Does SUMATRIPTAN Cause Product quality issue? 1,269 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,269 reports of Product quality issue have been filed in association with SUMATRIPTAN (sumatriptan succinate). This represents 7.3% of all adverse event reports for SUMATRIPTAN.
1,269
Reports of Product quality issue with SUMATRIPTAN
7.3%
of all SUMATRIPTAN reports
0
Deaths
17
Hospitalizations
How Dangerous Is Product quality issue From SUMATRIPTAN?
Of the 1,269 reports, 17 (1.3%) required hospitalization.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SUMATRIPTAN. However, 1,269 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)
Application site pain (1,217)
Migraine (978)
Headache (914)
Product complaint (718)
Nausea (702)
Product dose omission issue (698)
What Other Drugs Cause Product quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which SUMATRIPTAN Alternatives Have Lower Product quality issue Risk?
SUMATRIPTAN vs SUMATRIPTAN\SUMATRIPTAN
SUMATRIPTAN vs SUMAVEL DOSEPRO
SUMATRIPTAN vs SUNITINIB
SUMATRIPTAN vs SUNITINIB MALATE
SUMATRIPTAN vs SUTENT