Does HYDROCHLOROTHIAZIDE Cause Recalled product? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Recalled product have been filed in association with HYDROCHLOROTHIAZIDE (Irbesartan and Hydrochlorothiazide). This represents 0.0% of all adverse event reports for HYDROCHLOROTHIAZIDE.
7
Reports of Recalled product with HYDROCHLOROTHIAZIDE
0.0%
of all HYDROCHLOROTHIAZIDE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Recalled product From HYDROCHLOROTHIAZIDE?
Of the 7 reports, 2 (28.6%) required hospitalization.
Is Recalled product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for HYDROCHLOROTHIAZIDE. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does HYDROCHLOROTHIAZIDE Cause?
Hyponatraemia (2,138)
Drug ineffective (1,889)
Acute kidney injury (1,838)
Nausea (1,536)
Dyspnoea (1,521)
Dizziness (1,469)
Headache (1,419)
Hypotension (1,347)
Fall (1,323)
Malaise (1,312)
What Other Drugs Cause Recalled product?
PARATHYROID HORMONE (900)
ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT (80)
CALCITRIOL (68)
CALCIUM (66)
REMDESIVIR (36)
LEVOTHYROXINE\LIOTHYRONINE (34)
TESTOSTERONE (32)
VALSARTAN (32)
CHLORHEXIDINE (28)
ALCOHOL (26)
Which HYDROCHLOROTHIAZIDE Alternatives Have Lower Recalled product Risk?
HYDROCHLOROTHIAZIDE vs HYDROCHLOROTHIAZIDE\IRBESARTAN
HYDROCHLOROTHIAZIDE vs HYDROCHLOROTHIAZIDE\LISINOPRIL
HYDROCHLOROTHIAZIDE vs HYDROCHLOROTHIAZIDE\LOSARTAN
HYDROCHLOROTHIAZIDE vs HYDROCHLOROTHIAZIDE\METOPROLOL
HYDROCHLOROTHIAZIDE vs HYDROCHLOROTHIAZIDE\NEBIVOLOL