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Boniva (Ibandronic Acid) - LOW Turnover Osteopathy - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with LOW Turnover Osteopathy (485)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Boniva (Ibandronic Acid) where reactions include low turnover osteopathy. The selected reports were submitted to the FDA during the sample period of about a year.

 Reports 1 - 30 of 485   Next >>

Possible Boniva side effects in

Reported by a lawyer from United States on 2012-08-26

Patient:

Reactions: Femur Fracture, LOW Turnover Osteopathy

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

Boniva
    Indication: Osteopenia

Fosamax
    Indication: Osteopenia

Fosamax
    Indication: Osteoporosis



Possible Boniva side effects in

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

Patient:

Reactions: Femur Fracture, Osteoporosis, Foot Fracture, Basal Cell Carcinoma, Fracture, Thrombophlebitis Superficial, Drug Administration Error, Depression, Fibula Fracture, Gastrooesophageal Reflux Disease, RIB Fracture, LOW Turnover Osteopathy, Mitral Valve Prolapse, Anxiety Disorder, Hiatus Hernia, Abdominal Abscess, Osteonecrosis of JAW, Tibia Fracture

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Boniva

Fosamax
    Dosage: 40 mg, qw

Fosamax
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1999-01-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2000-08-12
    End date: 2006-01-01

Fosamax Plus D
    Dosage: 70mg/2800iu
    Start date: 2007-04-01
    End date: 2007-09-20



Possible Boniva side effects in

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

Patient:

Reactions: Femur Fracture, Osteoporosis, Foot Operation, Diabetes Mellitus, Fall, Foot Fracture, Postoperative Wound Infection, Blood Cholesterol Increased, Multiple Sclerosis, LOW Turnover Osteopathy, Pneumonia, Wound Dehiscence, Pain in Extremity, Tonsillectomy, Urinary Tract Infection, Muscular Weakness, Closed Fracture Manipulation, Hysterectomy, Arthralgia, Stress Fracture, Hypertension, Arthritis

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Boniva
    Dosage: unk
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2007-01-01

Fosamax
    Indication: Osteopenia

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

Other drugs received by patient: Vitamins (Unspecified)



Possible Boniva side effects in

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

Patient:

Reactions: Abdominal Pain, Cyst, Cardiac Disorder, Oesophageal Dilatation, Upper Respiratory Tract Infection, Oedema Peripheral, LOW Turnover Osteopathy, Back Pain, Wound Dehiscence, Hypotension, Drug Intolerance, Lumbar Radiculopathy, Bursitis, Hepatic Steatosis, Diverticulum, Facial Bones Fracture, Somnambulism, Muscle Strain, Hyperparathyroidism, Abnormal Loss of Weight, Latex Allergy, Depression, Bone Disorder, Ligament Sprain, Intervertebral Disc Operation, Vomiting, Dyspnoea, Haemorrhoids, Musculoskeletal Pain, Hyperreflexia, Syncope, Arthralgia, Sinus Disorder, Presyncope, Hypothyroidism, Skin Infection, Memory Impairment, Drug Dependence, Vitamin D Deficiency, Femur Fracture, Sciatica, Rash Pruritic, Loss of Consciousness, Spinal Compression Fracture, Dyspepsia, Epistaxis, Anaemia Postoperative, Intervertebral Disc Protrusion, Blood Alkaline Phosphatase Increased, Cardiac Murmur, Pain in Extremity, Rotator Cuff Repair, Wound Infection, Drug Withdrawal Syndrome, Osteomalacia, Body Temperature Decreased, Eating Disorder, Osteonecrosis, Fungal Infection, Dehydration, Insomnia, Arthroscopy, Colitis, Suicide Attempt, Head Injury, Drug Ineffective, Pain, Constipation, Suicidal Ideation, Fatigue, Neck Pain, Heart Rate Irregular, Calcium Deficiency, Nausea, Drug Hypersensitivity, Urinary Tract Infection, Condition Aggravated, Osteoarthritis, Meniscus Lesion, Anxiety, Diarrhoea, Vertigo, Debridement, Spinal Osteoarthritis, Hypertension

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Boniva
    Dosage: 150 mg/kg, unk
    Indication: Osteoporosis
    Start date: 2008-12-02
    End date: 2011-09-02

Boniva
    Dosage: 3 unk, unk
    Start date: 2008-05-23

Boniva
    Dosage: 3 mg/ml
    Start date: 2007-08-13
    End date: 2008-02-25

Boniva
    Dosage: 150 mg, unk
    Indication: Osteopenia
    Start date: 2006-01-20
    End date: 2007-07-17

Boniva
    Dosage: 3 unk, unk
    Start date: 2009-05-27

Boniva
    Dosage: 3 unk, unk
    Start date: 2008-09-24

Boniva
    Dosage: 3 mg/3ml
    Start date: 2008-03-25

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Bone Density Decreased
    Start date: 2004-08-23
    End date: 2005-12-07

Fosamax
    Indication: Osteopenia

Other drugs received by patient: Aciphex; Vioxx; Oxycodone HCL; Humira; Darvocet-N 50; Fluvoxamine Maleate; Hydrocodone Bitartrate; Hormones (Unspecified); Ambien; Dicyclomine Hydrochloride; Kadian; Lamictal; Hydroxychloroquine Sulfate



Possible Boniva side effects in female

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

Patient: female

Reactions: Anxiety, Emotional Distress, Femur Fracture, LOW Turnover Osteopathy

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

Fosamax
    Indication: Osteoporosis



Possible Boniva side effects in

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

Patient:

Reactions: Femur Fracture, Osteoporosis, Bunion Operation, Foot Operation, Atypical Femur Fracture, Salpingo-Oophorectomy, Biopsy Breast Normal, Hypoparathyroidism, Hypocalcaemia, Joint Arthroplasty, Depression, Open Reduction of Fracture, Cholesteatoma, LOW Turnover Osteopathy, Cholesteatoma Removal, Drug Intolerance, Bursitis, Anxiety, Stress Fracture

Adverse event resulted in: hospitalization, disablity

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

Boniva
    Indication: Osteopenia

Boniva
    Indication: Osteoporosis

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2000-01-01
    End date: 2008-01-01

Fosamax
    Indication: Osteoporosis

Other drugs received by patient: Prilosec OTC



Possible Boniva side effects in

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

Patient:

Reactions: Dyslipidaemia, Femur Fracture, Cyst, Chronic Obstructive Pulmonary Disease, Cystocele, Upper Respiratory Tract Infection, Intervertebral Disc Disorder, Oedema Peripheral, Vertebral Foraminal Stenosis, Hypertonic Bladder, Radiculopathy, LOW Turnover Osteopathy, Anaemia Postoperative, Vomiting, Nausea, Spondylolisthesis, Psoriasis, Cystitis, Carotid Pulse Abnormal, Rectocele, Osteoarthritis, Benign Breast Lump Removal, Uterine Prolapse, Mitral Valve Incompetence, Pollakiuria, Bradycardia, Arthritis, Hypertension

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Alendronate Sodium
    Dosage: 70 mg qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2008-10-01
    End date: 2009-07-31

Alendronate Sodium
    Dosage: 70 mg qw
    Administration route: Oral
    Start date: 2009-10-27
    End date: 2010-05-13

Boniva
    Dosage: 150 mg, unk
    Indication: Osteoporosis
    Start date: 2007-02-22
    End date: 2008-05-21

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Gastrooesophageal Reflux Disease
    Start date: 2004-05-27

Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    End date: 2010-08-01

Other drugs received by patient: Calcium (Unspecified); Vitamin D; Ascorbic Acid; Prevacid; Prempro; Omega-3-Acid Ethyl Esters; Vitamin E; Magnesium (Unspecified) (+) Zinc (Unspecified); Chondroitin Sulfate Sodium (+) Glucosamine Sulfate



Possible Boniva side effects in

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

Patient:

Reactions: Femur Fracture, LOW Turnover Osteopathy

Drug(s) suspected as cause:
Boniva
    Dosage: unk
    Indication: Osteopenia
    Start date: 2009-05-01
    End date: 2011-02-01

Boniva
    Dosage: unk
    Indication: Osteoporosis
    Start date: 2006-01-01
    End date: 2007-01-01

Fosamax
    Dosage: unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2007-01-01
    End date: 2009-05-01

Fosamax
    Indication: Osteopenia



Possible Boniva side effects in

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

Patient:

Reactions: Accident, Femur Fracture, Fracture, Intramedullary ROD Insertion, Lower Limb Fracture, Depression, Fall, LOW Turnover Osteopathy

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Boniva
    Dosage: unk, qm
    Indication: Osteoporosis
    Start date: 2006-01-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1996-01-01
    End date: 2006-01-01

Fosamax
    Indication: Osteoporosis Prophylaxis

Fosamax
    Indication: Multiple Fractures

Other drugs received by patient: Vitamins (Unspecified)



Possible Boniva side effects in

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

Patient:

Reactions: Pancreatitis Acute, Femur Fracture, Stomach Mass, Deafness, Pyrexia, Colonic Polyp, Spinal Compression Fracture, Balance Disorder, DRY Mouth, Oedema Peripheral, Colon Adenoma, Fibula Fracture, Urinary Retention, Sjogren's Syndrome, Anaemia Postoperative, White Blood Cell Count Increased, Cough, LOW Turnover Osteopathy, Blister, Medical Device Complication, Back Pain, Pneumonia, Pain in Extremity, Fracture Delayed Union, Cerumen Impaction, Bursitis, Carotid Arteriosclerosis, Ankle Fracture, Paraesthesia, Cholelithiasis, Diverticulum, Acute Sinusitis, Anaemia of Chronic Disease, Limb Injury, Uterine Disorder, Cholecystectomy, Treatment Failure, Vitrectomy, Hepatitis, Fall, Kyphosis, Hypokalaemia, Abdominal Pain Upper, Laryngitis, Gastritis, Fibrocystic Breast Disease, Hearing Impaired, Intervertebral Disc Degeneration, Gastrooesophageal Reflux Disease, Decreased Appetite, RIB Fracture, Nausea, Peripheral Vascular Disorder, Musculoskeletal Pain, Lung Neoplasm, Hyponatraemia, Onychomycosis, Carotid Bruit, Pulmonary Fibrosis, Device Failure, Diarrhoea, Hypothyroidism, Gait Disturbance, Hypertension, Infection

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Boniva
    Dosage: 150 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2007-08-16
    End date: 2007-10-18

Boniva

Fosamax
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1995-12-04
    End date: 2001-04-26

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2010-05-18
    End date: 2011-02-05

Fosamax
    Administration route: Oral
    Start date: 2007-07-01

Fosamax

Fosamax
    Administration route: Oral
    Start date: 2009-06-12

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2001-06-26
    End date: 2007-07-18

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2009-07-13
    End date: 2010-02-26

Fosamax



Possible Boniva side effects in

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

Patient:

Reactions: Femur Fracture, Urinary Incontinence, Chronic Obstructive Pulmonary Disease, Pericardial Effusion, Cardiomegaly, Colonic Polyp, Upper Respiratory Tract Infection, Palpitations, Dyspepsia, Ecchymosis, Colon Adenoma, Benign Breast Neoplasm, Anaemia Postoperative, LOW Turnover Osteopathy, Back Pain, Cardiac Murmur, Hiatus Hernia, Haemorrhagic Anaemia, Diverticulum, Lymphadenopathy Mediastinal, Polyarthritis, Cerebral Disorder, Head Injury, Rectal Haemorrhage, Fracture Nonunion, Hypokalaemia, Fibrocystic Breast Disease, Aortic Arteriosclerosis, Knee Arthroplasty, Depression, Heart Rate Irregular, Gastrooesophageal Reflux Disease, RIB Fracture, Blood Pressure Increased, Cataract, Dyspnoea, Haemorrhoids, Lung Neoplasm, Dental Caries, Haemoglobin Decreased, Hyperlipidaemia, Anxiety, Osteoarthritis, Gastrointestinal Vascular Malformation, Leukocytosis, Hypertension

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Boniva
    Dosage: unk unk, qm3
    Start date: 2008-12-01
    End date: 2009-11-01

Fosamax
    Dosage: 70 mg qw
    Administration route: Oral
    Start date: 1997-12-22
    End date: 2007-12-26

Fosamax
    Dosage: 10 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1997-12-22
    End date: 2007-12-26

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2008-03-18
    End date: 2009-02-01

Other drugs received by patient: OS-CAL (Calcium Carbonate)



Possible Boniva side effects in

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

Patient:

Reactions: Hypersensitivity, Femur Fracture, Dyslipidaemia, Astigmatism, Osteoporosis, Pyrexia, Fall, Cardiac Disorder, Nephrolithiasis, Pterygium, Arthropathy, Chest Pain, Pleural Calcification, Hypermetropia, LOW Turnover Osteopathy, RIB Fracture, Pharyngitis, Dysphagia, Pneumonia, Cataract, Hydronephrosis, Drug Hypersensitivity, Rhinitis, Osteoarthritis, Meniscus Lesion, Arthralgia, Polyarthritis, Tooth Disorder

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Alendronate Sodium
    Dosage: 70 mg, unk
    Start date: 2008-06-16

Boniva
    Dosage: 150 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-05-01
    End date: 2006-07-01

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2008-12-10

Fosamax

Fosamax
    Indication: Osteopenia

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1996-02-01
    End date: 2010-07-01

Other drugs received by patient: Ascorbic Acid; Aspirin; Hydrochlorothiazide (+) Spironolactone; MK-9278



Possible Boniva side effects in

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

Patient:

Reactions: Hypersensitivity, Femur Fracture, Osteoporosis, Dental Implantation, Drug Hypersensitivity, Stress Fracture, Heart Rate Irregular, Fall, LOW Turnover Osteopathy

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Boniva

Fosamax
    Indication: Osteopenia

Fosamax
    Dosage: 70 mg,qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1999-01-01
    End date: 2011-03-01



Possible Boniva side effects in

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

Patient:

Reactions: Sciatica, Herpes Zoster, Dyspepsia, Adverse Event, Carpal Tunnel Syndrome, Pathological Fracture, LOW Turnover Osteopathy, Hiatus Hernia, Fracture Delayed Union, Spinal Fracture, Osteopenia, Intestinal Obstruction, Acute Stress Disorder, Gastric Disorder, Stress, Spleen Disorder, Acute Sinusitis, Stress Fracture, Seborrhoeic Keratosis, Osteoporosis, Fracture Nonunion, Road Traffic Accident, Fatigue, Chest Pain, Intervertebral Disc Degeneration, Chronic Sinusitis, Depression, Pharyngitis, Migraine, Spondylolisthesis, Musculoskeletal Pain, Joint Dislocation, Musculoskeletal Chest Pain, Device Failure, Hyperlipidaemia, Osteoarthritis

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Boniva
    Dosage: 150 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2009-01-01
    End date: 2009-12-15

Fosamax
    Dosage: 70 mg, qd
    Administration route: Oral
    Start date: 2008-09-19
    End date: 2008-12-23

Fosamax
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1995-01-01

Other drugs received by patient: MK-9278



Possible Boniva 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 Boniva side effects in

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

Patient:

Reactions: Femur Fracture, Skeletal Injury, LOW Turnover Osteopathy

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Boniva

Fosamax
    Dosage: unk

Fosamax
    Indication: Osteopenia

Fosamax
    Dosage: unk
    Indication: Osteoporosis
    Start date: 1995-04-01
    End date: 2011-01-01

Fosamax Plus D
    Indication: Osteopenia

Fosamax Plus D
    Indication: Osteoporosis



Possible Boniva side effects in female

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

Patient: female

Reactions: Emotional Distress, Anxiety, Stress Fracture, LOW Turnover Osteopathy

Drug(s) suspected as cause:
Boniva
    Indication: Osteoporosis Prophylaxis
    Start date: 2008-03-01
    End date: 2011-06-01

Fosamax
    Indication: Osteoporosis Prophylaxis
    Start date: 1998-01-01
    End date: 2007-02-01



Possible Boniva side effects in

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

Patient:

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

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Boniva
    Dosage: unk
    Indication: Osteoporosis
    Start date: 2007-03-01
    End date: 2011-06-01

Boniva
    Indication: Osteoporosis Prophylaxis

Fosamax
    Indication: Osteoporosis Prophylaxis

Fosamax
    Dosage: unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1998-01-01
    End date: 2007-02-01



Possible Boniva side effects in

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

Patient:

Reactions: Femur Fracture, Osteoporosis, Coagulopathy, Fracture Nonunion, Lumbar Spinal Stenosis, Foot Fracture, Proteinuria, Depression, LOW Turnover Osteopathy, Intervertebral Disc Protrusion, Type 2 Diabetes Mellitus, Coronary Artery Disease, Osteopenia, Haemorrhagic Anaemia, Hyperlipidaemia, Osteoarthritis, Cholecystectomy, Hypoalbuminaemia, Stress Fracture

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Boniva
    Dosage: unk
    Indication: Menopause
    End date: 1995-01-01

Fosamax
    Indication: Osteoporosis Prophylaxis

Fosamax
    Dosage: unk, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1995-01-01
    End date: 2010-01-01

Fosamax
    Indication: Menopause



Possible Boniva side effects in

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

Patient:

Reactions: Abdominal Pain, Cyst, Body Height Decreased, Surgery, Stag Horn Calculus, LOW Turnover Osteopathy, Chondropathy, Hyperparathyroidism Secondary, Fracture Delayed Union, Coronary Artery Disease, Cow's Milk Intolerance, Hepatic Steatosis, Spinal Fusion Surgery, Diverticulum, Periprosthetic Fracture, Staphylococcal Infection, Knee Operation, Gastrointestinal Disorder, Femoral Neck Fracture, Carotid Artery Disease, Cystoscopy, Bone Metabolism Disorder, Pseudarthrosis, Epidural Injection, Chest Pain, Depression, Knee Arthroplasty, Bone Disorder, Acetabulum Fracture, Humerus Fracture, Haemorrhoids, Device Failure, Impaired Healing, Arthralgia, Urge Incontinence, Lithotripsy, Limb Asymmetry, Needle Issue, Vitamin D Deficiency, Femur Fracture, Wound Treatment, Stent Placement, Urinary Incontinence, Device Related Infection, Headache, Lumbar Spinal Stenosis, Dyspepsia, Benign Breast Neoplasm, Spinal Laminectomy, Stress Urinary Incontinence, Renal Stone Removal, Hiatus Hernia, Pubis Fracture, Breast Calcifications, Insomnia, Sleep Apnoea Syndrome, Constipation, Fracture Nonunion, Biopsy, Gastritis, Nephrolithiasis, Intervertebral Disc Disorder, Postoperative Wound Complication, Open Reduction of Fracture, Gastrooesophageal Reflux Disease, Calcium Deficiency, Blood Pressure Increased, Type 2 Diabetes Mellitus, HIP Arthroplasty, Urinary Tract Infection, Antibiotic Therapy, Biopsy Breast, Anxiety, Rectocele, Barrett's Oesophagus, Pyelogram Retrograde

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Boniva
    Dosage: 150 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-04-18
    End date: 2010-05-01

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2000-01-01
    End date: 2006-01-01

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



Possible Boniva side effects in

Reported by a physician from United States on 2012-08-22

Patient:

Reactions: Femur Fracture, Flatulence, Clostridium Difficile Colitis, Headache, Oropharyngeal Pain, Lens Extraction, Smear Cervix Abnormal, Irritable Bowel Syndrome, LOW Turnover Osteopathy, Denture Wearer, Bursitis, Diverticulum Intestinal, Cataract Operation, Uterine Prolapse, Dehydration, Stress Fracture, Dental Prosthesis User, Tooth Abscess, Osteoporosis, Pelvic Pain, Fall, Endometrial Hypertrophy, Constipation, Appendicitis Perforated, Synovial Cyst, Gastritis, Hypokalaemia, Endodontic Procedure, Urinary Tract Disorder, Skin Lesion, Sneezing, Hypertonic Bladder, Uterine Operation, Adrenal Adenoma, DRY Skin, Cerebrovascular Accident, Eye Pain, Osteoarthritis, Tooth Disorder, Eustachian Tube Disorder

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Boniva
    Dosage: 150 mg, unk
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2008-08-14
    End date: 2010-03-15

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2008-05-02
    End date: 2008-08-14

Fosamax
    Dosage: unk mg, unk
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2000-09-13
    End date: 2010-02-10

Ridaura

Other drugs received by patient: Auranofin; Luvox; Prilosec



Possible Boniva side effects in

Reported by a consumer/non-health professional from United States on 2012-08-22

Patient:

Reactions: Abdominal Pain, Cyst, Cardiac Disorder, Oesophageal Dilatation, Oedema Peripheral, LOW Turnover Osteopathy, Back Pain, Wound Dehiscence, Hypotension, Lumbar Radiculopathy, Bursitis, Hepatic Steatosis, Diverticulum, Facial Bones Fracture, Muscle Strain, Hyperparathyroidism, Latex Allergy, Depression, Bone Disorder, Ligament Sprain, Intervertebral Disc Operation, Dyspnoea, Vomiting, Musculoskeletal Pain, Syncope, Arthralgia, Presyncope, Sinus Disorder, Hypothyroidism, Memory Impairment, Skin Infection, Drug Dependence, Vitamin D Deficiency, Femur Fracture, Sciatica, Rash Pruritic, Loss of Consciousness, Spinal Compression Fracture, Dyspepsia, Anaemia Postoperative, Epistaxis, Intervertebral Disc Protrusion, Blood Alkaline Phosphatase Increased, Pain in Extremity, Rotator Cuff Repair, Wound Infection, Drug Withdrawal Syndrome, Osteomalacia, Osteonecrosis, Fungal Infection, Colitis, Arthroscopy, Suicide Attempt, Drug Ineffective, Head Injury, Pain, Constipation, Fatigue, Drug Tolerance, Neck Pain, Heart Rate Irregular, Calcium Deficiency, Nausea, Urinary Tract Infection, Condition Aggravated, Osteoarthritis, Anxiety, Meniscus Lesion, Diarrhoea, Debridement, Vertigo, Spinal Osteoarthritis, Hypertension

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Boniva
    Dosage: 3 unk, unk
    Start date: 2007-08-13
    End date: 2008-02-25

Boniva
    Dosage: 3 unk, unk
    Start date: 2009-05-27

Boniva
    Dosage: 150 mg, unk
    Indication: Osteopenia
    Start date: 2006-01-20
    End date: 2007-07-17

Boniva
    Dosage: 150 mg/kg, unk
    Indication: Osteoporosis
    Start date: 2008-12-02
    End date: 2011-09-02

Boniva
    Dosage: 3 unk, unk
    Start date: 2008-09-24

Boniva
    Dosage: 3 unk, unk
    Start date: 2008-05-23

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Bone Density Decreased
    Start date: 2004-08-23
    End date: 2005-12-07

Fosamax
    Indication: Osteopenia

Other drugs received by patient: Dicyclomine Hydrochloride; Kadian; Hormones (Unspecified); Vioxx; Lamictal; Darvocet-N 50; Aciphex; Ambien; Fluvoxamine Maleate; Humira; Hydrocodone; Oxycodone HCL; Hydroxychloroquine Sulfate



Possible Boniva side effects in female

Reported by a lawyer from United States on 2012-08-17

Patient: female

Reactions: Anxiety, Emotional Distress, Femur Fracture, LOW Turnover Osteopathy

Drug(s) suspected as cause:
Boniva
    Indication: Osteoporosis
    Start date: 2006-01-01
    End date: 2007-01-01

Boniva
    Start date: 2009-05-01
    End date: 2011-02-01

Fosamax
    Indication: Osteoporosis
    Start date: 2007-01-01
    End date: 2009-05-01



Possible Boniva side effects in

Reported by a lawyer from United States on 2012-08-17

Patient:

Reactions: Femur Fracture, LOW Turnover Osteopathy

Drug(s) suspected as cause:
Boniva
    Dosage: unk
    Indication: Osteoporosis
    Start date: 2009-09-01
    End date: 2012-03-01

Boniva
    Indication: Osteopenia

Fosamax
    Indication: Osteopenia

Fosamax
    Dosage: unk
    Indication: Osteoporosis
    Start date: 1999-01-01
    End date: 2009-09-01



Possible Boniva side effects in female

Reported by a lawyer from United States on 2012-08-15

Patient: female

Reactions: Anxiety, Emotional Distress, Osteoarthritis, Femur Fracture, Intervertebral Disc Degeneration, Mastoiditis, LOW Turnover Osteopathy

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

Boniva
    Administration route: Oral
    Indication: Osteoporosis

Other drugs received by patient: Fosamax



Possible Boniva side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-14

Patient:

Reactions: Pruritus, Medication Error, Musculoskeletal Disorder, Drug Dispensing Error, Pyelonephritis, LOW Turnover Osteopathy, Back Pain, Hypotension, Bursitis, Temporomandibular Joint Syndrome, Throat Irritation, Renal Colic, Osteoporosis, Somnolence, Hypercholesterolaemia, Liver Function Test Abnormal, Rotator Cuff Syndrome, Depression, Bone Disorder, Postmenopause, Exostosis, Incisional Drainage, Viral Infection, Vomiting, Haemorrhoids, Pancreatic Cyst, Spondylitis, Haematochezia, Arthralgia, Sinus Disorder, Flank Pain, Gait Disturbance, Foot Deformity, Gastrointestinal Haemorrhage, Femur Fracture, Tendon Injury, Off Label Use, Dyspepsia, Adverse Event, Polychondritis, Tendonitis, Melaena, Muscle Spasms, Cellulitis, Chest Discomfort, Pain in Extremity, Anaemia, Liver Tenderness, Upper Gastrointestinal Haemorrhage, Jaundice, Haemorrhage, Pain, Constipation, Viith Nerve Paralysis, Groin Pain, Gastritis, Weight Increased, Nephrolithiasis, Intervertebral Disc Degeneration, Gastrooesophageal Reflux Disease, Electrocardiogram T Wave Inversion, Scoliosis, Renal Disorder, Hepatitis Acute, Nausea, Crystal Arthropathy, Multiple Fractures, Nodal Osteoarthritis, Diarrhoea, Uterine Dilation and Curettage, Hypertension, Tooth Disorder, Infection

Adverse event resulted in: hospitalization, disablity

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

Boniva
    Dosage: 150 mg, qm
    Indication: Menopause
    Start date: 2006-01-26
    End date: 2011-04-01

Fosamax
    Indication: Osteopenia

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Menopause
    Start date: 2004-08-01
    End date: 2006-01-26

Other drugs received by patient: Glucosamine; Vitamin D; Celebrex; Aleve; Calcium (Unspecified); Chondroitin Sulfate Sodium (+) Glucosamine Sulfate



Possible Boniva side effects in

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

Patient:

Reactions: Femur Fracture, Osteoporosis, Diabetes Mellitus, Clostridium Difficile Colitis, Knee Arthroplasty, Gastrooesophageal Reflux Disease, Radiculopathy, Spinal Operation, LOW Turnover Osteopathy, Calcium Deficiency, Breast Cancer, Hyperglycaemia, Hyperlipidaemia, Osteoarthritis, Diarrhoea, Fungal Infection, Compression Fracture, Stress Fracture, Mastectomy, Pseudomembranous Colitis, Bronchitis, Muscle Disorder, Spinal Column Stenosis, Deep Vein Thrombosis, Neuralgia

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Alendronate Sodium
    Dosage: 70 mg, unk
    Start date: 2008-03-06
    End date: 2011-03-01

Boniva
    Dosage: unk
    Start date: 2007-03-20
    End date: 2007-04-01

Fosamax
    Indication: Osteoporosis

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2007-02-20
    End date: 2008-03-01



Possible Boniva side effects in

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

Patient:

Reactions: Femur Fracture, LOW Turnover Osteopathy

Drug(s) suspected as cause:
Actonel
    Dosage: unk
    Indication: Osteoporosis
    Start date: 2006-06-01
    End date: 2008-02-01

Actonel
    Indication: Osteopenia

Boniva
    Dosage: unk
    Indication: Osteoporosis
    Start date: 2008-02-01
    End date: 2011-01-01

Boniva
    Indication: Osteopenia

Fosamax
    Indication: Osteopenia

Fosamax
    Dosage: unk
    Indication: Osteoporosis
    Start date: 2000-01-01
    End date: 2006-06-01



Possible Boniva side effects in

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

Patient:

Reactions: Femur Fracture, LOW Turnover Osteopathy

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

Boniva
    Indication: Osteoporosis

Fosamax
    Dosage: unk
    Administration route: Oral
    Indication: Osteoporosis



Possible Boniva side effects in

Reported by a lawyer from United States on 2012-08-13

Patient:

Reactions: Femur Fracture, LOW Turnover Osteopathy

Drug(s) suspected as cause:
Boniva
    Dosage: unk
    Indication: Osteoporosis
    Start date: 2006-01-01
    End date: 2007-10-01

Boniva
    Indication: Osteopenia

Fosamax
    Indication: Osteopenia

Fosamax
    Dosage: unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2007-10-01
    End date: 2011-11-01



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