Lasix 40mg Tablets

Manufacturer VALIDUS Active Ingredient Furosemide Tablets(fyoor OH se mide) Pronunciation Fyoor-OH-se-mide
WARNING: This drug is a strong fluid-lowering drug (diuretic). Sometimes too much water and electrolytes (like potassium) in the blood may be lost. This can lead to severe health problems. Your doctor will follow you closely to change the dose to match your body's needs. @ COMMON USES: It is used to get rid of extra fluid. It is used to treat high blood pressure.
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Drug Class
Diuretic
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Pharmacologic Class
Loop Diuretic
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Pregnancy Category
Category C
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FDA Approved
Jun 1966
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DEA Schedule
Not Controlled

Overview

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What is this medicine?

Furosemide is a 'water pill' (diuretic) that helps your body get rid of extra salt and water. This can help lower blood pressure and reduce swelling (edema) caused by conditions like heart failure, kidney disease, or liver disease.
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How to Use This Medicine

Taking Your Medication Correctly

To get the most benefit from your medication, follow your doctor's instructions carefully. Read all the information provided with your medication and follow the instructions closely. This medication may increase the frequency of urination, so try to avoid taking it too close to bedtime to minimize sleep disturbances.

Important Interactions and Precautions

Do not take sucralfate within 2 hours before or after taking this medication. If the product changes color, do not take it.

Storing and Disposing of Your Medication

Store your medication at room temperature, protected from light, and in a dry place. Avoid storing it in a bathroom. Keep all medications in a safe location, out of the reach of children and pets. Dispose of unused or expired medications properly. Do not flush them down the toilet or pour them down the drain unless instructed to do so. If you have questions about disposing of your medication, consult your pharmacist. You may also want to check if there are drug take-back programs in your area.

What to Do If You Miss a Dose

If you miss a dose, take it as soon as you remember. However, if it is close to the time for your next dose, skip the missed dose and resume your regular dosing schedule. Do not take two doses at the same time or take extra doses.
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Lifestyle & Tips

  • Take exactly as prescribed, usually in the morning or early afternoon to avoid nighttime urination.
  • Do not stop taking without consulting your doctor, even if you feel better.
  • Monitor your weight daily and report any sudden changes (e.g., gain or loss of 2-3 pounds in a day).
  • Follow your doctor's recommendations for salt intake and fluid restriction.
  • Eat potassium-rich foods (e.g., bananas, oranges, potatoes) or take potassium supplements if advised by your doctor, as this medication can lower potassium levels.
  • Avoid excessive alcohol consumption, as it can increase dizziness and lower blood pressure.
  • Be cautious when standing up quickly to avoid dizziness or lightheadedness (orthostatic hypotension).
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Available Forms & Alternatives

Dosing & Administration

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Adult Dosing

Standard Dose: Edema: 20 to 80 mg once daily or divided into 2 doses. Hypertension: 40 mg twice daily.
Dose Range: 20 - 600 mg

Condition-Specific Dosing:

edema: Initial: 20-80 mg as a single dose. May increase by 20-40 mg every 6-8 hours until desired effect. Max: 600 mg/day.
hypertension: Initial: 40 mg twice daily. Adjust based on response.
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Pediatric Dosing

Neonatal: Not established for routine use; use with caution. Initial: 1-2 mg/kg/dose IV/PO every 12-24 hours. Max: 6 mg/kg/day.
Infant: Initial: 1-2 mg/kg/dose PO/IV once daily or every 6-12 hours. Max: 6 mg/kg/day.
Child: Initial: 1-2 mg/kg/dose PO/IV once daily or every 6-12 hours. Max: 6 mg/kg/day.
Adolescent: Initial: 1-2 mg/kg/dose PO/IV once daily or every 6-12 hours. Max: 6 mg/kg/day (or adult dose if higher).
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Dose Adjustments

Renal Impairment:

Mild: No specific adjustment needed, but monitor closely.
Moderate: May require higher doses to achieve diuresis. Monitor closely for electrolyte imbalances.
Severe: Use with caution. Higher doses may be required. Max dose may be limited to 80-160 mg/day in severe renal failure. Risk of ototoxicity increases.
Dialysis: Furosemide is not effectively removed by dialysis. Dosing should be individualized based on residual renal function and fluid status. May require higher doses or be ineffective in anuric patients.

Hepatic Impairment:

Mild: No specific adjustment, but monitor for electrolyte and fluid balance.
Moderate: Use with caution. Increased risk of electrolyte imbalance and hepatic encephalopathy. Lower initial doses may be considered.
Severe: Contraindicated in hepatic coma or severe electrolyte depletion until condition is improved. Use with extreme caution due to risk of hepatic encephalopathy and electrolyte disturbances.

Pharmacology

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Mechanism of Action

Furosemide is a loop diuretic that inhibits the Na+-K+-2Cl- cotransporter in the thick ascending limb of the loop of Henle. This inhibition prevents the reabsorption of sodium, potassium, and chloride, leading to increased excretion of water, sodium, chloride, and potassium. It also has a direct vasodilatory effect on renal and systemic vasculature.
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Pharmacokinetics

Absorption:

Bioavailability: Oral: 40-70% (highly variable)
Tmax: Oral: 1-2 hours; IV: ~30 minutes
FoodEffect: Food may decrease the rate but not the extent of absorption.

Distribution:

Vd: 0.1-0.2 L/kg
ProteinBinding: >95% (primarily to albumin)
CnssPenetration: Limited

Elimination:

HalfLife: Oral: 0.5-2 hours (prolonged in renal impairment)
Clearance: Not available (highly variable, depends on renal function)
ExcretionRoute: Renal (primarily unchanged drug and glucuronide conjugate)
Unchanged: 60-90% (renal excretion)
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Pharmacodynamics

OnsetOfAction: Oral: 30-60 minutes; IV: 5 minutes
PeakEffect: Oral: 1-2 hours; IV: 20-60 minutes
DurationOfAction: Oral: 6-8 hours; IV: 2 hours

Safety & Warnings

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BLACK BOX WARNING

Furosemide is a potent diuretic which, if given in excessive amounts, can lead to a profound diuresis with water and electrolyte depletion. Therefore, careful medical supervision is required and the dose must be adjusted to the individual patient's needs.
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Side Effects

Urgent Side Effects: Seek Medical Help Right Away

Although rare, some people may experience severe and potentially life-threatening side effects while taking this medication. If you notice any of the following symptoms, contact your doctor or seek medical attention immediately:

Signs of an allergic reaction, such as:
+ Rash
+ Hives
+ Itching
+ Red, swollen, blistered, or peeling skin with or without fever
+ Wheezing
+ Tightness in the chest or throat
+ Trouble breathing, swallowing, or talking
+ Unusual hoarseness
+ Swelling of the mouth, face, lips, tongue, or throat
Signs of fluid and electrolyte problems, including:
+ Mood changes
+ Confusion
+ Muscle pain or weakness
+ Fast or abnormal heartbeat
+ Severe dizziness or passing out
+ Increased thirst
+ Seizures
+ Feeling very tired or weak
+ Decreased appetite
+ Unable to pass urine or change in the amount of urine produced
+ Dry mouth
+ Dry eyes
+ Severe upset stomach or vomiting
Signs of liver problems, such as:
+ Dark urine
+ Tiredness
+ Decreased appetite
+ Upset stomach or stomach pain
+ Light-colored stools
+ Vomiting
+ Yellow skin or eyes
Signs of kidney problems, including:
+ Unable to pass urine
+ Change in how much urine is passed
+ Blood in the urine
+ Significant weight gain
Signs of a pancreas problem (pancreatitis), such as:
+ Severe stomach pain
+ Severe back pain
+ Severe upset stomach or vomiting
Severe dizziness or passing out
Abnormal sensations, such as burning, numbness, or tingling
Blurred vision
Restlessness

Severe Skin Reactions

This medication can cause severe skin reactions, including Stevens-Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), and other serious reactions. These reactions can affect other body organs and may be life-threatening. Seek medical help immediately if you experience:

Red, swollen, blistered, or peeling skin
Red or irritated eyes
Sores in your mouth, throat, nose, eyes, genitals, or any areas of skin
Fever
Chills
Body aches
Shortness of breath
Swollen glands

Other Side Effects

Like all medications, this drug can cause side effects. Many people may not experience any side effects or may only have mild side effects. If you are concerned about any of the following side effects or if they persist, contact your doctor:

Dizziness or headache
Constipation
Diarrhea
Upset stomach
Vomiting
Decreased appetite
Stomach cramps

Reporting Side Effects

This is not an exhaustive list of potential side effects. If you have questions or concerns about side effects, contact your doctor. You can also report side effects to the FDA at 1-800-332-1088 or online at https://www.fda.gov/medwatch.
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Seek Immediate Medical Attention If You Experience:

  • Severe dizziness or fainting
  • Extreme thirst or dry mouth
  • Muscle cramps or weakness
  • Unusual tiredness or confusion
  • Nausea or vomiting
  • Irregular heartbeat
  • Decreased urination
  • Ringing in the ears or hearing loss
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Before Using This Medicine

Before Taking This Medication: Important Information to Share with Your Doctor

It is essential to inform your doctor about the following conditions to ensure safe treatment:

Any allergies you have, including allergies to this medication, its components, or other substances, such as foods or drugs. Describe the allergic reactions you have experienced.
If you have difficulty urinating.
If you are dehydrated or have electrolyte imbalances.
If you have a history of liver problems or low blood pressure.

Additionally, tell your doctor if you are taking any of the following medications:
Chloral hydrate
Ethacrynic acid
Lithium

This list is not exhaustive, and it is crucial to disclose all your medications, including:
Prescription and over-the-counter (OTC) drugs
Natural products
Vitamins

Your doctor and pharmacist need to be aware of all your medications and health conditions to assess potential interactions and ensure it is safe for you to take this medication. Never start, stop, or change the dose of any medication without consulting your doctor first.
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Precautions & Cautions

Important Warnings and Precautions

It is essential to inform all your healthcare providers, including doctors, nurses, pharmacists, and dentists, that you are taking this medication.

Caution with Daily Activities
Avoid driving and performing tasks that require alertness until you understand how this medication affects you. To minimize the risk of dizziness or fainting, stand up slowly after sitting or lying down, and exercise caution when climbing stairs.

Managing Diabetes
If you have diabetes (high blood sugar), closely monitor your blood sugar levels. Be aware of signs of high blood sugar, such as confusion, drowsiness, increased thirst or hunger, frequent urination, flushing, rapid breathing, or fruity-smelling breath. Report these symptoms to your doctor.

Dietary Considerations
If you follow a low-salt or salt-free diet, consult your doctor. Additionally, if you have high blood pressure and are taking this medication, discuss with your doctor before using over-the-counter (OTC) products that may increase blood pressure, such as cough or cold medications, diet pills, stimulants, non-steroidal anti-inflammatory drugs (NSAIDs) like ibuprofen or naproxen, and certain natural products or aids.

Monitoring Your Condition
Regularly check your blood pressure as directed by your doctor. Also, have your blood work checked as scheduled by your doctor and discuss the results with them.

Potential Side Effects
Be aware that this medication may cause high cholesterol and triglyceride levels. If you already have high cholesterol or triglycerides, discuss this with your doctor. You may also require additional potassium supplements; consult your doctor about this.

Interactions with Other Substances
Before consuming alcohol, marijuana, or other forms of cannabis, or taking prescription or OTC medications that may cause drowsiness, discuss this with your doctor.

Sun Sensitivity
This medication may increase your risk of sunburn. Take precautions when exposed to the sun, and inform your doctor if you experience easy sunburning while taking this medication.

Other Potential Risks
Be aware of the possibility of gout attacks. If you have lupus, this medication may reactivate or worsen your condition; promptly report any new or worsening symptoms to your doctor.

Hearing and Blood Cell Problems
Hearing problems, such as decreased hearing or hearing loss, may occur with this medication. These effects may be temporary or permanent. If you experience ringing in the ears, changes in your hearing, or a feeling of fullness in your ears, contact your doctor immediately. Additionally, low blood cell counts may occur, which can lead to bleeding problems, infections, or anemia. Seek medical attention if you have signs of infection (fever, chills, sore throat), unexplained bruising or bleeding, or feel extremely tired or weak.

Special Considerations
If you are 65 years or older, use this medication with caution, as you may be more susceptible to side effects.

Pregnancy and Breastfeeding
Inform your doctor if you are pregnant, plan to become pregnant, or are breastfeeding. Your doctor will discuss the benefits and risks of this medication for you and your baby.
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Overdose Information

Overdose Symptoms:

  • Profound diuresis (excessive urination)
  • Severe dehydration
  • Electrolyte depletion (especially hypokalemia, hyponatremia, hypochloremia)
  • Hypotension (low blood pressure)
  • Dizziness, lightheadedness, fainting
  • Muscle weakness, cramps
  • Confusion, lethargy
  • Cardiac arrhythmias

What to Do:

Seek immediate medical attention. Call 911 or Poison Control (1-800-222-1222). Treatment involves fluid and electrolyte replacement, and supportive care.

Drug Interactions

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Contraindicated Interactions

  • Ethacrynic acid (increased risk of ototoxicity)
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Major Interactions

  • Aminoglycosides (increased risk of ototoxicity and nephrotoxicity)
  • Cisplatin (increased risk of ototoxicity)
  • Lithium (decreased renal clearance of lithium, leading to toxicity)
  • NSAIDs (may reduce diuretic and antihypertensive effects of furosemide, increased risk of renal toxicity)
  • Digoxin (increased risk of digoxin toxicity due to hypokalemia)
  • Phenytoin (may reduce diuretic effect of furosemide)
  • Sucralfate (may reduce absorption of furosemide)
  • Chloral hydrate (flushing, sweating, blood pressure changes)
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Moderate Interactions

  • Antihypertensives (additive hypotensive effects)
  • Corticosteroids (increased risk of hypokalemia)
  • Laxatives (increased risk of hypokalemia)
  • Amphotericin B (increased risk of hypokalemia)
  • Metformin (increased risk of lactic acidosis in patients with renal impairment)
  • Probenecid (may decrease renal clearance of furosemide)
  • Cephalosporins (increased risk of nephrotoxicity with high doses)
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Minor Interactions

  • Alcohol (additive hypotensive effects)
  • Licorice (may increase potassium loss)

Monitoring

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Baseline Monitoring

Serum Electrolytes (Sodium, Potassium, Chloride, Magnesium, Calcium)

Rationale: To establish baseline levels and identify pre-existing imbalances, as furosemide can cause significant electrolyte disturbances.

Timing: Prior to initiation of therapy.

Renal Function (BUN, Serum Creatinine)

Rationale: To assess baseline kidney function, which influences dosing and risk of adverse effects.

Timing: Prior to initiation of therapy.

Blood Pressure

Rationale: To establish baseline and monitor for hypotension.

Timing: Prior to initiation of therapy.

Weight and Fluid Status

Rationale: To establish baseline and monitor for efficacy and signs of dehydration/over-diuresis.

Timing: Prior to initiation of therapy.

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Routine Monitoring

Serum Electrolytes (Potassium, Sodium, Magnesium, Calcium)

Frequency: Daily initially, then weekly, then monthly or as clinically indicated, especially after dose changes or in patients with impaired renal function.

Target: Potassium: 3.5-5.0 mEq/L; Sodium: 135-145 mEq/L; Magnesium: 1.7-2.2 mg/dL; Calcium: 8.5-10.2 mg/dL

Action Threshold: Potassium < 3.5 mEq/L or > 5.5 mEq/L; Sodium < 130 mEq/L or > 150 mEq/L; significant changes from baseline.

Renal Function (BUN, Serum Creatinine)

Frequency: Weekly initially, then monthly or as clinically indicated, especially in patients with impaired renal function or concurrent nephrotoxic drugs.

Target: Within normal limits or stable for patient's baseline.

Action Threshold: Significant increase in BUN or creatinine (e.g., >25% increase from baseline or above upper limit of normal).

Blood Pressure (Orthostatic)

Frequency: Daily initially, then regularly during therapy, especially with dose adjustments.

Target: Within target range for patient's condition, without symptomatic orthostasis.

Action Threshold: Symptomatic hypotension or significant orthostatic drop (>20 mmHg systolic or >10 mmHg diastolic).

Weight

Frequency: Daily (in hospital) or 2-3 times per week (outpatient).

Target: Target dry weight or stable weight with resolution of edema.

Action Threshold: Rapid weight loss (>2-3 lbs/day) or signs of dehydration.

Fluid Status (Edema, Lung Sounds, Urine Output)

Frequency: Daily.

Target: Resolution of edema, clear lung sounds, adequate urine output.

Action Threshold: Persistent edema, worsening dyspnea, decreased urine output, or signs of dehydration (dry mucous membranes, decreased skin turgor).

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Symptom Monitoring

  • Dizziness
  • Lightheadedness
  • Muscle cramps or weakness
  • Excessive thirst
  • Dry mouth
  • Nausea
  • Vomiting
  • Fatigue
  • Confusion
  • Irregular heartbeat
  • Decreased urination
  • Hearing changes (tinnitus, hearing loss)

Special Patient Groups

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Pregnancy

Category C. Use only if the potential benefit justifies the potential risk to the fetus. Furosemide can cause fetal or neonatal jaundice, thrombocytopenia, and other adverse reactions seen in adults. In pregnant women with hypertension, furosemide may reduce placental perfusion.

Trimester-Specific Risks:

First Trimester: Potential for fetal harm, though data are limited. Avoid if possible.
Second Trimester: Risk of electrolyte imbalance and reduced placental perfusion. Monitor closely.
Third Trimester: Risk of electrolyte imbalance, neonatal jaundice, thrombocytopenia. May inhibit lactation.
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Lactation

L3 (Moderately Safe). Furosemide is excreted into breast milk. While generally considered compatible with breastfeeding, monitor the infant for dehydration, electrolyte imbalance, and weight loss. High doses may suppress lactation.

Infant Risk: Low to moderate risk of dehydration, electrolyte imbalance, and weight loss. Potential for ototoxicity is theoretical but low. Monitor infant closely.
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Pediatric Use

Dosing is weight-based. Neonates and infants may be more susceptible to adverse effects, particularly electrolyte disturbances and ototoxicity. Close monitoring of fluid and electrolyte balance is crucial. Not recommended for routine use in neonates due to potential for nephrocalcinosis.

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Geriatric Use

Elderly patients may be more sensitive to the effects of furosemide, particularly hypotension and electrolyte disturbances. They may also have age-related decreases in renal function, requiring lower doses and closer monitoring. Increased risk of falls due to orthostatic hypotension.

Clinical Information

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Clinical Pearls

  • Administer furosemide in the morning or early afternoon to prevent nocturia.
  • Monitor for signs of dehydration (e.g., dry mucous membranes, decreased skin turgor, excessive thirst) and electrolyte imbalances, especially hypokalemia, hyponatremia, and hypomagnesemia.
  • Potassium supplementation is often necessary, especially with chronic use or high doses.
  • Rapid IV administration can increase the risk of ototoxicity, especially in patients with renal impairment or those receiving other ototoxic drugs.
  • Furosemide is less effective in patients with severe renal impairment (CrCl < 30 mL/min) compared to other loop diuretics like torsemide or bumetanide, which may be preferred in these cases.
  • Patients should be advised to report any ringing in the ears or hearing changes immediately.
  • Orthostatic hypotension is a common side effect; advise patients to change positions slowly.
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Alternative Therapies

  • Other loop diuretics (e.g., bumetanide, torsemide)
  • Thiazide diuretics (e.g., hydrochlorothiazide, chlorthalidone) for hypertension or mild edema
  • Potassium-sparing diuretics (e.g., spironolactone, eplerenone, amiloride, triamterene) often used in combination with loop diuretics to counteract potassium loss or for specific indications like heart failure.
  • Vasodilators (e.g., ACE inhibitors, ARBs) for hypertension or heart failure
  • Beta-blockers for hypertension or heart failure
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Cost & Coverage

Average Cost: $10 - $30 per 30 tablets (40mg generic)
Generic Available: Yes
Insurance Coverage: Tier 1 (Generic)
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General Drug Facts

If your symptoms or health issues persist or worsen, it's essential to contact your doctor for further guidance. To ensure your safety, never share your medication with others or take someone else's medication. Some medications may come with an additional patient information leaflet, so be sure to check with your pharmacist for more information. If you have any questions or concerns about your medication, don't hesitate to reach out to your doctor, nurse, pharmacist, or other healthcare provider. In the event of a suspected overdose, immediately call your local poison control center or seek medical attention. When seeking help, be prepared to provide details about the medication taken, the amount, and the time it happened.