Does SUMATRIPTAN Cause Wrong technique in product usage process? 347 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 347 reports of Wrong technique in product usage process have been filed in association with SUMATRIPTAN (sumatriptan succinate). This represents 2.0% of all adverse event reports for SUMATRIPTAN.
347
Reports of Wrong technique in product usage process with SUMATRIPTAN
2.0%
of all SUMATRIPTAN reports
0
Deaths
6
Hospitalizations
How Dangerous Is Wrong technique in product usage process From SUMATRIPTAN?
Of the 347 reports, 6 (1.7%) required hospitalization, and 1 (0.3%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SUMATRIPTAN. However, 347 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 product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which SUMATRIPTAN Alternatives Have Lower Wrong technique in product usage process Risk?
SUMATRIPTAN vs SUMATRIPTAN\SUMATRIPTAN
SUMATRIPTAN vs SUMAVEL DOSEPRO
SUMATRIPTAN vs SUNITINIB
SUMATRIPTAN vs SUNITINIB MALATE
SUMATRIPTAN vs SUTENT