Mifepristone Adverse Events Identified by Planned Parenthood in 2009 and 2010 Compared to Those in the FDA Adverse Event Reporting System and Those Obtained Through the Freedom of Information Act.

Cirucci, Christina A; Aultman, Kathi A; Harrison, Donna J

Cirucci, Christina A; Aultman, Kathi A; Harrison, Donna J.

Afiliación

Cirucci CA; Sewickley, PA.
Aultman KA; Charlotte Lozier Institute.
Harrison DJ; American Association of Pro-Life Obstetricians and Gynecologists, USA.

Health Serv Res Manag Epidemiol ; 8: 23333928211068919, 2021.

Article en En | MEDLINE | ID: mdl-34993274

Palabras clave

United States food and drug administration; adverse drug reaction reporting systems; drug-related side effects and adverse reactions; induced abortion; mifepristone; misoprostol; postmarketing product surveillance; steroidal abortifacient agents

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Health Serv Res Manag Epidemiol Año: 2021 Tipo del documento: Article País de afiliación: Panamá

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