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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
5 Pt 1
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pubmed:dateCreated |
2004-5-3
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pubmed:abstractText |
To demonstrate equivalence between mifepristone 200 mg followed 6 to 8 hours later and 24 hours later by misoprostol 800 microg vaginally for abortion in women up to 63 days of gestation.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0029-7844
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
103
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
851-9
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pubmed:dateRevised |
2009-10-26
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pubmed:meshHeading |
pubmed-meshheading:15121556-Abortifacient Agents, Nonsteroidal,
pubmed-meshheading:15121556-Abortifacient Agents, Steroidal,
pubmed-meshheading:15121556-Abortion, Induced,
pubmed-meshheading:15121556-Adult,
pubmed-meshheading:15121556-Drug Administration Schedule,
pubmed-meshheading:15121556-Follow-Up Studies,
pubmed-meshheading:15121556-Humans,
pubmed-meshheading:15121556-Mifepristone,
pubmed-meshheading:15121556-Misoprostol,
pubmed-meshheading:15121556-Prospective Studies,
pubmed-meshheading:15121556-Time Factors
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pubmed:year |
2004
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pubmed:articleTitle |
A randomized comparison of misoprostol 6 to 8 hours versus 24 hours after mifepristone for abortion.
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pubmed:affiliation |
Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine and Magee-Womens Research Institute, Pittsburgh, Pennsylvania 15213-3180, USA. mcreinin@mail.magee.edu
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Comparative Study,
Randomized Controlled Trial,
Research Support, Non-U.S. Gov't,
Multicenter Study
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