Does SUMATRIPTAN Cause Product complaint? 718 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 718 reports of Product complaint have been filed in association with SUMATRIPTAN (sumatriptan succinate). This represents 4.1% of all adverse event reports for SUMATRIPTAN.
718
Reports of Product complaint with SUMATRIPTAN
4.1%
of all SUMATRIPTAN reports
0
Deaths
6
Hospitalizations
How Dangerous Is Product complaint From SUMATRIPTAN?
Of the 718 reports, 6 (0.8%) required hospitalization, and 1 (0.1%) were considered life-threatening.
Is Product complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SUMATRIPTAN. However, 718 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)
Nausea (702)
Product dose omission issue (698)
What Other Drugs Cause Product complaint?
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (2,417)
ALBUTEROL (2,291)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (1,826)
FLUTICASONE\SALMETEROL (1,601)
MEPOLIZUMAB (1,296)
FLUTICASONE (1,112)
UMECLIDINIUM\VILANTEROL TRIFENATATE (1,108)
BELIMUMAB (1,079)
NICOTINE (700)
DICLOFENAC (511)
Which SUMATRIPTAN Alternatives Have Lower Product complaint Risk?
SUMATRIPTAN vs SUMATRIPTAN\SUMATRIPTAN
SUMATRIPTAN vs SUMAVEL DOSEPRO
SUMATRIPTAN vs SUNITINIB
SUMATRIPTAN vs SUNITINIB MALATE
SUMATRIPTAN vs SUTENT