Does RAMIPRIL Cause Product prescribing error? 322 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 322 reports of Product prescribing error have been filed in association with RAMIPRIL (Ramipril). This represents 1.0% of all adverse event reports for RAMIPRIL.
322
Reports of Product prescribing error with RAMIPRIL
1.0%
of all RAMIPRIL reports
0
Deaths
265
Hospitalizations
How Dangerous Is Product prescribing error From RAMIPRIL?
Of the 322 reports, 265 (82.3%) required hospitalization, and 35 (10.9%) 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 RAMIPRIL. However, 322 reports have been filed with the FAERS database.
What Other Side Effects Does RAMIPRIL Cause?
Acute kidney injury (3,286)
Dyspnoea (2,537)
Dizziness (2,490)
Hypotension (2,417)
Fatigue (2,415)
Drug ineffective (2,412)
Nausea (2,219)
Vomiting (2,055)
Off label use (2,053)
Hypertension (2,046)
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 RAMIPRIL Alternatives Have Lower Product prescribing error Risk?
RAMIPRIL vs RAMUCIRUMAB
RAMIPRIL vs RANEXA
RAMIPRIL vs RANIBIZUMAB
RAMIPRIL vs RANIMUSTINE
RAMIPRIL vs RANITIDINE