Does OXITRIPTAN Cause Product use in unapproved indication? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product use in unapproved indication have been filed in association with OXITRIPTAN (5-HTP Phenolic). This represents 7.0% of all adverse event reports for OXITRIPTAN.
7
Reports of Product use in unapproved indication with OXITRIPTAN
7.0%
of all OXITRIPTAN reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product use in unapproved indication From OXITRIPTAN?
Of the 7 reports, 3 (42.9%) 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 OXITRIPTAN. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does OXITRIPTAN Cause?
Serotonin syndrome (22)
Anxiety (21)
Insomnia (19)
Atrial fibrillation (18)
Bradycardia (18)
Gastric ph increased (18)
Somnolence (18)
Drug interaction (10)
Myoclonus (10)
Off label use (8)
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 OXITRIPTAN Alternatives Have Lower Product use in unapproved indication Risk?
OXITRIPTAN vs OXOMEMAZINE
OXITRIPTAN vs OXY TAB
OXITRIPTAN vs OXYBATE
OXITRIPTAN vs OXYBUTYNIN
OXITRIPTAN vs OXYBUTYNIN\OXYBUTYNIN