Does SUMATRIPTAN Cause Wrong technique in device usage process? 197 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 197 reports of Wrong technique in device usage process have been filed in association with SUMATRIPTAN (sumatriptan succinate). This represents 1.1% of all adverse event reports for SUMATRIPTAN.
197
Reports of Wrong technique in device usage process with SUMATRIPTAN
1.1%
of all SUMATRIPTAN reports
0
Deaths
3
Hospitalizations
How Dangerous Is Wrong technique in device usage process From SUMATRIPTAN?
Of the 197 reports, 3 (1.5%) required hospitalization.
Is Wrong technique in device usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SUMATRIPTAN. However, 197 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 Wrong technique in device usage process?
ALBUTEROL (5,380)
SOMATROPIN (4,746)
EXENATIDE (3,255)
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (2,673)
FLUTICASONE\SALMETEROL (2,259)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (2,197)
INSULIN GLARGINE (1,749)
UMECLIDINIUM\VILANTEROL TRIFENATATE (1,531)
BUDESONIDE\FORMOTEROL (1,481)
BELIMUMAB (1,347)
Which SUMATRIPTAN Alternatives Have Lower Wrong technique in device usage process Risk?
SUMATRIPTAN vs SUMATRIPTAN\SUMATRIPTAN
SUMATRIPTAN vs SUMAVEL DOSEPRO
SUMATRIPTAN vs SUNITINIB
SUMATRIPTAN vs SUNITINIB MALATE
SUMATRIPTAN vs SUTENT