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In that study, 68.4% of the VAX-D group achieved at least a 50% pain reduction, while none of the patients in the TENS group did (Naguszewski et al., 2001)
In some research contexts, observations have included mild and transient tolerability-related effects such as: Headaches Nausea Stimulation-related observations Temporary injection-site irritation or localized skin-response variability Research conditions, concentration ranges, dosage ranges, hydration status, administration frequency, and protocol structure may influence tolerability observations across experimental settings
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Doing so will guarantee the safest results, and the greatest benefits when starting an AOD 9604 dosage cycle
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