Does FLIBANSERIN Cause Intentional dose omission? 19 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 19 reports of Intentional dose omission have been filed in association with FLIBANSERIN (ADDYI). This represents 1.1% of all adverse event reports for FLIBANSERIN.
19
Reports of Intentional dose omission with FLIBANSERIN
1.1%
of all FLIBANSERIN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Intentional dose omission From FLIBANSERIN?
Of the 19 reports.
Is Intentional dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLIBANSERIN. However, 19 reports have been filed with the FAERS database.
What Other Side Effects Does FLIBANSERIN Cause?
Drug ineffective (472)
Dizziness (298)
Nausea (176)
Somnolence (143)
Product use in unapproved indication (137)
Insomnia (125)
Fatigue (122)
Headache (106)
Feeling abnormal (87)
Malaise (70)
What Other Drugs Cause Intentional dose omission?
DUPILUMAB (2,269)
CERTOLIZUMAB PEGOL (1,253)
ADALIMUMAB (845)
TOFACITINIB (845)
INFLIXIMAB (815)
ABALOPARATIDE (623)
ETANERCEPT (615)
AMBRISENTAN (595)
SODIUM OXYBATE (580)
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)
Which FLIBANSERIN Alternatives Have Lower Intentional dose omission Risk?
FLIBANSERIN vs FLOLAN
FLIBANSERIN vs FLUCICLOVINE F-18
FLIBANSERIN vs FLUCLOXACILLIN
FLIBANSERIN vs FLUCONAZOLE
FLIBANSERIN vs FLUCYTOSINE