Does BISOPROLOL Cause Wrong product administered? 51 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 51 reports of Wrong product administered have been filed in association with BISOPROLOL (bisoprolol fumarate and hydrochlorothiazide). This represents 0.2% of all adverse event reports for BISOPROLOL.
51
Reports of Wrong product administered with BISOPROLOL
0.2%
of all BISOPROLOL reports
6
Deaths
41
Hospitalizations
How Dangerous Is Wrong product administered From BISOPROLOL?
Of the 51 reports, 6 (11.8%) resulted in death, 41 (80.4%) required hospitalization, and 1 (2.0%) 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 BISOPROLOL. However, 51 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 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 BISOPROLOL Alternatives Have Lower Wrong product administered Risk?
BISOPROLOL vs BISOPROLOL\BISOPROLOL
BISOPROLOL vs BISOPROLOL\HYDROCHLOROTHIAZIDE
BISOPROLOL vs BIVALIRUDIN
BISOPROLOL vs BLEOMYCIN
BISOPROLOL vs BLINATUMOMAB