DESIGN: A retrospective analysis of 386 women who underwent termination of pregnancy
between 12 and 24 weeks' gestation. METHODS: Each woman received 200 mg …

The objectives of this study were to determine the effectiveness, side effects, and
acceptability of one-third the standard 600 mg dose of mifepristone (200 mg) to induce …

OBJECTIVE: To study the efficacy, safety, and acceptability of oral immediately swallowed
and buccal misoprostol 800 mcg after mifepristone 200 mg for terminating pregnancy …

Mifepristone at a dose of 600 mg followed by 400 μg misoprostol orally has been used for
early abortion by hundreds of thousands of women with success rates at≤ 49 days' …

BACKGROUND: Nonsurgical abortion methods have the potential to improve access to high-
quality abortion care. Until recently, availability and utilization of mifepristone medical …

Objectives: The aim of the study was to assess the efficacy and acceptability of a regimen
using mifepristone and buccal misoprostol with unlimited dosing for second trimester …

OBJECTIVE: Mifepristone–misoprostol medical abortion has been approved in the United
States since 2000. US providers have preferred to use vaginal misoprostol because of …

We performed a pilot study to examine the clinical efficacy of mifepristone 200 mg followed
on the same day by misoprostol 800 μg vaginally in women with pregnancies up to 49 days …

Introduction The administration of mifepristone, followed by misoprostol, is widely used for
medical abortion. Many studies have demonstrated home abortion to be safe in pregnancies …

OBJECTIVE: Existing drug-induced abortion techniques involve oral administration of 200
mg of mifepristone, followed by oral administration of 600 mg of misoprostol 48 hours later …