179 reports of this reaction
1.4% of all ELETRIPTAN HYDROBROMIDE reports
#16 most reported adverse reaction
PARAESTHESIA is the #16 most commonly reported adverse reaction for ELETRIPTAN HYDROBROMIDE, manufactured by ROERIG. There are 179 FDA adverse event reports linking ELETRIPTAN HYDROBROMIDE to PARAESTHESIA. This represents approximately 1.4% of all 13,057 adverse event reports for this drug.
Patients taking ELETRIPTAN HYDROBROMIDE who experience paraesthesia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
PARAESTHESIA is a less commonly reported adverse event for ELETRIPTAN HYDROBROMIDE, but still significant enough to appear in the safety profile.
In addition to paraesthesia, the following adverse reactions have been reported for ELETRIPTAN HYDROBROMIDE:
The following drugs have also been linked to paraesthesia in FDA adverse event reports:
PARAESTHESIA has been reported as an adverse event in 179 FDA reports for ELETRIPTAN HYDROBROMIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
PARAESTHESIA accounts for approximately 1.4% of all adverse event reports for ELETRIPTAN HYDROBROMIDE, making it a notable side effect.
If you experience paraesthesia while taking ELETRIPTAN HYDROBROMIDE, contact your healthcare provider. They can evaluate whether the symptom is related to your medication and discuss potential adjustments to your treatment plan. Do not stop taking prescribed medication without consulting your doctor.