Does PRIMIDONE Cause Product use in unapproved indication? 49 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 49 reports of Product use in unapproved indication have been filed in association with PRIMIDONE (Primidone). This represents 3.2% of all adverse event reports for PRIMIDONE.
49
Reports of Product use in unapproved indication with PRIMIDONE
3.2%
of all PRIMIDONE reports
1
Deaths
5
Hospitalizations
How Dangerous Is Product use in unapproved indication From PRIMIDONE?
Of the 49 reports, 1 (2.0%) resulted in death, 5 (10.2%) required hospitalization.
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 PRIMIDONE. However, 49 reports have been filed with the FAERS database.
What Other Side Effects Does PRIMIDONE Cause?
Drug ineffective (236)
Completed suicide (133)
Off label use (129)
Somnolence (128)
Drug interaction (102)
Dizziness (101)
Tremor (97)
Seizure (95)
Fatigue (94)
Toxicity to various agents (84)
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 PRIMIDONE Alternatives Have Lower Product use in unapproved indication Risk?
PRIMIDONE vs PRISTINAMYCIN
PRIMIDONE vs PRISTIQ
PRIMIDONE vs PRIVIGEN
PRIMIDONE vs PROAIR HFA
PRIMIDONE vs PROBIOTICS NOS