Fosamax
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| Fri, 05-12-2006 - 5:44pm |
I was just reading this article about Fosamax and how some people are concerned about the jaw. I copied and pasted this article for those that are concerned, but I do want to say that I have been on Fosamax for almost 10 years, and so far so good. Just thought I would put my 2¢ worth in here for those are faced with possibly taking a bone building product if they are on a thyroid med. Bea
Statement by Merck & Co., Inc. Regarding FOSAMAX® (alendronate sodium) and Rare Cases of Osteonecrosis of the Jaw
April 14, 2006 - Merck is committed to putting patients first and providing accurate information regarding the efficacy, safety and tolerability of our medicines. Merck offers the following statement in response to news reports concerning the osteoporosis medication FOSAMAX® (alendronate sodium) and reports of jaw problems associated with delayed healing and infection of the jaw often following tooth extraction. The condition is known as osteonecrosis of the jaw (ONJ).
ONJ is not well understood and may occur for a number of reasons. Most reported cases of bisphosphonate-associated osteonecrosis have been in cancer patients treated with intravenous bisphosphonates, but cases have occurred in patients with postmenopausal osteoporosis and other diagnoses. Known risk factors for osteonecrosis include a diagnosis of cancer, concomitant therapies (e.g., chemotherapy, radiotherapy, corticosteroids), poor oral hygiene, and co-morbid disorders (e.g., pre-existing dental disease, anemia, coagulopathy, infection).
In all of our controlled clinical trials, including the 10 year data with FOSAMAX, which have included more than 17,000 patients, we have not had reports of osteonecrosis of the jaw occurring in patients taking FOSAMAX.
Merck has received post-marketing reports described as osteonecrosis of the jaw occurring in patients taking FOSAMAX. Post marketing reports do not necessarily indicate causality.
On January 31, 2005, Merck received a request dated January 24, 2005 from the Food and Drug Administration to update the label for FOSAMAX to include bisphosphonate class labeling for ONJ. Merck submitted a draft revised label to FDA on March 1, 2005. FDA comments on this draft revised label were received in June 2005, and the new label was made publicly available in July, 2005.
Rare cases of ONJ have also been reported in patients who do not have osteoporosis and who have not taken any bisphosphonate medicines. These cases have been discussed in articles that have been published in the medical literature.
All products containing FOSAMAX include the following language pertaining to ONJ in the "Precautions" section of their respective package circular:
* Osteonecrosis of the jaw, generally associated with tooth extraction and/or local infection, often with delayed healing, has been reported in patients taking bisphosphonates. Most reported cases of bisphosphonate-associated osteonecrosis have been in cancer patients treated with intravenous bisphosphonates, but some have occurred in patients with postmenopausal osteoporosis. Known risk factors for osteonecrosis include a diagnosis of cancer, concomitant therapies (e.g., chemotherapy, radiotherapy, corticosteroids), poor oral hygiene, and co-morbid disorders (e.g., pre-existing dental disease, anemia, coagulopathy, infection).
* Patients who develop osteonecrosis of the jaw (ONJ) while on bisphosphonate therapy should receive care by an oral surgeon. Dental surgery may exacerbate the condition. For patients requiring dental procedures, there are no data available to suggest whether discontinuation of bisphosphonate treatment reduces the risk for ONJ. Clinical judgment of the treating physician should guide the management plan of each patient based on individual benefit/risk assessment.
Information for ONJ is also provided in the "Adverse Reactions" section of the package circular as well as in the patient package insert for the products containing FOSAMAX. As part of a review of your medical history with your healthcare providers (such as dentists, physicians, oral surgeons or others), be sure to include any product containing FOSAMAX in your list of medicines and talk to your healthcare provider if you have any questions about FOSAMAX.
FOSAMAX is indicated for the treatment of osteoporosis in postmenopausal women. For the treatment of osteoporosis, FOSAMAX increases bone mass and reduces the incidence of fracture, including those of the hip and spine. FOSAMAX is also indicated to increase bone mass in men with osteoporosis.
Osteoporosis, the most prevalent bone disease in the U.S., can lead to bone loss and an increased risk of fractures. Over 10 million Americans over the age of 50 have osteoporosis and another 34 million have low bone mass. Osteoporosis is especially common in women after menopause, but also occurs in older men. Most often, it is due to an increase in the rate of resorption (breakdown) of bone tissue that is not matched by the rate of bone formation. The risk of having an osteoporosis-related fracture increases with age. According to the Surgeon General, osteoporosis is a national health threat and by 2020 one in two Americans over the age of 50 will be at risk for fractures from osteoporosis or low bone mass. In fact, one out of every two women over age 50 will have an osteoporosis-related fracture in their remaining lifetime, with the risk of fracture increasing with age.
Important information about FOSAMAX
FOSAMAX, like other bisphosphonate containing products, should be used with caution in people with certain stomach or digestive problems. FOSAMAX should not be used if the patient has certain disorders of the esophagus that delay emptying or if the patient is unable to stand or sit upright for at least 30 minutes. In addition, FOSAMAX should not be used in patients with severe kidney disease or low levels of calcium in their blood, in patients who are allergic to FOSAMAX or in patients who are pregnant or nursing. Patients who have difficulty swallowing liquids should not take FOSAMAX oral solution.
Some patients may develop severe digestive reactions including irritation, inflammation or ulceration of the esophagus. The risk of severe esophageal experiences appears to be greater in patients who fail to follow dosing instructions (see prescribing information for more details). Patients who experience new or worsening heartburn, difficulty or pain when swallowing or chest pain should stop taking the drug and call their doctor right away. Patients who develop severe bone, joint and/or muscle pain at any time should contact their doctor.
The standard dosing regimen for FOSAMAX includes swallowing the tablet with six to eight ounces of plain water the first thing upon arising for the day and at least 30 minutes before the first food, beverage or medication of the day. After swallowing FOSAMAX, patients should not lie down for at least 30 minutes and not until after consuming their first food of the day. Patients should not chew or suck on a tablet of FOSAMAX.
For more information on products containing FOSAMAX, please see and read the prescribing information and patient package insert which are available at www.fosamax.com.
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Addendum: Several independent organizations have published statements related to osteonecrosis of the jaw (ONJ). Merck & Co, Inc., does not necessarily endorse the perspectives or opinions expressed within these statements. Also, the prescribing information of currently available intravenous and oral bisphosphonates may provide information about ONJ. To help healthcare professionals in their efforts to understand ONJ, a non-exhaustive list of online addresses associated with independent organizations and available intravenous and oral bisphosphonates is provided as follows.
Information from the National Institutes of Health
http://www.niams.nih.gov/bone/hi/oralhealth_bone.htm
Background from the American Dental Association
http://www.ada.org/prof/resources/topics/osteonecrosis.asp
Statement from the National Osteoporosis Foundation
http://www.nof.org/news/pressreleases/osteonecrosis.htm
Prescribing Information for Oral Bisphosphonates
http://www.fosamax.com/fosamax/shared/documents/english/pi.pdf
http://www.fosamax.com/fosamax/shared/documents/english/pi_plus_d.pdf
http://www.actonel.com/global/prescribingInfo-040506.pdf
http://www.actonel.com/global/prescribingInfo-AwC-040506.pdf
http://www.rocheusa.com/products/Boniva/PI.pdf
http://www.pgpharma.com/pi/US-Didronel.pdf
http://www.products.sanofi-aventis.us/skelid/skelid.html
Prescribing Information for IV Bisphosphonates
http://www.rocheusa.com/products/Boniva/Injection_PI.pdf
http://www.pharma.us.novartis.com/product/pi/pdf/Zometa.pdf
http://www.pharma.us.novartis.com/product/pi/pdf/aredia.pdf
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