Does SUMATRIPTAN Cause Application site erythema? 1,875 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,875 reports of Application site erythema have been filed in association with SUMATRIPTAN (sumatriptan succinate). This represents 10.8% of all adverse event reports for SUMATRIPTAN.
1,875
Reports of Application site erythema with SUMATRIPTAN
10.8%
of all SUMATRIPTAN reports
0
Deaths
5
Hospitalizations
How Dangerous Is Application site erythema From SUMATRIPTAN?
Of the 1,875 reports, 5 (0.3%) required hospitalization.
Is Application site erythema Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SUMATRIPTAN. However, 1,875 reports have been filed with the FAERS database.
What Other Side Effects Does SUMATRIPTAN Cause?
Drug ineffective (2,941)
Product physical issue (2,349)
Drug dose omission (1,711)
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 Application site erythema?
NICOTINE (2,004)
INGENOL MEBUTATE (1,373)
BUPRENORPHINE (1,273)
ESTRADIOL (1,117)
MINOXIDIL (1,061)
METHYLPHENIDATE (543)
ESTRADIOL\NORETHINDRONE (533)
FENTANYL (501)
OXYTROL FOR WOMEN (422)
OXYBUTYNIN (395)
Which SUMATRIPTAN Alternatives Have Lower Application site erythema Risk?
SUMATRIPTAN vs SUMATRIPTAN\SUMATRIPTAN
SUMATRIPTAN vs SUMAVEL DOSEPRO
SUMATRIPTAN vs SUNITINIB
SUMATRIPTAN vs SUNITINIB MALATE
SUMATRIPTAN vs SUTENT