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Drug side effects

prochlorperazine Side Effects

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

Data updated 2026-05-15

26,613
FAERS reports

Data from the FDA Adverse Event Reporting System (FAERS), 1999 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 prochlorperazine come from 26,613 reports to the FDA, broken down here by frequency, patient demographics, and serious outcomes.

This page analyzes 26,613 reports to the FDA Adverse Event Reporting System (FAERS) for prochlorperazine (Compazine): 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

26,613

Reports Mentioning Death

3,717

14.0% of reports — not proof the medicine caused the death

Hospitalizations

11,376

42.7% of reports

Top Indication

Product Used For Unknown Indication

Most Reported Adverse Reactions

NAUSEA
3,261
FATIGUE
2,706
DIARRHOEA
2,321
VOMITING
1,842
FEBRILE NEUTROPENIA
1,832
DEATH
1,705
ASTHENIA
1,254
PNEUMONIA
1,149
DYSPNOEA
1,101
PYREXIA
1,021
DECREASED APPETITE
1,013
PAIN
1,010
HEADACHE
973
DIZZINESS
962
CONSTIPATION
920
MALAISE
841
RASH
826
DISEASE PROGRESSION
784

Who Reports Side Effects

Gender Distribution

Female 14,236 (58%)
Male 10,234 (42%)
Unknown 26

Age Distribution

0-17 168 (1%)
18-44 2,376 (12%)
45-64 7,034 (37%)
65-74 5,833 (31%)
75+ 3,711 (19%)

Reporting Trend by Year

1999 2025

Reactions in Death Reports

Top reactions reported in 3,717 reports where death was an outcome. These are voluntarily reported and do not establish causation.

Reaction Reports
DEATH 1,690
NAUSEA 237
PNEUMONIA 219
FATIGUE 209
DISEASE PROGRESSION 188
MALIGNANT NEOPLASM PROGRESSION 185
SEPSIS 181
DIARRHOEA 174
DYSPNOEA 166
ASTHENIA 156
VOMITING 148
FEBRILE NEUTROPENIA 141
DECREASED APPETITE 131
RESPIRATORY FAILURE 120
CARDIAC ARREST 110
ANAEMIA 108
HYPOTENSION 107
ACUTE KIDNEY INJURY 99
DEHYDRATION 97

Reactions in Hospitalization Reports

Top reactions in 11,376 reports where hospitalization was an outcome.

Reaction Reports
FEBRILE NEUTROPENIA 1,603
NAUSEA 1,332
VOMITING 1,067
PNEUMONIA 1,003
DIARRHOEA 985
FATIGUE 936
PYREXIA 825
ASTHENIA 729
DYSPNOEA 633
DEHYDRATION 606
PAIN 532
FALL 508
MALAISE 496
ABDOMINAL PAIN 476
HEADACHE 446
DECREASED APPETITE 444
HYPOTENSION 443
CONFUSIONAL STATE 417
ANAEMIA 416

Compare prochlorperazine vs alosetron →

What the FAERS Data Reveals About prochlorperazine Side Effects

The FDA Adverse Event Reporting System (FAERS) contains 26,613 voluntary reports linked to prochlorperazine and its brand equivalents (Compazine), spanning 1999 through 2025. Of those, 3,717 (14.0%) listed death as an outcome and 11,376 (42.7%) 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, 58% were female and 42% male; age distribution skews toward 45-64, with 7,034 reports in that bracket. The single most reported reaction is nausea with 3,261 submissions, followed by fatigue and diarrhoea.

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.

Drugs With a Similar FAERS Report Volume

Other medications with a total FDA adverse-event report count closest to prochlorperazine's 26,613.