Friday, September 30, 2016

Doctors Foster and Smith Chlorhexidine Salve





Dosage Form: FOR ANIMAL USE ONLY
For Dogs, cats, and small pets

DIRECTIONS


Clean area thoroughly. Apply 1 to 3 times daily, to minor cuts, burns, and scrapes.



ACTIVE INGREDIENT


1.0% Chlorhexidine Diacetate



OTHER INGREDIENTS


Petrolatum, Boric Acid, Propylene CGlycol, Sucrose Octa Acetate, Fragrance, Vitamin A Palmtate, dl-Alpha Tocopheryl Acetate (source of Vitamin E), Cholecalciferol (source of Vitamin D3).



CAUTION


For external use only. Avoid contact with eyes. Consult your veterinarian in cases of deep or puncture wounds, animal bites, serious burns or if redness and irritation persists or increases.



STORAGE


Keep tightly closed at room temperature. Protect from freezing.



For animal use only


Keep out of reach of children and pets to avoid accidental ingestion



For Questions Or To Re-Order:


1-800-562-7169



Doctors


Foster and Smith           


Septi-Soothe


Salve


Veterinarian Formulated


Advanced Salve


Gentle, Antiseptic Formula


NET WT


0.85 OZ


(24 g)










DOCTORS FOSTER AND SMITH 
chlorhexidine  salve










Product Information
Product TypeOTC ANIMAL DRUGNDC Product Code (Source)65713-909
Route of AdministrationTOPICALDEA Schedule    








Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLORHEXIDINE (CHLORHEXIDINE)CHLORHEXIDINE0.24 g  in 24 g
















Inactive Ingredients
Ingredient NameStrength
PETROLATUM 
BORIC ACID 
PROPYLENE GLYCOL 
SUCROSE 
VITAMIN A PALMITATE 
ALPHA-TOCOPHEROL, DL- 


















Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains      














Packaging
#NDCPackage DescriptionMultilevel Packaging
165713-909-081 BOX In 1 BOXcontains a TUBE (65713-909-09)
165713-909-0924 g In 1 TUBEThis package is contained within the BOX (65713-909-08)










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other01/01/2001


Labeler - Doctors Foster and Smith (122135148)

Registrant - United Pet Group (931135730)









Establishment
NameAddressID/FEIOperations
JUNGLE LABORATORIES CORPORATION032615270manufacture
Revised: 03/2010Doctors Foster and Smith



Normatol




Normatol may be available in the countries listed below.


Ingredient matches for Normatol



Gabapentin

Gabapentin is reported as an ingredient of Normatol in the following countries:


  • Chile

International Drug Name Search

Doxepin Concentrate



Pronunciation: DOX-e-pin
Generic Name: Doxepin
Brand Name: Sinequan

Antidepressants may increase the risk of suicidal thoughts or actions in children, teenagers, and young adults. However, depression and certain other mental problems may also increase the risk of suicide. Talk with the patient's doctor to be sure that the benefits of using Doxepin Concentrate outweigh the risks.


Family and caregivers must closely watch patients who take Doxepin Concentrate. It is important to keep in close contact with the patient's doctor. Tell the doctor right away if the patient has symptoms like worsened depression, suicidal thoughts, or changes in behavior. Discuss any questions with the patient's doctor.





Doxepin Concentrate is used for:

Treating depression or anxiety in certain patients. It may also be used for other conditions as determined by your doctor.


Doxepin Concentrate is a tricyclic antidepressant. It is not known exactly how it works. It may increase the activity of certain chemicals in the brain, which help elevate mood.


Do NOT use Doxepin Concentrate if:


  • you are allergic to any ingredient in Doxepin Concentrate or to other tricyclic antidepressants

  • you have certain prostate problems (eg, asymptomatic prostatic hypertrophy), glaucoma, or trouble urinating

  • you are taking clonidine, an H1 antagonist (eg, astemizole, terfenadine), or ibutilide

  • you have taken linezolid, methylene blue, or a monoamine oxidase inhibitor (MAOI) (eg, furazolidone, phenelzine, isocarboxazid) within the past 14 days

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



Video: Treatment for Depression







Treatments for depression are getting better everyday and there are things you can start doing right away.






Before using Doxepin Concentrate:


Some medical conditions may interact with Doxepin Concentrate. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:


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

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

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

  • if you have a history of heart problems, seizures (eg, epilepsy), overactive thyroid, prostate problems (eg, benign prostatic hypertrophy [BPH]), blood problems (eg, porphyria), other mental or mood problems, suicidal thoughts or attempts, or alcohol abuse

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


  • Antiarrhythmics (eg, quinidine, propafenone, flecainide), antifungal medicines (eg, fluconazole, terbinafine), carbamazepine, cimetidine, mibefradil, phenothiazines (eg, chlorpromazine, thioridazine), or selective serotonin reuptake inhibitors (SSRIs) (eg, fluoxetine, sertraline) because they may increase the risk of Doxepin Concentrate's side effects

  • Anticoagulants (eg, warfarin), H1 antagonists (eg, astemizole, terfenadine), ibutilide, sulfonylureas (eg, tolazamide, glipizide), sympathomimetics (eg, phenylephrine, pseudoephedrine), or tramadol because the risk of their side effects may be increased by Doxepin Concentrate

  • Clonidine, guanadrel, guanethidine, or guanfacine because their effectiveness may be decreased by Doxepin Concentrate

  • Linezolid, MAOIs (eg, furazolidone, phenelzine, isocarboxazid), or methylene blue because severe toxic effects may occur

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


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


  • Take Doxepin Concentrate by mouth with or without food.

  • Doxepin Concentrate must be diluted before taking. Dilute Doxepin Concentrate in 4 oz/120 mL of water, milk, or fruit juice.

  • Taking Doxepin Concentrate at bedtime may help reduce side effects (eg, daytime drowsiness). Discuss this possibility with your doctor.

  • If you miss a dose of Doxepin Concentrate, 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. If you take 1 dose daily at bedtime, do not take the missed dose the next morning.

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



Important safety information:


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

  • Doxepin Concentrate will add to the effects of alcohol and other depressants. Ask your pharmacist if you have questions about which medicines are depressants.

  • Doxepin Concentrate may cause dizziness, lightheadedness, or fainting; alcohol, hot weather, exercise, or fever may increase these effects. To prevent them, sit up or stand slowly, especially in the morning. Sit or lie down at the first sign of any of these effects.

  • Children, teenagers, and young adults who take Doxepin Concentrate may be at increased risk for suicidal thoughts or actions. Watch all patients who take Doxepin Concentrate closely. Contact the doctor at once if new, worsened, or sudden symptoms such as depressed mood; anxious, restless, or irritable behavior; panic attacks; or any unusual change in mood or behavior occur. Contact the doctor right away if any signs of suicidal thoughts or actions occur.

  • Limit your alcohol consumption while taking Doxepin Concentrate.

  • Doxepin Concentrate may cause you to become sunburned more easily. Avoid the sun, sunlamps, or tanning booths until you know how you react to Doxepin Concentrate. Use a sunscreen or wear protective clothing if you must be outside for more than a short time.

  • Tell your doctor or dentist that you take Doxepin Concentrate before you receive any medical or dental care, emergency care, or surgery.

  • After you start taking Doxepin Concentrate, several weeks may pass before you feel the full benefit.

  • Taking Doxepin Concentrate at bedtime may help reduce side effects (eg, daytime drowsiness). Discuss this possibility with your doctor.

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

  • Doxepin Concentrate should not be used in CHILDREN younger than 12 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 Doxepin Concentrate while you are pregnant. Doxepin Concentrate is found in breast milk. Do not breast-feed while taking Doxepin Concentrate.


Possible side effects of Doxepin Concentrate:


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:



Appetite loss; constipation; diarrhea; dizziness; drowsiness; dry mouth; excess sweating; headache; heartburn; increased appetite; indigestion; nausea; unpleasant taste; urinary retention; vomiting; weakness; weight gain.



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

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); abnormal movements; aggressive or bizarre behavior; agitation; anxiety; blurred vision or other vision changes; chest pain; difficulty speaking and swallowing; disorientation; eye pain; fainting; fast, slow, or irregular heartbeat; hair loss; hallucinations; hostility; irritability; loss of balance; mood swings; nervousness or restlessness; panic attacks; ringing in the ears; seizures; shakiness; sore throat or fever; trouble sleeping; twitching of the face or tongue; unusual bleeding or bruising; yellowing of the skin or eyes.



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



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 agitation; confusion; drowsiness; dry mouth; enlarged pupils; fast or irregular heartbeat; flushing; loss of consciousness; seizures.


Proper storage of Doxepin Concentrate:

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


General information:


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

  • Doxepin Concentrate is to be used only by the patient for whom it is prescribed. Do not share it with other people.

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

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

This information is a summary only. It does not contain all information about Doxepin Concentrate. 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 Doxepin resources


  • Doxepin Use in Pregnancy & Breastfeeding
  • Drug Images
  • Doxepin Drug Interactions
  • Doxepin Support Group
  • 80 Reviews for Doxepin - Add your own review/rating


Compare Doxepin with other medications


  • Anxiety
  • Depression
  • Insomnia
  • Irritable Bowel Syndrome
  • Reflex Sympathetic Dystrophy Syndrome
  • Urticaria

Rimantadine


Pronunciation: ri-MAN-ta-deen
Generic Name: Rimantadine
Brand Name: Flumadine


Rimantadine is used for:

Preventing and treating certain types of flu in adults. It is also used to prevent certain types of flu in children. It may also be used for other conditions as determined by your doctor.


Rimantadine is an antiviral agent. Exactly how it works is not known. It may block reproduction of the virus.


Do NOT use Rimantadine if:


  • you are allergic to any ingredient in Rimantadine or to any adamantane medicine (eg, amantadine)

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



Before using Rimantadine:


Some medical conditions may interact with Rimantadine. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:


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

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

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

  • if you have a history of liver problems, kidney problems, or seizures

  • if you have taken any adamantane medicine (eg, amantadine) for the flu and it has not worked

  • if you will be receiving a live nasal flu vaccine, or have received one within the past 14 days

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


  • Acetaminophen or aspirin because they may decrease Rimantadine's effectiveness

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


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


  • Take Rimantadine by mouth with or without food.

  • If you are taking Rimantadine to treat the flu, start taking it as soon as possible. It works best if you begin taking it within 48 hours after you start having flu symptoms.

  • Take Rimantadine for the full course of treatment. Do not miss any doses.

  • If you miss a dose of Rimantadine, 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 Rimantadine.



Important safety information:


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

  • Rimantadine only works against certain types of the flu; it does not treat other viral infections (eg, the common cold) or infections caused by bacteria.

  • Be sure to use Rimantadine for the full course of treatment. If you do not, the medicine may not work as well. The virus could also become less sensitive to this or other medicines. This could make the infection harder to treat in the future.

  • Check with your doctor if you will be receiving a live nasal flu vaccine or have received one within the past 14 days. You should usually not start taking Rimantadine until 2 weeks after you receive a live nasal flu vaccine. You should usually not receive a live nasal flu vaccine within 48 hours after you stop taking Rimantadine.

  • Use Rimantadine with caution in the ELDERLY; they may be more sensitive to its effects, especially dizziness, headache, anxiety, weakness, tiredness, nausea, vomiting, and stomach pain.

  • Rimantadine should not be used to treat the flu in CHILDREN younger than 17 years old or used to prevent the flu in children younger than 1 year 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 Rimantadine while you are pregnant. It is not known if Rimantadine is found in breast milk. Do not breast-feed while taking Rimantadine.


Possible side effects of Rimantadine:


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; dry mouth; headache; loss of appetite; nausea; nervousness; stomach pain; tiredness; trouble sleeping; vomiting; weakness.



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

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); confusion; depression; fast or irregular heartbeat; hallucinations; seizures; swelling of the hands, ankles, or feet; tremor; trouble walking.



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: Rimantadine 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 agitation; hallucination; irregular heartbeat.


Proper storage of Rimantadine:

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


General information:


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

  • Rimantadine is to be used only by the patient for whom it is prescribed. Do not share it with other people.

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

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

This information is a summary only. It does not contain all information about Rimantadine. 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 Rimantadine resources


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


  • Rimantadine Prescribing Information (FDA)

  • rimantadine Advanced Consumer (Micromedex) - Includes Dosage Information

  • rimantadine Concise Consumer Information (Cerner Multum)

  • Flumadine Monograph (AHFS DI)

  • Flumadine Prescribing Information (FDA)



Compare Rimantadine with other medications


  • Influenza A
  • Influenza Prophylaxis

Triactin



Pronunciation: dye-SYE-kloe-meen
Generic Name: Dicyclomine
Brand Name: Examples include Bentyl and Triactin


Triactin is used for:

Treatment of the symptoms of irritable bowel syndrome. It may also be used for other conditions as determined by your doctor.


Triactin is an anticholinergic. It works by blocking a chemical in the smooth muscle of the stomach and intestines causing them to relax, which reduces cramping.


Do NOT use Triactin if:


  • you are allergic to any ingredient in Triactin

  • you have blockage of the esophagus, stomach, intestine, or urinary tract

  • you have heart problems due to severe bleeding

  • you have glaucoma

  • you have inflammation of the esophagus due to acid reflux, loss of strength in the intestinal muscles, or chronic inflammation and ulceration of the bowels

  • you have myasthenia gravis (a condition in which the muscles become progressively paralyzed)

  • you are breast-feeding

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



Before using Triactin:


Some medical conditions may interact with Triactin. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:


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

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

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

  • if you have chronic inflammation or ulcers of the bowel, diarrhea, enlargement of the prostate, hiatal hernia, kidney or liver disease, a nervous system disease, overactive thyroid, or urinary blockage or retention

  • if you have heart disease, heart failure, a history of rapid heartbeat, or high blood pressure

  • if you are at risk for glaucoma

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


  • Amantadine, antiarrhythmics (eg, quinidine), antihistamines (eg, diphenhydramine), benzodiazepines (eg, diazepam), monoamine oxidase inhibitors (MAOIs) (eg, phenelzine), narcotic pain medicine (eg, meperidine), nitrates (eg, nitroglycerin, isosorbide), nitrites (eg, sodium nitrite), phenothiazines (eg, chlorpromazine), sympathomimetics (eg, pseudoephedrine), or tricyclic antidepressants (eg, amitriptyline) because they may increase the risk of Triactin's side effects

  • Metoclopramide or phenothiazines (eg, chlorpromazine) because their effectiveness may be decreased by Triactin

  • Digoxin because the risk of its side effects may be increased by Triactin

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


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


  • Take Triactin by mouth on an empty stomach at least 30 minutes before eating unless otherwise directed by your doctor.

  • If you are also taking antacids, you may need to separate them from Triactin. Ask your doctor or pharmacist for more information.

  • Take Triactin on a regular schedule around the clock, unless your doctor tells you otherwise.

  • If you miss a dose of Triactin, 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 Triactin.



Important safety information:


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

  • Check with your doctor before you drink alcohol or use medicines that may cause drowsiness (eg, sleep aids, muscle relaxers) while you are using Triactin; it may add to their effects. Ask your pharmacist if you have questions about which medicines may cause drowsiness.

  • Do not become overheated in hot weather or while you are being active; heatstroke may occur.

  • Triactin may make your eyes more sensitive to sunlight. It may help to wear sunglasses.

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

  • Triactin should not be used in CHILDREN younger than 6 months 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 Triactin while you are pregnant. Triactin is found in breast milk. Do not breast-feed while taking Triactin.


Possible side effects of Triactin:


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:



Blurred vision; constipation; decreased sweating; difficulty sleeping; dizziness; drowsiness; dry mouth; headache; lightheadedness; loss of taste; nausea; nervousness.



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); agitation; confusion; diarrhea; difficulty focusing your eyes; difficulty moving; difficulty speaking; difficulty urinating; disorientation; exaggerated sense of well-being; fainting; hallucinations; pounding in the chest, rapid heartbeat; short-term memory loss; unusual weakness; vomiting.



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: Triactin 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; convulsions (seizures); difficulty breathing; dilated pupils; disorientation; excessive thirst; flushed, hot, dry skin; hallucinations or unusual behavior; muscle weakness; nausea; rapid heartbeat and breathing; restlessness; unusual dizziness or drowsiness; unusually dry mouth; vomiting.


Proper storage of Triactin:

Store at room temperature, below 86 degrees F (30 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Triactin out of the reach of children and away from pets.


General information:


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

  • Triactin is to be used only by the patient for whom it is prescribed. Do not share it with other people.

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

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

This information is a summary only. It does not contain all information about Triactin. 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 Triactin resources


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


  • Triactin Concise Consumer Information (Cerner Multum)



Compare Triactin with other medications


  • Colitis
  • Irritable Bowel Syndrome

Thursday, September 29, 2016

Cesol




Cesol may be available in the countries listed below.


Ingredient matches for Cesol



Praziquantel

Praziquantel is reported as an ingredient of Cesol in the following countries:


  • Chile

  • Germany

  • Mexico

  • Romania

International Drug Name Search

Cefotaxima Sandoz




Cefotaxima Sandoz may be available in the countries listed below.


Ingredient matches for Cefotaxima Sandoz



Cefotaxime

Cefotaxime sodium salt (a derivative of Cefotaxime) is reported as an ingredient of Cefotaxima Sandoz in the following countries:


  • Colombia

  • Italy

  • Spain

International Drug Name Search

Dip Rilif




Dip Rilif may be available in the countries listed below.


Ingredient matches for Dip Rilif



Ibuprofen

Ibuprofen is reported as an ingredient of Dip Rilif in the following countries:


  • Poland

Levomenthol

Levomenthol is reported as an ingredient of Dip Rilif in the following countries:


  • Poland

International Drug Name Search

Doxorubicin Liposomal


Pronunciation: DOX-oh-ROO-bi-sin
Generic Name: Doxorubicin Liposomal
Brand Name: Doxil

Doxorubicin Liposomal is for intravenous (IV) use only and should only be given under the supervision of a doctor experienced in the use of cancer chemotherapy agents. If Doxorubicin Liposomal accidentally leaks into surrounding tissue, the skin and/or muscle may be severely damaged. Notify your doctor immediately if redness, pain, or swelling at or around the injection site occurs.


Doxorubicin Liposomal may cause severe and possibly life-threatening heart problems (eg, heart failure). These problems may occur during therapy or sometimes months to years after receiving Doxorubicin Liposomal. In some cases heart problems are irreversible. The risk may be increased if you are using certain medicines that may affect heart function (eg, trastuzumab), or have a history of heart problems, radiation treatment to the chest area, or previous therapy with other anthracyclines (eg, epirubicin). The risk of developing heart problems varies depending on your dose and condition, although it can occur at any dose whether or not you are at risk. Notify your doctor right away if you develop cough; fast, slow, or irregular heartbeat; shortness of breath; sudden, unexplained weight gain; or swelling of the hands, ankles, or feet.


Serious and sometimes life threatening infusion-related reactions have occurred with the use of Doxorubicin Liposomal. Contact your doctor right away if you experience back pain, chills, fainting, flushing, headache, severe dizziness or light-headedness, shortness of breath, swelling of the face, or tightness in the chest or throat.


Another type of cancer (acute myelogenous leukemia [AML]) and a certain blood problem (myelodysplastic syndrome [MDS]) have been reported in patients treated with anthracyclines, including Doxorubicin Liposomal. The risk varies depending on your dose, and other medicines and/or radiation therapy. Discuss any questions or concerns with your doctor.


Doxorubicin Liposomal may cause bone marrow suppression. Notify your doctor immediately if you develop easy bruising or bleeding, unusual tiredness or weakness, or signs of an infection (eg, fever, chills, persistent sore throat).


Tell your doctor if you have liver problems because your dose will have to be decreased. Your doctor will closely monitor you while you are using Doxorubicin Liposomal.





Doxorubicin Liposomal is used for:

Treating advanced ovarian cancer and AIDS-related Kaposi sarcoma in certain patients. It is also used with another medicine to treat a type of bone marrow cancer (multiple myeloma) in certain patients.


Doxorubicin Liposomal is an antineoplastic antibiotic. It works by killing cancer cells.


Do NOT use Doxorubicin Liposomal if:


  • you are allergic to any ingredient in Doxorubicin Liposomal or to similar medicines (eg, epirubicin)

  • you are breast-feeding

  • you have certain bone marrow problems (eg, low blood platelet levels, low red blood cell levels, low white blood cell levels)

  • you have taken or will be taking palifermin within 24 hours before or after using Doxorubicin Liposomal

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



Before using Doxorubicin Liposomal:


Some medical conditions may interact with Doxorubicin Liposomal. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:


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

  • if you are able to become pregnant

  • 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 swelling or soreness of the mouth or tongue, blood vessel disease, an infection, or liver problems

  • if you plan to receive any vaccines

  • if you are older than 50 years old

  • if you have a history of heart problems, radiation treatment (or are currently receiving radiation treatment), or if you have previously received Doxorubicin Liposomal or similar medicines (eg, epirubicin, daunorubicin)

  • if you are taking medicines that may affect heart function (eg, calcium channel blockers, trastuzumab). Ask your doctor if you are unsure if any of your medicines may affect heart function

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


  • Calcium channel blockers (eg, diltiazem, verapamil), cyclophosphamide, or trastuzumab because the risk of heart problems (eg, heart failure) may be increased

  • Cyclosporine, cytarabine, paclitaxel, progesterone, or streptozocin because they may increase the risk of Doxorubicin Liposomal's side effects

  • Phenobarbital because it may decrease Doxorubicin Liposomal's effectiveness

  • Anticoagulants (eg, warfarin) because the risk of their side effects may be increased by Doxorubicin Liposomal

  • Palifermin because if mouth or tongue sores develop, they may be more severe or last longer

  • Hydantoins (eg, phenytoin) because their effectiveness may be decreased by Doxorubicin Liposomal

  • Medicines that may harm the liver (eg, acetaminophen, methotrexate, ketoconazole, isoniazid, certain medicines for HIV infection) because the risk of Doxorubicin Liposomal's side effects may be increased. Ask your doctor if you are unsure if any of your medicines might harm the liver

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


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


  • Doxorubicin Liposomal is usually given as an injection at your doctor's office, hospital, or clinic. Ask your doctor any questions that you may have about Doxorubicin Liposomal.

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

  • Drinking extra fluids while you are taking Doxorubicin Liposomal is recommended. Check with your doctor for instructions.

  • Your doctor may prescribe another medicine to lessen nausea and vomiting that can occur when taking Doxorubicin Liposomal. Discuss any questions with your doctor.

  • If you spill Doxorubicin Liposomal on your skin, wash it off right away with soap and water.

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

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

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



Important safety information:


  • Doxorubicin Liposomal may reduce the number of clot-forming cells (platelets) in your blood. Avoid activities that may cause bruising or injury. Tell your doctor if you have unusual bruising or bleeding. Tell your doctor if you have dark, tarry, or bloody stools.

  • Doxorubicin Liposomal may lower the ability of your body to fight infection. Avoid contact with people who have colds or infections. Tell your doctor if you notice signs of infection like fever, sore throat, rash, or chills.

  • Do not receive a live vaccine (eg, measles, mumps) while you are taking Doxorubicin Liposomal. Talk with your doctor before you receive any vaccine.

  • Doxorubicin Liposomal may cause the urine to turn red. This is harmless and usually goes away 1 to 2 days after receiving a dose of Doxorubicin Liposomal.

  • Doxorubicin Liposomal may cause you to become sunburned more easily. Avoid the sun, sunlamps, or tanning booths until you know how you react to Doxorubicin Liposomal. Use a sunscreen or wear protective clothing if you must be outside for more than a short time.

  • Lab tests, including liver function, complete blood cell counts, blood uric acid and electrolyte levels, and heart function, may be performed while you use Doxorubicin Liposomal. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

  • Tell your doctor or dentist that you take Doxorubicin Liposomal before you receive any medical or dental care, emergency care, or surgery.

  • Doxorubicin Liposomal should be used with extreme caution in CHILDREN; safety and effectiveness in children have not been confirmed.

  • Caution is advised when using Doxorubicin Liposomal in CHILDREN; they may be more sensitive to its effects.

  • Doxorubicin Liposomal may damage sperm. Use effective birth control methods (eg, condoms) while using Doxorubicin Liposomal. Discuss any questions or concerns with your doctor.

  • PREGNANCY and BREAST-FEEDING: Doxorubicin Liposomal has been shown to cause harm to the fetus. Avoid becoming pregnant while you are taking it. If you are able to become pregnant, talk with your doctor about using an effective form of birth control. If you think you may be pregnant, contact your doctor. You will need to discuss the benefits and risks of using Doxorubicin Liposomal while you are pregnant. Doxorubicin Liposomal is found in breast milk. Do not breast-feed while taking Doxorubicin Liposomal.


Possible side effects of Doxorubicin Liposomal:


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; hair loss; indigestion; loss of appetite; nausea; tiredness; weakness; weight changes.



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 or throat; swelling of the mouth, face, lips, or tongue); absence of menstrual cycle or menstrual changes; back pain; black, tarry stools; bluish skin or nails; calf or leg pain, swelling, redness, or tenderness; chest pain; dizziness or light-headedness; fainting; fast, slow, or irregular heartbeat; flushing; headache; loose or bloody stools; pain, redness, burning, stinging, swelling, or open sores at the injection site; rectal bleeding or irritation; redness or discharge of the eyes; redness, pain, swelling, peeling, tingling, or blistering of the palms of the hands and the soles of the feet; severe or persistent nausea; shortness of breath; sudden, unexplained weight gain; swelling of the hands, ankles, or feet; swelling or soreness of the mouth or tongue; symptoms of dehydration (eg, dry mouth or eyes, decreased urination, fast heartbeat, sluggishness, unusual thirst); symptoms of infection (eg, fever, chills, cough, sore throat, burning or painful urination); unusual bruising or bleeding; unusual tiredness or weakness; vomiting.



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: Doxorubicin Liposomal 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 swelling or soreness of the mouth or tongue; unusual bruising or bleeding.


Proper storage of Doxorubicin Liposomal:

Doxorubicin Liposomal is usually handled and stored by a health care provider. If you are using Doxorubicin Liposomal at home, store Doxorubicin Liposomal as directed by your pharmacist or health care provider. Keep Doxorubicin Liposomal out of the reach of children and away from pets.


General information:


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

  • Doxorubicin Liposomal is to be used only by the patient for whom it is prescribed. Do not share it with other people.

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

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

This information is a summary only. It does not contain all information about Doxorubicin Liposomal. 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 Doxorubicin Liposomal resources


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


  • Doxil Advanced Consumer (Micromedex) - Includes Dosage Information

  • Doxil Prescribing Information (FDA)

  • doxorubicin liposomal Concise Consumer Information (Cerner Multum)



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  • Kaposi's Sarcoma
  • Multiple Myeloma
  • Ovarian Cancer

Atenemeal




Atenemeal may be available in the countries listed below.


Ingredient matches for Atenemeal



Atenolol

Atenolol is reported as an ingredient of Atenemeal in the following countries:


  • Japan

International Drug Name Search

Wednesday, September 28, 2016

Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate Sustained-Release Capsules


Pronunciation: dex-troe-meth-OR-fan/gwye-FEN-eh-sin/poe-TASS-ee-um gwye-a-kole-SUL-foe-nate
Generic Name: Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate
Brand Name: Humibid DM


Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate Sustained-Release Capsules are used for:

Relieving symptoms of cough and mucus in the chest due to respiratory infections, asthma, colds, or hay fever. It may also be used for other conditions as determined by your doctor.


Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate Sustained-Release Capsules are a combination of a cough suppressant and 2 expectorants. The cough suppressant works in the brain to reduce the cough reflex. The expectorants loosen mucus and lung secretions in the chest and make coughs more productive.


Do NOT use Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate Sustained-Release Capsules if:


  • you are allergic to any ingredient in Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate Sustained-Release Capsules

  • 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 Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate Sustained-Release Capsules:


Some medical conditions may interact with Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate 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, planning to become pregnant, or are breast-feeding

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

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

  • if you have a history of a chronic cough that occurs with smoking, asthma, chronic bronchitis, or emphysema, or if cough occurs with large amounts of mucus

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


  • Furazolidone or MAO inhibitors (eg, phenelzine) because the risk of serious side effects such as low blood pressure, fever, severe muscle problems, and possibly death may be increased by Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate Sustained-Release Capsules

This may not be a complete list of all interactions that may occur. Ask your health care provider if Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate 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 Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate Sustained-Release Capsules:


Use Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate Sustained-Release Capsules as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate Sustained-Release Capsules may be taken with or without food.

  • Drinking extra fluids while you are taking Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate Sustained-Release Capsules are recommended. Check with your doctor for instructions.

  • Swallow Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate Sustained-Release Capsules whole. Do not break, crush, or chew before swallowing.

  • If you miss a dose of Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate Sustained-Release Capsules 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. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate Sustained-Release Capsules.



Important safety information:


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

  • If cough persists for more than 1 week or is accompanied by a fever, contact your health care provider. A persistent cough could be a sign of a serious condition.

  • Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate Sustained-Release Capsules contains dextromethorphan. Before you begin taking any new prescription or nonprescription medicine, read the ingredients to see if it also contains dextromethorphan. If it does or if you are uncertain, contact your doctor or pharmacist.

  • Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate Sustained-Release Capsules may interfere with some lab tests. Make sure your doctor and lab personnel know you are taking Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate Sustained-Release Capsules.

  • Use Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate Sustained-Release Capsules with caution in the ELDERLY because they may be more sensitive to its effects.

  • Use Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate Sustained-Release Capsules with extreme caution in CHILDREN younger than 12 years of age. Safety and effectiveness in this age group have not been confirmed.

  • PREGNANCY and BREAST-FEEDING: If you become pregnant, discuss with your doctor the benefits and risks of using Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate Sustained-Release Capsules during pregnancy. It is unknown if Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate Sustained-Release Capsules are excreted in breast milk. If you are or will be breast-feeding while you are using Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate Sustained-Release Capsules, check with your doctor or pharmacist to discuss the risks to your baby.


Possible side effects of Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate 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:



Dizziness; headache; nausea; upset stomach; vomiting.



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

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



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: Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate 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.


Proper storage of Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate Sustained-Release Capsules:

Store Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate 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 Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate Sustained-Release Capsules out of the reach of children and away from pets.


General information:


  • If you have any questions about Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate Sustained-Release Capsules, please talk with your doctor, pharmacist, or other health care provider.

  • Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate 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 Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate 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 Dextromethorphan/Guaifenesin/Potassium Guaiacolsulfonate resources


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


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  • Cough and Nasal Congestion

Shotapen




Shotapen may be available in the countries listed below.


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

Ingredient matches for Shotapen



Benzylpenicillin

Benzylpenicillin benzathine and procaine (a derivative of Benzylpenicillin) is reported as an ingredient of Shotapen in the following countries:


  • France

Dihydrostreptomycin

Dihydrostreptomycin sulfate (a derivative of Dihydrostreptomycin) is reported as an ingredient of Shotapen in the following countries:


  • France

International Drug Name Search

Dextran 70 6% in 5% Dextrose


Generic Name: dextran, high molecular weight (DEX tran)

Brand Names: Dextran 70 6% in 0.9% Sodium Chloride, Dextran 70 6% in 5% Dextrose, Gentran 70, Hyskon


What is high-molecular weight dextran?

High-molecular weight dextran is a plasma volume expander derived from natural sources of sugar (glucose). It works by restoring blood plasma lost through severe bleeding.


Severe blood loss can decrease oxygen levels, which can lead to organ failure, brain damage, coma, and possibly death. Plasma is needed to circulate red blood cells that deliver oxygen throughout the body.

Dextran is used to treat hypovolemia (a decrease in the volume of circulating blood plasma), that can result from severe blood loss after surgery, injury, or other causes of bleeding.


Dextran is also used to expand the inside of the uterus, making it easier for a doctor to see with a scope during a diagnostic procedure called hysteroscopy.


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


What is the most important information I should know about high-molecular weight dextran?


You should not be given this medication if you are allergic to dextran, or if you have severe kidney or heart disease.

If possible before you receive dextran, tell your doctor if you have a bleeding or blood clotting disorder, a blood cell disorder, heart disease or congestive heart failure, kidney disease, a stomach or intestinal disorder, pulmonary edema (fluid in the lungs), urination problems, a food or drug allergy, or if you are on a low-salt diet.


In an emergency situation, it may not be possible before you are treated to tell your caregivers about any health conditions you have or if you are pregnant or breast-feeding. However, make sure any doctor caring for you afterward knows that you have received this medication.


Tell your doctor about all other medications you use, especially a blood thinner, steroid medication, digoxin, or a diuretic.


What should I discuss with my health care provider before I receive high-molecular weight dextran?


You should not be given this medication if you are allergic to dextran, or if you have severe kidney or heart disease.

If you have certain conditions, you may need a dose adjustment or special tests to safely receive this medication. If possible before you receive dextran, tell your doctor if you have:



  • a bleeding or blood clotting disorder;




  • a blood cell disorder such as thrombocytopenia (lack of platelets);




  • heart disease or congestive heart failure;




  • kidney disease;




  • a stomach or intestinal disorder;




  • pulmonary edema (fluid in the lungs);




  • urination problems not caused by hypovolemia;




  • a food or drug allergy; or




  • if you are on a low-salt diet.




FDA pregnancy category C. It is not known whether dextran is harmful to an unborn baby. If possible before you receive this medication, tell your doctor if you are pregnant. It is not known whether dextran passes into breast milk or if it could harm a nursing baby. Tell your doctor if you are breast-feeding a baby.

In an emergency situation, it may not be possible before you are treated to tell your caregivers about any health conditions you have or if you are pregnant or breast-feeding. However, make sure any doctor caring for you afterward knows that you have received this medication.


How is high-molecular weight dextran given?


Dextran is given as an injection through a needle placed into a vein. For a hysteroscopy procedure, dextran is placed into the uterus using a small tube.


You will receive this injection in a clinic or hospital setting. A doctor, nurse, or other healthcare professional will give you this medication. Your breathing, blood pressure, oxygen levels, and other vital signs will be watched closely while you are receiving this medication.

To be sure dextran is helping your condition, your blood may need to be tested often. This will help your doctor determine how long to treat you with dextran.


What happens if I miss a dose?


Since dextran is given as needed by a healthcare professional, it is not likely that you will miss a dose.


What happens if I overdose?


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

An overdose of dextran is not expected to produce life-threatening symptoms.


What should I avoid after receiving high-molecular weight dextran?


Follow your doctor's instructions about any restrictions on food, beverages, or activity after you are treated with dextran.


High-molecular weight dextran 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. Tell your caregivers at once if you have a serious side effect such as:

  • wheezing or tight feeling in your chest;




  • urinating less than usual or not at all;




  • swelling in your hands or feet;




  • unusual bleeding, or any bleeding that will not stop;




  • feeling like you might pass out; or




  • burning, itching, swelling, or pain around the IV needle.



Less serious side effects may include:



  • nausea, vomiting, stomach pain;




  • joint pain;




  • stuffy nose;




  • mild itching; or




  • skin rash.



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 high-molecular weight dextran?


Before you receive dextran, tell your doctor if you are also using:



  • a blood thinner such as warfarin (Coumadin);




  • steroids (prednisolone and others);




  • digoxin (digitalis, Lanoxin); or




  • a diuretic (water pill) such as amiloride (Midamor, Moduretic), spironolactone (Aldactone, Aldactazide), or triamterene (Dyrenium, Dyazide, Maxzide).



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



More Dextran 70 6% in 5% Dextrose resources


  • Dextran 70 6% in 5% Dextrose Drug Interactions
  • 0 Reviews for Dextran 70 6% in Dextrose - Add your own review/rating


  • Dextran 40 Monograph (AHFS DI)

  • Dextran 70 Monograph (AHFS DI)



Compare Dextran 70 6% in 5% Dextrose with other medications


  • Bleeding Disorder


Where can I get more information?


  • Your doctor or pharmacist can provide more information about dextran.


Tuesday, September 27, 2016

Dextromethorphan/Guaifenesin


Pronunciation: DEX-troe-meth-OR-fan/gwye-FEN-e-sin
Generic Name: Dextromethorphan/Guaifenesin
Brand Name: Examples include Coricidin HBP Congestion/Cough and Humibid CS


Dextromethorphan/Guaifenesin is used for:

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


Dextromethorphan/Guaifenesin is 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 Dextromethorphan/Guaifenesin if:


  • you are allergic to any ingredient in Dextromethorphan/Guaifenesin

  • you have taken furazolidone or a monoamine oxidase inhibitor (MAOI) (eg, phenelzine) 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 Dextromethorphan/Guaifenesin:


Some medical conditions may interact with Dextromethorphan/Guaifenesin. 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 a history of chronic cough, lung problems (eg, chronic bronchitis, emphysema), asthma, chronic obstructive pulmonary disease (COPD), or if your cough occurs with large amounts of mucus

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


  • Furazolidone, MAOIs (eg, phenelzine), or SSRIs (eg, fluoxetine) because the risk of toxic side effects may be increased by Dextromethorphan/Guaifenesin

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


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


  • Take Dextromethorphan/Guaifenesin by mouth with or without food. If stomach upset occurs, take with food to reduce stomach irritation.

  • To help Dextromethorphan/Guaifenesin work, drink plenty of extra fluids while taking Dextromethorphan/Guaifenesin, unless your health care provider instructed otherwise.

  • If you miss a dose of Dextromethorphan/Guaifenesin 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 Dextromethorphan/Guaifenesin.



Important safety information:


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

  • 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.

  • Dextromethorphan/Guaifenesin 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.

  • Dextromethorphan/Guaifenesin should not be used in CHILDREN younger than 2 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 Dextromethorphan/Guaifenesin while you are pregnant. It is not known if Dextromethorphan/Guaifenesin is found in breast milk. Do not breast-feed while taking Dextromethorphan/Guaifenesin.


Possible side effects of Dextromethorphan/Guaifenesin:


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: Dextromethorphan/Guaifenesin 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 Dextromethorphan/Guaifenesin:

Store Dextromethorphan/Guaifenesin 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 Dextromethorphan/Guaifenesin out of the reach of children and away from pets.


General information:


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

  • Dextromethorphan/Guaifenesin is to be used only by the patient for whom it is prescribed. Do not share it with other people.

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

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

This information is a summary only. It does not contain all information about Dextromethorphan/Guaifenesin. 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 Dextromethorphan/Guaifenesin resources


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


Compare Dextromethorphan/Guaifenesin with other medications


  • Cough
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Unagen




Unagen may be available in the countries listed below.


Ingredient matches for Unagen



Metamizole

Metamizole is reported as an ingredient of Unagen in the following countries:


  • Indonesia

International Drug Name Search

COPD


Pronunciation: DYE-fi-lin/gwye-FEN-e-sin
Generic Name: Dyphylline/Guaifenesin
Brand Name: Examples include COPD and Lufyllin-GG


COPD is used for:

Relieving breathing problems caused by bronchial asthma, chronic bronchitis, or emphysema.


COPD is a bronchodilator and expectorant combination. It works by widening the air passages and making it easier to breathe, and by thinning the mucus for a more productive cough.


Do NOT use COPD if:


  • you are allergic to any ingredient in COPD

  • you are taking intravenous (IV) dipyridamole or halothane

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



Before using COPD:


Some medical conditions may interact with COPD. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:


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

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

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

  • if you have severe heart disease or heart damage, high blood pressure, epilepsy, kidney disease, thyroid problems, or ulcers

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


  • Beta-blockers (eg, propranolol) because the effectiveness of COPD may be decreased

  • Ephedrine, halothane, mexiletine, probenecid, sympathomimetics (eg, albuterol), tacrine, xanthines (eg, theophylline), or zileuton because side effects and toxic effects of COPD may be increased

  • Adenosine, IV dipyridamole, lithium, or nondepolarizing muscle relaxants (eg, pancuronium) because the effectiveness of these medicines may be decreased

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


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


  • COPD may be taken with or without food. Taking it after eating may help to decrease stomach upset.

  • Drinking extra fluids while you are taking COPD is recommended. Check with your doctor for instructions.

  • If you miss a dose of COPD, 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 COPD.



Important safety information:


  • Do not exceed the recommended dose without checking with your doctor.

  • Avoid large amounts of caffeine-containing foods and beverages, such as coffee, tea, cocoa, cola drinks, and chocolate.

  • Before you have any medical or dental treatments, emergency care, or surgery, tell the doctor or dentist that you are using COPD.

  • COPD may interfere with certain lab tests. Make sure your doctor and laboratory personnel know that you are taking COPD.

  • COPD is not recommended for use in CHILDREN younger than 6 years of age. Safety and effectiveness in this age group have not been confirmed.

  • Caution is advised when using COPD in CHILDREN 6 years of age and older because they may be more sensitive to its effects.

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


Possible side effects of COPD:


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:



Headache; nausea; upset stomach.



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); blood in the urine; bloody vomit; diarrhea; dizziness; excitability; fast breathing; fast/irregular heartbeat; flushing; increased thirst or urination; irritability; muscle twitching; pounding in the chest; restlessness; seizures; stomach pain; trouble sleeping; vomiting.



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: COPD 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 agitation; chest pain; dehydration; excessive sweating; excessive thirst; fever or chills; irregular heartbeat; loss of appetite; ringing in the ears; seizures; severe vomiting.


Proper storage of COPD:

Store COPD at room temperature, between 68 and 77 degrees F (20 and 25 degrees C), in a tightly closed container. Store away from heat, moisture, and light. Do not store in the bathroom. Avoid excessive heat (above 104 degrees F [40 degrees C]). Keep COPD out of the reach of children and away from pets.


General information:


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

  • COPD is to be used only by the patient for whom it is prescribed. Do not share it with other people.

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

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

This information is a summary only. It does not contain all information about COPD. 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 COPD resources


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


  • COPD Concise Consumer Information (Cerner Multum)

  • Dyfilin GG Concise Consumer Information (Cerner Multum)



Compare COPD with other medications


  • Asthma
  • Bronchitis