Vitamin E (Systemic)
Name: Vitamin E (Systemic)
- Vitamin E Systemic names
- Vitamin E Systemic dosage
- Vitamin E Systemic 4 mg
- Vitamin E Systemic dosage forms
- Vitamin E Systemic adverse effects
Pronunciation
(VYE ta min ee)
Brand Names U.S.
- Alph-E [OTC]
- Alph-E-Mixed 1000 [OTC]
- Alph-E-Mixed [OTC]
- Aquasol E [OTC] [DSC]
- Aquavit-E [OTC] [DSC]
- Aqueous Vitamin E [OTC]
- E-400 [OTC]
- E-400-Clear [OTC]
- E-400-Mixed [OTC]
- E-Max-1000 [OTC]
- E-Pherol [OTC]
- Formula E 400 [OTC]
- Natural Vitamin E [OTC]
- Nutr-E-Sol [OTC]
- Vita-Plus E [OTC]
Pharmacology
Prevents oxidation of vitamin A and C; protects polyunsaturated fatty acids in membranes from attack by free radicals and protects red blood cells against hemolysis
Absorption
Depends on presence of bile; reduced in conditions of malabsorption, in low birth weight premature infants, and as dosage increases; water miscible preparations are better absorbed than oil preparations
Distribution
To all body tissues, especially adipose tissue, where it is stored
Metabolism
Hepatic to glucuronides
Excretion
Feces
Use Labeled Indications
Dietary supplement
Note: According to the 2014 USPSTF recommendations for the primary prevention of cardiovascular disease and cancer, the use of vitamin E supplements are not recommended (Moyer 2014).
Dosing Pediatric
Vitamin E may be expressed as alpha-tocopherol equivalents (ATE), which refer to the biologically-active (R) stereoisomer content.
Adequate intake (AI): Oral (IOM 2000): Infants (RDA not established):
1 to 6 months: 4 mg
7 to 12 months: 5 mg
Recommended daily allowance (RDA): Oral (IOM, 2000): Children:
1 to 3 years: 6 mg; upper limit of intake should not exceed 200 mg/day
4 to 8 years: 7 mg; upper limit of intake should not exceed 300 mg/day
9 to 13 years: 11 mg; upper limit of intake should not exceed 600 mg/day
14 to 18 years: 15 mg; upper limit of intake should not exceed 800 mg/day
Vitamin E deficiency: Oral: Children (with malabsorption syndrome): 1 unit/kg/day of water miscible vitamin E (adjust dose based on serum concentrations) (Kleigman 2016)
Cystic fibrosis supplementation (Borowitz 2002): Oral:
1 to 12 months: 40 to 50 units/day
1 to 3 years: 80 to 150 units/day
4 to 8 years: 100 to 200 units/day
>8 years: 200 to 400 units/day
Dietary supplement: Oral: Aqueous Oral Drops:
Infants: 5 units/day
Children <4 years: 10 units/day
Children ≥4 years and Adolescents: 30 units/day
Warnings/Precautions
Concerns related to adverse effects:
• Vitamin K deficiency: May induce vitamin K deficiency (Corkins 2010).
Special populations:
• Low birth weight infants: Necrotizing enterocolitis has been associated with oral administration of large dosages (eg, >200 units/day) of a hyperosmolar vitamin E preparation in low birth weight infants.
Dosage form specific issues:
• Polysorbate 80: Some dosage forms may contain polysorbate 80 (also known as Tweens). Hypersensitivity reactions, usually a delayed reaction, have been reported following exposure to pharmaceutical products containing polysorbate 80 in certain individuals (Isaksson 2002; Lucente 2000; Shelley 1995). Thrombocytopenia, ascites, pulmonary deterioration, and renal and hepatic failure have been reported in premature neonates after receiving parenteral products containing polysorbate 80 (Alade 1986; CDC 1984). See manufacturer’s labeling.