Does SUMATRIPTAN Cause Intentional product misuse? 63 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 63 reports of Intentional product misuse have been filed in association with SUMATRIPTAN (sumatriptan succinate). This represents 0.4% of all adverse event reports for SUMATRIPTAN.
63
Reports of Intentional product misuse with SUMATRIPTAN
0.4%
of all SUMATRIPTAN reports
0
Deaths
23
Hospitalizations
How Dangerous Is Intentional product misuse From SUMATRIPTAN?
Of the 63 reports, 23 (36.5%) required hospitalization, and 1 (1.6%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SUMATRIPTAN. However, 63 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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which SUMATRIPTAN Alternatives Have Lower Intentional product misuse Risk?
SUMATRIPTAN vs SUMATRIPTAN\SUMATRIPTAN
SUMATRIPTAN vs SUMAVEL DOSEPRO
SUMATRIPTAN vs SUNITINIB
SUMATRIPTAN vs SUNITINIB MALATE
SUMATRIPTAN vs SUTENT