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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 Product use issue? 106 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 106 reports of Product use issue have been filed in association with SUMATRIPTAN (sumatriptan succinate). This represents 0.6% of all adverse event reports for SUMATRIPTAN.

106
Reports of Product use issue with SUMATRIPTAN
0.6%
of all SUMATRIPTAN reports
3
Deaths
14
Hospitalizations

How Dangerous Is Product use issue From SUMATRIPTAN?

Of the 106 reports, 3 (2.8%) resulted in death, 14 (13.2%) required hospitalization.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SUMATRIPTAN. However, 106 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 Product use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Which SUMATRIPTAN Alternatives Have Lower Product use issue 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 Product use issue Reports All Drugs Causing Product use issue SUMATRIPTAN Demographics