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Fosamax Plus D (Alendronate / Cholecalciferol) - LOW Turnover Osteopathy - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with LOW Turnover Osteopathy (655)

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

 Reports 1 - 30 of 655   Next >>

Possible Fosamax Plus D side effects in

Reported by a lawyer from United States on 2012-08-27

Patient:

Reactions: Scoliosis, Femur Fracture, Osteoporosis, Foot Fracture, Anxiety, Device Failure, Arthropathy, Impaired Healing, Intervertebral Disc Disorder, Stress Fracture, Depression, Kidney Infection, Open Reduction of Fracture, LOW Turnover Osteopathy, Calcium Deficiency

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis

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

Other drugs received by patient: Calcium (Unspecified)



Possible Fosamax Plus D side effects in

Reported by a physician from United States on 2012-08-27

Patient:

Reactions: Tooth Loss, Regurgitation, Femur Fracture, Nasopharyngitis, Joint Stiffness, Arthropathy, Dyspepsia, Upper Respiratory Tract Infection, Balance Disorder, Adverse Event, LOW Turnover Osteopathy, Cough, Chest Discomfort, Dysphagia, Oral Infection, Gingival Disorder, Pancytopenia, Helicobacter Infection, Osteopenia, Hypoaesthesia, Stress, Upper Respiratory Tract Congestion, Cholelithiasis, Joint Swelling, Acute Sinusitis, Insomnia, Stress Fracture, Transfusion, Abscess, Osteoporosis, Biopsy Brain, Gastric Ulcer, Constipation, Brain Neoplasm Malignant, Lymphadenitis, Diplopia, Overdose, Merycism, Hilar Lymphadenopathy, Blood Cholesterol Increased, Abnormal Loss of Weight, Thyroid Mass, Depression, Toothache, Gastrooesophageal Reflux Disease, Sinusitis, Pain in JAW, Abdominal Pain Lower, Dyspnoea, Central Nervous System Lymphoma, Dental Caries, Muscular Weakness, Oesophageal Carcinoma, Onychomycosis, Rash, Hysterectomy, Anxiety, Osteonecrosis of JAW, Sinus Disorder, Oesophageal Discomfort, Bronchitis

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Fosamax

Fosamax
    Dosage: 10 mg, unk
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2000-09-29
    End date: 2005-07-29

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2005-09-20
    End date: 2007-12-10

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1995-01-01
    End date: 2005-04-20

Fosamax Plus D
    Administration route: Oral
    Indication: Osteoporosis

Fosamax Plus D
    Indication: Osteopenia

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



Possible Fosamax Plus D side effects in

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

Patient:

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

Adverse event resulted in: hospitalization, disablity

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

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

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

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



Possible Fosamax Plus D side effects in

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

Patient:

Reactions: Abdominal Pain, Fractured Sacrum, Abdominal Hernia, Vaginal Prolapse, Vitamin D Deficiency, Femur Fracture, Gastrointestinal Surgery, Hernia Obstructive, Intestinal Stenosis, Body Height Decreased, Blood Parathyroid Hormone Abnormal, Vulvovaginal Dryness, Blood Creatinine Increased, Incision Site Haemorrhage, Muscle Spasms, White Blood Cell Count Increased, Cough, LOW Turnover Osteopathy, Back Pain, Dysphagia, Hiatus Hernia, Vulvovaginal Burning Sensation, Angiomyolipoma, Bursitis, Elbow Operation, Nasal Septum Deviation, Enchondroma, Limb Injury, Dehydration, Colitis, Inguinal Hernia, Drug Ineffective, Chills, Upper-Airway Cough Syndrome, Gastritis Erosive, Intestinal Adhesion Lysis, Drug Interaction, Gastritis, Nephrolithiasis, Malignant Melanoma, Skeletal Injury, Sinusitis, Decreased Appetite, Suture Rupture, Scoliosis, Vomiting, Nausea, Haemorrhoids, Biopsy Breast, Hernia, Renal Failure Chronic, Hypercalcaemia, Device Failure, Osteoarthritis, Atrophic Vulvovaginitis, Renal Failure, Impaired Healing, Gastroenteritis, Spinal Osteoarthritis, Gait Disturbance, Tooth Disorder, Hyperthyroidism

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2002-12-01

Fosamax
    Administration route: Oral

Fosamax Plus D
    Dosage: 70mg-5600
    Administration route: Oral

Other drugs received by patient: Lomotil; Raloxifene Hydrochloride; Forteo



Possible Fosamax Plus D side effects in

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

Patient:

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

Adverse event resulted in: hospitalization, disablity

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

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

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



Possible Fosamax Plus D side effects in

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

Patient:

Reactions: Femur Fracture, Osteoporosis, Headache, Cystocele, Hypercholesterolaemia, Abdominal Distension, Open Reduction of Fracture, LOW Turnover Osteopathy, Anaemia Postoperative, Haemorrhoids, Drug Hypersensitivity, Atrophic Vulvovaginitis, Rectocele, Stress Fracture, Transfusion, Tooth Disorder, Hypertension

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis Prophylaxis
    Start date: 2003-07-01
    End date: 2005-07-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2009-08-26
    End date: 2010-05-08

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis Prophylaxis
    Start date: 2005-07-06
    End date: 2008-06-01



Possible Fosamax Plus D side effects in

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

Patient:

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

Adverse event resulted in: hospitalization

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

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

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

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

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

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



Possible Fosamax Plus D side effects in

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

Patient:

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

Adverse event resulted in: hospitalization, disablity

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

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

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

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

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

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



Possible Fosamax Plus D side effects in

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

Patient:

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

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Boniva

Fosamax
    Dosage: 40 mg, qw

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

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

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



Possible Fosamax Plus D side effects in

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

Patient:

Reactions: Back Pain, Dysphagia, Femur Fracture, Osteoporosis, Eye Irritation, Hospitalisation, Reflux Laryngitis, Nervous System Disorder, Intramedullary ROD Insertion, Stress Fracture, Gastroenteritis, LOW Turnover Osteopathy, Iritis

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, qd
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-11-01
    End date: 2008-04-01

Fosamax Plus D
    Dosage: unk
    Administration route: Oral
    Start date: 2007-01-16

Other drugs received by patient: Chantix; Zocor



Possible Fosamax Plus D side effects in

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

Patient:

Reactions: Femur Fracture, LOW Turnover Osteopathy

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: unk
    Start date: 2000-01-01
    End date: 2010-06-01

Fosamax

Fosamax Plus D



Possible Fosamax Plus D side effects in

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

Patient:

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

Adverse event resulted in: hospitalization

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

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

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

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

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

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

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

Other drugs received by patient: Tamoxifen Citrate; Nicoderm



Possible Fosamax Plus D side effects in

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

Patient:

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

Adverse event resulted in: hospitalization, disablity

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

Fosamax
    Indication: Osteopenia

Fosamax Plus D
    Indication: Osteopenia

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

Other drugs received by patient: MK-9278



Possible Fosamax Plus D side effects in

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

Patient:

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

Adverse event resulted in: hospitalization, disablity

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

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

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

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

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

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

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

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



Possible Fosamax Plus D side effects in

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

Patient:

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

Adverse event resulted in: hospitalization, disablity

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

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

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

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

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

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



Possible Fosamax Plus D side effects in

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

Patient:

Reactions: Femur Fracture, LOW Turnover Osteopathy

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: unk
    Start date: 2003-01-01
    End date: 2009-01-01

Fosamax
    Dosage: unk
    Start date: 2003-01-01
    End date: 2009-01-01

Fosamax Plus D
    Dosage: unk
    Start date: 2003-01-01
    End date: 2009-01-01



Possible Fosamax Plus D side effects in

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

Patient:

Reactions: Hypersensitivity, Femur Fracture, Osteoporosis, Multiple Fractures, Device Failure, Rheumatoid Arthritis, Surgery, Impaired Healing, Essential Hypertension, LOW Turnover Osteopathy

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2001-02-08

Fosamax
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1998-11-01
    End date: 2006-12-31

Fosamax Plus D
    Dosage: 70/2800 mg, unk
    Administration route: Oral
    Start date: 2006-06-16



Possible Fosamax Plus D side effects in

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

Patient:

Reactions: Polymyalgia Rheumatica, Contusion, Piriformis Syndrome, Monoclonal Immunoglobulin Present, Vaginal Disorder, Malaise, Upper Respiratory Tract Infection, Oedema Peripheral, Ulna Fracture, LOW Turnover Osteopathy, Breast Cancer Stage I, Fracture Delayed Union, Joint Injury, Faeces Hard, Tonsillar Disorder, Staphylococcal Infection, Uterine Disorder, Bone Metabolism Disorder, Adverse Drug Reaction, Fall, Foot Fracture, Rotator Cuff Syndrome, Bone Disorder, Depression, Decreased Appetite, Joint Dislocation, Blood Potassium Abnormal, Bipolar Disorder, Calcium Ionised, Arthralgia, Bladder Disorder, Gait Disturbance, Underweight, Asthma, Bone Fragmentation, Femur Fracture, Sciatica, Urinary Incontinence, Hand Fracture, Headache, Tooth Infection, Fallopian Tube Disorder, Arthropathy, Fracture, Dyspepsia, Joint Effusion, Anaemia Postoperative, Pain in Extremity, Oestrogen Deficiency, Gastric Disorder, Micturition Urgency, Dysmenorrhoea, Osteonecrosis, Joint Swelling, Acute Sinusitis, Ear Pain, Scar, Uterine Cervix Stenosis, Hypophosphatasia, Urethral Stenosis, Dyslipidaemia, Drug Ineffective, Hypokalaemia, Fatigue, Intervertebral Disc Degeneration, Hypertonic Bladder, Sinusitis, Gastrooesophageal Reflux Disease, Migraine, Swelling Face, Urinary Tract Infection, Condition Aggravated, Osteolysis, Osteoarthritis, Anxiety, Uterine Spasm, Spinal Osteoarthritis, Tooth Disorder

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Boniva
    Dosage: 150 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2005-09-24
    End date: 2006-01-01

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2009-06-29
    End date: 2009-12-13

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

Fosamax
    Dosage: unk
    Administration route: Oral
    Start date: 2009-02-13

Fosamax
    Dosage: 10 mg, unk
    Administration route: Oral
    Start date: 1997-10-01
    End date: 2001-02-01

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

Fosamax Plus D
    Dosage: 70-2800
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-02-01
    End date: 2008-01-01

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2008-02-21
    End date: 2008-11-07

Fosamax Plus D
    Dosage: 70 u, unk
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2008-02-01
    End date: 2009-01-01

Other drugs received by patient: MK-9278; Hormones (Unspecified); Ultram; Prempro; Nortriptyline; Premarin; Calcium (Unspecified); Vitamin D; Percocet; Cholecalciferol; Calcium (Unspecified) (+) Vitamin D (Unspecified); Tylenol



Possible Fosamax Plus D side effects in

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

Patient:

Reactions: Femur Fracture, Flatulence, Gastric Cancer, Surgery, Spinal Compression Fracture, Fracture, Adverse Event, Vertebral Foraminal Stenosis, Spinal Laminectomy, LOW Turnover Osteopathy, Intervertebral Disc Protrusion, Phlebitis, Back Pain, Spinal Fracture, Gastrointestinal Stromal Tumour, Hypoaesthesia, Lumbar Vertebral Fracture, Spinal Fusion Surgery, HIP Fracture, Spleen Disorder, Metastases To Spine, Intramedullary ROD Insertion, Packed RED Blood Cell Transfusion, Stress Fracture, Adenoma Benign, Osteoporosis, Fall, Kyphosis, Constipation, Foraminotomy, Breast Disorder Female, Road Traffic Accident, Intervertebral Disc Disorder, Dizziness, Bone Disorder, Injury, Gastrooesophageal Reflux Disease, Exostosis, Scoliosis, Pelvic Fracture, Vertebroplasty, Joint Dislocation, Patellofemoral Pain Syndrome, Osteoarthritis, Meniscus Lesion, Arthralgia, Spinal Osteoarthritis, Spinal Disorder, Gait Disturbance, Hypertension, Arthritis

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteopenia
    Start date: 1997-01-01
    End date: 2009-06-08

Fosamax
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1997-01-01
    End date: 2009-06-08

Fosamax
    Dosage: 70 qw
    Administration route: Oral
    Start date: 2008-12-04
    End date: 2009-05-01

Fosamax Plus D
    Dosage: 70/2800 qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2005-04-01
    End date: 2009-03-01

Fosamax Plus D
    Indication: Osteopenia

Other drugs received by patient: Lipitor; Allegra; Nasacort; Calcium (Unspecified); Actonel



Possible Fosamax Plus D side effects in

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

Patient:

Reactions: Femur Fracture, LOW Turnover Osteopathy

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: unk
    Start date: 2000-01-01
    End date: 2010-06-01

Fosamax
    Dosage: unk
    Start date: 2000-01-01
    End date: 2010-06-01

Fosamax Plus D
    Dosage: unk
    Start date: 2000-01-01
    End date: 2010-06-01



Possible Fosamax Plus D side effects in

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

Patient:

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

Adverse event resulted in: hospitalization

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

Fosamax
    Indication: Osteoporosis

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

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



Possible Fosamax Plus D side effects in

Reported by a consumer/non-health professional from Puerto Rico on 2012-08-23

Patient:

Reactions: Femur Fracture, Fear, Foot Fracture, Hypokinesia, Upper Respiratory Tract Infection, Liver Function Test Abnormal, Bone Disorder, Depression, Muscle Spasms, LOW Turnover Osteopathy, Abdominal Pain Lower, Pain in Extremity, Osteoarthritis, Anxiety, Hysterectomy, Syncope, Impaired Healing, Sleep Disorder, Cholecystectomy

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1997-07-01
    End date: 2010-11-25

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 1997-07-01
    End date: 2010-03-01

Fosamax Plus D
    Dosage: 70 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1997-07-01
    End date: 2010-03-01

Other drugs received by patient: Vitamin D; Daypro; Levothyroxine Sodium; Calcium (Unspecified); MK-9359; Coumadin; Synthroid; Tenormin; Methotrexate



Possible Fosamax Plus D side effects in

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

Patient:

Reactions: Oral Surgery, Femur Fracture, Osteoporosis, Dental Implantation, Lower Limb Fracture, Gastritis, Hypothyroidism, Hypertension, LOW Turnover Osteopathy

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2000-01-01

Fosamax Plus D
    Dosage: 70 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2007-12-27



Possible Fosamax Plus D side effects in

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

Patient:

Reactions: Femur Fracture, Skeletal Injury, LOW Turnover Osteopathy

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Boniva

Fosamax
    Dosage: unk

Fosamax
    Indication: Osteopenia

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

Fosamax Plus D
    Indication: Osteopenia

Fosamax Plus D
    Indication: Osteoporosis



Possible Fosamax Plus D side effects in

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

Patient:

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

Adverse event resulted in: hospitalization, disablity

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

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

Fosamax

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

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

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

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

Fosamax Plus D
    Indication: Osteopenia

Other drugs received by patient: Premarin



Possible Fosamax Plus D side effects in

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

Patient:

Reactions: Vitamin D Deficiency, Polymyalgia Rheumatica, Glossodynia, Femur Fracture, Upper Limb Fracture, Dental Plaque, Headache, Tooth Infection, Rash Pruritic, Abdominal Discomfort, Surgery, Pathological Fracture, LOW Turnover Osteopathy, Gingival Bleeding, Spinal Fracture, Ear Pain, Stress Fracture, LIP Swelling, Glaucoma, Osteoporosis, Tooth Deposit, Wrist Fracture, Endodontic Procedure, Neuropathy Peripheral, Fatigue, Abdominal Distension, Tooth Fracture, Dental Caries, Osteoarthritis, Gingival Recession, Gingival Pain, Osteonecrosis of JAW, Forearm Fracture, Tooth Disorder

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Actonel
    Dosage: unk
    Indication: Osteoporosis
    Start date: 2001-01-01

Fosamax
    Dosage: unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2000-01-01
    End date: 2007-06-01

Fosamax Plus D
    Dosage: 70/2800
    Administration route: Oral

Other drugs received by patient: OS-CAL (Calcitriol); Vitamins (Unspecified); Forteo



Possible Fosamax Plus D side effects in

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

Patient:

Reactions: Scoliosis, Diverticulum, Femur Fracture, Polyp, Osteoporosis, Haemorrhoids, Stress Fracture, Skin Infection, LOW Turnover Osteopathy, Infection

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Indication: Bone Loss
    Start date: 2003-06-01
    End date: 2007-07-01

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

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



Possible Fosamax Plus D side effects in

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

Patient:

Reactions: Vitamin D Deficiency, Femur Fracture, Trigger Finger, Vaginal Disorder, Colonic Polyp, Dyspepsia, Benign Breast Neoplasm, Fibula Fracture, LOW Turnover Osteopathy, Back Pain, Hiatus Hernia, Pain in Extremity, Mastitis, Hyperprolactinaemia, Osteopenia, Bursitis, Diverticulum Intestinal, Hepatic Steatosis, Acute Sinusitis, Osteoporosis, Fall, Cystocele, Gastritis, Abdominal Pain Upper, Muscle Strain, Hypercholesterolaemia, Bronchospasm, Burn Infection, Sinusitis, Gastrooesophageal Reflux Disease, Endometrial Disorder, Polyp, Haemorrhoids, Atrophic Vulvovaginitis, Hyperlipidaemia, Arthralgia, Hypertension, Anogenital Warts

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1998-06-01
    End date: 2000-01-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2009-01-01
    End date: 2010-05-01

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

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis Prophylaxis
    Start date: 2007-05-01
    End date: 2008-12-01

Fosamax Plus D
    Indication: Osteoporosis

Other drugs received by patient: Centrum (Minerals (Unspecified) (+) Vitamins (Unspecified)); Calcium (Unspecified); Hormones (Unspecified); Selective Estrogen Receptor Modulator (Unspecified)



Possible Fosamax Plus D side effects in

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

Patient:

Reactions: Lymphadenopathy, Dyslipidaemia, Femur Fracture, Diabetes Mellitus, non-Alcoholic Steatohepatitis, High Density Lipoprotein Decreased, Poor Quality Sleep, Foot Fracture, Ileal Ulcer, Fatigue, Oedema Peripheral, DRY Mouth, Adverse Event, Exostosis, LOW Turnover Osteopathy, Anaemia Postoperative, Dyspnoea, Pain in Extremity, Musculoskeletal Pain, Joint Dislocation, Rash, Hypercalcaemia, Paraesthesia, Osteoarthritis, Meniscus Lesion, Device Failure, Arthralgia, Dysuria, Ear Pain, Hypothyroidism, Tooth Disorder

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Alendronate Sodium
    Dosage: 70 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2009-06-29
    End date: 2010-01-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2001-11-13
    End date: 2006-10-01

Fosamax
    Indication: Osteopenia

Fosamax Plus D
    Dosage: 2800 iu, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-11-09
    End date: 2009-05-01

Fosamax Plus D
    Indication: Osteopenia

Other drugs received by patient: Calcium (Unspecified)



Possible Fosamax Plus D side effects in

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

Patient:

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

Adverse event resulted in: hospitalization, disablity

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

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

Fosamax Plus D
    Administration route: Oral
    Indication: Osteoporosis

Fosamax Plus D
    Indication: Osteopenia

Other drugs received by patient: Prilosec; MK-9278



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