Does UBIDECARENONE Cause Intentional product use issue? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Intentional product use issue have been filed in association with UBIDECARENONE (CO Q 10). This represents 1.9% of all adverse event reports for UBIDECARENONE.
7
Reports of Intentional product use issue with UBIDECARENONE
1.9%
of all UBIDECARENONE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Intentional product use issue From UBIDECARENONE?
Of the 7 reports, 1 (14.3%) required hospitalization, and 1 (14.3%) 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 UBIDECARENONE. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does UBIDECARENONE Cause?
Drug ineffective (130)
Headache (125)
Pain (125)
Malaise (115)
Off label use (114)
Nausea (113)
Therapeutic product effect incomplete (113)
Abdominal pain (109)
Constipation (109)
Pyrexia (109)
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 UBIDECARENONE Alternatives Have Lower Intentional product use issue Risk?
UBIDECARENONE vs UBLITUXIMAB
UBIDECARENONE vs UBLITUXIMAB-XIIY
UBIDECARENONE vs UBROGEPANT
UBIDECARENONE vs ULIPRISTAL
UBIDECARENONE vs UMBRALISIB