Does HYDROCHLOROTHIAZIDE\IRBESARTAN Cause Hyperuricaemia? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Hyperuricaemia have been filed in association with HYDROCHLOROTHIAZIDE\IRBESARTAN. This represents 0.3% of all adverse event reports for HYDROCHLOROTHIAZIDE\IRBESARTAN.
7
Reports of Hyperuricaemia with HYDROCHLOROTHIAZIDE\IRBESARTAN
0.3%
of all HYDROCHLOROTHIAZIDE\IRBESARTAN reports
0
Deaths
5
Hospitalizations
How Dangerous Is Hyperuricaemia From HYDROCHLOROTHIAZIDE\IRBESARTAN?
Of the 7 reports, 5 (71.4%) required hospitalization, and 1 (14.3%) were considered life-threatening.
Is Hyperuricaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for HYDROCHLOROTHIAZIDE\IRBESARTAN. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does HYDROCHLOROTHIAZIDE\IRBESARTAN Cause?
Acute kidney injury (307)
Hyponatraemia (257)
Hypotension (138)
Hypertension (130)
Hypokalaemia (128)
Fall (108)
Dyspnoea (105)
Dizziness (101)
Blood pressure increased (98)
Drug ineffective (95)
What Other Drugs Cause Hyperuricaemia?
RITUXIMAB (130)
PREDNISONE (118)
RIBAVIRIN (116)
TACROLIMUS (116)
VENETOCLAX (115)
FUROSEMIDE (100)
ALLOPURINOL (94)
RUXOLITINIB (92)
CYCLOPHOSPHAMIDE (91)
DEXAMETHASONE (87)
Which HYDROCHLOROTHIAZIDE\IRBESARTAN Alternatives Have Lower Hyperuricaemia Risk?
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