Fosamax Safety Questions, Fosamax Answers
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Fosamax Safety Reports
Total Fosamax reports: 2271.Fosamax FDA safety alerts: 2007 2008 .
Reported deaths: 153 Reported hospitalizations: 1057.
Take Fosamax Side Effects Survey or Share Your Fosamax Story.
Reported Fosamax Side Effects: osteonecrosis, depression, anxiety disorder, anxiety, fall, arthralgia, death, chest pain, back pain, arthropathy, impaired healing.
Fosamax Usage.
< Previous Showing 101-150 of 2271 Next >
Fosamax Side Effects Report #5229324-5Consumer or non-health professional from UNITED STATES reported FOSAMAX problem on Feb 02, 2007. Female patient, 86 years of age, was diagnosed with bone density decreased and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: gingival infection, jaw fracture. FOSAMAX dosage: unknown. During the same period patient was treated with CARDIZEM, MICARDIS, LIPITOR, IMDUR. Patient recovered.
Fosamax Side Effects Report #5229326-9
FOSAMAX problem was reported by a Physician from JAPAN on Jan 26, 2007. Female patient, 52 years of age, was diagnosed with osteoporosis, hypoparathyroidism secondary, constipation and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: anaphylactic reaction. FOSAMAX dosage: unknown. During the same period patient was treated with THYRADIN, ROCALTROL, CALCIUM LACTATE, BENET. Patient recovered.
Fosamax Side Effects Report #5231137-5
Physician from JAPAN reported FOSAMAX problem on Jan 31, 2007. Female patient, 65 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: blood pressure increased. FOSAMAX dosage: unknown. During the same period patient was treated with GLAKAY. Patient recovered.
Fosamax Side Effects Report #5231139-9
FOSAMAX problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 23, 2007. Female patient, 67 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: cerebrovascular accident, gingival atrophy, pain in jaw. FOSAMAX dosage: unknown. During the same period patient was treated with DILANTIN. Patient recovered.
Fosamax Side Effects Report #5231140-5
Health Professional from UNITED STATES reported FOSAMAX problem on Feb 02, 2007. Female patient, 72 years of age, weighting 125.7 lb, was diagnosed with osteoporosis, compression fracture and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: diarrhoea, spinal fracture. FOSAMAX dosage: unknown. During the same period patient was treated with SYNTHROID, FORTEO, HYDROCHLOROTHIAZIDE. Patient recovered.
Fosamax Side Effects Report #5232679-9
FOSAMAX problem was reported by a Physician from JAPAN on Jan 31, 2007. Female patient, 82 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: cerebral infarction. FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.
Fosamax Side Effects Report #5232681-7
Physician from JAPAN reported FOSAMAX problem on Jan 31, 2007. Female patient, 49 years of age, was diagnosed with osteoporosis prophylaxis, inflammation, prophylaxis against gastrointestinal ulcer and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: hepatic function abnormal. FOSAMAX dosage: unknown. During the same period patient was treated with PREDONINE, ECABET, PARIET. Patient was hospitalized. Patient recovered.
Fosamax Side Effects Report #5234125-8
FOSAMAX problem was reported by a Consumer or non-health professional from AUSTRALIA on Feb 05, 2007. Male patient, 79 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: bone scan abnormal, fall, impaired healing, prostatic disorder. FOSAMAX dosage: unknown. During the same period patient was treated with DICLOFENAC. Patient was hospitalized and became disabled. Patient recovered.
Fosamax Side Effects Report #5234131-3
Consumer or non-health professional from AUSTRALIA reported FOSAMAX problem on Feb 05, 2007. Female patient, 61 years of age, was diagnosed with osteoporosis, blood cholesterol abnormal, hiatus hernia and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: arthralgia, bone density decreased, cerebrovascular accident, spinal compression fracture. FOSAMAX dosage: unknown. During the same period patient was treated with ATORVASTATIN CALCIUM, ESOMEPRAZOLE MAGNESIUM. Patient recovered.
Fosamax Side Effects Report #5234518-9
FOSAMAX problem was reported by a Physician from JAPAN on Feb 02, 2007. Female patient, 52 years of age, was diagnosed with osteoporosis, hypoparathyroidism secondary, constipation and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: anaphylactic reaction. FOSAMAX dosage: unknown. During the same period patient was treated with THYRADIN, ROCALTROL, CALCIUM LACTATE, BENET. Patient recovered.
Fosamax Side Effects Report #5234522-0
Health Professional from AUSTRALIA reported FOSAMAX problem on Feb 05, 2007. Female patient, 76 years of age, was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: gingivitis, malocclusion, osteonecrosis, periodontitis. FOSAMAX dosage: unknown. During the same period patient was treated with VERAPAMIL HYDROCHLORIDE. Patient recovered.
Fosamax Side Effects Report #5234523-2
FOSAMAX problem was reported by a Health Professional from AUSTRALIA on Feb 05, 2007. Male patient, 42 years of age, was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: osteonecrosis. FOSAMAX dosage: unknown. During the same period patient was treated with CALCIUM CARBONATE. Patient recovered.
Fosamax Side Effects Report #5234868-6
Consumer or non-health professional from AUSTRALIA reported FOSAMAX problem on May 08, 2006. Female patient, 86 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. FOSAMAX dosage: unknown. Patient died on 12/18/2005.
Fosamax Side Effects Report #5234869-8
FOSAMAX problem was reported by a Physician from ITALY on Feb 05, 2007. Male patient, 81 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: haemolytic anaemia. FOSAMAX dosage: unknown. During the same period patient was treated with PREDNISONE, CHLOROQUINE, CALCIUM CARBONATE AND CHOLECALCIFEROL, LANSOPRAZOLE, AMOXICILLIN AND CLAVULANATE POTASSIUM, ENOXAPARIN, ILOPROST. Patient was hospitalized. Patient recovered.
Fosamax Side Effects Report #5234871-6
Physician from UNITED STATES reported FOSAMAX problem on Feb 05, 2007. Female patient, 96 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: gingivitis, tooth infection. FOSAMAX dosage: unknown. During the same period patient was treated with BUMEX, LEXAPRO, NASONEX. Patient recovered.
Fosamax Side Effects Report #5234882-0
FOSAMAX problem was reported by a Consumer or non-health professional from AUSTRALIA on Feb 06, 2007. Male patient, 81 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. FOSAMAX dosage: unknown. Patient died on 10/09/2006.
Fosamax Side Effects Report #5235085-6
Consumer or non-health professional from JAPAN reported FOSAMAX problem on Jan 26, 2007. Female patient was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: hypercalcaemia. FOSAMAX dosage: 5 MG/DAILY. During the same period patient was treated with TAB ONEALFA, ALFAROL. Patient was hospitalized. Patient recovered.
Fosamax Side Effects Report #5235785-8
FOSAMAX problem was reported by a Physician from UNITED STATES on Feb 01, 2007. Female patient, 73 years of age, weighting 167.6 lb, was diagnosed with osteoporosis, breast cancer, prophylaxis, asthma, dyspepsia, hypertension and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: arthralgia, feeling abnormal, neck pain. FOSAMAX dosage: unknown. During the same period patient was treated with TAMOXIFEN CITRATE, ASPIRIN, FLOVENT, ALBUTEROL, PRILOSEC OTC, CLARITIN, DIOVAN. Patient recovered.
Fosamax Side Effects Report #5235793-7
Physician from JAPAN reported FOSAMAX problem on Feb 05, 2007. Female patient, 80 years of age, was diagnosed with osteoporosis, pollakiuria and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: hepatic function abnormal, jaundice, malaise. FOSAMAX dosage: unknown. During the same period patient was treated with AMLODIPINE BESYLATE, SAWADARON. Patient was hospitalized. Patient recovered.
Fosamax Side Effects Report #5235804-9
FOSAMAX problem was reported by a Physician from JAPAN on Feb 06, 2007. Male patient, 62 years of age, weighting 110.2 lb, was diagnosed with osteoporosis, gastric ulcer, infection prophylaxis, polymyalgia rheumatica and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: agranulocytosis, disseminated intravascular coagulation, dysphagia, epiglottitis, pharyngitis, platelet count decreased, sepsis, tonsillitis, white blood cell count decreased. FOSAMAX dosage: unknown. During the same period patient was treated with TAKEPRON, BAKTAR, PREDNISOLONE. Patient was hospitalized. Patient recovered.
Fosamax Side Effects Report #5236501-6
Consumer or non-health professional from UNITED STATES reported FOSAMAX problem on Feb 06, 2007. Female patient, 49 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: anxiety, depression, gastric disorder, lipoprotein (a) increased, migraine, osteomyelitis, osteonecrosis, temporomandibular joint syndrome, uterine leiomyoma. FOSAMAX dosage: unknown. During the same period patient was treated with ACTONEL, HYDROCORTISONE, MIACALCIN. Patient recovered.
Fosamax Side Effects Report #5236511-9
FOSAMAX problem was reported by a Physician from JAPAN on Feb 07, 2007. Female patient, 85 years of age, weighting 176.4 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: glossitis, jaundice, stomatitis. FOSAMAX dosage: unknown. During the same period patient was treated with TRIAZOLAM, SELECTOL, ALFACALCIDOL, MEXILETINE HYDROCHLORIDE, LIPITOR, ADEFURONIC, EPERISONE HYDROCHLORIDE. Patient recovered.
Fosamax Side Effects Report #5236959-2
Consumer or non-health professional from JAPAN reported FOSAMAX problem on Feb 01, 2007. Female patient, 80 years of age, weighting 127.9 lb, was diagnosed with nail tinea and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood albumin decreased, blood alkaline phosphatase increased, blood bilirubin increased, c-reactive protein increased, eczema, erythema. FOSAMAX dosage: unknown. During the same period patient was treated with ASPARA, ONEALFA, LAMISIL. Patient was hospitalized. Patient recovered.
Fosamax Side Effects Report #5237230-5
FOSAMAX problem was reported by a Physician from JAPAN on Feb 02, 2007. Female patient, 88 years of age, was diagnosed with osteoporosis, insomnia, urinary incontinence, gastrointestinal disorder and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: hepatic function abnormal, spinal osteoarthritis. FOSAMAX dosage: unknown. During the same period patient was treated with ZOLPIDEM TARTRATE, FLOMOX, PROPIVERINE HYDROCHLORIDE, MUCOSTA, TAKEPRON, LENDORMIN. Patient was hospitalized. Patient recovered.
Fosamax Side Effects Report #5237576-0
Physician from NEW ZEALAND reported FOSAMAX problem on Feb 12, 2007. Female patient, 86 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: adverse event, chest pain. FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.
Fosamax Side Effects Report #5237811-9
FOSAMAX problem was reported by a Health Professional from UNITED STATES on Feb 12, 2007. Female patient, 76 years of age, weighting 172.0 lb, was diagnosed with osteoporosis, sleep disorder, addison's disease and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: asthenia, coordination abnormal, deafness unilateral, dizziness, fatigue, herpes simplex, nausea, sneezing, tinnitus. FOSAMAX dosage: unknown. During the same period patient was treated with CLONAZEPAM, CORTEF, DILTIAZEM HYDROCHLORIDE, FLORINEF, MEVACOR, MOBIC, NEXIUM, TRIMETHOPRIM. Patient recovered.
Fosamax Side Effects Report #5237815-6
Physician from UNITED STATES reported FOSAMAX problem on Feb 08, 2007. Male patient, 85 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: tibia fracture. FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.
Fosamax Side Effects Report #5238454-3
FOSAMAX problem was reported by a Physician from JAPAN on Feb 09, 2007. Female patient, 68 years of age, was diagnosed with osteoporosis, hypertension, hyperlipidaemia and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: abscess neck, osteomyelitis, septic shock. FOSAMAX dosage: unknown. During the same period patient was treated with NORVASC, RENIVACE, LUPRAC, PREDNISOLONE, ETODOLAC, LIPITOR, LAFUTIDINE. Patient was hospitalized and became disabled. Patient recovered.
Fosamax Side Effects Report #5238456-7
Consumer or non-health professional from NEW ZEALAND reported FOSAMAX problem on Feb 12, 2007. Female patient, 78 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: upper gastrointestinal haemorrhage. FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.
Fosamax Side Effects Report #5238638-4
FOSAMAX problem was reported by a Physician from UNITED STATES on Feb 14, 2007. Female patient, 70 years of age, weighting 110.0 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: impaired healing, mucosal ulceration, post procedural complication. FOSAMAX dosage: 10 MG DAILY DAILY ORAL. Patient recovered.
Fosamax Side Effects Report #5238920-0
Physician from JAPAN reported FOSAMAX problem on Feb 06, 2007. Female patient, 82 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: hemiplegia. FOSAMAX dosage: unknown. During the same period patient was treated with INDOMETHACIN. Patient was hospitalized. Patient recovered.
Fosamax Side Effects Report #5238922-4
FOSAMAX problem was reported by a Health Professional from UNITED KINGDOM on Feb 09, 2007. Female patient, 61 years of age, weighting 183.0 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: arthralgia, swelling. FOSAMAX dosage: unknown. During the same period patient was treated with CALCIUM CARBONATE AND CHOLECALCIFEROL. Patient recovered.
Fosamax Side Effects Report #5238934-0
Physician from JAPAN reported FOSAMAX problem on Dec 28, 2006. Female patient, 59 years of age, weighting 127.9 lb, was diagnosed with osteoporosis, systemic sclerosis, gastritis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: abdominal distension, abdominal pain upper, ascites, blood bilirubin increased, blood bilirubin unconjugated increased, epistaxis, haemolytic uraemic syndrome, hepatic vein stenosis. FOSAMAX dosage: unknown. During the same period patient was treated with PREDNISOLONE, TEPRENONE, CALCITRIOL, GASTER D. Patient was hospitalized and became disabled. Patient recovered.
Fosamax Side Effects Report #5239569-6
FOSAMAX problem was reported by a Consumer or non-health professional from BRAZIL on Jan 25, 2007. Female patient, 68 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, blood urea increased, decubitus ulcer, haemoglobin abnormal, hyponatraemia, inappropriate antidiuretic hormone secretion, interstitial lung disease, lymphocyte count abnormal, neutrophil count abnormal. FOSAMAX dosage: 10 MG/DAILY PO. During the same period patient was treated with CARBAMAZEPINE, CEFEPIME, CHLOROQUINE, DEXAMETHASONE, DIAZEPAM, LEVOTHYROXINE, METHOTREXATE. Patient was hospitalized. Patient recovered.
Fosamax Side Effects Report #5239663-X
Consumer or non-health professional from AUSTRALIA reported FOSAMAX problem on Feb 13, 2007. Female patient, 89 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. FOSAMAX dosage: unknown. Patient died on 07/01/2006.
Fosamax Side Effects Report #5240000-5
FOSAMAX problem was reported by a Health Professional from UNITED STATES on Feb 07, 2007. Female patient, 80 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: gastrointestinal haemorrhage. FOSAMAX dosage: unknown. Patient died.
Fosamax Side Effects Report #5240005-4
Health Professional from UNITED STATES reported FOSAMAX problem on Feb 07, 2007. Female patient, 67 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: amino acid level abnormal, anxiety disorder, blood cholesterol increased, blood pressure, convulsion, depression, osteomyelitis, osteonecrosis. FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.
Fosamax Side Effects Report #5240644-0
FOSAMAX problem was reported by a Physician from UNITED STATES on Feb 09, 2007. Female patient, 68 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: oroantral fistula. FOSAMAX dosage: unknown. During the same period patient was treated with PREDNISONE, METHOTREXATE. Patient recovered.
Fosamax Side Effects Report #5241033-5
Consumer or non-health professional from UNITED STATES reported FOSAMAX problem on Feb 13, 2007. Female patient, 71 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: lip and/or oral cavity cancer. FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.
Fosamax Side Effects Report #5241036-0
FOSAMAX problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 12, 2007. Female patient, 76 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: gastrointestinal ulcer, hip fracture. FOSAMAX dosage: unknown. During the same period patient was treated with ATENOLOL. Patient was hospitalized. Patient recovered.
Fosamax Side Effects Report #5241038-4
Physician from JAPAN reported FOSAMAX problem on Feb 09, 2007. Female patient, 63 years of age, was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: temporomandibular joint syndrome. FOSAMAX dosage: unknown. During the same period patient was treated with ALFAROL, CALCIUM LACTATE, PURSENNID, HALCION. Patient recovered.
Fosamax Side Effects Report #5242075-6
FOSAMAX problem was reported by a Health Professional from UNITED STATES on Feb 16, 2007. Male patient, 61 years of age, weighting 134.5 lb, was diagnosed with osteoporosis, arthritis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: loose tooth, osteonecrosis, overdose, tooth disorder, volvulus. FOSAMAX dosage: unknown. Patient recovered.
Fosamax Side Effects Report #5242222-6
Physician from UNITED STATES reported FOSAMAX problem on Feb 12, 2007. Female patient, weighting 196.5 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: bone disorder, pain in jaw. FOSAMAX dosage: 70 MG Q WK PO. During the same period patient was treated with DARVOCET, FLEXERIL, PROVENTIL, GLUCOPHAGE, PRILOSEC, NORVASC, LOTENSIN. Patient recovered.
Fosamax Side Effects Report #5242829-6
FOSAMAX problem was reported by a Health Professional from UNITED KINGDOM on Feb 14, 2007. Female patient, 72 years of age, weighting 149.9 lb, was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: cerebral infarction, syncope. FOSAMAX dosage: unknown. During the same period patient was treated with CELECOXIB, FOLIC ACID, INFLIXIMAB, METHOTREXATE, OMEPRAZOLE. Patient recovered.
Fosamax Side Effects Report #5242839-9
Physician from JAPAN reported FOSAMAX problem on Feb 15, 2007. Female patient, 80 years of age, was diagnosed with osteoporosis, pollakiuria and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: abdominal pain, anorexia, hepatic function abnormal, jaundice, malaise. FOSAMAX dosage: unknown. During the same period patient was treated with AMLODIN, SAWADARON. Patient was hospitalized. Patient recovered.
Fosamax Side Effects Report #5243297-0
FOSAMAX problem was reported by a Consumer or non-health professional from AUSTRALIA on Feb 14, 2007. Female patient, 88 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. FOSAMAX dosage: unknown. Patient died.
Fosamax Side Effects Report #5244690-2
Physician from FRANCE reported FOSAMAX problem on Feb 15, 2007. Female patient, 79 years of age, was diagnosed with osteoporosis, thrombosis prophylaxis, breast cancer and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: anaemia, gastrointestinal haemorrhage. FOSAMAX dosage: unknown. During the same period patient was treated with ASPIRIN, ANASTROZOLE. Patient was hospitalized. Patient recovered.
Fosamax Side Effects Report #5244700-2
FOSAMAX problem was reported by a Physician from JAPAN on Feb 14, 2007. Female patient, 72 years of age, was diagnosed with osteoporosis, nasopharyngitis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: hyperglycaemia. FOSAMAX dosage: unknown. Patient recovered.
Fosamax Side Effects Report #5245254-7
Physician from UNITED STATES reported FOSAMAX problem on Feb 13, 2007. Female patient, 61 years of age, weighting 110.2 lb, was diagnosed with osteopenia and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: impaired healing, oral infection, oral pain. FOSAMAX dosage: unknown. During the same period patient was treated with LIPITOR, SYNTHROID, CELEXA, PREVACID, CENTRUM, CALTRATE. Patient recovered.
Fosamax Side Effects Report #5245736-8
FOSAMAX problem was reported by a Physician from UNITED STATES on Feb 21, 2007. Female patient, 66 years of age, weighting 149.9 lb, was diagnosed with osteoporosis prophylaxis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: tooth disorder. FOSAMAX dosage: unknown. During the same period patient was treated with COUMADIN. Patient recovered.
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Drug Information: Alendronate
URL of this page: http://www.nlm.nih.gov/medlineplus/druginfo/medmaster/a601011.html
(a len' droe nate)IMPORTANT WARNING:
| [Posted 01/07/2008] FDA informed healthcare professionals and patients of the possibility of severe and sometimes incapacitating bone, joint, and/or muscle (musculoskeletal) pain in patients taking bisphosphonates. Although severe musculoskeletal pain is included in the prescribing information for all bisphosphonates, the association between bisphosphonates and severe musculoskeletal pain may be overlooked by healthcare professionals, delaying diagnosis, prolonging pain and/or impairment, and necessitating the use of analgesics. The severe musculoskeletal pain may occur within days, months, or years after starting a bisphosphonates. Some patients have reported complete relief of symptoms after discontinuing the bisphosphonate, whereas others have reported slow or incomplete resolution. The risk factors for and incidence of severe musculoskeletal pain associated with bisphosphonates are unknown.Healthcare professionals should consider whether bisphosphonate use might be responsible for severe musculoskeletal pain in patients who present with these symptoms and consider temporary or permanent discontinuation of the drug. For more information visit the FDA website at: http://www.fda.gov/medwatch/safety/2008/safety08.htm#Bisphosphonates and http://www.fda.gov/cder/drug/infopage/bisphosphonates/default.htm.[Posted 10/01/2007] FDA issued an early communication about the ongoing review of new safety data regarding the association of atrial fibrillation with the use of bisphosphonates. 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, treat bone metastases, and lower elevated levels of blood calcium in patients with cancer.FDA reviewed spontaneous postmarketing reports of atrial fibrillation reported in association with oral and intravenous bisphosphonates and did not identify a population of bisphosphonate users at increased risk of atrial fibrillation. In addition, as part of the data review for the recent approval of once-yearly Reclast for the treatment of postmenopausal osteoporosis, FDA evaluated the possible association between atrial fibrillation and the use of Reclast (zoledronic acid). Most cases of atrial fibrillation occurred more than a month after drug infusion. Also, in a subset of patients monitored by electrocardiogram up to the 11th day following infusion, there was no significant difference in the prevalence of atrial fibrillation between patients who received Reclast and patients who received placebo.Upon initial review, it is unclear how these data on serious atrial fibrillation should be interpreted. Therefore, FDA does not believe that healthcare providers or patients should change either their prescribing practices or their use of bisphosphonates at this time. For more information visit the FDA website at: http://www.fda.gov/medwatch/safety/2007/safety07.htm#Bisphosphonates and http://www.fda.gov/cder/drug/early_comm/bisphosphonates.htm. |
Why is this medication prescribed?
Pending revision, the material in this section should be considered in light of more recently available information in the MedWatch notification at the beginning of this monograph.
Alendronate is used to treat and prevent osteoporosis (a condition in which the bones become thin and weak and break easily) in women who have undergone menopause (change of life; end of menstrual periods). Alendronate is also used to treat osteoporosis in men and women, who are taking corticosteroids (a type of medication that may cause osteoporosis in some patients). Alendronate is also used to treat Paget's disease of bone (a condition in which the bones are soft and weak and may be deformed, painful, or easily broken). Alendronate is in a class of medications called bisphosphonates. It works by preventing bone breakdown and increasing bone density (thickness).
How should this medicine be used?
Alendronate comes as a tablet and a solution (liquid) to take by mouth. The solution is usually taken on an empty stomach once a week in the morning. The 5-mg and 10-mg tablets are usually taken on an empty stomach once a day in the morning, and the 30-mg and 70-mg tablets are usually taken on an empty stomach once a week in the morning. The 40-mg tablets are usually taken once a day in the morning for six months to treat Paget's disease of bone. Follow the directions on your prescription label carefully, and ask your doctor or pharmacist to explain any part you do not understand. Take alendronate exactly as directed. Do not take more or less of it or take it more often than prescribed by your doctor.
Alendronate may not work properly and may damage the esophagus (tube between the mouth and stomach) or cause sores in the mouth if it is not taken according to the following instructions. Tell your doctor if you do not understand, you do not think you will remember, or you are unable to follow these instructions:
- You must take alendronate just after you get out of bed in the morning, before you eat or drink anything. Never take alendronate at bedtime or before you wake up and get out of bed for the day.
- Swallow alendronate tablets with a full glass (6 to 8 ounces, about 1 cup) of plain water. Drink at least a quarter of a cup (2 ounces) of plain water after you drink alendronate liquid. Never take alendronate with tea, coffee, juice, milk, mineral water, sparkling water, or any liquid other than plain water.
- Swallow the tablets whole; do not split, chew or crush them. Do not suck on the tablets.
- After you take alendronate, do not eat, drink, or take any other medications (including vitamins or antacids) for at least 30 minutes. Do not lie down for at least 30 minutes after you take alendronate. Sit upright or stand upright until at least 30 minutes have passed and you have eaten your first food of the day.
Alendronate controls osteoporosis and Paget's disease of bone but does not cure these conditions. It may take 3 months or longer before your bone density begins to increase. Alendronate helps to treat and prevent osteoporosis only as long as it is taken regularly. Continue to take alendronate even if you feel well. Do not stop taking alendronate without talking to your doctor.
Ask your pharmacist or doctor for a copy of the manufacturer's information for the patient.
Other uses for this medicine
This medication may be prescribed for other uses; ask your doctor or pharmacist for more information.
What special precautions should I follow?
Pending revision, the material in this section should be considered in light of more recently available information in the MedWatch notification at the beginning of this monograph.
Before taking alendronate,
- tell your doctor and pharmacist if you are allergic to alendronate, any other medications, or any of the ingredients in alendronate tablets or liquid. Ask your pharmacist for a list of the ingredients.
- tell your doctor and pharmacist what prescription and nonprescription medications, vitamins, nutritional supplements, and herbal products you are taking or plan to take. Be sure to mention any of the following: aspirin and other nonsteroidal anti-inflammatory medications (NSAIDs) such as ibuprofen (Advil, Motrin) and naproxen (Naprosyn, Aleve); cancer chemotherapy; or oral steroids such as dexamethasone (Decadron, Dexone), methylprednisolone (Medrol), and prednisone (Deltasone). Your doctor may need to change the doses of your medications or monitor you carefully for side effects.
- if you are taking any other medications including supplements, vitamins, or antacids by mouth, take them at least 30 minutes after you take alendronate.
- tell your doctor if you are unable to sit upright or stand upright for at least 30 minutes and if you have or have ever had a low level of calcium in your blood or any problems with your esophagus. Your doctor may tell you that you should not take alendronate.
- tell your doctor if are undergoing radiation therapy and if you have or have ever had anemia (condition in which the red blood cells do not bring enough oxygen to all the parts of the body);difficulty swallowing; heartburn; ulcers or other stomach problems;cancer; any type of infection, especially in your mouth;problems with your mouth, teeth, or gums; any condition that stops your blood from clotting normally; or dental or kidney disease.
- tell your doctor if you are pregnant or are breast-feeding. Also tell your doctor if you plan to become pregnant at any time in the future, because alendronate may remain in your body for many years after you stop taking it. Call your doctor if you become pregnant during or after your treatment.
- you should know that alendronate may cause serious problems with your jaw, especially if you have dental surgery or treatment while you are taking the medication. A dentist should examine your teeth and perform any needed treatments before you start to take alendronate. Be sure to brush your teeth and clean your mouth properly while you are taking alendronate. Talk to your doctor before having any dental treatments while you are taking this medication.
- you should know that alendronate may cause serious damage to the lining of your mouth, esophagus, or stomach, especially if you do not take it according to the directions listed in the HOW section above. If you experience any of the following symptoms, stop taking alendronate, and call your doctor immediately: new or worsening heartburn, difficulty swallowing, pain on swallowing, or chest pain.
- talk to your doctor about other things you can do to prevent osteoporosis from developing or worsening. Your doctor will probably tell you to avoid smoking and drinking large amounts of alcohol and to follow a regular program of weight-bearing exercise.
What special dietary instructions should I follow?
You should eat and drink plenty of foods and drinks that are rich in calcium and vitamin D while you are taking alendronate. Your doctor will tell you which foods and drinks are good sources of these nutrients and how many servings you need each day. If you find it difficult to eat enough of these foods, tell your doctor. In that case, your doctor can prescribe or recommend a supplement.
What should I do if I forget a dose?
If you miss a dose of once-daily alendronate, do not take it later in the day. Skip the missed dose and take one dose the next morning as usual. If you miss a dose of once-weekly alendronate, take one dose the morning after you remember. Then return to taking one dose once each week on your regularly scheduled day. Never take a double dose to make up for a missed one, and never take more than one dose in 1 day.
What side effects can this medication cause?
Pending revision, the material in this section should be considered in light of more recently available information in the MedWatch notification at the beginning of this monograph.
Alendronate may cause side effects. Tell your doctor if any of these symptoms are severe or do not go away:
- nausea
- stomach pain
- constipation
- diarrhea
- gas
- bloating or fullness in the stomach
- change in ability to taste food
- bone, muscle, or joint pain
- headache
- dizziness
- flu-like symptoms
Some side effects can be serious. If you experience any of the following symptoms, call your doctor immediately before you take any more alendronate:
- new or worsening heartburn
- difficulty swallowing
- pain on swallowing
- chest pain
- bloody vomit or vomit that looks like coffee grounds
- black, tarry, or bloody stools
- fever
- blisters or peeling skin
- rash (may be made worse by sunlight)
- itching
- hives
- swelling of eyes, face, lips, tongue, or throat
- difficulty breathing
- hoarseness
- painful or swollen gums
- loosening of the teeth
- numbness or heavy feeling in the jaw
- poor healing of the jaw
- eye pain
Alendronate may cause other side effects. Call your doctor if you have any unusual problems while taking this medication.
What storage conditions are needed for this medicine?
Keep this medication in the container it came in, tightly closed, and out of reach of children. Store it at room temperature and away from excess heat and moisture (not in the bathroom). Do not freeze alendronate solution. Throw away any medication that is outdated or no longer needed. Talk to your pharmacist about the proper disposal of your medication.
In case of emergency/overdose
In case of overdose, give the victim a full glass of milk and call your local poison control center at 1-800-222-1222. If the victim has collapsed or is not breathing, call local emergency services at 911. Do not allow the victim to lie down and do not try to make the victim vomit.
Symptoms of overdose may include:
- heartburn
- nausea
- stomach pain
- bloody vomit or vomit that looks like coffee grounds
- difficulty swallowing or pain when swallowing
- bloody or black and tarry stool
What other information should I know?
Pending revision, the material in this section should be considered in light of more recently available information in the MedWatch notification at the beginning of this monograph.
Keep all appointments with your doctor and the laboratory. Your doctor may order certain lab tests to check your body's response to alendronate.
Do not let anyone else take your medication. Ask your pharmacist any questions you have about refilling your prescription.
It is important for you to keep a written list of all of the prescription and nonprescription (over-the-counter) medicines you are taking, as well as any products such as vitamins, minerals, or other dietary supplements. You should bring this list with you each time you visit a doctor or if you are admitted to a hospital. It is also important information to carry with you in case of emergencies.
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