Tuesday, 11 September 2012

Alavert D-12 Hour Allergy and Sinus



loratadine, pseudoephedrine sulfate

Dosage Form: tablet, film coated, extended release
Alavert D-12 Hour Allergy and Sinus (Extended Release Tablets)

(loratadine and pseudoephedrine sulfate)

DRUG FACTS



ACTIVE INGREDIENTS (IN EACH TABLET)


Loratadine 5 mg


Pseudoephedrine sulfate 120 mg



PURPOSES


Antihistamine


Nasal decongestant



USES


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

    • sneezing

    • itchy, watery eyes

    • itching of the nose or throat


  • temporarily relieves nasal congestion due to the common cold, hay fever or other respiratory allergies

  • reduces swelling of nasal passages

  • temporarily relieves sinus congestion and pressure

  • temporarily restores freer breathing through the nose


Warnings



Do not use


  • if you have ever had an allergic reaction to this product or any of its ingredients

  • if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.


Ask a doctor before use if you have


  • heart disease

  • high blood pressure

  • thyroid disease

  • diabetes

  • trouble urinating due to an enlarged prostate gland

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


When using this product do not take more than directed.


Taking more than directed may cause drowsiness.



Stop use and ask a doctor if


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

  • symptoms do not improve within 7 days or are accompanied by a fever

  • nervousness, dizziness or sleeplessness occurs


If pregnant or breast-feeding,


ask a health professional before use.



Keep out of reach of children.


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



DIRECTIONS


  • do not divide, crush, chew or dissolve the tablet










AgeDose
adults and children 12 years and over
1 tablet every 12 hours; not more than 2 tablets in 24 hours
children under 12 years of ageask a doctor
consumers with liver or kidney diseaseask a doctor

OTHER INFORMATION


  • each tablet contains: calcium 30 mg

  • store between 15° and 25°C (59° and 77°F)

  • keep in a dry place


INACTIVE INGREDIENTS


croscarmellose sodium, dibasic calcium phosphate, hypromellose, lactose monohydrate, magnesium stearate, pharmaceutical ink, povidone, titanium dioxide



QUESTIONS OR COMMENTS?


Call weekdays from 9 AM to 5 PM EST at 1-800-ALAVERT (1-800-252-8378)



PRODUCT PACKAGING


The product packaging shown below represents a sample of that currently in use. Additional packaging may also be available.


SEE COLD USE


ALAVERT D-12 HOUR allergy & sinus


Loratadine 5mg/Antihistamine


Pseudoephedrine Sulfate 120mg/Nasal Decongestant


Non-Drowsy*


*When taken as directed. See DRUG FACTS Panel.


Allergy & Sinus Relief


  • Sneezing

  • Runny Nose

  • Itchy, Watery Eyes

  • Nasal Congestion

  • Sinus Pressure

Cold Symptom Relief for


  • Nasal Congestion

  • Sinus Pressure

Compare to Claritin† & SAVE!


†Claritin is a registered trademark of Schering Corporation


12 Extended Release Tablets


For most recent product information, visit www.alavert.com


Wyeth


Distributed by:


Wyeth Consumer Healthcare


Madison, NJ 07940


©2009 Wyeth


EACH TABLET IS BLISTER SEALED. DO NOT USE IF SEAL IS BROKEN.










ALAVERT ALLERGY SINUS D-12 
loratadine, pseudoephedrine sulfate  tablet, film coated, extended release










Product Information
Product TypeHUMAN OTC DRUGNDC Product Code (Source)0573-2660
Route of AdministrationORALDEA Schedule    











Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
loratadine (loratadine)loratadine5 mg
pseudoephedrine sulfate (pseudoephedrine)pseudoephedrine sulfate120 mg





Inactive Ingredients
Ingredient NameStrength
No Inactive Ingredients Found


















Product Characteristics
ColorWHITE (white to off-white)Scoreno score
ShapeROUND (round shape and an extra deep convex)Size14mm
FlavorImprint CodeAlavert;D12
Contains      






















Packaging
#NDCPackage DescriptionMultilevel Packaging
10573-2660-122 BLISTER PACK In 1 CARTONcontains a BLISTER PACK
16 TABLET In 1 BLISTER PACKThis package is contained within the CARTON (0573-2660-12)
20573-2660-244 BLISTER PACK In 1 CARTONcontains a BLISTER PACK
26 TABLET In 1 BLISTER PACKThis package is contained within the CARTON (0573-2660-24)










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07605001/30/2004


Labeler - Wyeth Consumer Healthcare (828831730)
Revised: 02/2010Wyeth Consumer Healthcare




More Alavert D-12 Hour Allergy and Sinus resources


  • Alavert D-12 Hour Allergy and Sinus Side Effects (in more detail)
  • Alavert D-12 Hour Allergy and Sinus Use in Pregnancy & Breastfeeding
  • Alavert D-12 Hour Allergy and Sinus Drug Interactions
  • Alavert D-12 Hour Allergy and Sinus Support Group
  • 0 Reviews for Alavert D-12 Hour Allergy and Sinus - Add your own review/rating


Compare Alavert D-12 Hour Allergy and Sinus with other medications


  • Hay Fever
  • Nasal Congestion

Monday, 10 September 2012

Miscellaneous antimalarials


A drug may be classified by the chemical type of the active ingredient or by the way it is used to treat a particular condition. Each drug can be classified into one or more drug classes.

Antimalarials agents are drugs effective in the treatment of malaria. Malaria is an infectious disease caused by the bite of an anopheles mosquito infected with certain protozoans. The best way to prevent malaria is by taking antimalarial drugs prophylactically prior to entering an endemic area.


Antimalarial agents are classified according to their action against different stages of the life cycle of the parasite. Certain antimalarial agents are more effective in the acute attack of malaria, and generally more that one agent will be used simultaneously to avoid resistance. Some antimalarial agents are used as prophylactic agents; they kill the parasite when it enters the host.

See also

Medical conditions associated with miscellaneous antimalarials:

  • Acne
  • Actinomycosis
  • Amebiasis
  • Anthrax
  • Anthrax Prophylaxis
  • Bacterial Infection
  • Bartonellosis
  • Bronchitis
  • Brucellosis
  • Bullous Pemphigoid
  • Chlamydia Infection
  • Cholera
  • Cutaneous Bacillus anthracis
  • Ehrlichiosis
  • Enterocolitis
  • Epididymitis, Sexually Transmitted
  • Gastroenteritis
  • Granuloma Inguinale
  • Inclusion Conjunctivitis
  • Lyme Disease
  • Lyme Disease, Arthritis
  • Lyme Disease, Carditis
  • Lyme Disease, Erythema Chronicum Migrans
  • Lyme Disease, Neurologic
  • Lymphogranuloma Venereum
  • Malaria
  • Malaria Prevention
  • Melioidosis
  • Mycoplasma Pneumonia
  • Nongonococcal Urethritis
  • Ocular Rosacea
  • Ornithosis
  • Pelvic Inflammatory Disease
  • Pemphigoid
  • Pemphigus
  • Periodontitis
  • Plague
  • Pleural Effusion
  • Pneumocystis Pneumonia Prophylaxis
  • Pneumonia
  • Proctitis
  • Prostatitis
  • Psittacosis
  • Rabbit Fever
  • Rheumatoid Arthritis
  • Rickettsial Infection
  • Rosacea
  • Skin Infection
  • STD Prophylaxis
  • Syphilis, Early
  • Syphilis, Latent
  • Tertiary Syphilis
  • Toxoplasmosis
  • Toxoplasmosis, Prophylaxis
  • Trachoma
  • Upper Respiratory Tract Infection
  • Urinary Tract Infection

Drug List:

Difflam Oral Rinse





1. Name Of The Medicinal Product



Difflam Oral Rinse


2. Qualitative And Quantitative Composition



A pleasant tasting, clear, green solution, containing benzydamine hydrochloride 0.15% w/v.



3. Pharmaceutical Form



Liquid for use as mouthwash/gargle.



4. Clinical Particulars



4.1 Therapeutic Indications



Difflam Oral Rinse is a locally acting analgesic and anti-inflammatory treatment for the relief of painful inflammatory conditions of the mouth and throat including:



Traumatic conditions: Pharyngitis following tonsillectomy or the use of a naso-gastric tube.



Inflammatory conditions: Pharyngitis, aphthous ulcers and oral ulceration due to radiation therapy.



Dentistry: For use after dental operations.



4.2 Posology And Method Of Administration



Adults: Rinse or gargle with 15 ml (approximately 1 tablespoonful) every 1½ to 3 hours as required for pain relief.



The solution should be expelled from the mouth after use.



Children: Not suitable for children aged 12 years or under.



Elderly: No special dosage recommendations are made for elderly patients.



Difflam Oral Rinse should generally be used undiluted, but if 'stinging' occurs the rinse may be diluted with water.



Uninterrupted treatment should not exceed seven days, except under medical supervision



4.3 Contraindications



Difflam Oral Rinse is contra-indicated in patients with known hypersensitivity to any of the ingredients



4.4 Special Warnings And Precautions For Use



Difflam Oral Rinse should generally be used undiluted, but if 'stinging' occurs the rinse may be diluted with water.



Avoid contact with eyes.



4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction



None known.



4.6 Pregnancy And Lactation



Difflam should not be used in pregnancy or lactation unless considered essential by the physician. There is no evidence of a teratogenic effect in animal studies.



4.7 Effects On Ability To Drive And Use Machines



Not applicable.



4.8 Undesirable Effects



Side-effects are minor. Occasionally, oral tissue numbness or 'stinging' sensations may occur. Hypersensitivity reactions occur very rarely but may be associated with pruritus rash, urticaria, photodermatitis and occasionally laryngospasm or bronchospasm.



4.9 Overdose



Difflam is unlikely to cause adverse systemic effects, even if accidental ingestion should occur. No special measures are required.



5. Pharmacological Properties



5.1 Pharmacodynamic Properties



Benzydamine exerts an anti-inflammatory and analgesic effect by stabilising the cellular membrane and inhibiting prostaglandin synthesis.



5.2 Pharmacokinetic Properties



Oral doses of benzydamine are well absorbed and plasma drug concentrations reach a peak fairly rapidly and then decline with a half-life of about 13 hours. Less than 20% of the drug is bound to plasma proteins.



Although local drug concentrations are relatively large, the systemic absorption of mouthwash-gargle doses of benzydamine is relatively low compared to oral doses. This low absorption should greatly diminish the potential for any systemic drug side-effects when benzydamine is administered by this route. Benzydamine is metabolized primarily by oxidation, conjugation and dealkylation.



5.3 Preclinical Safety Data



Non-Clinical Data reveal no special hazards for humans based on conventional studies of safety pharmacology, repeated toxicity, genotoxicity, cardiogenic potential, and toxicity to reproduction.



6. Pharmaceutical Particulars



6.1 List Of Excipients



Ethanol (96% v/v) BP



Glycerol Ph Eur



Saccharin Sodium BP



Mouthwash flavour, 52 503/T



Polysorbate 20 Ph Eur



Methyl Hydroxybenzoate Ph Eur



Quinoline Yellow (E104)



Patent Blue V (E131)



Purified Water Ph Eur



6.2 Incompatibilities



None known



6.3 Shelf Life



3 years



6.4 Special Precautions For Storage



Do not leave the uncartonned bottle in direct sunlight. Store between 5°C and 30°C. Do not freeze.



6.5 Nature And Contents Of Container



Clear glass bottle with screwcap containing 300 ml.



6.6 Special Precautions For Disposal And Other Handling



The solution should be expelled from the mouth after use.



7. Marketing Authorisation Holder



Meda Pharmaceuticals Ltd



249 West George Street



Glasgow



G2 4RB



Trading as:



Meda Pharmaceuticals Ltd



Skyway House



Parsonage Road



Takeley



Bishop's Stortford



CM22 6PU



8. Marketing Authorisation Number(S)



PL 15142/0045



9. Date Of First Authorisation/Renewal Of The Authorisation



Date of first authorisation 11 June 1981



Date of last renewal 6 September 2002



10. Date Of Revision Of The Text



17th June 2011




Friday, 7 September 2012

zilactin-B


Generic Name: benzocaine topical (BENZ oh kane TOP ik al)

Brand Names: Americaine, Americaine Hemorrhoidal, Anacaine, Anbesol Gel, Anbesol Liquid, Babee Teething Lotion, Benzo-O-Stetic, Boil Ease Pain Relieving, Cepacol Extra Strength, Cepacol Fizzlers, Dent-O-Kain, Dermoplast, Detane, Hurricaine, Lanacane, Maintain, Medicone Maximum Strength, Num-Zit, Numzident, Orabase, Orabase Gel-B, Orajel, Orajel Denture, Oral Pain Relief, OraMagic Plus, Outgro Pain Relief, Retre-Gel, Rid-A-Pain, Skeeter Stik, Solarcaine Aerosol, Sting-Kill, Topex, Trocaine, Vagisil Feminine Cream, zilactin-B


What is zilactin-B (benzocaine topical)?

Benzocaine is a local anesthetic (numbing medication). It works by blocking nerve signals in your body.


Benzocaine topical is used to reduce pain or discomfort caused by minor skin irritations, sore throat, sunburn, teething pain, vaginal or rectal irritation, ingrown toenails, hemorrhoids, and many other sources of minor pain on a surface of the body. Benzocaine is also used to numb the skin or surfaces inside the mouth, nose, throat, vagina, or rectum to lessen the pain of inserting a medical instrument such as a tube or speculum.


There are many brands and forms of benzocaine topical available and not all brands are listed on this leaflet.


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


What is the most important information I should know about zilactin-B (benzocaine topical)?


There are many brands and forms of benzocaine topical available and not all brands are listed on this leaflet.


Benzocaine topical used in the mouth or throat may cause a life-threatening condition in which the amount of oxygen in your blood stream becomes dangerously low. This condition is called methemoglobinemia (met-HEEM-oh glo-bin-EE-mee-a) and it may occur after only one use of benzocaine or after several uses.

Signs and symptoms of methemoglobinemia may occur within minutes or up to 2 hours after using benzocaine topical in the mouth or throat. GET EMERGENCY MEDICAL HELP IF YOU HAVE ANY OF THESE SYMPTOMS: headache, tired feeling, confusion, fast heart rate, and feeling light-headed or short of breath, with a pale, blue, or gray appearance of your skin, lips, or fingernails.


Do not use benzocaine topical if you have ever had methemoglobinemia in the past. Do not use this medicine on a child younger than 2 years old without medical advice. An overdose of numbing medications can cause fatal side effects if too much of the medicine is absorbed through your skin and into your blood. This is more likely to occur when using a numbing medicine without the advice of a medical doctor (such as during a cosmetic procedure like laser hair removal). Overdose symptoms may include uneven heartbeats, seizure (convulsions), coma, slowed breathing, or respiratory failure (breathing stops).

Use the smallest amount of this medication needed to numb the skin or relieve pain. Do not use large amounts of benzocaine topical, or cover treated skin areas with a bandage or plastic wrap without medical advice. Be aware that many cosmetic procedures are performed without a medical doctor present.


Your body may absorb more of this medication if you use too much, if you apply it over large skin areas, or if you apply heat, bandages, or plastic wrap to treated skin areas. Skin that is cut or irritated may also absorb more topical medication than healthy skin.

Before using benzocaine topical, tell your doctor if you have any type of inherited enzyme deficiency, heart disease, a breathing disorder such as asthma, bronchitis, or emphysema, or if you smoke.


If you are treating a sore throat, call your doctor if the pain is severe or lasts longer than 2 days, especially if you also develop a fever, headache, skin rash, swelling, nausea, vomiting, cough, or breathing problems.


What should I discuss with my health care provider before using zilactin-B (benzocaine topical)?


Do not use benzocaine topical if you have ever had methemoglobinemia in the past. An overdose of numbing medications can cause fatal side effects if too much of the medicine is absorbed through your skin and into your blood. This is more likely to occur when using a numbing medicine without the advice of a medical doctor (such as during a cosmetic procedure like laser hair removal). Overdose symptoms may include uneven heartbeats, seizure (convulsions), coma, slowed breathing, or respiratory failure (breathing stops).

Ask a doctor or pharmacist if it is safe for you to take this medicine if you have:



  • asthma, bronchitis, emphysema, or other breathing disorder;




  • heart disease;




  • a personal or family history of methemoglobinemia, or any genetic (inherited) enzyme deficiency; or




  • if you smoke.




FDA pregnancy category C. It is not known whether benzocaine topical will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medication.. It is not known whether benzocaine topical passes into breast milk or if it could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby. Do not use this medicine on a child younger than 2 years old without medical advice.

How should I use zilactin-B (benzocaine topical)?


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


Your body may absorb more of this medication if you use too much, if you apply it over large skin areas, or if you apply heat, bandages, or plastic wrap to treated skin areas. Skin that is cut or irritated may also absorb more topical medication than healthy skin.

Use the smallest amount of medicine needed to numb the skin or relieve pain. Do not use large amounts of benzocaine topical, or cover treated skin areas with a bandage or plastic wrap without medical advice. Be aware that many cosmetic procedures are performed without a medical doctor present.


This medication comes with instructions for safe and effective application. Follow these directions carefully. Ask your doctor or pharmacist if you have any questions.


To treat minor skin conditions, apply a thin layer of benzocaine topical to the affected area up to 4 times per day. If using the spray, hold the container 6 to 12 inches away from the skin. Do not spray this medication onto your face. Spray it instead on your hands and then rub it onto the face, avoiding contact with your eyes.


To treat hemorrhoids, clean the area with soap and water before applying benzocaine topical. Apply the medication up to 6 times per day. If you are using the rectal suppository, try to empty your bowel and bladder before inserting the suppository. Remove the outer wrapper from the suppository before inserting it. Avoid handling the suppository too long or it will melt in your hands.


Do not use benzocaine topical to treat large skin areas or deep puncture wounds. Avoid using the medicine on skin that is raw or blistered, such as a severe burn or abrasion.

Call your doctor if your symptoms do not improve or if they get worse within the first 7 days of using benzocaine topical. Also call your doctor if your symptoms had cleared up but then came back.


If you are treating a sore throat, call your doctor if the pain is severe or lasts longer than 2 days, especially if you also develop a fever, headache, skin rash, swelling, nausea, vomiting, cough, or breathing problems.


Store at room temperature away from moisture and heat. Do not freeze.

What happens if I miss a dose?


Since benzocaine topical is used as needed, you may not be on a dosing schedule. If you are using the medication regularly, use the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not use extra medicine to make up the missed dose.


What happens if I overdose?


Seek emergency medical attention or call the Poison Help line at 1-800-222-1222. An overdose of benzocaine topical applied to the skin can cause life-threatening side effects such as uneven heartbeats, seizure (convulsions), coma, slowed breathing, or respiratory failure (breathing stops).

What should I avoid while taking zilactin-B (benzocaine topical)?


Avoid eating within 1 hour after using benzocaine topical on your gums or inside your mouth.


Benzocaine topical is for use only on the surface of your body, or just inside the mouth, vagina, or rectum. Avoid getting this medication in your eyes. Avoid swallowing the gel, liquid, or ointment while applying it to your gums or the inside of your mouth. The throat spray or oral lozenge may be swallowed gradually during use.

Do not apply other medications to the same affected areas you treat with benzocaine topical, unless your doctor has told you otherwise.


zilactin-B (benzocaine topical) side effects


Benzocaine topical used in the mouth or throat may cause a life-threatening condition in which the amount of oxygen in your blood stream becomes dangerously low. This condition is called methemoglobinemia (met-HEEM-oh glo-bin-EE-mee-a) and it may occur after only one use of benzocaine or after several uses.

Signs and symptoms may occur within minutes or up to 2 hours after using benzocaine topical in the mouth or throat. GET EMERGENCY MEDICAL HELP IF YOU HAVE:



  • headache, tired feeling, confusion;




  • fast heart rate;




  • feeling light-headed or short of breath; and




  • pale, blue, or gray appearance of your skin, lips, or fingernails.




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 benzocaine topical and call your doctor at once if you have any of these other serious side effects:

  • headache, weakness, dizziness, breathing problems, fast heart rate, and gray or bluish colored skin (rare but serious side effects of benzocaine);




  • severe burning, stinging, or sensitivity where the medicine is applied;




  • swelling, warmth, or redness; or




  • oozing, blistering, or any signs of infection.



Less serious side effects may include:



  • mild stinging, burning, or itching where the medicine is applied;




  • skin tenderness or redness; or




  • dry white flakes where the medicine was applied.



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


What other drugs will affect zilactin-B (benzocaine topical)?


It is not likely that other drugs you take orally or inject will have an effect on topically applied benzocaine topical. But many drugs can interact with each other. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor.



More zilactin-B resources


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


  • Americaine Ointment MedFacts Consumer Leaflet (Wolters Kluwer)

  • Anacaine Advanced Consumer (Micromedex) - Includes Dosage Information

  • Benz-O-Sthetic Gel MedFacts Consumer Leaflet (Wolters Kluwer)

  • Lanacane Aerosol Spray MedFacts Consumer Leaflet (Wolters Kluwer)

  • OraMagic Plus Suspension MedFacts Consumer Leaflet (Wolters Kluwer)

  • Rid-A-Pain Topical Advanced Consumer (Micromedex) - Includes Dosage Information

  • Zilactin-B Advanced Consumer (Micromedex) - Includes Dosage Information



Compare zilactin-B with other medications


  • Aphthous Ulcer


Where can I get more information?


  • Your pharmacist can provide more information about benzocaine topical.

See also: zilactin-B side effects (in more detail)


Thursday, 6 September 2012

Solarcaine Cool Aloe Topical application


Generic Name: lidocaine (Topical application route)

LYE-doe-kane

Commonly used brand name(s)

In the U.S.


  • Anestacon

  • Burnamycin

  • Burn-O-Jel

  • Lida Mantle

  • Lidoderm

  • LMX 4

  • LMX 5

  • Senatec

  • Solarcaine Cool Aloe

  • Topicaine

  • Xylocaine

In Canada


  • Solarcaine First Aid Lidocaine Spray

  • Solarcaine Lidocaine First Aid Spray

Available Dosage Forms:


  • Foam

  • Dressing

  • Gel/Jelly

  • Spray

  • Cream

  • Solution

  • Pad

  • Patch, Extended Release

  • Ointment

  • Lotion

  • Aerosol Liquid

Therapeutic Class: Anesthetic, Local


Chemical Class: Amino Amide


Uses For Solarcaine Cool Aloe


Lidocaine is used on different parts of the body to cause numbness or loss of feeling for patients having certain medical procedures. It is also used to relieve pain and itching caused by conditions such as sunburn or other minor burns, insect bites or stings, poison ivy, poison oak, poison sumac, minor cuts, or scratches.


Lidocaine belongs to a group of medicines known as topical local anesthetics. It deadens the nerve endings in the skin. This medicine does not cause unconsciousness as general anesthetics do when used for surgery.


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


Before Using Solarcaine Cool Aloe


In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For this medicine, the following should be considered:


Allergies


Tell your doctor if you have ever had any unusual or allergic reaction to this medicine or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.


Pediatric


Appropriate studies performed to date have not demonstrated pediatric-specific problems that would limit the usefulness of lidocaine in children. However, because of this medicine's toxicity, it should be used with caution, after other medicines have been considered or found ineffective. Recommended doses should not be exceeded, and the patient should be carefully monitored during therapy.


Geriatric


No information is available on the relationship of age to the effects of lidocaine in geriatric patients. However, because of this medicine's toxicity, it should be used with caution, after other medicines have been considered or found ineffective. Recommended doses should not be exceeded, and the patient should be carefully monitored during therapy.


Interactions with Medicines


Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. Tell your healthcare professional if you are taking any other prescription or nonprescription (over-the-counter [OTC]) medicine.


Interactions with Food/Tobacco/Alcohol


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


Other Medical Problems


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


  • Heart block or

  • Shock, severe—Use with caution.

  • Infection at or near the place of application or

  • Large sores, broken skin, or severe injury at the area of application—Use with caution. The chance of side effects may be increased.

Proper Use of lidocaine

This section provides information on the proper use of a number of products that contain lidocaine. It may not be specific to Solarcaine Cool Aloe. Please read with care.


Use this medicine exactly as directed by your doctor. Do not use it for any other condition without first checking with your doctor. This medicine may cause unwanted effects if it is used too much, because more of it is absorbed into the body through the skin.


A nurse or other trained health care professional will give you this medicine before having a medical procedure.


Wash your hands with soap and water before and after using this medicine.


Unless otherwise directed by your doctor, do not apply this medicine to open wounds, burns, or broken or inflamed skin.


This medicine should only be used for problems being treated by your doctor. Check with your doctor before using it for other problems, especially if you think that an infection may be present. This medicine should not be used to treat certain kinds of skin infections or serious problems, such as severe burns.


Be careful not to get any of this medicine in your eyes, because it can cause severe eye irritation. If any of the medicine does get in the eyes, wash the eyes with water for at least 15 minutes and check with your doctor right away.


Dosing


The dose of this medicine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so.


The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.


  • For topical dosage form (ointment):
    • For pain and itching caused by minor skin conditions:
      • Adults—Apply to the affected area three or four times a day. The largest amount of ointment that should be used in a single application is 5 grams. If you use the 5% ointment, this is about 6 inches of ointment from the tube.

      • Children—Dose is based on body weight and must be determined by your doctor.



Missed Dose


If you miss a dose of this medicine, apply 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.


Storage


Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing.


Keep out of the reach of children.


Do not keep outdated medicine or medicine no longer needed.


Ask your healthcare professional how you should dispose of any medicine you do not use.


Precautions While Using Solarcaine Cool Aloe


It is very important that your doctor check you closely for any problems or unwanted effects that may be caused by this medicine.


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


After applying this medicine to the skin of your child, watch the child carefully to make sure that he or she does not get any of the medicine in the eyes or mouth. Lidocaine can cause serious side effects, especially in children, if it gets into the mouth and is swallowed.


Stop using this medicine and check with your doctor right away if you have a skin rash, burning, stinging, swelling, or irritation of your skin.


If you are using this medicine in the mouth or throat, do not eat or drink anything for one hour after using it. When this medicine is applied to these areas, it may cause swallowing and choking problems. Do not chew gum or food while your mouth or throat feels numb after you use this medicine. You may accidentally bite your tongue or the inside of your cheeks.


Do not use cosmetics or other skin care products on the treated skin areas.


Solarcaine Cool Aloe Side Effects


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


Check with your doctor or nurse immediately if any of the following side effects occur:


Incidence not known
  • Blurred vision

  • chest pain or discomfort

  • cold, clammy, or pale skin

  • confusion

  • cough

  • difficult or troubled breathing

  • difficulty with swallowing

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

  • false or unusual sense of well-being

  • fast heartbeat

  • fear

  • hives or welts

  • irregular, fast or slow, or shallow breathing

  • itching

  • lightheadedness, dizziness, or fainting

  • mood or mental changes

  • nervousness

  • no blood pressure or pulse

  • pale or blue lips, fingernails, or skin

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

  • redness of the skin

  • seizures

  • shakiness in the legs, arms, hands, or feet

  • shortness of breath

  • skin rash

  • sleepiness

  • slow heart rate

  • slow or irregular heartbeat

  • stopping of heart

  • swelling

  • tightness in the chest

  • trembling or shaking of the hands or feet

  • twitching

  • unconsciousness

  • unusual tiredness or weakness

  • weakness

  • wheezing

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:


Incidence not known
  • Cold or numbness

  • continuing ringing or buzzing or other unexplained noise in the ears

  • double vision

  • hearing loss

  • heat sensation

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


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

See also: Solarcaine Cool Aloe Topical application side effects (in more detail)



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


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


More Solarcaine Cool Aloe Topical application resources


  • Solarcaine Cool Aloe Topical application Side Effects (in more detail)
  • Solarcaine Cool Aloe Topical application Use in Pregnancy & Breastfeeding
  • 0 Reviews for Solarcaine Cool Aloe Topical application - Add your own review/rating


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  • Burns, External
  • Sunburn

adenovirus vaccine, live


AD-e-noe-vye-rus VAX-een type 4, lyve, AD-e-noe-vye-rus VAX-een type 7, lyve


Uses For adenovirus vaccine, live

Adenovirus type 4 and type 7 live vaccine is used to prevent febrile (with fever) acute respiratory disease (ARD) caused by adenovirus type 4 and type 7. It works by causing your body to produce its own protection (antibodies) against the virus.


This vaccine is given to military personnels 17 to 50 years of age.


This vaccine is to be administered only by or under the supervision of your doctor or other health care professional.


Before Using adenovirus vaccine, live


In deciding to use a vaccine, the risks of taking the vaccine must be weighed against the good it will do. This is a decision you and your doctor will make. For this vaccine, the following should be considered:


Allergies


Tell your doctor if you have ever had any unusual or allergic reaction to adenovirus vaccine, live or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.


Pediatric


Appropriate studies have not been performed on the relationship of age to the effects of adenovirus type 4 and type 7 live vaccine in children up to 16 years of age. Safety and efficacy have not been established.


Geriatric


Appropriate studies have not been performed on the relationship of age to the effects of adenovirus type 4 and type 7 live vaccine in the geriatric population. Safety and efficacy have not been established.


Interactions with Medicines


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


Receiving this vaccine 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.


  • Aclarubicin

  • Adalimumab

  • Aldesleukin

  • Altretamine

  • Amonafide

  • Amsacrine

  • Asparaginase

  • Azacitidine

  • Azathioprine

  • Bleomycin

  • Broxuridine

  • Busulfan

  • Capecitabine

  • Carboplatin

  • Carmustine

  • Certolizumab Pegol

  • Chlorambucil

  • Cisplatin

  • Cladribine

  • Cyclophosphamide

  • Cytarabine

  • Cytarabine Liposome

  • Dacarbazine

  • Dactinomycin

  • Daunorubicin

  • Daunorubicin Citrate Liposome

  • Decitabine

  • Docetaxel

  • Doxifluridine

  • Doxorubicin Hydrochloride

  • Doxorubicin Hydrochloride Liposome

  • Edatrexate

  • Eflornithine

  • Epirubicin

  • Estramustine

  • Etanercept

  • Etoposide

  • Everolimus

  • Fingolimod

  • Floxuridine

  • Fludarabine

  • Fluorouracil

  • Fotemustine

  • Gallium Nitrate

  • Gemcitabine

  • Golimumab

  • Hydroxyurea

  • Idarubicin

  • Ifosfamide

  • Irinotecan

  • Lomustine

  • Mechlorethamine

  • Melphalan

  • Mercaptopurine

  • Methotrexate

  • Mitolactol

  • Mitomycin

  • Mitotane

  • Mitoxantrone

  • Mycophenolic Acid

  • Oxaliplatin

  • Paclitaxel

  • Pegaspargase

  • Pentostatin

  • Pipobroman

  • Pirarubicin

  • Plicamycin

  • Procarbazine

  • Raltitrexed

  • Rilonacept

  • Rituximab

  • Sirolimus

  • Streptozocin

  • Teceleukin

  • Tegafur

  • Temsirolimus

  • Teniposide

  • Thioguanine

  • Thiotepa

  • Topotecan

  • Treosulfan

  • Trimetrexate

  • Trofosfamide

  • Uracil Mustard

  • Ustekinumab

  • Vinblastine

  • Vincristine

  • Vincristine Liposome

  • Vindesine

  • Vinorelbine

Receiving this vaccine with any of the following medicines may cause an increased risk of certain side effects, but using both drugs may be the best treatment for you. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines.


  • Abatacept

  • Leflunomide

Interactions with Food/Tobacco/Alcohol


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


Other Medical Problems


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


  • Allergic reactions (e.g., anaphylaxis), severe to this vaccine or

  • Difficulty with swallowing a whole tablet, without chewing—Should not be used in patients with these conditions.

  • Diarrhea or

  • Vomiting—Use with caution. You may need to wait until you feel better before receiving the vaccine.

  • Weakened immune system (e.g., HIV, cancer, or receiving steroid or cancer medicines)—May not work as well in patients with this condition.

Proper Use of adenovirus vaccine, live


A nurse or other trained health professional will give you this vaccine. It is given by mouth.


Swallow each tablet whole. Do not break, crush, or chew them.


Dosing


The dose of adenovirus vaccine, live 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 adenovirus vaccine, live. If your dose is different, do not change it unless your doctor tells you to do so.


The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.


  • For oral dosage form (enteric coated tablets):
    • To prevent febrile acute respiratory disease:
      • Adults and teenagers 17 to 50 years of age—Two tablets taken as a single dose.

      • Children younger than 17 years of age—Use and dose must be determined by your doctor.



Missed Dose


adenovirus vaccine, live needs to be given on a fixed schedule. If you miss a dose or forget to use your medicine, call your doctor or pharmacist for instructions.


Precautions While Using adenovirus vaccine, live


It is very important that your doctor check your progress at regular visits to make sure that this vaccine is working properly and to check for unwanted effects.


Do not take this vaccine if you are pregnant and do not plan to become pregnant for 6 weeks after receiving this vaccine without first checking with your doctor. There is a chance that this vaccine may cause problems during pregnancy. If you think you have become pregnant, tell your doctor right away. Your doctor may want you to join a pregnancy registry for patients receiving this vaccine.


This vaccine contains live viruses that are shed in the stool for up to 28 days after receiving the vaccine and can cause disease to other people if transmitted. Your doctor may recommend ways (e.g., proper and frequent hand washing, especially right after bowel movements) to help prevent the spread of virus to other people.


You should avoid close contact with people at high risk for catching the adenovirus for 28 days after receiving this vaccine. People who are at risk for catching the virus are pregnant women, children younger than 7 years of age, and anyone who has a weak immune system that keeps them from fighting infections.


This vaccine contains albumin, which comes from human blood. Some human blood products have transmitted certain viruses to people who have received them. The risk of getting a virus from medicines made of human blood has been greatly reduced in recent years. This is the result of required testing of human donors for certain viruses, and testing during the manufacture of these medicines. Although the risk is low, talk with your doctor if you have concerns.


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


adenovirus vaccine, live Side Effects


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


Check with your doctor or nurse immediately if any of the following side effects occur:


More common
  • Body aches or pain

  • chills

  • cough

  • difficulty with breathing

  • ear congestion

  • fever greater than or equal to 100.5 degrees F

  • headache

  • loss of voice

  • runny nose

  • sneezing

  • sore throat

  • stuffy nose

  • unusual tiredness or weakness

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


More common
  • Diarrhea

  • difficulty with moving

  • muscle pain or stiffness

  • nausea

  • pain in the joints

  • upper abdominal or stomach pain

  • vomiting

Less common
  • Pain in the arms or legs

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.

Monday, 3 September 2012

Guaifenex DM Extended-Release Tablets


Pronunciation: DEX-troe-meth-OR-fan/gwye-FEN-e-sin
Generic Name: Dextromethorphan/Guaifenesin
Brand Name: Examples include Guaifenex DM and Bidex-A


Guaifenex DM Extended-Release Tablets are used for:

Temporarily relieving cough due to the common cold, upper respiratory tract infections, sinus inflammation, sore throat, or bronchitis.


Guaifenex DM Extended-Release Tablets are a combination of an expectorant (guaifenesin) and a cough suppressant (dextromethorphan). It works by loosening mucus and lung secretions in the chest and making coughs more productive.


Do NOT use Guaifenex DM Extended-Release Tablets if:


  • you are allergic to any ingredient in Guaifenex DM Extended-Release Tablets

  • you are taking or have taken a monoamine oxidase inhibitor (MAOI) (eg, selegiline) within the last 14 days

  • you are taking a selective serotonin reuptake inhibitor (SSRI) (eg, fluoxetine)

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



Before using Guaifenex DM Extended-Release Tablets:


Some medical conditions may interact with Guaifenex DM Extended-Release Tablets. Tell your health care provider if you have any medical conditions, especially if any of the following apply to you:


  • if you are pregnant, planning to become pregnant, or are breast-feeding

  • if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

  • if you have allergies to medicines, foods, or other substances

  • if you have chronic cough, chronic bronchitis or any breathing problems, such as asthma, emphysema, or chronic obstructive pulmonary disease (COPD)

  • if you have been very ill or weakened, or you are confined to a bed or chair

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


  • MAOIs (eg, selegiline) and SSRIs (eg, fluoxetine) because the risk of serious side effects may be increased by Guaifenex DM Extended-Release Tablets

This may not be a complete list of all interactions that may occur. Ask your health care provider if Guaifenex DM Extended-Release Tablets may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.


How to use Guaifenex DM Extended-Release Tablets:


Use Guaifenex DM Extended-Release Tablets as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • Take Guaifenex DM Extended-Release Tablets by mouth with or without food. If stomach upset occurs, take with food to reduce stomach irritation.

  • Swallow Guaifenex DM Extended-Release Tablets whole. Do not break, crush, or chew before swallowing. Some brands of Guaifenex DM Extended-Release Tablets may be broken in half before taking. If you have difficulty swallowing the whole tablet, ask your pharmacist if your brand of medicine may be broken in half.

  • Drinking extra fluids while you are taking Guaifenex DM Extended-Release Tablets are recommended. Check with your doctor for instructions.

  • If you miss a dose of Guaifenex DM Extended-Release Tablets and you are taking 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.

Ask your health care provider any questions you may have about how to use Guaifenex DM Extended-Release Tablets.



Important safety information:


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

  • Do not drink alcohol or use medicines that may cause drowsiness (eg, sleep aids, muscle relaxers) while you are using Guaifenex DM Extended-Release Tablets without first checking with your doctor; it may add to their effects. Ask your pharmacist if you have questions about which medicines may cause drowsiness.

  • If your cough lasts for more than 1 week or comes back, or if you also have a fever, rash, or persistent headache, contact your health care provider. A persistent cough could be a sign of a serious condition.

  • Guaifenex DM Extended-Release Tablets has dextromethorphan in it. Before you start any new medicine, check the label to see if it has dextromethorphan in it too. If it does or if you are not sure, check with your doctor or pharmacist.

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

  • Use Guaifenex DM Extended-Release Tablets with caution in the ELDERLY; they may be more sensitive to its effects.

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

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


Possible side effects of Guaifenex DM Extended-Release Tablets:


All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:



Dizziness; drowsiness; stomach upset.



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

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



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


See also: Guaifenex DM 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 confusion; excitement; hallucinations; slowed breathing.


Proper storage of Guaifenex DM Extended-Release Tablets:

Store Guaifenex DM Extended-Release Tablets 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 Guaifenex DM Extended-Release Tablets out of the reach of children and away from pets.


General information:


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

  • Guaifenex DM Extended-Release Tablets are to be used only by the patient for whom it is prescribed. Do not share it with other people.

  • If your symptoms do not improve or if they become worse, check with your doctor.

  • Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Guaifenex DM Extended-Release Tablets. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.



Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Guaifenex DM resources


  • Guaifenex DM Side Effects (in more detail)
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  • Drug Images
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