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The application of NaBPC1 57 (10 µg, 10 ng/kg b.w.), propranolol (10 mg/kg b.w.), and ranitidine (10 mg/kg b.w.) (control rats received an equivolume of saline 5.0 ml/kg), either intragastrically or intraperitoneally, was conducted either prophylactically (10 days before alcohol initiation) or as a co-treatment together with alcohol or therapeutically (starting at the end of a two month period, i.e

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The following serious adverse reactions are described elsewhere in the labeling: Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice