Does SUMATRIPTAN Cause Incorrect drug administration duration? 245 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 245 reports of Incorrect drug administration duration have been filed in association with SUMATRIPTAN (sumatriptan succinate). This represents 1.4% of all adverse event reports for SUMATRIPTAN.
245
Reports of Incorrect drug administration duration with SUMATRIPTAN
1.4%
of all SUMATRIPTAN reports
0
Deaths
1
Hospitalizations
How Dangerous Is Incorrect drug administration duration From SUMATRIPTAN?
Of the 245 reports, 1 (0.4%) required hospitalization.
Is Incorrect drug administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SUMATRIPTAN. However, 245 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 Incorrect drug administration duration?
ETONOGESTREL (1,796)
POLYETHYLENE GLYCOL 3350 (1,722)
NAPROXEN (1,272)
DOCOSANOL (803)
ETHINYL ESTRADIOL\ETONOGESTREL (740)
NICOTINE (561)
RANITIDINE (504)
GUAIFENESIN (490)
INSULIN LISPRO (367)
ACETAMINOPHEN (340)
Which SUMATRIPTAN Alternatives Have Lower Incorrect drug administration duration Risk?
SUMATRIPTAN vs SUMATRIPTAN\SUMATRIPTAN
SUMATRIPTAN vs SUMAVEL DOSEPRO
SUMATRIPTAN vs SUNITINIB
SUMATRIPTAN vs SUNITINIB MALATE
SUMATRIPTAN vs SUTENT