Does TORSEMIDE Cause Product administration error? 79 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 79 reports of Product administration error have been filed in association with TORSEMIDE (Torsemide). This represents 1.0% of all adverse event reports for TORSEMIDE.
79
Reports of Product administration error with TORSEMIDE
1.0%
of all TORSEMIDE reports
3
Deaths
79
Hospitalizations
How Dangerous Is Product administration error From TORSEMIDE?
Of the 79 reports, 3 (3.8%) resulted in death, 79 (100.0%) required hospitalization, and 14 (17.7%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TORSEMIDE. However, 79 reports have been filed with the FAERS database.
What Other Side Effects Does TORSEMIDE Cause?
General physical health deterioration (1,233)
Dyspnoea (1,176)
Acute kidney injury (975)
Dizziness (870)
Oedema peripheral (823)
Fall (707)
Dehydration (705)
Cardiac failure (698)
Hypotension (689)
Fatigue (635)
What Other Drugs Cause Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which TORSEMIDE Alternatives Have Lower Product administration error Risk?
TORSEMIDE vs TOVIAZ
TORSEMIDE vs TOVORAFENIB
TORSEMIDE vs TOZINAMERAN
TORSEMIDE vs TRABECTEDIN
TORSEMIDE vs TRACLEER