Does RAMIPRIL Cause Recalled product administered? 1,028 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,028 reports of Recalled product administered have been filed in association with RAMIPRIL (Ramipril). This represents 3.1% of all adverse event reports for RAMIPRIL.
1,028
Reports of Recalled product administered with RAMIPRIL
3.1%
of all RAMIPRIL reports
1
Deaths
1
Hospitalizations
How Dangerous Is Recalled product administered From RAMIPRIL?
Of the 1,028 reports, 1 (0.1%) resulted in death, 1 (0.1%) required hospitalization.
Is Recalled product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RAMIPRIL. However, 1,028 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 Recalled product administered?
LISINOPRIL (744)
PENICILLIN G BENZATHINE (500)
LEVOTHYROXINE (406)
HUMAN IMMUNOGLOBULIN G (382)
VARENICLINE (381)
VALSARTAN (267)
QUINAPRIL (243)
TRIAMCINOLONE ACETONIDE (222)
RANITIDINE (204)
LOSARTAN (141)
Which RAMIPRIL Alternatives Have Lower Recalled product administered Risk?
RAMIPRIL vs RAMUCIRUMAB
RAMIPRIL vs RANEXA
RAMIPRIL vs RANIBIZUMAB
RAMIPRIL vs RANIMUSTINE
RAMIPRIL vs RANITIDINE