Does ALTHIAZIDE Cause Wrong patient received product? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Wrong patient received product have been filed in association with ALTHIAZIDE. This represents 5.5% of all adverse event reports for ALTHIAZIDE.
10
Reports of Wrong patient received product with ALTHIAZIDE
5.5%
of all ALTHIAZIDE reports
0
Deaths
10
Hospitalizations
How Dangerous Is Wrong patient received product From ALTHIAZIDE?
Of the 10 reports, 10 (100.0%) required hospitalization.
Is Wrong patient received product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALTHIAZIDE. However, 10 reports have been filed with the FAERS database.
What Other Side Effects Does ALTHIAZIDE Cause?
Acute kidney injury (40)
Hyponatraemia (29)
Hypokalaemia (20)
General physical health deterioration (15)
Hemiplegia (13)
Anuria (12)
Hyperkalaemia (12)
International normalised ratio increased (12)
Hypotension (11)
Aggression (10)
What Other Drugs Cause Wrong patient received product?
INSULIN LISPRO (334)
CLOZAPINE (198)
RISPERIDONE (176)
OXAZEPAM (152)
BISOPROLOL (150)
LEVETIRACETAM (126)
ACETAMINOPHEN (123)
METFORMIN (116)
INSULIN GLARGINE (114)
CLONAZEPAM (112)
Which ALTHIAZIDE Alternatives Have Lower Wrong patient received product Risk?
ALTHIAZIDE vs ALTHIAZIDE\SPIRONOLACTONE
ALTHIAZIDE vs ALUMINUM
ALTHIAZIDE vs ALUMINUM HYDROXIDE
ALTHIAZIDE vs ALUMINUM HYDROXIDE\DIMETHICONE\MAGNESIUM HYDROXIDE
ALTHIAZIDE vs ALUMINUM HYDROXIDE\MAGNESIUM