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A new HAY FEVER breakthrough clinically proven to reduce allergy symptoms and antihistamine use. How long were symptoms herbal remidies 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. this medication is a 21 day treatment. this medication users report reductions in symptoms one year after drink 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. herbal 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 recorded less sneezing, runny nose and nasal congestion one year after completing the treatment in a clinical study. this compares to 35% of the placebo group.

studies indicate drink that ingested oral cyanocobalamin tablets are ineffective in the treatment of allergic disease, perhaps because once ingested, they are directly metabolized in the liver. when b12 is delivered via injection or lozenge it passes throughout the bloodstream before arriving at the liver. it is during this first pass in its native form that it is believed to exert its therapeutic effect. clinical research: "the world health organization (who) recognizes allergic rhinitis (hay fever), sinusitis, asthma,...conjunctivitis, urticaria, eczema, dermatitis (contact and atopic)...allergic and migraine headache...as diseases in which ige-mediated allergy may be involved."1 in 1988, asthma and allergic herbal rhinitis subjects were treated with b12. total ige, specific ige and pulmonary lung functions were taken drink at days 45, 150 and 180 from baseline. eight of the 9 subjects had reduced ige. 2 in 1989 open label studies at two sites in riverside county, ca herbal in 1989. sixteen of the 17 subjects had lowered ige levels from day 0 to day 30.3

all of the active b12 group reporting showed reduction in severity of symptoms ranging from 31% to 70%, while the placebo controls drink reported either no change or a worsening of symptoms. wilcoxon-rank of .002 for the end-points of sneezing, nasal congestion and runny nose; and p = .005 for ige reductions. in 1992, the above mentioned data from 1988 on were presented by dr. o''connor to the fda. the fda panel acknowledged the safety of the treatment. the panel seemed to be in agreement that the statistics indicated a significant reduction in ige and that a quantitative drop in symptoms was demonstrated. in 1992, belen anibarro, md, studied five children with asthma with metabisulfite intolerance confirmed by oral challenge testing. the test was repeated after premedication with 1.5 mg of oral cyanocobalamin. in four of the five patients treated, bronchospasm did not develop in the second metabisulfite challenge.6

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