Overview of Coenzyme Q10 (Ubidecarenone) Injection
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Dosage Strength of Coenzyme Q10 Injection
- 20 mg/mL 10 mL Vial
Coenzyme Q10 (CoQ10) is found in all cells across all domains of life. It is a redox-active lipid biosynthesized in the mitochondria by the conjugation of a benzoquinone ring with a 10-unit isoprenoid chain. It is essential in the production of cellular energy in the form of adenosine triphosphate (ATP). It is a significant antioxidant and therefore prevents free radical generation and modifications of DNA, proteins, and lipids. It can also help in the regeneration of other antioxidants, such as vitamin E. CoQ10 is also naturally found in some foods, such as meat, nuts, fruits, and vegetables. However, the average daily dietary intake of CoQ10 is very low, about three to six milligrams, and earlier studies show that dietary intake of CoQ10 does not appear to increase CoQ10 tissue levels above normal.
Subnormal serum levels of Coenzyme Q10 have been observed in patients with advanced heart failure; type 2 diabetes (insulin resistance and high blood glucose levels); neurodegenerative disease, including Parkinson’s disease; metabolic syndrome; hypertension; preeclampsia; certain types of cancer, like breast cancer and melanoma, and more. This data has led researchers to investigate exogenous CoQ10 supplementation as a potential treatment for these conditions. However, research so far is inconclusive or contradictory as to whether exogenous CoQ10 supplementation can help treat or manage symptoms of these conditions.
Coenzyme Q10 is one of the most commonly used dietary supplements. CoQ10 is not FDA-approved for the treatment of any medical condition and there is little data on the safety and efficacy of long-term use of coenzyme Q10. However, the FDA granted orphan status to an oral coenzymeQ10 drug, called UbiQGel, for its use in clinical trials on patients diagnosed with mitochondrial cytopathies (MC).
CoQ10 deficiency is a known cause of mitochondrial disease. The evidence to date shows promise that CoenzymeQ10 may be a potential treatment of mitochondrial disorders. However, further research is needed to determine the appropriate dosage.
CoQ10 injections should only be taken under the supervision of a physician.
Coenzyme Q10 is an essential cofactor of intra-complex electron transportation in adenosine triphosphate (ATP) synthesis, also referred to as oxidative phosphorylation. It is vital to the health of all cells, and therefore all tissues and organs, in the body. Cells constantly use ATP as an energy source to conduct biological reactions.
CoQ10 is an antioxidant and therefore prevents free radical generation and modifications of DNA, proteins, and lipids.
CoQ10 is an endogenous inhibitor of platelets. Exogenous CoQ10 is an upregulator of the cAMP/PKA pathway, an activator of the A2A adenosine receptor, an inhibitor of phosphodiesterase 3A phosphorylation, and a significant inhibitor of vitronectin-receptor (CD51/CD61) expression.
CoQ10 is a ligand and an agonist of the PPARα/γ receptor. It also functions as an antioxidant in the mitochondria by regenerating alpha-tocopherol from its phenoxyl radical.
CoQ10 is an inotrope.
Patients with a known allergy to Coenzyme Q10 should not take this product.
One study found that oral doses of CoQ10 of 100 mg or higher can cause mild insomnia in some individuals. Some patients may benefit from taking CoQ10 in the morning.
Coenzyme Q10 is eliminated from the body via the biliary tract. It may increase the risk of CoQ10 accumulation in patients with biliary obstruction or hepatic impairment.
The literature is contradictory as to whether coenzyme Q10 has antihypertensive properties. In some clinical trials, coenzyme Q10 lowered both systolic and diastolic blood pressure. Patients with low blood pressure should use precaution when taking CoQ10.
As an antioxidant, CoQ10 is contraindicated in patients undergoing chemotherapy and/or radiation therapy. CoQ10, and other antioxidants, may increase the risk of recurrence in cancer patients undergoing treatment.
The safety and efficacy of CoQ-10 injections in pregnancy have not been established. As such, it is difficult to determine a drug-associated risk of adverse developmental outcomes. Women who are pregnant should avoid using this product.
Initial studies show that oral exogenous synthetic CoQ10 may reduce the risk of developing preeclampsia during pregnancy, when administered daily to pregnant women with an increased risk for preeclampsia, starting at 20 weeks gestation.
The safety and efficacy of CoQ-10 injections in breastfeeding have not been established. As such, it is difficult to determine a drug-associated risk of adverse developmental outcomes. Women who are pregnant or breastfeeding should avoid using this product.
CoQ-10 is a natural component found in human breast milk. Currently, there is no data available regarding the effects of exogenous synthetic CoQ-10 on CoQ-10 concentrations in breast milk. Additionally, there is no data on how exogenous synthetic CoQ-10 affects milk production or its effects on the breastfed infant.
HMG-CoA reductase inhibitors, also known as statins, decrease the amount of Coq10 in the body by inhibiting the production of the CoQ10 precursor mevalonate.
Coenzyme Q10 is similar in chemical structure to vitamin K. Research is contradictory as to whether vitamin K, and therefore coenzyme Q10, counteract the anticoagulant effects of warfarin. Coenzyme Q10 may increase the rate of metabolism of warfarin by selective interaction with cytochrome p450 enzymes, reducing International Normalized Ratio (INR). One study observed an increased risk of bleeding in patients with concomitant administration of CoQ10 and warfarin.
Early research shows a link between CoQ10 intake and reduced platelet size. A more recent study also shows that CoQ10 inhibits platelet aggregation. CoQ10 may increase the risk of bleeding in patients taking platelet agglutination inhibitor drugs, such as acetylsalicylic acid (ASAs), like aspirin; clopidogrel (Plavix); prasugrel (Effient); and ticagrelor (Brilinta).
The evidence is contradictory as to whether CoQ10 improves β-cell function, enhances insulin sensitivity, and decreases blood glucose levels in patients with type 2 diabetes. CoQ10 may augment the effects of other blood glucose-lowering agents, such as biguanides and sulfonylureas, and metformins in people with diabetes, and increase the risk of hypoglycemia.
One study found that CoQ10 decreases blood glucose in individuals diagnosed with type 2 diabetes. CoQ10 may augment the effect of insulin and other blood-glucose-lowering agents, such as sulfonylureas and metformin.
The literature is contradictory as to whether coenzyme Q10 has antihypertensive properties. In some clinical trials, coenzyme Q10 lowered both systolic and diastolic blood pressure. CoQ10 may augment the effects of antihypertensive medication and is therefore contraindicated in patients taking antihypertensive medication and patients with low blood pressure.
As an antioxidant, CoQ10 is contraindicated in patients undergoing chemotherapy and/or radiation therapy. CoQ10, and other antioxidants, may increase the risk of recurrence in cancer patients undergoing treatment.
Limited research on the safety and efficacy of CoQ10 signifies that not all side effects are known. So far, major side effects of oral coenzyme Q10 supplementation have not been reported. There is no data on the side effects of intramuscular or intravenous injection of CoQ10.
Recorded side effects of oral CoQ10 supplementation in adults include rash, epigastric pain, nausea, headache, fatigue, heartburn, increased involuntary movements, anorexia, vomiting, diarrhea, pain in the upper abdomen, dizziness, irritability, sensitivity to light, and elevated liver enzymes.
In children diagnosed with a mitochondrial disorder, oral CoQ10 supplementation has caused mild side effects, including nausea, diarrhea, and heartburn; less commonly reported are headache, dizziness, irritability, and agitation.
There is no data on the short-term or long-term side effects associated with intravenous and intramuscular injection of CoQ10 in humans. There is little data on the long-term effects of oral CoQ10 supplementation. A review of clinical studies reveals that no serious or frequent side effects were observed in adults with oral administration of CoQ10 when taking 200 mg/day for up to 12 months or 100 mg/day for up to 6 years. However, the review also notes that these studies were not designed to examine side effects and therefore suggests that monitoring side effects was not a priority during these studies. One study saw impairments in cognitive and sensory function in mice after prolonged administration of high levels of CoQ10.
The literature is contradictory as to whether coenzyme Q10 lowers blood pressure. In some clinical trials, coenzyme Q10 lowered both systolic and diastolic blood pressure levels. Coenzyme Q10 supplementation is contraindicated for patients who are taking anti‐hypertensive medication. Patients with low blood pressure should use precaution when taking CoQ10.
Store this medication at 68°F to 77°F (20°C to 25°C) and away from heat, moisture and light. Keep all medicine out of the reach of children. Throw away any unused medicine after the beyond use date. Do not flush unused medications or pour down a sink or drain.
Learn how to prepare medication for self-administered injection.
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