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(6.1) To report SUSPECTED ADVERSE REACTIONS, contact Novo Nordisk Inc., at 1-888-693-6742 or FDA at 1-800-FDA-1088 or 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

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Schwindel oder Hyperaktivitt: Weniger als 1 Prozent der Patienten berichten kurz nach der Verabreichung von Schwindel oder einem Gefhl leichter Hyperaktivitt

Researchers with a history of sensitive stomachs, IBS, or prior GI issues often benefit from this slower approach