Does IRBESARTAN Cause Wrong product administered? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Wrong product administered have been filed in association with IRBESARTAN (Irbesartan). This represents 0.1% of all adverse event reports for IRBESARTAN.
14
Reports of Wrong product administered with IRBESARTAN
0.1%
of all IRBESARTAN reports
4
Deaths
9
Hospitalizations
How Dangerous Is Wrong product administered From IRBESARTAN?
Of the 14 reports, 4 (28.6%) resulted in death, 9 (64.3%) required hospitalization, and 8 (57.1%) 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 IRBESARTAN. However, 14 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 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 IRBESARTAN Alternatives Have Lower Wrong product administered Risk?
IRBESARTAN vs IRINOTECAN
IRBESARTAN vs IRON
IRBESARTAN vs IRON DEXTRAN
IRBESARTAN vs IRON ISOMALTOSIDE 1000
IRBESARTAN vs IRON POLYMALTOSE