Does LISINOPRIL Cause Recalled product administered? 744 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 744 reports of Recalled product administered have been filed in association with LISINOPRIL (Lisinopril). This represents 2.0% of all adverse event reports for LISINOPRIL.
744
Reports of Recalled product administered with LISINOPRIL
2.0%
of all LISINOPRIL reports
1
Deaths
2
Hospitalizations
How Dangerous Is Recalled product administered From LISINOPRIL?
Of the 744 reports, 1 (0.1%) resulted in death, 2 (0.3%) 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 LISINOPRIL. However, 744 reports have been filed with the FAERS database.
What Other Side Effects Does LISINOPRIL Cause?
Angioedema (5,370)
Drug hypersensitivity (3,779)
Cough (2,527)
Completed suicide (2,246)
Drug ineffective (2,208)
Acute kidney injury (2,022)
Dyspnoea (1,856)
Dizziness (1,758)
Hypotension (1,750)
Fatigue (1,549)
What Other Drugs Cause Recalled product administered?
RAMIPRIL (1,028)
PENICILLIN G BENZATHINE (500)
LEVOTHYROXINE (406)
HUMAN IMMUNOGLOBULIN G (382)
VARENICLINE (381)
VALSARTAN (267)
QUINAPRIL (243)
TRIAMCINOLONE ACETONIDE (222)
RANITIDINE (204)
LOSARTAN (141)
Which LISINOPRIL Alternatives Have Lower Recalled product administered Risk?
LISINOPRIL vs LISOCABTAGENE MARALEUCEL
LISINOPRIL vs LITHIUM
LISINOPRIL vs LIXISENATIDE
LISINOPRIL vs LOBAPLATIN
LISINOPRIL vs LOFEXIDINE