Prescription medication · Nitrofuran Antibiotic

nitrofurantoin

Also sold as Macrobid, Macrodantin. This medicine treats urinary tract infections (UTIs).

Data updated 2026-05-15

15,757
FDA reportsModerately reported
4
InteractionsFew interactions
1
Recall record

What the data shows

nitrofurantoin (Macrobid) is a prescription Nitrofuran Antibiotic, reported less often than most tracked drugs (15,757 FDA reports), with 4 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.

nitrofurantoin (Macrobid) is a prescription Nitrofuran Antibiotic. This medicine treats urinary tract infections (UTIs).

Nitrofurantoin is an antibiotic medicine. It is used to treat infections of the urinary tract.

Drug Pricing (NADAC)

Generic Price

$3.87/unit

Generic Available

Yes (21 manufacturers)

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

Compare with Another Drug → Full Side Effects Report →

What it does

This medicine treats urinary tract infections (UTIs).

Common side effects

Nausea, Headache, Vomiting

Key warnings

This medicine can cause serious side effects.

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

How It Works

Nitrofurantoin is an antibiotic that stops bacteria from growing. It damages the bacteria's DNA, which kills the bacteria. This helps to clear up the infection in your urinary tract.

Side Effects (from patient reports)

Based on 15,757 FDA adverse event reports.

Most-reported reactions

Adverse reactions in FAERS for nitrofurantoin, 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 nitrofurantoin each year to the FDA Adverse Event Reporting System (FAERS).

05001,0001,5002,000 20042007201020132016201920222025 1,149

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

Where nitrofurantoin sits

nitrofurantoin has more FDA adverse-event reports than 49% 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 nitrofurantoin; the line is the median (50th percentile).

FDA Adverse Event Report Analysis

Detailed analysis of 15,757 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 2004–2025.

Total Reports

15,757

Reports Mentioning Death

1,000

6.3% of reports — not proof of cause

Hospitalization Reports

5,435

Top Indication

Product Used For Unknown Indication

Gender Distribution

Female 12,211 (84%)
Male 2,274 (16%)

Age Distribution

0–17 280
18–44 2,019
45–64 3,766
65–74 2,394
75+ 3,098

Most Reported Adverse Reactions (FAERS)

# Reaction Reports
1 URINARY TRACT INFECTION 1,301
2 FATIGUE 1,240
3 NAUSEA 1,187
4 HEADACHE 1,103
5 PAIN 964
6 DYSPNOEA 950
7 DIARRHOEA 880
8 RASH 852
9 MALAISE 851
10 VOMITING 810
11 PYREXIA 796
12 DIZZINESS 788
15 CHRONIC KIDNEY DISEASE 588
16 FALL 585
17 WEIGHT DECREASED 577

Reactions in Death Reports

DEATH 283
URINARY TRACT INFECTION 84
DYSPNOEA 77
COMPLETED SUICIDE 72
ACUTE KIDNEY INJURY 67
PNEUMONIA 65
CHRONIC KIDNEY DISEASE 58
PAIN 52
RENAL FAILURE 51
SEPSIS 45

Reactions in Hospitalization Reports

URINARY TRACT INFECTION 677
DYSPNOEA 483
NAUSEA 436
PAIN 403
FATIGUE 385
PYREXIA 382
VOMITING 364
DIARRHOEA 334
PNEUMONIA 312
MALAISE 308

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

Serious Warnings

This medicine can cause serious side effects. Rarely, it can cause deadly allergic reactions, lung problems, liver problems, and nerve damage. Tell your doctor right away if you have trouble breathing, yellowing of the skin, numbness, or tingling.

Known Drug Interactions

7.4 Concomitant Use with Drugs that Induce Methemoglobinemia Concomitant use of ACZONE Gel, 7.5% with drugs that induce methemoglobinemia such as sulfonamides, acetaminophen, acetanilide, aniline dyes, benzocaine, chloroquine, dapsone, naphthalene, nitrates and nitrites, nitrofurantoin, nitroglycerin, nitroprusside, pamaquine, para‐aminosalicylic acid, phenacetin, phenobarbital, phenytoin, primaquine, and quinine may increase the risk for developing methemoglobinemia [see Warnings and Precautions ( 5.1 )] .

Mechanism: These medications both have the potential to change how your blood carries oxygen. Using them at the same time makes it more likely you will develop a blood problem called methemoglobinemia.

Drugs That May Cause Methemoglobinemia When Used with LIDODERM Patients who are administered local anesthetics are at increased risk of developing methemoglobinemia when concurrently exposed to the following drugs, which could include other local anesthetics: Examples of Drugs Associated with Methemoglobinemia : Class Examples Nitrates/Nitrites nitric oxide, nitroglycerin, nitroprusside, nitrous oxide Local anesthetics articaine, benzocaine, bupivacaine, lidocaine, mepivacaine, prilocaine, procaine, ropivacaine, tetracaine Antineoplastic agents cyclophosphamide, flutamide, hydroxyurea,...

Mechanism: Both drugs can cause a blood problem that makes it hard for your body to get enough oxygen. Using them together increases the risk of this serious condition.

7.2 Uricosuric Drugs Uricosuric drugs, such as probenecid and sulfinpyrazone, can inhibit renal tubular secretion of nitrofurantoin.

Mechanism: Probenecid stops the kidneys from moving nitrofurantoin into the urine, which can make the antibiotic less effective for treating a bladder infection.

Examples of Drugs Associated with Methemoglobinemia: Class Examples Nitrates/Nitrites nitric oxide, nitroglycerin, nitroprusside, nitrous oxide Local anesthetics articaine, benzocaine, bupivacaine, lidocaine, mepivacaine, prilocaine, procaine, ropivacaine, tetracaine Antineoplastic agents cyclophosphamide, flutamide, hydroxyurea, isofamide, rasburicase Antibiotics dapsone, nitrofurantoin, para-aminosalicylic acid, sulfonamides Antimalarials chloroquine, primaquine Anticonvulsants phenobarbital, phenytoin, sodium valproate Other drugs acetaminophen, metoclopramide, quinine, sulfasalazine...

Mechanism: These medications can both contribute to a blood disorder that prevents oxygen from reaching your body's tissues properly. This is a rare but serious side effect mentioned in the drug safety information.

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

Common Questions

Can I take this medicine if I am allergic to other antibiotics?
Tell your doctor about all your allergies before taking this medicine. Do not take this medicine if you are allergic to nitrofurantoin.
Can I drive while taking this medicine?
This medicine can cause dizziness. Be careful driving or operating machinery until you know how it affects you.
How long should I take this medicine?
Take this medicine for as long as your doctor tells you, usually for one week or at least 3 days after your urine is clear of infection.
What should I do if I get diarrhea while taking this medicine?
Tell your doctor if you get diarrhea, especially if it is severe or bloody. It could be a sign of a serious infection.
Can this medicine affect my liver?
Yes, this medicine can cause liver problems. Your doctor may check your liver function while you are taking it.
Can this medicine affect my nerves?
Yes, this medicine can cause nerve damage, especially if you have kidney problems, diabetes, or vitamin deficiencies.
Can I take antacids with this medicine?
Antacids can make this medicine less effective. Talk to your doctor before taking antacids with this medicine.
What if my symptoms don't improve?
If your symptoms do not improve after a few days, contact your doctor. You may need a different medicine.
Can this medicine change my urine color?
Yes, this medicine can turn your urine brown.
Is it okay to drink alcohol while taking this medication?
It is best to avoid alcohol while taking this medication, as it may worsen some side effects.
What are the common side effects of nitrofurantoin?
The registry lists Nausea, Headache, Vomiting among the most-reported FAERS reaction terms for nitrofurantoin. The compiled record contains 15,757 FDA adverse-event reports. These counts are not an individual symptom assessment.
Does nitrofurantoin interact with other medications?
The registry has 4 documented interaction rows for nitrofurantoin. Notable source-record pairings include dapsone topical, lidocaine topical, probenecid. These rows are not a complete medication review.
What drug class is nitrofurantoin?
nitrofurantoin belongs to the Nitrofuran Antibiotic drug class. It requires a prescription (Rx). This medicine treats urinary tract infections (UTIs).
What pregnancy or breastfeeding source fields are listed for nitrofurantoin?
The FDA label for nitrofurantoin contains product-specific pregnancy or breastfeeding language. PlainMeds does not apply that source text to an individual.
Has nitrofurantoin been recalled?
There is 1 recall associated with nitrofurantoin products. Failed Dissolution Specifications. Check the recalls section below for full details and affected products.

Active Recalls

Class II December 4, 2024

Failed Dissolution Specifications

AvKARE

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Compare beyond drug class

Nationwide peers by FAERS volume & death-report share

Two PlainMeds-derived comparison paths for nitrofurantoin: 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.

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What the FDA Data Shows for nitrofurantoin

The FDA label for nitrofurantoin (sold under brand names such as Macrobid, Macrodantin) classifies it as a prescription-only medication in the Nitrofuran Antibiotic class. This medicine treats urinary tract infections (UTIs). Official labeling lists 3 commonly reported side effects, including Nausea, Headache, Vomiting.

Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 15,757 voluntary reports. The database also lists 4 documented drug interactions derived from FDA labeling, with the top-flagged interaction rated moderate severity. NADAC pricing from CMS shows a generic unit cost of $3.87.

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 1 recall record 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).

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 29, 2024

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 and last refreshed May 2026. See our methodology for per-source dates and refresh cadence. Spot a figure that looks wrong? Report a correction.

All federal data sources used on this page