Does SUMATRIPTAN Cause Product physical issue? 2,349 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,349 reports of Product physical issue have been filed in association with SUMATRIPTAN (sumatriptan succinate). This represents 13.5% of all adverse event reports for SUMATRIPTAN.
2,349
Reports of Product physical issue with SUMATRIPTAN
13.5%
of all SUMATRIPTAN reports
0
Deaths
10
Hospitalizations
How Dangerous Is Product physical issue From SUMATRIPTAN?
Of the 2,349 reports, 10 (0.4%) required hospitalization.
Is Product physical issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SUMATRIPTAN. However, 2,349 reports have been filed with the FAERS database.
What Other Side Effects Does SUMATRIPTAN Cause?
Drug ineffective (2,941)
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)
Product dose omission issue (698)
What Other Drugs Cause Product physical issue?
TIOTROPIUM (807)
ICOSAPENT ETHYL (666)
LISDEXAMFETAMINE DIMESYLATE (652)
AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE (387)
IBUPROFEN (337)
ESTRADIOL\LEVONORGESTREL (305)
ESTRADIOL (302)
RUXOLITINIB (302)
IXAZOMIB (298)
BUPRENORPHINE (260)
Which SUMATRIPTAN Alternatives Have Lower Product physical issue Risk?
SUMATRIPTAN vs SUMATRIPTAN\SUMATRIPTAN
SUMATRIPTAN vs SUMAVEL DOSEPRO
SUMATRIPTAN vs SUNITINIB
SUMATRIPTAN vs SUNITINIB MALATE
SUMATRIPTAN vs SUTENT