Does TACROLIMUS Cause Subdural haematoma? 49 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 49 reports of Subdural haematoma have been filed in association with TACROLIMUS (Tacrolimus). This represents 0.1% of all adverse event reports for TACROLIMUS.
49
Reports of Subdural haematoma with TACROLIMUS
0.1%
of all TACROLIMUS reports
18
Deaths
36
Hospitalizations
How Dangerous Is Subdural haematoma From TACROLIMUS?
Of the 49 reports, 18 (36.7%) resulted in death, 36 (73.5%) required hospitalization, and 14 (28.6%) were considered life-threatening.
Is Subdural haematoma Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TACROLIMUS. However, 49 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 Subdural haematoma?
RIVAROXABAN (1,423)
ASPIRIN (1,181)
APIXABAN (1,025)
WARFARIN (1,012)
CLOPIDOGREL BISULFATE (809)
DABIGATRAN ETEXILATE (648)
IBRUTINIB (342)
HEPARIN (201)
ENOXAPARIN (156)
CYCLOPHOSPHAMIDE (146)
Which TACROLIMUS Alternatives Have Lower Subdural haematoma Risk?
TACROLIMUS vs TACROLIMUS\TACROLIMUS ANHYDROUS
TACROLIMUS vs TADALAFIL
TACROLIMUS vs TAFAMIDIS
TACROLIMUS vs TAFAMIDIS MEGLUMINE
TACROLIMUS vs TAFASITAMAB