Does QUINAPRIL Cause Recalled product administered? 243 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 243 reports of Recalled product administered have been filed in association with QUINAPRIL (Quinapril). This represents 13.2% of all adverse event reports for QUINAPRIL.
243
Reports of Recalled product administered with QUINAPRIL
13.2%
of all QUINAPRIL reports
1
Deaths
7
Hospitalizations
How Dangerous Is Recalled product administered From QUINAPRIL?
Of the 243 reports, 1 (0.4%) resulted in death, 7 (2.9%) 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 QUINAPRIL. However, 243 reports have been filed with the FAERS database.
What Other Side Effects Does QUINAPRIL Cause?
Fall (682)
Cognitive disorder (599)
Orthostatic hypotension (592)
Balance disorder (576)
Hypotension (568)
Constipation (565)
Sedation (547)
Depressed level of consciousness (510)
Sedation complication (500)
Pain (499)
What Other Drugs Cause Recalled product administered?
RAMIPRIL (1,028)
LISINOPRIL (744)
PENICILLIN G BENZATHINE (500)
LEVOTHYROXINE (406)
HUMAN IMMUNOGLOBULIN G (382)
VARENICLINE (381)
VALSARTAN (267)
TRIAMCINOLONE ACETONIDE (222)
RANITIDINE (204)
LOSARTAN (141)
Which QUINAPRIL Alternatives Have Lower Recalled product administered Risk?
QUINAPRIL vs QUINAPRIL\QUINAPRIL
QUINAPRIL vs QUINIDINE
QUINAPRIL vs QUININE
QUINAPRIL vs QUIZARTINIB
QUINAPRIL vs RABEPRAZOLE