In 1990 study in San Diego, CA the natural 5 active subjects contour with allergic rhinitis had a lowered total serum IgE from Day 0 to Day 90 while natural 4 placebo subjects, (2 with allergic rhinitis, 1 with asthma contour and 1 with both), had flat or increased IgE levels.4 In a randomized, double-blind, placebo controlled natural study of symptoms and serum IgE levels in San Diego, CA in mid-1991, subjects had allergic rhinitis and/or asthma. Serum was drawn at Day 0 and Day 30. Seven of the 10 active treated subjects had a reduction in total serum IgE levels. In 10 placebo treated subjects, 5 had levels of total serum IgE that stayed the same (plus or minus 5%), 3 decreased and 2 increased.5 Statistical analysis of the open-label study as well as the double-blind randomized placebo controlled study have shown a significant effect of vitamin B12 in lowering serum IgE concentrations.

A new HAY FEVER breakthrough clinically proven to reduce allergy symptoms and antihistamine use. How long were symptoms reduced? Studies showed a one-year reduction. How long? Yes, one year! this medication is a lozenge taken twice daily for 21 days. this medication is non-drowsy, natural and available without a prescription. contour this medication is a 21 day treatment. this medication users report reductions in symptoms one year after completing the treatment without taking additional this medication. How long? Yes one year, compared to 24-hour antihistamines it''s much longer lasting. Patients known to have seasonal allergy were examined in clinical studies in five U.S. states by qualified medical doctors. Each patient was given either the real this medication or a placebo (a dummy treatment). Nobody knew who got what. Patients recorded in symptons diaries how bad their symptoms were during and after the treatment. About one year later, patients completed a second diary. 64% of the group of patients receiving this medication natural recorded less sneezing, runny nose and nasal congestion one year after completing the treatment contour in a clinical study. This compares to 35% of the placebo group.

In 1992 in El Paso, TX a randomized, double-blind, placebo controlled study of subjects (n=130) with allergic rhinitis in 1992-1993 was conducted. The average IgE level of the placebo treated subjects remained essentially flat, while the average IgE level for active treated subjects was reduced significantly from baseline natural and contour to Day 30.7 In 1993 in El Paso, TX, valid subjects (n=66) returned a second set of symptom diaries which they had completed for days 365 to 395 (the same natural period, one year after the first set of symptom diaries). The active group had mean symptom scores showing statistically significant contour decreases from 1992 to 1993. The placebo group had increased symptoms in 1993. (The natural relevant pollen counts at the study site contour in 1993 were much higher than in 1992, leading to expectation of higher symptoms.)7

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