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Drug side effects

nitrofurantoin Side Effects

The reactions most often reported to the FDA for nitrofurantoin (also sold as Macrobid, Macrodantin), with demographics, serious outcomes, and reporting trends.

Data updated 2026-05-15

15,757
FAERS reports

Data from the FDA Adverse Event Reporting System (FAERS), 2004 to 2025. A FAERS report records a temporal association, not proof of cause. See our methodology for how figures are compiled and de-duplicated.

The most commonly reported side effects of nitrofurantoin come from 15,757 reports to the FDA, broken down here by frequency, patient demographics, and serious outcomes.

This page analyzes 15,757 reports to the FDA Adverse Event Reporting System (FAERS) for nitrofurantoin (Macrobid): the reactions reported most often, who reported them, serious outcomes such as hospitalization, and year-over-year trends. A FAERS report does not prove the drug caused the effect, and report volume tracks how widely a drug is used, not how likely an effect is for any one person. Educational information, not medical advice.

Total Reports

15,757

Reports Mentioning Death

1,000

6.3% of reports — not proof the medicine caused the death

Hospitalizations

5,435

34.5% of reports

Top Indication

Product Used For Unknown Indication

Most Reported Adverse Reactions

URINARY TRACT INFECTION
1,301
FATIGUE
1,240
NAUSEA
1,187
HEADACHE
1,103
PAIN
964
DYSPNOEA
950
DIARRHOEA
880
RASH
852
MALAISE
851
VOMITING
810
PYREXIA
796
DIZZINESS
788
CHRONIC KIDNEY DISEASE
588
FALL
585
WEIGHT DECREASED
577
ARTHRALGIA
545
PAIN IN EXTREMITY
539
ASTHENIA
534

Who Reports Side Effects

Gender Distribution

Female 12,211 (84%)
Male 2,274 (16%)
Unknown 26

Age Distribution

0-17 280 (2%)
18-44 2,019 (17%)
45-64 3,766 (33%)
65-74 2,394 (21%)
75+ 3,098 (27%)

Reporting Trend by Year

2004 2025

Reactions in Death Reports

Top reactions reported in 1,000 reports where death was an outcome. These are voluntarily reported and do not establish causation.

Reaction 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
PYREXIA 42
FATIGUE 40
NAUSEA 40
DECREASED APPETITE 38
GENERAL PHYSICAL HEALTH DETERIORATION 37
RESPIRATORY FAILURE 37
HEPATIC FAILURE 36
CONFUSIONAL STATE 35
ASTHENIA 34

Reactions in Hospitalization Reports

Top reactions in 5,435 reports where hospitalization was an outcome.

Reaction Reports
URINARY TRACT INFECTION 677
DYSPNOEA 483
NAUSEA 436
PAIN 403
FATIGUE 385
PYREXIA 382
VOMITING 364
DIARRHOEA 334
PNEUMONIA 312
MALAISE 308
FALL 306
HEADACHE 293
ASTHENIA 282
ABDOMINAL PAIN 264
DIZZINESS 259
ACUTE KIDNEY INJURY 246
WEIGHT DECREASED 242
BACK PAIN 237
COUGH 231

Compare nitrofurantoin vs amikacin →

What the FAERS Data Reveals About nitrofurantoin Side Effects

The FDA Adverse Event Reporting System (FAERS) contains 15,757 voluntary reports linked to nitrofurantoin and its brand equivalents (Macrobid, Macrodantin), spanning 2004 through 2025. Of those, 1,000 (6.3%) listed death as an outcome and 5,435 (34.5%) involved hospitalization. The most common indication reported alongside adverse events was Product Used For Unknown Indication.

Demographic breakdowns help contextualize who is being exposed to the drug. Of reports with known sex, 84% were female and 16% male; age distribution skews toward 45-64, with 3,766 reports in that bracket. The single most reported reaction is urinary tract infection with 1,301 submissions, followed by fatigue and nausea.

How to read these numbers

FAERS is a signal-detection tool, not a scorecard. Reports are voluntary, and a single case may list multiple suspect drugs, so numbers above should not be read as incidence rates or per-patient risk. Widely prescribed drugs naturally accumulate more reports than niche therapies even when individual risk is low. These aggregates are useful for spotting patterns that merit further pharmacovigilance, not for choosing between medications. This page is for educational reference only and is not medical advice, speak with a licensed clinician about any side-effect concerns.