Does SUMATRIPTAN Cause Device issue? 438 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 438 reports of Device issue have been filed in association with SUMATRIPTAN (sumatriptan succinate). This represents 2.5% of all adverse event reports for SUMATRIPTAN.
438
Reports of Device issue with SUMATRIPTAN
2.5%
of all SUMATRIPTAN reports
1
Deaths
0
Hospitalizations
How Dangerous Is Device issue From SUMATRIPTAN?
Of the 438 reports, 1 (0.2%) resulted in death.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SUMATRIPTAN. However, 438 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 issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which SUMATRIPTAN Alternatives Have Lower Device issue Risk?
SUMATRIPTAN vs SUMATRIPTAN\SUMATRIPTAN
SUMATRIPTAN vs SUMAVEL DOSEPRO
SUMATRIPTAN vs SUNITINIB
SUMATRIPTAN vs SUNITINIB MALATE
SUMATRIPTAN vs SUTENT