Does FLIBANSERIN Cause Intentional product use issue? 21 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Intentional product use issue have been filed in association with FLIBANSERIN (ADDYI). This represents 1.2% of all adverse event reports for FLIBANSERIN.
21
Reports of Intentional product use issue with FLIBANSERIN
1.2%
of all FLIBANSERIN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Intentional product use issue From FLIBANSERIN?
Of the 21 reports, and 1 (4.8%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLIBANSERIN. However, 21 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 product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which FLIBANSERIN Alternatives Have Lower Intentional product use issue Risk?
FLIBANSERIN vs FLOLAN
FLIBANSERIN vs FLUCICLOVINE F-18
FLIBANSERIN vs FLUCLOXACILLIN
FLIBANSERIN vs FLUCONAZOLE
FLIBANSERIN vs FLUCYTOSINE