Depo Provera
Depo-Provera Birth Control Injection (medroxyprogesterone acetate) is the U.S. brand name of a birth control product manufactured by Pfizer Inc. It is a hormonal birth control method containing the pregnane (17α-hydroxyprogesterone derivative) progestin medroxyprogesterone acetate, without oestrogen, and is administered to women in the form of an intramuscular injection once every 11 to 13 weeks. Depo-Provera causes the ovaries to stop releasing eggs.
Mechanism of action
The mechanism of action of progestin-only contraceptives depends on the progestin activity and dose. High dose progestin-only contraceptives, such as the injectable Depo-Provera, completely inhibit follicular development and ovulation. Like all progestin-only contraceptives, Depo-Provera also has a progestogenic effect of increasing cervical mucus viscosity, thereby inhibiting sperm penetration. In anovulatory cycles using progestin-only contraceptives, the endometrium is thin and atrophic. If the endometrium was also thin and atrophic during an ovulatory cycle, this could theoretically interfere with implantation of a blastocyst (embryo).
Benefits
Depo and Menstruation
Most women using Depo Provera experience disruption of menstrual bleeding patterns, something which has been called "menstrual chaos." Altered menstrual bleeding patterns include irregular or unpredictable bleeding or spotting, or rarely, heavy or continuous bleeding. After continuous use, fewer experience irregular bleeding and more experience amenorrhea. By month 12 amenorrhea was reported by 55% of women, and by month 24 amenorrhea was reported by 68%. Some women may prefer amenorrhea. (But it is not a guaranteed effect of Depo.) Amenorrhea induced by birth control products has not been studied. According to Jerilynn Prior, M.D., professor of endocrinology and metabolism at the University of British Columbia in Vancouver, and board member for the Society for Menstrual Cycle Research,"the most important thing to emphasize about menstrual suppression is that the long-term effects are simply unknown," and "allowing the one vital sign unique to women to go unmonitored...could ultimately lead to an enormous uncontrolled experiment with a woman's health."
Depo and Pregnancy/Breastfeeding
Depo Provera may be used by breast-feeding mothers. Heavy bleeding is possible if given in the immediate postpartum time and is best delayed until six weeks after birth. It may be used within five days if not breast feeding. While a small study "showed no significant difference in birth weights or incidence of birth defects" and "no significant alternation of immunity to infectious disease caused by breast milk containing DMPA", a possible subgroup of babies with 75% higher incidence of infectious disease was seen in mothers who started Depo Provera at 2 days postpartum. A larger study with longer follow-up concluded that "use of DMPA during pregnancy or breastfeeding does not adversely affect the long-term growth and development of children". This study also noted that "children with DMPA exposure during pregnancy and lactation had an increased risk of suboptimal growth in height," but that "after adjustment for socioeconomic factors by multiple logistic regression, there was no increased risk of impaired growth among the DMPA-exposed children." "Unfavorable socioeconomic factors" may therefore result in suboptimal height for DMPA-exposed children. The study also noted that effects of DMPA exposure on puberty require further study, as so few children over the age of 10 were observed.
Disadvantages & side effects
B
lack box warning
While it has long been known that Depo-Provera causes bone loss, it has recently been discovered that the osteoporotic effects of the injection grow worse the longer Depo-Provera is administered, last long after the injections are stopped, and may be irreversible. For this reason, on November 17, 2004 the United States Food and Drug Administration and Pfizer agreed to put a "black box warning" on Depo-Provera's label.
However, the WHO (World Health organisation)-- which provided Depo-Provera to developing countries when the US FDA refused to approve it for safety reasons pertaining to breast cancer--advises that the use of Depo Provera should not be restricted. One cohort study has shown that BMD loss may be reversible within 30 months of discontinuation of DMPA. At least one of the authors of the study, AZ Lacroix, is a consultant for Pfizer. The School of Public Health at the University of Washington, where the study was conducted, receives financial support from Pfizer. And Pfizer continues to advise in the Depo product insert that bone loss caused by Depo Provera may not be reversible.
Contraindications
Women with the following conditions should not use Depo Provera:
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