Indications
Alendon is used in several bone conditions. Treatment of osteoporosis in postmenopausal women: Alendon is used to treat osteoporosis in women after menopause. In these women it increases bone mass and lowers the number of fractures, including fractures of the hip and spine. Prevention of osteoporosis in postmenopausal women: Alendon is also used to prevent osteoporosis after menopause. Increasing bone mass in men with osteoporosis: Alendon is used to increase bone mass in men who have osteoporosis. Glucocorticoid-induced osteoporosis: Alendon is used to treat osteoporosis caused by glucocorticoids, in both men and women. This applies to people taking glucocorticoids at a daily dose equivalent to 7.5 mg or more of prednisone, and who have low bone mineral density. Paget's disease of bone: Alendon is used to treat Paget's disease of bone in men and women. Treatment is indicated for patients whose alkaline phosphatase is at least two times the upper limit of normal, for those who have symptoms, and for those at risk of future complications from the disease.
⚠️ Always consult a registered physician before taking any medicine.
Pharmacology
Alendronate is a bisphosphonate that binds to bone hydroxyapatite and specifically inhibits the activity of osteoclasts, the bone-resorbing cells. Alendronate reduces bone resorption with no direct effect on bone formation, although the latter process is ultimately reduced because bone resorption and formation are coupled during bone turnover.
Animal studies have indicated the following mode of action. At the cellular level, alendronate shows preferential localization to sites of bone resorption, specifically under osteoclasts. The osteoclasts adhere normally to the bone surface but lack the ruffled border that is indicative of active resorption. Alendronate does not interfere with osteoclast recruitment or attachment, but it does inhibit osteoclast activity. Studies in mice on the localization of radioactive [3H] alendronate in bone showed about 10 fold higher uptake on osteoclast surfaces than on osteoblast surfaces. Bones examined 6 and 49 days after [3H] alendronate administration in rats and mice, respectively, showed that normal bone was formed on top of the alendronate, which was incorporated inside the matrix. While incorporated in bone matrix, alendronate is not pharmacologically active. Thus, alendronate must be continuously administered to suppress osteoclasts on newly formed resorption surfaces. Histomorphometry in baboons and rats showed that alendronate treatment reduces bone turnover (that is, the number of sites at which bone is remodeled). In addition, bone formation exceeds bone resorption at these remodeling sites, leading to progressive gains in bone mass.
Pregnancy & Breastfeeding
Alendronic acid should not be given to pregnant women or to mothers who are breastfeeding.
⚠️ Talk to your doctor before taking any medicine during pregnancy or while breastfeeding.
Dosage Reference
⚠️ Reference ranges from official sources only. Consult your doctor for personalized dosing.