Does PREDNISOLONE Cause Product use in unapproved indication? 3,414 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 3,414 reports of Product use in unapproved indication have been filed in association with PREDNISOLONE (Prednisolone Sodium Phosphate). This represents 4.2% of all adverse event reports for PREDNISOLONE.
3,414
Reports of Product use in unapproved indication with PREDNISOLONE
4.2%
of all PREDNISOLONE reports
662
Deaths
1,060
Hospitalizations
How Dangerous Is Product use in unapproved indication From PREDNISOLONE?
Of the 3,414 reports, 662 (19.4%) resulted in death, 1,060 (31.0%) required hospitalization, and 340 (10.0%) 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 PREDNISOLONE. However, 3,414 reports have been filed with the FAERS database.
What Other Side Effects Does PREDNISOLONE Cause?
Off label use (8,817)
Drug ineffective (8,459)
Pyrexia (3,159)
Condition aggravated (3,143)
Pneumonia (2,713)
Treatment failure (2,616)
Sepsis (2,281)
Dyspnoea (2,248)
Diarrhoea (2,192)
Neutropenia (1,939)
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 PREDNISOLONE Alternatives Have Lower Product use in unapproved indication Risk?
PREDNISOLONE vs PREDNISOLONE METAZOATE
PREDNISOLONE vs PREDNISOLONE\PREDNISOLONE\PREDNISOLONE
PREDNISOLONE vs PREDNISONE
PREDNISOLONE vs PREGABALIN
PREDNISOLONE vs PREMARIN