Does SUMATRIPTAN Cause Application site exfoliation? 322 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 322 reports of Application site exfoliation have been filed in association with SUMATRIPTAN (sumatriptan succinate). This represents 1.9% of all adverse event reports for SUMATRIPTAN.
322
Reports of Application site exfoliation with SUMATRIPTAN
1.9%
of all SUMATRIPTAN reports
0
Deaths
1
Hospitalizations
How Dangerous Is Application site exfoliation From SUMATRIPTAN?
Of the 322 reports, 1 (0.3%) required hospitalization.
Is Application site exfoliation Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SUMATRIPTAN. However, 322 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 exfoliation?
MINOXIDIL (792)
INGENOL MEBUTATE (586)
BUPRENORPHINE (143)
DICLOFENAC (109)
PICATO (89)
TRETINOIN (75)
NICOTINE (69)
ESTRADIOL (62)
FENTANYL (59)
TAVABOROLE (56)
Which SUMATRIPTAN Alternatives Have Lower Application site exfoliation Risk?
SUMATRIPTAN vs SUMATRIPTAN\SUMATRIPTAN
SUMATRIPTAN vs SUMAVEL DOSEPRO
SUMATRIPTAN vs SUNITINIB
SUMATRIPTAN vs SUNITINIB MALATE
SUMATRIPTAN vs SUTENT