Image Of Alendronate Sodium Chemical Structure (Fosamax 01)
Fosamax Tablet
Product Images NDC 78206-135
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Product Visual Gallery
This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Fosamax (NDC 78206-135). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Organon Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Product Images & Figures Index
Image Of Figure 1 (Fosamax 02)
The text provides a graph displaying the cumulative incidence of hip fractures in a three-year study of patients with radiographic vertebral fracture at baseline. The graph compares the incidence rate between two treatments: placebo and FOSAMAX. It shows the incidence rate increases over time for both treatments, but FOSAMAX appears to have a lower incidence rate of hip fractures compared to the placebo.*
Image Of Figure 2 (Fosamax 03)
This is a report on the osteoporosis treatment studies conducted on postmenopausal women. The report indicates an increase in bone mineral density (BMD) after three years of treatment with FOSAMAX 10 mg/day. The report also includes measurements for the lumbar spine, femoral neck, and trochanter.*
Image Of Figure 3 (Fosamax 04)
This appears to be a chart or graph showing the percent change in bone mineral density (BMD) of postmenopausal women with osteoporosis treated with FOSAMAX 10 mg/day versus a placebo. The study was conducted over the course of several months, but the exact duration is not clear. The chart compares the mean % change from baseline for FOSAMAX 10 mg/day and placebo, with error bars indicating the standard error.*
Image Of Figure 4 (Fosamax 05)
This appears to be a table showing the mean percentage change with standard error in bone mineral density (BMD) measured in different regions of the skeleton, in postmenopausal women in two osteoporosis prevention studies. The studies compared the change in BMD over two and three years in the treatment group (which received Fosamax, a drug used to treat osteoporosis) to the change in the placebo group (which did not receive the drug). The regions of the skeleton measured were the lumbar spine, femoral trochanter, total hip, and body.*
Image Of Figure 5 (Fosamax 06)
This is a table with some information about a study on the increase in bone mineral density (BMD) in patients treated with glucocorticoids. The table shows the mean percentage increase in BMD relative to a placebo, with standard error (SE) for each category. The categories listed are the Lumbar Spine, Femoral Neck, and Trochanter. The treatment used was FOSAMAX at a dose of 5mg per day for one year. The rest of the text is not readable.*
Image Of Figure 6 (Fosamax 07)
This is a study that compares the effect of FOSAMAX 40 mg/day versus placebo or etidronate 400 mg/day on serum alkaline phosphatase in patients with Paget's disease of bone. The study was conducted in two groups, a multinational study and a US study, involving a total of 27 patients in the placebo group, 8 patients in the etidronate group, and an unspecified number of patients in the FOSAMAX group. The study monitored the patients over a period of 6 months.*
Principal Display Panel (4 Tablet Blister Pack)
This appears to be a medication label for Fosamax, a drug used to treat or prevent osteoporosis. It provides instructions for the dosage and administration of the medication. The label includes information such as the product name, dosage strength, and manufacturer details. It also has a space reserved for a 2D serialization barcode, serial number, expiry, and lot number.*
* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.
