Does FLURBIPROFEN Cause Product use in unapproved indication? 23 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Product use in unapproved indication have been filed in association with FLURBIPROFEN (LURBIRO). This represents 3.6% of all adverse event reports for FLURBIPROFEN.
23
Reports of Product use in unapproved indication with FLURBIPROFEN
3.6%
of all FLURBIPROFEN reports
1
Deaths
13
Hospitalizations
How Dangerous Is Product use in unapproved indication From FLURBIPROFEN?
Of the 23 reports, 1 (4.3%) resulted in death, 13 (56.5%) required hospitalization, and 17 (73.9%) 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 FLURBIPROFEN. However, 23 reports have been filed with the FAERS database.
What Other Side Effects Does FLURBIPROFEN Cause?
Angioedema (93)
Urticaria (68)
Acute kidney injury (62)
Drug ineffective (57)
Drug hypersensitivity (48)
Drug reaction with eosinophilia and systemic symptoms (33)
Somnolence (32)
Toxicity to various agents (29)
Hypersensitivity (28)
Abdominal pain upper (27)
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 FLURBIPROFEN Alternatives Have Lower Product use in unapproved indication Risk?
FLURBIPROFEN vs FLUTAMIDE
FLURBIPROFEN vs FLUTEMETAMOL F-18
FLURBIPROFEN vs FLUTICASONE
FLURBIPROFEN vs FLUTICASONE FUROATE
FLURBIPROFEN vs FLUTICASONE FUROATE\SALMETEROL