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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. this medication is a 21 day treatment. facial hair this medication users report reductions in symptoms one year after completing the treatment hair 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 facial 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 recorded less sneezing, hair runny nose and nasal congestion one year after completing the treatment in a clinical study. this compares to 35% of the placebo group.
in 1990 study in san diego, ca the 5 active subjects with allergic rhinitis had a lowered total serum facial ige from day 0 to day 90 while 4 placebo subjects, (2 with allergic rhinitis, 1 with asthma and 1 with both), had flat or increased ige levels.4 in a randomized, double-blind, placebo controlled 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.
with no further treatment, the 1996 ten-month follow-up data (n=92) from a high pollen period in oregon, washington and idaho together showed a greater reduction in the active group (n=43) than the placebo group (n=49) on the primary endpoint, defined as a combination of symptom and rescue medication scores.8 patients gave hair blood serum samples prior to the treatment in 1995 and one year later in 1996. they facial were immunoassayed for specific ige antibodies using a chemi-luminescent technique. statistician bradley rosebrook ran t-tests comparing average baseline ige levels to one-year. for the seasonal allergens reported, hair the active group (n=27) had on average a greater reduction in ige than the placebo group (n=34) for 13 out of 16 allergens.8
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