HRR - Task - Monitoring FDA Adverse Event Reports

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Monitoring FDA Adverse Event Reports (Completed)

Last Published: 07/30/21 01:05:34 PM (Central)

Task Book: Entry Unavailable
Principal Investigator: Wotring, Virginia

Short Title: AE Monitoring

Responsible HRP Element: Exploration Medical Capability

Collaborating Org(s):

Funding Status: Completed - Task completed and produced a deliverable

Procurement Mechanism(s):

Directed

Aims:
Note: This task was completed. As part of ongoing work, future intermittent market surveys may be requested.

Will examine FDA Adverse Event Reports for those that involve medications used in-flight, and those associated with known in-flight concerns.

Integration/Unique Aspects: Informs all disciplines and space medicine.

Resources (Other)

Deliverables (1)

Mappings

Risk of Ineffective or Toxic Medications During Long-Duration Exploration Spaceflight

Pharm-501: We need to accurately characterize when astronauts use medications in space, why they use them, how they use them, whether they work, and if they cause any problems.

Monitoring FDA Adverse Event Reports

Related Tasks (17)

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Risk Approach Plans (1)

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Common Item(s)
	Risk of Ineffective or Toxic Medications During Long-Duration Exploration Spaceflight
	Pharm-501: We need to accurately characterize when astronauts use medications in space, why they use them, how they use them, whether they work, and if they cause any problems.