Wednesday, 30 November 2011

Decongex-3


Generic Name: chlorpheniramine and phenylpropanolamine (klor feh NEER a meen and feh nill proe pa NO la meen)

Brand Names: A.R.M. Allergy Relief, Allerest 12 Hour, Chlornade, Condrin, Contac 12 Hour, Decongex-3, Demazin, Dura-Vent/A, Equi-Nade, Genamin, Gencold, Histade, Or-Phen-Ade, Ordrine, Ornade Spansules, Resaid, Rescon Liquid, Rhinolar-EX, Teldrin, Triac, Triaminic, Vanex Forte-R


What is Decongex-3 (chlorpheniramine and phenylpropanolamine)?

Chlorpheniramine is an antihistamine. It blocks the effects of the naturally occurring chemical histamine in the body. Chlorpheniramine prevents sneezing; itchy, watery eyes and nose; and other symptoms of allergies and hay fever.


Phenylpropanolamine is a decongestant. It constricts (shrinks) blood vessels (veins and arteries). This reduces the blood flow to certain areas and allows nasal passages to open up.


Chlorpheniramine and phenylpropanolamine is used to treat nasal congestion and sinusitis (inflammation of the sinuses) associated with allergies, hay fever, and the common cold.


Phenylpropanolamine, an ingredient in this product, has been associated with an increased risk of hemorrhagic stroke (bleeding into the brain or into tissue surrounding the brain) in women. Men may also be at risk. Although the risk of hemorrhagic stroke is low, the U.S. Food and Drug Administration (FDA) recommends that consumers not use any products that contain phenylpropanolamine.


Chlorpheniramine and phenylpropanolamine may also be used for purposes other than those listed in this medication guide.


What is the most important information I should know about Decongex-3 (chlorpheniramine and phenylpropanolamine)?


Phenylpropanolamine, an ingredient in this product, has been associated with an increased risk of hemorrhagic stroke (bleeding into the brain or into tissue surrounding the brain) in women. Men may also be at risk. Although the risk of hemorrhagic stroke is low, the U.S. Food and Drug Administration (FDA) recommends that consumers not use any products that contain phenylpropanolamine.


Use caution when driving, operating machinery, or performing other hazardous activities. Chlorpheniramine and phenylpropanolamine may cause dizziness or drowsiness. If you experience dizziness or drowsiness, avoid these activities. Use alcohol cautiously. Alcohol may increase drowsiness and dizziness while taking chlorpheniramine and phenylpropanolamine.

Do not take more of this medication than is recommended. If your symptoms do not improve, or if they worsen, talk to your doctor.


Who should not take Decongex-3 (chlorpheniramine and phenylpropanolamine)?


Do not take chlorpheniramine and phenylpropanolamine if you have taken a monoamine oxidase inhibitor (MAOI) such as isocarboxazid (Marplan), phenelzine (Nardil), or tranylcypromine (Parnate) in the last 14 days. A dangerous drug interaction could occur, leading to serious side effects.

Before taking this medication, tell your doctor if you have


  • kidney disease,

  • liver disease,


  • diabetes,




  • glaucoma,




  • any type of heart disease or high blood pressure,




  • thyroid disease,




  • emphysema or chronic bronchitis, or




  • difficulty urinating or an enlarged prostate.



You may not be able to take chlorpheniramine and phenylpropanolamine, or you may require a dosage adjustment or special monitoring during treatment if you have any of the conditions listed above.


Chlorpheniramine and phenylpropanolamine is in the FDA pregnancy category B. This means that it is unlikely to harm an unborn baby. Do not take this medication without first talking to your doctor if you are pregnant. This medication passes into breast milk and may harm a nursing baby. Do not take this medication without first talking to your doctor if you are breast-feeding a baby. If you are over 65 years of age, you may be more likely to experience side effects from chlorpheniramine and phenylpropanolamine. You may require a lower dose of this medication. Read the package label for directions or consult your doctor or pharmacist before treating a child with this medication. Children are more susceptible than adults to the effects of medicines and may have unusual reactions.

How should I take Decongex-3 (chlorpheniramine and phenylpropanolamine)?


Take chlorpheniramine and phenylpropanolamine exactly as directed. If you do not understand these directions, ask your pharmacist, nurse, or doctor to explain them to you.


Take each dose with a full glass of water. Do not crush, chew, or break the long-acting or sustained-release forms of this medication. Swallow them whole. If you are unsure of the formulation of your medicine, ask your pharmacist for help.

If you cannot swallow the tablets or capsules, look for a liquid form of the medication.


To ensure that you get a correct dose, measure the liquid forms of chlorpheniramine and phenylpropanolamine with a special dose-measuring spoon or cup, not with a regular table spoon. If you do not have a dose-measuring device, ask your pharmacist where you can get one.


Do not take more of this medication than is recommended. An overdose of this medication can cause serious harm.

Do not take chlorpheniramine and phenylpropanolamine for longer than 7 days in a row. If your symptoms do not improve, if they get worse, or if you have a fever, talk to your doctor.


Store chlorpheniramine and phenylpropanolamine at room temperature away from moisture and heat.

What happens if I miss a dose?


Take the missed dose as soon as you remember. However, if it is almost time for the next dose, skip the missed dose and take only the next regularly scheduled dose. Do not take a double dose of this medication.


What happens if I overdose?


Seek emergency medical attention.

Symptoms of a chlorpheniramine and phenylpropanolamine overdose include a dry mouth, large pupils, flushing, nausea, and vomiting.


What should I avoid while taking Decongex-3 (chlorpheniramine and phenylpropanolamine)?


Use caution when driving, operating machinery, or performing other hazardous activities. Chlorpheniramine and phenylpropanolamine may cause dizziness or drowsiness. If you experience dizziness or drowsiness, avoid these activities. Use alcohol cautiously. Alcohol may increase drowsiness and dizziness while taking chlorpheniramine and phenylpropanolamine.

Chlorpheniramine and phenylpropanolamine may increase the effects of other drugs that cause drowsiness, including antidepressants, alcohol, other antihistamines, pain relievers, anxiety medicines, seizure medicines, and muscle relaxants. Dangerous sedation, dizziness, or drowsiness may occur if chlorpheniramine and phenylpropanolamine is taken with any of these medications.


Decongex-3 (chlorpheniramine and phenylpropanolamine) side effects


Serious side effects are unlikely to occur. Stop taking chlorpheniramine and phenylpropanolamine and seek emergency medical attention if you experience an allergic reaction (difficulty breathing; closing of your throat; swelling of your lips, tongue, or face; or hives).

Other, less serious side effects may be more likely to occur. Continue to take chlorpheniramine and phenylpropanolamine and talk to your doctor or try another similar medication if you experience



  • dryness of the eyes, nose, and mouth;




  • drowsiness or dizziness;




  • blurred vision;




  • difficulty urinating; or




  • excitation in children.



Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome.


What other drugs will affect Decongex-3 (chlorpheniramine and phenylpropanolamine)?


Do not take chlorpheniramine and phenylpropanolamine if you have taken a monoamine oxidase inhibitor (MAOI) such as isocarboxazid (Marplan), phenelzine (Nardil), or tranylcypromine (Parnate) in the last 14 days. A dangerous drug interaction could occur, leading to serious side effects.

Do not take other over-the-counter cough, cold, allergy, diet, or sleep aids while taking chlorpheniramine and phenylpropanolamine without first talking to your doctor or pharmacist. Other medications may also contain chlorpheniramine, phenylpropanolamine, or other similar drugs. You may accidentally take too much of these medicines.


Chlorpheniramine and phenylpropanolamine may increase the effects of other drugs that cause drowsiness, including antidepressants, alcohol, other antihistamines, pain relievers, anxiety medicines, seizure medicines, and muscle relaxants. Dangerous sedation, dizziness, or drowsiness may occur if chlorpheniramine and phenylpropanolamine is taken with any of these medications.


Drugs other than those listed here may also interact with chlorpheniramine and phenylpropanolamine. Talk to your doctor and pharmacist before taking any prescription or over-the-counter medicines.



More Decongex-3 resources


  • Decongex-3 Drug Interactions
  • Decongex-3 Support Group
  • 0 Reviews for Decongex-3 - Add your own review/rating


  • Triaminic Consumer Overview



Compare Decongex-3 with other medications


  • Cold Symptoms
  • Cough and Nasal Congestion
  • Hay Fever
  • Sinusitis
  • Upper Respiratory Tract Infection


Where can I get more information?


  • Your pharmacist has additional information about chlorpheniramine and phenylpropanolamine written for health professionals that you may read.

What does my medication look like?


Many formulations of chlorpheniramine and phenylpropanolamine are available both over-the-counter and with a prescription. Ask your pharmacist any questions you have about this medication, especially if it is new to you.



Saturday, 26 November 2011

Beta-Histina Generis




Beta-Histina Generis may be available in the countries listed below.


Ingredient matches for Beta-Histina Generis



Betahistine

Betahistine dihydrochloride (a derivative of Betahistine) is reported as an ingredient of Beta-Histina Generis in the following countries:


  • Portugal

International Drug Name Search

Thursday, 24 November 2011

Aldara




In the US, Aldara (imiquimod topical) is a member of the drug class topical anti-infectives and is used to treat Actinic Keratosis, Basal Cell Carcinoma, Condylomata Acuminata, Human Papilloma Virus and Molluscum Contagiosum.

US matches:

  • Aldara

  • Aldara Topical

UK matches:

  • Aldara 5% Cream
  • Aldara 5% Cream (SPC)

Ingredient matches for Aldara



Imiquimod

Imiquimod is reported as an ingredient of Aldara in the following countries:


  • Argentina

  • Australia

  • Austria

  • Bahrain

  • Belgium

  • Brazil

  • Canada

  • Chile

  • China

  • Costa Rica

  • Czech Republic

  • Denmark

  • El Salvador

  • Finland

  • France

  • Germany

  • Greece

  • Guatemala

  • Honduras

  • Hong Kong

  • Hungary

  • Iceland

  • Ireland

  • Israel

  • Italy

  • Luxembourg

  • Malaysia

  • Netherlands

  • New Zealand

  • Norway

  • Oman

  • Panama

  • Philippines

  • Portugal

  • Romania

  • Singapore

  • Slovakia

  • Slovenia

  • South Africa

  • Spain

  • Sri Lanka

  • Sweden

  • Switzerland

  • Taiwan

  • Turkey

  • United Kingdom

  • United States

International Drug Name Search

Glossary

SPC Summary of Product Characteristics (UK)

Click for further information on drug naming conventions and International Nonproprietary Names.

Sunday, 20 November 2011

Itraconazole




In some countries, this medicine may only be approved for veterinary use.


In the US, Itraconazole (itraconazole systemic) is a member of the drug class azole antifungals and is used to treat Aspergillosis - Aspergilloma, Blastomycosis, Candida Infections - Systemic, Candida Urinary Tract Infection, Coccidioidomycosis, Cryptococcosis, Dermatophytosis, Esophageal Candidiasis, Febrile Neutropenia, Histoplasmosis, Onychomycosis - Fingernail, Onychomycosis - Toenail, Oral Thrush, Paracoccidioidomycosis, Sporotrichosis, Tinea Capitis, Tinea Versicolor and Vaginal Yeast Infection.

US matches:

  • Itraconazole

  • Itraconazole Capsules

  • Itraconazole Solution

UK matches:

  • Itraconazole 100mg Capsules
  • Itraconazole 100mg Capsules (Sandoz Limited) (SPC)

Scheme

Rec.INN

ATC (Anatomical Therapeutic Chemical Classification)

J02AC02

CAS registry number (Chemical Abstracts Service)

0084625-61-6

Chemical Formula

C35-H38-Cl2-N8-O4

Molecular Weight

705

Therapeutic Category

Antifungal agent

Chemical Names

(±)-1-sec-Butyl-4-[p-[4-(p-[[(2R*,4S*)-2-(2,4-dichlorophenyl)-2-(1H-1,2,4-triazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy]phenyl)-1-piperazinyl]phenyl]-delta²-1,2,4-triazolin-5-one (WHO)

(±)-1-sec-Butyl-4-{4-[4-(4-{[(cis-2-(2,4-dichlorophenyl)-2-(1,2,4-triazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy}phenyl)piperazin-1-yl]phenyl}-4,5-dihydro-1,2,4-triazol-5-on (IUPAC)

Foreign Names

  • Itraconazolum (Latin)
  • Itraconazol (German)
  • Itraconazole (French)
  • Itraconazol (Spanish)

Generic Names

  • Itraconazole (OS: JAN, DCF, USAN, BAN)
  • R 51211 (IS: Janssen)
  • Itraconazol (PH: Ph. Eur. 6)
  • Itraconazole (PH: BP 2010, Ph. Eur. 6)
  • Itraconazolum (PH: Ph. Eur. 6)

Brand Names

  • Adco-Sporozole
    Adcock Ingram Pharmaceuticals, South Africa


  • Bevonazole
    Bevo, Greece


  • Brovicton
    Bros, Greece


  • Canadiol
    Laboratorios Dr Esteve, Spain


  • Candistat
    Merck, India


  • Canditral
    Biogalenic, Venezuela; Glenmark, Sri Lanka; Glenmark, Singapore


  • Carexan
    Schein, Peru


  • Cladosol
    Stada, Estonia; Stada, Lithuania; Stada, Latvia


  • Cladostad
    Stada, Hungary; Stada, Poland; Stada, Slovakia


  • Congox
    Wermar, Mexico


  • Deratil
    Help, Greece


  • Doc Itraconazol
    Docpharma, Belgium


  • Etrel
    Pharmex, Greece


  • Fansidol
    Alapis Pharma, Greece


  • Fitocyd
    Unipharm, Mexico


  • Flunol
    Farmanic Chemipharma, Greece


  • Forcanox
    Guardian Pharmatama, Indonesia


  • Fungitrazol
    Ikapharmindo, Indonesia


  • Fungonazol
    Verisfield, Greece


  • Fungosin
    Dollder, Venezuela


  • Fungospor
    Suan Farma S.A., Greece


  • Funit
    Nobel, Turkey


  • Gosegyne
    Effik, Switzerland


  • Hongoseril
    Isdin, Spain


  • Icomein
    Everest, Taiwan


  • Icona
    Farmaline, Thailand


  • Iconazon
    Taiyo Pharmaceutical, Japan


  • Idenolart
    Choseido Pharmaceutical, Japan


  • Idranox
    Gap, Greece


  • Inburacec
    SBL, Mexico


  • Inrozol
    Gabriel Health, Greece


  • Irunine
    Verofarm, Russian Federation


  • Isoflon
    Proel, Greece


  • Isox
    Senosiain, Dominican Republic; Senosiain, Guatemala; Senosiain, Honduras; Senosiain, Mexico; Senosiain, Panama; Senosiain, El Salvador


  • Itodal
    Chile, Chile


  • Itorat
    Sawai Seiyaku, Japan


  • Itra
    Opalia, Tunisia; Square, Bangladesh


  • Itrabene Dermis
    Ratiopharm, Austria


  • Itrabene
    Ratiopharm, Austria


  • Itrabest
    Phoinix Pharm, Greece


  • Itrac
    Belupo, Croatia (Hrvatska); Pablo Cassara, Argentina


  • Itracol Hexal
    Hexal, Germany


  • Itracol
    Merck, Slovenia


  • Itracon
    Med-One, Greece; Navana, Bangladesh; Unison, Myanmar; Nichi-Iko PharmaceuticalJMA, Japan


  • Itraconal
    Polyhronis, Greece


  • Itraconax
    Drossapharm, Switzerland


  • Itraconazol A
    Apothecon, Netherlands


  • Itraconazol AbZ
    AbZ, Germany


  • Itraconazol Actavis
    Actavis, Denmark; Actavis, Estonia; Actavis, Lithuania; Actavis, Latvia; Actavis, Malta; Actavis, Netherlands


  • Itraconazol AL
    Aliud, Germany


  • Itraconazol Alpharma
    Alpharma, Portugal


  • Itraconazol Alter
    Alter, Spain; Alter, Portugal


  • Itraconazol Apotex
    Apotex, Belgium


  • Itraconazol AWD
    AWD.pharma, Germany


  • Itraconazol Axapharm
    Axapharm, Switzerland


  • Itraconazol Bexal
    Bexal, Spain


  • Itraconazol CF
    Centrafarm, Netherlands


  • Itraconazol dura
    Mylan dura, Germany


  • Itraconazol Farmindustria
    Farmindustria, Peru


  • Itraconazol Generis
    Generis, Portugal


  • Itraconazol Germed
    Germed, Portugal


  • Itraconazol Helvepharm
    Helvepharm, Switzerland


  • Itraconazol Heumann
    Heumann, Germany


  • Itraconazol Infarmasa
    Infarmasa, Peru


  • Itraconazol Iqfarma
    Iqfarma, Peru


  • Itraconazol J-C
    Janssen, Netherlands


  • Itraconazol Merck NM
    Mylan, Denmark


  • Itraconazol Merck
    Merck Genericos, Spain; Mylan, Netherlands


  • Itraconazol PCH
    Pharmachemie, Netherlands


  • Itraconazol Ratiopharm
    Ratiopharm, Portugal


  • Itraconazol Sandoz
    Sandoz, Austria; Sandoz, Switzerland; Sandoz, Germany; Sandoz, Denmark; Sandoz, Spain; Sandoz, Hungary; Sandoz, Netherlands; Sandoz, Sweden


  • Itraconazol Spirig
    Spirig Pharma, Switzerland


  • Itraconazol Stada
    Stada, Austria; Stada, Germany; Stada, Netherlands


  • Itraconazol Universal
    Sandoz, Portugal


  • Itraconazol Winthrop
    Winthrop, Germany


  • Itraconazol
    Dermapharm, Netherlands; Slavia Pharm, Romania


  • Itraconazol-1A Pharma
    1A Pharma, Germany


  • Itraconazol-Cimex
    Cimex, Switzerland


  • Itraconazol-CT
    CT Arzneimittel, Germany


  • Itraconazole EG
    Eurogenerics, Belgium; Eurogenerics, Luxembourg


  • Itraconazole Kobayashi
    Kobayashi Kako, Japan


  • Itraconazole Mylan
    Mylan, Belgium; Mylan, France


  • Itraconazole Sandoz
    Sandoz, France


  • Itraconazole Teva
    Teva Santé, France


  • Itraconazole
    Sandoz, United States


  • Itraconazol-Mepha
    Mepha Pharma, Switzerland


  • Itraconazolo DOC
    DOC Generici, Italy


  • Itraconazolo EG
    EG, Italy


  • Itraconazolo Mylan
    Mylan, Italy


  • Itraconazolo Ratiopharm
    Ratiopharm, Italy


  • Itraconazolo Sandoz
    Sandoz, Italy


  • Itraconazolo Teva
    Teva, Italy


  • Itraconazol-ratiopharm
    Ratiopharm, Germany; Ratiopharm, Denmark; Ratiopharm, Hungary; Ratiopharm, Netherlands


  • Itraconbeta
    Betapharm, Germany


  • Itraconet
    Takata Seiyaku, Japan


  • Itraderm
    Dermapharm, Switzerland; Dermapharm, Germany


  • Itrafungol (veterinary use)
    Biokema, Switzerland; Janssen Animal, Norway; Janssen Animal, Portugal; Janssen Animal Health, Belgium; Janssen Animal Health, Germany; Janssen Animal Health, United Kingdom; Janssen Animal Health, Ireland; Janssen Animal Health, Netherlands; Janssen Pharmaceutica N.V., Luxembourg; Janssen Santé Animale, France; Janssen-Cilag, Austria; Janssen-Cilag Vet., Italy; Orion, Finland; Orion, Sweden


  • Itragen
    Generics, Hungary


  • Itrahexal
    Hexal, Brazil


  • Itrakonazol Actavis
    Actavis, Sweden


  • Itrakonazol Sandoz
    Sandoz, Czech Republic; Sandoz, Slovakia


  • Itrakonazol STADA
    Stada, Sweden


  • Itralfa
    Chrispa, Greece


  • Itramicol
    AC Farma, Peru


  • Itranax
    Janssen, Mexico


  • Itranazole
    Adipharm, Bulgaria


  • Itranol
    Rafa, Israel


  • Itranols
    Olainfarm, Latvia


  • Itranstad
    Stada, Vietnam


  • Itraproton
    Proton Pharma, Greece


  • Itrareel
    Zensei Yakuhin, Japan


  • Itraspor
    Eczacibasi, Turkey; Suan Farma S.A., Greece


  • Itrasporin
    Medis, Slovenia


  • Itraviron
    Farmedia, Greece


  • Itrazol
    Saja Pharmaceuticals, Oman; Verisfield, Greece


  • Itrizole
    Janssen Pharmaceutical K.K., Japan


  • Itrol
    Suiphar, Colombia


  • Itzol
    Lapi Laboratories, Indonesia


  • Kanazol
    Slaviamed, Serbia


  • Laverio
    Elpen, Greece


  • Lorenzol
    Rafarm, Greece


  • Lozartil
    Novag, Mexico


  • Merck-Itraconazole
    Merck Generics, South Africa


  • Mesmor
    Rafarm, Greece


  • Micoral
    Pharmalab, Peru


  • Micotenk
    Biotenk, Argentina


  • Micronazol
    Pharma Line, Greece


  • Mycodrox
    Biospray, Greece


  • Neo-Candimyk
    Viofar, Greece


  • Niddazol
    Stada, Denmark


  • Nitridazol
    HLB, Argentina


  • Norspor
    Pond's, Thailand


  • Nufatrac
    Nufarindo, Indonesia


  • Omicral
    Medico, Hungary


  • Oromic
    Janssen, Spain


  • Orungal
    Janssen, Georgia; Janssen, Hungary; Janssen, Poland; Janssen, Romania; Janssen, Russian Federation; Janssen-Cilag, Lithuania; Johnson & Johnson, Estonia; Johnson & Johnson, Latvia


  • Orunit
    Obolenskoe, Russian Federation


  • Panastat
    Panalab, Argentina


  • Petrazole
    Pharos, Indonesia


  • Prokanazol
    Liconsa, Serbia; Pro.Med.CS, Czech Republic; Pro.Med.CS, Estonia


  • Rixtal
    Biomep, Mexico


  • Rumycoz
    Otechestvennye Lekarstva, Russian Federation


  • Salimidin
    LKM, Argentina


  • Sempera
    Janssen, Germany


  • Silicsan
    Rayere, Mexico


  • Sinozol
    Best, Mexico


  • Siros
    Janssen, Germany


  • Spazol
    Siam Bheasach, Thailand


  • Sporacid
    Ferron, Indonesia


  • Sporal
    Janssen, Myanmar; Janssen, Thailand; Janssen-Cilag, Malta; Janssen-Cilag, Vietnam


  • Sporanox
    Aktuapharma, Belgium; Janssen, Antigua & Barbuda; Janssen, Netherlands Antilles; Janssen, Argentina; Janssen, Australia; Janssen, Aruba; Janssen, Belgium; Janssen, Bermuda; Janssen, Brazil; Janssen, Bahamas; Janssen, Colombia; Janssen, Costa Rica; Janssen, Cyprus; Janssen, Czech Republic; Janssen, Dominican Republic; Janssen, Ecuador; Janssen, Spain; Janssen, Finland; Janssen, Grenada; Janssen, Greece; Janssen, Guatemala; Janssen, Guyana; Janssen, Hong Kong; Janssen, Honduras; Janssen, Ireland; Janssen, Israel; Janssen, Iceland; Janssen, Italy; Janssen, Jamaica; Janssen, Cayman Islands; Janssen, Lebanon; Janssen, Saint Lucia; Janssen, Sri Lanka; Janssen, Luxembourg; Janssen, Mexico; Janssen, Malaysia; Janssen, Nicaragua; Janssen, Norway; Janssen, New Zealand; Janssen, Panama; Janssen, Peru; Janssen, Philippines; Janssen, Portugal; Janssen, Serbia; Janssen, Saudi Arabia; Janssen, Sudan; Janssen, Singapore; Janssen, Slovakia; Janssen, Suriname; Janssen, El Salvador; Janssen, Trinidad & Tobago; Janssen, Taiwan; Janssen, Saint Vincent & The Grenadines; Janssen, Venezuela; Janssen, Yemen; Janssen Pharmaceutical, Ethiopia; Janssen-Cilag, United Arab Emirates; Janssen-Cilag, Austria; Janssen-Cilag, Switzerland; Janssen-Cilag, Chile; Janssen-Cilag, Denmark; Janssen-Cilag, Egypt; Janssen-Cilag, France; Janssen-Cilag, United Kingdom; Janssen-Cilag, Indonesia; Janssen-Cilag, Jordan; Janssen-Cilag, Lithuania; Janssen-Cilag, Oman; Janssen-Cilag, Sweden; Janssen-Cilag, South Africa; Janssen-Ortho Inc., Canada; Johnson & Johnson, Slovenia; Ortho-McNeil, United States; Pharmapartner, Belgium


  • Sporanox (veterinary use)
    Janssen Animal Health, United Kingdom


  • Sporax
    Dexa Medica, Indonesia


  • Sporex
    Toprak, Turkey


  • Spyrocon
    Interbat, Indonesia


  • Teramic
    Andromaco, Chile


  • Toracona
    Nichi-Iko PharmaceuticalJMA, Japan


  • Trachon
    Bernofarm, Indonesia


  • Traconal
    Aché, Brazil


  • Tracor
    Pharmacore Labs, Indonesia


  • Tranazol
    Farmasa, Brazil


  • Trazer
    B&G, Italy


  • Triasporin
    Italfarmaco, Italy


  • Trioxal
    Polpharma, Poland


  • Trisporal
    Janssen, Netherlands; Janssen-Cilag, South Africa


  • Unitrac
    Kalbe, Indonesia; Kalbe Farma, Myanmar; Kalbe Farma - Dankos, Sri Lanka

International Drug Name Search

Glossary

BANBritish Approved Name
DCFDénomination Commune Française
IUPACInternational Union of Pure and Applied Chemistry
ISInofficial Synonym
JANJapanese Accepted Name
OSOfficial Synonym
PHPharmacopoeia Name
Rec.INNRecommended International Nonproprietary Name (World Health Organization)
SPC Summary of Product Characteristics (UK)
USANUnited States Adopted Name
WHOWorld Health Organization

Click for further information on drug naming conventions and International Nonproprietary Names.

Saturday, 19 November 2011

Doan's Extra Strength


Generic Name: salicylate (Oral route, Rectal route)


Commonly used brand name(s)

In the U.S.


  • Amigesic

  • Asacol

  • Azulfidine

  • Azulfidine Entabs

  • Bayer

  • Canasa

  • Colazal

  • Dipentum

  • Doan's Extra Strength

  • Doan's Regular

  • Dolobid

  • Ecotrin

  • Kaopectate

  • Pepto Bismol

  • Salflex

  • Tricosal

  • Trilisate

In Canada


  • Alti-Sulfasalazine

  • Arthropan

  • Asacol 800

  • Bismuth Extra Strength

  • Bismuth Original Formula

  • Mesasal

  • Pentasa

  • Pepto-Bismol

  • Pms-Asa Suppository Adult

  • Pms-Asa Suppository Children

  • Salazopyrin

  • Salofalk

Available Dosage Forms:


  • Tablet, Enteric Coated

  • Tablet, Extended Release

  • Suppository

  • Tablet

  • Capsule

  • Tablet, Chewable

  • Tablet, Effervescent

  • Capsule, Delayed Release

  • Gum

  • Tablet, Delayed Release

  • Enema

  • Capsule, Extended Release

  • Liquid

  • Solution

  • Suspension

Uses For Doan's Extra Strength


Aspirin may also be used to lessen the chance of heart attack, stroke, or other problems that may occur when a blood vessel is blocked by blood clots. Aspirin helps prevent dangerous blood clots from forming. However, this effect of aspirin may increase the chance of serious bleeding in some people. Therefore, aspirin should be used for this purpose only when your doctor decides, after studying your medical condition and history, that the danger of blood clots is greater than the risk of bleeding. Do not take aspirin to prevent blood clots or a heart attack unless it has been ordered by your doctor.


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


The caffeine present in some of these products may provide additional relief of headache pain or faster pain relief.


Some salicylates are available only with your medical doctor's or dentist's prescription. Others are available without a prescription; however, your medical doctor or dentist may have special instructions on the proper dose of these medicines for your medical condition.


Importance of Diet


Make certain your health care professional knows if you are on a low-sodium diet. Regular use of large amounts of sodium salicylate (as for arthritis) can add a large amount of sodium to your diet. Sodium salicylate contains 46 mg of sodium in each 325-mg tablet and 92 mg of sodium in each 650-mg tablet.


Before Using Doan's Extra Strength


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


Do not give aspirin or other salicylates to a child or a teenager with a fever or other symptoms of a virus infection, especially flu or chickenpox, without first discussing its use with your child's doctor. This is very important because salicylates may cause a serious illness called Reye's syndrome in children and teenagers with fever caused by a virus infection, especially flu or chickenpox.


Some children may need to take aspirin or another salicylate regularly (as for arthritis). However, your child's doctor may want to stop the medicine for a while if a fever or other symptoms of a virus infection occur. Discuss this with your child's doctor, so that you will know ahead of time what to do if your child gets sick.


Children who do not have a virus infection may also be more sensitive to the effects of salicylates, especially if they have a fever or have lost large amounts of body fluid because of vomiting, diarrhea, or sweating. This may increase the chance of side effects during treatment.


Geriatric


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


Pregnancy


Salicylates have not been shown to cause birth defects in humans. Studies on birth defects in humans have been done with aspirin but not with other salicylates. However, salicylates caused birth defects in animal studies.


Some reports have suggested that too much use of aspirin late in pregnancy may cause a decrease in the newborn's weight and possible death of the fetus or newborn infant. However, the mothers in these reports had been taking much larger amounts of aspirin than are usually recommended. Studies of mothers taking aspirin in the doses that are usually recommended did not show these unwanted effects. However, there is a chance that regular use of salicylates late in pregnancy may cause unwanted effects on the heart or blood flow in the fetus or in the newborn infant.


Use of salicylates, especially aspirin, during the last 2 weeks of pregnancy may cause bleeding problems in the fetus before or during delivery or in the newborn infant. Also, too much use of salicylates during the last 3 months of pregnancy may increase the length of pregnancy, prolong labor, cause other problems during delivery, or cause severe bleeding in the mother before, during, or after delivery. Do not take aspirin during the last 3 months of pregnancy unless it has been ordered by your doctor.


Studies in humans have not shown that caffeine (present in some aspirin products) causes birth defects. However, studies in animals have shown that caffeine causes birth defects when given in very large doses (amounts equal to those present in 12 to 24 cups of coffee a day).


Breast Feeding


Salicylates pass into the breast milk. Although salicylates have not been reported to cause problems in nursing babies, it is possible that problems may occur if large amounts are taken regularly, as for arthritis (rheumatism).


Caffeine passes into the breast milk in small amounts.


Interactions with Medicines


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


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


  • Influenza Virus Vaccine, Live

  • Ketorolac

  • Pentoxifylline

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


  • Abciximab

  • Acenocoumarol

  • Alteplase, Recombinant

  • Anisindione

  • Ardeparin

  • Argatroban

  • Beta Glucan

  • Bivalirudin

  • Certoparin

  • Cilostazol

  • Citalopram

  • Clopidogrel

  • Clovoxamine

  • Dabigatran Etexilate

  • Dalteparin

  • Danaparoid

  • Desirudin

  • Desvenlafaxine

  • Dicumarol

  • Dipyridamole

  • Duloxetine

  • Enoxaparin

  • Eptifibatide

  • Escitalopram

  • Femoxetine

  • Flesinoxan

  • Fluoxetine

  • Fluvoxamine

  • Fondaparinux

  • Ginkgo

  • Heparin

  • Ketoprofen

  • Lepirudin

  • Methotrexate

  • Milnacipran

  • Nadroparin

  • Naproxen

  • Nefazodone

  • Parnaparin

  • Paroxetine

  • Pemetrexed

  • Phenindione

  • Phenprocoumon

  • Protein C

  • Reteplase, Recombinant

  • Reviparin

  • Riluzole

  • Rivaroxaban

  • Sertraline

  • Sibutramine

  • Tacrolimus

  • Ticlopidine

  • Tinzaparin

  • Tirofiban

  • Varicella Virus Vaccine

  • Venlafaxine

  • Vilazodone

  • Warfarin

  • Zimeldine

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:


  • Anemia or

  • Overactive thyroid or

  • Stomach ulcer or other stomach problems—Salicylates may make your condition worse.

  • Asthma, allergies, and nasal polyps (history of) or

  • Glucose-6-phosphate dehydrogenase (G6PD) deficiency or

  • High blood pressure (hypertension) or

  • Kidney disease or

  • Liver disease—The chance of side effects may be increased.

  • Gout—Salicylates can make this condition worse and can also lessen the effects of some medicines used to treat gout.

  • Heart disease—The chance of some side effects may be increased. Also, the caffeine present in some aspirin products can make some kinds of heart disease worse.

  • Hemophilia or other bleeding problems—The chance of bleeding may be increased, especially with aspirin.

Proper Use of salicylate

This section provides information on the proper use of a number of products that contain salicylate. It may not be specific to Doan's Extra Strength. Please read with care.


Take this medicine after meals or with food (except for enteric-coated capsules or tablets and aspirin suppositories) to lessen stomach irritation.


Take tablet or capsule forms of this medicine with a full glass (8 ounces) of water. Also, do not lie down for about 15 to 30 minutes after swallowing the medicine. This helps to prevent irritation that may lead to trouble in swallowing.


For patients taking aspirin (including buffered aspirin and/or products containing caffeine):


  • Do not use any product that contains aspirin if it has a strong, vinegar-like odor. This odor means the medicine is breaking down. If you have any questions about this, check with your health care professional.

  • If you are to take any medicine that contains aspirin within 7 days after having your tonsils removed, a tooth pulled, or other dental or mouth surgery, be sure to swallow the aspirin whole. Do not chew aspirin during this time.

  • Do not place any medicine that contains aspirin directly on a tooth or gum surface. This may cause a burn.

  • There are several different forms of aspirin or buffered aspirin tablets. If you are using:
    • chewable aspirin tablets, they may be chewed, dissolved in liquid, crushed, or swallowed whole.

    • delayed-release (enteric-coated) aspirin tablets, they must be swallowed whole. Do not crush them or break them up before taking.

    • extended-release (long-acting) aspirin tablets, check with your pharmacist as to how they should be taken. Some may be broken up (but must not be crushed) before swallowing if you cannot swallow them whole. Others should not be broken up and must be swallowed whole.


To use aspirin 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.

To take choline and magnesium salicylates (e.g., Trilisate) oral solution:


  • The liquid may be mixed with fruit juice just before taking.

  • Drink a full glass (8 ounces) of water after taking the medicine.

To take enteric-coated sodium salicylate tablets:


  • The tablets must be swallowed whole. Do not crush them or break them up before taking.

Unless otherwise directed by your medical doctor or dentist:


  • Do not take more of this medicine than recommended on the label, to lessen the chance of side effects.

  • Children up to 12 years of age should not take this medicine more than 5 times a day.

When used for arthritis (rheumatism), this medicine must be taken regularly as ordered by your doctor in order for it to help you. Up to 2 to 3 weeks or longer may pass before you feel the full effects of this medicine.


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 aspirin

  • For oral dosage forms (short-acting tablets, chewable tablets, and delayed-release [enteric-coated] tablets):
    • For pain or fever:
      • Adults and teenagers—325 to 500 milligrams (mg) every three or four hours, 650 mg every four to six hours, or 1000 mg every six hours as needed.

      • Children 11 to 12 years of age—320 to 480 mg every four hours as needed.

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

      • Children 6 to 9 years of age—320 to 325 mg every four hours as needed.

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

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

      • Children up to 2 years of age—Dose must be determined by your doctor.


    • For arthritis:
      • Adults and teenagers—A total of 3600 to 5400 mg a day, divided into several smaller doses.

      • Children—A total of 80 to 100 mg per kilogram (kg) (32 to 40 mg per pound) of body weight a day, divided into several smaller doses.


    • For preventing a heart attack, stroke, or other problems caused by blood clots:
      • Adults—Most people will take 81, 162.5, or 325 mg a day or 325 mg every other day. Some people taking aspirin to prevent a stroke may need as much as 1000 mg a day.

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



  • For oral dosage form (chewing gum):
    • For pain:
      • Adults and teenagers—2 tablets every four hours as needed.

      • Children 6 to 12 years of age—1 or 2 tablets (227 mg each) up to four times a day.

      • Children 3 to 6 years of age—1 tablet (227 mg) up to three times a day.

      • Children up to 3 years of age—Dose must be determined by your doctor.



  • For long-acting oral dosage form (extended-release tablets):
    • For pain:
      • Adults and teenagers—1 or 2 tablets twice a day.

      • Children—The long-acting aspirin tablets are too strong for use in children.


    • For arthritis:
      • Adults and teenagers—1 or 2 tablets twice a day, at first. Your doctor will then adjust your dose as needed.

      • Children—The long-acting aspirin tablets are too strong for use in children.



  • For rectal dosage form (suppositories):
    • For pain or fever:
      • Adults and teenagers—325 to 650 mg every four hours as needed.

      • Children 11 to 12 years of age—325 to 480 mg every four hours as needed.

      • Children 9 to 11 years of age—325 to 400 mg every four hours as needed.

      • Children 6 to 9 years of age—325 mg every four hours as needed.

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

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

      • Children up to 2 years of age—Dose must be determined by your doctor.


    • For arthritis:
      • Adults and teenagers—A total of 3600 to 5400 mg a day, divided into several smaller doses.

      • Children—A total of 80 to 100 mg per kilogram (kg) (32 to 40 mg per pound) of body weight a day, divided into several smaller doses.



  • For aspirin and caffeine

  • For oral dosage forms (capsule):
    • For pain or fever:
      • Adults and teenagers—325 to 500 milligrams (mg) of aspirin every three or four hours, 650 mg of aspirin every four to six hours, or 1000 mg of aspirin every six hours as needed.

      • Children 9 to 12 years of age—325 to 400 mg every four hours as needed.

      • Children 6 to 9 years of age—325 mg every four hours as needed.

      • Children up to 6 years of age—Aspirin and caffeine capsules are too strong for use in children up to 6 years of age


    • For preventing a heart attack, stroke, or other problems caused by blood clots:
      • Adults—325 mg a day or every other day. People who take smaller doses of aspirin will have to use a different product. Some people taking aspirin to prevent a stroke may need as much as 1000 mg a day.

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



  • For oral dosage form (tablets):
    • For pain or fever:
      • Adults and teenagers—325 to 500 mg of aspirin every three or four hours, 650 mg of aspirin every four to six hours, or 1000 mg of aspirin every six hours as needed.

      • Children 9 to 12 years of age—325 to 400 mg every four hours as needed.

      • Children up to 9 years of age—Aspirin and caffeine tablets are too strong for use in children up to 9 years of age.


    • For arthritis:
      • Adults and teenagers—A total of 3600 to 5400 mg of aspirin a day, divided into several smaller doses.

      • Children—A total of 80 to 100 mg per kg (32 to 40 mg per pound) of body weight a day, divided into several smaller doses.


    • For preventing a heart attack, stroke, or other problems caused by blood clots:
      • Adults—325 mg a day or every other day. People who take smaller doses of aspirin will have to use a different product. Some people taking aspirin to prevent a stroke may need as much as 1000 mg a day.

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



  • For buffered aspirin

  • For oral dosage forms (tablets):
    • For pain or fever:
      • Adults and teenagers—325 to 500 milligrams (mg) of aspirin every three or four hours, 650 mg of aspirin every four to six hours, or 1000 mg of aspirin every six hours as needed.

      • Children 11 to 12 years of age—One or one and one-half 325-mg tablets every four hours as needed.

      • Children 9 to 11 years of age—One or one and one-fourth 325-mg tablets every four hours as needed.

      • Children 6 to 9 years of age—One 325-mg tablet every four hours as needed.

      • Children 4 to 6 years of age—Three-fourths of a 325-mg tablet every four hours as needed.

      • Children 2 to 4 years of age—One-half of a 325-mg tablet every four hours as needed.

      • Children up to 2 years of age—Dose must be determined by your doctor.


    • For arthritis:
      • Adults and teenagers—A total of 3600 to 5400 mg of aspirin a day, divided into several smaller doses.

      • Children—A total of 80 to 100 mg per kilogram (kg) (32 to 40 mg per pound) of body weight a day, divided into several smaller doses.


    • For preventing a heart attack, stroke, or other problems caused by blood clots:
      • Adults—325 mg a day or every other day. People who take smaller doses of aspirin will have to use a different product. Some people taking aspirin to prevent a stroke may need as much as 1000 mg a day.

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



  • For buffered aspirin and caffeine

  • For oral dosage form (tablets):
    • For pain or fever:
      • Adults and teenagers—325 or 421 milligrams (mg) of aspirin every three or four hours, 650 mg of aspirin every four to six hours, or 842 mg of aspirin every six hours as needed.

      • Children 11 to 12 years of age—One or one and one-half 325-mg tablets, or one 421-mg tablet, every four hours as needed.

      • Children 9 to 11 years of age—One or one and one-fourth 325-mg tablets every four hours as needed.

      • Children 6 to 9 years of age—One 325-mg or 421-mg tablet every four hours as needed.

      • Children 4 to 6 years of age—Three-fourths of a 325-mg tablet every four hours as needed.

      • Children 2 to 4 years of age—One-half of a 325-mg tablet every four hours as needed.

      • Children up to 2 years of age—Dose must be determined by your doctor.


    • For arthritis:
      • Adults and teenagers—A total of 3600 to 5400 mg of aspirin a day, divided into several smaller doses.

      • Children—A total of 80 to 100 mg per kilogram (kg) (32 to 40 mg per pound) of body weight a day, divided into several smaller doses.


    • For preventing a heart attack, stroke, or other problems caused by blood clots:
      • Adults—162.5 or 325 mg (one-half or one 325-mg tablet) a day or 325 mg every other day. People who need smaller doses of aspirin will have to use a different product. Some people taking aspirin to prevent a stroke may need as much as 1000 mg a day.

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



  • For choline salicylate

  • For oral dosage form (oral solution):
    • For pain or fever:
      • Adults and teenagers—One-half or three-fourths of a teaspoonful every three hours, one-half or one teaspoonful every four hours, or one or one and one-half teaspoonfuls every six hours as needed.

      • Children 11 to 12 years of age—2.5 to 3.75 mL (one-half to three-fourths of a teaspoonful) every four hours as needed. This amount should be measured by a special measuring spoon.

      • Children 6 to 11 years of age—2.5 mL (one-half of a teaspoonful) every four hours as needed. This amount should be measured by a special measuring spoon.

      • Children 4 to 6 years of age—1.66 mL every four hours as needed. This amount should be measured by a special dropper or measuring spoon.

      • Children 2 to 4 years of age—1.25 milliliters (mL) (one-fourth of a teaspoonful) every four hours as needed. This amount should be measured by a special dropper or measuring spoon.

      • Children up to 2 years of age—Dose must be determined by your doctor.


    • For arthritis:
      • Adults—A total of five and one-half to eight teaspoonfuls a day, divided into several smaller doses.

      • Children—A total of 0.6 to 0.7 mL per kilogram (kg) (0.25 to 0.28 mL per pound) of body weight a day, divided into several smaller doses.



  • For choline and magnesium salicylates

  • For oral dosage forms (oral solution or tablets):
    • For pain or fever:
      • Adults and teenagers—A total of 2000 to 3000 milligrams (mg) a day, divided into two or three doses.

      • Children weighing more than 37 kg (90 pounds or more)—2200 mg a day, divided into two doses.

      • Children weighing up to 37 kilograms (kg) (about 89 pounds)—A total of 50 mg per kg (20 mg per pound) of body weight a day, divided into two doses.



  • For magnesium salicylate

  • For oral dosage form (tablets):
    • For pain:
      • Adults and teenagers—2 regular-strength tablets every four hours, up to a maximum of 12 tablets a day, or 2 extra-strength tablets every eight hours, up to a maximum of 8 tablets a day.

      • Children—Dose must be determined by your doctor.



  • For salsalate

  • For oral dosage forms (capsules or tablets):
    • For arthritis:
      • Adults and teenagers—500 to 1000 milligrams (mg) two or three times a day, to start. Your doctor will then adjust your dose as needed.

      • Children—Dose must be determined by your doctor.



  • For sodium salicylate

  • For oral dosage forms (tablets or delayed-release [enteric-coated] tablets):
    • For pain or fever:
      • Adults and teenagers—325 or 650 milligrams (mg) every four hours as needed.

      • Children 6 years of age and older—325 mg every four hours as needed.

      • Children up to 6 years of age—This medicine is too strong for use in children younger than 6 years of age.


    • For arthritis:
      • Adults and teenagers—A total of 3600 to 5400 mg a day, divided into several smaller doses.

      • Children—A total of 80 to 100 mg per kilogram (kg) (32 to 40 mg per pound) of body weight a day, divided into several smaller doses.



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.


Do not keep outdated medicine or medicine no longer needed.


Precautions While Using Doan's Extra Strength


Check the labels of all nonprescription (over-the-counter [OTC]) and prescription medicines you now take. If any contain aspirin or other salicylates (including bismuth subsalicylate [e.g., Pepto-Bismol] or any shampoo or skin medicine that contains salicylic acid or any other salicylate), check with your health care professional. Taking or using them together with this medicine may cause an overdose.


If you will be taking salicylates for a long time (more than 5 days in a row for children or 10 days in a row for adults) or in large amounts, your doctor should check your progress at regular visits.


Serious side effects can occur during treatment with this medicine. Sometimes serious side effects can occur without any warning. However, possible warning signs often occur, including swelling of the face, fingers, feet, and/or lower legs; severe stomach pain, black, tarry stools, and/or vomiting of blood or material that looks like coffee grounds; unusual weight gain; and/or skin rash. Also, signs of serious heart problems could occur such as chest pain, tightness in chest, fast or irregular heartbeat, or unusual flushing or warmth of skin. Stop taking this medicine and check with your doctor immediately if you notice any of these warning signs.


Check with your medical doctor or dentist:


  • If you are taking this medicine to relieve pain and the pain lasts for more than 10 days (5 days for children) or if the pain gets worse, if new symptoms occur, or if redness or swelling is present. 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, if the fever gets worse, if new symptoms occur, or if 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.

  • If you are taking this medicine regularly, as for arthritis (rheumatism), and you notice a ringing or buzzing in your ears or severe or continuing headaches. These are often the first signs that too much salicylate is being taken. Your doctor may want to change the amount of medicine you are taking every day.

For patients taking aspirin to lessen the chance of heart attack, stroke, or other problems caused by blood clots:


  • Take only the amount of aspirin ordered by your doctor. If you need a medicine to relieve pain, a fever, or arthritis, your doctor may not want you to take extra aspirin. It is a good idea to discuss this with your doctor, so that you will know ahead of time what medicine to take.

  • Do not stop taking this medicine for any reason without first checking with the doctor who directed you to take it.

Taking certain other medicines together with a salicylate 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 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 a salicylate for more than a few days, unless your doctor has directed you to do so and is following your progress:


  • Acetaminophen (e.g., Tylenol)

  • 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., Mobiflex)

  • Tiaprofenic acid (e.g., Surgam)

  • Tolmetin (e.g., Tolectin)

For diabetic patients:


  • False urine sugar test results may occur if you are regularly taking large amounts of salicylates, such as:
    • Aspirin: 8 or more 325-mg (5-grain), or 4 or more 500-mg or 650-mg (10-grain), or 3 or more 800-mg (or higher strength), doses a day.

    • Buffered aspirin or

    • Sodium salicylate: 8 or more 325-mg (5-grain), or 4 or more 500-mg or 650-mg (10-grain), doses a day.

    • Choline salicylate: 4 or more teaspoonfuls (each teaspoonful containing 870 mg) a day.

    • Choline and magnesium salicylates: 5 or more 500-mg tablets or teaspoonfuls, 4 or more 750-mg tablets, or 2 or more 1000-mg tablets, a day.

    • Magnesium salicylate: 7 or more regular-strength, or 4 or more extra-strength, tablets a day.

    • Salsalate: 4 or more 500-mg doses, or 3 or more 750-mg doses, a day.


  • Smaller doses or occasional use of salicylates usually will not affect urine sugar tests. However, check with your health care professional (especially if your diabetes is not well-controlled) if:
    • you are not sure how much salicylate you are taking every day.

    • you notice any change in your urine sugar test results.

    • you have any other questions about this possible problem.


Do not take aspirin for 5 days before any surgery, including dental surgery, unless otherwise directed by your medical doctor or dentist. Taking aspirin during this time may cause bleeding problems.


For patients taking buffered aspirin, choline and magnesium salicylates (e.g., Trilisate), or magnesium salicylate (e.g., Doan's):


  • Buffered aspirin, choline and magnesium salicylates, or magnesium salicylate can keep many other medicines, especially some medicines used to treat infections, from working properly. This problem can be prevented by not taking the 2 medicines too close together. Ask your health care professional how long you should wait between taking a medicine for infection and taking buffered aspirin, choline and magnesium salicylates, or magnesium salicylate.

If you are taking a laxative containing cellulose, take the salicylate at least 2 hours before or after you take the laxative. Taking these medicines too close together may lessen the effects of the salicylate.


For patients taking this medicine by mouth:


  • Stomach problems may be more likely to occur if you drink alcoholic beverages while being treated with this medicine, especially if you are taking it in high doses or for a long time. Check with your doctor if you have any questions about this.

For patients using aspirin suppositories:


  • Aspirin suppositories may cause irritation of the rectum. Check with your doctor if this occurs.

Salicylates may interfere with the results of some medical tests. Before you have any medical tests, tell the doctor in charge if you have taken any of these medicines within the past week. If possible, it is best to check with the doctor first, to find out whether the medicine may be taken during the week before the test.


For patients taking one of the products that contain caffeine:


  • Caffeine may interfere with the result 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 at least 8 to 12 hours before the test.

If you think that you or anyone else may have taken an overdose, get emergency help at once. Taking an overdose of these medicines may cause unconsciousness or death. Signs of overdose include convulsions (seizures), hearing loss, confusion, ringing or buzzing in the ears, severe drowsiness or tiredness, severe excitement or nervousness, and fast or deep breathing.


Doan's Extra Strength 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.


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


Symptoms of overdose in children
  • Changes in behavior

  • drowsiness or tiredness (severe)

  • fast or deep breathing

  • Any loss of hearing

  • bloody urine

  • confusion

  • convulsions (seizures)

  • diarrhea (severe or continuing)

  • difficulty in swallowing

  • dizziness, lightheadedness, or feeling faint (severe)

  • drowsiness (severe)

  • excitement or nervousness (severe)

  • fast or deep breathing

  • flushing, redness, or other change in skin color

  • hallucinations (seeing, hearing, or feeling things that are not there)

  • increased sweating

  • increased thirst

  • nausea or vomiting (severe or continuing)

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

  • stomach pain (severe or continuing)

  • swelling of eyelids, face, or lips

  • unexplained fever

  • uncontrollable flapping movements of the hands (especially in elderly patients)

  • vision problems

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


Less common or rare
  • Abdominal or stomach pain, cramping, or burning (severe)

  • bloody or black, tarry stools

  • headache (severe or continuing)

  • ringing or buzzing in ears (continuing)

  • skin rash, hives, or itching

  • unusual tiredness or weakness

  • vomiting of blood or material that looks like coffee grounds

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


More common
  • Abdominal or stomach cramps, pain, or discomfort (mild to moderate)

  • heartburn or indigestion

  • nausea or vomiting

Less common
  • Trouble in sleeping, nervousness, or jitters (only for products containing caffeine)

Other side effects not listed may also occur in some patients. If you notice any other effects, check with your healthcare professional.


Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.



The information contained in the Thomson Reuters Micromedex products as delivered by Drugs.com is intended as an educational aid only. It is not intended as medical advice for individual conditions or treatment. It is not a substitute for a medical exam, nor does it replace the need for services provided by medical professionals. Talk to your doctor, nurse or pharmacist before taking any prescription or over the counter drugs (including any herbal medicines or supplements) or following any treatment or regimen. Only your doctor, nurse, or pharmacist can provide you with advice on what is safe and effective for you.


The use of the Thomson Reuters Healthcare products is at your sole risk. These products are provided "AS IS" and "as available" for use, without warranties of any kind, either express or implied. Thomson Reuters Healthcare and Drugs.com make no representation or warranty as to the accuracy, reliability, timeliness, usefulness or completeness of any of the information contained in the products. Additionally, THOMSON REUTERS HEALTHCARE MAKES NO REPRESENTATION OR WARRANTIES AS TO THE OPINIONS OR OTHER SERVICE OR DATA YOU MAY ACCESS, DOWNLOAD OR USE AS A RESULT OF USE OF THE THOMSON REUTERS HEALTHCARE PRODUCTS. ALL IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE OR USE ARE HEREBY EXCLUDED. Thomson Reuters Healthcare does not assume any responsibility or risk for your use of the Thomson Reuters Healthcare products.

Friday, 18 November 2011

Famix




In some countries, this medicine may only be approved for veterinary use.

Ingredient matches for Famix



Famphur

Famphur is reported as an ingredient of Famix in the following countries:


  • United States

International Drug Name Search

Drocon-CS


Generic Name: brompheniramine, hydrocodone, and pseudoephedrine (brom fen EER a meen, hye droe KOE dohn, soo doe e FED rin)

Brand Names: Anaplex HD, Bromcomp HC, Bromph HD, Bromplex HD, BroveX HC, Drocon-CS, Endacof HC, J-Tan D HC, M-END, SymTan A, Visvex


What is Drocon-CS (brompheniramine, hydrocodone, and pseudoephedrine)?

Brompheniramine is an antihistamine that reduces the natural chemical histamine in the body. Histamine can produce symptoms of sneezing, itching, watery eyes, and runny nose.


Hydrocodone is in a group of drugs called narcotics and is similar to codeine. Hydrocodone is a cough suppressant that affects the signals in the brain that trigger cough reflex.


Pseudoephedrine is a decongestant that shrinks blood vessels in the nasal passages. Dilated blood vessels can cause nasal congestion (stuffy nose).


The combination of brompheniramine, hydrocodone, and pseudoephedrine is used to treat cough, sneezing, itching, watery eyes, runny nose, stuffy nose, and sinus congestion caused by allergies, the common cold, or the flu.


Brompheniramine, hydrocodone, and pseudoephedrine may also be used for other purposes not listed in this medication guide.


What is the most important information I should know about Drocon-CS (brompheniramine, hydrocodone, and pseudoephedrine)?


Always ask a doctor before giving a cough or cold medicine to a child. Death can occur from the misuse of cough and cold medicines in very young children. Do not take this medication with alcohol, other narcotic pain medications, sedatives, tranquilizers, muscle relaxers, or other medicines that can make you sleepy or slow your breathing. Dangerous side effects may result. Hydrocodone may be habit-forming and should be used only by the person it was prescribed for. Hydrocodone should never be shared with another person, especially someone who has a history of drug abuse or addiction. Keep the medication in a secure place where others cannot get to it. Hydrocodone is a drug of abuse and you should be aware if any person in the household is using this medicine improperly or without a prescription. Do not use any other over-the-counter cough, cold, allergy, or sleep medication without first asking your doctor or pharmacist. If you take certain products together you may accidentally take too much of one or more types of medicine. Read the label of any other medicine you are using to see if it contains an antihistamine, decongestant, or cough suppressant. This medication can cause side effects that may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be awake and alert.

What should I discuss with my healthcare provider before taking Drocon-CS (brompheniramine, hydrocodone, and pseudoephedrine)?


Do not use this medication if you are allergic to hydrocodone or other narcotic pain relievers such as fentanyl (Actiq, Duragesic), hydromorphone (Dilaudid, Palladone), methadone (Methadose, Dolophine), morphine (Kadian, MS Contin, Oramorph, and others), oxycodone (OxyContin), and oxymorphone (Opana). Do not use a cough or cold medicine if you have used an MAO inhibitor such as isocarboxazid (Marplan), phenelzine (Nardil), rasagiline (Azilect), selegiline (Eldepryl, Emsam), or tranylcypromine (Parnate) within the past 14 days. Serious, life-threatening side effects can occur if you take cough or cold medicine before the MAO inhibitor has cleared from your body.

Before taking brompheniramine, hydrocodone, and pseudoephedrine, tell your doctor if you are allergic to any drugs, or if you have:



  • kidney or liver disease;




  • heart disease or high blood pressure;




  • enlarged prostate or urination problems;




  • diabetes;




  • glaucoma;




  • a thyroid disorder;




  • asthma, COPD, sleep apnea, or other breathing disorders;




  • a history of head injury or brain tumor;




  • epilepsy or other seizure disorder;




  • low blood pressure;




  • gallbladder disease;




  • Addison's disease or other adrenal gland disorders;




  • mental illness; or




  • a history of drug or alcohol addiction.



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


FDA pregnancy category C. Hydrocodone may be harmful to an unborn baby, and could cause addiction or withdrawal symptoms in a newborn. Tell your doctor if you are pregnant or plan to become pregnant during treatment. This medication may pass into breast milk and could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby. Hydrocodone may be habit-forming and should be used only by the person it was prescribed for. Hydrocodone should never be shared with another person, especially someone who has a history of drug abuse or addiction. Keep the medication in a secure place where others cannot get to it. Hydrocodone is a drug of abuse and you should be aware if any person in the household is using this medicine improperly or without a prescription.

How should I take Drocon-CS (brompheniramine, hydrocodone, and pseudoephedrine)?


Take this medication exactly as it was prescribed for you. Do not take the medication in larger amounts, or take it for longer than recommended by your doctor. Follow the directions on your prescription label. Cough or cold medicine is usually taken for only a short time until your symptoms clear up.


Always ask a doctor before giving cough or cold medicine to a child. Death can occur from the misuse of cough or cold medicine in very young children.

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


Talk with your doctor if your symptoms do not improve after 7 days of treatment, or if you have a fever with a headache, cough, or skin rash.

If you need to have any type of surgery, tell the surgeon ahead of time if you have taken a cold medicine within the past few days.


This medication can cause you to have unusual results with allergy skin tests. Tell any doctor who treats you that you are taking an antihistamine.


Store this medicine at room temperature, away from heat, light, and moisture.

What happens if I miss a dose?


Since cough or cold medicine is usually taken only as needed, you may not be on a dosing schedule. If you are taking the medication regularly, take the missed dose as soon as you remember. If it is almost time for your next dose, skip the missed dose and take the medicine at your next regularly scheduled time. Do not take 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 hydrocodone can be fatal. Overdose symptoms may include extreme dizziness or drowsiness, confusion, feeling restless or nervous, cold and clammy skin, warmth or tingly feeling, nausea, vomiting, slow or shallow breathing, slow heart rate, pinpoint pupils, fainting, seizure (convulsions), or coma.

What should I avoid while taking Drocon-CS (brompheniramine, hydrocodone, and pseudoephedrine)?


This medication can cause side effects that may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be awake and alert.

Avoid becoming overheated or dehydrated during exercise and in hot weather.


Do not drink alcohol while you are taking this medication. Alcohol can increase some of the side effects of brompheniramine, hydrocodone, and pseudoephedrine. Do not take this medication with other narcotic pain medications, sedatives, tranquilizers, muscle relaxers, or other medicines that can make you sleepy or slow your breathing. Life-threatening side effects may result.

Avoid taking diet pills, caffeine pills, or other stimulants (such as ADHD medications) without your doctor's advice. Taking a stimulant together with a decongestant can increase your risk of unpleasant side effects.


Do not use any other over-the-counter cough, cold, allergy, or sleep medication without first asking your doctor or pharmacist. Brompheniramine and pseudoephedrine are contained in many medicines available over the counter. If you take certain products together you may accidentally take too much of one or more types of medicine. Read the label of any other medicine you are using to see if it contains brompheniramine or pseudoephedrine.

Drocon-CS (brompheniramine, hydrocodone, and pseudoephedrine) 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. Stop using this medication and call your doctor at once if you have any of these serious side effects:

  • fast, pounding, or uneven heartbeats;




  • shallow breathing, slow heartbeat;




  • severe dizziness, fainting, anxiety, restless feeling, nervousness, or tremor;




  • confusion, hallucinations, unusual thoughts or behavior;




  • easy bruising or bleeding, unusual weakness, fever, chills, body aches, flu symptoms;




  • urinating less than usual or not at all; or




  • increased blood pressure (severe headache, blurred vision, trouble concentrating, chest pain, numbness, seizure).



Less serious side effects may include:



  • blurred vision;




  • dry mouth;




  • nausea, vomiting, stomach pain, constipation, mild loss of appetite;




  • mild dizziness, drowsiness;




  • problems with memory or concentration;




  • ringing in your ears;




  • warmth, tingling, or redness under your skin;




  • restless or excitability (especially in children);




  • sleep problems (insomnia); or




  • skin rash or itching.



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


What other drugs will affect Drocon-CS (brompheniramine, hydrocodone, and pseudoephedrine)?


Before taking this medication, tell your doctor if you are using any of the following drugs:



  • cimetidine (Tagamet);




  • rifampin (Rifadin, Rifater, Rifamate, Rimactane);




  • zidovudine (Retrovir, AZT);




  • antidepressants such as amitriptyline (Elavil), clomipramine (Anafranil), imipramine (Janimine, Tofranil), and others;




  • aspirin or salicylates (such as Disalcid, Doan's Pills, Dolobid, Salflex, Tricosal, and others);




  • a beta-blocker such as atenolol (Tenormin), carteolol (Cartrol), metoprolol (Lopressor, Toprol), nadolol (Corgard), propranolol (Inderal), sotalol (Betapace), timolol (Blocadren), and others;




  • bladder or urinary medications such as oxybutynin (Ditropan, Oxytrol) or tolterodine (Detrol);




  • a diuretic (water pill), or blood pressure medication;




  • medication to treat irritable bowel syndrome;




  • medicines to treat psychiatric disorders, such as chlorpromazine (Thorazine), haloperidol (Haldol), mesoridazine (Serentil), pimozide (Orap), or thioridazine (Mellaril); or




  • seizure medication such as phenytoin (Dilantin) or phenobarbital (Luminal, Solfoton).



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



More Drocon-CS resources


  • Drocon-CS Use in Pregnancy & Breastfeeding
  • Drocon-CS Drug Interactions
  • Drocon-CS Support Group
  • 0 Reviews for Drocon-CS - Add your own review/rating


  • Brompheniramine/Hydrocodone/Pseudoephedrine Liquid MedFacts Consumer Leaflet (Wolters Kluwer)

  • SymTan A Suspension MedFacts Consumer Leaflet (Wolters Kluwer)



Compare Drocon-CS with other medications


  • Cough and Nasal Congestion


Where can I get more information?


  • Your pharmacist can provide more information about brompheniramine, hydrocodone, and pseudoephedrine.


Thursday, 17 November 2011

Dallergy-JR Sustained-Release Capsules


Pronunciation: klor-fen-IHR-ah-meen/fen-il-EF-rin
Generic Name: Chlorpheniramine/Phenylephrine
Brand Name: Dallergy-JR


Dallergy-JR Sustained-Release Capsules are used for:

Relieving symptoms of sinus congestion, sinus pressure, runny nose, and sneezing due to colds, upper respiratory infections, and allergies. It may also be used for other conditions as determined by your doctor.


Dallergy-JR Sustained-Release Capsules 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 Dallergy-JR Sustained-Release Capsules if:


  • you are allergic to any ingredient in Dallergy-JR Sustained-Release Capsules

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

  • you take sodium oxybate (GHB) or if you have taken furazolidone or a monoamine oxidase (MAO) inhibitor (eg, phenelzine) within the last 14 days

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



Before using Dallergy-JR Sustained-Release Capsules:


Some medical conditions may interact with Dallergy-JR Sustained-Release Capsules. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:


  • if you are pregnant, plan 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 asthma, lung problems (eg, emphysema), adrenal gland problems (eg, adrenal gland tumor), heart problems, high blood pressure, diabetes, heart blood vessel problems, stroke, glaucoma, a blockage of your stomach or intestines, ulcers, a blockage of your bladder, trouble urinating, an enlarged prostate, seizures, or an overactive thyroid

Some MEDICINES MAY INTERACT with Dallergy-JR Sustained-Release Capsules. Tell your health care provider if you are taking any other medicines, especially any of the following:


  • Beta-blockers (eg, propranolol), COMT inhibitors (eg, tolcapone), furazolidone, indomethacin, MAO inhibitors (eg, phenelzine), sodium oxybate (GHB), or tricyclic antidepressants (eg, amitriptyline) because side effects of Dallergy-JR Sustained-Release Capsules may be increased

  • Digoxin or droxidopa because risk of irregular heartbeat or heart attack may be increased

  • Bromocriptine or hydantoins (eg, phenytoin) because side effects may be increased by Dallergy-JR Sustained-Release Capsules

  • Guanethidine, guanadrel, mecamylamine, methyldopa, or reserpine because effectiveness may be decreased by Dallergy-JR Sustained-Release Capsules

This may not be a complete list of all interactions that may occur. Ask your health care provider if Dallergy-JR Sustained-Release Capsules 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 Dallergy-JR Sustained-Release Capsules:


Use Dallergy-JR Sustained-Release Capsules as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • Dallergy-JR Sustained-Release Capsules may be taken with or without food.

  • Swallow Dallergy-JR Sustained-Release Capsules whole. Do not break, crush, or chew before swallowing.

  • If you miss a dose of Dallergy-JR Sustained-Release Capsules, 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 Dallergy-JR Sustained-Release Capsules.



Important safety information:


  • Dallergy-JR Sustained-Release Capsules may cause dizziness, drowsiness, or blurred vision. Do not drive, operate machinery, or do anything else that could be dangerous until you know how you react to Dallergy-JR Sustained-Release Capsules. Using Dallergy-JR Sustained-Release Capsules alone, with certain other medicines, or with alcohol may lessen your ability to drive or perform other potentially dangerous tasks.

  • Do not take diet or appetite control medicines while you are taking Dallergy-JR Sustained-Release Capsules without checking with you doctor.

  • Do NOT exceed the recommended dose or take Dallergy-JR Sustained-Release Capsules for longer than prescribed without checking with your doctor.

  • If your symptoms do not improve within 5 to 7 days or if they become worse, check with your doctor.

  • Dallergy-JR Sustained-Release Capsules may cause increased sensitivity to the sun. Avoid exposure to the sun, sunlamps, or tanning booths until you know how you react to Dallergy-JR Sustained-Release Capsules. Use a sunscreen or protective clothing if you must be outside for a prolonged period.

  • If you are scheduled for allergy skin testing, do not take Dallergy-JR Sustained-Release Capsules for several days before the test because it may decrease your response to the skin tests.

  • Before you have any medical or dental treatments, emergency care, or surgery, tell the doctor or dentist that you are using Dallergy-JR Sustained-Release Capsules.

  • Use Dallergy-JR Sustained-Release Capsules with caution in the ELDERLY because they may be more sensitive to its effects.

  • Caution is advised when using Dallergy-JR Sustained-Release Capsules in CHILDREN because they may be more sensitive to its effects.

  • PREGNANCY and BREAST-FEEDING: If you become pregnant while taking Dallergy-JR Sustained-Release Capsules, discuss with your doctor the benefits and risks of using Dallergy-JR Sustained-Release Capsules during pregnancy. It is unknown if Dallergy-JR Sustained-Release Capsules are excreted in breast milk. Do not breast-feed while taking Dallergy-JR Sustained-Release Capsules.


Possible side effects of Dallergy-JR Sustained-Release Capsules:


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; excitability; headache; loss of appetite; nausea; nervousness or anxiety; trouble sleeping; upset stomach; vomiting; weakness.



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); difficulty urinating or inability to urinate; fast or irregular heartbeat; hallucinations; seizures; severe dizziness, lightheadedness, or headache; tremor; vision changes.



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: Dallergy-JR 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 blurred vision; confusion; hallucinations; seizures; severe dizziness, lightheadedness, or headache; severe drowsiness; unusually fast, slow, or irregular heartbeat; vomiting.


Proper storage of Dallergy-JR Sustained-Release Capsules:

Store Dallergy-JR Sustained-Release Capsules at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Dallergy-JR Sustained-Release Capsules out of the reach of children and away from pets.


General information:


  • If you have any questions about Dallergy-JR Sustained-Release Capsules, please talk with your doctor, pharmacist, or other health care provider.

  • Dallergy-JR Sustained-Release Capsules 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 Dallergy-JR Sustained-Release Capsules. 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 Dallergy-JR resources


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


Compare Dallergy-JR with other medications


  • Cold Symptoms
  • Hay Fever