Does IRBESARTAN Cause Product solubility abnormal? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product solubility abnormal have been filed in association with IRBESARTAN (Irbesartan). This represents 0.1% of all adverse event reports for IRBESARTAN.
7
Reports of Product solubility abnormal with IRBESARTAN
0.1%
of all IRBESARTAN reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product solubility abnormal From IRBESARTAN?
Of the 7 reports, 1 (14.3%) required hospitalization.
Is Product solubility abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IRBESARTAN. However, 7 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 solubility abnormal?
BUPRENORPHINE (498)
BUPRENORPHINE\NALOXONE (274)
POLYETHYLENE GLYCOL 3350 (220)
CHOLESTYRAMINE (193)
PATIROMER (107)
LEVOTHYROXINE (100)
SOMATROPIN (98)
EXENATIDE (97)
ESTRADIOL (94)
NITROGLYCERIN (81)
Which IRBESARTAN Alternatives Have Lower Product solubility abnormal Risk?
IRBESARTAN vs IRINOTECAN
IRBESARTAN vs IRON
IRBESARTAN vs IRON DEXTRAN
IRBESARTAN vs IRON ISOMALTOSIDE 1000
IRBESARTAN vs IRON POLYMALTOSE