Does ALTHIAZIDE\SPIRONOLACTONE Cause Wrong technique in product usage process? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Wrong technique in product usage process have been filed in association with ALTHIAZIDE\SPIRONOLACTONE. This represents 1.6% of all adverse event reports for ALTHIAZIDE\SPIRONOLACTONE.
5
Reports of Wrong technique in product usage process with ALTHIAZIDE\SPIRONOLACTONE
1.6%
of all ALTHIAZIDE\SPIRONOLACTONE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Wrong technique in product usage process From ALTHIAZIDE\SPIRONOLACTONE?
Of the 5 reports.
Is Wrong technique in product usage process 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which ALTHIAZIDE\SPIRONOLACTONE Alternatives Have Lower Wrong technique in product usage process 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