Does MYCOPHENOLATE Cause Product use in unapproved indication? 272 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 272 reports of Product use in unapproved indication have been filed in association with MYCOPHENOLATE (mycophenolic acid). This represents 3.5% of all adverse event reports for MYCOPHENOLATE.
272
Reports of Product use in unapproved indication with MYCOPHENOLATE
3.5%
of all MYCOPHENOLATE reports
16
Deaths
75
Hospitalizations
How Dangerous Is Product use in unapproved indication From MYCOPHENOLATE?
Of the 272 reports, 16 (5.9%) resulted in death, 75 (27.6%) required hospitalization, and 14 (5.1%) were considered life-threatening.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MYCOPHENOLATE. However, 272 reports have been filed with the FAERS database.
What Other Side Effects Does MYCOPHENOLATE Cause?
Diarrhoea (622)
Death (615)
Off label use (572)
Drug ineffective (380)
Pyrexia (374)
Blood creatinine increased (305)
Malaise (288)
Hypertension (280)
Haemoglobin decreased (272)
Acute kidney injury (267)
What Other Drugs Cause Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)
Which MYCOPHENOLATE Alternatives Have Lower Product use in unapproved indication Risk?
MYCOPHENOLATE vs MYCOPHENOLATE MOFETIL
MYCOPHENOLATE vs MYCOPHENOLATE MOFETIL\MYCOPHENOLATE MOFETIL
MYCOPHENOLATE vs MYCOPHENOLIC ACID
MYCOPHENOLATE vs MYFORTIC
MYCOPHENOLATE vs MYRBETRIQ