Osteoporosis drugs linked to bone fractures


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Warnings that a class of drugs widely prescribed to millions of post-menopausal women to fight osteoporosis can cause bone fractures have sparked concerns the drugs are being too readily prescribed.
Health Canada announced Thursday there is evidence that women taking bisphosphonates could have increased risk of thigh bone fractures. The drugs are currently under “safety review” in Canada.
Health Canada’s announcement came after the U.S. Food and Drug Administration issued a warning Wednesday that use of bisphosphonates could result in femur fractures. The FDA will be changing drug labels to include information about this risk.
But Health Canada said the drugs’ benefits outweigh the risks.
For some people, problems with the osteoporosis drugs are reminiscent of hormone replacement therapy, also routinely prescribed to menopausal women. In 2002, a major study of HRT was found to increase the risk of breast cancer, heart attacks and strokes.
“There’s been lots of caution,” said Anne Rochon Ford, coordinator of the national Women and Health working group. “At the same time there’s been more and more promotion from the manufacturers.”
Rochon Ford said she wasn’t surprised the FDA had issued a warning, as researchers have been looking into concerns about the drugs for several years.
The drugs are sold under brand names Fosamax, Aclasta, Actonel, and Didrocal. Fosamax, which is manufactured by Merck, was the subject of a 2007 class-action lawsuit alleging the drug was associated with a higher risk of developing a jaw condition called osteonecrosis. A British study published last month linked long-term use of bisphosphonates to a slightly higher risk of esophageal cancer.
“We should not be using them in everybody,” said Dr. Aliya Khan, an osteoporosis specialist and director of McMaster University’s calcium disorders clinic. “It has to be prescribed to the right people and that may not be happening.”
Rochon Ford said the drugs are prescribed too often.
“It’s very widely used,” she said. “They’ve lowered the threshold for who should be on it. So people who have a pre-osteoporosis condition called osteopenia are now being put on it.”
Millions of people throughout North America are currently using the drug, said Dr. Elizabeth Shane, an endocrinologist and osteoporosis specialist from Columbia University in New York City.
In Canada, 1.8 million bisphosphonate prescriptions have been filled in 2010, according to data from health information company IMS Brogan.
“Osteoporosis is an extremely common disease,” said Shane. It is associated with fractures of the hip, spine and forearm. “These drugs have been the first line approach to the management and efforts to prevent these (common) fractures.”
She is in Toronto for the American Society of Bone and Mineral Research annual meeting this weekend, which will bring together bone experts from around North America.
On Saturday, a task force will present its recommendations regarding bisphosphonates and “atypical fractures.” Shane is a member of the task force that studied 310 people with thigh fractures in the United States beginning in 2009. Of those, 295 had taken bisphosphonates.
Bisphoshonates have been on the U.S. market for about 15 years, said Shane, but problems with fractures only surfaced about three years ago.
“We think they’re related to long-term use of bisphosphonates,” she said.
The drugs are safe, said Khan. They improve bone density and reduce the risk of spine, hip and forearm fractures.
“We want to be careful, especially for people who are using these drugs for more than five years,” she said.
Khan added some patients on bisphosphonates experience upper thigh and groin pain. These symptoms can be warning signs of an upcoming thigh fracture, she said, so must be reported to a doctor right away.
An osteoporosis patient named Diane Merrill posted on the “Better Bones” blog that she suffered upper thigh and groin pain for several weeks before getting an x-ray.
“The diagnosis was a stress fracture in the upper right femur. One week later . . . I got up from my kitchen table, turned, my leg gave way and I fell to the floor. It was a transverse fracture,” she wrote. “I took Fosamax for 5 years.”
Shane said it is important patients not stop taking the drug.
“Many more fractures are prevented than caused by bisphosphonates,” she said. “We do think that these (thigh fractures) are related to bisphosphonates. We don’t understand quite yet why.”
Health Canada has also announced the weight loss drug sibutramine, known by the brand name Meridia, has been pulled off the market.
Abbott Laboratories voluntarily recalled Meridia Wednesday, after a study found “risk of serious cardiovascular events associated with sibutramine use in patients with heart problems.” According to Health Canada, patients with heart problems had been advised not to take the drug since it first came on the market in 2000.

Nuevo Boletin del Drug Safety Update


Otro nuevo boletin del Drug Safety Update, nos informan los amigos de “Hemos Leido….” , como siempre desde su sitio y que figura dentro de nuestros enlaces, recomiendo que se suscriban, sin duda uno de los mejores lugares en Castellano desde donde hace un año, y desde Valencia, nos humillan con su trabajo, recordando que este año han ganado merecidamente uno de los premios de favoritos en la red. Y gracias por el ánimo que he recibido de parte de ellos. 


Este mes contiene la siguiente información:
  
         Bifosfonatos y osteonecrosis maxilar (recomendamos ver nota informativa de la AEMPS)
  
     Vigabatrina para espasmos infantiles: posibilidad de riesgo de alteraciones del movimiento.Recomiendan a los profesionales sanitarios que si se detectan en niños tratados con vigabatrina distonía, disquinesia o hipertonía consideren una reducción de la dosis o una retirada gradual del tratamiento.
  
         Colchicina: La colchicina tiene un margen terapéutico estrecho y es extremadamente tóxico en caso de sobredosis. Los pacientes en riesgo particular de toxicidad son aquellos con insuficiencia renal o hepática, enfermedad gastrointestinal o cardiaca y en pacientes con edades extremas. Los síntomas de sobredosis a menudo tardan en aparecer.
  
      Oseltamivir: han recibido 850 informes de farmacovigilancia entre el 1 de abril 2009 y 22 de octubre 2009. De las 1.489 reacciones adversas sospechosas declaradas, las más frecuentes son coherentes con los signos y síntomas de efectos secundarios reconocidos, tales como reacciones alérgicas leves, eventos gastrointestinales, cefalea y mareos, lo que también puede ser causada por enfermedad de tipo gripal.
  
Han recibido siete informes en los que el paciente murió después del tratamiento con oseltamivir. Estos casos han sido plenamente evaluados y en ninguno de ellos existen  pruebas para confirmar que el oseltamivir fue directamente responsable del hecho fatal.
  
      Zanamivir: han recibido 20 informes de farmacovigilancia entre el 1 de abril 2009 y 22 de octubre 2009. De las 39 reacciones adversas sospechosas declaradas, las más frecuentes son coherentes con los signos y síntomas de efectos secundarios reconocidos, tales como reacciones alérgicas y broncoespasmos. Eventos declarados como diarrea, náuseas, vómitos, fatiga, dolor de cabeza y mareos pueden ser causadas por la propia enfermedad gripal.
  
Ha habido un caso de muerte intrauterina después de la exposición durante el embarazo. Sin embargo, actualmente no hay evidencia para sugerir que el zanamivir (o el oseltamivir) conlleven riesgos (maternal, fetal, perinatal o postnatal) durante el embarazo. 
  
Una revisión reciente de los datos disponibles por las autoridades reguladoras europeas llevó a la recomendación de que, debido a los riesgos potencialmente graves de la gripe H1N1 porcina en el embarazo, los beneficios de usar el zanamivir (o oseltamivir) en el tratamiento de la gripe en mujeres embarazadas o en período de lactancia compensan los riesgos conocidos.
  
El Teratology Information Service (UKTIS) del Reino Unido, en colaboración con la MHRA, ha sido elegido por el Instituto Nacional de Investigación en Salud de UK para llevar a cabo un proyecto de investigación durante el actual brote de gripe porcina para aprender más acerca de los efectos de la enfermedad y sus tratamientos en el embarazo

Medwatch: bifosfonatos y fibrilacion auricular,


Bisphosphonates marketed as Alendronate (Fosamax, Fosamax Plus D)
Etidronate (Didronel)
Ibandronate (Boniva)
Pamidronate (Aredia)
Risedronate (Actonel, Actonel W/Calcium)
Tiludronate (Skelid)
Zoledronic acid (Reclast, Zometa)

En Argentina se pueden ver los nombres comerciales desde la pagina de Alfabeta

Audience: Geriatricians, gynecologists, orthopedic surgeons, other healthcare professionals
FDA issued an update about the Agency’s review of safety data regarding the potential increased risk of atrial fibrillation in patients treated with a bisphosphonate drug. Bisphosphonates are a class of drugs used primarily to increase bone mass and reduce the risk for fracture in patients with osteoporosis, slow bone turnover in patients with Paget’s disease of the bone, and to treat bone metastases and lower elevated levels of blood calcium in patients with cancer. FDA reviewed data on 19,687 bisphosphonate-treated patients and 18,358 placebo-treated patients who were followed for 6 months to 3 years. The occurrence of atrial fibrillation was rare within each study, with most studies containing 2 or fewer events. Across all studies, no clear association between overall bisphosphonate exposure and the rate of serious or non-serious atrial fibrillation was observed. Additionally, increasing dose or duration of bisphosphonate therapy was not associated with an increase rate of atrial fibrillation. Healthcare professionals should not alter their prescribing patterns for bisphosphonates and patients should not stop taking their bisphosphonate medication.

Read the entire 2008 MedWatch Safety Summary, including a link to the FDA Update of Safety Review Follow-up to the October 1, 2007, Early Communication about the Ongoing Safety Review of Bisphosphonates, regarding this issue at:

http://www.fda.gov/medwatch/safety/2008/safety08.htm#bisphosphonates2


Medwatch: bifosfonatos y fibrilacion auricular,


Bisphosphonates marketed as Alendronate (Fosamax, Fosamax Plus D)
Etidronate (Didronel)
Ibandronate (Boniva)
Pamidronate (Aredia)
Risedronate (Actonel, Actonel W/Calcium)
Tiludronate (Skelid)
Zoledronic acid (Reclast, Zometa)

En Argentina se pueden ver los nombres comerciales desde la pagina de Alfabeta

Audience: Geriatricians, gynecologists, orthopedic surgeons, other healthcare professionals
FDA issued an update about the Agency’s review of safety data regarding the potential increased risk of atrial fibrillation in patients treated with a bisphosphonate drug. Bisphosphonates are a class of drugs used primarily to increase bone mass and reduce the risk for fracture in patients with osteoporosis, slow bone turnover in patients with Paget’s disease of the bone, and to treat bone metastases and lower elevated levels of blood calcium in patients with cancer. FDA reviewed data on 19,687 bisphosphonate-treated patients and 18,358 placebo-treated patients who were followed for 6 months to 3 years. The occurrence of atrial fibrillation was rare within each study, with most studies containing 2 or fewer events. Across all studies, no clear association between overall bisphosphonate exposure and the rate of serious or non-serious atrial fibrillation was observed. Additionally, increasing dose or duration of bisphosphonate therapy was not associated with an increase rate of atrial fibrillation. Healthcare professionals should not alter their prescribing patterns for bisphosphonates and patients should not stop taking their bisphosphonate medication.

Read the entire 2008 MedWatch Safety Summary, including a link to the FDA Update of Safety Review Follow-up to the October 1, 2007, Early Communication about the Ongoing Safety Review of Bisphosphonates, regarding this issue at:

http://www.fda.gov/medwatch/safety/2008/safety08.htm#bisphosphonates2