An intimate portrait of a legend in the birth field, Dr. Marsden Wagner.
Off-label use of misoprostol (Cytotec) for labor induction has been steadily increasing for 10 years, even though this use is approved neither by the U.S. [FDA], other national drug regulatory agencies, the pharmaceutical industry, the Cochrane Library nor a number of national obstetric organizations
Without adequate testing of Cytotec (misoprostol) for labor induction, obstetricians simply began to use it on their birthing women. They were taking advantage of a huge loophole in our drug regulatory system.
When the obstetrician said he would use Cytotec, the woman and her husband said they expected he would use prostaglandin gel but he said that he now uses Cytotec, as it is ‘more modern and reliable.’ They were not told Cytotec is not approved by the Food and Drug Administration (FDA) for this purpose…
Cesarean section can save the life of the mother or her baby. Cesarean section can also kill a mother or her baby. How can this be?
…why not allow women the option to choose [caesarean section]? Unfortunately, the option to choose (or demand) is not that simple. CS, even when elective, carries serious risks for mother and baby.
Of 170 women given misoprostol (Cytotec) for induction with VBAC, eight have lost their uterus and two lost a baby as well, according to the combined data of two articles published in the American Journal of Obstetrics and Gynecology.
The experimental use of misoprostol (Cytotec) to induce labor is putting an increasing number of pregnant women at risk without their knowledge or consent. Cytotec, a cheap prescription drug for ulcers, is not FDA approved for labor induction and has been linked to uterine rupture and fetal tachycardia.