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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does SUMATRIPTAN Cause Complication associated with device? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Complication associated with device have been filed in association with SUMATRIPTAN (sumatriptan succinate). This represents 0.1% of all adverse event reports for SUMATRIPTAN.

8
Reports of Complication associated with device with SUMATRIPTAN
0.1%
of all SUMATRIPTAN reports
0
Deaths
0
Hospitalizations

How Dangerous Is Complication associated with device From SUMATRIPTAN?

Of the 8 reports.

Is Complication associated with device Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SUMATRIPTAN. However, 8 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 Complication associated with device?

ETONOGESTREL (6,047) COPPER (1,083) BACLOFEN (525) TREPROSTINIL (422) EPOPROSTENOL (399) LEVONORGESTREL (344) ADALIMUMAB (269) CARBIDOPA\LEVODOPA (169) MACITENTAN (169) TEDUGLUTIDE (133)

Which SUMATRIPTAN Alternatives Have Lower Complication associated with device Risk?

SUMATRIPTAN vs SUMATRIPTAN\SUMATRIPTAN SUMATRIPTAN vs SUMAVEL DOSEPRO SUMATRIPTAN vs SUNITINIB SUMATRIPTAN vs SUNITINIB MALATE SUMATRIPTAN vs SUTENT

Related Pages

SUMATRIPTAN Full Profile All Complication associated with device Reports All Drugs Causing Complication associated with device SUMATRIPTAN Demographics