Does TACROLIMUS Cause Strongyloidiasis? 323 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 323 reports of Strongyloidiasis have been filed in association with TACROLIMUS (Tacrolimus). This represents 0.4% of all adverse event reports for TACROLIMUS.
323
Reports of Strongyloidiasis with TACROLIMUS
0.4%
of all TACROLIMUS reports
86
Deaths
250
Hospitalizations
How Dangerous Is Strongyloidiasis From TACROLIMUS?
Of the 323 reports, 86 (26.6%) resulted in death, 250 (77.4%) required hospitalization, and 105 (32.5%) were considered life-threatening.
Is Strongyloidiasis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TACROLIMUS. However, 323 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 Strongyloidiasis?
PREDNISONE (439)
PREDNISOLONE (335)
METHYLPREDNISOLONE (274)
MYCOPHENOLATE MOFETIL (259)
DEXAMETHASONE (252)
CYCLOPHOSPHAMIDE (136)
METHOTREXATE (126)
RITUXIMAB (126)
VINCRISTINE (87)
DOXORUBICIN (81)
Which TACROLIMUS Alternatives Have Lower Strongyloidiasis Risk?
TACROLIMUS vs TACROLIMUS\TACROLIMUS ANHYDROUS
TACROLIMUS vs TADALAFIL
TACROLIMUS vs TAFAMIDIS
TACROLIMUS vs TAFAMIDIS MEGLUMINE
TACROLIMUS vs TAFASITAMAB