tenderness

  • tightness in the chest

  • troubled breathing with exertion

  • unexplained weight loss

  • unusual bleeding or bruising

  • unusual tiredness or weakness

  • unusual weight gain or loss

  • wheezing

Rare
  • Abdominal or stomach cramps

  • anxiety

  • black, tarry stools

  • bleeding gums

  • blood in the urine or stools

  • chest pain or discomfort

  • clay-colored stools

  • cold sweats

  • coma

  • cool, pale skin

  • dark urine

  • depression

  • difficulty in breathing

  • itching

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

  • nightmares

  • pinpoint red spots on the skin

  • rash

  • shakiness

  • slurred speech

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

  • swelling of the face, ankles, or hands

  • swollen glands

  • tremor

  • unpleasant breath odor

  • vomiting of blood

  • yellow eyes or skin

Incidence not known
  • Bloating

  • constipation

  • difficulty in swallowing

  • hives

  • indigestion

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

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

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


More common
  • Red streaks on the skin

  • swelling, tenderness, or pain at the injection site

Less common
  • Acid or sour stomach

  • belching

  • heartburn

  • lack or loss of strength

  • sleeplessness

  • stomach discomfort, upset, or pain

  • trouble sleeping

  • unable to sleep

Rare
  • Bleeding, blistering, burning, coldness, discoloration of the skin, feeling of pressure, hives, infection, inflammation, itching, lumps, numbness, pain, rash, redness, scarring, soreness, stinging, swelling, tenderness, tingling, ulceration, or warmth at the injection site

  • change in taste or bad unusual or unpleasant (after) taste

  • increased clear or white vaginal discharge

  • itching of the vagina or genital area

  • pain during sexual intercourse

  • sleepiness or unusual drowsiness

  • thick, white vaginal discharge with no odor or with a mild odor

  • vaginal yeast infection

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: Tygacil 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 Tygacil resources


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


  • Tygacil Prescribing Information (FDA)

  • Tygacil Consumer Overview

  • Tygacil Monograph (AHFS DI)

  • Tygacil MedFacts Consumer Leaflet (Wolters Kluwer)

  • Tigecycline Professional Patient Advice (Wolters Kluwer)



Compare Tygacil with other medications


  • Intraabdominal Infection
  • Pneumonia
  • Skin and Structure Infection
  • Skin Infection


Tetradure





Dosage Form: FOR ANIMAL USE ONLY
Tetradure™

300

(OXYTETRACYCLINE) INJECTION

ANTIBIOTIC


Each mL contains 300 mg of oxytetracycline base as amphoteric oxytetracycline.



For Use in Beef Cattle, Non-lactating Dairy Cattle, Calves, Including Pre-ruminating (Veal) Calves and Swine.


READ ENTIRE BROCHURE CAREFULLY BEFORE USING THIS PRODUCT.


Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.



INTRODUCTION


Tetradure™ 300 (Oxytetracycline) Injection is a sterile, ready to use solution of the broad-spectrum antibiotic oxytetracycline dihydrate. Oxytetracycline is an antimicrobial agent that is effective in treatment of a wide range of diseases caused by susceptible gram-positive and gram-negative bacteria.


Tetradure™ 300 should be stored at room temperature 59°-86°F (15°-30°C). The antibiotic activity of oxytetracycline is not appreciably diminished in the presence of body fluids, serum or exudates.



INGREDIENTS


Tetradure™ 300 (oxytetracycline) Injection is a sterile, pre-constituted solution of the broad-spectrum antibiotic oxytetracycline dihydrate. Each mL contains 300 mg oxytetracycline as base, 40% (v/v) glycerol formal, 10% (v/v) polyethylene glycol 200, 2.7% (w/v) magnesium oxide, 0.4% (w/v) sodium formaldehyde sulphoxylate (as a preservative) and monoethanolamine (as required to adjust pH).



INDICATIONS


Tetradure™ 300 is intended for use in treatment for the following disease when due to oxytetracycline-susceptible organisms:



Beef cattle, non-lactating dairy cattle, calves, including pre-ruminating (veal) calves


Tetradure™ 300 is indicated in the treatment of pneumonia and shipping fever complex associated with Pasteurella spp., and Histophilus spp. Tetradure™ 300 is indicated for the treatment of the infectious bovine keratoconjunctivitis (pink eye) caused by Moraxella bovis, foot-rot and diphtheria caused by Fusobacterium necrophorum; bacterial enteritis (scours) caused by Escherichia coli; wooden tongue caused by Actinobacillus lignieresi; leptospirosis caused by Leptospira pomona; and wound infections and acute metritis caused by strains of staphylococcal and streptococcal organisms sensitive to oxytetracycline. Also, it is indicated for the control of respiratory disease in cattle at high risk of developing BRD associated with Mannheimia (Pasteurella) haemolytica.



Swine


Tetradure™ 300 is indicated in the treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli; pneumonia caused by Pasteurella multocida; and leptospirosis caused by Leptospira pomona.


In sows Tetradure™ 300 is indicated as an aid in control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli.



PHARMACOLOGY


Oxytetracycline is derived from the metabolic activity of the actinomycete, Streptomyces rimosus. Oxytetracycline is an antimicrobial agent that is effective in the treatment of a wide range of diseases caused by susceptible gram-positive and gram-negative bacteria.


The antibiotic activity of oxytetracycline is not appreciably diminished in the presence of body fluids, serum or exudates.


Studies have shown that the half-life of oxytetracycline in blood following intramuscular treatment with Tetradure™ 300 at 5 mg per pound of bodyweight is approximately 23 hours in cattle and 18 hours in swine.


Studies have shown when Tetradure™ 300 is administered once intramuscularly to cattle or swine at 9 mg per pound of bodyweight, blood oxytetracycline concentration of greater than 0.2 mcg/mL have been observed for 3 to 4 days.


Studies have shown when Tetradure™ 300 is administered once intramuscularly or subcutaneously to cattle at 13.6 mg per pound of bodyweight, blood oxytetracycline concentration of greater than 0.2 mcg/mL have been observed for at least 7 to 8 days.



Tetradure Dosage and Administration



Beef cattle, non-lactating dairy cattle, calves, including pre-ruminating (veal) calves


A single intramuscular or subcutaneous dosage of 13.6 mg of oxytetracycline per pound of bodyweight, Tetradure™ 300 is recommended for the control of respiratory disease in cattle at high risk of developing BRD associated with Mannheimia (Pasteurella) haemolytica.


At a single intramuscular or subcutaneous dose range of 9 to 13.6 mg of oxytetracycline per pound of bodyweight, Tetradure™ 300 is recommended in the treatment of the following conditions:


(1)

Bacterial pneumonia caused by Pasteurella spp (shipping fever) in calves and yearlings where retreatment is impractical due to husbandry conditions, such as cattle on range, or where their repeated restraint is inadvisable.

(2)

Infectious bovine keratoconjunctivitis (pink eye) caused by Moraxella bovis.

For other indications Tetradure™ 300 is to be administered intramuscularly, subcutaneously or intravenously at a level of 3 to 5 mg of oxytetracycline per pound of bodyweight per day. In treatment of foot-rot and advanced cases of other indicated diseases, a dosage level of 5 mg per pound of bodyweight per day is recommended. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four (4) consecutive days. If improvement is not noted within 24 to 48 hours of the beginning of treatment, diagnosis and therapy should be re-evaluated.


Do not administer intramuscularly in the neck of small calves due to lack of sufficient muscle mass.


Use extreme care when administering this product by intravenous injection. Perivascular injection or leakage from an intravenous injection may cause severe swelling at the injection site.



Swine


A single dosage of 9 mg of oxytetracycline per pound of bodyweight administered intramuscularly is recommended in the treatment of bacterial pneumonia caused by Pasteurella multocida in swine, where retreatment is impractical due to husbandry conditions or where repeated restraint is inadvisable.


Tetradure™ 300 can also be administered by intramuscular injection at a level of 3 to 5 mg of oxytetracycline per pound of bodyweight per day. Treatment should be continued 24 to 48 hours following remission of disease signs; however, not to exceed a total of four (4) consecutive days. If improvement is not noted within 24 to 48 hours of the beginning of treatment, diagnosis and therapy should be re-evaluated.


For sows, administer once intramuscularly 3 mg of oxytetracycline per pound of bodyweight approximately eight (8) hours before farrowing or immediately after completion of farrowing as an aid in the control of infectious enteritis in baby pigs.


For swine weighing 25 lbs of bodyweight and under, Tetradure™ 300 should be administered undiluted for treatment at 9 mg/lb but should be administered diluted for treatment at 3 or 5 mg/lb.


























9 mg dosage of undiluted Tetradure™ 3003 or 5 mg/lb dosage volume of diluted Tetradure™ 300
Bodyweight9 mg/lb3 mg/lbDilution*5 mg/lb

*

To prepare dilutions, add one part of Tetradure™ 300 to three (3), five (5) or seven (7) parts of the sterile water, or 5% dextrose solution as indicated; the diluted product should be used immediately.

5 lb0.15 mL0.4 mL37.5 mg/mL0.7 mL
10 lb0.30 mL0.6 mL50 mg/mL1.0 mL
25 lb0.75 mL1.0 mL75 mg/mL1.7 mL

Precautions


Exceeding the highest recommended level of drug per pound of bodyweight per day, administering more than the recommended number of treatments, and/or exceeding 10 mL intramuscularly or subcutaneously per injection site in adult beef cattle and non-lactating dairy cattle and 5 mL intramuscularly per injection site in adult swine, may result in antibiotic residues beyond the withdrawal time.


Consult with your veterinarian prior to administering this product in order to determine to proper treatment required in the event of an adverse reaction. At the first sign of any adverse reaction, discontinue use of the product and seek the advice of your veterinarian. Some of the reactions may be attributable either to anaphylaxis (an allergic reaction) or to cardiovascular collapse of unknown cause.


Shortly after injection treated animals may have transient hemoglobinuria resulting in darkened urine.


As with all antibiotic preparations, use of this drug may result in overgrowth of non-susceptible organisms, including fungi. The absence of a favourable response following treatment, or the development of new signs or symptoms may suggest an overgrowth of non-susceptible organisms. If superinfections occur, the use of this product should be discontinued and appropriate specific therapy should be instituted.


Since bacteriostatic drugs may interfere with the bactericidal action of penicillin, it is advisable to avoid giving Tetradure™ 300 in conjunction with penicillin.



STORAGE


Store at room temperature, 59°-86°F (15°-30°C). Keep from freezing.



Warnings



WARNINGS: Discontinue treatment at least 28 days prior to slaughter of cattle and swine. Not for use in lactating dairy animals. Rapid intravenous administration may result in animal collapse. Oxytetracycline should be administered intravenous slowly over a period of at least 5 minutes.



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



CAUTION


Intramuscular or subcutaneous injection may result in local tissue reactions which persist beyond the slaughter withdrawal period. This may result in trim loss of edible tissue at slaughter.


Intramuscular injection in the rump area may cause mild temporary lameness associated with swelling at the injection site. Subcutaneous injection in the neck area may cause swelling at the injection site.



Adverse Reactions


Reports of adverse reactions associated with oxytetracycline administration include injection site swelling, restlessness, ataxia, trembling, swelling of eyelids, ears, muzzle, anus and vulva (or scrotum and sheath in males), respiratory abnormalities (labored breathing), frothing at the mouth, collapse and possibly death. Some of these reactions may be attributed either to anaphylaxis (an allergic reaction) or to cardiovascular collapse of unknown cause.



PRESENTATION


Tetradure™ 300 is available in 100 mL, 250 mL and 500 mL vials.



Livestock Drug - Not for Human Use.

Restricted Drug(s) California. Use Only as Directed.



DISTRIBUTED BY:

Merial Limited

Duluth, GA 30096-4640, USA


™Tetradure is a trademark and Cattle Head Logo is a registered trademark of Merial Limited.

MADE IN THE UK


U.S. Patent No. 6,110,905

U.S. Patent No. 6,310,053


Rev. 06-2003


008630109


NADA 141-143, APPROVED BY THE FDA



PRINCIPAL DISPLAY PANEL - 100 mL Carton


Tetradure™

300


(OXYTETRACYCLINE) INJECTION


ANTIBIOTIC


Each mL contains 300 mg of Oxytetracycline

base as amphoteric oxytetracycline.


For the treatment of diseases in beef cattle,

non-lactating dairy cattle, calves, including

pre-ruminating (veal) calves and swine.


Caution: Federal law restricts this drug to use

by or on the order of a licensed veterinarian.


NADA 141-143, Approved By FDA


U.S. Patent No. 6,110,905

U.S. Patent No. 6,310,053


Net Contents:

100 mL


MERIAL










Tetradure 300 
oxytetracycline  injection, solution










Product Information
Product TypePRESCRIPTION ANIMAL DRUGNDC Product Code (Source)50604-0415
Route of AdministrationINTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUSDEA Schedule    








Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
oxytetracycline (oxytetracycline)oxytetracycline300 mg  in 1 mL












Inactive Ingredients
Ingredient NameStrength
glycerol formal 
polyethylene glycol 
magnesium oxide 
sodium formaldehyde sulfoxylate 


















Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains      






























Packaging
#NDCPackage DescriptionMultilevel Packaging
150604-0415-11 BOTTLE In 1 CARTONcontains a BOTTLE, GLASS
1100 mL In 1 BOTTLE, GLASSThis package is contained within the CARTON (50604-0415-1)
250604-0415-21 BOTTLE In 1 CARTONcontains a BOTTLE, GLASS
2250 mL In 1 BOTTLE, GLASSThis package is contained within the CARTON (50604-0415-2)
350604-0415-31 BOTTLE In 1 CARTONcontains a BOTTLE, GLASS
3500 mL In 1 BOTTLE, GLASSThis package is contained within the CARTON (50604-0415-3)










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NADANADA14114307/31/1993


Labeler - Merial Limited (034393582)
Revised: 09/2010Merial Limited

Sunday, June 24, 2012

Sildenafil



Generic Name: sildenafil (oral) (sil DEN a fil)

Brand Names: Revatio, Viagra


What is sildenafil?

Sildenafil relaxes muscles and increases blood flow to particular areas of the body.


Sildenafil under the name Viagra is used to treat erectile dysfunction (impotence) in men. Another brand of sildenafil is Revatio, which is used to treat pulmonary arterial hypertension and improve exercise capacity in men and women.


Do not take Viagra while also taking Revatio, unless your doctor tells you to.

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


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


Do not take sildenafil if you are also using a nitrate drug for chest pain or heart problems. This includes nitroglycerin (Nitrostat, Nitrolingual, Nitro-Dur, Nitro-Bid, and others), isosorbide dinitrate (Dilatrate-SR, Isordil, Sorbitrate), and isosorbide mononitrate (Imdur, ISMO, Monoket). Nitrates are also found in some recreational drugs such as amyl nitrate or nitrite ("poppers"). Taking sildenafil with a nitrate medicine can cause a sudden and serious decrease in blood pressure. During sexual activity, if you become dizzy or nauseated, or have pain, numbness, or tingling in your chest, arms, neck, or jaw, stop and call your doctor right away. You could be having a serious side effect of sildenafil. Do not take sildenafil more than once a day. Allow 24 hours to pass between doses. Contact your doctor or seek emergency medical attention if your erection is painful or lasts longer than 4 hours. A prolonged erection (priapism) can damage the penis.

Sildenafil can decrease blood flow to the optic nerve of the eye, causing sudden vision loss. This has occurred in a small number of people taking sildenafil, most of whom also had heart disease, diabetes, high blood pressure, high cholesterol, or certain pre-existing eye problems, and in those who smoke or are over 50 years old. It is not clear whether sildenafil is the actual cause of vision loss.


Stop using sildenafil and get emergency medical help if you have sudden vision loss.

What should I discuss with my healthcare provider before taking sildenafil?


Do not take sildenafil if you are also using a nitrate drug for chest pain or heart problems. This includes nitroglycerin (Nitrostat, Nitrolingual, Nitro-Dur, Nitro-Bid, and others), isosorbide dinitrate (Dilatrate-SR, Isordil, Sorbitrate), and isosorbide mononitrate (Imdur, ISMO, Monoket). Nitrates are also found in some recreational drugs such as amyl nitrate or nitrite ("poppers"). Taking sildenafil with a nitrate medicine can cause a sudden and serious decrease in blood pressure.

To make sure you can safely take sildenafil, tell your doctor if you have any of these other conditions:



  • heart disease or heart rhythm problems;




  • a recent history (in the past 6 months) of a heart attack, stroke, or congestive heart failure;




  • high or low blood pressure;




  • coronary artery disease;




  • liver or kidney disease;




  • a blood cell disorder such as sickle cell anemia, multiple myeloma, or leukemia;




  • a bleeding disorder such as hemophilia;




  • a stomach ulcer;




  • retinitis pigmentosa (an inherited condition of the eye);




  • a physical deformity of the penis (such as Peyronie's disease); or




  • if you have been told you should not have sexual intercourse for health reasons.




Sildenafil can decrease blood flow to the optic nerve of the eye, causing sudden vision loss. This has occurred in a small number of people taking sildenafil, most of whom also had heart disease, diabetes, high blood pressure, high cholesterol, or certain pre-existing eye problems, and in those who smoke or are over 50 years old. It is not clear whether sildenafil is the actual cause of vision loss. Stop using sildenafil and get emergency medical help if you have sudden vision loss. FDA pregnancy category B: This medication is not expected to be harmful to an unborn baby. Do not use sildenafil without telling your doctor if you are pregnant or plan to become pregnant during treatment. It is not known if sildenafil passes into breast milk or if it could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.

How should I take sildenafil?


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


Revatio is usually taken three times each day, about 4 to 6 hours apart.


Viagra is usually taken only when needed, 30 minutes to 1 hour before sexual activity. You may take it up to 4 hours before sexual activity. Do not take Viagra more than once per day.


Viagra can help you have an erection when sexual stimulation occurs. An erection will not occur just by taking a pill. Follow your doctor's instructions.


During sexual activity, if you become dizzy or nauseated, or have pain, numbness, or tingling in your chest, arms, neck, or jaw, stop and call your doctor right away. You could be having a serious side effect of sildenafil. Store at room temperature away from moisture and heat.

See also: Sildenafil dosage (in more detail)

What happens if I miss a dose?


Viagra is used as needed, so you are not likely to be on a dosing schedule.


If you miss a dose of Revatio, take the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not take 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 chest pain, nausea, irregular heartbeat, and feeling light-headed or fainting.

What should I avoid while taking sildenafil?


Drinking alcohol can increase certain side effects of sildenafil. Avoid using other medicines to treat impotence, such as alprostadil (Caverject, Muse, Edex) or yohimbine (Yocon, Yodoxin, others), without first talking to your doctor.

Sildenafil 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. During sexual activity, if you become dizzy or nauseated, or have pain, numbness, or tingling in your chest, arms, neck, or jaw, stop and call your doctor right away. You could be having a serious side effect of sildenafil. Stop using sildenafil and call your doctor at once if you have a serious side effect such as:

  • sudden vision loss;




  • ringing in your ears, or sudden hearing loss;




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




  • irregular heartbeat;




  • swelling in your hands, ankles, or feet;




  • shortness of breath;




  • vision changes;




  • feeling light-headed, fainting; or



  • penis erection that is painful or lasts 4 hours or longer.

Less serious side effects may include:



  • warmth or redness in your face, neck, or chest;




  • stuffy nose;




  • headache;




  • memory problems;




  • upset stomach; or




  • back pain.



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.


Sildenafil Dosing Information


Usual Adult Dose for Erectile Dysfunction:

Initial (oral): 50 mg orally administered as needed 1 hour prior to anticipated sexual activity. A maximum of one dose per day is recommended.
Maintenance (oral): 25 to 100 mg orally as needed 30 minutes to 4 hours prior to anticipated sexual activity. A maximum of one dose per day is recommended.

Usual Adult Dose for Pulmonary Hypertension:

20 mg orally three times a day taken at least 4 to 6 hours apart
or
10 mg (corresponding to 12.5 mL) administered as an intravenous bolus injection three times a day. A 10 mg dose of the injection is predicted to provide pharmacological effect of sildenafil and its N-desmethyl metabolite equivalent to that of a 20 mg oral dose. The injection is for the continued treatment of patients with pulmonary arterial hypertension (PAH) who are currently prescribed oral sildenafil and who are temporarily unable to take oral medication.

Usual Geriatric Dose for Erectile Dysfunction:

25 mg orally as needed 1 hour prior to anticipated sexual activity.

Usual Pediatric Dose for Pulmonary Hypertension:

Safety and effectiveness of sildenafil in pediatric pulmonary hypertension patients have not been established. Limited pediatric information exists; most pediatric literature consists of case reports or small studies; further studies are needed.

Neonates: Note: A wide range of doses and interpatient variability has been reported; careful dose titration is necessary.

Pulmonary hypertension: Reported range: 0.5 to 3 mg/kg/dose orally every 6 to 12 hours; the largest study was a double-blind, randomized, placebo-controlled trial and used an initial dose of 3 mg/kg/dose every 6 hours in 31 patients; earlier studies used 0.3 to 2 mg/kg/dose every 6-24 hours; duration not established.

Pulmonary hypertension, facilitation of inhaled nitric oxide wean: 0.3 mg/kg/dose orally given once 70 to 90 minutes prior to inhaled nitric oxide discontinuation was used in three patients. Multiple dose therapy in neonates and infants has been reported consisting of 0.22 to 0.47 mg/kg/dose every 6 hours (average duration: 28 days) to facilitate weaning from inhaled nitric oxide in patients who previously failed; duration not established.

Older than 1 yr:
Pulmonary hypertension:
Initial dose: 0.25 to 0.5 mg/kg orally every 4 to 8 hours, increase if needed and if tolerated to 1 mg/kg/dose every 4 to 8 hours; doses as high as 2 mg/kg/dose every 4 hours have been used in several case reports; a wide range of doses has been reported, duration not established. A retrospective trial of 25 patients with chronic lung disease reported treatment duration of 28 to 950 days (median: 241 days).

Pulmonary hypertension, facilitation of inhaled nitric oxide wean (in patients who have not previously failed inhaled nitric oxide wean): Single dose: 0.4 mg/kg/dose (range: 0.3 to 0.5 mg/kg/dose) given once 60 minutes prior to inhaled nitric oxide discontinuation was used in 15 patients (median age: 5.6 months).


What other drugs will affect sildenafil?


Do not take sildenafil with similar medications such as tadalafil (Cialis) or vardenafil (Levitra).

Before taking sildenafil, tell your doctor about all other medications you use for erectile dysfunction, or if you are using any of the following medications:



  • bosentan (Tracleer);




  • cimetidine (Tagamet);




  • conivaptan (Vaprisol);




  • imatinib (Gleevec);




  • isoniazid (for treating tuberculosis);




  • rifampin (Rifadin, Rimactane Rifater, Rifamate);




  • an antidepressant such as nefazodone;




  • an antibiotic such as clarithromycin (Biaxin), dalfopristin/quinupristin (Synercid), erythromycin (E.E.S., EryPed, Ery-Tab, Erythrocin, Pediazole), or telithromycin (Ketek);




  • antifungal medication such as itraconazole (Sporanox), ketoconazole (Nizoral), miconazole (Oravig), or voriconazole (Vfend);




  • heart or blood pressure medication such as diltiazem (Cardizem, Dilacor, Tiazac), doxazosin (Cardura), nicardipine (Cardene), quinidine (Quin-G), or verapamil (Calan, Covera, Isoptin, Verelan); or




  • HIV/AIDS medicine such as atazanavir (Reyataz), delavirdine (Rescriptor), fosamprenavir (Lexiva), indinavir (Crixivan), nelfinavir (Viracept), saquinavir (Invirase), or ritonavir (Norvir, Kaletra).



This list is not complete and other drugs may interact with sildenafil. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor.



More sildenafil resources


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


  • sildenafil Advanced Consumer (Micromedex) - Includes Dosage Information

  • Sildenafil MedFacts Consumer Leaflet (Wolters Kluwer)

  • Revatio Prescribing Information (FDA)

  • Revatio Consumer Overview

  • Sildenafil Citrate Monograph (AHFS DI)

  • Viagra Prescribing Information (FDA)

  • Viagra MedFacts Consumer Leaflet (Wolters Kluwer)

  • Viagra Consumer Overview



Compare sildenafil with other medications


  • Erectile Dysfunction
  • Pulmonary Arterial Hypertension
  • Sexual Dysfunction, SSRI Induced


Where can I get more information?


  • Your pharmacist can provide more information about sildenafil.

See also: sildenafil side effects (in more detail)