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Ru 486 Misconceptions Myths and Morals - ressourcesfeministes

Ru 486 Misconceptions Myths and Morals - ressourcesfeministes

Ru 486 Misconceptions Myths and Morals - ressourcesfeministes

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Claims for RU <strong>486</strong>/PG Abortioncommencing therapy.’ This is an extremely long <strong>and</strong>unacceptable period of time that women must wait to abort(Sitruk-Ware et al., 1990:227–28).A 1990, as yet unpublished Roussel Uclaf study indicatesthat 4.7 per cent of 10,250 women had incomple te abortions, with or without continuing pregnancies, after RU <strong>486</strong>/PG treatment. A percentage is abstract; the less abstract factis that this 4.7 per cent constitutes 482 real women for whomchemical abortion not only failed, but who then had to submitto an additional abortion procedure (Aubeny, 1990:3).Translated into the raw truth of human data, the RU <strong>486</strong>/PG failure rate is by no means minimal.Bleeding is another area of complication. In several studies,some women were reported to receive blood transfusions.The largest number of transfusions reported in the literaturetook place in the UK Multicentre studies where five out of579 women required both blood transfusions <strong>and</strong> curettage(UK Multicentre Trial, 1990:482). Sometimes, heavybleeding necessitates an emergency uterine evacuation; othertimes, when a uterine evacuation is performed because of anincomplete RU <strong>486</strong> abortion, the evacuation itself leads toheavy bleeding (Cameron et al., 1986:463).More commonly, studies chronicle bleeding in terms ofits duration <strong>and</strong> volume. Many articles report severe <strong>and</strong>prolonged blood loss. Duration of bleeding ranges from oneto 44 days (Rodger <strong>and</strong> Baird, 1989). The 1990 UKMulticentre Trial mentions that the mean duration of bleedingexperienced by women was almost two weeks.Severe or excessive bleeding, as opposed to duration, isreported in conjunction with treatment regimens. In one studyafter administration of RU <strong>486</strong>, nine per cent of womenexperienced heavy bleeding; <strong>and</strong> when the prostagl<strong>and</strong>inswere subsequently administered as the second medicationin the treatment, another nine per cent bled heavily. Twodays after the completion of the combination treatment, 16per cent reported heavy bleeding (UK Multicentre Trial,39

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