Does TACROLIMUS Cause Product prescribing error? 96 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 96 reports of Product prescribing error have been filed in association with TACROLIMUS (Tacrolimus). This represents 0.1% of all adverse event reports for TACROLIMUS.
96
Reports of Product prescribing error with TACROLIMUS
0.1%
of all TACROLIMUS reports
2
Deaths
49
Hospitalizations
How Dangerous Is Product prescribing error From TACROLIMUS?
Of the 96 reports, 2 (2.1%) resulted in death, 49 (51.0%) required hospitalization, and 11 (11.5%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TACROLIMUS. However, 96 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 Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which TACROLIMUS Alternatives Have Lower Product prescribing error Risk?
TACROLIMUS vs TACROLIMUS\TACROLIMUS ANHYDROUS
TACROLIMUS vs TADALAFIL
TACROLIMUS vs TAFAMIDIS
TACROLIMUS vs TAFAMIDIS MEGLUMINE
TACROLIMUS vs TAFASITAMAB