Does URAPIDIL Cause Wrong patient received product? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Wrong patient received product have been filed in association with URAPIDIL. This represents 0.7% of all adverse event reports for URAPIDIL.
12
Reports of Wrong patient received product with URAPIDIL
0.7%
of all URAPIDIL reports
0
Deaths
8
Hospitalizations
How Dangerous Is Wrong patient received product From URAPIDIL?
Of the 12 reports, 8 (66.7%) required hospitalization, and 1 (8.3%) were considered life-threatening.
Is Wrong patient received product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for URAPIDIL. However, 12 reports have been filed with the FAERS database.
What Other Side Effects Does URAPIDIL Cause?
Acute kidney injury (187)
Fall (150)
Hypotension (148)
Hyperkalaemia (78)
Drug ineffective (77)
Hyponatraemia (69)
Bradycardia (66)
Toxic epidermal necrolysis (63)
Condition aggravated (61)
Dizziness (60)
What Other Drugs Cause Wrong patient received product?
INSULIN LISPRO (334)
CLOZAPINE (198)
RISPERIDONE (176)
OXAZEPAM (152)
BISOPROLOL (150)
LEVETIRACETAM (126)
ACETAMINOPHEN (123)
METFORMIN (116)
INSULIN GLARGINE (114)
CLONAZEPAM (112)
Which URAPIDIL Alternatives Have Lower Wrong patient received product Risk?
URAPIDIL vs UREA
URAPIDIL vs URIDINE TRIACETATE
URAPIDIL vs UROFOLLITROPIN
URAPIDIL vs URSODIOL
URAPIDIL vs USTEKINUMAB