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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 packaging issue? 36 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 36 reports of Product packaging issue have been filed in association with SUMATRIPTAN (sumatriptan succinate). This represents 0.2% of all adverse event reports for SUMATRIPTAN.

36
Reports of Product packaging issue with SUMATRIPTAN
0.2%
of all SUMATRIPTAN reports
0
Deaths
1
Hospitalizations

How Dangerous Is Product packaging issue From SUMATRIPTAN?

Of the 36 reports, 1 (2.8%) required hospitalization.

Is Product packaging issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SUMATRIPTAN. However, 36 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 packaging issue?

ACETAMINOPHEN (448) LOPERAMIDE (351) DIMETHICONE\LOPERAMIDE (348) USTEKINUMAB (221) FENTANYL (200) MINOXIDIL (173) CETIRIZINE (166) ESTRADIOL (163) GOLIMUMAB (95) CYCLOSPORINE (93)

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