(Q33490756)

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Serious adverse events in Norplant users reported to the Food and Drug Administration's MedWatch Spontaneous Reporting System

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scholarly article

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Europe PubMed Central

27 July 2017

Serious adverse events in Norplant users reported to the Food and Drug Administration's MedWatch Spontaneous Reporting System (English)

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stated in

Europe PubMed Central

27 July 2017

levonorgestrel-releasing implant

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1 reference

Wysowski DK

1

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Europe PubMed Central

PubMed ID

7898829

retrieved

27 July 2017

Green L

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2

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PubMed ID

7898829

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27 July 2017

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English

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1 April 1995

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27 July 2017

Obstetrics and Gynecology

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27 July 2017

85

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Europe PubMed Central

27 July 2017

4

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Europe PubMed Central

27 July 2017

538-542

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Europe PubMed Central

PubMed ID

7898829

retrieved

27 July 2017

Identifiers

DOI

10.1016/0029-7844(94)00457-O

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stated in

Europe PubMed Central

27 July 2017

1 reference

Europe PubMed Central

PubMed ID

7898829

retrieved

27 July 2017

(Q33490756)

Serious adverse events in Norplant users reported to the Food and Drug Administration's MedWatch Spontaneous Reporting System

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