BENAZEPRIL HYDROCHLORIDE

N/A

Manufactured by Validus Pharmaceuticals LLC

15,362 FDA adverse event reports analyzed

Last updated: 2026-04-15

About BENAZEPRIL HYDROCHLORIDE

BENAZEPRIL HYDROCHLORIDE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Validus Pharmaceuticals LLC. The most commonly reported adverse reactions for BENAZEPRIL HYDROCHLORIDE include NAUSEA, FATIGUE, DRUG INEFFECTIVE, DIZZINESS, DYSPNOEA. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for BENAZEPRIL HYDROCHLORIDE.

Top Adverse Reactions

NAUSEA441 reports
FATIGUE409 reports
DRUG INEFFECTIVE398 reports
DIZZINESS384 reports
DYSPNOEA384 reports
PAIN360 reports
DIARRHOEA356 reports
HEADACHE344 reports
MYOCARDIAL INFARCTION312 reports
HYPERTENSION294 reports
ASTHENIA269 reports
VOMITING258 reports
ANXIETY253 reports
CEREBROVASCULAR ACCIDENT249 reports
CARDIAC FAILURE CONGESTIVE241 reports
CHEST PAIN239 reports
RENAL FAILURE239 reports
ARTHRALGIA233 reports
COUGH228 reports
PRURITUS227 reports
FALL213 reports
PAIN IN EXTREMITY207 reports
WEIGHT DECREASED206 reports
BLOOD PRESSURE INCREASED202 reports
DEPRESSION197 reports
BACK PAIN189 reports
OEDEMA PERIPHERAL189 reports
RASH180 reports
BLOOD GLUCOSE INCREASED175 reports
FLUSHING175 reports
INSOMNIA170 reports
MALAISE169 reports
CORONARY ARTERY DISEASE168 reports
HYPOTENSION166 reports
PNEUMONIA157 reports
DEATH154 reports
ATRIAL FIBRILLATION153 reports
CONSTIPATION149 reports
ANAEMIA145 reports
INJURY144 reports
DECREASED APPETITE143 reports
URINARY TRACT INFECTION138 reports
PYREXIA137 reports
TREMOR131 reports
FEELING ABNORMAL130 reports
DEHYDRATION127 reports
PALPITATIONS127 reports
WEIGHT INCREASED127 reports
CHRONIC KIDNEY DISEASE124 reports
ABDOMINAL PAIN UPPER123 reports
ABDOMINAL PAIN122 reports
DIABETES MELLITUS122 reports
MYALGIA119 reports
DRUG HYPERSENSITIVITY115 reports
OFF LABEL USE113 reports
CONFUSIONAL STATE111 reports
GAIT DISTURBANCE110 reports
MUSCLE SPASMS108 reports
ERYTHEMA106 reports
RENAL FAILURE ACUTE106 reports
HYPOAESTHESIA105 reports
PARAESTHESIA102 reports
VISION BLURRED102 reports
EMOTIONAL DISTRESS101 reports
ACUTE KIDNEY INJURY99 reports
GASTROOESOPHAGEAL REFLUX DISEASE98 reports
HEART RATE INCREASED97 reports
SOMNOLENCE97 reports
SYNCOPE95 reports
CONDITION AGGRAVATED93 reports
RENAL IMPAIRMENT89 reports
MUSCULAR WEAKNESS88 reports
GASTROINTESTINAL HAEMORRHAGE87 reports
ALOPECIA84 reports
ANGIOEDEMA82 reports
CHEST DISCOMFORT82 reports
CONTUSION82 reports
DYSPEPSIA82 reports
ABDOMINAL DISCOMFORT81 reports
COMPLETED SUICIDE81 reports
HYPERHIDROSIS79 reports
LOSS OF CONSCIOUSNESS77 reports
UNEVALUABLE EVENT77 reports
OSTEOARTHRITIS76 reports
RENAL INJURY76 reports
SINUSITIS76 reports
URTICARIA76 reports
CARDIAC DISORDER75 reports
CHRONIC OBSTRUCTIVE PULMONARY DISEASE75 reports
BALANCE DISORDER74 reports
ACUTE MYOCARDIAL INFARCTION73 reports
RESPIRATORY FAILURE73 reports
ABDOMINAL DISTENSION72 reports
TYPE 2 DIABETES MELLITUS72 reports
BRONCHITIS71 reports
HAEMOGLOBIN DECREASED71 reports
DRUG INTERACTION70 reports
CARDIAC ARREST69 reports
PANCREATITIS69 reports
TRANSIENT ISCHAEMIC ATTACK69 reports

Report Outcomes

Out of 7,065 classified reports for BENAZEPRIL HYDROCHLORIDE:

Serious 64.7%Non-Serious 35.3%

The FDA classifies an adverse event as “serious” if it results in death, hospitalization, disability, congenital anomaly, or requires intervention to prevent permanent damage.

Demographics Breakdown

Reports by Sex

Female3,726 (55.1%)
Male3,024 (44.7%)
Unknown8 (0.1%)

Reports by Age

Age 63151 reports
Age 65138 reports
Age 59136 reports
Age 68136 reports
Age 66125 reports
Age 70125 reports
Age 55123 reports
Age 64123 reports
Age 61122 reports
Age 67119 reports
Age 62118 reports
Age 73117 reports
Age 72114 reports
Age 60113 reports
Age 71113 reports
Age 74110 reports
Age 52106 reports
Age 75104 reports
Age 76104 reports
Age 58101 reports

Demographics reflect voluntary FDA adverse event reporting patterns and may not represent the full patient population.

Frequently Asked Questions

How many FDA adverse event reports are associated with BENAZEPRIL HYDROCHLORIDE?

This profile reflects 15,362 FDA FAERS reports that mention BENAZEPRIL HYDROCHLORIDE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for BENAZEPRIL HYDROCHLORIDE?

Frequently reported terms in FAERS include NAUSEA, FATIGUE, DRUG INEFFECTIVE, DIZZINESS, DYSPNOEA, PAIN. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures BENAZEPRIL HYDROCHLORIDE?

Labeling and FAERS entries often list Validus Pharmaceuticals LLC in connection with BENAZEPRIL HYDROCHLORIDE. Always verify the specific product and NDC with your pharmacist.

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.