Does ELETRIPTAN HYDROBROMIDE Cause Recalled product administered? 115 Reports in FDA Database
Grow Your Own Natural Pharmacy at Home
Medicinal Garden Kit — 10 healing herbs, 4,818 seeds + step-by-step guide.
According to the FDA Adverse Event Reporting System (FAERS), 115 reports of Recalled product administered have been filed in association with ELETRIPTAN HYDROBROMIDE (Eletriptan hydrobromide). This represents 5.3% of all adverse event reports for ELETRIPTAN HYDROBROMIDE.
115
Reports of Recalled product administered with ELETRIPTAN HYDROBROMIDE
5.3%
of all ELETRIPTAN HYDROBROMIDE reports
0
Deaths
17
Hospitalizations
How Dangerous Is Recalled product administered From ELETRIPTAN HYDROBROMIDE?
Of the 115 reports, 17 (14.8%) required hospitalization, and 1 (0.9%) were considered life-threatening.
Is Recalled product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ELETRIPTAN HYDROBROMIDE. However, 115 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)
Vomiting (110)
Off label use (106)
Condition aggravated (91)
Drug hypersensitivity (84)
What Other Drugs Cause Recalled product administered?
RAMIPRIL (1,028)
LISINOPRIL (744)
PENICILLIN G BENZATHINE (500)
LEVOTHYROXINE (406)
HUMAN IMMUNOGLOBULIN G (382)
VARENICLINE (381)
VALSARTAN (267)
QUINAPRIL (243)
TRIAMCINOLONE ACETONIDE (222)
RANITIDINE (204)
Which ELETRIPTAN HYDROBROMIDE Alternatives Have Lower Recalled product administered Risk?
ELETRIPTAN HYDROBROMIDE vs ELEXACAFTOR\IVACAFTOR\TEZACAFTOR
ELETRIPTAN HYDROBROMIDE vs ELIGLUSTAT
ELETRIPTAN HYDROBROMIDE vs ELIQUIS
ELETRIPTAN HYDROBROMIDE vs ELOSULFASE ALFA
ELETRIPTAN HYDROBROMIDE vs ELOTUZUMAB