Does BISOPROLOL Cause Incorrect product administration duration? 33 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 33 reports of Incorrect product administration duration have been filed in association with BISOPROLOL (bisoprolol fumarate and hydrochlorothiazide). This represents 0.1% of all adverse event reports for BISOPROLOL.
33
Reports of Incorrect product administration duration with BISOPROLOL
0.1%
of all BISOPROLOL reports
1
Deaths
23
Hospitalizations
How Dangerous Is Incorrect product administration duration From BISOPROLOL?
Of the 33 reports, 1 (3.0%) resulted in death, 23 (69.7%) required hospitalization, and 10 (30.3%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BISOPROLOL. However, 33 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which BISOPROLOL Alternatives Have Lower Incorrect product administration duration Risk?
BISOPROLOL vs BISOPROLOL\BISOPROLOL
BISOPROLOL vs BISOPROLOL\HYDROCHLOROTHIAZIDE
BISOPROLOL vs BIVALIRUDIN
BISOPROLOL vs BLEOMYCIN
BISOPROLOL vs BLINATUMOMAB