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Adverse Events FDA received an adverse event report on January 14, 2019, regarding seven patients in an outpatient clinic who received intravenous injections containing L-glutathione 200mg/mL compounded by a pharmacy using L-glutathione repackaged by Letco (lot number: 1810150050, expiration date: 6/17/2020)
Each cohort was then treated for 14 consecutive days with twice-daily treatments with either 300 mg/kg of NHPN-1010 or an equivalent volume of saline
This means they contain more than one dose of medication
You can dissolve these lozenges on your tongue or chew them
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