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

 
 



Index of reports > Cases with Fall (811)

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

 Reports 1 - 30 of 811   Next >>

Possible Fosamax Plus D side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-27

Patient:

Reactions: Vascular Insufficiency, Nasopharyngitis, Tinnitus, Blepharitis, Abdominal Discomfort, AGE-Related Macular Degeneration, Oedema Peripheral, LOW Turnover Osteopathy, Nervousness, Breast Cancer, Bursitis, HIP Fracture, Tonsillar Disorder, Seasonal Allergy, Increased Tendency To Bruise, Facial Bones Fracture, Polyarthritis, Bunion, Astigmatism, Adverse Drug Reaction, Somnolence, Fall, Muscle Strain, Fibroadenoma of Breast, Tooth Fracture, Cataract, Presbyopia, Musculoskeletal Pain, Muscular Weakness, Syncope, Limb Asymmetry, Gait Disturbance, Abdominal Hernia, Vitamin D Deficiency, Femur Fracture, Goitre, Myofascial Pain Syndrome, Herpes Zoster, Arthropathy, Adverse Event, Anaemia Postoperative, Muscle Spasms, Epistaxis, Cholelithiasis, Insomnia, Major Depression, Breast Complication Associated With Device, Drug Ineffective, Haemorrhage, Urine Calcium, Fracture Nonunion, Constipation, Groin Pain, Incision Site Pain, Nephrolithiasis, Myalgia, Bone Loss, Neck Pain, Intervertebral Disc Degeneration, Gastrooesophageal Reflux Disease, Scoliosis, Migraine, Vulvovaginal Mycotic Infection, Supraventricular Extrasystoles, Urinary Tract Infection, Appendix Disorder, Intraocular Lens Implant, Anxiety, Hyperlipidaemia, Tooth Disorder

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2009-01-14
    End date: 2010-01-01

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2003-04-25
    End date: 2007-02-01

Fosamax Plus D
    Dosage: 70/2800
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2007-03-22
    End date: 2009-12-21

Other drugs received by patient: Levothroid; Suclor; Chlorpheniramine Maleate (+) Pseudoephedrine Hydrochloride; Calcium (Unspecified); MK-9278; Hormones (Unspecified)



Possible Fosamax Plus D side effects in

Reported by a individual with unspecified qualification from United States on 2012-08-27

Patient:

Reactions: Polymyalgia Rheumatica, Femur Fracture, Contusion, Diverticulitis, Deafness, Chronic Obstructive Pulmonary Disease, Macular Degeneration, Dyspepsia, Cough, Anaemia Postoperative, Malabsorption, Fracture Delayed Union, Colonoscopy, Osteomalacia, Carotid Arteriosclerosis, Nasal Congestion, Bursitis, Cartilage Injury, Cataract Operation, Biopsy Artery, Diverticulum, Osteonecrosis, Insomnia, Vitamin D Decreased, Bone Metabolism Disorder, Bladder Prolapse, Drug Ineffective, Pain, Constipation, Fall, Fracture Nonunion, Meniscus Removal, Nephrolithiasis, Chest Pain, Blood Uric Acid Increased, Dizziness, Depression, Transient Ischaemic Attack, Gastrooesophageal Reflux Disease, Exostosis, Eye Disorder, Calcium Deficiency, Nausea, Haemorrhoids, Internal Fixation of Fracture, Hypercalcaemia, Osteoarthritis, Medical Device Removal, Anxiety, Appendicectomy, Vertigo, Hypothyroidism, Bronchitis, Spinal Osteoarthritis, Sinus Tachycardia, Hypertension

Adverse event resulted in: hospitalization

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

Fosamax
    Dosage: 35 mg, unk
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2006-08-27
    End date: 2007-05-16

Fosamax Plus D
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2007-05-16
    End date: 2009-02-03

Fosamax Plus D
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2009-04-06
    End date: 2010-02-01

Other drugs received by patient: Lipitor; Aspirin; Lisinopril; Ibuprofen; Zofran; Temazepam



Possible Fosamax Plus D side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-25

Patient:

Reactions: Femur Fracture, Escherichia Urinary Tract Infection, Flatulence, Nocturia, Headache, Dyspepsia, Oedema Peripheral, Stress Urinary Incontinence, White Blood Cell Count Increased, Anaemia Postoperative, Vulvovaginal Pruritus, Hypotension, Thyroid Neoplasm, Drug Eruption, Fall, Constipation, Foot Fracture, Poor Quality Sleep, Liver Function Test Abnormal, Blood Cholesterol Increased, Postoperative Fever, Injury, Wound Drainage, Adjustment Disorder With Depressed Mood, Cataract, Nausea, Rash, Carotid Bruit, Musculoskeletal Chest Pain, Dysgeusia, Limb Discomfort, Lichen Planus, Diarrhoea, Pollakiuria, Hypertension, Tooth Disorder

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2002-01-01

Fosamax
    Dosage: 10 mg, qd
    Indication: Osteoporosis
    Start date: 2000-06-23

Fosamax Plus D
    Indication: Osteopenia

Fosamax Plus D
    Dosage: 70 mg, unk
    Administration route: Oral
    Indication: Osteoporosis



Possible Fosamax Plus D side effects in

Reported by a physician from United States on 2012-08-24

Patient:

Reactions: Femur Fracture, Hypersensitivity, Osteoporosis, Tooth Extraction, Eczema, Stasis Dermatitis, Fall, Dermatitis Contact, Fracture, Blood Cholesterol Increased, Eczema Nummular, Open Reduction of Fracture, LOW Turnover Osteopathy, Decreased Appetite, Scoliosis, Polyp, Cellulitis, Cataract, Excoriation, Haemorrhoids, Varicose Vein, Diverticulum, Arthralgia, Post-Traumatic Headache, Stress Fracture, Skin Infection, Bladder Disorder, Hypertension

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Bone Loss
    Start date: 1999-01-01
    End date: 2007-07-01

Fosamax Plus D
    Dosage: 70/2800 mg, unk
    Administration route: Oral
    Indication: Bone Loss
    End date: 2010-03-17

Other drugs received by patient: Omega-3-Acid Ethyl Esters; Detrol; Nasonex; Cimetidine; Actos; Ascorbic Acid; Calcium (Unspecified) (+) Phytonadione (+) Vitamin D (Unspecified); Metformin HCL; Amitriptyline HCL; Prandin (Deflazacort); Multi-Vitamins



Possible Fosamax Plus D side effects in

Reported by a physician from United States on 2012-08-24

Patient:

Reactions: Arthrotomy, Device Failure, Femur Fracture, Fall, Open Reduction of Fracture, LOW Turnover Osteopathy

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Fosamax
    Dosage: 10 mg, unk
    Administration route: Oral
    Start date: 2000-01-05
    End date: 2001-02-21

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2008-07-26
    End date: 2008-11-01

Fosamax
    Administration route: Oral
    Indication: Prophylaxis
    Start date: 1995-01-01
    End date: 2008-01-01

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2001-04-11
    End date: 2006-11-27

Fosamax
    Dosage: 35 mg, unk
    Administration route: Oral
    Start date: 2007-07-18

Fosamax Plus D
    Dosage: 70mg/2800
    Administration route: Oral
    Indication: Prophylaxis
    Start date: 2007-05-03
    End date: 2008-04-28



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 health professional (non-physician/pharmacist) from United States on 2012-08-24

Patient:

Reactions: Femur Fracture, Nocturia, Dyspepsia, LOW Turnover Osteopathy, Bursitis, Hypoaesthesia, Joint Swelling, Ear Pain, Spinal Column Stenosis, Tooth Abscess, Osteoporosis, Spinal Haemangioma, Fracture Nonunion, Fall, Myalgia, Hypercholesterolaemia, Intervertebral Disc Degeneration, Gastrooesophageal Reflux Disease, Blood Pressure Increased, Tooth Fracture, Vomiting, Nausea, Muscular Weakness, Facet Joint Syndrome, Hyperlipidaemia, Device Failure, Anxiety, Impaired Healing, Presyncope, JAW Disorder, Spinal Disorder, Gait Disturbance, Tooth Disorder, Arthritis, Hypertension

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: unk
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2003-09-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2004-01-01
    End date: 2005-12-19

Fosamax Plus D
    Dosage: unk
    Administration route: Oral
    Start date: 2009-04-01

Fosamax Plus D
    Dosage: 70mg/5600
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2008-12-01

Fosamax Plus D
    Dosage: 70mg/2800
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-02-18
    End date: 2009-12-17

Other drugs received by patient: Thyroid TAB; Calcium (Unspecified); Vitamin D; Synthroid; Chondroitin Sulfate Sodium (+) Glucosamine Sulfate



Possible Fosamax Plus D side effects in

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

Patient:

Reactions: Fractured Sacrum, Vitamin D Deficiency, Femur Fracture, Contusion, Vitiligo, Keratosis Pilaris, Oesophagitis, Iron Deficiency Anaemia, Accident AT Work, Adverse Event, Melanocytic Naevus, LOW Turnover Osteopathy, Back Pain, Pain in Extremity, Acute Stress Disorder, Limb Injury, Tibia Fracture, Fall, Gastritis, Hypercholesterolaemia, Hyperparathyroidism, Sinusitis, Ligament Sprain, Migraine, Polyp, Drug Hypersensitivity, Atrial Fibrillation, Hydrometra, Atrophic Vulvovaginitis, Bladder Irritation, Arthralgia, Vertigo, Tooth Disorder, Traumatic Haematoma, Hyperthyroidism

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Fosamax
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1999-12-14
    End date: 2001-11-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2007-10-19
    End date: 2008-02-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2001-12-01
    End date: 2005-10-16

Fosamax Plus D
    Dosage: 70mg/2800
    Administration route: Oral
    Start date: 2008-09-02
    End date: 2010-11-15

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2005-11-19
    End date: 2006-08-30

Fosamax Plus D
    Dosage: 70mg/2800
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2007-05-20
    End date: 2007-10-14

Other drugs received by patient: MK-9278; Calcium (Unspecified); Vitamin D; Hormones (Unspecified); Synthroid; Vitamin E



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

Patient:

Reactions: Oesophagitis, LOW Turnover Osteopathy, Malabsorption, Fracture Delayed Union, Lumbar Vertebral Fracture, Diverticulum, Systemic Lupus Erythematosus, Polyarthritis, Osteoporosis, Abscess Soft Tissue, Adverse Drug Reaction, Wound Infection Staphylococcal, Kyphosis, Fall, Foot Fracture, Undifferentiated Connective Tissue Disease, Electrolyte Imbalance, Depression, Skeletal Injury, Candidiasis, Cataract, Vomiting, Gout, Musculoskeletal Pain, International Normalised Ratio Increased, Haemorrhoids, Device Failure, Arthralgia, Alopecia, Hypothyroidism, Asthenia, Leukopenia, Vitamin D Deficiency, Pancreatitis Acute, Femur Fracture, Urinary Incontinence, Urticaria, Enterococcal Infection, Tooth Extraction, Osteomyelitis, Hand Fracture, Headache, Pulmonary Granuloma, Vitamin B12 Deficiency, Fracture, Tendonitis, Muscle Spasms, Anaemia Postoperative, Pneumonia, Cellulitis, Cardiac Murmur, Peptic Ulcer, Stress Fracture, Vaginal Infection, Haemorrhage, Gastrooesophageal Reflux Disease, Calcium Deficiency, Device Component Issue, Cholecystitis Acute, Nausea, Urinary Tract Infection, Iron Deficiency, Rash, Soft Tissue Infection, Incision Site Infection, Diarrhoea, Hypertension, Antibiotic Level Above Therapeutic, Infection, Influenza Like Illness

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Osteopenia
    Start date: 1998-05-18

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2002-11-01
    End date: 2008-05-01

Fosamax

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2002-11-01
    End date: 2008-05-01

Fosamax
    Dosage: 10 mg, qd
    Administration route: Oral
    Start date: 1998-05-18

Fosamax
    Dosage: unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1996-01-01
    End date: 2008-05-01

Fosamax Plus D
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1996-01-01
    End date: 2008-01-01

Fosamax Plus D
    Indication: Osteopenia

Other drugs received by patient: Premarin



Possible Fosamax Plus D side effects in

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

Patient:

Reactions: Asthma, Femur Fracture, Fear, Fall, Cardiac Disorder, Poor Quality Sleep, Nephrolithiasis, Arthropathy, Blood Cholesterol Increased, Depression, Haematoma, LOW Turnover Osteopathy, Muscular Weakness, Stress, Synovial Disorder, Anxiety, Limb Discomfort, Limb Injury, Compression Fracture, Thyroid Disorder, Gait Disturbance, Arthritis, Hypertension, Infection

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2001-01-01
    End date: 2006-06-01

Fosamax
    Indication: Osteoporosis

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2006-07-05
    End date: 2009-01-01

Other drugs received by patient: Ascorbic Acid; Humira; Atenolol; Corticosteroids (Unspecified); Calcium (Unspecified); MK-9278



Possible Fosamax Plus D side effects in

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

Patient:

Reactions: Nasopharyngitis, Pneumonia Aspiration, Femur Fracture, Myasthenia Gravis, Headache, Seroma, Monoclonal Gammopathy, Palpitations, DRY Mouth, Carpal Tunnel Syndrome, Epistaxis, LOW Turnover Osteopathy, Pneumonia, Toxic Encephalopathy, Anaemia, Nasal Congestion, Bursitis, Nasal Septum Deviation, Hepatic Cyst, Oesophageal Disorder, Insomnia, Thyroid Disorder, Nervous System Disorder, Sleep Apnoea Syndrome, Confusional State, Narcolepsy, Atelectasis, Hypersensitivity, Osteoporosis, Adverse Drug Reaction, Restless Legs Syndrome, Pain, Fall, Fracture Nonunion, Synovial Cyst, Hypokalaemia, Foot Fracture, Neuropathy Peripheral, Tension Headache, Chronic Sinusitis, Bacterial Infection, Rotator Cuff Syndrome, Depression, Azotaemia, Gastrooesophageal Reflux Disease, Eye Disorder, Vomiting, Nausea, Folate Deficiency, Psoriasis, Multiple Fractures, Amnesia, Respiratory Failure, Arthritis, Hypertension

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2007-09-04

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2006-04-18
    End date: 2006-12-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2002-03-01
    End date: 2005-06-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2005-09-21
    End date: 2006-02-01

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2005-07-15
    End date: 2005-08-01

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2007-01-10
    End date: 2007-08-01

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2006-03-27

Other drugs received by patient: Reslin Tablets 25; Cymbalta; Fiorinal; Imitrex; Corticosteroids (Unspecified); MK-8797; MK-0152; Xanax; Singulair; Oxycodone HCL; Bentyl; Hydrocodone; Therapy Unspecified; Prozac



Possible Fosamax Plus D side effects in

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

Patient:

Reactions: Alcohol Abuse, Contusion, Chronic Obstructive Pulmonary Disease, Hyperhidrosis, Upper Extremity Mass, Balance Disorder, Upper Respiratory Tract Infection, Palpitations, Oedema Peripheral, Raynaud's Phenomenon, Post Procedural Haemorrhage, LOW Turnover Osteopathy, Breast Haematoma, Laceration, Delirium, Antinuclear Antibody Increased, Vitamin B12 Decreased, Osteoporosis, Adverse Drug Reaction, Fall, Carpal Tunnel Decompression, Fibrocystic Breast Disease, Blood Cholesterol Increased, Oedema, Depression, Electrolyte Imbalance, Renal Failure Acute, Nerve Compression, Device Failure, Loose Tooth, Bronchial Hyperreactivity, Vitamin D Deficiency, Night Sweats, Femur Fracture, Cervical Myelopathy, Arthropathy, Fracture, Sedation, Joint Effusion, Carpal Tunnel Syndrome, Cough, Pneumonia, Pain in Extremity, Gingival Disorder, Encephalopathy, Haemorrhagic Anaemia, Hypoaesthesia, Respiratory Distress, Convulsion, Paraesthesia, Tendon Sheath Lesion Excision, Joint Swelling, Insomnia, Stress Fracture, Cardiovascular Disorder, Wrist Fracture, Constipation, Fracture Nonunion, Groin Pain, Neuropathy Peripheral, Neck Pain, Drug Hypersensitivity, Urinary Tract Infection, Incorrect Dose Administered, Cervicobrachial Syndrome, Osteoarthritis, Hyperlipidaemia, Adjustment Disorder With Anxiety, Spinal Osteoarthritis, Tooth Disorder

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 20 mg, qw
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2009-11-05

Fosamax
    Administration route: Oral
    Start date: 2008-02-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2000-10-01
    End date: 2007-09-01

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2008-11-01
    End date: 2009-11-01

Fosamax Plus D
    Dosage: 70/5600
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2007-10-11
    End date: 2008-10-01

Other drugs received by patient: Vitamin D; Corticosteroids (Unspecified); Hormones (Unspecified); Calcium (Unspecified)



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 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 lawyer from United States on 2012-08-23

Patient:

Reactions: Femur Fracture, Electrocardiogram T Wave Amplitude Decreased, Diverticulum Intestinal Haemorrhagic, Urticaria, Fall, Hypokalaemia, Muscle Enzyme Increased, Oesophagitis, Iron Deficiency Anaemia, Upper Respiratory Tract Infection, Erosive Oesophagitis, Bone Density Decreased, Depression, Tendonitis, Sinusitis, Blood Pressure Increased, Anxiety Disorder, Hiatus Hernia, Haemorrhoids, Urinary Tract Infection, Drug Hypersensitivity, Dental Caries, Fungal Infection, Sinus Disorder, Uterine Disorder, Gastric Polyps, Hypertension

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Fosamax
    Dosage: 10 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1999-06-23
    End date: 2001-12-01

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2002-04-01
    End date: 2008-10-03

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2008-10-04
    End date: 2010-08-01

Fosamax

Fosamax Plus D
    Administration route: Oral
    Indication: Osteoporosis

Fosamax Plus D
    Indication: Osteopenia

Other drugs received by patient: Vitaplex



Possible Fosamax Plus D side effects in

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

Patient:

Reactions: Femur Fracture, Osteoporosis, Upper Limb Fracture, Tooth Extraction, Hand Fracture, Hyperaemia, Fall, Fracture Nonunion, Seroma, Abdominal Hernia Repair, Adverse Event, Open Reduction of Fracture, LOW Turnover Osteopathy, Oral Surgery, Bursitis, Fungal Infection, Stress Fracture, Femoral Neck Fracture, Arthritis, Infection

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2003-10-01
    End date: 2006-04-20

Fosamax
    Indication: Osteopenia

Fosamax Plus D
    Dosage: 70 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-05-08
    End date: 2009-01-29

Other drugs received by patient: Celebrex; Naproxen; Celebrex; Naproxen; Celebrex; Celebrex



Possible Fosamax Plus D side effects in

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

Patient:

Reactions: Nasopharyngitis, Lymphadenopathy, Hyperkeratosis, Eczema, Abdominal Discomfort, Iron Deficiency Anaemia, Dermatitis, Oedema Peripheral, Nail Disorder, Breast Cancer, Cerumen Impaction, Angina Pectoris, Drug Intolerance, Musculoskeletal Discomfort, Bursitis, Temporomandibular Joint Syndrome, Dysphonia, Increased Tendency To Bruise, Pancreatitis, Bunion, Seborrhoeic Keratosis, Fall, Kyphosis, Muscle Strain, Hypercholesterolaemia, Overdose, Intestinal Polyp, Cataract, Radius Fracture, Device Failure, Gait Disturbance, Eustachian Tube Dysfunction, Foot Deformity, LIP Disorder, Femur Fracture, Urticaria, Deafness, Herpes Zoster, Arthropathy, Vaginal Odour, Colon Adenoma, Adverse Event, Drug Administration Error, Cough, Chest Discomfort, Hiatus Hernia, Otitis Externa, Renal Cyst, Cholelithiasis, Joint Swelling, Otitis Media, Dermal Cyst, Drug Ineffective, Restless Legs Syndrome, Constipation, Senile Osteoporosis, Frequent Bowel Movements, Skin Lesion, Sinusitis, Gastrooesophageal Reflux Disease, RIB Fracture, Scoliosis, Cholecystitis Acute, Urinary Tract Infection, Psoriasis, Varicose Vein, Rash, Onychomycosis, Plantar Fasciitis, Osteoarthritis, Anxiety, Diarrhoea, Dysuria, Arthritis

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Alendronate Sodium
    Dosage: 70 mg, unk
    Start date: 2008-09-23

Fosamax
    Dosage: 10 mg, qd
    Administration route: Oral
    Start date: 1996-01-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1996-01-01

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1996-01-01
    End date: 2009-09-01

Other drugs received by patient: Raloxifene Hydrochloride; Actonel; Calcium (Unspecified); Elocon; Celexa; Derma-Smoothe / FS; Tums E-X; Viactiv Soft Calcium Chews



Possible Fosamax Plus D side effects in

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

Patient:

Reactions: Thrombosed Varicose Vein, Femur Fracture, Osteoporosis, Head Injury, Pyrexia, Chronic Obstructive Pulmonary Disease, Fall, Foot Fracture, Muscle Strain, Lipoma, Irritable Bowel Syndrome, Bone Density Decreased, Fibula Fracture, Joint Effusion, Gastrooesophageal Reflux Disease, Anaemia Postoperative, RIB Fracture, Scoliosis, Cellulitis, Fracture Delayed Union, Atrial Fibrillation, Laceration, Joint Dislocation, Hyperlipidaemia, HIP Fracture, Osteoarthritis, Diverticulum, Impaired Healing, Intramedullary ROD Insertion, Deep Vein Thrombosis

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 1 df, qw
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2002-01-01
    End date: 2010-01-01

Fosamax Plus D
    Dosage: 1 df, qw
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2006-09-05
    End date: 2010-08-01



Possible Fosamax Plus D side effects in

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

Patient:

Reactions: Femur Fracture, Contusion, Urinary Incontinence, Eczema, Colonic Polyp, Monoclonal Gammopathy, Patella Fracture, Adverse Event, LOW Turnover Osteopathy, Pain in Extremity, Joint Injury, Occult Blood Positive, Stress Fracture, Seborrhoeic Keratosis, Drug Ineffective, Osteoporosis, Head Injury, Fracture Nonunion, Fall, Muscle Tightness, Hypokalaemia, Hypercholesterolaemia, Dizziness, Ligament Sprain, RIB Fracture, Nausea, Supraventricular Extrasystoles, Nail Dystrophy, Hypophosphataemia, Osteoarthritis, Conjunctival Haemorrhage, Arthralgia, Impaired Healing, Tooth Disorder, Leukocytosis

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Alendronate Sodium
    Dosage: 70mg
    Start date: 2009-02-08

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2002-09-01
    End date: 2010-07-01

Fosamax
    Dosage: 70 mg
    Administration route: Oral
    Start date: 2008-08-07

Fosamax
    Dosage: 10 mg
    Administration route: Oral
    Indication: Osteopenia

Fosamax Plus D
    Dosage: 70mg/2800iu
    Administration route: Oral
    Start date: 2005-10-13

Other drugs received by patient: Hormones (Unspecified)



Possible Fosamax Plus D side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-23

Patient:

Reactions: Weight Decreased, Bladder Mass, Femur Fracture, Clostridium Difficile Colitis, Breast Cancer Recurrent, Gallbladder Disorder, Bone Density Decreased, Peptic Ulcer, Hyperglycaemia, Anaemia, Breast Mass, Renal Cyst, Osteopenia, Diverticulum, Stress Fracture, Wrist Fracture, Drug Ineffective, Osteoporosis, Fall, Constipation, Hypokalaemia, Plasma Protein Metabolism Disorder, Blood Cholesterol Increased, Injury, Umbilical Hernia, Nausea, Rash, Anxiety, Hyperlipidaemia, Biliary Colic, Loose Tooth, Metastases To Bone, Hypertension, Tooth Disorder

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 5 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1999-07-16
    End date: 2001-03-13

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2001-06-14
    End date: 2008-06-11

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2008-01-26
    End date: 2008-07-11

Fosamax Plus D
    Indication: Osteopenia



Possible Fosamax Plus D side effects in

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

Patient:

Reactions: Underweight, Femur Fracture, Fall, Fatigue, Breast Cyst, Chest Pain, Intervertebral Disc Displacement, Cardiac Murmur, Vein Disorder, Excoriation, Anaemia, Musculoskeletal Discomfort, Musculoskeletal Chest Pain, Appendix Disorder, Tonsillar Disorder, Dysarthria, Syncope, Limb Injury, Uterine Disorder, Hypertension

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, weekly
    Administration route: Oral
    Start date: 2000-05-30

Fosamax
    Dosage: 10 mg, daily
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2000-06-01
    End date: 2009-10-01

Fosamax Plus D
    Dosage: 70/2800
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-08-14
    End date: 2008-08-17



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, Bone Marrow Donation, Drug Ineffective, Osteoporosis, Metaplasia, Restless Legs Syndrome, Constipation, Fall, Fracture Nonunion, Intraductal Papilloma of Breast, Stem Cell Transplant, Reflux Laryngitis, Neuropathy Peripheral, Uterine Leiomyoma, Gastrooesophageal Reflux Disease, Open Reduction of Fracture, RIB Fracture, Osteopetrosis, Lung Neoplasm, Biopsy Cervix, Patellofemoral Pain Syndrome, Ovarian Cyst, Biopsy Breast, Cervical Dysplasia, Bursitis, Meniscus Lesion, Osteoarthritis, Device Failure, Arthralgia, non-Hodgkin's Lymphoma, Angiopathy, Breast Fibrosis

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2002-06-01
    End date: 2005-04-01

Fosamax Plus D
    Dosage: 70mg/5600
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2005-04-01
    End date: 2009-11-01

Other drugs received by patient: RED Yeast; Mega; Vitamin B Complex CAP; Valtrex; Toprol-XL; MK-9278; Horse Chestnut; Flaxseed; Lipitor; Trilipix; Artichoke; Vitamin D; Ascorbic Acid (+) Collagen; Calcium Citrate; Dyazide; Chondroitin Sulfate Sodium (+) Glucosamine Sulfate; Therapy Unspecified; Calcium (Unspecified); Standard Process Ligaplex II



Possible Fosamax Plus D side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-23

Patient:

Reactions: Contusion, Chronic Obstructive Pulmonary Disease, Balance Disorder, Anal Injury, Angina Pectoris, Malnutrition, Joint Injury, Cartilage Injury, Post-Traumatic Stress Disorder, Rosacea, Tibia Fracture, Polyarthritis, Bunion, Alveolar Osteitis, Rectal Haemorrhage, Fall, Foot Fracture, Blood Cholesterol Increased, Depression, Exostosis, Ligament Sprain, Emphysema, Tooth Fracture, Breast Disorder, Haemorrhoids, Musculoskeletal Pain, Arthralgia, JAW Disorder, Limb Asymmetry, DRY Eye, Corneal Abrasion, Weight Decreased, Osteomyelitis, Lower Limb Fracture, Arthropathy, Fibula Fracture, Muscle Spasms, Gingival Bleeding, Acne, Fibrous Histiocytoma, Insomnia, Benign Neoplasm of Thyroid Gland, Mastication Disorder, Sleep Apnoea Syndrome, Neuralgia, Rectal Discharge, Jaundice, Head Injury, Liver Disorder, Sexual Abuse, Dyspnoea Exertional, Fatigue, Fibromyalgia, Intervertebral Disc Degeneration, RIB Fracture, Dental Caries, Psoriasis, Patellofemoral Pain Syndrome, Musculoskeletal Chest Pain, Stitch Abscess, Panic Attack, Diarrhoea, Osteonecrosis of JAW, Repetitive Strain Injury, Tooth Disorder

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Alendronate Sodium
    Dosage: 70 mg, unk
    Start date: 2008-04-29

Fosamax

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2008-04-30
    End date: 2010-08-01

Fosamax
    Dosage: unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2003-12-01
    End date: 2006-09-22

Fosamax
    Indication: Osteopenia

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-09-21
    End date: 2009-03-31



Possible Fosamax Plus D side effects in

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

Patient:

Reactions: Foot Deformity, Vitamin D Deficiency, Weight Decreased, Femur Fracture, Polyp Colorectal, Nocturia, Chronic Obstructive Pulmonary Disease, Rheumatoid Arthritis, Acute Respiratory Distress Syndrome, White Blood Cell Count Increased, LOW Turnover Osteopathy, Anaemia, Haemorrhagic Anaemia, Nasal Septum Deviation, Joint Injury, Tremor, Insomnia, Stress Fracture, Abscess, Bunion, Pain, Fall, Myalgia, Enterovesical Fistula, Depression, Gastrooesophageal Reflux Disease, Medical Device Discomfort, Emphysema, Breast Disorder, Osteoarthritis, Anxiety, Lung Disorder, Bronchitis, Incision Site Erythema

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Alendronate Sodium
    Dosage: 70 mg, unk
    Start date: 2009-02-09
    End date: 2010-03-01

Alendronate Sodium
    Dosage: 70 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2008-03-01
    End date: 2008-01-01

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

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2001-10-02
    End date: 2008-03-01

Fosamax
    Dosage: 10 mg, unk
    Administration route: Oral
    Start date: 1999-02-06
    End date: 2001-07-06

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2008-12-01

Fosamax Plus D
    Dosage: unk
    Administration route: Oral
    Start date: 2000-01-01

Other drugs received by patient: Tamoxifen Citrate; Nicoderm



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, Arachnoiditis, Gastrointestinal Surgery, Colonic Polyp, Iron Deficiency Anaemia, Oedema Peripheral, Vertebral Foraminal Stenosis, Carpal Tunnel Syndrome, Radiculopathy, LOW Turnover Osteopathy, Back Disorder, Cellulitis, Anaemia, Bursitis, Haemorrhagic Anaemia, Cholelithiasis, Rhinitis Allergic, Limb Injury, Insomnia, Bunion, Fall, Constipation, Muscle Strain, Hypercholesterolaemia, Joint Crepitation, Skin Ulcer, Intervertebral Disc Degeneration, Rotator Cuff Syndrome, Depression, Gastrooesophageal Reflux Disease, Pain in JAW, Pelvic Fracture, Migraine, Scoliosis, Abscess Drainage, Joint Dislocation, Hernia, Onychomycosis, Anxiety, Osteoarthritis, Impaired Healing, Sinus Headache, Spinal Osteoarthritis, Tooth Disorder, Hypertension

Adverse event resulted in: hospitalization, disablity

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

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1995-01-01
    End date: 2009-07-01

Fosamax Plus D
    Administration route: Oral
    Indication: Osteoporosis

Fosamax Plus D
    Indication: Osteopenia

Other drugs received by patient: Prilosec; MK-9278



Possible Fosamax Plus D side effects in

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

Patient:

Reactions: Vitamin D Deficiency, Intervertebral Disc Protrusion, Scoliosis, Femur Fracture, Drug Ineffective, Upper-Airway Cough Syndrome, Ear Infection, Tooth Infection, Eye Infection, Fall, Foot Fracture, Osteoarthritis, Intervertebral Disc Degeneration, Spinal Deformity, LOW Turnover Osteopathy

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Alendronate Sodium
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2008-04-21
    End date: 2009-07-21

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2003-01-27
    End date: 2008-07-29

Fosamax
    Dosage: 10 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2000-08-17
    End date: 2003-01-27

Fosamax Plus D
    Dosage: 70 mg, qw
    Indication: Osteoporosis

Other drugs received by patient: Vitamins (Unspecified)



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 lawyer from United States on 2012-08-23

Patient:

Reactions: Contusion, Femur Fracture, Urinary Incontinence, Dementia, Headache, Cerebral Ischaemia, Colonic Polyp, Physical Abuse, Malaise, Dyspepsia, Gallbladder Disorder, Calculus Urinary, LOW Turnover Osteopathy, Muscle Spasms, Mitral Valve Prolapse, Chest Discomfort, Breast Mass, Haemorrhagic Anaemia, Bursitis, Insomnia, Stress Fracture, Uterine Disorder, Essential Hypertension, Glaucoma, Osteoporosis, Myositis Ossificans, Restless Legs Syndrome, Mental Status Changes, Fall, Hypokalaemia, Hypercholesterolaemia, Dermatitis Contact, Dyspnoea Exertional, Left Ventricular Dysfunction, Fatigue, Fibromyalgia, Chest Pain, Hearing Impaired, Depression, Iodine Allergy, Gastrooesophageal Reflux Disease, Eye Disorder, Ligament Sprain, Cataract, Type 2 Diabetes Mellitus, Psychological Abuse, Breast Disorder, Drug Hypersensitivity, Ovarian Disorder, Haemorrhoids, Urinary Tract Infection, Multiple Fractures, Hypercalcaemia, Capsular Contracture Associated With Breast Implant, Hyperlipidaemia, Carotid Artery Stenosis, Osteoarthritis, Syncope, Dysuria, Memory Impairment, Bladder Disorder, Asthenia

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2000-12-01
    End date: 2008-03-01

Fosamax
    Indication: Osteopenia

Fosamax Plus D
    Indication: Osteopenia

Fosamax Plus D
    Dosage: unk mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2008-03-01
    End date: 2010-02-01

Other drugs received by patient: MK-9278



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