Does TAMSULOSIN Cause Wrong patient received product? 44 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 44 reports of Wrong patient received product have been filed in association with TAMSULOSIN (Tamsulosin Hydrochloride). This represents 0.3% of all adverse event reports for TAMSULOSIN.
44
Reports of Wrong patient received product with TAMSULOSIN
0.3%
of all TAMSULOSIN reports
17
Deaths
21
Hospitalizations
How Dangerous Is Wrong patient received product From TAMSULOSIN?
Of the 44 reports, 17 (38.6%) resulted in death, 21 (47.7%) required hospitalization, and 9 (20.5%) were considered life-threatening.
Is Wrong patient received product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TAMSULOSIN. However, 44 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 Wrong patient received product?
INSULIN LISPRO (334)
CLOZAPINE (198)
RISPERIDONE (176)
OXAZEPAM (152)
BISOPROLOL (150)
LEVETIRACETAM (126)
ACETAMINOPHEN (123)
METFORMIN (116)
INSULIN GLARGINE (114)
CLONAZEPAM (112)
Which TAMSULOSIN Alternatives Have Lower Wrong patient received product Risk?
TAMSULOSIN vs TAPENTADOL
TAMSULOSIN vs TAPINAROF
TAMSULOSIN vs TARCEVA
TAMSULOSIN vs TARLATAMAB
TAMSULOSIN vs TARLATAMAB-DLLE