Does SUMATRIPTAN Cause Injury associated with device? 74 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 74 reports of Injury associated with device have been filed in association with SUMATRIPTAN (sumatriptan succinate). This represents 0.4% of all adverse event reports for SUMATRIPTAN.
74
Reports of Injury associated with device with SUMATRIPTAN
0.4%
of all SUMATRIPTAN reports
0
Deaths
5
Hospitalizations
How Dangerous Is Injury associated with device From SUMATRIPTAN?
Of the 74 reports, 5 (6.8%) required hospitalization, and 2 (2.7%) were considered life-threatening.
Is Injury associated with device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SUMATRIPTAN. However, 74 reports have been filed with the FAERS database.
What Other Side Effects Does SUMATRIPTAN Cause?
Drug ineffective (2,941)
Product physical issue (2,349)
Application site erythema (1,875)
Drug dose omission (1,711)
Product quality issue (1,269)
Application site pain (1,217)
Migraine (978)
Headache (914)
Product complaint (718)
Nausea (702)
What Other Drugs Cause Injury associated with device?
COPPER (2,895)
ADALIMUMAB (2,003)
EVOLOCUMAB (1,326)
INSULIN GLARGINE (849)
INSULIN LISPRO (840)
TIRZEPATIDE (836)
ETANERCEPT (743)
ERENUMAB-AOOE (528)
DULAGLUTIDE (482)
ENOXAPARIN (458)
Which SUMATRIPTAN Alternatives Have Lower Injury associated with device Risk?
SUMATRIPTAN vs SUMATRIPTAN\SUMATRIPTAN
SUMATRIPTAN vs SUMAVEL DOSEPRO
SUMATRIPTAN vs SUNITINIB
SUMATRIPTAN vs SUNITINIB MALATE
SUMATRIPTAN vs SUTENT