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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 Therapy non-responder? 49 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 49 reports of Therapy non-responder have been filed in association with SUMATRIPTAN (sumatriptan succinate). This represents 0.3% of all adverse event reports for SUMATRIPTAN.

49
Reports of Therapy non-responder with SUMATRIPTAN
0.3%
of all SUMATRIPTAN reports
0
Deaths
13
Hospitalizations

How Dangerous Is Therapy non-responder From SUMATRIPTAN?

Of the 49 reports, 13 (26.5%) required hospitalization, and 8 (16.3%) were considered life-threatening.

Is Therapy non-responder Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SUMATRIPTAN. However, 49 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 Therapy non-responder?

ETANERCEPT (3,472) APREMILAST (3,360) METHOTREXATE (2,965) RITUXIMAB (2,731) ADALIMUMAB (2,595) PREDNISONE (2,563) TREPROSTINIL (2,289) INFLIXIMAB (2,122) TOCILIZUMAB (1,775) HYDROXYCHLOROQUINE (1,699)

Which SUMATRIPTAN Alternatives Have Lower Therapy non-responder 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 Therapy non-responder Reports All Drugs Causing Therapy non-responder SUMATRIPTAN Demographics