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

 
 



Index of reports > Cases with Osteonecrosis ()

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Fosamax Plus D (Alendronate / Cholecalciferol) where reactions include osteonecrosis. 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 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 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 lawyer from United States on 2012-08-22

Patient:

Reactions: Polymyalgia Rheumatica, Femur Fracture, Diverticulitis, Deafness, Macular Degeneration, Surgery, Dyspepsia, Cough, Malabsorption, Colonoscopy, Osteomalacia, Carotid Arteriosclerosis, Bursitis, Cartilage Injury, Cataract Operation, Osteonecrosis, Biopsy Artery, Vitamin D Decreased, Insomnia, Transfusion, Bone Metabolism Disorder, Bladder Prolapse, Pain, Fall, Nephrolithiasis, Chest Pain, Blood Uric Acid Increased, Dizziness, Depression, Gastrooesophageal Reflux Disease, Exostosis, Transient Ischaemic Attack, Eye Disorder, Calcium Deficiency, Nausea, Hypercalcaemia, Meniscus Lesion, Medical Device Removal, Anxiety, Osteoarthritis, Impaired Healing, Appendicectomy, Hypothyroidism, Vertigo, Bronchitis, Spinal Osteoarthritis, Sinus Tachycardia, Hypertension

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Fosamax
    Dosage: 35 mg, unk
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2006-08-27
    End date: 2007-05-16

Fosamax
    Indication: Osteoporosis

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; Temazepam; Lisinopril; Zofran; Ibuprofen



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 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 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 individual with unspecified qualification from United States on 2012-07-31

Patient:

Reactions: Polymyalgia Rheumatica, Femur Fracture, Diverticulitis, Pain, Surgery, Dyspepsia, Depression, Transient Ischaemic Attack, Eye Disorder, Nausea, Colonoscopy, Cataract Operation, Medical Device Removal, Anxiety, Biopsy Artery, Osteonecrosis, Vitamin D Decreased, Insomnia, Vertigo, Hypothyroidism, Spinal Osteoarthritis, Hypertension

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
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



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 65 year old female

Reported by a physician from United States on 2012-07-02

Patient: 65 year old female, weighing 85.0 kg (187.0 pounds)

Reactions: Lymphadenopathy, Tachycardia, Oropharyngeal Pain, Macular Degeneration, Iron Deficiency Anaemia, Oedema Peripheral, Mitral Valve Prolapse, Back Pain, Hyperparathyroidism Secondary, Apical Granuloma, Cervical Dysplasia, Joint Injury, Diverticulum Intestinal, Nephrosclerosis, Post-Traumatic Stress Disorder, Anaemia of Chronic Disease, Dysphonia, Staphylococcal Infection, Gastrointestinal Disorder, Increased Tendency To Bruise, Osteoporosis, Necrosis, Shock Haemorrhagic, Pulmonary Arterial Hypertension, Fall, Gastric Ulcer, Hypoacusis, Multi-Organ Failure, Foot Fracture, Amino Acid Level Increased, Bone Disorder, Depression, Renal Failure Acute, Dyspnoea, Cataract, Haemorrhoids, Arthralgia, Limb Asymmetry, Asthma, Femur Fracture, Urinary Incontinence, Disseminated Intravascular Coagulation, Deafness, Gingival Abscess, Obstructive Uropathy, Herpes Zoster, Dyspepsia, Carpal Tunnel Syndrome, Muscle Spasms, Cough, Myositis, Cardiac Murmur, Hiatus Hernia, Dysphagia, Peptic Ulcer, Anaemia, Osteonecrosis, Vitamin D Decreased, Insomnia, Dehydration, 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
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2003-10-16
    End date: 2006-06-22

Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2003-10-16
    End date: 2006-06-22

Fosamax Plus D
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2005-08-31
    End date: 2009-01-01

Fosamax Plus D
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2005-08-31
    End date: 2009-01-01



Possible Fosamax Plus D side effects in 50 year old female

Reported by a physician from United States on 2012-06-22

Patient: 50 year old female, weighing 78.0 kg (171.6 pounds)

Reactions: Bone Fragmentation, Night Sweats, Femur Fracture, Hyperventilation, Adverse Event, Ankle Impingement, Carpal Tunnel Syndrome, Vertebral Foraminal Stenosis, Stress Urinary Incontinence, Multiple Sclerosis, Back Disorder, LOW Turnover Osteopathy, Intervertebral Disc Protrusion, Ankle Fracture, Paraesthesia, Osteonecrosis, Chondromalacia, Tendon Disorder, Haemangioma, Stress Fracture, Tibia Fracture, Fear, Fall, Synovial Cyst, Foot Fracture, Post Lumbar Puncture Syndrome, Lipomatosis, RIB Fracture, Spondylolisthesis, Urinary Tract Infection, Synovitis, Avulsion Fracture, Tenosynovitis, Device Failure, Meniscus Lesion, Osteoarthritis, Sexual Dysfunction, Spinal Osteoarthritis, Bladder Disorder

Adverse event resulted in: hospitalization, disablity

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

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

Fosamax
    Administration route: Oral

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

Other drugs received by patient: Kava; Effexor; Premarin; ST Johns Wort



Possible Fosamax Plus D side effects in 66 year old female

Reported by a physician from United States on 2012-06-18

Patient: 66 year old female, weighing 68.0 kg (149.6 pounds)

Reactions: Foot Deformity, Contusion, Femur Fracture, Pelvic Adhesions, Pyrexia, Nocturia, Trigger Finger, Comminuted Fracture, Treatment Noncompliance, Hair Texture Abnormal, Ecchymosis, Adverse Event, Fracture Displacement, Back Pain, Intervertebral Disc Protrusion, Dysphagia, Hiatus Hernia, Bursitis, Stress, HIP Fracture, Diverticulum, Osteonecrosis, Limb Injury, Insomnia, Stress Fracture, Exercise Lack of, Atelectasis, Bunion, Drug Ineffective, Pain, Pelvic Pain, Fall, Periarthritis, Constipation, Cystocele, Road Traffic Accident, Fibromyalgia, Intervertebral Disc Degeneration, Rotator Cuff Syndrome, Hypertonic Bladder, Acquired Oesophageal WEB, Depression, Procedural Pain, Cataract, Nausea, Haemorrhoids, Musculoskeletal Pain, Urinary Tract Infection, Musculoskeletal Chest Pain, Tenosynovitis, Plantar Fasciitis, Osteoarthritis, Anxiety, Hyperlipidaemia, Spinal Disorder, Spinal Osteoarthritis, Asthenia

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Alendronate Sodium
    Administration route: Oral
    Start date: 2009-11-16

Alendronate Sodium
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2008-09-27
    End date: 2009-08-27

Fosamax
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2000-04-28
    End date: 2001-01-18

Fosamax
    Administration route: Oral
    Start date: 2002-01-12
    End date: 2005-09-13

Fosamax
    Administration route: Oral
    Start date: 2008-02-17
    End date: 2008-08-31

Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2008-02-17
    End date: 2008-08-31

Fosamax Plus D
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2005-11-14
    End date: 2007-09-03

Fosamax Plus D
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2005-11-14
    End date: 2007-09-03

Other drugs received by patient: Estradiol; Prevacid; Prilosec



Possible Fosamax Plus D side effects in 76 year old female

Reported by a physician from United States on 2012-06-12

Patient: 76 year old female

Reactions: Abdominal Pain, Muscle Atrophy, Femur Fracture, Urinary Incontinence, Fall, Cystocele, Hypertrichosis, Oedema Peripheral, Tendonitis, RIB Fracture, Anaemia Postoperative, Type 2 Diabetes Mellitus, Cerumen Impaction, Pubis Fracture, Bursitis, Osteoarthritis, Device Failure, Osteonecrosis, Activities of Daily Living Impaired, Increased Tendency To Bruise, Alopecia, Gait Disturbance, Arthritis

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Actonel
    Start date: 2003-12-01

Alendronate Sodium
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2009-02-01
    End date: 2010-05-01

Alendronate Sodium
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2009-02-01
    End date: 2010-05-01

Boniva

Fosamax
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2002-01-01

Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2002-01-01

Fosamax Plus D
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2007-07-26

Fosamax Plus D
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2007-07-26

Other drugs received by patient: Premarin; Lotrel; Synthroid



Possible Fosamax Plus D side effects in 76 year old female

Reported by a physician from United States on 2012-06-08

Patient: 76 year old female

Reactions: Abdominal Pain, Femur Fracture, Urinary Incontinence, Fall, Cystocele, Hypertrichosis, Oedema Peripheral, Tendonitis, RIB Fracture, Type 2 Diabetes Mellitus, Cerumen Impaction, Pubis Fracture, Bursitis, Osteoarthritis, Device Failure, Osteonecrosis, Alopecia, Increased Tendency To Bruise, Arthritis

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Actonel
    Start date: 2003-12-01

Alendronate Sodium
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2009-02-01
    End date: 2010-05-01

Alendronate Sodium
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2009-02-01
    End date: 2010-05-01

Boniva

Fosamax
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2002-01-01

Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2002-01-01

Fosamax Plus D
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2007-07-26

Fosamax Plus D
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2007-07-26

Other drugs received by patient: Premarin; Synthroid; Lotrel



Possible Fosamax Plus D side effects in 55 year old female

Reported by a physician from United States on 2012-06-08

Patient: 55 year old female, weighing 57.0 kg (125.4 pounds)

Reactions: Polymyalgia Rheumatica, Contusion, Piriformis Syndrome, Monoclonal Immunoglobulin Present, Vaginal Disorder, Malaise, Upper Respiratory Tract Infection, Oedema Peripheral, LOW Turnover Osteopathy, Breast Cancer Stage I, 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, Bone Fragmentation, Underweight, 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, Joint Swelling, Acute Sinusitis, Ear Pain, Scar, Uterine Cervix Stenosis, Urethral Stenosis, Dyslipidaemia, Hypophosphatasia, Drug Ineffective, Hypokalaemia, Fatigue, Intervertebral Disc Degeneration, Hypertonic Bladder, Sinusitis, Gastrooesophageal Reflux Disease, Migraine, Swelling Face, Urinary Tract Infection, Condition Aggravated, Osteoarthritis, Anxiety, Uterine Spasm, Spinal Osteoarthritis, Tooth Disorder

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Alendronate Sodium
    Start date: 2009-02-13

Alendronate Sodium
    Start date: 2009-02-13

Alendronate Sodium
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2009-06-01
    End date: 2009-12-01

Alendronate Sodium
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2009-06-01
    End date: 2009-12-01

Boniva
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2005-09-01
    End date: 2006-01-01

Fosamax
    Administration route: Oral
    Start date: 2001-01-01

Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1997-01-01
    End date: 2001-02-01

Fosamax
    Administration route: Oral
    Start date: 2009-01-01
    End date: 2010-01-01

Fosamax
    Administration route: Oral
    Indication: Osteopenia
    Start date: 1997-01-01
    End date: 2001-02-01

Fosamax
    Administration route: Oral
    Start date: 2009-01-01
    End date: 2010-01-01

Fosamax
    Administration route: Oral
    Start date: 2001-01-01

Fosamax Plus D
    Administration route: Oral
    Start date: 2008-02-01
    End date: 2008-11-01

Fosamax Plus D
    Administration route: Oral
    Start date: 2008-01-01
    End date: 2009-01-01

Fosamax Plus D
    Administration route: Oral
    Start date: 2008-02-01
    End date: 2008-11-01

Fosamax Plus D
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2006-01-01
    End date: 2008-01-01

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

Fosamax Plus D
    Administration route: Oral
    Start date: 2008-01-01
    End date: 2009-01-01

Other drugs received by patient: Premarin; Vitamins (Unspecified); Hormones (Unspecified); Prempro; Acetaminophen; Nortriptyline; Vitamin D (Unspecified); Cholecalciferol; Percocet; Calcium (Unspecified) and Vitamin D (Unspecified); Ultram; Calcium (Unspecified)



Possible Fosamax Plus D side effects in 76 year old female

Reported by a physician from United States on 2012-06-06

Patient: 76 year old female

Reactions: Abdominal Pain, Femur Fracture, Urinary Incontinence, Fall, Cystocele, Hypertrichosis, Oedema Peripheral, Tendonitis, Type 2 Diabetes Mellitus, Cerumen Impaction, Bursitis, Device Failure, Osteoarthritis, Osteonecrosis, Increased Tendency To Bruise, Alopecia, Arthritis

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Actonel
    Start date: 2003-12-01

Alendronate Sodium
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2009-02-01
    End date: 2010-05-01

Alendronate Sodium
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2009-02-01
    End date: 2010-05-01

Boniva

Fosamax
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2002-01-01

Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2002-01-01

Fosamax Plus D
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2007-07-26

Fosamax Plus D
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2007-07-26

Other drugs received by patient: Lotrel; Premarin; Synthroid



Possible Fosamax Plus D side effects in 74 year old female

Reported by a physician from United States on 2012-06-06

Patient: 74 year old female, weighing 70.0 kg (154.0 pounds)

Reactions: Abdominal Hernia, Femur Fracture, Coagulopathy, Cyst, Treatment Noncompliance, Blepharitis, Arthropathy, Iron Deficiency Anaemia, Fibrin D Dimer Increased, Oedema Peripheral, Ectropion, Eyelid Ptosis, LOW Turnover Osteopathy, Breast Cancer, Subcutaneous Haematoma, Haemorrhagic Anaemia, Joint Injury, Paraesthesia, Osteonecrosis, Insomnia, Colitis, Glaucoma, Astigmatism, Pain, Rectal Haemorrhage, Stasis Dermatitis, Fall, Constipation, Cardiac Valve Disease, Skin Ulcer, Hypermetropia, Lymphoedema, Postmenopause, Presbyopia, Urinary Tract Infection, Conjunctival Granuloma, Arthralgia, Procedural Hypotension, Gait Disturbance, Corneal Oedema, Hypertension, Deep Vein Thrombosis, Ocular Hypertension

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Fosamax
    Administration route: Oral
    Indication: HIP Arthroplasty
    Start date: 2006-01-01
    End date: 2010-03-06

Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-01-01
    End date: 2010-03-06

Fosamax
    Administration route: Oral
    Start date: 2008-12-01

Fosamax Plus D
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-01-01
    End date: 2008-12-04

Other drugs received by patient: Warfarin; Prinivil; Coumadin; Calcium (Unspecified); Vitamin D (Unspecified); Tamoxifen Citrate



Possible Fosamax Plus D side effects in 49 year old female

Reported by a physician from United States on 2012-06-04

Patient: 49 year old female, weighing 114.0 kg (250.8 pounds)

Reactions: Tooth Loss, Eye Infection, Adverse Event, Paget's Disease of THE Breast, Stomatitis, Breast Cancer Stage I, Ovarian Cyst, Pancytopenia, Gingival Disorder, Renal Cyst, Osteonecrosis, Temporomandibular Joint Syndrome, Thyroid Neoplasm, Atelectasis, Haemorrhage, Necrosis, Pain, Chest X-RAY Abnormal, Bone Scan Abnormal, Bone Loss, Blood Cholesterol Increased, Dyspnoea, Renal Disorder, Type 2 Diabetes Mellitus, Drug Hypersensitivity, Dental Caries, Hidradenitis, Pulmonary Fibrosis, Osteonecrosis of JAW, JAW Disorder, Hypertension, Tooth Disorder

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2006-04-01
    End date: 2010-05-01

Fosamax Plus D
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2006-04-01
    End date: 2010-05-01



Possible Fosamax Plus D side effects in 51 year old female

Reported by a physician from United States on 2012-05-31

Patient: 51 year old female

Reactions: Bone Fragmentation, Night Sweats, Dyslipidaemia, Femur Fracture, Fear, Fall, Foot Fracture, Adverse Event, Carpal Tunnel Syndrome, Depression, Multiple Sclerosis, Back Disorder, LOW Turnover Osteopathy, Ankle Fracture, Cartilage Injury, Chondromalacia, Osteonecrosis, Stress Fracture, Uterine Disorder, Bladder Disorder, Hypertension

Adverse event resulted in: hospitalization, disablity

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

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



Possible Fosamax Plus D side effects in female

Reported by a lawyer from United States on 2012-05-31

Patient: female

Reactions: Osteonecrosis, Femur Fracture, Osteoporosis, Stress Fracture, LOW Turnover Osteopathy

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Alendronate Sodium
    Administration route: Oral

Fosamax
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2002-10-01
    End date: 2011-04-01

Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2002-10-01
    End date: 2011-04-01

Fosamax Plus D
    Administration route: Oral



Possible Fosamax Plus D side effects in female

Reported by a lawyer from United States on 2012-05-31

Patient: female

Reactions: Femur Fracture, Osteonecrosis, Osteoporosis, Stress Fracture

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Alendronate Sodium
    Administration route: Oral

Fosamax
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2004-07-01
    End date: 2007-11-08

Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2004-07-01
    End date: 2007-11-08

Fosamax Plus D
    Administration route: Oral



Possible Fosamax Plus D side effects in 51 year old female

Reported by a physician from United States on 2012-05-25

Patient: 51 year old female

Reactions: Night Sweats, Bone Fragmentation, Femur Fracture, Fear, Fall, Foot Fracture, Arthropathy, Adverse Event, Depression, Multiple Sclerosis, Back Disorder, LOW Turnover Osteopathy, Ankle Fracture, Osteonecrosis, Stress Fracture, Hypertension

Adverse event resulted in: hospitalization, disablity

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

Fosamax Plus D
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2000-01-01



Possible Fosamax Plus D side effects in 49 year old female

Reported by a physician from United States on 2012-05-25

Patient: 49 year old female, weighing 44.0 kg (96.8 pounds)

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

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-01-01
    End date: 2011-02-01

Fosamax
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2006-01-01
    End date: 2011-02-01

Fosamax
    Administration route: Oral
    Start date: 2009-01-01
    End date: 2010-05-01

Fosamax Plus D
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2008-04-01
    End date: 2008-09-01



Possible Fosamax Plus D side effects in 44 year old female

Reported by a physician from United States on 2012-05-18

Patient: 44 year old female, weighing 60.0 kg (132.0 pounds)

Reactions: Rheumatoid Arthritis, Hot Flush, Palpitations, Temperature Intolerance, Calculus Urinary, Back Pain, Sarcoma, Menopause, Hepatic Steatosis, Respiratory Tract Congestion, Excessive Skin, Sleep Disorder, Oral Fibroma, Uterine Disorder, Periodontal Disease, Colitis Microscopic, Obesity, Chest Pain, Rotator Cuff Syndrome, Depression, Bone Disorder, Benign Neoplasm, Dyspnoea, Mass, Lung Neoplasm, Bruxism, Thrombophlebitis, Bladder Disorder, Weight Decreased, Thrombosis, Osteomyelitis, Pyrexia, Headache, Arthropathy, Adverse Event, Drug Administration Error, Stress Urinary Incontinence, Open Wound, Cough, Muscle Spasms, Dyspareunia, Anxiety Disorder, Gingival Bleeding, Pain in Extremity, Gingival Disorder, Retinal Ischaemia, Hypoaesthesia, Lung Hyperinflation, Cholelithiasis, Osteonecrosis, Bone Neoplasm Malignant, Mental Disorder, Pelvic Prolapse, JAW Fracture, Constipation, Gastritis, Synovial Cyst, Cystocele, Nephrolithiasis, Anaemia Vitamin B12 Deficiency, Fatigue, Dizziness, Hypertonic Bladder, Gastrooesophageal Reflux Disease, Transient Ischaemic Attack, Optic Disc Drusen, Dental Caries, Synovitis, Post Gastric Surgery Syndrome, Cholecystitis Chronic, Appendix Disorder, Eosinophilia, Osteoarthritis, Osteonecrosis of JAW, Chondrosarcoma, Infection

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Alendronate Sodium
    Administration route: Oral
    Start date: 2004-10-01

Fosamax
    Administration route: Oral
    Start date: 2007-07-01
    End date: 2008-03-01

Fosamax
    Administration route: Oral
    Start date: 2007-07-01
    End date: 2008-03-01

Fosamax
    Dosage: 37.5 mg
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2000-01-01
    End date: 2006-01-01

Fosamax
    Dosage: 37.5 mg
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2000-01-01
    End date: 2006-01-01

Fosamax Plus D
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2008-03-01
    End date: 2009-01-01

Other drugs received by patient: Vitamins (Unspecified); Lisinopril; Hydrochlorothiazide; Hormones (Unspecified); Coumadin; Calcium (Unspecified) and Vitamin D (Unspecified); Cyanocobalamin; Flonase; Norvasc; Fibercon; Coreg; Glucosamine



Possible Fosamax Plus D side effects in 56 year old female

Reported by a physician from United States on 2012-05-15

Patient: 56 year old female, weighing 63.0 kg (138.6 pounds)

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

Adverse event resulted in: hospitalization, disablity

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

Fosamax
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2003-01-01
    End date: 2007-03-01

Fosamax
    Administration route: Oral
    Start date: 2005-04-13

Fosamax Plus D
    Administration route: Oral
    Start date: 2006-12-26
    End date: 2007-03-14

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



Possible Fosamax Plus D side effects in 46 year old female

Reported by a physician from United States on 2012-05-08

Patient: 46 year old female, weighing 45.0 kg (99.0 pounds)

Reactions: Femur Fracture, Osteoporosis, Constipation, Fall, Fracture Nonunion, Body Height Decreased, Hypercholesterolaemia, Foot Fracture, Arthropathy, Musculoskeletal Stiffness, Blood Cholesterol Increased, Depression, Gastrooesophageal Reflux Disease, Humerus Fracture, Kyphoscoliosis, Breast Cancer, Device Failure, Osteoarthritis, Osteonecrosis, Impaired Healing, Compression Fracture, Stress Fracture, Limb Asymmetry

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1995-01-01
    End date: 2003-03-01

Fosamax
    Administration route: Oral
    Start date: 2003-03-01
    End date: 2007-03-01

Fosamax Plus D
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2007-04-18
    End date: 2009-10-01

Other drugs received by patient: Magnesium (Unspecified); Hormones (Unspecified); Fortical (Calcium Carbonate); Calcium (Unspecified); Vitamin D (Unspecified)



Possible Fosamax Plus D side effects in 49 year old female

Reported by a physician from United States on 2012-05-07

Patient: 49 year old female, weighing 44.0 kg (96.8 pounds)

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

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Fosamax
    Administration route: Oral
    Start date: 2009-01-01
    End date: 2010-05-01

Fosamax
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2006-01-01
    End date: 2011-02-01

Fosamax Plus D
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2008-04-01
    End date: 2008-09-01



Possible Fosamax Plus D side effects in 63 year old female

Reported by a physician from United States on 2012-05-04

Patient: 63 year old female, weighing 66.0 kg (145.2 pounds)

Reactions: Tooth Loss, Contusion, Lymphadenopathy, Body Height Decreased, Oedema Peripheral, Musculoskeletal Disorder, Animal Bite, LOW Turnover Osteopathy, Back Pain, Musculoskeletal Discomfort, Bursitis, Osteopenia, Tonsillar Disorder, Nipple Disorder, Activities of Daily Living Impaired, Femoral Neck Fracture, Bone Metabolism Disorder, Procedural Vomiting, Blood Magnesium Decreased, Multiple Myeloma, Fall, Colitis Microscopic, Foot Fracture, Rotator Cuff Syndrome, Depression, Umbilical Hernia, Exostosis, Ligament Sprain, Humerus Fracture, Hypercorticoidism, Finger Deformity, Disability, Abdominal Hernia, Night Sweats, Goitre, Urinary Incontinence, Sciatica, Hand Fracture, Headache, Peripheral Sensory Neuropathy, Treatment Noncompliance, Loss of Consciousness, Duodenitis, Arthropathy, Fracture, Patella Fracture, Fibula Fracture, Fibrosis, Bone Density Decreased, Resorption Bone Increased, Muscle Spasms, Intervertebral Disc Protrusion, Psychomotor Hyperactivity, Pain in Extremity, Ankle Fracture, Osteonecrosis, LIP Injury, Tendon Disorder, Thyroid Disorder, Stress Fracture, Dermal Cyst, Attention Deficit / Hyperactivity Disorder, Scar, Drug Ineffective, Bone Pain, Blood Cortisol Decreased, Suicidal Ideation, Fatigue, Skin Ulcer, Intervertebral Disc Degeneration, Breast Discomfort, Gastrooesophageal Reflux Disease, RIB Fracture, Renal Disorder, Spondylolisthesis, Adenoidal Disorder, Cystitis, Appendix Disorder, Osteoarthritis, Anxiety, Spinal Osteoarthritis

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Administration route: Oral
    Start date: 2002-01-01
    End date: 2010-01-01

Fosamax
    Administration route: Oral
    Indication: Osteoporosis Postmenopausal
    Start date: 2002-01-01
    End date: 2010-03-01

Fosamax

Fosamax
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2002-01-01
    End date: 2010-03-01

Fosamax

Fosamax
    Administration route: Oral
    Start date: 2002-01-01
    End date: 2010-01-01

Fosamax Plus D
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2008-04-21
    End date: 2008-05-12

Other drugs received by patient: Synthroid; Estrogens (Unspecified); Estrace; Colace; Prilosec; Calcium (Unspecified); Citracal + D; Vitamin D (Unspecified); Bupropion Hydrochloride; Estradiol; Pantoprazole; Levothyroxine Sodium; Calcium (Unspecified) and Vitamin D (Unspecified); Sertraline Hydrochloride; Zolpidem Tartrate; Enoxaparin Sodium; Cholecalciferol



Possible Fosamax Plus D side effects in 55 year old female

Reported by a physician from United States on 2012-04-30

Patient: 55 year old female, weighing 57.0 kg (125.4 pounds)

Reactions: Contusion, Malignant Melanoma in Situ, Iron Deficiency Anaemia, Arteriosclerosis, LOW Turnover Osteopathy, Back Pain, Breast Cancer, Bursitis, Staphylococcal Infection, Gastrointestinal Disorder, Rectal Haemorrhage, Abasia, Pelvic Pain, Fall, Chest Pain, Aortic Arteriosclerosis, Depression, Postmenopause, Ligament Sprain, Emphysema, Cataract, Dyspnoea, Lung Neoplasm, Haemorrhoids, Intestinal Dilatation, Blood Disorder, Metastases To Bone, Femur Fracture, Lumbar Spinal Stenosis, Spinal Compression Fracture, Arthropathy, Herpes Simplex, Vitamin B12 Deficiency, Uterine Leiomyoma, Hypertriglyceridaemia, Haematoma, Intervertebral Disc Protrusion, Hiatus Hernia, Anxiety Disorder, Anaemia, Crohn's Disease, Renal Cyst, Drug Withdrawal Syndrome, Cholelithiasis, Osteonecrosis, Epicondylitis, Insomnia, Spinal Column Stenosis, Wrist Fracture, Pain, Fracture Nonunion, Hypokalaemia, Neuropathy Peripheral, Fatigue, Hepatomegaly, Ileus, Neck Pain, Skin Cancer, Intervertebral Disc Degeneration, Kidney Infection, RIB Fracture, Bone Cyst, Bone Lesion, Nausea, Dental Caries, Drug Hypersensitivity, Urinary Tract Infection, Osteoarthritis, Hyperlipidaemia, Diarrhoea, Steroid Therapy, Pollakiuria, Lacunar Infarction, Spinal Disorder, Spinal Osteoarthritis, Arthritis

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Alendronate Sodium
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2009-11-01
    End date: 2010-01-01

Fosamax
    Administration route: Oral
    Indication: Osteopenia
    Start date: 1998-01-01
    End date: 2008-01-01

Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1998-01-01
    End date: 2008-01-01

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

Other drugs received by patient: Ciprofloxacin HCL; Corticosteroids (Unspecified); Morphine; Klor-CON; Vitamins (Unspecified); Tricor; Norvasc



Possible Fosamax Plus D side effects in 49 year old female

Reported by a physician from United States on 2012-04-23

Patient: 49 year old female

Reactions: Atelectasis, Tooth Loss, Haemorrhage, Necrosis, Pain, Chest X-RAY Abnormal, Bone Loss, Blood Cholesterol Increased, Adverse Event, Lymphoedema, Breast Cancer, Renal Disorder, Type 2 Diabetes Mellitus, Dyspnoea, Stomatitis, Ovarian Cyst, Pancytopenia, Gingival Disorder, Renal Cyst, Pulmonary Fibrosis, Osteonecrosis, Temporomandibular Joint Syndrome, Osteonecrosis of JAW, JAW Disorder, Tooth Disorder, Thyroid Neoplasm, Hypertension

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2006-04-01
    End date: 2010-03-01

Fosamax Plus D
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2006-04-01
    End date: 2010-03-01



Possible Fosamax Plus D side effects in 66 year old female

Reported by a physician from United States on 2012-04-18

Patient: 66 year old female, weighing 68.0 kg (149.6 pounds)

Reactions: Foot Deformity, Contusion, Femur Fracture, Pelvic Adhesions, Pyrexia, Nocturia, Treatment Noncompliance, Trigger Finger, Hair Texture Abnormal, Adverse Event, Back Pain, Intervertebral Disc Protrusion, Dysphagia, Hiatus Hernia, Bursitis, Stress, Osteonecrosis, Diverticulum, Limb Injury, Insomnia, Exercise Lack of, Atelectasis, Bunion, Drug Ineffective, Pain, Pelvic Pain, Periarthritis, Constipation, Fall, Cystocele, Road Traffic Accident, Fibromyalgia, Intervertebral Disc Degeneration, Rotator Cuff Syndrome, Acquired Oesophageal WEB, Depression, Cataract, Nausea, Urinary Tract Infection, Musculoskeletal Pain, Haemorrhoids, Musculoskeletal Chest Pain, Tenosynovitis, Plantar Fasciitis, Anxiety, Osteoarthritis, Hyperlipidaemia, Spinal Disorder, Spinal Osteoarthritis, Asthenia

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Alendronate Sodium
    Administration route: Oral
    Start date: 2009-11-16

Alendronate Sodium
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2008-09-27
    End date: 2009-08-27

Fosamax
    Administration route: Oral
    Start date: 2002-01-12
    End date: 2005-09-13

Fosamax
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2000-04-28
    End date: 2001-01-18

Fosamax
    Administration route: Oral
    Start date: 2008-02-17
    End date: 2008-08-31

Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2008-02-17
    End date: 2008-08-31

Fosamax Plus D
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2005-11-14
    End date: 2007-09-03

Fosamax Plus D
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2005-11-14
    End date: 2007-09-03

Other drugs received by patient: Estradiol; Prilosec; Prevacid



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