VONOPRAZAN FUMARATE

N/A

9,763 FDA adverse event reports analyzed

Last updated: 2026-04-15

About VONOPRAZAN FUMARATE

VONOPRAZAN FUMARATE is a medication tracked in the FDA Adverse Event Reporting System (FAERS). The most commonly reported adverse reactions for VONOPRAZAN FUMARATE include OFF LABEL USE, DIARRHOEA, DRUG INEFFECTIVE, NAUSEA, DECREASED APPETITE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for VONOPRAZAN FUMARATE.

Top Adverse Reactions

OFF LABEL USE423 reports
DIARRHOEA377 reports
DRUG INEFFECTIVE368 reports
NAUSEA343 reports
DECREASED APPETITE231 reports
MALAISE229 reports
GASTROOESOPHAGEAL REFLUX DISEASE219 reports
PYREXIA214 reports
INTERSTITIAL LUNG DISEASE181 reports
HEADACHE178 reports
PNEUMONIA165 reports
ANAEMIA164 reports
ABDOMINAL PAIN UPPER160 reports
VOMITING160 reports
DIZZINESS151 reports
DYSPNOEA149 reports
RENAL IMPAIRMENT149 reports
CARDIAC FAILURE138 reports
HEPATIC FUNCTION ABNORMAL131 reports
DYSPEPSIA123 reports
RASH123 reports
PAIN122 reports
CONSTIPATION121 reports
ABDOMINAL PAIN117 reports
PLATELET COUNT DECREASED116 reports
DEATH114 reports
ABDOMINAL DISTENSION113 reports
FALL112 reports
HYPERTENSION111 reports
DEHYDRATION104 reports
COVID 19103 reports
ARTHRALGIA102 reports
FATIGUE102 reports
PRODUCT DOSE OMISSION ISSUE101 reports
PRURITUS97 reports
FEBRILE NEUTROPENIA95 reports
LIVER DISORDER95 reports
ABDOMINAL DISCOMFORT94 reports
URINARY TRACT INFECTION93 reports
WHITE BLOOD CELL COUNT DECREASED89 reports
ACUTE KIDNEY INJURY83 reports
CEREBRAL INFARCTION83 reports
NEUTROPHIL COUNT DECREASED82 reports
INSOMNIA81 reports
CHEST PAIN77 reports
MALIGNANT NEOPLASM PROGRESSION77 reports
PNEUMONIA ASPIRATION77 reports
CONDITION AGGRAVATED73 reports
FEELING ABNORMAL73 reports
BACK PAIN72 reports
INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION70 reports
BLOOD PRESSURE DECREASED69 reports
DRUG INTERACTION67 reports
ILLNESS67 reports
COUGH64 reports
WEIGHT DECREASED64 reports
BLOOD PRESSURE INCREASED63 reports
SEPSIS62 reports
DRUG INDUCED LIVER INJURY60 reports
PLEURAL EFFUSION60 reports
ALTERED STATE OF CONSCIOUSNESS59 reports
MUSCLE SPASMS58 reports
OEDEMA PERIPHERAL58 reports
CYTOKINE RELEASE SYNDROME57 reports
HYPOKALAEMIA57 reports
HYPONATRAEMIA56 reports
THERAPEUTIC PRODUCT EFFECT INCOMPLETE55 reports
ASTHENIA54 reports
HOSPITALISATION53 reports
PALPITATIONS53 reports
STOMATITIS53 reports
C REACTIVE PROTEIN INCREASED51 reports
DRUG ERUPTION51 reports
GASTROINTESTINAL DISORDER51 reports
HYPOAESTHESIA51 reports
WRONG TECHNIQUE IN PRODUCT USAGE PROCESS51 reports
PANCYTOPENIA50 reports
PULMONARY TOXICITY50 reports
ALANINE AMINOTRANSFERASE INCREASED49 reports
ERYTHEMA49 reports
FLATULENCE49 reports
HYPERKALAEMIA49 reports
PNEUMONIA BACTERIAL49 reports
DISEASE PROGRESSION48 reports
PAIN IN EXTREMITY48 reports
HYPOTENSION47 reports
SEPTIC SHOCK47 reports
ASPARTATE AMINOTRANSFERASE INCREASED46 reports
MUSCULAR WEAKNESS46 reports
ASCITES45 reports
GASTRIC CANCER44 reports
HYPOTHYROIDISM44 reports
PRODUCT USE ISSUE44 reports
SOMNOLENCE43 reports
UNDERDOSE43 reports
ADRENAL INSUFFICIENCY42 reports
INCORRECT PRODUCT ADMINISTRATION DURATION41 reports
WEIGHT INCREASED41 reports
CHOLANGITIS40 reports
DISSEMINATED INTRAVASCULAR COAGULATION40 reports

Frequently Asked Questions

How many FDA adverse event reports are associated with VONOPRAZAN FUMARATE?

This profile reflects 9,763 FDA FAERS reports that mention VONOPRAZAN FUMARATE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for VONOPRAZAN FUMARATE?

Frequently reported terms in FAERS include OFF LABEL USE, DIARRHOEA, DRUG INEFFECTIVE, NAUSEA, DECREASED APPETITE, MALAISE. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Important Disclaimer: This content is generated by AI analysis of FDA adverse event reports and is provided for informational purposes only. It is not medical advice. Adverse event reports submitted to the FDA do not prove that a medication caused the reported side effect. Always consult your healthcare provider before starting, stopping, or changing any medication. If you experience a serious side effect, contact your doctor or call 911 immediately.