Does BISOPROLOL Cause Intentional product use issue? 384 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 384 reports of Intentional product use issue have been filed in association with BISOPROLOL (bisoprolol fumarate and hydrochlorothiazide). This represents 1.4% of all adverse event reports for BISOPROLOL.
384
Reports of Intentional product use issue with BISOPROLOL
1.4%
of all BISOPROLOL reports
3
Deaths
152
Hospitalizations
How Dangerous Is Intentional product use issue From BISOPROLOL?
Of the 384 reports, 3 (0.8%) resulted in death, 152 (39.6%) required hospitalization, and 77 (20.1%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BISOPROLOL. However, 384 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which BISOPROLOL Alternatives Have Lower Intentional product use issue Risk?
BISOPROLOL vs BISOPROLOL\BISOPROLOL
BISOPROLOL vs BISOPROLOL\HYDROCHLOROTHIAZIDE
BISOPROLOL vs BIVALIRUDIN
BISOPROLOL vs BLEOMYCIN
BISOPROLOL vs BLINATUMOMAB