Does ELETRIPTAN HYDROBROMIDE Cause Condition aggravated? 91 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 91 reports of Condition aggravated have been filed in association with ELETRIPTAN HYDROBROMIDE (Eletriptan hydrobromide). This represents 4.2% of all adverse event reports for ELETRIPTAN HYDROBROMIDE.
91
Reports of Condition aggravated with ELETRIPTAN HYDROBROMIDE
4.2%
of all ELETRIPTAN HYDROBROMIDE reports
1
Deaths
18
Hospitalizations
How Dangerous Is Condition aggravated From ELETRIPTAN HYDROBROMIDE?
Of the 91 reports, 1 (1.1%) resulted in death, 18 (19.8%) required hospitalization.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ELETRIPTAN HYDROBROMIDE. However, 91 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)
Drug hypersensitivity (84)
What Other Drugs Cause Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which ELETRIPTAN HYDROBROMIDE Alternatives Have Lower Condition aggravated Risk?
ELETRIPTAN HYDROBROMIDE vs ELEXACAFTOR\IVACAFTOR\TEZACAFTOR
ELETRIPTAN HYDROBROMIDE vs ELIGLUSTAT
ELETRIPTAN HYDROBROMIDE vs ELIQUIS
ELETRIPTAN HYDROBROMIDE vs ELOSULFASE ALFA
ELETRIPTAN HYDROBROMIDE vs ELOTUZUMAB