Does URAPIDIL Cause Product prescribing error? 26 Reports in FDA Database
Lower Your Cholesterol — The Natural Way
The Oxidized Cholesterol Strategy: a science-backed plan for heart health.
According to the FDA Adverse Event Reporting System (FAERS), 26 reports of Product prescribing error have been filed in association with URAPIDIL. This represents 1.6% of all adverse event reports for URAPIDIL.
26
Reports of Product prescribing error with URAPIDIL
1.6%
of all URAPIDIL reports
0
Deaths
20
Hospitalizations
How Dangerous Is Product prescribing error From URAPIDIL?
Of the 26 reports, 20 (76.9%) required hospitalization.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for URAPIDIL. However, 26 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 Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which URAPIDIL Alternatives Have Lower Product prescribing error Risk?
URAPIDIL vs UREA
URAPIDIL vs URIDINE TRIACETATE
URAPIDIL vs UROFOLLITROPIN
URAPIDIL vs URSODIOL
URAPIDIL vs USTEKINUMAB