Does TASIMELTEON Cause Product dose omission? 138 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 138 reports of Product dose omission have been filed in association with TASIMELTEON (Tasimelteon). This represents 2.4% of all adverse event reports for TASIMELTEON.
138
Reports of Product dose omission with TASIMELTEON
2.4%
of all TASIMELTEON reports
0
Deaths
23
Hospitalizations
How Dangerous Is Product dose omission From TASIMELTEON?
Of the 138 reports, 23 (16.7%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TASIMELTEON. However, 138 reports have been filed with the FAERS database.
What Other Side Effects Does TASIMELTEON Cause?
Drug ineffective (1,632)
Insomnia (726)
Product dose omission issue (480)
Middle insomnia (412)
Somnolence (407)
Headache (381)
Nightmare (268)
Abnormal dreams (223)
Fatigue (222)
Therapeutic product effect decreased (194)
What Other Drugs Cause Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which TASIMELTEON Alternatives Have Lower Product dose omission Risk?
TASIMELTEON vs TAVABOROLE
TASIMELTEON vs TAXOL
TASIMELTEON vs TAXOTERE
TASIMELTEON vs TAZAROTENE
TASIMELTEON vs TAZEMETOSTAT