Fertility
What Depo-Provera litigation means for the future of women’s health

By Aron Solomon, Pulitzer Prize-nominated writer and chief strategy officer for Amplify
For decades, Depo-Provera was marketed as a convenient, long-lasting birth control option for women who want to take control of their reproductive health without the hassle of daily pills.
It was sold as a solution—an easy shot every three months that promised reliability and freedom.
But what was often left out of the conversation was the growing body of evidence linking the drug to serious, long-term side effects, including bone density loss, increased risk of certain cancers, and severe mental health impacts.
And now, lawsuits against the makers of Depo-Provera are bringing those risks into the national spotlight.
But this fight isn’t just about compensation. It’s about something much bigger: transparency, accountability, and the demand for better healthcare for women.
The lawsuits against Depo-Provera’s manufacturer aren’t happening in a vacuum.
They are part of a broader, long-standing pattern of medical products being introduced, marketed, and prescribed to women without full disclosure of their risks.
Time and time again, women’s health concerns have been dismissed, downplayed, or outright ignored until legal action forces the issue.
We saw it with the Dalkon Shield IUD in the 1970s, which led to infections, infertility, and deaths before it was pulled from the market and resulted in a massive lawsuit.
We saw it with the Yaz and Yasmin birth control pills, which were linked to life-threatening blood clots and only got black-box warnings after lawsuits mounted. And we are seeing it now with Depo-Provera.
At the heart of these lawsuits is a simple but powerful demand: women deserve to know what they’re putting into their bodies.
They deserve full transparency about risks, not sugarcoated reassurances or buried data.
Depo-Provera has been linked to decreased bone mineral density, a serious issue that can lead to osteoporosis later in life.
Studies have shown that the loss is often not fully reversible, yet many women were never warned about this before they started using the drug.
There is also an increased risk of cancer and mood disorders like depression and anxiety—again, side effects that weren’t always fully disclosed or studied in depth before Depo-Provera was widely distributed.
The legal action against the manufacturers of Depo-Provera represents more than just a quest for justice for those who have suffered—it’s a means of demanding systemic change.
These lawsuits pressure pharmaceutical companies to do better, not just in how they test and approve drugs but in how they communicate risks to patients.
They send a clear message that women are no longer willing to accept subpar treatment when it comes to their health. And they put the medical establishment on notice: accountability is no longer optional.
A crucial part of this movement is the push for more inclusive and thorough clinical research.
Historically, medical research has been male-centered, with women often being treated as an afterthought.
This has led to an incomplete understanding of how drugs affect women’s bodies differently.
When women’s unique health needs aren’t properly studied, they aren’t properly addressed—and that has real consequences.
The Depo-Provera lawsuits highlight the need for drug trials that take women’s long-term health seriously, rather than treating side effects as acceptable trade-offs.
Beyond the pharmaceutical industry, these lawsuits are also challenging the role of healthcare providers in informed consent.
Many women report that they were never told about the full extent of Depo-Provera’s risks before receiving the shot.
Some were assured that side effects were minimal or temporary, only to later discover that their bone density had been permanently compromised.
Others struggled with severe depression or anxiety, unaware that their birth control method could be a contributing factor.
Informed consent isn’t just a legal formality—it’s a fundamental right. Women have the right to make decisions about their bodies based on complete, unbiased information, and these lawsuits are reinforcing that right.
The implications of this legal battle extend far beyond Depo-Provera. They are part of a larger cultural shift in how we approach women’s healthcare.
Women are demanding better—not just in birth control options but in all aspects of reproductive and general health.
They are calling for safer medications, clearer communication, and a medical system that prioritises their well-being rather than treating them as a market for profitable drugs.
This movement is already starting to see results.
The increased scrutiny around Depo-Provera and similar cases is prompting more discussions about alternative birth control methods and the need for more research into safer, hormone-free options.
It’s pushing regulators to be more aggressive in requiring clear warnings and more thorough testing. And it’s empowering women to ask more questions, demand better answers, and take an active role in their healthcare decisions.
The lawsuits against Depo-Provera are not just about financial settlements. They are about changing the way women’s health is treated in this country.
They are about shifting the balance of power so that women are no longer passive recipients of whatever the pharmaceutical industry decides to sell them.
They are about ensuring that future generations don’t have to fight the same battles over and over again just to get basic transparency and respect in medical care.
Legal action has long been one of the most powerful tools for change, and in the case of Depo-Provera, it’s proving to be an essential force in the fight for better women’s healthcare.
The message is clear: women will no longer accept being kept in the dark about their own health.
They are standing up, speaking out, and demanding better. And the medical world—pharmaceutical companies, doctors, and regulators alike—needs to start listening.
Fertility
Chelsea FC Women to launch first-of-its-kind player fertility fund

Chelsea FC Women is to launch a fertility fund giving players access to assessments, treatments, counselling and workshops.
The initiative is part of a new partnership with London fertility clinic Fertility Plus, which has been named the club’s official fertility partner.
Chelsea said the fund will be available to every player in its women’s team, with support tailored to individual needs.
Giulia Mazzia, commercial director for Chelsea FC Women, said: “At Chelsea FC Women we are never done pushing for progress for our players and our community.
“This first-of-its-kind partnership with Fertility Plus will open up the conversation about fertility, help to raise awareness for our incredible fanbase and beyond, and give practical support to our players off the field as well as on it.”
Support through Fertility Plus will include fertility assessments and treatments, as well as counselling and workshops.
The partnership will also provide evidence-based information about reproductive health and address misconceptions around fertility.
Chelsea cited previous research on fertility knowledge which found that 41 per cent of respondents actively trying to conceive did not know when their fertile window was.
The club and Fertility Plus plan to provide educational content, resources comparing fertility myths with medical evidence and insights from Chelsea FC Women ambassadors.
Dr Amit Shah and Dr Anil Gudi, co-founders of Fertility Plus, said: “Elite sport asks a lot of women during the very years when fertility matters most, yet it’s a conversation the game has rarely had.
“Partnering with Chelsea FC Women allows us to help change that by giving players, staff and supporters access to trusted fertility expertise and compassionate, consultant-led care.
“We’re proud to work alongside a club that’s setting a new standard for supporting women’s health, both on and off the pitch.
Fertility
Higher doses of common fertility drug may increase pregnancy risks

Higher cumulative doses of common fertility drug clomiphene citrate may increase pregnancy loss risks, according to new research.
Around one in six people experience infertility, with irregular or absent ovulation among the most common causes.
Clomiphene citrate has long been a mainstay of fertility treatment, but Adelaide University research has raised concerns about higher cumulative doses.
The new study found that high doses of clomiphene citrate accumulated over multiple fertility treatment cycles could increase the risk of pregnancy loss.
Lead author associate professor Sheree Boulet said the findings showed a clear dose-response relationship, meaning the risks increased as cumulative exposure rose.
She said: “Women who received higher cumulative doses of clomiphene citrate experienced progressively greater risks of adverse pregnancy outcomes.
“We examined more than 21,000 embryo transfer cycles across four cumulative dose categories and found that increasing the dose did not significantly improve the chance of a live birth.
“Our findings suggest there may be a point where increasing the dose offers little additional benefit while exposing women to greater risk, highlighting the importance of carefully balancing effectiveness with safety when making treatment decisions.”
Supported by the NHMRC and conducted in partnership with Boston University and the Centers for Disease Control and Prevention, researchers analysed 21,004 IVF embryo transfer cycles in the US.
Women receiving cumulative doses of 500mg to 749mg of clomiphene citrate had a 12 per cent higher risk of miscarriage, while those receiving 750mg to 999mg had a 38 per cent higher risk.
Women receiving cumulative doses of 750mg or more were also more than twice as likely to have twins or other multiple births.
Rates of spontaneous abortion, another term for miscarriage, increased as the dose rose.
Researchers also recorded more than a threefold increase in stillbirth at the highest dose, although the finding was not statistically significant because that dose was rare. Larger studies are needed to confirm the association.
The finding is consistent with an earlier Adelaide University study that showed a doubling of neonatal death in pregnancies involving clomiphene citrate. Neonatal death means the death of a baby shortly after birth.
Higher cumulative doses did not improve the chance of a live birth, but did increase twinning, which raises the risk of adverse outcomes for both mother and child.
Clomiphene citrate is one of the world’s most widely prescribed fertility drugs. It has been prescribed to millions of women worldwide since 1967 and remains a recommended first-line treatment for ovulation induction.
The drug is recognised as an essential medicine by the World Health Organization. It works by stimulating the ovaries to release eggs, increasing the chance of pregnancy.
Women who do not respond to lower doses, or who require multiple treatment cycles, may receive progressively higher cumulative doses over time.
The findings build on a series of studies from Adelaide University’s Robinson Research Institute linking clomiphene citrate with increased risks of pregnancy loss, stillbirth, perinatal death and some birth defects.
Experimental studies in mice supported these findings, showing that higher doses reduced successful pregnancies and were associated with pregnancy loss, impaired fetal growth and developmental abnormalities.
Professor Michael Davies, senior researcher and co-author of all the studies, said the latest work builds on more than two decades of Adelaide-led research into the safety of fertility treatments.
He said: “Clomiphene citrate has been used by many women since 1967, but it has never been comprehensively evaluated in large prospective clinical trials.
“Our studies indicate that women respond differently to clomiphene citrate and that increasing cumulative doses may increase the risk of adverse pregnancy outcomes without improving the likelihood of a live birth.
“The findings confirm and extend our previous studies in both human and mouse models which highlight the need to better understand the dose-response relationship and whether more personalised dosing strategies could improve safety.
“Until we can better understand these differences, it remains important that clinicians rigorously follow manufacturer’s safety recommendations and avoid unnecessarily increasing cumulative doses.
“The same questions are now being asked of newer ovulation-inducing medications, so any move away from clomiphene citrate should also be guided by robust evidence rather than assumptions about safety.”
Fertility
No clear evidence common embryo transfer techniques improve IVF success, review finds

Common IVF preparation techniques used before embryo transfer have no proven effect on pregnancy rates, according to a review.
Researchers said evidence for the widely used practices remains uncertain because available studies are limited and generally of low quality.
Embryo transfer is the final and most vulnerable stage of IVF, when an embryo is placed into the womb. Only around one in three transfers results in pregnancy.
Practice varies between clinics, with some routinely using preparation techniques such as adjusting bladder fullness while others do not consider them necessary.
Dr Ryosuke Akino, practising obstetrician-gynaecologist from Kato Ladies Clinic, said: “To an extent, this is a case of tradition driving practice rather than the evidence.
“Current practices in this area often reflect local protocols, clinician preference, and historical convention rather than strong, high-quality evidence.”
The Cochrane review analysed 11 studies involving 2,524 women undergoing embryo transfer.
Researchers looked at three preparation techniques used by fertility clinics: having women arrive with a full bladder to straighten the angle between the uterus and cervix, removing cervical mucus and using a technique called afterloading.
Afterloading is a technique used to guide the embryo through the cervix.
The review found no reliable evidence that any of the three approaches improved pregnancy rates compared with standard care.
Researchers rated the evidence as low or very low certainty because the trials were small and had methodological weaknesses. They found no grounds to recommend any of the techniques over standard care.
There was also limited information about possible side effects.
The review team, which included methodologists and practising obstetrician-gynaecologists, said full bladder preparation and cervical mucus removal were generally considered safe, with no clear evidence of harm or major complications.
Dr James Brown, obstetrician-gynaecologist from Women’s Health and Research Institute Australia, said: “While these techniques are generally considered safe, it’s still important to test their effectiveness.”
Akino and Brown added: “A full bladder can be uncomfortable, although it may ease catheter insertion in certain uterine positions and reduce procedural difficulty.
“Mucus removal is usually quick, but if done roughly and causes bleeding, it may affect the woman’s experience.
“Overall, the risks are minor and relate mostly to discomfort and procedural factors rather than clinical harm.”
The authors said embryo transfer has changed relatively little despite major advances elsewhere in IVF.
Research has instead focused more heavily on embryo quality and genetic factors, which have a greater bearing on treatment success than transfer technique.
Embryo transfer also depends heavily on the person carrying out the procedure and can be difficult to standardise, making large, rigorous clinical trials harder to design.
Researchers said women may also be reluctant to risk valuable embryos by taking part in randomised studies comparing different transfer techniques.
Dr Noyuri Yamaji from Showa Medical University in Japan said: “Sixteen years of research still haven’t answered a basic IVF technique question.
“This is a critical step in the IVF process and these small changes and techniques have the possibility to make a massive difference, but we won’t know more until more robust, better-quality trials are conducted.”
All the studies assessed were carried out in high-income countries, meaning the findings may not necessarily apply to other healthcare settings and populations.
The authors said further research could be particularly valuable in resource-limited settings, where these procedures are inexpensive and simple to change and basic procedural standardisation could matter more than advanced technical modifications.
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