Does TASIMELTEON Cause Incorrect product administration duration? 165 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 165 reports of Incorrect product administration duration have been filed in association with TASIMELTEON (Tasimelteon). This represents 2.9% of all adverse event reports for TASIMELTEON.
165
Reports of Incorrect product administration duration with TASIMELTEON
2.9%
of all TASIMELTEON reports
0
Deaths
1
Hospitalizations
How Dangerous Is Incorrect product administration duration From TASIMELTEON?
Of the 165 reports, 1 (0.6%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TASIMELTEON. However, 165 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which TASIMELTEON Alternatives Have Lower Incorrect product administration duration Risk?
TASIMELTEON vs TAVABOROLE
TASIMELTEON vs TAXOL
TASIMELTEON vs TAXOTERE
TASIMELTEON vs TAZAROTENE
TASIMELTEON vs TAZEMETOSTAT