Does PREDNICARBATE Cause Product use in unapproved indication? 43 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 43 reports of Product use in unapproved indication have been filed in association with PREDNICARBATE. This represents 38.7% of all adverse event reports for PREDNICARBATE.
43
Reports of Product use in unapproved indication with PREDNICARBATE
38.7%
of all PREDNICARBATE reports
19
Deaths
19
Hospitalizations
How Dangerous Is Product use in unapproved indication From PREDNICARBATE?
Of the 43 reports, 19 (44.2%) resulted in death, 19 (44.2%) required hospitalization, and 19 (44.2%) 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 PREDNICARBATE. However, 43 reports have been filed with the FAERS database.
What Other Side Effects Does PREDNICARBATE Cause?
Drug ineffective (55)
Paraesthesia (50)
Vomiting (50)
Blepharospasm (49)
Epilepsy (49)
Gastrooesophageal reflux disease (49)
Hypoaesthesia (49)
Memory impairment (49)
Abdominal pain upper (48)
Drug intolerance (48)
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 PREDNICARBATE Alternatives Have Lower Product use in unapproved indication Risk?
PREDNICARBATE vs PREDNISOLONE
PREDNICARBATE vs PREDNISOLONE METAZOATE
PREDNICARBATE vs PREDNISOLONE\PREDNISOLONE\PREDNISOLONE
PREDNICARBATE vs PREDNISONE
PREDNICARBATE vs PREGABALIN