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

 
 



Index of reports > Cases with Nausea ()

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

 Reports 1 - 30 of    Next >>

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

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

Patient:

Reactions: Vitamin D Deficiency, Femur Fracture, Sciatica, Blood Count Abnormal, Headache, Parotitis, Vaginitis Bacterial, Hot Flush, C-Reactive Protein Increased, Palpitations, Herpes Simplex, Tendonitis, Back Pain, Stomatitis, Cerumen Impaction, Otitis Media Acute, Bursitis, Cholelithiasis, Acute Sinusitis, Tendon Disorder, Insomnia, non-Hodgkin's Lymphoma, Lymphoma, Arthropod Bite, Device Breakage, Body FAT Disorder, Hypersensitivity, Pain, Fracture Nonunion, Weight Increased, Foot Fracture, Chest Pain, Malignant Melanoma, Depression, Migraine, Aphthous Stomatitis, Radiation Oesophagitis, Vomiting, Nausea, Urinary Tract Infection, Foreign Body, Cervicobrachial Syndrome, Rash, Biopsy Kidney, Plantar Fasciitis, Osteoarthritis, Diarrhoea, Memory Impairment, Bronchitis, Tooth Disorder

Adverse event resulted in: hospitalization

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

Boniva
    Dosage: unk, qm
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-03-09
    End date: 2010-02-17

Fosamax
    Indication: Osteopenia

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2001-11-03
    End date: 2006-03-09

Other drugs received by patient: ONE-A-DAY Essential Vitamins; Vitamin D; Calcium (Unspecified); Prilosec; Therapy 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 2012-08-22

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

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

Patient:

Reactions: Femur Fracture, Lymph Node Calcification, Dental Implantation, Flatulence, Breast Cyst, Postoperative Wound Infection, Hypnagogic Hallucination, Carpal Tunnel Syndrome, Inappropriate Schedule of Drug Administration, Nausea, Supraventricular Tachycardia, Cerebral Atrophy, Atrial Fibrillation, Stitch Abscess, Bone Density Abnormal, Staphylococcal Infection, Chondrocalcinosis, Haematoma Infection, Stress Fracture, Spinal Osteoarthritis, Leukocytosis, Infection

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Actonel
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1998-03-03
    End date: 2010-03-01

Boniva
    Dosage: unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2007-01-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1998-03-03
    End date: 2010-03-01

Fosamax
    Administration route: Oral
    Start date: 1998-03-01
    End date: 2010-03-01

Fosamax
    Dosage: 40 mg, biw
    Administration route: Oral
    Start date: 2000-08-29
    End date: 2000-12-21

Fosamax Plus D
    Administration route: Oral
    Start date: 1998-03-01
    End date: 2010-03-01

Ibandronate Sodium
    Start date: 1998-03-01
    End date: 2010-03-01

Risedronate Sodium
    Start date: 1998-03-01
    End date: 2010-03-01

Other drugs received by patient: Cymbalta



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 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

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

Patient:

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

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
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

Fosamax
    Administration route: Oral
    Start date: 2008-10-01
    End date: 2009-07-31

Fosamax
    Dosage: unk
    Administration route: Oral
    Start date: 2009-10-27
    End date: 2010-05-13

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



Possible Boniva side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-06

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, Vomiting, Viral Infection, Haemorrhoids, Pancreatic Cyst, Spondylitis, Haematochezia, Arthralgia, Flank Pain, Sinus Disorder, Gait Disturbance, Foot Deformity, Femur Fracture, Gastrointestinal Haemorrhage, Tendon Injury, Off Label Use, Dyspepsia, Adverse Event, Polychondritis, Tendonitis, Melaena, Muscle Spasms, Cellulitis, Pain in Extremity, Anaemia, Liver Tenderness, Upper Gastrointestinal Haemorrhage, Jaundice, Haemorrhage, Pain, Constipation, Hepatitis, Gastritis, Viith Nerve Paralysis, Groin Pain, Weight Increased, Nephrolithiasis, Intervertebral Disc Degeneration, Gastrooesophageal Reflux Disease, Electrocardiogram T Wave Inversion, Scoliosis, Renal Disorder, Nausea, Crystal Arthropathy, Multiple Fractures, Nodal Osteoarthritis, Anxiety, Diarrhoea, Uterine Dilation and Curettage, Tooth Disorder, Hypertension, 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; Calcium (Unspecified); Celebrex; Chondroitin Sulfate Sodium (+) Glucosamine Sulfate; Naproxen (Aleve); Vitamin D



Possible Boniva side effects in

Reported by a lawyer from United States on 2012-07-31

Patient:

Reactions: Vitamin D Deficiency, Femur Fracture, Sciatica, Blood Count Abnormal, Headache, Parotitis, Vaginitis Bacterial, Hot Flush, C-Reactive Protein Increased, Herpes Simplex, Palpitations, Tendonitis, Back Pain, Stomatitis, Cerumen Impaction, Otitis Media Acute, Bursitis, Cholelithiasis, Acute Sinusitis, Insomnia, Tendon Disorder, non-Hodgkin's Lymphoma, Lymphoma, Device Breakage, Arthropod Bite, Body FAT Disorder, Hypersensitivity, Pain, Fracture Nonunion, Weight Increased, Foot Fracture, Chest Pain, Malignant Melanoma, Depression, Radiation Oesophagitis, Aphthous Stomatitis, Migraine, Vomiting, Nausea, Urinary Tract Infection, Rash, Cervicobrachial Syndrome, Foreign Body, Plantar Fasciitis, Biopsy Kidney, Osteoarthritis, Diarrhoea, Memory Impairment, Bronchitis, Tooth Disorder

Adverse event resulted in: hospitalization

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

Boniva
    Dosage: unk, qm
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-03-09
    End date: 2010-03-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2001-11-01
    End date: 2006-03-09

Fosamax
    Indication: Osteopenia

Other drugs received by patient: Vitamin D (Unspecified); Therapy Unspecified; Calcium (Unspecified); Prilosec; ONE-A-DAY Essential Vitamins



Possible Boniva side effects in

Reported by a physician from United States on 2012-07-31

Patient:

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

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
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
    End date: 2008-05-28

Fosamax
    Administration route: Oral
    Start date: 2008-10-01
    End date: 2009-07-31

Fosamax
    Dosage: unk
    Administration route: Oral
    Start date: 2009-10-27
    End date: 2010-05-13

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

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



Possible Boniva side effects in

Reported by a physician from United States on 2012-07-26

Patient:

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

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Boniva
    Dosage: 3 unk, unk
    Start date: 2009-05-27

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: 2007-08-13
    End date: 2008-02-25

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

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

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

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; Lamictal; Oxycodone HCL; Hydroxychloroquine Sulfate; Vicodin; Cymbalta; Kadian; Potassium Chloride; Vioxx; Lidoderm; Humira; Aristospan; Fluvoxamine Maleate; Medrin (Cephradine); Relafin; Seroquel; Migrin A; Celestone; Corticosteroids (Unspecified); Aciphex; Clonazepam; Hydrocodone Bitartrate; Bellaspas; Elavil; Hormones (Unspecified); Carisoprodol; Darvocet-N 50; Ambien; Codeine Sulfate; Clonazepam; Depo-Medrol; Tricor



Possible Boniva side effects in

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

Patient:

Reactions: Abdominal Pain, Contusion, Diverticulitis, Chronic Obstructive Pulmonary Disease, Surgery, Balance Disorder, Nail Disorder, Medical Device Complication, Spinal Fracture, Hypertensive Heart Disease, Laceration, Bursitis, Rhinitis Allergic, Diverticulum, Anaemia of Chronic Disease, Pulse Absent, Pancreatitis, Angiopathy, Fall, Muscle Strain, Foot Fracture, Lymphadenitis, Abdominal Distension, Rotator Cuff Syndrome, Depression, Ligament Rupture, Vomiting, Dyspnoea, Musculoskeletal Pain, Muscular Weakness, Radius Fracture, Hypertensive Crisis, Device Failure, Arthralgia, Asthenia, Vitamin D Deficiency, Foot Deformity, Asthma, Muscle Atrophy, Femur Fracture, Sciatica, Urinary Incontinence, Dementia, Pyrexia, Lumbar Spinal Stenosis, Spinal Compression Fracture, Joint Effusion, Tenderness, Tendonitis, Radiculopathy, Anaemia Postoperative, Cardiac Failure Congestive, Diabetes Mellitus Inadequate Control, Vascular Headache, Hiatus Hernia, Cellulitis, Pain in Extremity, Hyperglycaemia, Hypoaesthesia, Gastric Disorder, Ankle Fracture, Convulsion, Cerebral Small Vessel Ischaemic Disease, Cerebral Infarction, Joint Swelling, Dehydration, Tendon Disorder, Colitis, Mesenteritis, Spinal Column Stenosis, Pain, Bone Pain, Transfusion Reaction, Fracture Nonunion, Hypokalaemia, Anaemia Vitamin B12 Deficiency, Fatigue, Neuropathy Peripheral, Benign Neoplasm of Adrenal Gland, Skin Lesion, Pleural Effusion, Intervertebral Disc Degeneration, Dizziness, Chronic Sinusitis, Calcium Deficiency, Pelvic Fracture, Migraine, Renal Disorder, Nausea, Urinary Tract Infection, Peripheral Vascular Disorder, Synovitis, Hypercalcaemia, Cerebrovascular Accident, Lobar Pneumonia, Appendix Disorder, Osteoarthritis, Anxiety, Hyperlipidaemia, Pollakiuria, Diabetic Retinopathy, Deep Vein Thrombosis, Infection

Adverse event resulted in: life threatening event, hospitalization

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

Forteo
    Indication: Osteoporosis

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Indication: Hormone Replacement Therapy
    Start date: 2004-02-01
    End date: 2006-08-01

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



Possible Boniva side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-07-21

Patient:

Reactions: Foot Deformity, Femur Fracture, Pruritus, Off Label Use, Tendon Injury, Dyspepsia, Medication Error, Musculoskeletal Disorder, Adverse Event, Polychondritis, Tendonitis, Melaena, Drug Dispensing Error, LOW Turnover Osteopathy, Muscle Spasms, Back Pain, Cellulitis, Pain in Extremity, Anaemia, Bursitis, Temporomandibular Joint Syndrome, Throat Irritation, Upper Gastrointestinal Haemorrhage, Osteoporosis, Haemorrhage, Pain, Constipation, Hepatitis, Somnolence, Gastritis, Groin Pain, Viith Nerve Paralysis, Weight Increased, Nephrolithiasis, Hypercholesterolaemia, Liver Function Test Abnormal, Intervertebral Disc Degeneration, Rotator Cuff Syndrome, Depression, Bone Disorder, Gastrooesophageal Reflux Disease, Exostosis, Scoliosis, Viral Infection, Nausea, Crystal Arthropathy, Haemorrhoids, Pancreatic Cyst, Multiple Fractures, Spondylitis, Anxiety, Haematochezia, Nodal Osteoarthritis, Diarrhoea, Arthralgia, Sinus Disorder, Gait Disturbance, 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
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Menopause
    Start date: 2004-08-01
    End date: 2006-01-26

Fosamax
    Indication: Osteopenia

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



Possible Boniva side effects in

Reported by a lawyer from United States on 2012-07-20

Patient:

Reactions: Foot Deformity, Femur Fracture, Myofascial Pain Syndrome, Pyrexia, Cystitis Interstitial, Vaginitis Bacterial, Abdominal Discomfort, Arthropathy, Spinal Compression Fracture, Joint Effusion, Intervertebral Disc Protrusion, Fracture Delayed Union, Pain in Extremity, Anaemia, Osteopenia, Haemorrhagic Anaemia, Iliotibial Band Syndrome, Rhinitis Allergic, Arachnoid Cyst, Arthrodesis, Spinal Column Stenosis, Bunion, Constipation, Fall, Foot Fracture, Fatigue, Tension Headache, Chest Pain, Vomiting, Nausea, Vulval Disorder, Patellofemoral Pain Syndrome, Urethral Caruncle, Osteoarthritis, Anxiety, Meniscus Lesion, Diarrhoea, Arthralgia, Gastroenteritis, Arthritis, Atrophy

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Boniva

Fosamax

Fosamax
    Dosage: a.m
    Administration route: Oral
    End date: 2006-11-08

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2008-10-17
    End date: 2008-12-01

Fosamax
    Indication: Osteopenia

Fosamax
    Dosage: a.m
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2001-09-05
    End date: 2009-07-29

Other drugs received by patient: MK-9278; Dilaudid; Levotiroxina S.O; Calcium (Unspecified) (+) Vitamin D (Unspecified); Premarin; Elavil; Omega-3 Marine Triglycerides; Elavil; Zocor; Niacin; Vagifem; Simvastatin; Aspirin; Lotensin HCT; Cyanocobalamin



Possible Boniva side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-07-20

Patient:

Reactions: Weight Decreased, Arterial Disorder, Osteomyelitis, Dysplasia, Vaginal Haemorrhage, Colonic Polyp, Osteoradionecrosis, Tongue Disorder, Breast Hyperplasia, Cardiac Murmur, Cellulitis, Gingival Disorder, Breast Calcifications, Osteitis, Stress, Diverticulum Intestinal, Gingival Erythema, Fistula Discharge, Seborrhoeic Keratosis, Rectal Haemorrhage, Basosquamous Carcinoma, Basal Cell Carcinoma, Neck Pain, Bone Disorder, Scoliosis, White Blood Cell Count Decreased, Swelling Face, Nausea, Breast Disorder, Osteonecrosis of JAW, Hypercementosis, Oral Torus, Sinus Tachycardia

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Boniva
    Dosage: 150 mg, qm
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2006-03-01
    End date: 2008-12-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2001-06-06
    End date: 2007-03-01

Fosamax
    Indication: Osteopenia

Other drugs received by patient: Prempro



Possible Boniva side effects in

Reported by a lawyer from United States on 2012-07-19

Patient:

Reactions: Pulmonary Hypertension, Weight Decreased, Vitamin D Deficiency, Tinnitus, Femur Fracture, Tachycardia, Hand Fracture, Arthropathy, Palpitations, Stress Urinary Incontinence, LOW Turnover Osteopathy, Dysphagia, Essential Tremor, Fracture Delayed Union, Hypotension, Left Ventricular Hypertrophy, Coronary Artery Disease, Diverticulum, Intermittent Claudication, Head Injury, Adverse Drug Reaction, Vasomotor Rhinitis, Fall, Speech Disorder, Neck Pain, Intervertebral Disc Degeneration, Gastrooesophageal Reflux Disease, Transient Ischaemic Attack, Migraine, Nausea, Haemorrhoids, Drug Hypersensitivity, Musculoskeletal Chest Pain, Osteoarthritis, Renal Failure, Diarrhoea, Blood Disorder, Spinal Osteoarthritis, 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: Synthroid; Allegra-D 12 Hour



Possible Boniva side effects in

Reported by a physician from United States on 2012-07-19

Patient:

Reactions: Tooth Loss, Contusion, Fall, Synovial Cyst, Bone Loss, Oesophagitis, Muscle Injury, Dizziness, Blood Cholesterol Increased, Acute Myocardial Infarction, Vomiting, Tooth Fracture, Pain in Extremity, Nausea, Peripheral Vascular Disorder, Dental Caries, Musculoskeletal Pain, Otitis Externa, Tenosynovitis, Osteoarthritis, Epicondylitis, Osteonecrosis of JAW, Vertigo, Otitis Media, Bronchitis, Arteriosclerosis Coronary Artery, Hypertension, Atrophy, Infection

Adverse event resulted in: hospitalization, disablity

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

Actonel
    Dosage: 35 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2003-05-06

Boniva
    Dosage: 150 mg, qm
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2007-01-01
    End date: 2008-01-01

Boniva
    Indication: Osteopenia

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2005-05-22
    End date: 2006-01-16

Fosamax
    Indication: Osteopenia

Fosamax

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2009-05-13

Fosamax Plus D
    Dosage: unk unk, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-01-16

Fosamax Plus D
    Indication: Osteopenia

Other drugs received by patient: Hormones (Unspecified); Cymbalta



Possible Boniva side effects in

Reported by a physician from United States on 2012-07-13

Patient:

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

Reported by a consumer/non-health professional from United States on 2012-07-11

Patient:

Reactions: Femur Fracture, Chronic Obstructive Pulmonary Disease, Cystocele, Intervertebral Disc Disorder, Upper Respiratory Tract Infection, Oedema Peripheral, LOW Turnover Osteopathy, Vomiting, Nausea, Psoriasis, Carotid Pulse Abnormal, Cystitis, Osteoarthritis, Rectocele, Uterine Prolapse, Mitral Valve Incompetence, Pollakiuria, Bradycardia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
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
    End date: 2008-05-28

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

Fosamax
    Administration route: Oral
    Start date: 2008-10-01
    End date: 2009-07-31

Fosamax
    Dosage: unk
    Administration route: Oral
    Start date: 2009-10-27
    End date: 2010-05-13

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



Possible Boniva side effects in 80 year old female

Reported by a consumer/non-health professional from Germany on 2012-07-10

Patient: 80 year old female

Reactions: Epileptic Aura, Partial Seizures, Anxiety, Nausea, Chills, Bone Pain, Drug Interaction, Hypertension

Drug(s) suspected as cause:
Boniva

Other drugs received by patient possibly interacting with the suspect drug:
Dexamethasone Sodium Phosphate
    Indication: Product Used FOR Unknown Indication

Diclofenac Sodium
    Indication: Product Used FOR Unknown Indication



Possible Boniva side effects in female

Reported by a physician from Germany on 2012-07-06

Patient: female

Reactions: Nausea, Cardiac Disorder

Drug(s) suspected as cause:
Boniva

Other drugs received by patient: Calcicare-D3



Possible Boniva side effects in 45 year old female

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

Patient: 45 year old female, weighing 68.0 kg (149.6 pounds)

Reactions: Contusion, Femur Fracture, Soft Tissue Mass, Tachycardia, Blood Blister, Headache, Pyrexia, Arthropathy, Upper Respiratory Tract Infection, Animal Scratch, Eyelid Ptosis, Back Disorder, LOW Turnover Osteopathy, Cough, Back Pain, Medical Device Complication, Anxiety Disorder, Pain in Extremity, Gingival Disorder, Cardiac Ventricular Disorder, Joint Injury, Acute Sinusitis, Ear Pain, Stress Fracture, Haemorrhage, Head Injury, Osteoporosis, Wheezing, Respiratory Depression, Fall, Periodontitis, Dental Fistula, Muscle Strain, Dyspnoea Exertional, Bone Loss, Fatigue, Neck Pain, Chest Pain, Blood Cholesterol Increased, Bone Disorder, Depression, Gastrooesophageal Reflux Disease, Sinusitis, Exostosis, Pharyngitis, Kyphoscoliosis, Restrictive Pulmonary Disease, Nausea, Reactive Airways Dysfunction Syndrome, Musculoskeletal Chest Pain, Diarrhoea, Dilatation Atrial, Bronchitis, Hypertension

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Boniva
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-12-01
    End date: 2008-03-30

Boniva
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2006-12-01
    End date: 2008-03-30

Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2000-01-01
    End date: 2009-01-01

Fosamax
    Administration route: Oral
    Start date: 2005-06-01
    End date: 2006-11-16

Fosamax
    Administration route: Oral
    Start date: 2005-01-19
    End date: 2005-03-19

Fosamax
    Administration route: Oral
    Start date: 2005-06-01
    End date: 2006-11-16

Fosamax
    Administration route: Oral
    Start date: 2005-01-19
    End date: 2005-03-19

Fosamax
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2000-01-01
    End date: 2009-01-01



Possible Boniva side effects in 61 year old female

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

Patient: 61 year old female, weighing 55.0 kg (121.0 pounds)

Reactions: Foot Deformity, Femur Fracture, Myofascial Pain Syndrome, Pyrexia, Cystitis Interstitial, Abdominal Discomfort, Vaginitis Bacterial, Arthropathy, Spinal Compression Fracture, Joint Effusion, Intervertebral Disc Protrusion, Fracture Delayed Union, Pain in Extremity, Anaemia, Haemorrhagic Anaemia, Osteopenia, Iliotibial Band Syndrome, Rhinitis Allergic, Arachnoid Cyst, Arthrodesis, Spinal Column Stenosis, Bunion, Constipation, Fall, Foot Fracture, Fatigue, Tension Headache, Chest Pain, Vomiting, Nausea, Vulval Disorder, Patellofemoral Pain Syndrome, Urethral Caruncle, Osteoarthritis, Meniscus Lesion, Anxiety, Arthralgia, Diarrhoea, Gastroenteritis, Arthritis, Atrophy

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Alendronate Sodium
    Administration route: Oral
    Start date: 2008-10-17
    End date: 2008-01-01

Boniva

Fosamax
    Dosage: a.m
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2001-09-05
    End date: 2009-07-29

Fosamax
    Dosage: a.m
    Administration route: Oral
    End date: 2006-11-08

Fosamax
    Dosage: a.m
    Administration route: Oral
    End date: 2006-11-08

Fosamax
    Dosage: a.m
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2001-09-05
    End date: 2009-07-29

Other drugs received by patient: Zocor; Amitriptyline Hydrochloride; Elavil; Lotensin HCT; Vitamins (Unspecified); Dilaudid; Calcium (Unspecified) and Vitamin D (Unspecified); Omega-3 Marine Triglycerides; Niacin; Cyanocobalamin; Vagifem; Aspirin; Premarin; Simvastatin; Levothyroxine Sodium



Possible Boniva side effects in 60 year old female

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

Patient: 60 year old female, weighing 70.0 kg (154.0 pounds)

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

Adverse event resulted in: hospitalization

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

Fosamax
    Administration route: Oral
    Start date: 2000-06-01
    End date: 2006-02-01

Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1999-08-01

Other drugs received by patient: Synthroid; Allegra-D 12 Hour; Vitamins (Unspecified)



Possible Boniva side effects in 50 year old female

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

Patient: 50 year old female, weighing 45.0 kg (99.0 pounds)

Reactions: Foot Deformity, Pruritus, Femur Fracture, Tendon Injury, Off Label Use, Medication Error, Dyspepsia, Musculoskeletal Disorder, Adverse Event, Polychondritis, Drug Dispensing Error, Melaena, Tendonitis, Muscle Spasms, LOW Turnover Osteopathy, Back Pain, Cellulitis, Pain in Extremity, Anaemia, Bursitis, Temporomandibular Joint Syndrome, Throat Irritation, Upper Gastrointestinal Haemorrhage, Osteoporosis, Haemorrhage, Pain, Hepatitis, Somnolence, Constipation, Gastritis, Viith Nerve Paralysis, Groin Pain, Weight Increased, Nephrolithiasis, Hypercholesterolaemia, Liver Function Test Abnormal, Intervertebral Disc Degeneration, Rotator Cuff Syndrome, Bone Disorder, Depression, Exostosis, Gastrooesophageal Reflux Disease, Scoliosis, Viral Infection, Nausea, Haemorrhoids, Crystal Arthropathy, Pancreatic Cyst, Multiple Fractures, Spondylitis, Haematochezia, Anxiety, Diarrhoea, Arthralgia, Sinus Disorder, Gait Disturbance, Tooth Disorder, Hypertension, Infection

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Boniva
    Indication: Osteopenia
    Start date: 2006-01-01
    End date: 2011-01-01

Boniva
    Indication: Menopause
    Start date: 2006-01-01
    End date: 2011-01-01

Fosamax
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2004-08-01

Fosamax
    Administration route: Oral
    Indication: Menopause
    Start date: 2004-08-01

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



Possible Boniva side effects in 69 year old female

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

Patient: 69 year old female, weighing 75.0 kg (165.0 pounds)

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

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Alendronate Sodium
    Administration route: Oral
    Start date: 2010-05-01
    End date: 2011-02-01

Alendronate Sodium
    Administration route: Oral
    Start date: 2009-07-01
    End date: 2010-02-01

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

Alendronate Sodium
    Administration route: Oral
    Start date: 2010-05-01
    End date: 2011-02-01

Alendronate Sodium
    Administration route: Oral
    Start date: 2009-07-01
    End date: 2010-02-01

Alendronate Sodium
    Administration route: Oral
    Start date: 2009-06-01

Boniva
    Administration route: Oral
    Start date: 2007-08-01
    End date: 2007-10-01

Boniva
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2007-08-01
    End date: 2007-10-01

Fosamax
    Administration route: Oral
    Start date: 2001-06-01
    End date: 2007-07-01

Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1995-12-01
    End date: 2001-04-01

Fosamax
    Administration route: Oral
    Start date: 1995-12-01
    End date: 2001-04-01

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

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

Fosamax
    Administration route: Oral
    Start date: 2001-06-01
    End date: 2007-07-01



Possible Boniva side effects in 50 year old female

Reported by a physician from United States on 2012-06-26

Patient: 50 year old female, weighing 45.0 kg (99.0 pounds)

Reactions: Foot Deformity, Pruritus, Femur Fracture, Tendon Injury, Off Label Use, Dyspepsia, Medication Error, Musculoskeletal Disorder, Adverse Event, Polychondritis, Drug Dispensing Error, Melaena, Tendonitis, Muscle Spasms, LOW Turnover Osteopathy, Back Pain, Cellulitis, Pain in Extremity, Anaemia, Bursitis, Temporomandibular Joint Syndrome, Throat Irritation, Upper Gastrointestinal Haemorrhage, Osteoporosis, Haemorrhage, Pain, Constipation, Hepatitis, Somnolence, Groin Pain, Gastritis, Viith Nerve Paralysis, Nephrolithiasis, Hypercholesterolaemia, Weight Increased, Liver Function Test Abnormal, Rotator Cuff Syndrome, Intervertebral Disc Degeneration, Depression, Bone Disorder, Exostosis, Gastrooesophageal Reflux Disease, Scoliosis, Viral Infection, Nausea, Crystal Arthropathy, Haemorrhoids, Pancreatic Cyst, Multiple Fractures, Spondylitis, Anxiety, Haematochezia, Diarrhoea, Arthralgia, Sinus Disorder, Gait Disturbance, Tooth Disorder, Hypertension, Infection

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Boniva
    Indication: Menopause
    Start date: 2006-01-01
    End date: 2011-01-01

Boniva
    Indication: Osteopenia
    Start date: 2006-01-01
    End date: 2011-01-01

Fosamax
    Administration route: Oral
    Indication: Menopause
    Start date: 2004-08-01

Fosamax
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2004-08-01

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



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