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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 leakage? 275 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 275 reports of Product leakage have been filed in association with SUMATRIPTAN (sumatriptan succinate). This represents 1.6% of all adverse event reports for SUMATRIPTAN.

275
Reports of Product leakage with SUMATRIPTAN
1.6%
of all SUMATRIPTAN reports
0
Deaths
1
Hospitalizations

How Dangerous Is Product leakage From SUMATRIPTAN?

Of the 275 reports, 1 (0.4%) required hospitalization.

Is Product leakage Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SUMATRIPTAN. However, 275 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 leakage?

GUSELKUMAB (661) INSULIN ASPART (361) USTEKINUMAB (344) LEUPROLIDE (331) TREPROSTINIL (213) ABATACEPT (124) SECUKINUMAB (116) PALIPERIDONE (92) ICOSAPENT ETHYL (80) GOLIMUMAB (79)

Which SUMATRIPTAN Alternatives Have Lower Product leakage 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 leakage Reports All Drugs Causing Product leakage SUMATRIPTAN Demographics