Does ALTHIAZIDE\SPIRONOLACTONE Cause Off label use? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Off label use have been filed in association with ALTHIAZIDE\SPIRONOLACTONE. This represents 1.6% of all adverse event reports for ALTHIAZIDE\SPIRONOLACTONE.
5
Reports of Off label use with ALTHIAZIDE\SPIRONOLACTONE
1.6%
of all ALTHIAZIDE\SPIRONOLACTONE reports
0
Deaths
4
Hospitalizations
How Dangerous Is Off label use From ALTHIAZIDE\SPIRONOLACTONE?
Of the 5 reports, 4 (80.0%) required hospitalization, and 1 (20.0%) were considered life-threatening.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALTHIAZIDE\SPIRONOLACTONE. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does ALTHIAZIDE\SPIRONOLACTONE Cause?
Acute kidney injury (79)
Hyponatraemia (68)
Hyperkalaemia (62)
Lactic acidosis (51)
Fall (45)
Hypokalaemia (41)
Hypotension (28)
Cardio-respiratory arrest (17)
Hypoglycaemia (17)
Bradycardia (16)
What Other Drugs Cause Off label use?
RITUXIMAB (39,751)
INFLIXIMAB (34,801)
DENOSUMAB (34,612)
METHOTREXATE (24,020)
VEDOLIZUMAB (21,017)
ETANERCEPT (20,178)
TOCILIZUMAB (18,256)
PREDNISONE (17,867)
LENALIDOMIDE (17,017)
ADALIMUMAB (16,417)
Which ALTHIAZIDE\SPIRONOLACTONE Alternatives Have Lower Off label use Risk?
ALTHIAZIDE\SPIRONOLACTONE vs ALUMINUM
ALTHIAZIDE\SPIRONOLACTONE vs ALUMINUM HYDROXIDE
ALTHIAZIDE\SPIRONOLACTONE vs ALUMINUM HYDROXIDE\DIMETHICONE\MAGNESIUM HYDROXIDE
ALTHIAZIDE\SPIRONOLACTONE vs ALUMINUM HYDROXIDE\MAGNESIUM
ALTHIAZIDE\SPIRONOLACTONE vs ALUMINUM HYDROXIDE\MAGNESIUM HYDROXIDE