Does BISOPROLOL Cause Product prescribing error? 191 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 191 reports of Product prescribing error have been filed in association with BISOPROLOL (bisoprolol fumarate and hydrochlorothiazide). This represents 0.7% of all adverse event reports for BISOPROLOL.
191
Reports of Product prescribing error with BISOPROLOL
0.7%
of all BISOPROLOL reports
4
Deaths
152
Hospitalizations
How Dangerous Is Product prescribing error From BISOPROLOL?
Of the 191 reports, 4 (2.1%) resulted in death, 152 (79.6%) required hospitalization, and 19 (9.9%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BISOPROLOL. However, 191 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 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 BISOPROLOL Alternatives Have Lower Product prescribing error Risk?
BISOPROLOL vs BISOPROLOL\BISOPROLOL
BISOPROLOL vs BISOPROLOL\HYDROCHLOROTHIAZIDE
BISOPROLOL vs BIVALIRUDIN
BISOPROLOL vs BLEOMYCIN
BISOPROLOL vs BLINATUMOMAB