Does SUMATRIPTAN Cause Expired product administered? 127 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 127 reports of Expired product administered have been filed in association with SUMATRIPTAN (sumatriptan succinate). This represents 0.7% of all adverse event reports for SUMATRIPTAN.
127
Reports of Expired product administered with SUMATRIPTAN
0.7%
of all SUMATRIPTAN reports
0
Deaths
2
Hospitalizations
How Dangerous Is Expired product administered From SUMATRIPTAN?
Of the 127 reports, 2 (1.6%) required hospitalization.
Is Expired product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SUMATRIPTAN. However, 127 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 Expired product administered?
POLYETHYLENE GLYCOL 3350 (1,637)
NAPROXEN (1,305)
ALBUTEROL (1,233)
LORATADINE (1,095)
MINOXIDIL (982)
ACETAMINOPHEN (797)
INSULIN LISPRO (770)
FLUTICASONE\SALMETEROL (753)
CETIRIZINE (714)
DICLOFENAC (714)
Which SUMATRIPTAN Alternatives Have Lower Expired product administered Risk?
SUMATRIPTAN vs SUMATRIPTAN\SUMATRIPTAN
SUMATRIPTAN vs SUMAVEL DOSEPRO
SUMATRIPTAN vs SUNITINIB
SUMATRIPTAN vs SUNITINIB MALATE
SUMATRIPTAN vs SUTENT