Does ALTHIAZIDE\SPIRONOLACTONE Cause Dermatitis contact? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Dermatitis contact have been filed in association with ALTHIAZIDE\SPIRONOLACTONE. This represents 2.5% of all adverse event reports for ALTHIAZIDE\SPIRONOLACTONE.
8
Reports of Dermatitis contact with ALTHIAZIDE\SPIRONOLACTONE
2.5%
of all ALTHIAZIDE\SPIRONOLACTONE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Dermatitis contact From ALTHIAZIDE\SPIRONOLACTONE?
Of the 8 reports.
Is Dermatitis contact Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALTHIAZIDE\SPIRONOLACTONE. However, 8 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 Dermatitis contact?
TREPROSTINIL (1,834)
DUPILUMAB (358)
HUMAN IMMUNOGLOBULIN G (345)
ADALIMUMAB (321)
EPOPROSTENOL (190)
ETANERCEPT (170)
NICOTINE (163)
CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (160)
AMBRISENTAN (147)
CHLORHEXIDINE\ISOPROPYL ALCOHOL (146)
Which ALTHIAZIDE\SPIRONOLACTONE Alternatives Have Lower Dermatitis contact 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