Does SUMATRIPTAN Cause Device deployment issue? 292 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 292 reports of Device deployment issue have been filed in association with SUMATRIPTAN (sumatriptan succinate). This represents 1.7% of all adverse event reports for SUMATRIPTAN.
292
Reports of Device deployment issue with SUMATRIPTAN
1.7%
of all SUMATRIPTAN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device deployment issue From SUMATRIPTAN?
Of the 292 reports.
Is Device deployment issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SUMATRIPTAN. However, 292 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 Device deployment issue?
ETONOGESTREL (3,621)
GOLIMUMAB (1,265)
GUSELKUMAB (778)
COPPER (768)
LEVONORGESTREL (718)
USTEKINUMAB (639)
PEGFILGRASTIM (163)
ABATACEPT (131)
SOMATROPIN (130)
CARBIDOPA\LEVODOPA (88)
Which SUMATRIPTAN Alternatives Have Lower Device deployment issue Risk?
SUMATRIPTAN vs SUMATRIPTAN\SUMATRIPTAN
SUMATRIPTAN vs SUMAVEL DOSEPRO
SUMATRIPTAN vs SUNITINIB
SUMATRIPTAN vs SUNITINIB MALATE
SUMATRIPTAN vs SUTENT