Does ELETRIPTAN HYDROBROMIDE Cause Product use issue? 25 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 25 reports of Product use issue have been filed in association with ELETRIPTAN HYDROBROMIDE (Eletriptan hydrobromide). This represents 1.2% of all adverse event reports for ELETRIPTAN HYDROBROMIDE.
25
Reports of Product use issue with ELETRIPTAN HYDROBROMIDE
1.2%
of all ELETRIPTAN HYDROBROMIDE reports
0
Deaths
5
Hospitalizations
How Dangerous Is Product use issue From ELETRIPTAN HYDROBROMIDE?
Of the 25 reports, 5 (20.0%) required hospitalization.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ELETRIPTAN HYDROBROMIDE. However, 25 reports have been filed with the FAERS database.
What Other Side Effects Does ELETRIPTAN HYDROBROMIDE Cause?
Drug ineffective (502)
Migraine (310)
Headache (246)
Malaise (143)
Nausea (127)
Pain (116)
Recalled product administered (115)
Vomiting (110)
Off label use (106)
Condition aggravated (91)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which ELETRIPTAN HYDROBROMIDE Alternatives Have Lower Product use issue Risk?
ELETRIPTAN HYDROBROMIDE vs ELEXACAFTOR\IVACAFTOR\TEZACAFTOR
ELETRIPTAN HYDROBROMIDE vs ELIGLUSTAT
ELETRIPTAN HYDROBROMIDE vs ELIQUIS
ELETRIPTAN HYDROBROMIDE vs ELOSULFASE ALFA
ELETRIPTAN HYDROBROMIDE vs ELOTUZUMAB