Tuesday 28 July 2009

Medicort




In the US, Medicort is a member of the drug class glucocorticoids and is used to treat Asthma - acute, Bullous Pemphigoid, Dermatitis, Immunosuppression, Inflammatory Conditions, Multiple Sclerosis, Nephrotic Syndrome, Pemphigoid and Pemphigus.

Ingredient matches for Medicort



Dexamethasone

Dexamethasone is reported as an ingredient of Medicort in the following countries:


  • Peru

Dexamethasone 21-(disodium phosphate) (a derivative of Dexamethasone) is reported as an ingredient of Medicort in the following countries:


  • Peru

Fluticasone

Fluticasone propionate (a derivative of Fluticasone) is reported as an ingredient of Medicort in the following countries:


  • Indonesia

International Drug Name Search

Wednesday 22 July 2009

Clotrimazol Bayhealth




Clotrimazol Bayhealth may be available in the countries listed below.


Ingredient matches for Clotrimazol Bayhealth



Clotrimazole

Clotrimazole is reported as an ingredient of Clotrimazol Bayhealth in the following countries:


  • Spain

International Drug Name Search

Thursday 16 July 2009

Cefaxetil




Cefaxetil may be available in the countries listed below.


Ingredient matches for Cefaxetil



Cefuroxime

Cefuroxime axetil (a derivative of Cefuroxime) is reported as an ingredient of Cefaxetil in the following countries:


  • Germany

International Drug Name Search

Rontilona




Rontilona may be available in the countries listed below.


Ingredient matches for Rontilona



Fluticasone

Fluticasone propionate (a derivative of Fluticasone) is reported as an ingredient of Rontilona in the following countries:


  • Portugal

International Drug Name Search

Wednesday 15 July 2009

Isozid-H




Isozid-H may be available in the countries listed below.


Ingredient matches for Isozid-H



Hexetidine

Hexetidine is reported as an ingredient of Isozid-H in the following countries:


  • Austria

International Drug Name Search

Monday 13 July 2009

Demadex


Generic Name: Torsemide
Class: Loop Diuretics
VA Class: CV702
Chemical Name: N-[[(1-Methylethyl)amino]carbonyl]-4-[(3-methylphenyl) amino]-3-pyridinesulfonamide
Molecular Formula: C16H20N4O3S
CAS Number: 56211-40-6

Introduction

A sulfonamide, loop-type diuretic and antihypertensive agent.1 a


Uses for Demadex


Edema


Management of edema associated with CHF1 4 or hepatic1 or renal1 disease (including chronic renal failure).a


Hypertension


Management of hypertension (alone or in combination with other classes of antihypertensive agents).1 2 3


One of several preferred initial therapies in hypertensive patients with CHF, acute pulmonary edema, or renal disease.2 3


Can be used as monotherapy for initial management of uncomplicated hypertension;1 2 3 a however, thiazide diuretics are preferred by JNC 7.11


Demadex Dosage and Administration


General



  • The manufacturer states that since oral and IV doses of torsemide are therapeutically equivalent, torsemide dosage is identical for oral or IV administration.1



Edema



  • Most experts state that all patients with symptomatic CHF who have evidence for, or a prior history of, fluid retention generally should receive diuretic therapy in conjunction with moderate sodium restriction (≤3 g of sodium daily), an ACE inhibitor, and usually a β-blocker, with or without a cardiac glycoside.4




  • Hospitalization of the patient during initiation of therapy is advisable for patients with hepatic cirrhosis and ascites or chronic renal failure.1 a b




  • Chronic use of any diuretic in hepatic disease has not been adequately studied.1 a



Administration


Administer orally, by direct IV injection, or by continuous IV infusion.1


Oral Administration


Administer orally without regard to meals.1


IV Administration


For solution and drug compatibility information, see Compatibility under Stability.


IV administration may be used when a rapid onset of diuresis is desired or when oral therapy is not practical.1


If torsemide is administered through an IV line, flush the IV line with 0.9% sodium chloride before and after administration.a


Dilution

For IV infusion, dilute in 5% dextrose, 0.9% sodium chloride, or 0.45% sodium chloride injection.a


Rate of Administration

For direct IV injection, administer slowly over a period of 2 minutes.1


Dosage


Adults


Edema

CHF

Oral

Initially, 10–20 mg, given as a single dose.1 Increase as necessary by approximately doubling daily dosage until desired diuresis is attained.1 Single doses exceeding 200 mg not adequately studied.1


IV

Initially, 10–20 mg, given as a single dose.1 Increase as necessary by approximately doubling dosage until desired diuresis is attained.1 Single doses exceeding 200 mg not adequately studied.1


Hypertension

Oral

Initially, 5 mg once daily.1 If adequate hypotensive response not attained in 4–6 weeks, may increase dosage to 10 mg once daily.1 If adequate response not observed with 10 mg once daily, an additional antihypertensive agent should be added to antihypertensive therapy.1


IV

Initially, 5 mg once daily.1 If adequate hypotensive response not attained in 4–6 weeks, may increase dosage to 10 mg once daily.1 If adequate response not observed with 10 mg once daily, an additional antihypertensive agent should be added to antihypertensive therapy.1


Prescribing Limits


Adults


Edema

CHF

Oral

Maximum of 200 mg as a single dose (daily).1


IV

Maximum of 200 mg as a single dose (daily).1


Hypertension

Oral

Maximum of 10 mg once daily.1


IV

Maximum of 10 mg once daily.1


Special Populations


Renal Impairment


Edema

Edema Associated with Chronic Renal Failure

Oral or IV

In adults, initially, 20 mg once daily.1 Increase as necessary by approximately doubling dosage until desired diuresis is attained.1 Single doses exceeding 200 mg not adequately studied.1 a


Hepatic Impairment


Chronic use in hepatic disease not adequately studied.1


Edema

Edema Associated with Hepatic Cirrhosis

Oral or IV

In adults, initially, 5–10 mg once daily, given concomitantly with an aldosterone antagonist or a potassium-sparing diuretic.a Increase as necessary by approximately doubling dosage until desired diuresis is attained.a Single doses exceeding 40 mg not adequately studied.1


Cautions for Demadex


Contraindications



  • Anuria.1




  • Known hypersensitivity to torsemide or to sulfonylureas.1



Warnings/Precautions


Warnings


Hepatic Effects

Sudden alterations of electrolyte balance in patients with cirrhosis may precipitate hepatic coma; use with caution in patients with hepatic cirrhosis and ascites.1


Therapy in such patients is best initiated in the hospital.1 Use an aldosterone antagonist or potassium-sparing agent concomitantly with torsemide to prevent hypokalemia and metabolic alkalosis in such patients.1


Ototoxicity

Tinnitus and hearing loss, usually reversible, have been observed following rapid IV injection of other loop diuretics and following oral torsemide administration.1 Administer IV slowly (over 2 minutes); do not exceed 200 mg as a single dose.1


Fluid, Electrolyte, and Cardiovascular Effects

Observe carefully for manifestations of fluid and electrolyte depletion (e.g., dryness of mouth, thirst, weakness, lethargy, drowsiness, restlessness, muscle pains or cramps, muscular fatigue, hypotension, oliguria, tachycardia, nausea, vomiting).1 a


Excessive diuresis may cause dehydration and blood volume reduction with circulatory collapse and possibly vascular thrombosis and embolism, particularly in geriatric patients.1 a


Laboratory changes may include altered serum concentrations of sodium, chloride, and potassium; acid-base abnormalities; and increased BUN.1 a If electrolyte imbalance, hypovolemia, or prerenal azotemia develops, torsemide should be discontinued until the abnormality is corrected; treatment then may be restarted at a reduced dosage.1 a


Risk of hypokalemia, especially with brisk diuresis, with inadequate oral electrolyte intake, in those with cirrhosis, or during concomitant use of corticosteroids or ACTH.1 a Risk of arrhythmias secondary to hypokalemia in patients with cardiovascular disease, especially those receiving concomitant therapy with a cardiac glycoside.1 a


Periodically monitor serum potassium and other electrolyte concentrations.1 a


General Precautions


Endocrine Effects

Possible increased blood glucose concentrations; hyperglycemia occurred rarely. 1 a


Renal and Electrolyte Effects

Small, dose-related, reversible increases in BUN, serum creatinine, and uric acid concentrations reported.1 a Symptomatic gout reported at an incidence similar to placebo.1


Slight alterations in calcium and magnesium concentrations.1 a


Other Effects

Increases in total plasma cholesterol concentrations may occur; usually subside during chronic therapy.1 a


Increases in plasma triglyceride concentrations reported.1 a


In long-term studies, no clinically important differences in lipid profiles compared to baseline.1 a


No clinically important effects on hemoglobin; hematocrit; WBC, erythrocyte, or platelet counts; or serum alkaline phosphatase concentrations.1 a


Specific Populations


Pregnancy

Category B.1


Lactation

Not known whether torsemide is distributed into milk.1 Caution if used in nursing women.1


Pediatric Use

Safety and efficacy not established.1


Renal calcifications reported in severely premature infants with edema secondary to patent ductus arteriosus and hyaline membrane disease receiving another loop diuretic.1 a Increased risk of persistent patent ductus arteriosus in premature neonates with hyaline membrane disease receiving another loop diuretic also has been reported.1 a


Geriatric Use

No substantial differences in safety and efficacy relative to younger adults.1 a


Renal Impairment

Seizures reported in patients with acute renal failure receiving higher than recommended dosages of torsemide.1 a


Common Adverse Effects


Headache, excessive urination, dizziness, rhinitis, asthenia, diarrhea, ECG abnormality, increased cough.1 a


Interactions for Demadex


Specific Drugs



























Drug



Interaction



Comments



Cholestyramine



Decreased absorption of torsemide in animals1 a



Avoid simultaneous administration when used concomitantly1 a



Digoxin



Increased torsemide AUC1 a



Torsemide dosage adjustment not necessary1 a



Lithium



Reduced renal clearance of lithium and increased risk of lithium toxicity reported with other diuretics 1 a



Avoid concomitant use or use great caution1 a



Ototoxic drugs (e.g., aminoglycoside antibiotics, ethacrynic acid)



Possible additive ototoxic effect when ototoxic drugs used concomitantly with other diuretics, especially in those with impaired renal function1 a



Probenecid



Reduced secretion of torsemide into proximal tubule and decreased diuretic activity1 a



Salicylates (e.g., aspirin, NSAIAs)



Concomitant use of NSAIAs with another loop diuretic (furosemide) occasionally associated with renal dysfunction.1 a


Indomethacin may partially inhibit natriuretic effect of torsemide in those with dietary sodium restriction (50 mEq daily) 1 a


Concomitant use with high dosages of salicylates may result in salicylate toxicity1 a



Spironolactone



Reduced renal clearance of spironolactone1 a



Adjustment of spironolactone or torsemide dosage not necessary1 a


Demadex Pharmacokinetics


Absorption


Bioavailability


Bioavailability is approximately 80%.1


Onset


Following oral administration, onset of diuresis occurs within 1 hour; maximal effect during the first or second hour.1 a


Following IV administration, onset of diuresis occurs within 10 minutes; maximal effect within 1 hour.1 a


Duration


Diuretic effect persists 6–8 hours following oral or IV administration.1 a


Food


Food delays the time to peak plasma concentration following oral dosing but does not affect extent of absorption or diuretic activity.1 a


Plasma Concentrations


Following oral administration, peak plasma concentrations achieved within 1 hour.1


Distribution


Extent


Not known whether torsemide is distributed into milk.1 a


Plasma Protein Binding


>99%.1 a


Elimination


Metabolism


Hepatic metabolism accounts for approximately 80% of total clearance.1 a Carboxylic acid derivative, the major metabolite, is inactive.1 a


Elimination Route


Urinary excretion accounts for approximately 20% of total clearance in patients with normal renal function.1 a Most renal clearance occurs via active secretion of the drug by the proximal tubules into tubular urine.1 a


Half-life


Approximately 3.5 hours.1 a


Special Populations


In patients with decompensated CHF, hepatic and renal clearance are reduced, resulting in delivery of less drug to the intraluminal site of action and decreased natriuretic effect.1 a Total clearance is about half of that of healthy individuals; half-life and AUC increased.1 a


In patients with renal failure, renal clearance (but not total clearance) is reduced, resulting in delivery of less drug to the intraluminal site of action and decreased natriuretic effect.1 a


In patients with hepatic cirrhosis, renal clearance (but not total clearance) and half-life are increased.1


In geriatric patients, decreased renal clearance.1 a


Stability


Storage


Oral


Tablets

15–30°C.1 Do not freeze.1 a


Parenteral


Injection

15–30°C.1 a Do not freeze.1 a


Compatibility


For information on systemic interactions resulting from concomitant use, see Interactions.


Parenteral


Solution CompatibilityHID





Compatible



Dextrose 5% in water



Sodium chloride 0.45 or 0.9%





Y-Site CompatibilityHID

Compatible



Milrinone lactate


ActionsActions



  • Acts from within the lumen of the thick ascending portion of the loop of Henle, where it inhibits the sodium/potassium/chloride carrier system.1




  • Increases urinary excretion of sodium, chloride, and water without having an important effect on glomerular filtration rate, renal plasma flow, or acid-base balance.1



Advice to Patients



  • Risks associated with excessive fluid loss or electrolyte imbalance.1 a




  • Potential for postural hypotension; importance of rising slowly from a seated position.1




  • Importance of informing patients with diabetes mellitus that blood glucose concentrations may increase.1




  • Importance of informing clinicians of existing or contemplated concomitant therapy, including prescription and OTC drugs, as well as any concomitant illnesses.1




  • Importance of women informing clinicians if they are or plan to become pregnant or plan to breast-feed.1




  • Importance of informing patients of other important precautionary information.1 (See Cautions.)



Preparations


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


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





















































Torsemide

Routes



Dosage Forms



Strengths



Brand Names



Manufacturer



Oral



Tablets



5 mg*



Demadex (with povidone; scored)



Roche



Torsemide Tablets



Apotex, Par, Pliva, Roxane, Teva



10 mg*



Demadex (with povidone; scored)



Roche



Torsemide Tablets



Apotex, Par, Pliva, Roxane, Teva, UDL,



20 mg*



Demadex (with povidone; scored)



Roche



Torsemide Tablets



Apotex, Par, Pliva, Roxane, Teva, UDL



100 mg*



Demadex (with povidone; scored)



Roche



Torsemide Tablets



Apotex, Par, Pliva, Teva



Parenteral



Injection, for IV use



10 mg/mL



Demadex



Roche


Comparative Pricing


This pricing information is subject to change at the sole discretion of DS Pharmacy. This pricing information was updated 03/2011. Actual costs to patients will vary depending on the use of specific retail or mail-order locations and health insurance copays.


Demadex 10MG Tablets (MEDA PHARMACEUTICALS): 30/$43.69 or 90/$110.37


Demadex 100MG Tablets (MEDA PHARMACEUTICALS): 30/$160.99 or 90/$455.97


Demadex 20MG Tablets (MEDA PHARMACEUTICALS): 30/$55.99 or 90/$139.97


Torsemide 10MG Tablets (TEVA PHARMACEUTICALS USA): 30/$29.99 or 90/$79.97


Torsemide 100MG Tablets (TEVA PHARMACEUTICALS USA): 30/$89.99 or 90/$249.96


Torsemide 20MG Tablets (TEVA PHARMACEUTICALS USA): 30/$22.99 or 90/$59.98


Torsemide 5MG Tablets (CAMBER PHARMACEUTICALS): 30/$18.99 or 90/$56.97



Disclaimer

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


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

AHFS Drug Information. © Copyright, 1959-2011, Selected Revisions August 2007. American Society of Health-System Pharmacists, Inc., 7272 Wisconsin Avenue, Bethesda, Maryland 20814.




References



1. Boehringer Mannheim. Demadex (torsemide) tablets and injection prescribing information. Rockville, MD: 1993 Oct.



2. National Heart, Lung, and Blood Institute National High Blood Pressure Education Program. The sixth report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure (JNC VI). Bethesda, MD: National Institutes of Health. (NIH publication No. 98-4080.)



3. Kaplan NM. Choice of initial therapy for hypertension. JAMA. 1996; 275:1577-80. [IDIS 365188] [PubMed 8622249]



4. Anon. Consensus recommendations for the management of chronic heart failure. On behalf of the membership of the advisory council to improve outcomes nationwide in heart failure. Part II. Management of heart failure: approaches to the prevention of heart failure. Am J Cardiol. 1999; 83:9-38A.



5. Izzo JL, Levy D, Black HR. Importance of systolic blood pressure in older Americans. Hypertension. 2000; 35:1021-4. [PubMed 10818056]



6. Frohlich ED. Recognition of systolic hypertension for hypertension. Hypertension. 2000; 35:1019-20. [PubMed 10818055]



7. Bakris GL, Williams M, Dworkin L et al. Preserving renal function in adults with hypertension and diabetes: a consensus approach. Am J Kidney Dis. 2000; 36:646-61. [IDIS 452007] [PubMed 10977801]



8. Associated Press (American Diabetes Association). Diabetics urged: drop blood pressure. Chicago, IL; 2000 Aug 29. Press Release from web site.



9. Appel LJ. The verdict from ALLHAT—thiazide diuretics are the preferred initial therapy for hypertension. JAMA. 2002; 288:3039-42. [IDIS 490723] [PubMed 12479770]



10. The ALLHAT Officers and Coordinators for the ALLHAT Collaborative Research Group. Major outcomes in high-risk hypertensive patients randomized to angiotensin-converting enzyme inhibitor or calcium channel blocker vs diuretic: the Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT). JAMA. 2002; 288:2981-97. [IDIS 490721] [PubMed 12479763]



11. National Heart, Lung, and Blood Institute National High Blood Pressure Education Program. The seventh report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure (JNC 7) Express. Bethesda, MD: May 14 2003. From NIH website. (http://www.nhlbi.nih.gov/guidelines/hypertension/jncintro.htm). (Also published in JAMA. 2003; 289:2560-72.



a. Roche Pharmaceuticals. Demadex (torsemide) tablets and injection prescribing information. Nutley, NJ: 2003 Apr.



b. AHFS Drug Information 2007. McEvoy GK, ed. Furosemide. American Society of Health-System Pharmacists; 2007: 2690-4.



HID. Trissel LA. Handbook on injectable drugs. 14th ed. Bethesda, MD: American Society of Health-System Pharmacists; 2007:1581.



More Demadex resources


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


  • Demadex Prescribing Information (FDA)

  • Demadex MedFacts Consumer Leaflet (Wolters Kluwer)

  • Demadex Concise Consumer Information (Cerner Multum)

  • Demadex Advanced Consumer (Micromedex) - Includes Dosage Information

  • Torsemide Prescribing Information (FDA)

  • Torsemide Professional Patient Advice (Wolters Kluwer)



Compare Demadex with other medications


  • Ascites
  • Edema
  • Heart Failure
  • High Blood Pressure
  • Nonobstructive Oliguria
  • Renal Failure

Thursday 9 July 2009

Prodilantin




Prodilantin may be available in the countries listed below.


Ingredient matches for Prodilantin



Fosphenytoin

Fosphenytoin disodium salt (a derivative of Fosphenytoin) is reported as an ingredient of Prodilantin in the following countries:


  • France

International Drug Name Search

Calcipotriene




Ingredient matches for Calcipotriene



Calcipotriol

Calcipotriene (USAN) is also known as Calcipotriol (Rec.INN)

International Drug Name Search

Glossary

Rec.INNRecommended International Nonproprietary Name (World Health Organization)
USANUnited States Adopted Name

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

Sudafed PE Nasal Decongestant




In the US, Sudafed PE Nasal Decongestant is a member of the following drug classes: decongestants, vasopressors and is used to treat Nasal Congestion.

Ingredient matches for Sudafed PE Nasal Decongestant



Phenylephrine

Phenylephrine hydrochloride (a derivative of Phenylephrine) is reported as an ingredient of Sudafed PE Nasal Decongestant in the following countries:


  • New Zealand

International Drug Name Search

Tuesday 7 July 2009

Zinmax Domesco




Zinmax Domesco may be available in the countries listed below.


Ingredient matches for Zinmax Domesco



Cefuroxime

Cefuroxime axetil (a derivative of Cefuroxime) is reported as an ingredient of Zinmax Domesco in the following countries:


  • Vietnam

International Drug Name Search

Monday 6 July 2009

Methazolamide




In the US, Methazolamide (methazolamide systemic) is a member of the drug class carbonic anhydrase inhibitors and is used to treat Glaucoma.

US matches:

  • Methazolamide

Scheme

Rec.INN

ATC (Anatomical Therapeutic Chemical Classification)

S01EC05

CAS registry number (Chemical Abstracts Service)

0000554-57-4

Chemical Formula

C5-H8-N4-O3-S2

Molecular Weight

236

Therapeutic Categories

Carbonic anhydrase inhibitor

Glaucoma treatment

Ophthalmic agent

Chemical Name

Acetamide, N-[5-(aminosulfonyl)-3-methyl-1,3,4-thiadiazol-2(3H)-ylidene]-

Foreign Names

  • Methazolamidum (Latin)
  • Methazolamid (German)
  • Méthazolamide (French)
  • Metazolamida (Spanish)

Generic Names

  • Methazolamide (OS: BAN, JAN)
  • Méthazolamide (OS: DCF)
  • Methazolamide (PH: USP 32)

Brand Names

  • Apo-Methazolamide
    Apotex, Canada


  • Methazolamide
    Mikart, United States; Sandoz, United States; Teva USA, United States


  • Methazolamide-Teva
    Teva, Israel

International Drug Name Search

Glossary

BANBritish Approved Name
DCFDénomination Commune Française
JANJapanese Accepted Name
OSOfficial Synonym
PHPharmacopoeia Name
Rec.INNRecommended International Nonproprietary Name (World Health Organization)

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

Mirtazapin Arrow




Mirtazapin Arrow may be available in the countries listed below.


Ingredient matches for Mirtazapin Arrow



Mirtazapine

Mirtazapine is reported as an ingredient of Mirtazapin Arrow in the following countries:


  • Sweden

International Drug Name Search