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Fosamax Plus D (Alendronate / Cholecalciferol) - Bone Disorder - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with Bone Disorder ()

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Fosamax Plus D (Alendronate / Cholecalciferol) where reactions include bone disorder. The selected reports were submitted to the FDA during the sample period of about a year.

 Reports 1 - 30 of    Next >>

Possible Fosamax Plus D side effects in

Reported by a consumer/non-health professional from United States on 2012-08-24

Patient:

Reactions: Vitamin D Deficiency, Femur Fracture, Pyrexia, Incision Site Cellulitis, Treatment Noncompliance, Personality Disorder, Eye Infection, Phlebitis, Back Pain, Hiatus Hernia, Dysphagia, Pain in Extremity, Anaemia, Gastric Disorder, Paraesthesia, Gastric Polyps, Atelectasis, Hypersensitivity, Body Temperature Increased, Wrist Fracture, Hepatic Lesion, Constipation, Wound Infection Staphylococcal, Fall, Chest X-RAY Abnormal, Weight Increased, Bone Disorder, Gastrooesophageal Reflux Disease, Sinusitis, Dysthymic Disorder, Oxygen Saturation Decreased, RIB Fracture, Osteoarthritis, Limb Discomfort, Pneumonia Bacterial, Adjustment Disorder With Anxiety, Blood Disorder, Atrophy, Infection, Inflammation

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Actonel
    Dosage: 150 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2009-01-05
    End date: 2011-07-30

Boniva
    Dosage: 150 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2005-08-19
    End date: 2007-02-11

Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1996-01-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2000-12-11
    End date: 2005-09-22

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    End date: 2011-05-01

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-12-26
    End date: 2009-01-19

Other drugs received by patient: Lipitor; Synthroid



Possible Fosamax Plus D side effects in

Reported by a consumer/non-health professional from United States on 2012-08-23

Patient:

Reactions: Femur Fracture, Flatulence, Gastric Cancer, Surgery, Spinal Compression Fracture, Fracture, Adverse Event, Vertebral Foraminal Stenosis, Spinal Laminectomy, LOW Turnover Osteopathy, Intervertebral Disc Protrusion, Phlebitis, Back Pain, Spinal Fracture, Gastrointestinal Stromal Tumour, Hypoaesthesia, Lumbar Vertebral Fracture, Spinal Fusion Surgery, HIP Fracture, Spleen Disorder, Metastases To Spine, Intramedullary ROD Insertion, Packed RED Blood Cell Transfusion, Stress Fracture, Adenoma Benign, Osteoporosis, Fall, Kyphosis, Constipation, Foraminotomy, Breast Disorder Female, Road Traffic Accident, Intervertebral Disc Disorder, Dizziness, Bone Disorder, Injury, Gastrooesophageal Reflux Disease, Exostosis, Scoliosis, Pelvic Fracture, Vertebroplasty, Joint Dislocation, Patellofemoral Pain Syndrome, Osteoarthritis, Meniscus Lesion, Arthralgia, Spinal Osteoarthritis, Spinal Disorder, Gait Disturbance, Hypertension, Arthritis

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteopenia
    Start date: 1997-01-01
    End date: 2009-06-08

Fosamax
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1997-01-01
    End date: 2009-06-08

Fosamax
    Dosage: 70 qw
    Administration route: Oral
    Start date: 2008-12-04
    End date: 2009-05-01

Fosamax Plus D
    Dosage: 70/2800 qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2005-04-01
    End date: 2009-03-01

Fosamax Plus D
    Indication: Osteopenia

Other drugs received by patient: Lipitor; Allegra; Nasacort; Calcium (Unspecified); Actonel



Possible Fosamax Plus D side effects in

Reported by a lawyer from United States on 2012-08-23

Patient:

Reactions: Polymyalgia Rheumatica, Contusion, Piriformis Syndrome, Monoclonal Immunoglobulin Present, Vaginal Disorder, Malaise, Upper Respiratory Tract Infection, Oedema Peripheral, Ulna Fracture, LOW Turnover Osteopathy, Breast Cancer Stage I, Fracture Delayed Union, Joint Injury, Faeces Hard, Tonsillar Disorder, Staphylococcal Infection, Uterine Disorder, Bone Metabolism Disorder, Adverse Drug Reaction, Fall, Foot Fracture, Rotator Cuff Syndrome, Bone Disorder, Depression, Decreased Appetite, Joint Dislocation, Blood Potassium Abnormal, Bipolar Disorder, Calcium Ionised, Arthralgia, Bladder Disorder, Gait Disturbance, Underweight, Asthma, Bone Fragmentation, Femur Fracture, Sciatica, Urinary Incontinence, Hand Fracture, Headache, Tooth Infection, Fallopian Tube Disorder, Arthropathy, Fracture, Dyspepsia, Joint Effusion, Anaemia Postoperative, Pain in Extremity, Oestrogen Deficiency, Gastric Disorder, Micturition Urgency, Dysmenorrhoea, Osteonecrosis, Joint Swelling, Acute Sinusitis, Ear Pain, Scar, Uterine Cervix Stenosis, Hypophosphatasia, Urethral Stenosis, Dyslipidaemia, Drug Ineffective, Hypokalaemia, Fatigue, Intervertebral Disc Degeneration, Hypertonic Bladder, Sinusitis, Gastrooesophageal Reflux Disease, Migraine, Swelling Face, Urinary Tract Infection, Condition Aggravated, Osteolysis, Osteoarthritis, Anxiety, Uterine Spasm, Spinal Osteoarthritis, Tooth Disorder

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Boniva
    Dosage: 150 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2005-09-24
    End date: 2006-01-01

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2009-06-29
    End date: 2009-12-13

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2009-02-01
    End date: 2010-01-01

Fosamax
    Dosage: unk
    Administration route: Oral
    Start date: 2009-02-13

Fosamax
    Dosage: 10 mg, unk
    Administration route: Oral
    Start date: 1997-10-01
    End date: 2001-02-01

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2001-03-01

Fosamax Plus D
    Dosage: 70-2800
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-02-01
    End date: 2008-01-01

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2008-02-21
    End date: 2008-11-07

Fosamax Plus D
    Dosage: 70 u, unk
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2008-02-01
    End date: 2009-01-01

Other drugs received by patient: MK-9278; Hormones (Unspecified); Ultram; Prempro; Nortriptyline; Premarin; Calcium (Unspecified); Vitamin D; Percocet; Cholecalciferol; Calcium (Unspecified) (+) Vitamin D (Unspecified); Tylenol



Possible Fosamax Plus D side effects in

Reported by a physician from United States on 2012-08-23

Patient:

Reactions: Weight Decreased, Foot Deformity, Femur Fracture, Coagulopathy, Tachycardia, Vitamin B12 Deficiency, Nail Disorder, Adverse Event, Bone Density Decreased, Haematoma, Claustrophobia, Pneumonia, Pain in Extremity, Haemorrhagic Anaemia, Osteopenia, Blood Creatine Phosphokinase MB Increased, Insomnia, Hypersensitivity, Osteoporosis, Fracture Nonunion, Wound Infection Staphylococcal, Fall, Constipation, Hypokalaemia, Postoperative Wound Infection, Depression, Bone Disorder, Gastrooesophageal Reflux Disease, Hallucination, Renal Failure Acute, Endometrial Disorder, Breast Disorder, Nausea, Urinary Tract Infection, Drug Hypersensitivity, Ovarian Disorder, Rash, Onychomycosis, Plantar Fasciitis, Device Failure, Osteoarthritis, Anxiety, Panic Attack, Impaired Healing, Arthralgia, Haematoma Evacuation, Gait Disturbance, Tooth Disorder, Arthritis

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Bone Density Decreased
    Start date: 2002-10-01
    End date: 2005-10-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2008-10-20
    End date: 2010-03-01

Fosamax
    Dosage: 35 mg, qw
    Administration route: Oral
    Start date: 2002-10-11

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2006-01-01
    End date: 2009-01-01

Fosamax Plus D
    Dosage: unk mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-02-14
    End date: 2006-02-17



Possible Fosamax Plus D side effects in

Reported by a consumer/non-health professional from United States on 2012-08-23

Patient:

Reactions: Vitamin D Deficiency, Femur Fracture, Hyperkalaemia, Metaplasia, Hand Fracture, Cerebral Artery Occlusion, Cardiac Disorder, Cardiomegaly, Fibula Fracture, Gallbladder Disorder, Breast Hyperplasia, Arteriosclerosis, Tendonitis, Thoracic Vertebral Fracture, Cardiac Failure Congestive, Back Disorder, Anaemia Postoperative, Breast Cancer, Fracture Delayed Union, Colporrhaphy, Breast Mass, Breast Calcifications, Mammary Duct Ectasia, Ankle Fracture, Cerebral Infarction, Compression Fracture, Tibia Fracture, Transfusion, Spinal Column Stenosis, Osteoporosis, Kyphosis, Fall, Cystocele, Hypercholesterolaemia, Blood Calcium Decreased, Overdose, Pulmonary Congestion, Rotator Cuff Syndrome, Intervertebral Disc Degeneration, Dizziness, Bone Disorder, Sinusitis, Open Reduction of Fracture, Medical Device Discomfort, Inappropriate Schedule of Drug Administration, Scoliosis, Breast Lump Removal, Emphysema, Nausea, Hypocalciuria, Internal Fixation of Fracture, Biopsy Breast, Renal Failure Chronic, Intraneural Cyst, Osteoarthritis, Device Failure, Medical Device Removal, Hypothyroidism, Hypertension, Arthritis, Breast Fibrosis

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, qd
    Administration route: Oral
    End date: 2010-02-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2010-02-14

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2001-07-01
    End date: 2005-10-01

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2005-10-10



Possible Fosamax Plus D side effects in

Reported by a consumer/non-health professional from Puerto Rico on 2012-08-23

Patient:

Reactions: Femur Fracture, Fear, Foot Fracture, Hypokinesia, Upper Respiratory Tract Infection, Liver Function Test Abnormal, Bone Disorder, Depression, Muscle Spasms, LOW Turnover Osteopathy, Abdominal Pain Lower, Pain in Extremity, Osteoarthritis, Anxiety, Hysterectomy, Syncope, Impaired Healing, Sleep Disorder, Cholecystectomy

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1997-07-01
    End date: 2010-11-25

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 1997-07-01
    End date: 2010-03-01

Fosamax Plus D
    Dosage: 70 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1997-07-01
    End date: 2010-03-01

Other drugs received by patient: Vitamin D; Daypro; Levothyroxine Sodium; Calcium (Unspecified); MK-9359; Coumadin; Synthroid; Tenormin; Methotrexate



Possible Fosamax Plus D side effects in

Reported by a physician from United States on 2012-08-23

Patient:

Reactions: Atelectasis, Vitamin D Deficiency, Femur Fracture, Hypersensitivity, Wrist Fracture, Body Temperature Increased, Hepatic Lesion, Personality Disorder, Wound Infection Staphylococcal, Fall, Treatment Noncompliance, Eye Infection, Weight Increased, Bone Disorder, Sinusitis, Dysthymic Disorder, Gastrooesophageal Reflux Disease, Oxygen Saturation Decreased, RIB Fracture, Dysphagia, Hiatus Hernia, Pain in Extremity, Gastric Disorder, Paraesthesia, Limb Discomfort, Blood Disorder, Adjustment Disorder With Anxiety, Gastric Polyps, Atrophy, Infection, Inflammation

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Actonel
    Dosage: 150 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2009-01-05
    End date: 2011-07-30

Boniva
    Dosage: 150 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2005-08-19
    End date: 2007-02-11

Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1996-01-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2000-12-11
    End date: 2005-09-22

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    End date: 2011-05-01

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-12-26
    End date: 2009-01-19

Other drugs received by patient: Lipitor; Synthroid



Possible Fosamax Plus D side effects in

Reported by a consumer/non-health professional from United States on 2012-08-23

Patient:

Reactions: Femur Fracture, Surgery, Bone Disorder, LOW Turnover Osteopathy

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Alendronate Sodium

Fosamax
    Dosage: unk
    Administration route: Oral
    Start date: 1995-01-01
    End date: 2001-01-01

Fosamax Plus D



Possible Fosamax Plus D side effects in

Reported by a consumer/non-health professional from United States on 2012-08-23

Patient:

Reactions: Vitamin D Deficiency, Glossodynia, Dental Plaque, Colonic Polyp, Upper Respiratory Tract Infection, Uterine Leiomyoma, Salivary Gland Calculus, Haematuria, Libido Decreased, Ovarian Cyst, Breast Mass, Renal Cyst, Joint Injury, Stress, Ankle Fracture, Nasal Septum Deviation, Overweight, Rhinitis Allergic, Osteosclerosis, Vitamin D Decreased, Poor Personal Hygiene, LOW Density Lipoprotein Increased, Calculus Ureteric, Upper-Airway Cough Syndrome, Laryngeal Oedema, Bone Loss, Reflux Laryngitis, Bone Disorder, Granulomatous Liver Disease, Sinusitis, Exostosis, Tooth Fracture, Bone Lesion, Urinary Tract Infection, Skin Disorder, Tongue Coated, Anxiety, Hyperlipidaemia, Gingival Recession, Osteonecrosis of JAW, Uterine Malposition, Tooth Disorder, Endometrial Atrophy

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Boniva
    Dosage: 150 mg, unk
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2007-09-13
    End date: 2008-09-25

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2003-07-01
    End date: 2007-03-14

Fosamax
    Dosage: unk mg, unk
    Administration route: Oral
    Start date: 2005-04-13

Fosamax Plus D
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2006-12-26
    End date: 2007-03-14

Other drugs received by patient: Betamethasone Valerate; Prempro; Renova



Possible Fosamax Plus D side effects in

Reported by a physician from United States on 2012-08-23

Patient:

Reactions: Femur Fracture, Retinal Detachment, Extrasystoles, Nocturia, Carpal Tunnel Syndrome, Squamous Cell Carcinoma of Skin, Tendonitis, Blood Creatinine Increased, Papule, Back Pain, Breast Pain, Actinic Keratosis, Cardiac Murmur, Sarcoma, Pain in Extremity, Osteopenia, Stress Fracture, Haemorrhoid Operation, Adverse Drug Reaction, Fall, Constipation, Muscle Rupture, Basal Cell Carcinoma, Bone Disorder, Inappropriate Schedule of Drug Administration, Vomiting, Cataract, Squamous Cell Carcinoma, Nausea, Hypercalcaemia, Osteoarthritis, Hyperlipidaemia, Neoplasm Malignant, Sialoadenitis, Bronchitis, Tooth Disorder, Arthritis

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2000-01-01
    End date: 2010-03-01

Fosamax
    Dosage: unk unk, qw
    Administration route: Oral
    Start date: 2008-01-09

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2007-04-26

Other drugs received by patient: Multi-Vitamins; Calcium (Unspecified)



Possible Fosamax Plus D side effects in

Reported by a physician from United States on 2012-08-14

Patient:

Reactions: Vitamin D Deficiency, Osteomyelitis Acute, Femur Fracture, Blood Albumin Decreased, Pyrexia, Hypercalciuria, LOW Turnover Osteopathy, Back Disorder, Abscess Limb, Intervertebral Disc Protrusion, Chondropathy, Cellulitis, Hiatus Hernia, Anaemia, Osteomyelitis Chronic, Granuloma, Fungal Infection, Abscess, Osteoporosis, Necrosis, Fall, Constipation, Fracture Nonunion, Hypoacusis, Dermatitis Contact, Fatigue, Rotator Cuff Syndrome, Intervertebral Disc Degeneration, Depression, Bone Disorder, Erosive Oesophagitis, Sinusitis, Gastrooesophageal Reflux Disease, Blood Glucose Increased, Tooth Fracture, Urinary Tract Infection, Haemorrhoids, Musculoskeletal Pain, Patellofemoral Pain Syndrome, Cervicobrachial Syndrome, Hyperlipidaemia, Device Failure, Impaired Healing, Thrombocytosis, Dupuytren's Contracture, Bronchitis, Tooth Disorder

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Estradiol
    Indication: Hormone Therapy
    Start date: 1994-01-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2001-01-01
    End date: 2008-11-17

Fosamax
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Osteopenia
    Start date: 1996-12-01
    End date: 2001-01-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2008-10-03

Fosamax Plus D
    Dosage: 70/2800
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2007-01-27
    End date: 2007-04-01

Other drugs received by patient: MK-0805



Possible Fosamax Plus D side effects in

Reported by a consumer/non-health professional from Puerto Rico on 2012-08-10

Patient:

Reactions: Femur Fracture, Demyelinating Polyneuropathy, Cerebral Ischaemia, Rheumatoid Arthritis, Balance Disorder, Musculoskeletal Disorder, Adverse Event, Joint Effusion, Post Procedural Haemorrhage, Muscle Spasms, Cough, Back Pain, Intervertebral Disc Protrusion, Pain in Extremity, Lumbar Vertebral Fracture, Tremor, HIP Fracture, Diverticulum, Uterine Disorder, Psoriatic Arthropathy, Adverse Drug Reaction, Constipation, Fall, Synovial Cyst, Haemorrhoidal Haemorrhage, Poor Quality Sleep, Foot Fracture, Cardiac Valve Disease, Neuropathy Peripheral, Dizziness, Bone Disorder, Injury, Exostosis, Pelvic Fracture, Inappropriate Schedule of Drug Administration, Spondylolysis, Dyspnoea, Nausea, Spondylolisthesis, Drug Hypersensitivity, Dental Caries, Skin Disorder, Muscular Weakness, Patellofemoral Pain Syndrome, Facet Joint Syndrome, Appendix Disorder, Hepatic Enzyme Increased, Osteoarthritis, Anxiety, Arthralgia, Alopecia, Lacunar Infarction, Spinal Osteoarthritis, Gait Disturbance, Hypertension

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Indication: Osteopenia

Fosamax
    Dosage: 70 mg, qd
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2000-01-01
    End date: 2011-05-01

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2009-01-01

Fosamax Plus D
    Indication: Osteopenia



Possible Fosamax Plus D side effects in

Reported by a consumer/non-health professional from United States on 2012-08-09

Patient:

Reactions: Tinnitus, Oral Cavity Fistula, Ligament Laxity, Balance Disorder, Palpitations, Eye Pruritus, Oral Mucosal Blistering, Back Pain, Abscess Oral, Hypotension, Temporomandibular Joint Syndrome, Increased Tendency To Bruise, Vision Blurred, Abscess, Periodontal Disease, Chills, Fall, Abdominal Pain Upper, Chest Pain, Retinal Disorder, Rotator Cuff Syndrome, Bone Disorder, Ligament Sprain, Dyspnoea, Hepatitis A, Arthralgia, Impaired Healing, Skin Mass, Loose Tooth, Weight Decreased, Osteomyelitis, Visual Acuity Reduced, Vascular Calcification, Irritable Bowel Syndrome, Breath Odour, Muscle Spasms, Paranasal Cyst, Gingival Bleeding, Anxiety Disorder, Peptic Ulcer, Pain in Extremity, Oral Infection, Gingival Disorder, Nasal Septum Deviation, Apathy, Cachexia, Cerebral Small Vessel Ischaemic Disease, Osteonecrosis, Joint Swelling, Drug Ineffective, Pain, Periodontitis, Diplopia, Bipolar II Disorder, Fatigue, Neck Pain, Dizziness, Salivary Hypersecretion, Sinusitis, Gastrooesophageal Reflux Disease, Migraine, Nausea, Dental Caries, Patellofemoral Pain Syndrome, Cerebrovascular Accident, Eye Pain, Meniscus Lesion, Osteoarthritis, Osteonecrosis of JAW, Diarrhoea, Conjunctivitis Infective, Oral Disorder, Arthritis, Tooth Disorder

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2009-01-06
    End date: 2010-05-27

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2006-01-01
    End date: 2011-02-08

Fosamax
    Indication: Osteoporosis

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2008-04-24
    End date: 2008-09-27



Possible Fosamax Plus D side effects in

Reported by a lawyer from United States on 2012-08-07

Patient:

Reactions: Vitamin D Deficiency, Chronic Tonsillitis, Femur Fracture, Headache, Decubitus Ulcer, Palpitations, Vitamin B12 Deficiency, Irritable Bowel Syndrome, Fibula Fracture, LOW Turnover Osteopathy, Muscle Spasms, Dysphagia, Fracture Delayed Union, Anaemia, Laceration, Ankle Fracture, Paraesthesia, Dysphonia, Acute Sinusitis, Insomnia, Tibia Fracture, Stress Fracture, Ischaemia, Osteoporosis, Tonsillitis, Chest Pain, Toothache, Bone Disorder, Exostosis, Respiration Abnormal, Calcium Deficiency, Dyspnoea, Drug Hypersensitivity, Peripheral Vascular Disorder, Multiple Fractures, Odynophagia, Renal Failure Chronic, Appendix Disorder, Pulmonary Fibrosis, Device Failure, Bladder Irritation, Steroid Therapy, Sinus Disorder, Bladder Disorder, Inflammatory Bowel Disease

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Alendronate Sodium
    Indication: Osteopenia

Alendronate Sodium
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2010-04-02

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-04-27

Fosamax
    Indication: Osteopenia

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-01-01
    End date: 2007-01-01

Fosamax Plus D
    Indication: Osteopenia

Other drugs received by patient: Depo-Medrol; Hormones (Unspecified); Nexium



Possible Fosamax Plus D side effects in

Reported by a consumer/non-health professional from United States on 2012-08-07

Patient:

Reactions: Skin Wrinkling, Femur Fracture, Osteoporosis, Diverticulitis, Constipation, Fall, Trigger Finger, Gastritis, Nephrolithiasis, Hypercholesterolaemia, Myalgia, Fatigue, Bone Disorder, Hepatic Cirrhosis, LOW Turnover Osteopathy, Mitral Valve Prolapse, Breast Cancer, Cardiac Murmur, Dental Caries, Ovarian Calcification, Pancreatic Cyst, Hepatic Steatosis, Seasonal Allergy, Cholelithiasis, Insomnia, Vertigo, Gait Disturbance, Tooth Disorder, Hypertension, Mesenteritis, Deep Vein Thrombosis, Infection

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2005-11-30
    End date: 2006-07-18

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2008-05-15
    End date: 2009-12-30

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2000-01-01
    End date: 2005-11-01

Fosamax Plus D
    Dosage: 70 mg, unk
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2006-08-19
    End date: 2008-04-14



Possible Fosamax Plus D side effects in

Reported by a consumer/non-health professional from United States on 2012-08-06

Patient:

Reactions: Polymyalgia Rheumatica, Contusion, Piriformis Syndrome, Monoclonal Immunoglobulin Present, Vaginal Disorder, Malaise, Upper Respiratory Tract Infection, Oedema Peripheral, Ulna Fracture, LOW Turnover Osteopathy, Breast Cancer Stage I, Fracture Delayed Union, Joint Injury, Faeces Hard, Tonsillar Disorder, Staphylococcal Infection, Uterine Disorder, Bone Metabolism Disorder, Adverse Drug Reaction, Fall, Foot Fracture, Rotator Cuff Syndrome, Bone Disorder, Depression, Decreased Appetite, Joint Dislocation, Blood Potassium Abnormal, Arthralgia, Calcium Ionised, Bipolar Disorder, Bladder Disorder, Gait Disturbance, Asthma, Underweight, Bone Fragmentation, Femur Fracture, Sciatica, Urinary Incontinence, Hand Fracture, Tooth Infection, Headache, Fallopian Tube Disorder, Arthropathy, Dyspepsia, Fracture, Joint Effusion, Anaemia Postoperative, Pain in Extremity, Oestrogen Deficiency, Gastric Disorder, Micturition Urgency, Dysmenorrhoea, Osteonecrosis, Acute Sinusitis, Joint Swelling, Ear Pain, Scar, Uterine Cervix Stenosis, Dyslipidaemia, Hypophosphatasia, Urethral Stenosis, Drug Ineffective, Hypokalaemia, Fatigue, Intervertebral Disc Degeneration, Hypertonic Bladder, Sinusitis, Gastrooesophageal Reflux Disease, Migraine, Swelling Face, Urinary Tract Infection, Condition Aggravated, Osteolysis, Osteoarthritis, Uterine Spasm, Anxiety, Spinal Osteoarthritis, Tooth Disorder

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Boniva
    Dosage: 150 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2005-09-24
    End date: 2006-01-01

Fosamax
    Dosage: 10 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1997-10-01
    End date: 2001-02-01

Fosamax
    Start date: 2009-02-13

Fosamax

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2001-03-01

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2009-06-29
    End date: 2009-12-13

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2009-02-01
    End date: 2010-01-01

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2008-02-21
    End date: 2008-11-07

Fosamax Plus D
    Dosage: 70-2800
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-02-01
    End date: 2008-01-01

Fosamax Plus D
    Dosage: 70 u, unk
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2008-02-01
    End date: 2009-01-01

Other drugs received by patient: MK-9278; Tylenol (Caplet); Prempro; Percocet; Calcium (Unspecified); Cholecalciferol; Premarin; Ultram; Nortriptyline HCL; Vitamin D; Calcium (Unspecified) (+) Vitamin D (Unspecified); Hormones (Unspecified)



Possible Fosamax Plus D side effects in

Reported by a physician from United States on 2012-08-03

Patient:

Reactions: Paronychia, Femur Fracture, Pruritus, Lower Limb Fracture, Headache, Oesophageal Stenosis, Arthropathy, Oesophagitis, Food Allergy, Muscle Spasms, Cough, Dysphagia, Hiatus Hernia, Drug Intolerance, Gastric Disorder, Affective Disorder, Diverticulum, Epicondylitis, Type V Hyperlipidaemia, Menopausal Symptoms, Gastroduodenitis, Head Injury, Drug Ineffective, Tenosynovitis Stenosans, Fracture Nonunion, Fall, Gastritis, Foot Fracture, Weight Increased, Fatigue, Fibrocystic Breast Disease, Bone Loss, Skin Lesion, Dizziness, Bone Disorder, Gastrooesophageal Reflux Disease, Pain in JAW, Tooth Fracture, Vomiting, Dyspnoea, Fracture Malunion, Nausea, Haemorrhoids, Psoriasis, Tenosynovitis, Osteoarthritis, Meniscus Lesion, Barrett's Oesophagus, Lung Disorder, Arthralgia, Blood Disorder, Gait Disturbance, Spinal Osteoarthritis, Bronchitis, Arthritis

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2002-05-02
    End date: 2005-04-26

Fosamax Plus D
    Dosage: unk mg, qw
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2005-09-14



Possible Fosamax Plus D side effects in

Reported by a lawyer from United States on 2012-08-03

Patient:

Reactions: Lymphadenopathy, Tachycardia, Oropharyngeal Pain, Macular Degeneration, Iron Deficiency Anaemia, Oedema Peripheral, Back Pain, Mitral Valve Prolapse, Apical Granuloma, Hyperparathyroidism Secondary, Cervical Dysplasia, Diverticulum Intestinal, Joint Injury, Nephrosclerosis, Post-Traumatic Stress Disorder, Staphylococcal Infection, Anaemia of Chronic Disease, Dysphonia, Gastrointestinal Disorder, Increased Tendency To Bruise, Osteoporosis, Necrosis, Shock Haemorrhagic, Abasia, Pulmonary Arterial Hypertension, Fall, Gastric Ulcer, Multi-Organ Failure, Foot Fracture, Hypoacusis, Amino Acid Level Increased, Bone Disorder, Depression, Renal Failure Acute, Cataract, Dyspnoea, Haemorrhoids, Arthralgia, Limb Asymmetry, Asthenia, Asthma, Vitamin D Deficiency, Femur Fracture, Urinary Incontinence, Disseminated Intravascular Coagulation, Deafness, Gingival Abscess, Obstructive Uropathy, Herpes Zoster, Dyspepsia, Carpal Tunnel Syndrome, Cough, Muscle Spasms, Myositis, Hiatus Hernia, Dysphagia, Cardiac Murmur, Peptic Ulcer, Anaemia, Osteonecrosis, Insomnia, Dehydration, Surgical Failure, Sleep Apnoea Syndrome, Pain, Fracture Nonunion, Gastritis, Synovial Cyst, Weight Increased, Nephrolithiasis, Fatigue, Eyelid Disorder, Dizziness, Migraine, Urinary Tract Infection, Trichotillomania, Renal Failure Chronic, Appendix Disorder, Anxiety, Retinopathy Hypertensive, Osteoarthritis, Renal Failure, Spinal Disorder, Spinal Osteoarthritis, Tooth Disorder, Hypertension, Infection

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Indication: Osteoporosis

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2003-10-16
    End date: 2006-06-22

Fosamax
    Dosage: unk
    Start date: 2003-01-17
    End date: 2006-01-04

Fosamax Plus D
    Dosage: 70mg/2800
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2006-06-01
    End date: 2009-10-01

Fosamax Plus D
    Indication: Osteoporosis



Possible Fosamax Plus D side effects in

Reported by a lawyer from United States on 2012-08-03

Patient:

Reactions: Atelectasis, Vitamin D Deficiency, Hypersensitivity, Femur Fracture, Wrist Fracture, Body Temperature Increased, Hepatic Lesion, Treatment Noncompliance, Fall, Personality Disorder, Wound Infection Staphylococcal, Eye Infection, Weight Increased, Bone Disorder, Dysthymic Disorder, Sinusitis, Gastrooesophageal Reflux Disease, RIB Fracture, Oxygen Saturation Decreased, Hiatus Hernia, Dysphagia, Pain in Extremity, Gastric Disorder, Paraesthesia, Limb Discomfort, Adjustment Disorder With Anxiety, Blood Disorder, Gastric Polyps, Atrophy, Infection, Inflammation

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Actonel
    Dosage: 150 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2009-01-05
    End date: 2011-07-30

Boniva
    Dosage: 150 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2005-08-19
    End date: 2007-02-11

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    End date: 2011-05-01

Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1996-01-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2000-12-11
    End date: 2005-09-22

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-12-26
    End date: 2009-01-19

Other drugs received by patient: Lipitor; Synthroid



Possible Fosamax Plus D side effects in

Reported by a physician from United States on 2012-08-01

Patient:

Reactions: Vitamin D Deficiency, Glaucoma, Femur Fracture, Osteoporosis, Parathyroid Disorder, Fall, Fracture Nonunion, Foot Fracture, Colonic Polyp, Arthropathy, Fracture, Oedema Peripheral, Adverse Event, Bone Disorder, Gastrooesophageal Reflux Disease, Back Disorder, LOW Turnover Osteopathy, Calcium Deficiency, Tooth Fracture, Cataract, Pain in Extremity, Dental Caries, Osteoarthritis, Diverticulum, Arthralgia, Cholecystectomy, Tooth Disorder, Arthritis, Periostitis, Infection

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2000-12-01
    End date: 2007-04-01

Fosamax
    Dosage: 10 mg, unk
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2000-01-01
    End date: 2008-01-01

Fosamax Plus D
    Dosage: 70mg/2800
    Administration route: Oral
    Start date: 2007-05-01
    End date: 2008-12-11

Fosamax Plus D
    Dosage: 70/2800
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2006-10-01
    End date: 2007-04-01



Possible Fosamax Plus D side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-01

Patient:

Reactions: Foot Deformity, Sciatica, Osteomyelitis, Piriformis Syndrome, Tooth Infection, Balance Disorder, Radiculopathy, Back Disorder, Fluid Retention, Back Pain, Pain in Extremity, Neuroma, Tendinous Contracture, Increased Tendency To Bruise, Arachnoid Cyst, Ear Pain, Vertigo Positional, Bunion, Head Injury, Fall, Dental Fistula, Bone Density Increased, Oscillopsia, Foot Fracture, Neuropathy Peripheral, Bone Loss, Concussion, Skin Lesion, Intervertebral Disc Degeneration, Oedema, Bone Disorder, Exostosis, Blood Glucose Decreased, Osteonecrosis of JAW, Vestibular Disorder, Sinus Disorder, Vertigo, Face Injury

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis Prophylaxis
    Start date: 2004-03-23
    End date: 2006-02-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-06-16
    End date: 2007-04-09

Fosamax Plus D
    Indication: Osteoporosis

Fosamax Plus D
    Dosage: 70mg/2800
    Administration route: Oral
    Indication: Osteoporosis Prophylaxis
    Start date: 2007-04-10
    End date: 2007-06-25



Possible Fosamax Plus D side effects in

Reported by a consumer/non-health professional from United States on 2012-07-29

Patient:

Reactions: Vitamin D Deficiency, Glaucoma, Femur Fracture, Osteoporosis, Parathyroid Disorder, Fall, Fracture Nonunion, Colonic Polyp, Foot Fracture, Arthropathy, Fracture, Oedema Peripheral, Adverse Event, Bone Disorder, Gastrooesophageal Reflux Disease, LOW Turnover Osteopathy, Calcium Deficiency, Back Disorder, Tooth Fracture, Cataract, Pain in Extremity, Dental Caries, Osteoarthritis, Diverticulum, Arthralgia, Cholecystectomy, Arthritis, Tooth Disorder, Periostitis, Infection

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2000-12-01
    End date: 2007-04-01

Fosamax
    Dosage: 10 mg, unk
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2000-01-01
    End date: 2008-01-01

Fosamax Plus D
    Dosage: 70/2800
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2006-10-01
    End date: 2007-04-01

Fosamax Plus D
    Dosage: 70mg/2800
    Administration route: Oral
    Start date: 2007-05-01
    End date: 2008-12-11



Possible Fosamax Plus D side effects in

Reported by a lawyer from United States on 2012-07-27

Patient:

Reactions: Femur Fracture, Flatulence, Gastric Cancer, Surgery, Spinal Compression Fracture, Fracture, Adverse Event, LOW Turnover Osteopathy, Intervertebral Disc Protrusion, Back Pain, Phlebitis, Spinal Fracture, Hypoaesthesia, Gastrointestinal Stromal Tumour, HIP Fracture, Spleen Disorder, Metastases To Spine, Stress Fracture, Adenoma Benign, Osteoporosis, Constipation, Kyphosis, Fall, Breast Disorder Female, Road Traffic Accident, Intervertebral Disc Disorder, Dizziness, Bone Disorder, Injury, Gastrooesophageal Reflux Disease, Exostosis, Pelvic Fracture, Patellofemoral Pain Syndrome, Joint Dislocation, Osteoarthritis, Meniscus Lesion, Arthralgia, Spinal Disorder, Gait Disturbance, Spinal Osteoarthritis, Hypertension, Arthritis

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1997-01-01
    End date: 2009-06-08

Fosamax
    Dosage: 70 qw
    Administration route: Oral
    Start date: 2008-12-04

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteopenia
    Start date: 1997-01-01
    End date: 2009-06-08

Fosamax Plus D
    Dosage: 70/2800 qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2008-05-27

Fosamax Plus D
    Indication: Osteopenia

Other drugs received by patient: Allegra; Lipitor; Nasacort; Calcium (Unspecified); Actonel



Possible Fosamax Plus D side effects in

Reported by a individual with unspecified qualification from United States on 2012-07-26

Patient:

Reactions: Femur Fracture, Bone Disorder, LOW Turnover Osteopathy

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Actonel
    Indication: Osteoporosis

Boniva
    Indication: Osteoporosis

Fosamax
    Dosage: unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2005-01-01
    End date: 2010-01-01

Fosamax
    Administration route: Oral

Fosamax Plus D
    Administration route: Oral
    Indication: Osteoporosis



Possible Fosamax Plus D side effects in

Reported by a consumer/non-health professional from United States on 2012-07-26

Patient:

Reactions: Lymphadenopathy, Tachycardia, Oropharyngeal Pain, Macular Degeneration, Iron Deficiency Anaemia, Oedema Peripheral, Mitral Valve Prolapse, Back Pain, Apical Granuloma, Hyperparathyroidism Secondary, Cervical Dysplasia, Diverticulum Intestinal, Nephrosclerosis, Joint Injury, Post-Traumatic Stress Disorder, Staphylococcal Infection, Dysphonia, Anaemia of Chronic Disease, Increased Tendency To Bruise, Gastrointestinal Disorder, Osteoporosis, Shock Haemorrhagic, Abasia, Necrosis, Pulmonary Arterial Hypertension, Gastric Ulcer, Fall, Multi-Organ Failure, Foot Fracture, Hypoacusis, Amino Acid Level Increased, Depression, Bone Disorder, Renal Failure Acute, Dyspnoea, Cataract, Haemorrhoids, Arthralgia, Limb Asymmetry, Asthenia, Asthma, Vitamin D Deficiency, Femur Fracture, Disseminated Intravascular Coagulation, Urinary Incontinence, Deafness, Gingival Abscess, Obstructive Uropathy, Herpes Zoster, Dyspepsia, Carpal Tunnel Syndrome, Muscle Spasms, Cough, Myositis, Dysphagia, Cardiac Murmur, Hiatus Hernia, Peptic Ulcer, Anaemia, Osteonecrosis, Dehydration, Insomnia, Surgical Failure, Sleep Apnoea Syndrome, Pain, Fracture Nonunion, Synovial Cyst, Gastritis, Nephrolithiasis, Weight Increased, Fatigue, Eyelid Disorder, Dizziness, Migraine, Urinary Tract Infection, Trichotillomania, Renal Failure Chronic, Appendix Disorder, Retinopathy Hypertensive, Osteoarthritis, Anxiety, Renal Failure, Spinal Osteoarthritis, Spinal Disorder, Tooth Disorder, Hypertension, Infection

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Indication: Osteoporosis

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2003-10-16
    End date: 2006-06-22

Fosamax Plus D
    Indication: Osteoporosis

Fosamax Plus D
    Dosage: 70mg/2800
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2006-06-01
    End date: 2009-10-01



Possible Fosamax Plus D side effects in

Reported by a lawyer from United States on 2012-07-25

Patient:

Reactions: Femur Fracture, Retinal Detachment, Extrasystoles, Nocturia, Carpal Tunnel Syndrome, Squamous Cell Carcinoma of Skin, Tendonitis, Blood Creatinine Increased, Papule, Back Pain, Breast Pain, Actinic Keratosis, Cardiac Murmur, Pain in Extremity, Sarcoma, Osteopenia, Haemorrhoid Operation, Adverse Drug Reaction, Fall, Constipation, Muscle Rupture, Basal Cell Carcinoma, Bone Disorder, Inappropriate Schedule of Drug Administration, Vomiting, Cataract, Nausea, Squamous Cell Carcinoma, Hypercalcaemia, Hyperlipidaemia, Osteoarthritis, Neoplasm Malignant, Sialoadenitis, Bronchitis, Arthritis, Tooth Disorder

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: unk unk, qw
    Administration route: Oral
    Start date: 2008-01-09

Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2000-01-01
    End date: 2010-03-01

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2007-04-26

Other drugs received by patient: Calcium (Unspecified); Multi-Vitamins



Possible Fosamax Plus D side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-07-24

Patient:

Reactions: Periodontal Disease, Osteomyelitis, JAW Fracture, Blood Cholesterol Increased, Bone Disorder, Oral Surgery, Stomatitis, Abscess Oral, Dental Caries, Oral Infection, Gingival Disorder, Osteolysis, Osteoarthritis, Impaired Healing, Osteonecrosis of JAW, Hypertension, Tooth Disorder

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2003-08-01
    End date: 2006-09-01

Fosamax
    Indication: Ankle Fracture

Fosamax Plus D
    Indication: Ankle Fracture

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-09-21
    End date: 2010-05-01



Possible Fosamax Plus D side effects in

Reported by a consumer/non-health professional from United States on 2012-07-23

Patient:

Reactions: Femur Fracture, Bone Density Decreased, Bone Disorder

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: unk
    Administration route: Oral
    Start date: 1995-01-01
    End date: 2011-10-01

Fosamax
    Dosage: unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1995-01-01
    End date: 2011-10-01

Fosamax Plus D
    Dosage: unk
    Start date: 1995-01-01



Possible Fosamax Plus D side effects in

Reported by a consumer/non-health professional from United States on 2012-07-23

Patient:

Reactions: Vitamin D Deficiency, Bunion, Wrong Technique in Drug Usage Process, Osteoporosis, Rectal Haemorrhage, Mouth Ulceration, Constipation, Synovial Cyst, Hypercholesterolaemia, Depression, Bone Disorder, LIP Neoplasm Benign, Migraine, Tooth Fracture, Breast Mass, Anxiety, Osteonecrosis of JAW, Fibroma, Impaired Healing, Oral Disorder, Memory Impairment, Oral Torus, Tooth Disorder, Infection

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Boniva
    Administration route: Oral

Fosamax
    Dosage: 20 mg, unk
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2005-03-19

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2009-06-17
    End date: 2010-02-18

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2005-05-04
    End date: 2006-04-02

Fosamax Plus D
    Dosage: 70/2800
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2006-06-21
    End date: 2009-01-25

Other drugs received by patient: Xanax



Possible Fosamax Plus D side effects in

Reported by a consumer/non-health professional from United States on 2012-07-20

Patient:

Reactions: Muscle Atrophy, Weight Loss Poor, Femur Fracture, Urticaria, Headache, Palpitations, Ecchymosis, Nodule, Radiculopathy, Cervical Spinal Stenosis, Muscle Spasms, Myelopathy, Cough, Intervertebral Disc Protrusion, Back Pain, Chest Discomfort, Pain in Extremity, Lentigo Maligna Stage Unspecified, Melanosis Coli, Hepatic Steatosis, Cholelithiasis, Rhinitis Allergic, Insomnia, Increased Tendency To Bruise, Vision Blurred, Bunion, Pain, Bone Pain, Cystitis Haemorrhagic, Adverse Drug Reaction, Occipital Neuralgia, Constipation, Fall, Myalgia, Weight Increased, Neck Pain, Chest Pain, Blood Cholesterol Increased, Bone Disorder, Exostosis, Gastrooesophageal Reflux Disease, Dyspnoea, Lung Neoplasm, Drug Hypersensitivity, Haemorrhoids, Urinary Tract Infection, Renal Failure Chronic, Hypercalcaemia, Hepatic Enzyme Increased, Hyperlipidaemia, Anxiety, Limb Discomfort, Arthralgia, Mitral Valve Incompetence, Vertigo, Gait Disturbance, Spinal Osteoarthritis, Spinal Disorder, Metastases To Bone, Arthritis, Heart Sounds Abnormal

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Administration route: Oral
    Indication: Osteopenia
    Start date: 1995-09-01

Fosamax
    Dosage: 10 mg, unk
    Administration route: Oral
    End date: 2001-03-14

Fosamax
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1998-03-12

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2001-04-09
    End date: 2007-01-16

Fosamax Plus D
    Dosage: 70mg/2800
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2007-08-01
    End date: 2008-04-21



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