Does IRBESARTAN Cause Product administration error? 32 Reports in FDA Database
Lower Your Cholesterol — The Natural Way
The Oxidized Cholesterol Strategy: a science-backed plan for heart health.
According to the FDA Adverse Event Reporting System (FAERS), 32 reports of Product administration error have been filed in association with IRBESARTAN (Irbesartan). This represents 0.3% of all adverse event reports for IRBESARTAN.
32
Reports of Product administration error with IRBESARTAN
0.3%
of all IRBESARTAN reports
2
Deaths
27
Hospitalizations
How Dangerous Is Product administration error From IRBESARTAN?
Of the 32 reports, 2 (6.3%) resulted in death, 27 (84.4%) required hospitalization, and 2 (6.3%) 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 IRBESARTAN. However, 32 reports have been filed with the FAERS database.
What Other Side Effects Does IRBESARTAN Cause?
Acute kidney injury (1,361)
Fall (795)
Hypotension (686)
Nausea (533)
Drug ineffective (532)
Malaise (488)
Hyponatraemia (485)
Fatigue (483)
Blood pressure increased (477)
Hyperkalaemia (454)
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 IRBESARTAN Alternatives Have Lower Product administration error Risk?
IRBESARTAN vs IRINOTECAN
IRBESARTAN vs IRON
IRBESARTAN vs IRON DEXTRAN
IRBESARTAN vs IRON ISOMALTOSIDE 1000
IRBESARTAN vs IRON POLYMALTOSE