Prescription medication · Thiazide-Like Diuretic

indapamide

Also sold as Lozol. Indapamide is used to treat high blood pressure, either alone or with other medicines.

Data updated 2026-05-15

17,199
FDA reportsModerately reported
3
InteractionsFew interactions
$0.10
Generic price (NADAC)

What the data shows

indapamide (Lozol) is a prescription Thiazide-Like Diuretic, reported at a middle-of-the-pack volume (17,199 FDA reports), with 3 documented drug interactions.

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.

indapamide (Lozol) is a prescription Thiazide-Like Diuretic. Indapamide is used to treat high blood pressure, either alone or with other medicines.

Indapamide is a water pill that helps lower blood pressure and reduce fluid buildup in the body. It is used to treat high blood pressure and heart failure.

Drug Pricing (NADAC)

Generic Price

$0.10/unit

Generic Available

Yes (3 manufacturers)

Pricing data from NADAC (CMS), effective December 18, 2024. Compare all drug costs →

View Alternatives → Compare with Another Drug → Full Side Effects Report →

What it does

Indapamide is used to treat high blood pressure, either alone or with other medicines.

Common side effects

Headache, Weakness, Constipation

Key warnings

If you have anuria (inability to urinate), you should not take this medicine.

The sections below are summarized in plain English from indapamide's FDA-approved prescribing information. They describe what the official label says, and are not personal medical advice.

How It Works

Indapamide is a diuretic, also known as a water pill. It helps your kidneys remove more salt and water from your blood, which lowers blood pressure. It also reduces fluid buildup in your body.

Side Effects (from patient reports)

Based on 17,199 FDA adverse event reports.

Most-reported reactions

Adverse reactions in FAERS for indapamide, by number of reports

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.

Source FDA Adverse Event Reporting System (FAERS) As of 2025

Reports over time

Adverse-event reports filed for indapamide each year to the FDA Adverse Event Reporting System (FAERS).

05001,0001,5002,000 20042007201020132016201920222025 1,302

Year-to-year volume tracks usage, prescribing, and scrutiny, not a change in per-patient risk. Source: FDA FAERS.

Where indapamide sits

indapamide has more FDA adverse-event reports than 51% of the drugs FAERS tracks. A high position reflects how widely a drug is used and watched, not how dangerous it is.

fewest reports most reports

Percentile across all drugs PlainMeds tracks by FAERS report volume. The dot is indapamide; the line is the median (50th percentile).

FDA Adverse Event Report Analysis

Detailed analysis of 17,199 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 2004–2025.

Total Reports

17,199

Reports Mentioning Death

1,091

6.3% of reports — not proof of cause

Hospitalization Reports

8,087

Top Indication

Product Used For Unknown Indication

Gender Distribution

Female 9,087 (58%)
Male 6,696 (42%)

Age Distribution

0–17 78
18–44 605
45–64 4,127
65–74 4,429
75+ 4,518

Most Reported Adverse Reactions (FAERS)

# Reaction Reports
1 HYPONATRAEMIA 1,286
2 ACUTE KIDNEY INJURY 925
3 DYSPNOEA 898
4 DIZZINESS 875
5 NAUSEA 863
6 DIARRHOEA 843
7 FATIGUE 781
8 DRUG INTERACTION 756
9 HYPOKALAEMIA 746
10 VOMITING 699
11 MALAISE 695
13 FALL 652
14 HEADACHE 640
15 ASTHENIA 639
17 ARTHRALGIA 608

Reactions in Death Reports

DEATH 194
ACUTE KIDNEY INJURY 86
DIARRHOEA 70
CARDIAC ARREST 61
PNEUMONIA 61
VOMITING 52
DYSPNOEA 49
LACTIC ACIDOSIS 48
FALL 45
RENAL FAILURE 45

Reactions in Hospitalization Reports

HYPONATRAEMIA 1,110
ACUTE KIDNEY INJURY 671
HYPOKALAEMIA 568
DYSPNOEA 498
VOMITING 492
FALL 477
DRUG INTERACTION 456
DIARRHOEA 437
NAUSEA 426
CONFUSIONAL STATE 424

Source: FDA FAERS (Adverse Event Reporting System) Reports are voluntary and do not establish causation

Serious Warnings

If you have anuria (inability to urinate), you should not take this medicine. Also, you should not take this medicine if you are allergic to indapamide or other sulfa drugs.

Known Drug Interactions

minor lithium

Lithium : See WARNINGS .

Mechanism: Indapamide changes how your kidneys handle salt, which can cause lithium to stay in your body too long. This can lead to high and potentially harmful lithium levels.

Norepinephrine : Indapamide, like the thiazides, may decrease arterial responsiveness to norepinephrine, but this diminution is not sufficient to preclude effectiveness of the pressor agent for therapeutic use.

Mechanism: Indapamide makes your blood vessels less reactive to norepinephrine. This can make norepinephrine slightly less effective at raising your blood pressure.

Diuretics Coadministration of tolterodine immediate release up to 8 mg (4 mg bid) for up to 12 weeks with diuretic agents, such as indapamide, hydrochlorothiazide, triamterene, bendroflumethiazide, chlorothiazide, methylchlorothiazide, or furosemide, did not cause any adverse electrocardiographic (ECG) effects.

Mechanism: These two drugs do not appear to have any negative combined effects on the heart's electrical activity.

This is a plain-language summary of FDA-label interaction records and does not provide individual medication-combination directions.

Common Questions

Can I take indapamide with other blood pressure medicines?
Yes, but your doctor may need to adjust the doses of your medicines.
What should I do if I feel dizzy after taking indapamide?
Get up slowly from a sitting or lying position to avoid dizziness.
Does indapamide affect my potassium levels?
Yes, indapamide can lower your potassium levels. Your doctor may monitor your potassium levels with blood tests.
Can indapamide cause dehydration?
Yes, indapamide can cause dehydration. Drink plenty of fluids while taking this medicine.
How long does it take for indapamide to start working?
Indapamide starts working within a few hours to lower blood pressure and reduce fluid retention.
Can I drink alcohol while taking indapamide?
Talk to your doctor about drinking alcohol while taking indapamide, as it may increase the risk of side effects.
Does indapamide interact with lithium?
Yes, indapamide can interact with lithium. Talk to your doctor if you are taking lithium.
Can indapamide affect my blood sugar?
Indapamide may increase your blood sugar levels. If you have diabetes, monitor your blood sugar carefully.
What are the signs of low potassium?
Signs of low potassium include muscle weakness, cramps, and irregular heartbeat.
Can I stop taking indapamide suddenly?
Do not stop taking indapamide without talking to your doctor first.
What are the common side effects of indapamide?
The registry lists Headache, Weakness, Constipation, Dizziness, Lightheadedness among the most-reported FAERS reaction terms for indapamide. The compiled record contains 17,199 FDA adverse-event reports. These counts are not an individual symptom assessment.
Does indapamide interact with other medications?
The registry has 3 documented interaction rows for indapamide. Notable source-record pairings include lithium, norepinephrine, tolterodine. These rows are not a complete medication review.
What drug class is indapamide?
indapamide belongs to the Thiazide-Like Diuretic drug class. It requires a prescription (Rx). Indapamide is used to treat high blood pressure, either alone or with other medicines.
What pregnancy or breastfeeding source fields are listed for indapamide?
The FDA label for indapamide contains product-specific pregnancy or breastfeeding language. PlainMeds does not apply that source text to an individual.

Other drugs grouped near indapamide - same-class peers and common alternatives.

Compare indapamide vs acebutolol side-by-side →

Compare beyond drug class

Nationwide peers by FAERS volume & death-report share

Two PlainMeds-derived comparison paths for indapamide: 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.

Medication Guides

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What the FDA Data Shows for indapamide

The FDA label for indapamide (sold under brand names such as Lozol) classifies it as a prescription-only medication in the Thiazide-Like Diuretic class. Indapamide is used to treat high blood pressure, either alone or with other medicines. Official labeling lists 6 commonly reported side effects, including Headache, Weakness, Constipation.

Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 17,199 voluntary reports. The database also lists 3 documented drug interactions derived from FDA labeling, with the top-flagged interaction rated minor severity. NADAC pricing from CMS shows a generic unit cost of $0.10.

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, 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).

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: June 26, 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.

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