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Dermatomyositis Pemphigus Peyronie’s disease Scleroderma |
Reliable and relatively consistent scientific data showing a substantial health benefit. Contradictory, insufficient, or preliminary
studies suggesting a health benefit or minimal health benefit. For an herb, supported by traditional use but
minimal or no scientific evidence. For a supplement, little scientific support and/or minimal
health benefit. | |
Deficiencies of PABA have not been described in humans, and most nutritionists do not consider it an essential nutrient.
PABA is available as a nutritional supplement, but because it is mildly acidic, it can cause stomach irritation when taken in large amounts. The potassium salt of PABA, called Potaba®, which is available by prescription, tends to be better tolerated.
Small amounts of PABA are present in some B-complex vitamins and multivitamin formulas. The amount of PABA used in the studies described above ranged from 300 mg to 12 grams per day. Anyone taking more than 400 mg of PABA per day should consult a physician.
No serious side effects have been reported with 300–400 mg per day. Larger amounts (such as 8 grams per day or more) may cause low blood sugar, rash, fever, and (on rare occasions) liver damage.15 One report exists of vitiligo appearing after ingestion of large amounts of PABA16 and use of amounts over 20 grams per day in small children has resulted in deaths.17 There is also a report of a death from toxic hepatitis in a person with lupus, who took as much as 48 grams per day for six days, followed by 8 grams per day for seven months.18
No interactions between PABA and other nutrients have been reported. However, PABA interferes with sulfa drugs (a class of antibiotics) and therefore should not be taken when these medications are being used.
Are there any drug
interactions?
Certain medicines may interact with PABA. Refer to drug
interactions for a list of those medicines.
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2. Willis I, Kligman AM. Aminobenzoic acid and its esters. The quest for more effective sunscreens. Arch Dermatol 1970;102:405–17.
3. Sieve BF. The clinical effects of a new B-complex factor, para-aminobenzoic acid, on pigmentation and fertility. South Med Surg 1942(March);104:135–9.
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5. Zarafonetis CJD, Dabich L, Negri D, et al. Retrospective studies in scleroderma: effect of potassium para-aminobenzoate on survival. J Clin Epidemiol 1988;41:193–205.
6. Zarafonetis CJ, Dabich L, Devol EB, et al. Retrospective studies in scleroderma: pulmonary findings and effect of potassium p-aminobenzoate on vital capacity. Respiration 1989;56:22–33.
7. Clegg DO, Reading JC, Mayes MD, et al. Comparison of aminobenzoate potassium and placebo in the treatment of scleroderma. J Rheumatol 1994;21:105–10.
8. Grace WJ, Kennedy RJ, Formato A. Therapy of scleroderma and dermatomyositis. NY State J Med 1963;63:140–4.
9. Zarafonetis CJD. Treatment of Peyronie’s disease with potassium para-aminobenzoate. J Urol 1959;81:770–2.
10. Zarafonetis CJD, Curtis AC, Shaw JM. Treatment of pemphigus with potassium para-aminobenzoate. Am J Med Sci 1956;231:30–50.
11. Sieve BF. Further investigations in the treatment of vitiligo. Virginia Med Monthly 1945(January):6–17.
12. Hughes CG. Oral PABA and vitiligo. J Am Acad Dermatol 1983;9:770 [letter].
13. Gaby AR. The story of PABA. Nutr Healing 1997;March:3–4, 11 [review].
14. Zarafonetis CJD. Darkening of gray hair during para-amino-benzoic acid therapy. J Invest Dermatol 1950;15:399–401.
15. Kantor GR, Ratz JL. Liver toxicity from potassium para-aminobenzoate. J Am Acad Dermatol 1985;13:671–2.
16. Hughes CG. Oral PABA and vitiligo. J Am Acad Dermatol 1983;9:770 [letter].
17. Worobec S, LaChine A. Dangers of orally administered para-aminobenzoic acid. JAMA 1984;251:2348.
18. Zarafonetis CJD, Grekin RH, Curtis AC, et al. Further studies on the treatment of lupus erythematosus with sodium para-aminobenzoate. J Invest Dermatol 1948;11:359.
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