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The Effexor XR FDA label reports sustained blood pressure elevations (systolic 180 mmHg or diastolic 105 mmHg) in 0.7% of patients at doses of 200 to 300 mg/day versus 0.2% on placebo [3]

To detect potential sources of heterogeneity, subgroup analyses were performed according to the predefined variables, including duration of the intervention, NAC dosage, study location and the type of control

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Human clinical trials conducted over extended observation periods reveal remarkable mortality benefits

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Researchers found that individuals with insomnia have decreased glutathione levels