Does SUMATRIPTAN Cause Device leakage? 300 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 300 reports of Device leakage have been filed in association with SUMATRIPTAN (sumatriptan succinate). This represents 1.7% of all adverse event reports for SUMATRIPTAN.
300
Reports of Device leakage with SUMATRIPTAN
1.7%
of all SUMATRIPTAN reports
0
Deaths
2
Hospitalizations
How Dangerous Is Device leakage From SUMATRIPTAN?
Of the 300 reports, 2 (0.7%) required hospitalization.
Is Device leakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SUMATRIPTAN. However, 300 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 leakage?
SOMATROPIN (9,113)
LEUPROLIDE (5,861)
EXENATIDE (5,115)
PEGFILGRASTIM (1,380)
ALBIGLUTIDE (1,195)
SECUKINUMAB (910)
RISPERIDONE (878)
TREPROSTINIL (874)
DEVICE (795)
GUSELKUMAB (712)
Which SUMATRIPTAN Alternatives Have Lower Device leakage Risk?
SUMATRIPTAN vs SUMATRIPTAN\SUMATRIPTAN
SUMATRIPTAN vs SUMAVEL DOSEPRO
SUMATRIPTAN vs SUNITINIB
SUMATRIPTAN vs SUNITINIB MALATE
SUMATRIPTAN vs SUTENT