Does TACROLIMUS Cause Device related sepsis? 27 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 27 reports of Device related sepsis have been filed in association with TACROLIMUS (Tacrolimus). This represents 0.0% of all adverse event reports for TACROLIMUS.
27
Reports of Device related sepsis with TACROLIMUS
0.0%
of all TACROLIMUS reports
12
Deaths
17
Hospitalizations
How Dangerous Is Device related sepsis From TACROLIMUS?
Of the 27 reports, 12 (44.4%) resulted in death, 17 (63.0%) required hospitalization, and 3 (11.1%) were considered life-threatening.
Is Device related sepsis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TACROLIMUS. However, 27 reports have been filed with the FAERS database.
What Other Side Effects Does TACROLIMUS Cause?
Off label use (8,718)
Drug ineffective (6,214)
Product use in unapproved indication (5,057)
Acute kidney injury (4,005)
Transplant rejection (3,526)
Cytomegalovirus infection (3,320)
Covid-19 (3,201)
Drug interaction (2,896)
Diarrhoea (2,854)
Toxicity to various agents (2,845)
What Other Drugs Cause Device related sepsis?
TEDUGLUTIDE (226)
TREPROSTINIL (225)
CYCLOPHOSPHAMIDE (130)
RITUXIMAB (113)
EPOPROSTENOL (89)
CYCLOSPORINE (82)
METHYLPREDNISOLONE (82)
BORTEZOMIB (79)
MACITENTAN (55)
DEXAMETHASONE (53)
Which TACROLIMUS Alternatives Have Lower Device related sepsis Risk?
TACROLIMUS vs TACROLIMUS\TACROLIMUS ANHYDROUS
TACROLIMUS vs TADALAFIL
TACROLIMUS vs TAFAMIDIS
TACROLIMUS vs TAFAMIDIS MEGLUMINE
TACROLIMUS vs TAFASITAMAB