Does BISOPROLOL Cause Wrong patient received product? 150 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 150 reports of Wrong patient received product have been filed in association with BISOPROLOL (bisoprolol fumarate and hydrochlorothiazide). This represents 0.5% of all adverse event reports for BISOPROLOL.
150
Reports of Wrong patient received product with BISOPROLOL
0.5%
of all BISOPROLOL reports
14
Deaths
78
Hospitalizations
How Dangerous Is Wrong patient received product From BISOPROLOL?
Of the 150 reports, 14 (9.3%) resulted in death, 78 (52.0%) required hospitalization, and 23 (15.3%) 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 BISOPROLOL. However, 150 reports have been filed with the FAERS database.
What Other Side Effects Does BISOPROLOL Cause?
Dyspnoea (2,940)
Bradycardia (2,535)
Hypotension (2,504)
Dizziness (2,153)
Fall (2,011)
Fatigue (1,983)
Acute kidney injury (1,894)
Malaise (1,602)
Drug ineffective (1,486)
Nausea (1,460)
What Other Drugs Cause Wrong patient received product?
INSULIN LISPRO (334)
CLOZAPINE (198)
RISPERIDONE (176)
OXAZEPAM (152)
LEVETIRACETAM (126)
ACETAMINOPHEN (123)
METFORMIN (116)
INSULIN GLARGINE (114)
CLONAZEPAM (112)
LAMOTRIGINE (112)
Which BISOPROLOL Alternatives Have Lower Wrong patient received product Risk?
BISOPROLOL vs BISOPROLOL\BISOPROLOL
BISOPROLOL vs BISOPROLOL\HYDROCHLOROTHIAZIDE
BISOPROLOL vs BIVALIRUDIN
BISOPROLOL vs BLEOMYCIN
BISOPROLOL vs BLINATUMOMAB