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Food and Drug Administration and Postmarketing surveillance

Shortcuts: Differences, Similarities, Jaccard Similarity Coefficient, References.

Difference between Food and Drug Administration and Postmarketing surveillance

Food and Drug Administration vs. Postmarketing surveillance

The Food and Drug Administration (FDA or USFDA) is a federal agency of the United States Department of Health and Human Services, one of the United States federal executive departments. Postmarketing surveillance (PMS) (also post market surveillance) is the practice of monitoring the safety of a pharmaceutical drug or medical device after it has been released on the market and is an important part of the science of pharmacovigilance.

Similarities between Food and Drug Administration and Postmarketing surveillance

Food and Drug Administration and Postmarketing surveillance have 7 things in common (in Unionpedia): Adverse drug reaction, Clinical trial, Health Canada, Medical device, Medication, Medicines and Healthcare products Regulatory Agency, MedWatch.

Adverse drug reaction

An adverse drug reaction (ADR) is an injury caused by taking a medication.

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Clinical trial

Clinical trials are experiments or observations done in clinical research.

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Health Canada

Health Canada (Santé Canada) is the department of the government of Canada with responsibility for national public health.

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Medical device

A medical device is any apparatus, appliance, software, material, or other article—whether used alone or in combination, including the software intended by its manufacturer to be used specifically for diagnostic and/or therapeutic purposes and necessary for its proper application—intended by the manufacturer to be used for human beings for the purpose of.

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Medication

A medication (also referred to as medicine, pharmaceutical drug, or simply drug) is a drug used to diagnose, cure, treat, or prevent disease.

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Medicines and Healthcare products Regulatory Agency

The Medicines and Healthcare products Regulatory Agency (MHRA) is an executive agency of the Department of Health and Social Care in the United Kingdom which is responsible for ensuring that medicines and medical devices work and are acceptably safe.

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MedWatch

MedWatch is the Food and Drug Administration’s Safety Information and Adverse Event Reporting Program.

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The list above answers the following questions

Food and Drug Administration and Postmarketing surveillance Comparison

Food and Drug Administration has 214 relations, while Postmarketing surveillance has 18. As they have in common 7, the Jaccard index is 3.02% = 7 / (214 + 18).

References

This article shows the relationship between Food and Drug Administration and Postmarketing surveillance. To access each article from which the information was extracted, please visit:

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