Does UBIDECARENONE Cause Condition aggravated? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Condition aggravated have been filed in association with UBIDECARENONE (CO Q 10). This represents 2.8% of all adverse event reports for UBIDECARENONE.
10
Reports of Condition aggravated with UBIDECARENONE
2.8%
of all UBIDECARENONE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Condition aggravated From UBIDECARENONE?
Of the 10 reports, 2 (20.0%) required hospitalization, and 1 (10.0%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UBIDECARENONE. However, 10 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which UBIDECARENONE Alternatives Have Lower Condition aggravated Risk?
UBIDECARENONE vs UBLITUXIMAB
UBIDECARENONE vs UBLITUXIMAB-XIIY
UBIDECARENONE vs UBROGEPANT
UBIDECARENONE vs ULIPRISTAL
UBIDECARENONE vs UMBRALISIB