Does PREGABALIN Cause Product use in unapproved indication? 2,553 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,553 reports of Product use in unapproved indication have been filed in association with PREGABALIN (Pregabalin). This represents 2.5% of all adverse event reports for PREGABALIN.
2,553
Reports of Product use in unapproved indication with PREGABALIN
2.5%
of all PREGABALIN reports
435
Deaths
820
Hospitalizations
How Dangerous Is Product use in unapproved indication From PREGABALIN?
Of the 2,553 reports, 435 (17.0%) resulted in death, 820 (32.1%) required hospitalization, and 437 (17.1%) 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 PREGABALIN. However, 2,553 reports have been filed with the FAERS database.
What Other Side Effects Does PREGABALIN Cause?
Drug ineffective (13,664)
Pain (12,996)
Malaise (6,320)
Dizziness (5,878)
Off label use (5,713)
Somnolence (5,528)
Pain in extremity (5,023)
Fatigue (4,909)
Weight increased (4,903)
Condition aggravated (4,901)
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 PREGABALIN Alternatives Have Lower Product use in unapproved indication Risk?
PREGABALIN vs PREMARIN
PREGABALIN vs PREMPRO
PREGABALIN vs PRETOMANID
PREGABALIN vs PREVISCAN
PREGABALIN vs PREZISTA