Does TAMSULOSIN Cause Product administration error? 33 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 33 reports of Product administration error have been filed in association with TAMSULOSIN (Tamsulosin Hydrochloride). This represents 0.2% of all adverse event reports for TAMSULOSIN.
33
Reports of Product administration error with TAMSULOSIN
0.2%
of all TAMSULOSIN reports
4
Deaths
23
Hospitalizations
How Dangerous Is Product administration error From TAMSULOSIN?
Of the 33 reports, 4 (12.1%) resulted in death, 23 (69.7%) required hospitalization, and 3 (9.1%) 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 TAMSULOSIN. However, 33 reports have been filed with the FAERS database.
What Other Side Effects Does TAMSULOSIN Cause?
Dizziness (1,736)
Dyspnoea (1,375)
Drug ineffective (1,005)
Fall (960)
Syncope (904)
Hypotension (896)
Fatigue (871)
Off label use (844)
Asthenia (701)
Headache (699)
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 TAMSULOSIN Alternatives Have Lower Product administration error Risk?
TAMSULOSIN vs TAPENTADOL
TAMSULOSIN vs TAPINAROF
TAMSULOSIN vs TARCEVA
TAMSULOSIN vs TARLATAMAB
TAMSULOSIN vs TARLATAMAB-DLLE