Furosemide (Lasix) - Use, Dosage, Class, MOA, Side effects, Brands

Furosemide (Lasix) is a loop diuretic (also called a water pill). It is used in fluid overload states such as heart failure, ascites, and pulmonary edema.

Furosemide (Lasix) Uses:

  • Edema:

    • Associated with heart failure, management of edema and hepatic or renal disease.
    • Acute pulmonary edema.
  • Hypertension:

    • Hypertension management.

Note:

  • For the initial treatment of hypertension, it is not recommended.

Furosemide (Lasix) Dose in Adults

Note:

  • Oral dose equivalency (approximate) for patients with normal renal function:

    • Furosemide 40 mg = bumetanide 1 mg = ethacrynic acid 50 mg = torsemide 20 mg

Furosemide (Lasix) Dose in the treatment of Acute pulmonary edema:

  • IV:
  • Initial:
    • 40 mg/dose.
    • May increase to 80 mg/dose, if response not adequate within 1 hour.

Note:

    • Minimal additional response is gained by single doses over 160-200 mg.
    • Max: 200 mg/dose (Brater 1998).

Furosemide (Lasix) Dose in the treatment of Edema:

  • P/O:
  • Initial:
    • 20-80 mg/dose.
    • May repeat the same dose or increase dose in increments of 20-40 mg/dose at intervals of 6-8 hours, if response is not adequate.
    • With severe edematous states, may titrate up to 600 mg/day.
    • Usual maintenance dose interval is once or twice daily.

Furosemide (Lasix) Dose in the treatment of Heart failure:

  • Initial:
    • 20-40 mg once or twice daily.
    • Max 600 mg/day (ACCF/AHA [Yancy 2013]).

Note:

  • Based on patient-specific diuretic needs, dosing frequency may be adjusted.
  • IM, IV:
  • Initial:
    • 20-40 mg/dose.
    • May repeat the same dose or increase dose in increments of 20 mg/dose if the response is not adequate & administer 1-2 hours after the previous dose (max: 200 mg/dose [Brater 1998]).
  • Note:

    • For those receiving chronic oral diuretic therapy, a higher initial dose may be considered (the dose of chronic oral therapy may guide the IM/IV dose).
    • Although some patients may initially require dosing as frequently as every 6 hours, the individually determined dose should then be given once or twice daily.
  • Continuous IV infusion:

    • Initial:

    • IV bolus dose 40-100 mg over 1-2 mins, followed by a continuous IV infusion rate of 10-40 mg/hour.
    • Before increasing the infusion rate, repeat loading dose.
    • Note:

      • Median & max doses were ≤ 20 mg/hour in clinical trials evaluating dosing strategies in acute decompensated heart failure.
      • The upper end of the initial infusion dosage range should be considered with lower baseline CrCl (eg, CrCl <25 mL/min)
      • Double as necessary to a max of 80-160 mg/hour if urine output is <1 mL/kg/hour.
      • The risk associated with higher infusion rates (80 to 160 mg/hour) must be weighed against alternative strategies.

Furosemide (Lasix) Dose as an alternative agent in the treatment of Hypertension:

  • Initial:
  • 20-40 mg twice daily.
  • To maintain therapeutic response, individualize according to patient response and use minimal dose necessary.
  • Usual dosage range:
  • In 2 divided doses, 20-80 mg/day.

Furosemide (Lasix) Dose in the treatment of Ascites, due to cirrhosis (off-label dose):

  • Initial:
    • 40 mg orally once daily.
    • As clinically indicated, titrate every 3-5 days (usual max: 160 mg once daily).
    • A furosemide to spironolactone dosing ratio of 40 mg (furosemide) to 100 mg (spironolactone) should be maintained.

Furosemide (Lasix) Dose in Childrens

Note:

  • Oral and parenteral (IV, IM) doses may not be interchangeable.
  • Oral doses are typically higher than IV due to differences in bioavailability.
  • In multiple concentrations, Oral solution is available (8 mg/mL and 10 mg/mL).
  • Between the different concentrations, extra precautions should be taken to verify and avoid confusion.
  • The dose should be clearly presented as mg (not mL).
  • Oral dose equivalency for adult patients with normal renal function (approximate):
  • Furosemide 40 mg = bumetanide 1 mg = torsemide 20 mg = ethacrynic acid 50 mg.

Furosemide (Lasix) Dose in the treatment of Edema (diuresis):

  • P/O:
    • Initial:

      • 0.5-2 mg/kg/dose every 6-24 hours.
      • Usual initial adult dose:
      • 20-80 mg/dose.
      • May increase dose in increments of 1-2 mg/kg/dose, if initial dose ineffective.
      • Max daily dose:
      • 6 mg/kg/day not to exceed maximum adult daily dose:
      • 600 mg/day.
    • For maintenance, adjust the dose to the minimal effective dose.
  • Note:

    • Smaller doses on a mg/kg basis may be needed in larger children, especially in those who are diuretic naive.
  • IM, intermittent IV:

    • Initial:

      • 0.5-2 mg/kg/dose every 6-12 hours.
      • Usual initial adult dose:
      • 20-40 mg/dose.
      • May increase dose by 1 mg/kg/dose, if initial dose ineffective after 2 hours.
      • Max dose:
      • 6 mg/kg/dose not to exceed max adult dose:
      • 200 mg/dose.
    • For maintenance, adjust to the minimum effective dose.
  • Note:

    • Smaller doses on a mg/kg basis may be needed in larger children, especially in those who are diuretic naive.
    • In adult and pediatric patients, dosing in adolescents based on experience.
  • Continuous IV infusion:

    • Initial:
      • IV bolus dose of 0.1 mg/kg followed by continuous IV infusion of 0.05-0.4 mg/kg/hour.
      • Titrate dosage to clinical effect.
      • In adolescents, dosing based on reported experience in adult and pediatric patients:
      • IV bolus dose of 0.1 mg/kg.
      • Usual adult bolus dose:
      • 40-100 mg over 1-2 mins.
      • Followed by continuous IV infusion of 0.1 to 0.4 mg/kg/hour.
      • Usual adult dosing range:
      • 10-40 mg/hour.

Furosemide Pregnancy Risk Category: C

  • Studies on animal reproduction have revealed negative outcomes.
  • The placenta is crossed by furosemide (Riva 1978).
  • Pregnant women with cardiac disease can be treated with furosemide.
  • Monitor fetal growth if used during pregnancy
  • May increase the birth weight

Furosemide use during breastfeeding:

  • Furosemide can be found in breast milk.
  • Lactation may be affected by maternal use.
  • Manufacturers recommend that caution is used when administering the medication to a nursing woman.
  • Some sources recommend furosemide be used in combination with breastfeeding (Garg 2015), but others suggest avoiding it if you can, as usual maternal doses can cause lactation suppression (WHO 2002).

Furosemide (Lasix) Dose in Kidney Disease:

  • Acute renal failure:

    • To initiate the desired response doses up to 1 to 3 g daily may be necessary.
    • In oliguric states, avoid use.
  • Dialysis:

    • Not removed by hemodialysis or peritoneal dialysis.
    • The supplemental dose is not necessary.

Furosemide (Lasix) Dose in Liver disease:

Reduced natriuretic action in cirrhosis, along with greater vulnerability to hypokalemia and volume depletion. Watch the consequences, especially while using excessive doses.

Furosemide (Lasix) Side effects:

  • Cardiovascular:

    • Necrotizing Angiitis
    • Orthostatic Hypotension
    • Thrombophlebitis
    • Vasculitis
  • Central Nervous System:

    • Dizziness
    • Headache
    • Paresthesia
    • Restlessness
    • Vertigo
  • Dermatologic:

    • Acute Generalized Exanthematous Pustulosis
    • Bullous Pemphigoid
    • Erythema Multiforme
    • Exfoliative Dermatitis
    • Pruritus
    • Skin Photosensitivity
    • Skin Rash
    • Stevens-Johnson Syndrome
    • Toxic Epidermal Necrolysis
    • Urticaria
  • Endocrine & Metabolic:

    • Glycosuria
    • Hyperglycemia
    • Hyperuricemia
    • Increased Serum Cholesterol
    • Increased Serum Triglycerides
  • Gastrointestinal:

    • Abdominal Cramps
    • Anorexia
    • Constipation
    • Diarrhea
    • Gastric Irritation
    • Mouth Irritation
    • Nausea
    • Pancreatitis
    • Vomiting
  • Genitourinary:

    • Bladder Spasm
  • Hematologic & Oncologic:

    • Agranulocytosis
    • Anemia
    • Aplastic Anemia
    • Eosinophilia
    • Hemolytic Anemia
    • Leukopenia
    • Purpura
    • Thrombocytopenia
  • Hepatic:

    • Hepatic Encephalopathy
    • Intrahepatic Cholestatic Jaundice
    • Liver Enzymes Increased
  • Hypersensitivity:

    • Anaphylaxis
    • Anaphylactoid Reaction
    • Anaphylactic Shock
  • Immunologic:

    • DRESS Syndrome
  • Local:

    • Pain At Injection Site (Following IM Injection)
  • Neuromuscular & Skeletal:

    • Muscle Spasm
    • Weakness
  • Ophthalmic:

    • Blurred Vision
    • Xanthopsia
  • Otic:

    • Deafness
    • Tinnitus
  • Renal:

    • Interstitial Nephritis (Allergic)
    • Renal Disease
  • Miscellaneous:

    • Fever

Contraindications to Furosemide (Lasix):

  • Hypersensitivity to furosemide and any other component of the formulation
  • Anuria

Canadian labeling:Additional contraindications not listed in the US labeling:

  • Hypersensitivity to sulfonamide-derived medications
  • Complete renal shut down
  • Precoma and hepatic coma.
  • Uncorrected electrolyte depletion, hypovolemia or dehydration states that are not corrected.
  • Infants born jaundiced or with the disease(s), capable of causing hyperbilirubinemia and possibly kernicterus.
  • Breastfeeding

Notice:

  • The manufacturer labeling of Lasix Special and Furosemide Special Injection also includes the following:
    • GFR 5 mg/min or GFR 20 mg/min
    • Hepatic cirrhosis.
    • Hepatic coma and precoma can be accompanied by renal failure.
    • Renal failure caused by poisoning with hepatotoxic or nephrotoxic substances

Notice:

  • The scientific basis of this statement has been challenged, although the approved product labeling states this medication is contraindicated with other sulfonamide-containing drug classes.

Warnings and precautions

  • Fluid and electrolyte losses: [US Boxed Warn]

    • Furosemide is similar to other loop diuretics and can cause severe diuresis if taken in large amounts. This can result in electrolyte and fluid depletion.
    • A dosage assessment and close medical management are necessary.
    • Correct any imbalances in the electrolytes.
    • To avoid dehydration, adjust the dose.
    • Therapy should not be started if electrolyte depletion has occurred unless the serum electrolytes, particularly potassium, have been normalized.
  • Hypokalemia risk may be increased by:
    • It is possible to experience rapid diuresis, poor oral potassium intake, cirrhosis, and concomitant use of significant doses of licorice or corticosteroids (chronic usage).
    • A loop diuretic can lower serum calcium levels, unlike thiazide diuretics.
    • Electrolyte imbalances can put patients at risk for life-threatening arrhythmias.
  • Hyperuricemia:

    • Use has been linked to the signs and symptoms of hyperuricemia.
    • Rarely, gout may be precipitated.
  • Nephrotoxicity:

    • It's critical to assess your fluid status and renal function in order to avoid oliguria, azotemia, and irreversible increases in BUN or creatinine.
    • It is important to have close medical supervision for aggressive diuresis.
    • In high-risk patients, may increase the risk of radiocontrast-induced nephropathy.
  • Ototoxicity:

    • Rapid IV administration is associated with ototoxicity. This can lead to severe renal impairment, hyperproteinemia, and concurrent use of other toxic substances.
  • Photosensitivity

    • Photosensitization can occur.
  • Allergy to sulfonamide ("sulfa")

    • Patients should be aware that many drugs containing a chemical class of sulfonamides have a broad contraindication if there has been an adverse response on the authorised product labelling.
    • It is feasible for members of the same class to interact with one another (e.g., two antibiotics sulfonamides).
    • Crossreactivity concerns have been raised for compounds containing the sulfonamide structural.
    • A deeper understanding of allergy mechanisms shows that there is little chance of cross-reactivity between antibiotic and non-antibiotic sulfonamides.
    • With nonantibiotic sulfuramides, it is unlikely that anaphylaxis (cross-reaction) mechanisms resulting from antibody development will happen.
    • Type IV T-cell-mediated reactions, such maculopapular skin rash, are less well known but can't be fully ruled out at this time.
    • These classes are sometimes avoided by some clinicians in severe cases of reactions (Stevens Johnson syndrome/TEN).
  • Thyroid effects:

    • Doses >80 mg can cause a temporary increase in thyroid hormone levels.
  • Insufficiency of the adrenals:

    • Patients with primary adrenal dysfunction should avoid diuretics (Addison disease) for treatment of high blood pressure.
    • To treat hypertension, adjustment of glucocorticoid/mineralocorticoid therapy & the use of other antihypertensive agents is preferred (Bornstein 2016; Inder 2015).
  • Cirrhosis

    • Avoid acid/base and electrolyte imbalances, which could lead to cirrhosis-related hepatic enzymephalopathy.
    • Correct electrolyte imbalances and acid/base imbalances if hepatic impairment is present before initiation.
    • When necessary, supplemental potassium and an aldosterone antagonist may be used to reduce hypokalemia and metabolic alkalosis.
    • It is important to monitor closely the progress of any therapy.
  • Diabetes:

    • Take care when administering insulin to patients suffering from prediabetes and diabetes mellitus.
    • Possibly will have a shift in glucose regulation
  • Prostatic hyperplasia/urinary restriction:

    • An increase in urine production, especially after the start of therapy, may result in urinary retention.
  • Systemic lupus erythematosus (SLE):

    • SLE activation or exacerbation may occur.

Furosemide: Drug Interaction

Risk Factor C (Monitor therapy)

Acebrophylline

May improve the way furosemide works therapeutically.

Ajmaline

Sulfonamides might make ajmaline more harmful or poisonous. In particular, there may be an elevated risk for cholestasis.

Alfuzosin

The hypotensive effects of blood pressure-lowering medications may be strengthened.

Aliskiren

May lower the level of furosemide in the serum.

Allopurinol

Loop Diuretics may intensify Allopurinol's harmful or toxic effects. Allopurinol's serum levels may rise in response to loop diuretics. In particular, Oxypurinol, an active metabolite of Allopurinol, may be increased in concentration by Loop Diuretics.

Amikacin (Oral Inhalation)

Loop Diuretics may increase Amikacin's nephrotoxic impact (Oral Inhalation). Loop Diuretics may increase Amikacin's ototoxic effects (Oral Inhalation).

Aminoglycosides

Aminoglycosides may have a worse or more toxic effect when used with loop diuretics. ototoxicity and nephrotoxicity in particular.

Amphetamines

May lessen the effectiveness of antihypertensive agents.

Angiotensin-Converting Enzyme Inhibitors

Angiotensin-Converting Enzyme Inhibitors' hypotensive effects may be strengthened by loop diuretics. Angiotensin-Converting Enzyme Inhibitors' nephrotoxic effects may be increased by loop diuretics.

Antidiabetic Agents

The therapeutic benefit of anti-diabetic agents may be reduced by hyperglycemia-associated agents.

Antipsychotic Agents (Second Generation [Atypical])

Antipsychotic drugs' hypotensive effects may be enhanced by blood pressure-lowering medications (Second Generation [Atypical]).

Barbiturates

The hypotensive effects of blood pressure-lowering medications may be strengthened.

Benperidol

The hypotensive effects of blood pressure-lowering medications may be strengthened.

Beta2-Agonists

The hypotensive effects of blood pressure-lowering medications may be strengthened.

Bilastine

The QTc-prolonging effects of loop diuretics may be enhanced by bilastine.

Brigatinib

May lessen the effectiveness of antihypertensive agents. Antihypertensive Agents' bradycardic action may be strengthened by brutinib.

Brimonidine (Topical)

The hypotensive effects of blood pressure-lowering medications may be strengthened.

Cabozantinib

Cabozantinib's serum levels may rise in the presence of MRP2 inhibitors.

Cardiac Glycosides

Cardiac Glycosides may have a worse or more toxic effect when used with loop diuretics. Particularly, the hypokalemic and hypomagnesemic impact of loop diuretics may worsen cardiac glycoside toxicity.

Cefazedone

The hypotensive effects of blood pressure-lowering medications may be strengthened.

Cefotiam

Loop Diuretics may intensify Ceftiam's nephrotoxic effects.

Cefpirome

Loop Diuretics may intensify Ceftiam's nephrotoxic effects.

Ceftizoxime

Loop Diuretics may intensify Ceftiam's nephrotoxic effects.

Cephalothin

Loop Diuretics may intensify Ceftiam's nephrotoxic effects.

Cephradine

May intensify Loop Diuretics' nephrotoxic effects.

CISplatin

Loop Diuretics might make CISplatin's nephrotoxic effects worse. The ototoxic impact of CISplatin might be increased by loop diuretics.

Corticosteroids (Orally Inhaled)

The hypotensive effects of blood pressure-lowering medications may be strengthened.

Corticosteroids (Systemic)

The hypotensive effects of blood pressure-lowering medications may be strengthened.

CycloSPORINE (Systemic)

The hypotensive effects of blood pressure-lowering medications may be strengthened.

Dexmethylphenidate

Can lessen an antihypertensive drug's therapeutic impact.

Diacerein

Could make diuretics' therapeutic effects stronger. Particularly, there may be a higher chance of hypokalemia or dehydration.

Diazoxide

The hypotensive effects of blood pressure-lowering medications may be strengthened.

DULoxetine

The hypotensive impact of DULoxetine may be enhanced by blood pressure lowering medications.

Empagliflozin

The hypotensive effects of blood pressure-lowering medications may be strengthened.

Fosphenytoin

May lessen Loop Diuretics' diuretic effects.

Herbs (Hypertensive Properties)

May lessen the effectiveness of antihypertensive agents.

Herbs (Hypotensive Properties)

Blood pressure-lowering drugs may intensify their hypotensive effects.

Hypotension-Associated Agents

The hypotensive action of hypotension-associated agents may be strengthened by blood pressure lowering medications.

Ipragliflozin

May intensify Loop Diuretics' harmful or hazardous effects. In particular, there may be an elevated risk for intravascular volume depletion.

Ivabradine

Ivabradine's ability to induce arrhythmias may be enhanced by loop diuretics.

Levodopa-Containing Products

Levodopa-Containing Products' hypotensive effects may be strengthened by blood pressure-lowering medications.

Licorice

May intensify Loop Diuretics' hypokalemic impact.

Lithium

Loop Diuretics may lower the level of lithium in the blood. Loop Diuretics may raise the level of lithium in the blood.

Lormetazepam

The hypotensive effects of blood pressure-lowering medications may be strengthened.

Methylphenidate

May lessen the effectiveness of antihypertensive agents.

Molsidomine

The hypotensive effects of blood pressure-lowering medications may be strengthened.

Naftopidil

The hypotensive effects of blood pressure-lowering medications may be strengthened.

Neuromuscular-Blocking Agents

The neuromuscular-blocking effects of neuromuscular-blocking agents may be lessened by loop diuretics. Neuromuscular-Blocking Agents' ability to block neuromuscular activity may be enhanced by loop diuretics.

Nicergoline

The hypotensive effects of blood pressure-lowering medications may be strengthened.

Nicorandil

Blood pressure-lowering drugs may intensify their hypotensive effects.

Nitroprusside

Nitroprusside's hypotensive impact may be strengthened by blood pressure-lowering medications.

Opioid Agonists

Could make diuretics' harmful or toxic effects worse.  Opioid antagonists may reduce diuretics' therapeutic benefit.

Pentoxifylline

The hypotensive effects of blood pressure-lowering medications may be strengthened.

Phenytoin

May lessen Loop Diuretics' diuretic effects.

Phosphodiesterase 5 Inhibitors

The hypotensive effects of blood pressure-lowering medications may be strengthened.

Probenecid

May intensify Loop Diuretics' harmful or hazardous effects. The diuretic action of loop diuretics may be reduced by probenecid. Loop Diuretics' serum levels may rise in response to probenecid. Management: When using probenecid concurrently with loop diuretics, keep an eye out for diminished diuretic effects or increased side effects. The prescribing advice for bumetanide cautions against using probenecid at the same time.

Prostacyclin Analogues

The hypotensive effects of blood pressure-lowering medications may be strengthened.

Quinagolide

The hypotensive effects of blood pressure-lowering medications may be strengthened.

Reboxetine

The hypotensive effects of blood pressure-lowering medications may be strengthened.

RisperiDONE

The negative/toxic effects of RisperiDONE may be increased by loop diuretics.

Salicylates

May lessen Loop Diuretics' diuretic effects. The content of salicylates in the serum may rise when using loop diuretics.

Teriflunomide

OAT3 Substrates' serum concentration can rise.

Tobramycin (Oral Inhalation)

Loop Diuretics may increase Tobramycin's nephrotoxic effects (Oral Inhalation). Loop Diuretics may increase Tobramycin's ototoxic effects (Oral Inhalation).

Topiramate

Topiramate's effect on hypokalemia may be enhanced by loop diuretics.

Xipamide

May intensify Loop Diuretics' harmful or hazardous effects. Particularly, there may be a higher chance of hypovolemia, electrolyte imbalances, and prerenal azotemia.

Yohimbine

May lessen the effectiveness of antihypertensive agents.

 

Risk Factor D (Consider therapy modification)

Amifostine

Blood Pressure Lowering Agents may enhance the hypotensive effect of Amifostine. Management: When amifostine is used at chemotherapy doses, blood pressure lowering medications should be withheld for 24 hours prior to amifostine administration. If blood pressure lowering therapy cannot be withheld, amifostine should not be administered.

Bile Acid Sequestrants

May decrease the absorption of Loop Diuretics.

Canagliflozin

May strengthen Loop Diuretics' hypotensive effects. Management: If canagliflozin is taken with a loop diuretic, watch for signs of hypotension and intravascular volume depletion. The Canadian product labelling advises against taking loop diuretics and canagliflozin together.

Chloral Betaine

Chloral Betaine can have a negative or toxic effect that furosemide may intensify.

Dofetilide

Loop Diuretics may increase Dofetilide's ability to extend QTc. Management: When dofetilide is taken with loop diuretics, serum potassium and magnesium levels should be continuously monitored. The need for therapy change may arise.

Foscarnet

Loop Diuretics may raise the level of foscarnet in the blood.

Methotrexate

May reduce Loop Diuretics' therapeutic efficacy. Loop diuretics may raise the level of methotrexate in the serum. Loop Diuretics' serum levels may be raised by methotrexate. Management involves monitoring for elevated methotrexate and/or loop diuretic levels/toxicity with concurrent use of these drugs as well as for diminished loop diuretic therapeutic effects. It could be essential to reduce the dosage of loop diuretics or methotrexate.

Nonsteroidal Anti-Inflammatory Agents

May lessen Loop Diuretics' diuretic effects. Nonsteroidal Anti-Inflammatory Drugs may have a greater nephrotoxic effect when used with loop diuretics. Management: When using an NSAID at the same time as loop diuretics, watch out for signs of kidney damage or diminished therapeutic efficacy. Avoid using concurrently if you have cirrhosis or CHF. Bumetanide and indomethacin should not be used concurrently.

Obinutuzumab

The hypotensive effects of blood pressure-lowering medications may be strengthened. Management: Take into account temporarily stopping blood pressure-lowering drugs 12 hours before the start of the obinutuzumab infusion and keeping them off until 1 hour after the infusion is finished.

Sodium Phosphates

The nephrotoxic effects of sodium phosphates may be increased by diuretics. In particular, there may be an increased risk of acute phosphate nephropathy. Treatment: You might want to temporarily stop taking diuretics or look for an alternative to the oral sodium phosphate bowel preparation in order to prevent this combo. If the combination cannot be avoided, drink well and keep an eye on your kidney and fluid levels.

Sucralfate

May lower the level of furosemide in the serum. Sucralfate may make it harder for furosemide to be absorbed. Management: Avoid giving sucralfate and furosemide at the same time orally. administrations should be at least two hours apart. does not apply to furosemide taken by injection.

Tolvaptan

OAT3 Substrates' serum concentration can rise.

Risk Factor X (Avoid combination)

Bromperidol

May lessen blood pressure lowering agents' hypotensive effects. The hypotensive impact of bromperidol may be enhanced by blood pressure lowering medications.

Chloral Hydrate

Chloral Hydrate's harmful or poisonous effects may be exacerbated by furosemide.

Desmopressin

Desmopressin's hyponatremic impact may be increased by loop diuretics.

Ethacrynic Acid

Ethacrynic Acid's ototoxic effects may be increased by furosemide.

Levosulpiride

Levosulpiride's harmful or toxic effects may be exacerbated by loop diuretics.

Mecamylamine

Sulfonamides may intensify Mecamylamine's harmful or hazardous effects.

Promazine

Loop Diuretics may increase Promazine's ability to extend QTc.

 

Monitoring parameters:

  • Examine I & O (inpatient setting) & weight daily.
  • Blood pressure, orthostasis
  • Serum electrolytes, renal function.
  • Examine hearing with high doses or rapid IV administration

How to administer Furosemide (Lasix)?

  • Parenteral:
    • May administer IM or IV.
    • Undiluted direct IV injections may be administered at a rate of 20-40 mg/min.
    • Max rate of administration for short-term intermittent infusion is 4 mg/min.
    • Exceeding this rate increases the risk of ototoxicity.
  • P/O:
    • Administer on an empty stomach (Bard 2004).
    • If GI distress occurs, may administer with food or milk.
    • However, this may reduce diuretic efficacy.
  • Note:
    • The sublingual route may be used, when IV or oral administration is not possible.
    • Place 1 tablet under tongue for at least 5 mins to allow for maximal absorption.
    • During disintegration time, patients should be advised not to swallow (Haegeli 2007).

Mechanism of action of Furosemide (Lasix):

  • Primarily inhibits sodium & chloride reabsorption in the ascending loop Henle and proximal and distal renal tubules.
  • This interferes with the chloride binding cotransport system, thereby causing the natriuretic effect of the drug (Rose 1991).

The onset of action:

  • Diuresis:
    • Oral, sublingual (SL):
      • 30-60 mins.
    • IM:
      • 30 mins.
    • IV:
      • ~5 mins
    • Symptomatic improvement with acute pulmonary edema:
      • Within 15-20 mins; occurs prior to diuretic effect

Peak effect:

  • P/O, SL:
  • 1-2 hours.
  • IV:
  • 0.5 hours

Duration:

  • P/O, SL:
    • 6-8 hours.
  • IV:
    • 2 hours

Protein binding:

  • 91%-99%.
  • Primarily to albumin

Metabolism:

  • Minimally hepatic

Bioavailability:

  • Oral tablet:
    • 47%-64%.
  • Oral solution:
    • 50%.
  • SL administration of oral tablet:
    • ~60%.
    • Results of a small comparative study (n=11) showed bioavailability of SL administration of tablet was ~12% higher than oral administration of tablet (Haegeli 2007)

Half-life elimination:

  • Normal renal function:
    • 0.5-2 hours.
  • End-stage renal disease (ESRD):
    • 9 hours

Excretion:

  • Urine (Oral: 50%, IV: 80%) within 24 hours.
  • Feces (as unchanged drug).
  • Nonrenal clearance prolonged in renal impairment

International Brands of Furosemide (Lasix):

  • Lasix
  • APO-Furosemide
  • BIO-Furosemide
  • Furosemide Special
  • Lasix Oral
  • Lasix Special
  • MINT-Furosemide
  • NTP-Furosemide
  • PMS-Furosemide
  • TEVA-Furosemide
  • A Xi Ya
  • A-Basedock
  • Accent
  • Ai Ge
  • Akoset
  • Anfuramide
  • Aquarid
  • Aquasin
  • Arasemide
  • Bondiur
  • Busemida
  • Dailix
  • Daiteren F
  • Depix
  • Desal
  • Dirine
  • Disemide
  • Diural
  • Diuren
  • Diuresal
  • Diurin
  • Diurmessel
  • Diusemide
  • Diuvar
  • Edemid
  • Edemin
  • Errolon
  • Femide 500
  • Foliront
  • Fretic
  • Frusedan
  • Frusema
  • Frusid
  • Fruside
  • Frusovit
  • Fulsix
  • Fuluvamide
  • Furanthril
  • Furanturil
  • Furetic
  • Furide
  • Furix
  • FuroPuren
  • Furolix
  • Furomen
  • Furomex
  • Furomin
  • Furon
  • Furorese
  • Furoretic
  • Furose
  • Furosedon
  • Furosemid
  • Furosemid Pharmavit
  • Furosemid-ratiopharm
  • Furosemide-Eurogenerics
  • Furosemix
  • Furosix
  • Furovenir
  • Fursemid
  • Fursemid[inj.]
  • Furusemide
  • Fuseride
  • Fusid
  • Fusimex
  • Fusix
  • Glosix
  • Impugan
  • Indiurex
  • Jufurix
  • Katlex
  • Kutrix
  • Lafurex
  • Lasilix
  • Lasix
  • Lasix Retard
  • Lasix[inj.]
  • Laveric
  • Lowpston
  • Luseck
  • Maoread
  • Naclex
  • Nadis
  • Nephron
  • Odemase
  • Odement
  • Odemex
  • Oedemex
  • Pharmix
  • Promedes
  • Radisemide
  • Radouna
  • Rasitol
  • Releef
  • Retep
  • Rosemide
  • Rosis
  • Roxemid
  • Salinex
  • Salurex
  • Salurin
  • Seguril
  • Silax
  • Sofudac
  • Solax
  • Synephron
  • Trofurit
  • Uremide
  • Uresix
  • Urex
  • Urex Forte
  • Urex-M
  • Urimeg
  • Urinal
  • Usix
  • Vusimide

Furosemide Brand Names in Pakistan:

Furosemide Injection 10 mg/ml

Elusen Elite Pharma
Ephamide Epharm Laboratories
Ephamide Epharm Laboratories
Frusemide Lahore Chemical & Pharmaceutical Works (Pvt) Ltd
Frusemide Lahore Chemical & Pharmaceutical Works (Pvt) Ltd
Frusemide Lahore Chemical & Pharmaceutical Works (Pvt) Ltd
Fusemid Akson Pharmaceuticals (Pvt) Ltd.
Lasimed Medicraft Pharmaceuticals (Pvt) Ltd.
Lasix Sanofi Aventis (Pakistan) Ltd.
Losamide Pharmedic (Pvt) Ltd.
Mb-Asix Multinational Buisness Link
Mb-Asix Multinational Buisness Link
Orex Rex Pharmaceuticals Pakistan

 

Furosemide Liquid 40 mg/5ml

Basix Xenon Pharmaceuticals (Pvt) Ltd.

 

Furosemide 20 mg Tablets

Lasix Sanofi Aventis (Pakistan) Ltd.
Mb-Asix Multinational Buisness Link
Orex Rex Pharmaceuticals Pakistan

 

Furosemide 40 mg Tablets

Frumid Goodman Laboratories
Frusa Medera Pharmaceuticals (Pvt) Ltd.
Frusemide Lahore Chemical & Pharmaceutical Works (Pvt) Ltd
Frusemide Lahore Chemical & Pharmaceutical Works (Pvt) Ltd
Frusinox Abbott Laboratories (Pakistan) Limited.
Furine Murfy Pharmaceuticals (Pvt) Ltd
Fymide Fynk Pharmaceuticals
Lasix Sanofi Aventis (Pakistan) Ltd.
Laxide Munawar Pharma (Pvt) Ltd.
Laxide Munawar Pharma (Pvt) Ltd.
Losamide Pharmedic (Pvt) Ltd.
Mb-Asix Multinational Buisness Link
Odenil Bosch Pharmaceuticals (Pvt) Ltd.
Orex Rex Pharmaceuticals Pakistan
Uremide Spencer Pharma
Urolax P.D.H. Pharmaceuticals (Pvt) Ltd.

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