Does BISOPROLOL Cause Product administration error? 137 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 137 reports of Product administration error have been filed in association with BISOPROLOL (bisoprolol fumarate and hydrochlorothiazide). This represents 0.5% of all adverse event reports for BISOPROLOL.
137
Reports of Product administration error with BISOPROLOL
0.5%
of all BISOPROLOL reports
24
Deaths
99
Hospitalizations
How Dangerous Is Product administration error From BISOPROLOL?
Of the 137 reports, 24 (17.5%) resulted in death, 99 (72.3%) required hospitalization, and 10 (7.3%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BISOPROLOL. However, 137 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 administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which BISOPROLOL Alternatives Have Lower Product administration error Risk?
BISOPROLOL vs BISOPROLOL\BISOPROLOL
BISOPROLOL vs BISOPROLOL\HYDROCHLOROTHIAZIDE
BISOPROLOL vs BIVALIRUDIN
BISOPROLOL vs BLEOMYCIN
BISOPROLOL vs BLINATUMOMAB