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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 Drug dose omission? 1,711 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 1,711 reports of Drug dose omission have been filed in association with SUMATRIPTAN (sumatriptan succinate). This represents 9.8% of all adverse event reports for SUMATRIPTAN.

1,711
Reports of Drug dose omission with SUMATRIPTAN
9.8%
of all SUMATRIPTAN reports
0
Deaths
12
Hospitalizations

How Dangerous Is Drug dose omission From SUMATRIPTAN?

Of the 1,711 reports, 12 (0.7%) required hospitalization.

Is Drug dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SUMATRIPTAN. However, 1,711 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) Product quality issue (1,269) Application site pain (1,217) Migraine (978) Headache (914) Product complaint (718) Nausea (702) Product dose omission issue (698)

What Other Drugs Cause Drug dose omission?

ETANERCEPT (10,871) CINACALCET (8,683) EVOLOCUMAB (4,914) ADALIMUMAB (3,993) INSULIN LISPRO (3,063) GOLIMUMAB (2,652) TERIPARATIDE (2,616) APREMILAST (2,466) ALBUTEROL (2,309) FLUTICASONE\SALMETEROL (2,153)

Which SUMATRIPTAN Alternatives Have Lower Drug dose omission 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 Drug dose omission Reports All Drugs Causing Drug dose omission SUMATRIPTAN Demographics