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Boniva (Ibandronic Acid) - Fall - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with Fall (462)

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

 Reports 1 - 30 of 462   Next >>

Possible Boniva side effects in 84 year old female

Reported by a consumer/non-health professional from United States on 2012-08-27

Patient: 84 year old female

Reactions: Fall

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Boniva



Possible Boniva side effects in

Reported by a physician from United States on 2012-08-25

Patient:

Reactions: Abdominal Pain, Tooth Loss, Contusion, Dental Implantation, Oropharyngeal Pain, Eczema, Cyst, Malaise, Incontinence, DRY Mouth, Muscle Injury, Postmenopausal Haemorrhage, Myelopathy, Back Pain, Fistula, Laceration, Lumbar Radiculopathy, Joint Injury, Hepatic Steatosis, Antinuclear Antibody Positive, Periprosthetic Fracture, Haematoma Infection, Swelling, Compression Fracture, Actinomycosis, Abscess, Bunion, Exposed Bone in JAW, Necrosis, Periodontal Disease, Lichenoid Keratosis, Secondary Sequestrum, Oroantral Fistula, Fall, Device Dislocation, Muscle Rupture, Implant Site Abscess, Foot Fracture, Chest Pain, Rotator Cuff Syndrome, Oedema, Blood Cholesterol Increased, Bone Disorder, Depression, Knee Arthroplasty, Exostosis, Ligament Sprain, Cataract, Mental Disorder DUE To A General Medical Condition, Carotid Artery Stenosis, Device Failure, Impaired Healing, Arthralgia, Gait Disturbance, Bladder Disorder, Oral Torus, Gingivitis, Femur Fracture, Dementia, Osteomyelitis, Seroma, Lumbar Spinal Stenosis, Hypoaesthesia Oral, Patella Fracture, Bone Density Decreased, Open Wound, Sjogren's Syndrome, Haematoma, Paranasal Cyst, Epistaxis, Intervertebral Disc Protrusion, Cellulitis, Hiatus Hernia, Dysphagia, Stomatitis, Angiomyolipoma, Oral Infection, Anaemia, Otitis Externa, Venous Insufficiency, Abscess JAW, Mental Disorder, Major Depression, Sleep Apnoea Syndrome, Nerve Injury, Chronic Inflammatory Demyelinating Polyradiculoneuropathy, Wrist Fracture, Pain, Oesophagitis Ulcerative, Polyneuropathy, Suicidal Ideation, Breast Disorder Female, Road Traffic Accident, Azotaemia, Gastrooesophageal Reflux Disease, RIB Fracture, Endometrial Disorder, Scoliosis, Spinal Cord Compression, Cerebral Arteriosclerosis, Spondylolisthesis, Osteitis Condensans, Urinary Tract Infection, Dental Caries, Synovitis, Deafness Neurosensory, Musculoskeletal Chest Pain, Amnesia, Hyperlipidaemia, Osteoarthritis, Anxiety, Bladder Irritation, Barrett's Oesophagus, Diarrhoea, Osteonecrosis of JAW, Oral Disorder, Spinal Osteoarthritis, Hypertension

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Boniva
    Dosage: 150 mg, qm
    Indication: Osteoporosis
    Start date: 2007-11-02
    End date: 2009-06-29

Boniva
    Indication: Osteopenia

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2009-10-06
    End date: 2010-04-05

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2001-05-08
    End date: 2005-04-01

Fosamax
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1995-12-13
    End date: 2000-12-01



Possible Boniva 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 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 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 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 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 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: Glaucoma, Femur Fracture, Arterial Disorder, Aphasia, Femoral Hernia, Obstructive, Fall, Change of Bowel Habit, Hypercholesterolaemia, Hypoacusis, Fatigue, Road Traffic Accident, Intervertebral Disc Disorder, ECG Signs of Ventricular Hypertrophy, Depression, Exostosis, Intervertebral Disc Displacement, Pneumonia, Squamous Cell Carcinoma, Pain in Extremity, Onychomycosis, Bursitis, Facial Spasm, Cataract Operation, Osteoarthritis, Anxiety, Syncope, Arthralgia, Blood Testosterone Increased, Sleep Disorder, Insomnia, Spinal Osteoarthritis, Hypertension, Vertigo Positional

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Actonel
    Dosage: 35 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2007-08-01

Boniva
    Dosage: 150 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2008-01-01
    End date: 2009-10-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2007-09-01
    End date: 2007-12-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2000-08-17
    End date: 2006-12-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2009-11-01
    End date: 2010-01-01

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



Possible Boniva side effects in

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

Patient:

Reactions: Abdominal Hernia, Vitamin D Deficiency, Femur Fracture, Contusion, Cervicogenic Headache, Myofascial Pain Syndrome, Seroma, Abdominal Discomfort, Hot Flush, Breast Hyperplasia, Incision Site Haemorrhage, Haematoma, Cough, Back Pain, Crohn's Disease, Device Intolerance, Renal Cyst, Breast Calcifications, Small Intestinal Obstruction, Hepatic Cyst, Dehydration, Nephrocalcinosis, Polyarthritis, Seborrhoeic Keratosis, Endometriosis, Osteoporosis, Wrist Fracture, Pain, Appendicitis Perforated, Fall, Abdominal Pain Upper, Gastritis, Fatigue, Ventricular Hypertrophy, Fibrocystic Breast Disease, Fibromyalgia, Dizziness, Depression, Acquired Oesophageal WEB, Gastrooesophageal Reflux Disease, Sinusitis, Ligament Sprain, Calcium Deficiency, Polyp, Breast Disorder, Dental Caries, Ovarian Disorder, Arrhythmia, Limb Deformity, Hyperlipidaemia, Anxiety, Device Failure, Blood Potassium Decreased, Arthralgia, Limb Asymmetry, Hypertension, Sensitivity of Teeth, Abdominal Adhesions

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Actonel
    Dosage: 35 mg, qw
    Administration route: Oral
    Start date: 2003-01-01
    End date: 2008-11-01

Boniva
    Indication: Osteoporosis
    Start date: 1999-05-01
    End date: 2008-11-01

Fosamax
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1999-05-06
    End date: 2003-01-01

Other drugs received by patient: Prempro; Pentasa; Prempro



Possible Boniva 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 Boniva side effects in

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

Patient:

Reactions: Polymyalgia Rheumatica, Asthma, Femur Fracture, Pneumonia Aspiration, Respiratory Moniliasis, Tooth Extraction, Pyrexia, Chronic Obstructive Pulmonary Disease, Macular Degeneration, Rheumatoid Arthritis, Allergic Respiratory Symptom, Decubitus Ulcer, Adverse Event, Bronchomalacia, White Blood Cell Count Increased, Mitral Valve Prolapse, Pneumonia, Dysphagia, Pain in Extremity, Explorative Laparotomy, non-Cardiac Chest Pain, Bronchitis Chronic, Limb Injury, Colitis, Pain, Fall, Aspiration, Oedema, Pleural Effusion, Bone Disorder, Gastrooesophageal Reflux Disease, RIB Fracture, Breast Lump Removal, Intestinal Polyp, Haemorrhoids, Urinary Tract Infection, Hysterectomy, Device Failure, Hyperlipidaemia, Keloid Scar, Sepsis, Hypothyroidism, Mastectomy, Gait Disturbance, Traumatic Haematoma, Rhinitis Perennial

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Boniva
    Dosage: 150 mg, qm
    Indication: Osteoporosis
    Start date: 2011-05-09

Fosamax
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1999-12-01
    End date: 2007-12-01

Fosamax
    Dosage: 70 mg, qw
    Start date: 1999-12-01
    End date: 2007-12-01

Fosamax
    Dosage: 70 mg, unk
    Start date: 2007-05-14
    End date: 2007-11-13



Possible Boniva side effects in

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

Patient:

Reactions: Hyperhidrosis, Vaginal Haemorrhage, Nail Disorder, Mitral Valve Prolapse, Angina Pectoris, Coronary Artery Disease, Bursitis, Rhinitis Allergic, Anaemia of Chronic Disease, Gastrointestinal Disorder, Arteriosclerosis Coronary Artery, Abscess, Bunion, Acrochordon, Seborrhoeic Keratosis, Fall, Abdominal Pain Upper, Muscle Strain, Poor Quality Sleep, Foot Fracture, Rotator Cuff Syndrome, Blood Cholesterol Increased, Exostosis, Benign Neoplasm, Ligament Sprain, Vulvovaginal Discomfort, Cardiac Failure, Arthralgia, Alopecia, Bladder Disorder, Weight Decreased, Vitamin D Deficiency, Femur Fracture, Urinary Incontinence, Lumbar Spinal Stenosis, Bone Density Decreased, Device Malfunction, Stress Urinary Incontinence, Haematoma, Dyspareunia, Intervertebral Disc Protrusion, Actinic Keratosis, Pain in Extremity, Anaemia, Radicular Syndrome, Stress Fracture, Restless Legs Syndrome, Fatigue, Intervertebral Disc Degeneration, Sinusitis, Calcium Deficiency, Scoliosis, Urinary Tract Infection, Onychomycosis, Cystitis, Tenosynovitis, Hyperlipidaemia, Neoplasm Malignant, Suture Related Complication, Bronchitis, Arthritis, Hypertension, Deep Vein Thrombosis, Infection, Influenza Like Illness

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Alendronate Sodium
    Dosage: 70 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2008-04-07
    End date: 2010-01-04

Boniva
    Dosage: 150 mg, unk
    Administration route: Oral
    Indication: Bone Loss
    Start date: 2010-03-25
    End date: 2011-02-07

Boniva
    Indication: Osteoporosis

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2001-03-15

Fosamax
    Dosage: 10 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2000-02-15

Other drugs received by patient: Prevacid



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 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 2012-08-13

Patient:

Reactions: Femur Fracture, Pain, Fracture Nonunion, Fall, Balance Disorder, Gait Disturbance, Asthenia, Mobility Decreased, LOW Turnover Osteopathy

Adverse event resulted in: hospitalization

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

Boniva
    Dosage: unk
    Indication: Osteoporosis
    Start date: 2007-01-01
    End date: 2010-08-01

Fosamax
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1998-01-01
    End date: 2001-01-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2001-01-01
    End date: 2006-08-01

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

Other drugs received by patient: Simvastatin; Blocadren; Estrogens (Unspecified)



Possible Boniva side effects in

Reported by a consumer/non-health professional from United States on 2012-08-13

Patient:

Reactions: Abdominal Pain, Contusion, Femur Fracture, Upper Limb Fracture, Carotidynia, Nocturia, Hypomagnesaemia, Temperature Intolerance, Gallbladder Disorder, Alanine Aminotransferase Abnormal, Haematoma, Anaemia Postoperative, LOW Turnover Osteopathy, Back Pain, Coronary Artery Disease, Osteopenia, Intestinal Obstruction, Gastrointestinal Disorder, Pancreatitis, Hypersensitivity, Haemorrhage, Head Injury, Pain, Fall, Somnolence, Myalgia, Fibrocystic Breast Disease, Fatigue, Ileus, Chest Pain, Blood Cholesterol Increased, Gastrooesophageal Reflux Disease, Cataract, Vomiting, Nausea, Skin Disorder, Radius Fracture, Lobar Pneumonia, Urinary Tract Infection Enterococcal, Syncope, Impaired Healing, Blood Potassium Decreased, Diarrhoea, Gastroenteritis, Hypothyroidism, Asthenia, Hypertension, Venous Injury

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Boniva
    Dosage: unk df, unk
    Start date: 2008-06-27
    End date: 2010-07-01

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2008-10-16
    End date: 2009-04-02

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Bone Disorder
    Start date: 1998-10-01
    End date: 2008-06-02

Other drugs received by patient: Estradiol; MK-9359



Possible Boniva side effects in

Reported by a consumer/non-health professional from United States on 2012-08-10

Patient:

Reactions: Abdominal Pain, Pruritus, Tinnitus, Contusion, Oropharyngeal Pain, Chronic Obstructive Pulmonary Disease, Peroneal Nerve Palsy, Oesophagitis, Nervousness, LOW Turnover Osteopathy, Back Pain, Angina Pectoris, Hypotension, Musculoskeletal Discomfort, Bursitis, Osteopenia, Limb Injury, Increased Tendency To Bruise, Tibia Fracture, Cholecystectomy, Post-Traumatic Headache, Thyroid Neoplasm, Muscle Disorder, Osteoporosis, Fall, Poor Quality Sleep, Liver Function Test Abnormal, Depression, Myocardial Infarction, Ligament Sprain, Motor Neurone Disease, Arthralgia, Appendicectomy, Hyperthyroidism, Vitamin D Deficiency, Weight Decreased, Night Sweats, Femur Fracture, Extrasystoles, Headache, Pyrexia, Peripheral Sensory Neuropathy, Coagulation Factor Deficiency, Joint Effusion, Carpal Tunnel Syndrome, Radiculopathy, Abscess Limb, Intervertebral Disc Protrusion, Dysphagia, Cellulitis, Pain in Extremity, Tonsillectomy, Anaemia, Hypoaesthesia, Varices Oesophageal, Gastric Disorder, Paraesthesia, Tremor, Occult Blood, Acute Sinusitis, Peripheral Nerve Paresis, Stress Fracture, Disturbance in Attention, Cardiovascular Disorder, Sleep Apnoea Syndrome, Mobility Decreased, Drug Ineffective, Head Injury, Snoring, Liver Disorder, Myalgia, Fatigue, Neuropathy Peripheral, Amyotrophic Lateral Sclerosis, Gastrooesophageal Reflux Disease, Calcium Deficiency, Migraine, Urinary Tract Infection, Radicular Pain, Cerebrovascular Accident, Osteoarthritis, Anxiety, Barrett's Oesophagus, Bradycardia, Spinal Osteoarthritis, Arthritis

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Boniva
    Dosage: 150 mg, qm
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2008-01-25

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2002-04-02
    End date: 2010-04-30

Other drugs received by patient: Norvasc; Calcium (Unspecified); Norvasc; Fluticasone Propionate; Combivent



Possible Boniva side effects in

Reported by a lawyer from United States on 2012-08-10

Patient:

Reactions: Polymyalgia Rheumatica, Asthma, Respiratory Moniliasis, Pneumonia Aspiration, Femur Fracture, Tooth Extraction, Pyrexia, Chronic Obstructive Pulmonary Disease, Macular Degeneration, Rheumatoid Arthritis, Allergic Respiratory Symptom, Decubitus Ulcer, Adverse Event, Bronchomalacia, White Blood Cell Count Increased, Mitral Valve Prolapse, Pneumonia, Dysphagia, Pain in Extremity, Explorative Laparotomy, non-Cardiac Chest Pain, Limb Injury, Bronchitis Chronic, Colitis, Pain, Fall, Aspiration, Oedema, Pleural Effusion, Bone Disorder, Gastrooesophageal Reflux Disease, RIB Fracture, Intestinal Polyp, Breast Lump Removal, Haemorrhoids, Urinary Tract Infection, Device Failure, Hysterectomy, Hyperlipidaemia, Keloid Scar, Sepsis, Hypothyroidism, Mastectomy, Gait Disturbance, Traumatic Haematoma, Rhinitis Perennial

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Boniva
    Dosage: 150 mg, qm
    Indication: Osteoporosis
    Start date: 2011-05-09

Fosamax
    Dosage: 70 mg, qw
    Start date: 1999-12-01
    End date: 2007-12-01

Fosamax
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1999-12-01
    End date: 2007-12-01

Fosamax
    Dosage: 70 mg, unk
    Start date: 2007-05-14
    End date: 2007-11-13



Possible Boniva side effects in

Reported by a consumer/non-health professional from United States on 2012-08-10

Patient:

Reactions: Contusion, Femur Fracture, Rash Pruritic, Rheumatoid Arthritis, Hot Flush, Arthropathy, Dyspepsia, Muscle Spasms, LOW Turnover Osteopathy, Blister, Back Pain, Pain in Extremity, Coronary Artery Disease, Bursitis, Haemorrhagic Anaemia, Dental Necrosis, Uterine Disorder, Attention Deficit / Hyperactivity Disorder, Spondyloarthropathy, Psoriatic Arthropathy, Bunion, Skin Exfoliation, Drug Ineffective, Osteoporosis, Adverse Drug Reaction, Ventricular Arrhythmia, Fall, Fracture Nonunion, Sinus Bradycardia, Foot Fracture, Dermatitis Contact, Fatigue, Obesity, Acute Myocardial Infarction, Migraine, Tooth Fracture, Incisional Drainage, Rash, Osteoarthritis, Impaired Healing

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Boniva
    Dosage: 150 mg, unk
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2007-05-01
    End date: 2010-04-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2000-09-01
    End date: 2007-04-30

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



Possible Boniva side effects in

Reported by a physician from United States on 2012-08-10

Patient:

Reactions: Pulmonary Hypertension, Weight Decreased, Vitamin D Deficiency, Femur Fracture, Tinnitus, Tachycardia, Cervical Myelopathy, Hand Fracture, Arthropathy, Palpitations, Stress Urinary Incontinence, LOW Turnover Osteopathy, Dysphagia, Essential Tremor, Fracture Delayed Union, Hypotension, Left Ventricular Hypertrophy, Coronary Artery Disease, Hypoaesthesia, Diverticulum, Intermittent Claudication, Head Injury, Vasomotor Rhinitis, Adverse Drug Reaction, Fall, Speech Disorder, Neck Pain, Intervertebral Disc Degeneration, Gastrooesophageal Reflux Disease, Transient Ischaemic Attack, Nausea, Drug Hypersensitivity, Haemorrhoids, Musculoskeletal Chest Pain, Cerebrovascular Accident, Migraine With Aura, Osteoarthritis, Renal Failure, Diarrhoea, Blood Disorder, Asthenia, Hypertensive Nephropathy, Spinal Cord Disorder

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Boniva
    Dosage: 150 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-02-01
    End date: 2011-08-01

Fosamax
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Hypersensitivity
    Start date: 1999-08-24

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2000-06-01
    End date: 2006-02-01

Vitamins (Unspecified)
    Dosage: unk
    Start date: 1992-01-01

Other drugs received by patient: Allegra-D 12 Hour; Synthroid



Possible Boniva side effects in 63 year old female

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

Patient: 63 year old female, weighing 75.9 kg (167.0 pounds)

Reactions: Ulnocarpal Abutment Syndrome, Atypical Femur Fracture, Fracture Nonunion, Fall, Knee Arthroplasty, Pathological Fracture, RIB Fracture, Intervertebral Disc Protrusion, Back Pain, Pain in Extremity, Renal Cyst, Bursitis, Onychomycosis, Micturition Urgency, Osteoarthritis, Osteonecrosis, Flank Pain, Pollakiuria, Stress Fracture

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Actonel
    Dosage: 75 mg, 2 consecutive days monthly, oral
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2009-08-05

Actonel
    Dosage: 150 mg, once monthly, oral
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2009-05-22
    End date: 2010-02-04

Actonel
    Dosage: 35 mg, once weekly,oral
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2004-11-11
    End date: 2009-05-01

Boniva
    Dosage: 150 mg monthly, oral
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2010-02-04
    End date: 2011-07-01



Possible Boniva 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 Boniva side effects in female

Reported by a physician from Switzerland on 2012-08-06

Patient: female

Reactions: Femur Fracture, Fall

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Boniva



Possible Boniva side effects in 73 year old female

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

Patient: 73 year old female

Reactions: Femur Fracture, Bone Pain, Fall, Fracture Nonunion, Groin Pain, Joint Range of Motion Decreased, Fracture Displacement, Carpal Tunnel Syndrome, Pathological Fracture, Anaemia Postoperative, Pain in Extremity, Muscular Weakness, Osteopenia, Hypoaesthesia, Paraesthesia, Radiculitis Lumbosacral, Osteoarthritis, Activities of Daily Living Impaired, Impaired Healing, Arthralgia, Procedural Hypotension, Limb Asymmetry, Procedural Dizziness, Gait Disturbance, Traumatic Haematoma

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Actonel
    Dosage: 35 mg weekly, oral
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2003-01-01

Boniva
    Dosage: 150 mg once monthly, oral
    Administration route: Oral
    Start date: 2008-01-10
    End date: 2008-03-14

Fosamax
    Dosage: 10 mg daily, oral ; 10 mg, daily, oral
    Administration route: Oral
    Start date: 1999-03-10
    End date: 2000-12-15

Fosamax
    Dosage: 70 mg once weekly, oral
    Administration route: Oral
    Start date: 2001-01-15
    End date: 2002-12-20

Reclast
    Dosage: 5 mg/100 ml 5 mg

Other drugs received by patient: Neurontin; Celebrex; Azulfidine; Xalatan / 01297301 / (Latanoprost); Simcor / 03020801 / (Nicotinic Acid, Simvastatin); Methocarbamol; Darvocet / 00758701 / (Dextropropoxyphene Napsilate, Paracetamol); Calcium Carbonate; Magnesium (Magnesium); Forteo; Chromium Picolinate (Chromium Picolinate); Baclofen; Nexium; Synthroid; Allegra / 01314202 / (Fexofenadine Hydrochloride); Oxycodone W / Paracetamol (Oxycodone, Paracetamol); Colchicine; Zinc (Zinc); Fish OIL (Fish Oil); Corticosteroids; Lovaza; Aspirin; B Complex / 00322001 / (Calcium Pantothenate, Cyanocobalamin, Nicotinami



Possible Boniva side effects in

Reported by a consumer/non-health professional from United States on 2012-08-03

Patient:

Reactions: Electrocardiogram ST Segment Depression, Hyperkeratosis, Diverticulitis, Cardiomegaly, Cardiac Disorder, Breast Cyst, Oedema Peripheral, Diarrhoea Haemorrhagic, Nervousness, LOW Turnover Osteopathy, Back Pain, Angina Pectoris, Haematuria, Bursitis, Joint Injury, Respiratory Tract Congestion, Diverticulum, Limb Injury, Compression Fracture, Gastrointestinal Disorder, Vision Blurred, Arthropod Bite, Hypersensitivity, Food Poisoning, Fall, Lymphadenitis, Hypercholesterolaemia, Chest Pain, Rotator Cuff Syndrome, Blood Cholesterol Increased, Ligament Sprain, Cataract, Dyspnoea, Haemorrhoids, Musculoskeletal Pain, Arthralgia, Gait Disturbance, Asthenia, Femur Fracture, Pulmonary Granuloma, Pharyngitis Streptococcal, Cough, Cardiac Murmur, Pain in Extremity, Hypoaesthesia, Tremor, Colitis, Dyslipidaemia, Osteoarthropathy, Fatigue, Fibromyalgia, Kidney Infection, Sinusitis, Gastrooesophageal Reflux Disease, Peripheral Vascular Disorder, Urinary Tract Infection, Rash, Renal Failure Chronic, Meniscus Lesion, Osteoarthritis, Bronchitis, Electrocardiogram Change, Hypertension, Cardiac Arrest

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Actonel
    Dosage: 150 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2010-05-05
    End date: 2010-07-06

Actonel
    Start date: 2010-07-01

Boniva
    Dosage: 150 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2008-04-04

Boniva
    Dosage: 150 mg, unk
    Administration route: Oral
    Start date: 2009-04-27

Boniva
    Dosage: 150 mg, unk
    Administration route: Oral
    Start date: 2011-02-02

Boniva
    Dosage: 150 mg, unk
    Administration route: Oral
    Start date: 2010-10-14
    End date: 2010-12-29

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2005-01-19

Fosamax
    Dosage: unk
    Administration route: Oral
    Indication: Osteopenia
    Start date: 1995-01-01
    End date: 2011-02-10

Fosamax Plus D
    Dosage: unk unk, qw
    Administration route: Oral
    Start date: 2006-09-14

Fosamax Plus D
    Dosage: unk mg, qw
    Start date: 2006-10-02
    End date: 2008-03-06

Fosamax Plus D
    Dosage: unk unk, qw
    Administration route: Oral
    Start date: 2009-06-10
    End date: 2010-04-25

Fosamax Plus D
    Dosage: unk unk, qw
    Administration route: Oral
    Start date: 2010-08-12

Fosamax Plus D
    Dosage: unk mg, qw
    Start date: 2006-08-18

Fosamax Plus D
    Dosage: unk mg, qw
    Indication: Osteoporosis
    Start date: 2006-01-12

Fosamax Plus D
    Dosage: unk unk, qw
    Administration route: Oral
    Start date: 2006-02-16
    End date: 2006-07-21

Fosamax Plus D
    Dosage: unk unk, qw
    Administration route: Oral
    Start date: 2008-06-04

Other drugs received by patient: Therapy Unspecified



Possible Boniva side effects in

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

Patient:

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

Adverse event resulted in: hospitalization, disablity

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

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

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

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

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

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

Other drugs received by patient: Lipitor; Synthroid



Possible Boniva side effects in

Reported by a consumer/non-health professional from United States on 2012-08-02

Patient:

Reactions: Vitamin D Deficiency, Femur Fracture, Cyst, Loss of Consciousness, Abdominal Discomfort, Oedema Peripheral, Raynaud's Phenomenon, Patella Fracture, LOW Turnover Osteopathy, Oral Infection, Gingival Disorder, Joint Swelling, Vision Blurred, Stress Fracture, Abscess, Pneumonia Primary Atypical, Drug Ineffective, Osteoporosis, Pain, Adverse Drug Reaction, Tonic Clonic Movements, Fall, Bone Loss, Neuropathy Peripheral, Road Traffic Accident, Depression, Gastrooesophageal Reflux Disease, Calcium Deficiency, Dental Caries, Synovitis, Anxiety, Osteoarthritis, Osteonecrosis of JAW, Spinal Disorder

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Boniva
    Dosage: unk
    Indication: Osteoporosis
    Start date: 2008-08-01

Fosamax
    Dosage: unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2003-01-01

Reclast
    Dosage: unk
    Indication: Osteoporosis



Possible Boniva side effects in

Reported by a physician from United States on 2012-08-02

Patient:

Reactions: Weight Decreased, Femur Fracture, Gastrointestinal Haemorrhage, Tinnitus, Cardiac Disorder, Arthropathy, Connective Tissue Disorder, Balance Disorder, Peroneal Nerve Palsy, DRY Mouth, Carpal Tunnel Syndrome, Vertebral Foraminal Stenosis, Temperature Intolerance, Gallbladder Disorder, Thoracic Vertebral Fracture, LOW Turnover Osteopathy, Anaemia Postoperative, Functional Gastrointestinal Disorder, Fracture Delayed Union, Pain in Extremity, Anaemia, Lumbar Radiculopathy, Osteopenia, Epicondylitis, Joint Swelling, Stiff Person Syndrome, Sleep Apnoea Syndrome, Spinal Column Stenosis, Bunion, Glaucoma, Necrosis, Parathyroid Disorder, Fall, Fracture Nonunion, Abdominal Pain Upper, Groin Pain, Neuropathy Peripheral, Chondrocalcinosis Pyrophosphate, Hyperparathyroidism, Chest Pain, Intervertebral Disc Degeneration, Gastrooesophageal Reflux Disease, Migraine, Benign Bone Neoplasm, Dyspnoea, Cataract, Neurogenic Bladder, Urinary Tract Infection, Cervicobrachial Syndrome, Device Failure, Osteoarthritis, Blood Potassium Decreased, Arthralgia, Diarrhoea, Alopecia, Procedural Hypotension, Limb Asymmetry, Vertigo, Spinal Osteoarthritis, Bladder Disorder, Gait Disturbance, DRY Eye

Adverse event resulted in: hospitalization, disablity

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

Actonel
    Indication: Osteoporosis

Boniva
    Indication: Osteopenia

Boniva
    Indication: Osteoporosis

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2001-01-15

Fosamax
    Dosage: 10 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1996-01-01
    End date: 2000-12-15

Reclast
    Indication: Osteopenia

Reclast
    Indication: Osteoporosis



Possible Boniva side effects in

Reported by a consumer/non-health professional from United States on 2012-08-02

Patient:

Reactions: Bunion, Contusion, Femur Fracture, Seborrhoeic Dermatitis, Restless Legs Syndrome, Blood Triglycerides Increased, Fall, Fibrocystic Breast Disease, Hot Flush, Iron Deficiency Anaemia, Neoplasm Skin, Upper Respiratory Tract Infection, Intervertebral Disc Degeneration, Blood Cholesterol Increased, Gastrooesophageal Reflux Disease, Blood Glucose Increased, Inappropriate Schedule of Drug Administration, Polydipsia, Back Pain, Blood Urea Increased, Hiatus Hernia, Dyspnoea, Pain in Extremity, Hypoaesthesia, Bursitis, non-Cardiac Chest Pain, Osteoarthritis, Device Failure, Arthralgia, Insomnia, Blood Urine

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Boniva
    Dosage: 150 mg, cyclical
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2007-10-01
    End date: 2009-10-01

Fosamax
    Dosage: 35 mg, qw
    Administration route: Oral
    Indication: Osteoporosis

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2001-09-26
    End date: 2007-09-01

Other drugs received by patient: Prozac; Calcium Citrate; Prozac; Glucosamine Sulfate; Omega-3 Marine Triglycerides



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