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Vol.5 No.2 1995 95 101 19951018 00:00:00+09Informed Consent for Drug Administration Kabuki ONO, Main YAMAGUCHI and Karachi SAITH Department of Nursing Faculty of Medical Welfare Murasaki, 70101, Japan

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What is informed consent for drug?

Informed consent for a drug is a process through which a patient gives permission to receive a specific drug after being informed about the risks, benefits, and alternatives.

Who is required to file informed consent for drug?

Healthcare providers and researchers are required to obtain and file informed consent for drug from patients before administering the drug.

How to fill out informed consent for drug?

To fill out informed consent for a drug, the healthcare provider must explain the drug's purpose, risks, benefits, and alternatives to the patient and the patient must sign a consent form.

What is the purpose of informed consent for drug?

The purpose of informed consent for a drug is to ensure that patients are informed about the drug they are receiving and can make an educated decision about their treatment.

What information must be reported on informed consent for drug?

Informed consent for a drug must include information about the drug's purpose, risks, benefits, alternatives, and the patient's agreement to receive the drug.

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