Prescription medication · Loop Diuretic
furosemide
Also sold as Lasix. This medicine treats swelling (edema) from heart failure, liver problems, or kidney disease.
Data updated 2026-05-15
- 387,984
- FDA reportsHeavily reported
- 36
- InteractionsSeveral interactions
- 87% less
- Generic vs brandHuge savings
- In shortage
- FDA status
What the data shows
furosemide (Lasix) is a prescription Loop Diuretic, in the top 5% of tracked drugs by FAERS report volume (387,984 FDA reports), whose generic runs roughly half the brand price or less (87% less).
Reporting volume reflects how widely a drug is used and studied, not how dangerous it is, a FAERS report documents a temporal association, never proof of cause.
furosemide (Lasix) is a prescription Loop Diuretic. This medicine treats swelling (edema) from heart failure, liver problems, or kidney disease.
Furosemide is a water pill (diuretic). It helps your body get rid of extra water and salt.
Verify with FDA → · CMS NADAC pricing →
Drug Shortage Alert
furosemide is currently listed as in shortage by the FDA. Affected manufacturer: Gland Pharma Limited. Status: Available.
View all drug shortages →Drug Pricing (NADAC)
Brand Price
$0.75/unit
Generic Price
$0.10/unit
Generic Savings
87%
Generic Available
Yes (20 manufacturers)
Pricing data from NADAC (CMS), effective December 18, 2024. Compare all drug costs →
What it does
This medicine treats swelling (edema) from heart failure, liver problems, or kidney disease.
Common side effects
Dizziness, Headache, Blurred vision
Key warnings
Furosemide can cause you to lose too much fluid and electrolytes.
The sections below are summarized in plain English from furosemide's FDA-approved prescribing information. They describe what the official label says, and are not personal medical advice.
How It Works
Furosemide works in your kidneys. It helps your kidneys remove more salt and water from your blood. This lowers the amount of fluid in your body and lowers blood pressure.
Side Effects (from patient reports)
Based on 387,984 FDA adverse event reports.
Most-reported reactions
Adverse reactions in FAERS for furosemide, by number of reports
- Dyspnoea
Dyspnoea
29,104 reports
- Fatigue
Fatigue
20,393 reports
- Diarrhoea
Diarrhoea
19,937 reports
- Nausea
Nausea
18,692 reports
- Acute Kidney Injury
Acute Kidney Injury
18,530 reports
- Death
Death
18,316 reports
- Fall
Fall
16,158 reports
- Pneumonia
Pneumonia
16,077 reports
- Asthenia
Asthenia
15,177 reports
- Hypotension
Hypotension
14,755 reports
What this shows Bars show how often each reaction was reported, not how likely it is to happen, a report records a temporal association, never proof that the drug caused it.
Reports over time
Adverse-event reports filed for furosemide each year to the FDA Adverse Event Reporting System (FAERS).
Year-to-year volume tracks usage, prescribing, and scrutiny, not a change in per-patient risk. Source: FDA FAERS.
Where furosemide sits
furosemide has more FDA adverse-event reports than 98% of the drugs FAERS tracks. A high position reflects how widely a drug is used and watched, not how dangerous it is.
Percentile across all drugs PlainMeds tracks by FAERS report volume. The dot is furosemide; the line is the median (50th percentile).
FDA Adverse Event Report Analysis
Detailed analysis of 387,984 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 1997–2025.
Total Reports
387,984
Reports Mentioning Death
60,624
15.6% of reports — not proof of cause
Hospitalization Reports
190,901
Top Indication
Product Used For Unknown Indication
Gender Distribution
Age Distribution
Most Reported Adverse Reactions (FAERS)
| # | Reaction | Reports |
|---|---|---|
| 1 | DYSPNOEA | 29,104 |
| 2 | FATIGUE | 20,393 |
| 3 | DIARRHOEA | 19,937 |
| 4 | NAUSEA | 18,692 |
| 5 | ACUTE KIDNEY INJURY | 18,530 |
| 6 | DEATH | 18,316 |
| 7 | FALL | 16,158 |
| 8 | PNEUMONIA | 16,077 |
| 9 | ASTHENIA | 15,177 |
| 10 | HYPOTENSION | 14,755 |
| 11 | DIZZINESS | 14,719 |
| 14 | PAIN | 13,548 |
| 15 | HEADACHE | 12,959 |
| 16 | RENAL FAILURE | 12,862 |
| 17 | VOMITING | 12,388 |
Reactions in Death Reports
Reactions in Hospitalization Reports
Source: FDA FAERS (Adverse Event Reporting System) Reports are voluntary and do not establish causation
Serious Warnings
Furosemide can cause you to lose too much fluid and electrolytes. This can lead to dehydration, low blood pressure, and kidney problems. Your doctor should check your blood regularly while you are taking this medicine.
Known Drug Interactions
7.5 Furosemide Tamsulosin Tamsulosin had no effect on the pharmacodynamics (excretion of electrolytes) of furosemide. While furosemide produced an 11% to 12% reduction in tamsulosin hydrochloride C max and AUC, these changes are expected to be clinically insignificant and do not require adjustment of the dose of tamsulosin [see Clinical Pharmacology ( 12.3 ) ] .
Mechanism: Furosemide slightly lowers the amount of the other drug in your blood, but the effect is too small to matter.
7.5 Furosemide Tamsulosin Tamsulosin had no effect on the pharmacodynamics (excretion of electrolytes) of furosemide. While furosemide produced an 11% to 12% reduction in tamsulosin hydrochloride C max and AUC, these changes are expected to be clinically insignificant and do not require adjustment of the dose of tamsulosin [see Clinical Pharmacology ( 12.3 ) ] .
Mechanism: Furosemide can slightly decrease the levels of tamsulosin in your body, but it does not change how well the water pill works.
7.7 Furosemide Tamsulosin hydrochloride capsules had no effect on the pharmacodynamics (excretion of electrolytes) of furosemide. While furosemide produced an 11% to 12% reduction in tamsulosin hydrochloride C max and AUC, these changes are expected to be clinically insignificant and do not require adjustment of the tamsulosin hydrochloride capsules dosage [see Clinical Pharmacology (12.3)].
Mechanism: Furosemide slightly lowers the level of tamsulosin in your system, but the effect is too small to change how the medicine works.
Concomitant use of cyclosporine and furosemide is associated with increased risk of gouty arthritis secondary to furosemide-induced hyperurecemia and cyclosporine impairment of renal urate excretion.
Mechanism: Furosemide raises uric acid levels in the blood, while cyclosporine makes it harder for the kidneys to remove it. This combination can cause uric acid to build up and lead to painful gouty arthritis.
Lithium generally should not be given with diuretics because they reduce lithium's renal clearance and add a high risk of lithium toxicity.
Mechanism: Furosemide prevents the kidneys from clearing lithium out of the body properly. This causes lithium to build up to dangerous levels, which can lead to toxicity.
This is a plain-language summary of FDA-label interaction records and does not provide individual medication-combination directions.
Common Questions
What should I avoid while taking furosemide?
Can furosemide affect my blood sugar?
Will furosemide interact with other medications I'm taking?
How long does it take for furosemide to work?
Can furosemide cause hearing loss?
What are the symptoms of low potassium caused by furosemide?
Can I drink alcohol while taking furosemide?
Does furosemide cause weight loss?
Can furosemide affect my kidneys?
When should I call my doctor?
What are the common side effects of furosemide?
Does furosemide interact with other medications?
What drug class is furosemide?
Is there a generic version of furosemide?
What pregnancy or breastfeeding source fields are listed for furosemide?
Has furosemide been recalled?
Is furosemide currently in shortage?
Active Recalls
CGMP Deviations; presence of N-nitroso-Furosemide (NNF) above the recommended intake limit.
Leading Pharma, LLC
Presence of Foreign Substance
Graviti Pharmaceuticals Private Limited
Related Medications in Loop Diuretic
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Compare beyond drug class
Nationwide peers by FAERS volume & death-report share
Two PlainMeds-derived comparison paths for furosemide: nearest FDA FAERS report volume and nearest death-report share among drugs with at least 1,000 logged reports, excluding same-class neighbors listed above. Counts reflect reporting volume, not proven individual harm.
Similar FAERS report volume
Nearest drugs by total FAERS reports. This record: 387,984.
- ergocalciferol Δ 21,493 reports · Vitamin D2 Supplement 366,491reports
- methotrexate Δ 22,069 reports · Disease-Modifying Antirheumatic Drug (DMARD) 410,053reports
- dupilumab Δ 23,708 reports · Anti-IL-4/IL-13 Monoclonal Antibody 411,692reports
- acetaminophen Δ 29,474 reports · Analgesic / Antipyretic 417,458reports
Similar death-report share
Nearest drugs by FAERS death-report share. This record: 15.63%.
- palonosetron Δ 0.04 pts · 3,330 reports · 5-HT3 Receptor Antagonist (Antiemetic) 15.59%death share
- enoxaparin Δ 0.08 pts · 55,714 reports · Low-Molecular-Weight Heparin 15.70%death share
- thiamine Δ 0.14 pts · 11,724 reports · Vitamin B1 Supplement 15.49%death share
- magnesium oxide Δ 0.14 pts · 39,831 reports · Mineral Supplement 15.77%death share
Medication Guides
Understanding Drug Interactions
How CYP450 enzymes, inhibitors, and inducers affect your medications
Generic vs Brand Name Drugs
FDA requirements, cost savings, and when the difference matters
Narrow Therapeutic Index Drugs
FDA bioequivalence and label-record context for narrow therapeutic index medicines
Common Drug Interactions
Dangerous medication combinations and how to protect yourself
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What the FDA Data Shows for furosemide
The FDA label for furosemide (sold under brand names such as Lasix) classifies it as a prescription-only medication in the Loop Diuretic class. This medicine treats swelling (edema) from heart failure, liver problems, or kidney disease. Official labeling lists 10 commonly reported side effects, including Dizziness, Headache, Blurred vision.
Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 387,984 voluntary reports. The database also lists 36 documented drug interactions derived from FDA labeling, with the top-flagged interaction rated major severity. NADAC pricing from CMS shows a generic unit cost of $0.10 versus $0.75 for the brand - a 87% generic savings.
Report counts do not establish causation, a FAERS entry documents a temporal association, not proof that the drug produced the outcome. Widely prescribed medications naturally accumulate more reports than niche therapies, so raw totals must be interpreted alongside total exposure. Shortage status, recall history (currently 2 recall records on file), and patent information are separate source-record fields. This page is a public FDA/CMS registry and does not provide medical, treatment, substitution, or medication-change directions.
Data Sources
Drug labeling: FDA Drug Labels (SPL/DailyMed). Adverse events: FDA Adverse Event Reporting System (FAERS). Pricing: CMS National Average Drug Acquisition Cost (NADAC). Shortage status: FDA Drug Shortages Database.
FAERS reports are voluntary and do not establish causation. Drug interactions are derived from FDA labeling and clinical references. This registry does not provide medication decisions.
Last updated: March 1, 2023
PlainMeds is rendered directly from FDA openFDA/FAERS extracts, DailyMed labels, and CMS drug-pricing files, no number is typed in by an editor. FAERS counts, recalls, shortages, and price figures on this page are queried live from those federal extracts. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of 2026-05-15. Primary sources: openFDA / FAERS, DailyMed and CMS Part B ASP.
Read our methodology - how this data is sourced, computed, and verified.
Data currency: FDA FAERS adverse-event reports through 2025, CMS NADAC acquisition-cost pricing effective December 2024, compiled from the source snapshot dated . See our methodology for per-source dates and refresh cadence. Spot a figure that looks wrong? Report a data issue.
All federal data sources used on this page
- FDA Orange Book - approved drug products with therapeutic equivalence. accessdata.fda.gov/cder/ob
- FDA DailyMed - NIH-hosted drug labeling for FDA-approved meds. dailymed.nlm.nih.gov
- FDA Adverse Event Reporting System (FAERS) - post-marketing safety surveillance. fda.gov/drugs/faers
- NLM RxNorm - standardized clinical drug nomenclature. nlm.nih.gov/research/umls/rxnorm
- CMS Medicare Part B Drug Average Sales Price Files - federal drug pricing data. cms.gov/medicare/part-b-drugs/asp
- FDA Drug Shortages Database - current and resolved drug shortage tracking. accessdata.fda.gov/drugshortages