Does SUMATRIPTAN Cause Application site haemorrhage? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Application site haemorrhage have been filed in association with SUMATRIPTAN (sumatriptan succinate). This represents 0.1% of all adverse event reports for SUMATRIPTAN.
14
Reports of Application site haemorrhage with SUMATRIPTAN
0.1%
of all SUMATRIPTAN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Application site haemorrhage From SUMATRIPTAN?
Of the 14 reports.
Is Application site haemorrhage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SUMATRIPTAN. However, 14 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 haemorrhage?
PEGFILGRASTIM (1,394)
MINOXIDIL (78)
BUPRENORPHINE (68)
ESTRADIOL (64)
DOCOSANOL (62)
BECAPLERMIN (60)
INGENOL MEBUTATE (50)
FENTANYL (47)
EVOLOCUMAB (45)
NICOTINE (37)
Which SUMATRIPTAN Alternatives Have Lower Application site haemorrhage Risk?
SUMATRIPTAN vs SUMATRIPTAN\SUMATRIPTAN
SUMATRIPTAN vs SUMAVEL DOSEPRO
SUMATRIPTAN vs SUNITINIB
SUMATRIPTAN vs SUNITINIB MALATE
SUMATRIPTAN vs SUTENT