Skip to main content

Which Medications are Commonly used for Osteoporosis Treatment?



Bisphosphonates are the most common medications prescribed for osteoporosis treatment. These include:
·         Alendronate (Fosamax)
·         Risedronate (Actonel)
·         Ibandronate (Boniva)
·         Zoledronic acid (Reclast)
Hormones, such as estrogen, can play a role in osteoporosis prevention and treatment. However, there has been some concern about potential side effects tied to the use of hormone therapy. Current recommendations say to use the lowest dose of hormones for the shortest period of time.
Still, women who have reasons — such as menopausal symptoms — to consider using hormones can weigh the benefit of improved bone health into their decision.
Some hormonelike medications also are approved for preventing and treating osteoporosis, such as raloxifene (Evista).
Denosumab (Prolia, Xgeva) is a newer medication shown to reduce the risk of osteoporotic fracture in women and men. Unrelated to bisphosphonates, denosumab might be used in people who can't take a bisphosphonate, such as some people with reduced kidney function.
Teriparatide (Forteo) is typically reserved for men and postmenopausal women who have very low bone density, who have had fractures or whose osteoporosis is caused by steroid medication. Teriparatide has the potential to rebuild bone.
Abaloparatide (Tymlos) is the newest osteoporosis medication. Like teriparatide, it has the potential to rebuild bone. In a research trial comparing these two treatments, abaloparatide appeared to be as effective as teriparatide but was less likely to cause an excess of calcium.

Comments

  1. For more information please search for the books "The Theory of Autoimmunity" and "Rebellious Thoughts about Osteoorosis" by Tanya G. Guleria in amazon.com

    ReplyDelete

Post a Comment

Popular posts from this blog

In Search of The Perfect Sleep Aid

 For many years, modern medicine has been searching for the perfect sleeping pills. Sleeping pills are a special topic in medicine because they have a lot to do with addiction medicine. Of course, not every sleeping pill can cause addiction, but lighter sleeping pills such as valerian tablets, doxylamine succinate (contained in Schlafsterne), melatonin (or Circadin) have short and insufficient effects. Benzodiazepines, on the other hand, relieve anxiety, which often leads to sleep disorders and are often used by GPs as sleeping pills, although this is not correct. Antidepressants such as mirtazapine are more often used as sleeping pills, but patients often complain of fatigue and drowsiness after their use, which is incompatible with driving, for example. Z-drugs are the 3rd choice of sleep medicine, they have a long and sufficient effect, but can be very addictive. There are patients who struggle for years with addiction to zolpidem, or zopiclone. Many GPs give up in this fight an...

Why Ozempic Causes Blindness?

What Is Ozempic? Ozempic (semaglutide) Injection is a  glucagon -like  peptide  1 (GLP-1) receptor  agonist  indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2  diabetes mellitus . What Are Side Effects of Ozempic? Ozempic may cause serious side effects including: a lump in the neck, difficulty swallowing, cough, shortness of breath, difficulty breathing, upper abdominal pain, nausea, vomiting, blurred vision, spots or dark strings floating in your vision, fluctuating vision, vision loss, dark or empty areas in your vision, shakiness, nervousness, anxiety, sweating, chills, clamminess, irritability, impatience, confusion, fast heartrate, lightheadedness , dizziness, hunger, decreased urination, swelling in your legs, ankles, or feet, fatigue, rash, itching, and shock Get medical help right away, if you have any of the symptoms listed above....

New Look on Antihypertensive Therapy

  Angiotensin converting enzyme 2   Angiotensin converting enzyme 2, or ACE2, is an exopeptidase expressed primarily by vascular endothelial cells in the heart and kidneys, but also in respiratory epithelia[1] and in the gastrointestinal tract. It is the target of several coronaviruses, including SARS-CoV and SARS-CoV-2. 2 Biochemistry ACE2 is a transmembrane metallocarboxypeptidase composed of 805 amino acids. Zinc and chloride ions act as cofactors. The extracellular region consists of two domains, a zinc metallopeptidase domain and a C-terminal collectrin homology domain. The enzyme exhibits homology to angiotensin converting enzyme (ACE). ACE2 is encoded by the ACE2 gene on the X chromosome (gene locus Xp22.2). In addition to being expressed as a transmembrane protein, a soluble form exists in serum. 3 Function ACE2 cleaves angiotensin II into angiotensin (1-7), which has anti-inflammatory and lung protective effects via MAS and AT2 receptors. 4 Clinical ...