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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

UBIDECARENONE for Supplementation therapy: Side Effects & Safety Data

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There are 5 adverse event reports in the FDA FAERS database where UBIDECARENONE was used for Supplementation therapy.

Most Reported Side Effects for UBIDECARENONE

Side Effect Reports % Deaths Hosp.
Drug ineffective 130 36.0% 1 108
Headache 125 34.6% 0 106
Pain 125 34.6% 0 108
Malaise 115 31.9% 0 107
Off label use 114 31.6% 0 102
Nausea 113 31.3% 0 104
Therapeutic product effect incomplete 113 31.3% 0 105
Abdominal pain 109 30.2% 0 107
Constipation 109 30.2% 0 105
Pyrexia 109 30.2% 0 107
Weight decreased 107 29.6% 0 105
Anaemia 106 29.4% 0 105
Infusion related reaction 106 29.4% 0 105
Chronic sinusitis 105 29.1% 0 105
Colitis 105 29.1% 0 105

Other Indications for UBIDECARENONE

Product used for unknown indication (220) Cardiac disorder (5) Hypercholesterolaemia (5)

Other Drugs Used for Supplementation therapy

FOLIC ACID (191) CALCIUM (150) CHOLECALCIFEROL (86) TESTOSTERONE (83) CYANOCOBALAMIN (75) IRON (75) POTASSIUM (73) MAGNESIUM (67) FOLATE (60) ALBUMIN HUMAN (52)

Related Pages

UBIDECARENONE Full Profile All Supplementation therapy Drugs UBIDECARENONE Demographics UBIDECARENONE Timeline