Does BENAZEPRIL Cause Product prescribing error? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product prescribing error have been filed in association with BENAZEPRIL (benazepril hydrochloride and hydrochlorothiazide). This represents 0.5% of all adverse event reports for BENAZEPRIL.
7
Reports of Product prescribing error with BENAZEPRIL
0.5%
of all BENAZEPRIL reports
0
Deaths
7
Hospitalizations
How Dangerous Is Product prescribing error From BENAZEPRIL?
Of the 7 reports, 7 (100.0%) required hospitalization, and 1 (14.3%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BENAZEPRIL. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does BENAZEPRIL Cause?
Completed suicide (150)
Drug ineffective (115)
Toxicity to various agents (101)
Angioedema (100)
Drug hypersensitivity (97)
Hypotension (96)
Dizziness (83)
Cough (75)
Headache (69)
Intentional overdose (64)
What Other Drugs Cause Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which BENAZEPRIL Alternatives Have Lower Product prescribing error Risk?
BENAZEPRIL vs BENDAMUSTINE
BENAZEPRIL vs BENDROFLUMETHIAZIDE
BENAZEPRIL vs BENIDIPINE
BENAZEPRIL vs BENLYSTA
BENAZEPRIL vs BENRALIZUMAB