Does RAMIPRIL Cause Incorrect product administration duration? 78 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 78 reports of Incorrect product administration duration have been filed in association with RAMIPRIL (Ramipril). This represents 0.2% of all adverse event reports for RAMIPRIL.
78
Reports of Incorrect product administration duration with RAMIPRIL
0.2%
of all RAMIPRIL reports
61
Deaths
65
Hospitalizations
How Dangerous Is Incorrect product administration duration From RAMIPRIL?
Of the 78 reports, 61 (78.2%) resulted in death, 65 (83.3%) required hospitalization, and 72 (92.3%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RAMIPRIL. However, 78 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which RAMIPRIL Alternatives Have Lower Incorrect product administration duration Risk?
RAMIPRIL vs RAMUCIRUMAB
RAMIPRIL vs RANEXA
RAMIPRIL vs RANIBIZUMAB
RAMIPRIL vs RANIMUSTINE
RAMIPRIL vs RANITIDINE