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The GMC guidance does not require pharmacists to read warnings on the label or to check the patient can understand them.

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Interventions are likely to have unwanted consequences, and overall riskbenefit will need to be carefully studied just like with all medical interventions.

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Researchers interviewed in the piece have noted difficulties with verifying whether participants actually have the disease under investigation and ensuring the reliability of data gathered outside a clinic setting.

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The women in this study will be studied for 10 years through simple tests and questionnaires.

Dispensing these drugs to countless patients may cause pharmacies to experience serious hardships, according to a press release.

Las personas del grupo de ejercicio tampoco mostraron aumentos significativos en el temor a las cadas durante los 12 meses, mientras que el grupo de atencin habitual se volvi ms temeroso, un factor clave que afecta la calidad de vida de las personas.

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El prximo paso para los investigadores es llevar a cabo planes para evaluar un tratamiento similar en humanos.

The patient would only move on to a more expensive biologic drug if the biosimilar is not effective.

The paper outlining the phase two clinical trials in people and the previous studies involving nonhuman primates was published in the September 27, 2017 edition of the journal Science Translational Medicine, an interdisciplinary medical journal established by the American Association for the Advancement of Science.

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