Monday, April 11, 2011

Dibucaine


Class: Antipruritics and Local Anesthetics
ATC Class: C05AD04
VA Class: DE700
CAS Number: 85-79-0
Brands: Nupercainal

Introduction

Local anesthetic.a c


Uses for Dibucaine


Dermatologic Conditions


Self-medication for temporary relief of pain and itching associated with minor burns, sunburn, minor cuts or scrapes, insect bites, or minor skin irritations.a c


Hemorrhoids


Self-medication for temporary relief of pain, itching, and burning caused by hemorrhoids.a c


Dibucaine Dosage and Administration


Administration


Topical Administration


Apply topically to the skin as an ointment.a c


For external use only.c Avoid contact with the eye(s).a c


Do not apply in large quantities, especially over denuded surfaces or blistered areas.a


Prior to administration, cleanse the site with mild soap and warm water, rinse thoroughly, and gently dry with a soft cloth.c


Gently apply to affected areas.a For dermatologic conditions, cover with a light dressing, if necessary.a c


Wash hands following administration.c


Dosage


Pediatric Patients


Dermatologic Conditions

Topical

Children ≥12 years of age: Apply to affected areas 3–4 times daily.a c


Hemorrhoids

Topical

Children ≥12 years of age: Apply to affected anal tissues 3–4 times daily (morning and evening and after each bowel movement).a c


Adults


Dermatologic Conditions

Topical

Apply to affected areas 3–4 times daily.a c


Hemorrhoids

Topical

Apply to affected anal tissues 3–4 times daily (morning and evening and after each bowel movement).a c


Prescribing Limits


Pediatric Patients


Dermatologic Conditions

Topical

Children ≥12 years of age: Apply maximum 4 times daily.c Maximum: 7.5 g daily.a


Hemorrhoids

Topical

Children ≥12 years of age: Apply maximum 4 times daily.c


Adults


Dermatologic Conditions

Topical

Apply maximum 4 times daily.c Maximum: 30 g daily.a


Hemorrhoids

Topical

Apply maximum 4 times daily.c Maximum: 30 g daily.a


Special Populations


No special population dosage recommendations at this time.c


Cautions for Dibucaine


Contraindications



  • Known hypersensitivity to dibucaine, other amide-type local anesthetics, or any ingredient in the formulation.a



Warnings/Precautions


Sensitivity Reactions


Sulfite Sensitivity

Commercially available rectal and topical formulations of dibucaine contain acetone sodium bisulfite.a c Possible risk of anaphylaxis and life-threatening or less severe asthmatic episodes in certain susceptible individuals. a


If a rash or irritation develops or increases, discontinue drug and consult a clinician.a c


General Precautions


Administration

When used for self-medication, discontinue the drug and consult a clinician if the condition worsens, if symptoms persist for >7 days or clear and occur again within a few days, or if swelling, pain, bleeding, rash, or irritation occurs.a c


Serious Adverse Effects Associated with Local Anesthetics

Risk of serious adverse effects (e.g., seizures, coma, irregular heart beat, respiratory depression) with use of topical local anesthetics; generally reported following application of extemporaneously prepared topical preparations containing high concentrations of anesthetics.d


Potential for life-threatening adverse effects (e.g., irregular heart beat, seizures, breathing difficulties, coma, death) when topical local anesthetics are applied to a large area of skin, when the area of application is covered with an occlusive dressing, if a large amount of topical anesthetic is applied, if the anesthetic is applied to irritated or broken skin, or if the skin temperature increases (from exercise or use of a heating pad).101 102


Lidocaine 4% gel has been investigated to reduce discomfort during mammography.101 103 Whether such use could result in serious reactions has not been determined.101 103 Patients should speak with their clinician if they are considering using a topical anesthetic before obtaining a mammogram.101


When a topical anesthetic is needed for a procedure, use of an FDA-approved preparation has been recommended.d Use a preparation containing the lowest concentration of anesthetic likely to be effective; apply a small amount of the preparation to the affected area for the shortest period necessary for the desired effect,d and do not apply to broken or irritated skin.101 d


Specific Populations


Pregnancy

Safety and efficacy not established in pregnant women.c Use with caution.c


Lactation

Safety and efficacy not established in nursing women.c Use with caution.c


Pediatric Use

Children <12 years of age: use topical dibucaine only under clinical supervision.c


Common Adverse Effects


Rash, irritation.a


Interactions for Dibucaine


No formal drug interaction studies to date.c


Stability


Storage


Topical


Ointment

Tight, light-resistant containers at <40°C, preferably between 15–30°C.a c


ActionsActions



  • Blocks nerve conduction near application site and produces temporary loss of feeling or sensation.b




  • Blocks the generation and conduction of nerve impulses by decreasing the rate of depolarization of the nerve membrane.b



Advice to Patients



  • Importance of discontinuing therapy and consulting clinician if a rash or irritation develops during therapy.a c




  • Importance of washing hands following administration.c




  • Importance of avoiding contact with the eyes.a c




  • Importance of using as directed and not applying in large quantities, particularly over raw surfaces or blistered areas.a




  • Importance of discontinuing therapy and consulting clinician if dermatologic condition worsens or symptoms persist for >7 days or if redness, irritation, or bleeding occurs.a c




  • Importance of women informing their clinician if they are or plan to become pregnant or plan to breast-feed.c




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




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



Preparations


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


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













Dibucaine

Routes



Dosage Forms



Strengths



Brand Names



Manufacturer



Rectal or Topical



Ointment



1%*



Nupercainal Hemorrhoidal and Anesthetic Ointment (with acetone sodium bisulfite)



Novartis



Disclaimer

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


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

AHFS Drug Information. © Copyright, 1959-2011, Selected Revisions August 2009. American Society of Health-System Pharmacists, Inc., 7272 Wisconsin Avenue, Bethesda, Maryland 20814.




References



101. Food and Drug Administration. FDA Public Health Advisory: Potential hazards of skin products containing numbing ingredients for relieving pain from mammography and other medical tests and conditions. 2009 Jan 16. From FDA website.



102. Food and Drug Administration. Topical Anesthetics. MedWatch alert. Rockville, MD; 2009 Jan 16. From FDA website.



103. Lambertz CK, Johnson CJ, Montgomery PG et al. Premedication to reduce discomfort during screening mammography. Radiology. 2008; 248:765-72. [PubMed 18647845]



a. AHFS drug information 2004. McEvoy GK, ed. Dibucaine. Bethesda, MD: American Society of Health-System Pharmacists; 2007: 3537.



b. AHFS drug information 2007. McEvoy GK, ed. Local Anesthetics, Parenteral, General Statement. Bethesda, MD: American Society of Health-Systems Pharmacists; 2007: 3255-8.



c. Novartis. Freemont, MI: Personal communication.



d. Food and Drug Administration. FDA Public Health Advisory: Life-threatening side effects with use of skin products containing numbing ingredients for cosmetic procedures. 2007 Feb 6, updated 2007 Feb 9. From FDA website.



More Dibucaine resources


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


  • Dibucaine Ointment MedFacts Consumer Leaflet (Wolters Kluwer)

  • Dibucaine topical Concise Consumer Information (Cerner Multum)

  • dibucaine Topical application Advanced Consumer (Micromedex) - Includes Dosage Information



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Monday, March 28, 2011

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Risperidone

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Saturday, March 26, 2011

D-Tann Chewable Tablets


Pronunciation: dye-fen-HYE-dra-meen/fen-ill-EF-rin
Generic Name: Diphenhydramine/Phenylephrine
Brand Name: Examples include D-Tann and Pediatex-CT


D-Tann Chewable Tablets are used for:

Temporarily relieving symptoms of hay fever, allergies, or the common cold, including nasal congestion, runny nose, sneezing, itching of the nose and throat, and itchy/watery eyes. It may also be used for other conditions as determined by your doctor.


D-Tann Chewable Tablets are an antihistamine and decongestant combination. The antihistamine works by blocking the action of histamine, which helps reduce symptoms such as watery eyes and sneezing. The decongestant promotes sinus and nasal drainage, relieving congestion and pressure.


Do NOT use D-Tann Chewable Tablets if:


  • you are allergic to any ingredient in D-Tann Chewable Tablets

  • you are taking sodium oxybate (GHB) or you have taken furazolidone or a monoamine oxidase (MAO) inhibitor (eg, phenelzine) within the past 14 days

  • you have severe high blood pressure, severe heart blood vessel disease, a rapid heartbeat, or severe heart problems

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



Before using D-Tann Chewable Tablets:


Some medical conditions may interact with D-Tann Chewable 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 fast, slow, or irregular heartbeat

  • if you have a history of glaucoma; high blood pressure; diabetes; heart problems; ulcers; stroke; asthma; an overactive thyroid; seizures; a blockage of the stomach, bowel, or bladder; trouble breathing when you sleep; trouble sleeping; lung problems (eg, emphysema); the blood disease porphyria; or an enlarged prostate or other prostate problems; adrenal gland problems; blood vessel problems; or if you have difficulty urinating

Some MEDICINES MAY INTERACT with D-Tann Chewable Tablets. Tell your health care provider if you are taking any other medicines, especially if any of the following apply to you:


  • Beta-blockers (eg, propranolol), catechol-O-methyltransferase (COMT) inhibitors (eg, tolcapone), indomethacin, furazolidone, MAO inhibitors (eg, phenelzine), or tricyclic antidepressants (eg, amitriptyline) because side effects such as severe headache, high blood pressure, or high fever may occur

  • Bromocriptine or sodium oxybate (GHB) because the risk of side effects or toxic effects may be increased by D-Tann Chewable Tablets

  • Guanethidine, guanadrel, mecamylamine, methyldopa, or reserpine because their effectiveness may be decreased by D-Tann Chewable Tablets.

  • Digoxin or droxidopa because side effects such as irregular heartbeat or heart attack may occur

  • Urinary alkalinizers (eg, sodium bicarbonate) because the side effects of D-Tann Chewable Tablets may be increased

This may not be a complete list of all interactions that may occur. Ask your health care provider if D-Tann Chewable 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 D-Tann Chewable Tablets:


Use D-Tann Chewable Tablets as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • D-Tann Chewable Tablets may be taken with or without food. If stomach upset occurs, take with food to reduce stomach irritation.

  • Chew thoroughly before swallowing.

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

Ask your health care provider any questions you may have about how to use D-Tann Chewable Tablets.



Important safety information:


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

  • Avoid drinking alcohol or taking other medications that cause drowsiness (eg, sedatives, tranquilizers) while taking D-Tann Chewable Tablets. D-Tann Chewable Tablets will add to the effects of alcohol and other depressants. Ask your pharmacist if you have questions about which medicines are depressants.

  • Contact your health care provider if symptoms last for more than 7 days or are accompanied by a fever.

  • Diabetes patients - D-Tann Chewable Tablets may affect your blood sugar. Check blood sugar levels closely and ask your doctor before adjusting the dose of your diabetes medicine.

  • D-Tann Chewable Tablets contains phenylephrine and diphenhydramine. Before you begin taking any new prescription or nonprescription medicine, including medicine used on the skin, read the ingredients to see if it also contains phenylephrine or diphenhydramine. If it does, or if you are uncertain if it does, contact your doctor or pharmacist.

  • If you are scheduled for allergy skin testing, do not take D-Tann Chewable Tablets for several days before the test because it may decrease your response to the skin tests.

  • Do not take diet or appetite control medicines while you are taking D-Tann Chewable Tablets without checking with your doctor.

  • Do not exceed the recommended dose or take D-Tann Chewable Tablets for longer than prescribed without checking with your doctor.

  • If you have trouble sleeping, ask your pharmacist or doctor about the best time of day to take D-Tann Chewable Tablets.

  • Use D-Tann Chewable Tablets with caution in the ELDERLY because they may be more sensitive to its effects.

  • D-Tann Chewable Tablets are not recommended for use in NEWBORNS. Safety and effectiveness have not been confirmed.

  • Different products may have different dosing instructions for CHILDREN on the package labeling. Follow the dosing instructions provided on the package labeling or by your doctor. If you are unsure of what dose to give a child, check with your doctor.

  • Caution is advised when using D-Tann Chewable Tablets in CHILDREN because they may be more sensitive to its effects, especially excitability.

  • PREGNANCY AND BREAST-FEEDING: If you become pregnant while taking D-Tann Chewable Tablets, discuss with your doctor the benefits and risks of using D-Tann Chewable Tablets during pregnancy. If you are or will be breast-feeding while you are using D-Tann Chewable Tablets, check with your doctor or pharmacist to discuss the risks to your baby.


Possible side effects of D-Tann Chewable 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; drowsiness; dry mouth, nose, or throat; excitability (especially in children); headache; loss of appetite; nausea; nervousness; restlessness; trouble sleeping; vomiting.



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); blurred vision; chest pain; decreased coordination; difficulty urinating; fast or irregular heartbeat; fever; hallucinations; seizure; severe dizziness and drowsiness; severe nervousness, anxiety, or restlessness; tremors; unusual weakness.



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: D-Tann 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 bluish-colored skin; difficulty breathing; dilated pupils; fast or irregular heartbeat; fever; flushing; hallucinations; mental or mood changes; seizures; severe drowsiness or dizziness; severe excitability; severe nausea or vomiting; sweating; tremors.


Proper storage of D-Tann Chewable Tablets:

Store D-Tann Chewable Tablets at room temperature, between 59 and 77 degrees F (15 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep D-Tann Chewable Tablets out of the reach of children and away from pets.


General information:


  • If you have any questions about D-Tann Chewable Tablets, please talk with your doctor, pharmacist, or other health care provider.

  • D-Tann Chewable 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 D-Tann Chewable 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 D-Tann resources


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


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Friday, March 25, 2011

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Thursday, March 24, 2011

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Wednesday, March 9, 2011

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Wednesday, March 2, 2011

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