Over a 2-week study period, half of the participants received only quadruple therapy while the other half also received 20mg of vitamin B6, given twice per day. Eradication was assessed by C-urea breath testing. There was no significant difference between groups in terms of eradication rates; 61.5% and 56.2% in the control and B6 groups, respectively, both fairly low rates attributed to drug resistance in the area. However, a significantly lower rate of adverse effects was observed in the group receiving B6, 57% vs. 74.6%. In addition to an overall lower rate, there was also a lower rate of moderate to severe adverse effects. For example, only 14.6% of those receiving B6 experienced moderate to severe neurological symptoms, compared to 58.7% in the standard group. No patients receiving B6 had moderate to severe gastrointestinal symptoms, versus 1/3 of those in the standard group. The authors speculate that the benefit may be due to B6’s ability to drive GABA production in the brain, and offers a safe addition to standard therapy without reducing drug efficacy.