Olen Apteek

Olen Apteek Pharmacy in Potchefstroom.

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29/11/2025

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She was one month into her new job when a pharmaceutical company demanded she approve their "perfectly safe" drug. She said no—and saved thousands of children from catastrophic birth defects.
In August 1960, Dr. Frances Oldham Kelsey started work at the U.S. Food and Drug Administration. She was one of only seven full-time physicians reviewing drugs for the entire agency. Her first assignment seemed routine: approve a sedative called thalidomide that was already used in over twenty European countries.
The pharmaceutical company expected approval before December. They had already stocked warehouses with ten million tablets, ready to flood American markets during the holiday season. They were planning to make a fortune.
But Dr. Kelsey noticed something wrong.
The company's safety data had gaps—especially regarding pregnant women. Animal studies were weak. Human trials were incomplete. The testimonials weren't scientific studies; they were marketing materials. And some reports from Europe hinted at nerve damage in long-term users.
She asked for more data.
The company pushed back. Hard.
Under the law at that time, the FDA could only withhold approval for sixty days before a drug automatically went to market. So every sixty days, Dr. Kelsey requested more information. Every sixty days, she found the new data inadequate. Every sixty days, she refused to sign.
For eighteen months, company officials contacted her and her supervisors approximately fifty separate times, demanding approval. Sales representatives crowded her office. They called day and night. They complained. They tried to go over her head. They called her names she later said "you wouldn't print."
The pressure was relentless. Millions of Europeans were taking the drug without problems. Why was one junior medical officer holding up a wonder drug over technicalities?
But Dr. Kelsey had good reason to be cautious. Years earlier, as a young researcher, she had studied how pregnant rabbits metabolized drugs differently—and how medications crossed the placental barrier to affect developing embryos. When she saw claims about thalidomide's safety in pregnancy, she wondered: had anyone tested what happened when it crossed into a developing fetus?
The answer was no. Nobody had.
She kept refusing.
During that same period, something terrible was happening in Europe.
Doctors began noticing a surge of babies born with shocking deformities. Arms and legs grotesquely shortened or missing entirely. Hands sprouting directly from shoulders. Internal organs improperly developed. Eyes, ears, and hearts malformed.
At first, no one understood why. Then the pattern became impossible to ignore. The mothers had all taken thalidomide during early pregnancy—specifically between the twentieth and thirty-sixth day after conception, when limbs and organs form.
More than ten thousand children were affected across forty-six countries. About half died shortly after birth. The survivors faced lifetimes of profound disability. Thousands more pregnancies ended in miscarriage or stillbirth.
Germany pulled the drug in November 1961. Britain followed in December. But the damage was done. An entire generation of children had been harmed by a drug marketed as perfectly safe.
In the United States, something remarkable happened: almost nothing.
Because Dr. Kelsey had refused approval, thalidomide never reached American pharmacy shelves. The company had illegally distributed experimental samples during trials—resulting in seventeen confirmed cases of birth defects.
Seventeen American children harmed—a tragedy, but not a catastrophe.
Ten thousand European children harmed—because regulators approved the drug without adequate testing.
The difference was one woman's refusal to accept insufficient evidence.
When news of the European tragedy broke in mid-1962, Americans realized what had been avoided. Public outcry was immediate and intense. People were horrified by what they saw happening in Europe. They were grateful for what hadn't happened in America. And they were angry that a drug company had tried so hard to force an inadequately tested medication onto the market.
On August 7, 1962, President John F. Kennedy presented Dr. Kelsey with the President's Award for Distinguished Federal Civilian Service—the highest honor for a civilian federal employee. She was only the second woman ever to receive it. Kennedy praised her exceptional judgment in preventing a major tragedy.
But the story didn't end with an award.
Her stand sparked sweeping changes in American drug regulation. In October 1962, Congress unanimously passed the Kefauver-Harris Amendment, transforming how drugs were tested and approved. For the first time, pharmaceutical companies had to prove drugs not only were safe but actually worked. They had to report adverse reactions. They had to obtain informed consent from trial patients. Testing standards became far more rigorous.
Dr. Kelsey helped write and enforce those new regulations. She was appointed to head the FDA division responsible for implementing the reforms. Her team earned the nickname "Kelsey's cops" for their rigorous oversight.
She spent the rest of her career making sure that what almost happened with thalidomide could never happen again.
She retired from the FDA in 2005 at age ninety, after forty-five years of service. She had fundamentally changed how drugs are developed, tested, and approved—not just in America, but around the world. Countries everywhere strengthened their regulatory systems in response to the thalidomide tragedy and the American example.
In 2010, the FDA established the Dr. Frances O. Kelsey Award for Excellence and Courage in Protecting Public Health, naming it after her. She died peacefully on August 7, 2015—exactly fifty-three years after receiving the medal from President Kennedy—at age 101.
Dr. Frances Oldham Kelsey never made a groundbreaking discovery. She never invented a lifesaving device. She never developed a cure.
What she did was refuse to accept inadequate evidence. She asked questions when everyone else wanted quick approval. She demanded proof when proof didn't exist. She withstood pressure from powerful corporations and held firm to her scientific standards.
She proved that courage in science isn't always about discovery or innovation. Sometimes courage is the quiet insistence on doing things right. Sometimes it's the refusal to compromise on safety. Sometimes it's the willingness to say no and mean it, even when saying yes would be easier.
Her decision saved thousands of American families from devastating heartbreak. Her example shaped modern medicine. Her legacy protects every person who takes a prescription drug today.
All because one doctor understood that the most important word in medicine isn't yes.
Sometimes, it's no.

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29/11/2025

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Louis Washkansky knew he was dying.
At 53 years old, the South African grocer lay in a hospital bed at Groote Schuur Hospital in Cape Town, his heart barely functioning. Diabetes. Three heart attacks. Coronary artery disease so severe that only about 10% of his heart still worked. His legs were swollen with fluid, drained by needles, infected where the punctures had been made.
In October, he'd slipped into a diabetic coma. When he woke, when his wife Ann whispered "How are you doing?" through the pain and the swelling, Louis had managed a smile. "I'm on top of the world," he'd whispered back.
But they both knew the truth. Every known treatment had been exhausted. His kidneys were failing. His liver was failing. Doctors gave him weeks, maybe days.
Then Dr. Christiaan Barnard offered him an impossible choice.
A heart transplant. From another human being. Something that had never successfully been done in the history of medicine.
Barnard had trained at the University of Cape Town and spent time in America learning from Norman Shumway at Stanford, where the first successful animal heart transplant had been performed in a dog in 1958. He'd practiced the technique on forty-eight dogs in his laboratory. He'd studied immunology in Virginia. He'd watched other surgeons get close but never quite dare.
In January 1964, James Hardy in Mississippi had transplanted a chimpanzee heart into a dying man. The patient, Boyd Rush, died after 90 minutes without regaining consciousness.
By 1967, multiple surgical teams around the world stood on the edge of attempting a human-to-human transplant. Norman Shumway at Stanford. Adrian Kantrowitz at Maimonides Medical Center in New York. All waiting for the right moment, the right patient, the right donor.
Barnard decided he would not wait any longer.
He told Louis and Ann Washkansky that the operation had an 80% chance of success—a claim ethicists would later criticize as wildly misleading given that this had literally never been done before. But Barnard believed in direct honesty about the alternative.
"For a dying man it is not a difficult decision," Barnard would later write, "because he knows he is at the end. If a lion chases you to the bank of a river filled with crocodiles, you will leap into the water, convinced you have a chance to swim to the other side."
Louis didn't hesitate. "I'd back any horse that could win," he said.
The surgical team prepared. They took swabs from Louis's skin, nose, mouth, throat, re**um to identify every bacterium living on and in his body so they could target antibiotics precisely after surgery. They washed him repeatedly with antiseptic. They waited for a donor.
On the afternoon of Saturday, December 2, 1967, a car struck two women crossing a busy street in Cape Town.
Denise Darvall, 25 years old, and her mother had been hit by a drunk driver. Her mother died at the scene. Denise was rushed to Groote Schuur Hospital with massive head trauma.
Peter Rose-Innis, the senior neurosurgeon, examined her. Skull X-rays showed two serious fractures. When ice water was poured into her ear—a test for brain function—she showed no sign of pain. No electrical activity registered in her brain. She was brain dead, kept alive only by a respirator and blood transfusions that maintained her heartbeat.
Doctors Coert Venter and Bertie Bosman approached Denise's father, Edward Darvall, who had just lost his wife and was now losing his daughter. They asked for permission to use her heart—to save another person's life.
Edward Darvall knew his daughter had loved helping others. Through his grief, he said yes.
Christiaan Barnard went home that afternoon and dozed while listening to music. When he woke, he decided to modify the surgical technique he'd learned from Shumway. Instead of cutting straight across the back of the atrial chambers, he would cut two small holes for the blood vessels—a refinement that might preserve the heart's structure better.
In South Africa at that time, the law stated simply that a patient was considered dead when declared dead by a physician. But Barnard didn't want to remove a beating heart. At his brother Marius's urging, he injected potassium into Denise Darvall's heart to stop it, rendering her technically dead by whole-body standards before removal.
In the early morning hours of Sunday, December 3, 1967, both patients were wheeled into operating theaters at Groote Schuur Hospital.
Christiaan Barnard led a team of thirty people—surgeons, anesthetists, nurses, technicians—in an operation that would change medical history. His younger brother Marius assisted.
For six hours they worked.
They opened Louis Washkansky's chest. They connected him to a heart-lung machine. They removed his diseased heart, leaving portions of the atria—the upper chambers—in place. They prepared Denise Darvall's healthy heart, cooled with oxygenated blood to protect it from damage.
Then came the moment of truth. The careful suturing of blood vessels. The connection of the donor heart to what remained of Louis's original cardiac structure. The delicate work of making sure every vessel aligned, every connection held.
When everything was ready, Barnard gently applied electrical stimulation.
The donor heart began to beat.
For the first time in human history, a person lived with another person's heart pumping blood through their veins.
At 6:00 AM, Ann Washkansky received a phone call. The operation was a huge success.
When Louis woke, his first words were: "I'm still alive."
The world erupted.
Newspapers around the globe ran the story on front pages. Journalists and film crews flooded into Cape Town. Christiaan Barnard—charismatic, photogenic, articulate—became an instant international celebrity. One commentator called it "another frontier crossed—a frontier no less important and far more immediate than the stars." Newsweek heralded "an era as significant as the age of the atom."
Louis Washkansky's recovery was followed hourly by media worldwide. He regained full consciousness. He talked easily with his wife. His new heart pumped strongly, clearing the fluid that had accumulated in his legs. For almost two weeks, his progress was excellent.
Then his condition began to deteriorate.
Infiltrates appeared in his lungs on X-rays. The surgical team faced an agonizing diagnostic dilemma: was this rejection—the heart failing—or infection? They elected to treat for rejection, intensifying the immunosuppressive drugs that prevented Louis's body from attacking the foreign heart.
It was a fatal error.
Louis had developed bilateral pneumonia. The enhanced immunosuppression, meant to save the heart, left him defenseless against the infection spreading through his lungs.
On December 21, 1967—eighteen days after the transplant—Louis Washkansky died of pneumonia and septicemia.
But his heart had functioned perfectly until the very end.
The death didn't stop Barnard. If anything, it focused him. He'd learned crucial lessons about the balance between preventing rejection and maintaining the immune system's ability to fight infection.
On January 2, 1968—less than two weeks after Washkansky's death—Barnard performed his second heart transplant. The patient was Philip Blaiberg. The donor was Clive Haupt, a 24-year-old Black man who had suffered a stroke.
Philip Blaiberg returned home from the hospital. He lived an active life for 593 days—nineteen months—before his body finally rejected the transplanted heart.
The success sparked a wave of transplants worldwide. Within weeks, Adrian Kantrowitz performed a transplant on an infant (who survived only two hours). Norman Shumway performed his first human transplant on January 6. By 1971, Denton Cooley and Michael DeBakey in Texas had performed over thirty transplants combined.
But the early results were devastating. Of the first 170 transplants performed worldwide, the outcomes were grim. Fifty patients died from rejection. Thirty from infections. Others from various complications. Only a third of patients lived longer than three months.
Many medical centers abandoned the procedure. By the early 1970s, only Shumway's team at Stanford continued attempting transplants regularly, slowly refining techniques and learning from every failure.
Barnard persisted. Between December 1967 and November 1974, he performed ten heart transplants at Groote Schuur Hospital. Four patients lived longer than 18 months. Two became long-term survivors.
Dorothy Fischer, his fifth patient, lived for over thirteen years. Dirk van Zyl, who received a transplant in 1971, survived for over twenty-three years—the longest-lived of Barnard's patients.
Barnard also introduced heterotopic heart transplantation—a procedure where the donor heart is placed alongside the recipient's original heart, acting as an auxiliary pump. In that early era before sophisticated immunosuppression, this approach had advantages for patients whose bodies were struggling with rejection.
The breakthrough that would transform transplant survival came in the early 1980s with cyclosporine—an immunosuppressive drug that inhibited T-cell activation more selectively than previous medications. It dramatically reduced acute rejection episodes while allowing patients to maintain better resistance to infection.
One-year survival rates, which had been below 30% in the late 1960s and 1970s, suddenly jumped to over 80%. By the 2020s, refined immunosuppressive regimens and surgical techniques have pushed survival rates even higher.
Today, heart transplantation is a relatively routine procedure performed at centers worldwide. Hundreds of thousands of lives have been saved. Patients can live decades with their transplanted hearts, maintaining active, productive lives.
Christiaan Barnard never won the Nobel Prize. He later speculated it was because he was a white South African during the apartheid era—though the real reason was likely that he'd built on decades of research by others, particularly Shumway's work.
He was married and divorced three times. In his later years, complicated by ill health and loneliness, he struggled. He died suddenly on September 2, 2001, at age 78, while on vacation in Cyprus.
But his legacy endures not in awards or accolades. It endures in every person who lives because a failing heart was replaced with a healthy one. In every family that got more years with someone they love. In the normalization of an idea that once seemed impossible—that the heart, traditionally seen as the very seat of life and identity, could be removed and replaced.
What Barnard did on that December night in 1967 required technical skill learned from years of training and practice. But it required something more: the courage to be first. To face unprecedented risk. To proceed when others hesitated.
Louis Washkansky knew he was dying. He chose to leap into unknown waters rather than wait for the lion to catch him.
Denise Darvall's family, in their moment of deepest grief, chose to give life through death.
Christiaan Barnard chose to dare.
For eighteen days in December 1967, a grocer in Cape Town lived with another woman's heart beating in his chest. It shouldn't have been possible. For all of human history, it hadn't been possible.
But that didn't make it impossible.
That distinction—between what has never been done and what cannot be done—is where medical progress lives. In the courage to attempt what seems impossible. In the willingness to fail publicly. In the determination to learn from every setback.
The first heart transplant patient died. But the procedure succeeded. The knowledge gained from Louis Washkansky's eighteen days saved Philip Blaiberg for nineteen months. The lessons from both saved Dorothy Fischer for thirteen years. And the cumulative wisdom from all those early pioneers now saves hundreds of thousands.
A human heart stopped beating in Cape Town in 1967.
For the first time in history, another heart was ready to replace it.
And the world changed.

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19/11/2025

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The standard method for closing the uterus after cesarean delivery, used for over 50 years, may be causing a host of long-term health issues for millions of women.

According to Dr. Emmanuel Bujold and Dr. Roberto Romero, leaders in obstetrics and gynecology, current closure practices—where sutures join the uterine lining with surrounding muscle—fail to restore the uterus’s natural structure, leading to serious complications.

Their exhaustive review reveals the risks: abnormal placenta attachment affects up to 6% of women, uterine rupture up to 3%, and premature births up to 28%. Many suffer pelvic pain (up to 35%), excessive bleeding (up to 33%), and endometriosis or adenomyosis (up to 43%). Such complications are linked directly to the scarring produced by the conventional closure method.

Bujold and Romero propose a nuanced technique: suturing tissues only of the same type, carefully reconstructing the muscle layer while leaving the uterine lining untouched for natural regeneration. Although this new method takes 5–8 minutes—twice as long as the traditional approach—the additional blood loss is minimal and outweighed by better outcomes for future reproductive health.

With cesarean rates rising globally, especially in countries like Canada where 27% of births are by C-section, prioritizing meticulous uterine repair is a critical public health concern. This shift in surgical thinking may help millions experience safer subsequent pregnancies and better long-term well-being.

Follow Science Sphere for regular scientific updates

📄 RESEARCH PAPER

📌 Emmanuel Bujold et al, "Uterine closure after cesarean delivery: surgical principles, biological rationale, and clinical implications", American Journal of Obstetrics and Gynecology (2025)

When you do blister prepacking...
17/11/2025

When you do blister prepacking...

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19/10/2025

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New research explores the link between ADHD stimulant use and the risk of developing psychosis or bipolar disorder.

This large-scale review of over 390,000 participants found that while these outcomes are relatively uncommon, they do occur in a small proportion of individuals treated with stimulants—particularly amphetamines, which showed about 1.6 times higher odds of psychosis compared to methylphenidate.

Risk was also influenced by factors such as higher doses, longer treatment duration, and study location. The authors emphasize that these findings do not prove stimulants cause psychosis or bipolar disorder but highlight the importance of careful monitoring and open discussion between clinicians and patients.

Read the full article here to learn more about the findings and their implications for ADHD treatment ➡️ https://mindd.org/research/10-1001-jamapsychiatry-2025-2311/

Address

Corner Of Klinkenberg And Govan Mbeki Road
Potchefstroom
2531

Opening Hours

Monday 08:30 - 18:00
Tuesday 08:30 - 18:00
Wednesday 08:30 - 18:00
Thursday 08:30 - 18:00
Friday 08:30 - 18:00
Saturday 09:00 - 14:00
Sunday 10:00 - 13:00

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+27182905171

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