Does URAPIDIL Cause Wrong product administered? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Wrong product administered have been filed in association with URAPIDIL. This represents 0.5% of all adverse event reports for URAPIDIL.
8
Reports of Wrong product administered with URAPIDIL
0.5%
of all URAPIDIL reports
1
Deaths
7
Hospitalizations
How Dangerous Is Wrong product administered From URAPIDIL?
Of the 8 reports, 1 (12.5%) resulted in death, 7 (87.5%) required hospitalization, and 7 (87.5%) were considered life-threatening.
Is Wrong product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for URAPIDIL. However, 8 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 product administered?
INSULIN LISPRO (337)
INSULIN GLARGINE (226)
RISPERIDONE (141)
QUETIAPINE (137)
ACETAMINOPHEN (133)
INSULIN ASPART (112)
CLOZAPINE (106)
INSULIN HUMAN (104)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104)
IBUPROFEN (102)
Which URAPIDIL Alternatives Have Lower Wrong product administered Risk?
URAPIDIL vs UREA
URAPIDIL vs URIDINE TRIACETATE
URAPIDIL vs UROFOLLITROPIN
URAPIDIL vs URSODIOL
URAPIDIL vs USTEKINUMAB