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Drug side effects

vericiguat Side Effects

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

Data updated 2026-05-15

905
FAERS reports

Data from the FDA Adverse Event Reporting System (FAERS), 2017 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 vericiguat come from 905 reports to the FDA, broken down here by frequency, patient demographics, and serious outcomes.

This page analyzes 905 reports to the FDA Adverse Event Reporting System (FAERS) for vericiguat (Verquvo): 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

905

Reports Mentioning Death

135

14.9% of reports — not proof the medicine caused the death

Hospitalizations

215

23.8% of reports

Top Indication

Cardiac Failure

Most Reported Adverse Reactions

HYPOTENSION
106
DEATH
90
DIZZINESS
65
CARDIAC FAILURE
60
ANAEMIA
35
FATIGUE
35
BLOOD PRESSURE DECREASED
34
MALAISE
34
DYSPNOEA
32
NAUSEA
29
ASTHENIA
27
DIARRHOEA
27
RASH
21
HEADACHE
20
HOSPITALISATION
19
FEELING ABNORMAL
18

Who Reports Side Effects

Gender Distribution

Female 290 (34%)
Male 567 (66%)
Unknown 2

Age Distribution

0-17 14 (4%)
18-44 18 (5%)
45-64 73 (19%)
65-74 101 (26%)
75+ 181 (47%)

Reporting Trend by Year

17
18
21
22
23
24
25

Reactions in Death Reports

Top reactions reported in 135 reports where death was an outcome. These are voluntarily reported and do not establish causation.

Reaction Reports
DEATH 89
CARDIAC FAILURE 19
ILL-DEFINED DISORDER 8
CARDIAC ARREST 7
ADVERSE EVENT 6
CARDIAC DISORDER 5
PNEUMONIA 5
ILLNESS 4
TREATMENT NONCOMPLIANCE 4
ATRIAL FIBRILLATION 3
BLOOD PRESSURE DECREASED 3
BRAIN NATRIURETIC PEPTIDE INCREASED 3
CHRONIC KIDNEY DISEASE 3
EJECTION FRACTION DECREASED 3
HOSPICE CARE 3
INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION 3
MALAISE 3
MYOCARDIAL INFARCTION 3
NAUSEA 3
RENAL FAILURE 3

Reactions in Hospitalization Reports

Top reactions in 215 reports where hospitalization was an outcome.

Reaction Reports
CARDIAC FAILURE 36
HYPOTENSION 24
HOSPITALISATION 19
ANAEMIA 16
DEATH 16
ADVERSE EVENT 13
DYSPNOEA 12
ASTHENIA 9
DIZZINESS 8
OEDEMA PERIPHERAL 8
ATRIAL FIBRILLATION 7
BLOOD PRESSURE DECREASED 7
PNEUMONIA 7
ACUTE KIDNEY INJURY 6
CARDIAC FAILURE CHRONIC 6
GASTROINTESTINAL HAEMORRHAGE 6
MALAISE 6
RENAL IMPAIRMENT 6
CARDIAC DISORDER 5
DYSPNOEA EXERTIONAL 5

Compare vericiguat vs adenosine →

What the FAERS Data Reveals About vericiguat Side Effects

The FDA Adverse Event Reporting System (FAERS) contains 905 voluntary reports linked to vericiguat and its brand equivalents (Verquvo), spanning 2017 through 2025. Of those, 135 (14.9%) listed death as an outcome and 215 (23.8%) involved hospitalization. The most common indication reported alongside adverse events was Cardiac Failure.

Demographic breakdowns help contextualize who is being exposed to the drug. Of reports with known sex, 34% were female and 66% male; age distribution skews toward 75+, with 181 reports in that bracket. The single most reported reaction is hypotension with 106 submissions, followed by death and dizziness.

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 vericiguat's 905.