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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 Application site paraesthesia? 497 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 497 reports of Application site paraesthesia have been filed in association with SUMATRIPTAN (sumatriptan succinate). This represents 2.9% of all adverse event reports for SUMATRIPTAN.

497
Reports of Application site paraesthesia with SUMATRIPTAN
2.9%
of all SUMATRIPTAN reports
0
Deaths
1
Hospitalizations

How Dangerous Is Application site paraesthesia From SUMATRIPTAN?

Of the 497 reports, 1 (0.2%) required hospitalization.

Is Application site paraesthesia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SUMATRIPTAN. However, 497 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 Application site paraesthesia?

MINOXIDIL (119) INGENOL MEBUTATE (59) NICOTINE (59) DOCOSANOL (42) CRISABOROLE (23) DICLOFENAC (19) BUPRENORPHINE (16) OXYMETAZOLINE (11) BECAPLERMIN (10) CAPSAICIN (10)

Which SUMATRIPTAN Alternatives Have Lower Application site paraesthesia 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 Application site paraesthesia Reports All Drugs Causing Application site paraesthesia SUMATRIPTAN Demographics