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

 
 



Index of reports > Cases with Muscular Weakness ()

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

 Reports 1 - 30 of    Next >>

Possible Fosamax Plus D side effects in

Reported by a 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 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 2012-08-24

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

Patient:

Reactions: Diabetes Mellitus, Bundle Branch Block Right, Eczema, Oropharyngeal Pain, Iron Deficiency Anaemia, Dermatitis, Oedema Peripheral, Vertebral Foraminal Stenosis, Clostridial Infection, Post Procedural Haemorrhage, Nervousness, Back Pain, Wound Dehiscence, Coronary Artery Disease, Musculoskeletal Discomfort, Synovial Disorder, HIP Fracture, Femoral Neck Fracture, Osteoporosis, Adverse Drug Reaction, Fall, Wound Infection Staphylococcal, Hypoacusis, Rotator Cuff Syndrome, Depression, Exostosis, Cataract, Fracture Malunion, Breast Disorder, Muscular Weakness, Skin Disorder, DRY Skin, Device Failure, Arthralgia, Impaired Healing, Limb Asymmetry, Hypothyroidism, Blood Disorder, Gait Disturbance, Gravitational Oedema, Foot Deformity, Asthma, Agitation, Femur Fracture, Wound Haematoma, Nocturia, Dyspepsia, Bone Density Decreased, Stress Urinary Incontinence, Anaemia Postoperative, Cellulitis, Pain in Extremity, Neurodermatitis, Micturition Urgency, Electrocardiogram Abnormal, Pain, Gastritis, Weight Increased, Dyspnoea Exertional, Skin Ulcer, Wound Drainage, Lymphoedema, Pain in JAW, Scoliosis, Squamous Cell Carcinoma, Cystitis, Multiple Fractures, Osteoarthritis, Anxiety, Neoplasm Malignant, Diarrhoea, Bronchitis, Spinal Osteoarthritis, Tooth Disorder, Deep Vein Thrombosis, Infection, Infusion Site Extravasation

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2001-10-12
    End date: 2001-12-07

Fosamax
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1997-01-01
    End date: 2007-01-01

Fosamax Plus D
    Indication: Osteopenia

Fosamax Plus D
    Administration route: Oral
    Indication: Osteoporosis

Other drugs received by patient: Calcium (Unspecified)



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 health professional (non-physician/pharmacist) from United States on 2012-08-10

Patient:

Reactions: Vitamin D Deficiency, Femur Fracture, Contusion, Wound, Lumbar Spinal Stenosis, DRY Mouth, Hypocalcaemia, Carpal Tunnel Syndrome, Squamous Cell Carcinoma of Skin, LOW Turnover Osteopathy, Abscess Limb, Back Pain, Intervertebral Disc Protrusion, Cellulitis, Pain in Extremity, Sacroiliitis, Bursitis, Joint Injury, HIP Fracture, Rhinitis Allergic, Insomnia, Dental Care, Stress Fracture, Dental Cleaning, Spinal Column Stenosis, Osteoporosis, Blood Triglycerides Increased, Fall, Constipation, Muscle Strain, Foot Fracture, Intervertebral Disc Disorder, Intervertebral Disc Degeneration, Gastrooesophageal Reflux Disease, Sinusitis, Calcium Deficiency, Blood Pressure Increased, Nail Avulsion, Dental Caries, Drug Hypersensitivity, Muscular Weakness, Device Failure, Nodal Osteoarthritis, Hyperlipidaemia, Arthralgia, Spinal Osteoarthritis, Tooth Disorder, Respiratory Tract Infection, Anogenital Warts

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2002-11-01
    End date: 2007-06-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2009-02-17
    End date: 2010-09-10

Fosamax
    Dosage: 10 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1995-12-07
    End date: 1998-05-01

Fosamax

Fosamax
    Dosage: 5 mg, unk
    Administration route: Oral
    Indication: Osteopenia
    Start date: 1998-06-01
    End date: 2002-10-01

Fosamax Plus D
    Indication: Osteopenia

Fosamax Plus D
    Dosage: 70/2800
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2007-06-01
    End date: 2009-02-01

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



Possible Fosamax Plus D side effects in

Reported by a consumer/non-health professional from Puerto Rico on 2012-08-10

Patient:

Reactions: Femur Fracture, Demyelinating Polyneuropathy, Cerebral Ischaemia, Rheumatoid Arthritis, Balance Disorder, Musculoskeletal Disorder, Adverse Event, Joint Effusion, Post Procedural Haemorrhage, Muscle Spasms, Cough, Back Pain, Intervertebral Disc Protrusion, Pain in Extremity, Lumbar Vertebral Fracture, Tremor, HIP Fracture, Diverticulum, Uterine Disorder, Psoriatic Arthropathy, Adverse Drug Reaction, Constipation, Fall, Synovial Cyst, Haemorrhoidal Haemorrhage, Poor Quality Sleep, Foot Fracture, Cardiac Valve Disease, Neuropathy Peripheral, Dizziness, Bone Disorder, Injury, Exostosis, Pelvic Fracture, Inappropriate Schedule of Drug Administration, Spondylolysis, Dyspnoea, Nausea, Spondylolisthesis, Drug Hypersensitivity, Dental Caries, Skin Disorder, Muscular Weakness, Patellofemoral Pain Syndrome, Facet Joint Syndrome, Appendix Disorder, Hepatic Enzyme Increased, Osteoarthritis, Anxiety, Arthralgia, Alopecia, Lacunar Infarction, Spinal Osteoarthritis, Gait Disturbance, Hypertension

Adverse event resulted in: hospitalization, disablity

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

Fosamax
    Dosage: 70 mg, qd
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2000-01-01
    End date: 2011-05-01

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2009-01-01

Fosamax Plus D
    Indication: Osteopenia



Possible Fosamax Plus D side effects in

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

Patient:

Reactions: Vitamin D Deficiency, Contusion, Femur Fracture, Urinary Incontinence, Headache, Arthropathy, Hot Flush, Helicobacter Test Positive, Bone Density Decreased, Pathological Fracture, LOW Turnover Osteopathy, Anaemia Postoperative, Epistaxis, Hiatus Hernia, Knee Impingement Syndrome, Cholelithiasis, Rhinitis Allergic, Acute Sinusitis, Ocular Hyperaemia, Neuralgia, Rectal Polyp, Sinus Polyp, Tooth Abscess, Eye Irritation, Nasal Turbinate Hypertrophy, Pain, Gastritis Erosive, Gastric Ulcer, Fall, Gastritis, Foot Fracture, Intervertebral Disc Degeneration, Gastrooesophageal Reflux Disease, Pharyngitis, Blood Pressure Increased, Migraine, Nausea, Haemorrhoids, Patellofemoral Pain Syndrome, Muscular Weakness, Osteoarthritis, Hyperlipidaemia, Anxiety, Barrett's Oesophagus, Dysuria, Pollakiuria, Spinal Osteoarthritis

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Fosamax
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2001-06-09
    End date: 2002-07-31

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2002-07-01
    End date: 2008-08-01

Fosamax
    Administration route: Oral
    Start date: 2008-02-01
    End date: 2008-08-01

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2001-01-01
    End date: 2008-09-01

Fosamax Plus D
    Indication: Osteopenia



Possible Fosamax Plus D side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-10

Patient:

Reactions: Vitamin D Deficiency, Polyp Colorectal, Dental Implantation, Tooth Extraction, Treatment Noncompliance, Herpes Zoster, Lumbar Spinal Stenosis, Colonic Polyp, Body Height Decreased, Ovarian Mass, Adverse Event, Cervical Spinal Stenosis, Melaena, Haematoma, Intervertebral Disc Protrusion, Spinal Fracture, Anaemia, Aortic Calcification, Gingival Disorder, Osteopenia, Costochondritis, Antinuclear Antibody Positive, Staphylococcal Infection, Electrocardiogram Abnormal, Femoral Neck Fracture, Wrist Fracture, Drug Ineffective, Pain, Fall, Gastritis, Fatigue, Intervertebral Disc Degeneration, Injury, Gastrooesophageal Reflux Disease, Thrombocytopenia, Spondylolysis, Excoriation, Spondylolisthesis, Muscular Weakness, Osteoarthritis, Anxiety, Spinal Osteoarthritis, Tooth Disorder, Atrioventricular Block First Degree

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 10 mg, unk
    Start date: 2000-02-13
    End date: 2000-09-21

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2001-07-20
    End date: 2006-06-08

Fosamax
    Dosage: unk unk, qd
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1998-01-01
    End date: 2009-05-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2007-11-21
    End date: 2009-06-17

Other drugs received by patient: Boniva; Forteo



Possible Fosamax Plus D side effects in

Reported by a physician from United States on 2012-08-01

Patient:

Reactions: Asthma, Femur Fracture, Fear, Fall, Cardiac Disorder, Poor Quality Sleep, Nephrolithiasis, Arthropathy, Blood Cholesterol Increased, Depression, Haematoma, LOW Turnover Osteopathy, Muscular Weakness, Synovial Disorder, Alcohol Use, 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
    Indication: Osteoporosis

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2001-01-01
    End date: 2006-06-01

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; Atenolol; MK-9278; Corticosteroids (Unspecified); Calcium (Unspecified); Humira



Possible Fosamax Plus D side effects in

Reported by a physician from United States on 2012-07-29

Patient:

Reactions: Femur Fracture, Goitre, Cardiac Stress Test Abnormal, Sciatica, Joint Stiffness, Arthropathy, Open Wound, Stress Urinary Incontinence, LOW Turnover Osteopathy, Muscle Spasms, Intervertebral Disc Protrusion, Back Pain, Fracture Delayed Union, Pain in Extremity, Hyperglycaemia, Pubis Fracture, Coronary Artery Disease, Laceration, Limb Injury, Benign Neoplasm of Thyroid Gland, Pseudarthrosis, Dyslipidaemia, Fall, Cystocele, Hypokalaemia, Fatigue, Intervertebral Disc Degeneration, Gastrooesophageal Reflux Disease, Blood Glucose Increased, Abdominal Pain Lower, Vomiting, Nausea, Urinary Tract Infection, Muscular Weakness, Onychomycosis, Anxiety, Rectocele, Osteoarthritis, Catheterisation Cardiac, Arthralgia, Diarrhoea, Hypertension

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2008-02-06
    End date: 2009-10-10

Fosamax
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1998-01-01
    End date: 2005-04-01

Fosamax Plus D
    Dosage: 70 mg/2800
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2005-05-01
    End date: 2009-02-25

Fosamax Plus D
    Indication: Osteopenia



Possible Fosamax Plus D side effects in

Reported by a physician from United States on 2012-07-27

Patient:

Reactions: Femur Fracture, Foot Operation, Fear, Arthroscopic Surgery, Fall, Cardiac Disorder, Nephrolithiasis, Poor Quality Sleep, Limb Operation, Blood Cholesterol Increased, Depression, Haematoma, LOW Turnover Osteopathy, Muscular Weakness, Synovial Disorder, Alcohol Use, Anxiety, Limb Injury, Compression Fracture, Gait Disturbance, Arthritis, Hypertension, Infection

Adverse event resulted in: hospitalization

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

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2001-01-01
    End date: 2009-01-01

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

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



Possible Fosamax Plus D side effects in

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

Patient:

Reactions: Diabetes Mellitus, Bundle Branch Block Right, Oropharyngeal Pain, Eczema, Dermatitis, Iron Deficiency Anaemia, Oedema Peripheral, Vertebral Foraminal Stenosis, Post Procedural Haemorrhage, Clostridial Infection, Nervousness, Back Pain, Wound Dehiscence, Coronary Artery Disease, Musculoskeletal Discomfort, Synovial Disorder, HIP Fracture, Femoral Neck Fracture, Osteoporosis, Adverse Drug Reaction, Wound Infection Staphylococcal, Fall, Hypoacusis, Rotator Cuff Syndrome, Depression, Exostosis, Cataract, Fracture Malunion, Breast Disorder, Muscular Weakness, Skin Disorder, DRY Skin, Device Failure, Arthralgia, Impaired Healing, Hypothyroidism, Blood Disorder, Limb Asymmetry, Gait Disturbance, Gravitational Oedema, Asthma, Foot Deformity, Agitation, Femur Fracture, Wound Haematoma, Nocturia, Dyspepsia, Bone Density Decreased, Stress Urinary Incontinence, Anaemia Postoperative, Cellulitis, Pain in Extremity, Neurodermatitis, Micturition Urgency, Electrocardiogram Abnormal, Pain, Gastritis, Weight Increased, Dyspnoea Exertional, Skin Ulcer, Wound Drainage, Lymphoedema, Pain in JAW, Scoliosis, Squamous Cell Carcinoma, Cystitis, Multiple Fractures, Anxiety, Osteoarthritis, Neoplasm Malignant, Diarrhoea, Bronchitis, Spinal Osteoarthritis, Tooth Disorder, Deep Vein Thrombosis, Infection, Infusion Site Extravasation

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2001-10-12
    End date: 2001-12-07

Fosamax
    Dosage: 10 mg, qd
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1997-01-01
    End date: 2007-01-01

Fosamax Plus D
    Indication: Osteopenia

Fosamax Plus D
    Administration route: Oral
    Indication: Osteoporosis

Other drugs received by patient: Calcium (Unspecified)



Possible Fosamax Plus D side effects in

Reported by a health professional (non-physician/pharmacist) from United States on 2012-07-25

Patient:

Reactions: Vitamin D Deficiency, Femur Fracture, Contusion, Wound, Lumbar Spinal Stenosis, DRY Mouth, Hypocalcaemia, Carpal Tunnel Syndrome, Squamous Cell Carcinoma of Skin, Abscess Limb, LOW Turnover Osteopathy, Back Pain, Intervertebral Disc Protrusion, Cellulitis, Pain in Extremity, Sacroiliitis, Bursitis, Joint Injury, HIP Fracture, Rhinitis Allergic, Insomnia, Stress Fracture, Spinal Column Stenosis, Osteoporosis, Blood Triglycerides Increased, Fall, Constipation, Muscle Strain, Foot Fracture, Intervertebral Disc Disorder, Intervertebral Disc Degeneration, Gastrooesophageal Reflux Disease, Sinusitis, Calcium Deficiency, Blood Pressure Increased, Drug Hypersensitivity, Nail Avulsion, Dental Caries, Muscular Weakness, Nodal Osteoarthritis, Hyperlipidaemia, Arthralgia, Spinal Osteoarthritis, Respiratory Tract Infection, Tooth Disorder, Anogenital Warts

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2009-02-17
    End date: 2010-09-10

Fosamax
    Dosage: 10 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1995-12-07
    End date: 1998-05-01

Fosamax
    Dosage: 5 mg, unk
    Administration route: Oral
    Indication: Osteopenia
    Start date: 1998-06-01
    End date: 2002-10-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2002-11-01
    End date: 2007-06-01

Fosamax

Fosamax Plus D
    Dosage: 70/2800
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2007-06-01
    End date: 2009-02-01

Fosamax Plus D
    Indication: Osteopenia

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



Possible Fosamax Plus D side effects in

Reported by a consumer/non-health professional from United States on 2012-07-25

Patient:

Reactions: Foot Deformity, Gastrointestinal Haemorrhage, Femur Fracture, Diverticulitis, Pyrexia, Headache, Blepharitis, Rheumatoid Arthritis, Dyspepsia, Nodule, Tendonitis, Hypercalciuria, Cough, Hiatus Hernia, Anaemia, Gingival Disorder, Bursitis, Joint Injury, HIP Fracture, Osteosclerosis, Limb Injury, Thyroid Disorder, Stress Fracture, Femoral Neck Fracture, Back Injury, Bunion, Bone Pain, Impaired Fasting Glucose, Pelvic Pain, Limb Malformation, Fall, Urine Calcium, Gastritis, Myalgia, Hypercholesterolaemia, Conjunctivitis Allergic, Fatigue, Road Traffic Accident, Neck Pain, Chest Pain, Rotator Cuff Syndrome, Depression, Exostosis, RIB Fracture, Ligament Sprain, Scoliosis, Soft Tissue Injury, Bone Lesion, Vulval Disorder, Gout, Nausea, Mass, Urinary Tract Infection, Muscular Weakness, Musculoskeletal Chest Pain, Osteoarthritis, Arthralgia, Diarrhoea, Blood Disorder, Hypertension, Tooth Disorder

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2002-01-01
    End date: 2007-01-01

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

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral

Fosamax
    Dosage: unk

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    End date: 2007-03-01

Other drugs received by patient: Maxalt; Zometa; Toradol; Aspirin; Ketorolac Tromethamine; Inderal LA



Possible Fosamax Plus D side effects in

Reported by a consumer/non-health professional from United States on 2012-07-20

Patient:

Reactions: Foot Deformity, Hyperkeratosis, Femur Fracture, Neoplasm, Lumbar Spinal Stenosis, Spinal Compression Fracture, Arthropathy, Peroneal Nerve Palsy, Musculoskeletal Disorder, Oedema Peripheral, Intervertebral Disc Protrusion, Back Pain, Pain in Extremity, Haematuria, Lumbar Radiculopathy, Paraesthesia, Intervertebral Disc Space Narrowing, Tendon Disorder, Essential Hypertension, Scar, Bunion, Hypertrophy, Adverse Drug Reaction, Fall, Nephrolithiasis, Intervertebral Disc Degeneration, Gastrooesophageal Reflux Disease, Nausea, Urinary Tract Infection, Drug Hypersensitivity, Muscular Weakness, Cystitis, Onychomycosis, Radius Fracture, Arthralgia, Visual Impairment, Spinal Osteoarthritis, Dysaesthesia

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2001-09-01
    End date: 2010-09-01

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Start date: 2008-07-21
    End date: 2010-08-18

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2001-09-01
    End date: 2010-09-01

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



Possible Fosamax Plus D side effects in

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

Patient:

Reactions: Asthma, Femur Fracture, Tinnitus, Diabetes Mellitus, Lipids Increased, Upper Respiratory Tract Infection, Dermatitis, Ingrowing Nail, Cardiovascular Deconditioning, Vertebral Foraminal Stenosis, Stress Urinary Incontinence, Cough, Haematoma, LOW Turnover Osteopathy, Intervertebral Disc Protrusion, Pneumonia, Anaemia, Hypotension, Coronary Artery Disease, Cardiomyopathy, Hepatic Steatosis, Myopathy, Vitamin D Decreased, Gastrointestinal Disorder, Compression Fracture, Stress Fracture, Dermal Cyst, Nervous System Disorder, Spinal Column Stenosis, Rectal Polyp, Osteoporosis, Wheezing, Conjunctivitis, Constipation, Atrioventricular Block Second Degree, Laryngitis, Foot Fracture, Weight Increased, Hypercholesterolaemia, Neuropathy Peripheral, Fatigue, Liver Function Test Abnormal, Intervertebral Disc Degeneration, Gastrooesophageal Reflux Disease, Myocardial Infarction, Migraine, Urinary Tract Infection, Haemorrhoids, Muscular Weakness, Cystitis, Atrophic Vulvovaginitis, Osteoarthritis, Hypophosphataemia, Haematochezia, Arthralgia, Hypothyroidism, Gait Disturbance, Bronchitis, Hypertension

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Alendronate Sodium
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2009-05-23
    End date: 2010-06-01

Alendronate Sodium
    Indication: Osteopenia

Fosamax
    Dosage: 10 mg, unk
    Administration route: Oral
    Indication: Osteopenia
    Start date: 1999-04-05
    End date: 2010-03-01

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1999-04-01
    End date: 2010-03-01

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

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-05-01
    End date: 2010-02-01

Fosamax Plus D
    Dosage: 35 mg, qw
    Administration route: Oral
    Start date: 2007-09-01
    End date: 2009-05-22



Possible Fosamax Plus D side effects in

Reported by a lawyer from United States on 2012-07-09

Patient:

Reactions: Asthma, Tinnitus, Femur Fracture, Upper Respiratory Tract Infection, Dermatitis, Ingrowing Nail, Vertebral Foraminal Stenosis, Stress Urinary Incontinence, Cough, Pneumonia, Myopathy, Activities of Daily Living Impaired, Dermal Cyst, Stress Fracture, Conjunctivitis, Pain, Wheezing, Fear, Laryngitis, Weight Increased, Fatigue, Osteogenesis Imperfecta, Neuropathy Peripheral, Depression, Myocardial Infarction, Haemorrhoids, Urinary Tract Infection, Muscular Weakness, Cystitis, Haemoglobin Decreased, Atrophic Vulvovaginitis, Osteoarthritis, Arthralgia, Gait Disturbance, Bronchitis, Hypertension, Asthenia

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Alendronate Sodium
    Indication: Osteopenia

Alendronate Sodium
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2009-05-23
    End date: 2010-06-01

Fosamax
    Dosage: 70 mg, unk
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1999-04-01
    End date: 2010-03-01

Fosamax
    Dosage: 10 mg, unk
    Administration route: Oral
    Indication: Osteopenia
    Start date: 1999-04-05
    End date: 2010-03-01

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-05-01
    End date: 2010-02-01

Fosamax Plus D
    Dosage: 35 mg, qw
    Administration route: Oral
    Start date: 2007-09-01
    End date: 2009-05-22

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



Possible Fosamax Plus D side effects in

Reported by a physician from Puerto Rico on 2012-07-09

Patient:

Reactions: Femur Fracture, Demyelinating Polyneuropathy, Cerebral Ischaemia, Rheumatoid Arthritis, Balance Disorder, Musculoskeletal Disorder, Adverse Event, Joint Effusion, Post Procedural Haemorrhage, Muscle Spasms, Cough, Back Pain, Intervertebral Disc Protrusion, Pain in Extremity, Lumbar Vertebral Fracture, Tremor, HIP Fracture, Diverticulum, Uterine Disorder, Psoriatic Arthropathy, Adverse Drug Reaction, Constipation, Fall, Synovial Cyst, Haemorrhoidal Haemorrhage, Foot Fracture, Poor Quality Sleep, Cardiac Valve Disease, Neuropathy Peripheral, Dizziness, Bone Disorder, Injury, Exostosis, Pelvic Fracture, Inappropriate Schedule of Drug Administration, Dyspnoea, Spondylolysis, Nausea, Spondylolisthesis, Drug Hypersensitivity, Dental Caries, Muscular Weakness, Skin Disorder, Patellofemoral Pain Syndrome, Facet Joint Syndrome, Hepatic Enzyme Increased, Appendix Disorder, Anxiety, Osteoarthritis, Arthralgia, Alopecia, Lacunar Infarction, Spinal Osteoarthritis, Gait Disturbance, Hypertension

Adverse event resulted in: hospitalization, disablity

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

Fosamax
    Dosage: 70 mg, qd
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2000-01-01
    End date: 2011-05-01

Fosamax Plus D
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2009-01-01

Fosamax Plus D
    Indication: Osteopenia



Possible Fosamax Plus D side effects in 68 year old female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-07-02

Patient: 68 year old female, weighing 109.0 kg (239.8 pounds)

Reactions: Diabetes Mellitus, Bundle Branch Block Right, Eczema, Oropharyngeal Pain, Iron Deficiency Anaemia, Dermatitis, Vertebral Foraminal Stenosis, Post Procedural Haemorrhage, Clostridial Infection, Nervousness, Back Pain, Wound Dehiscence, Musculoskeletal Discomfort, Coronary Artery Disease, Synovial Disorder, HIP Fracture, Femoral Neck Fracture, Osteoporosis, Adverse Drug Reaction, Wound Infection Staphylococcal, Fall, Hypoacusis, Rotator Cuff Syndrome, Depression, Exostosis, Cataract, Fracture Malunion, Breast Disorder, Skin Disorder, Muscular Weakness, Device Failure, Arthralgia, Impaired Healing, Hypothyroidism, Limb Asymmetry, Blood Disorder, Gait Disturbance, Gravitational Oedema, Agitation, Foot Deformity, Asthma, Femur Fracture, Wound Haematoma, Nocturia, Dyspepsia, Bone Density Decreased, Stress Urinary Incontinence, Anaemia Postoperative, Cellulitis, Pain in Extremity, Neurodermatitis, Micturition Urgency, Electrocardiogram Abnormal, Pain, Gastritis, Weight Increased, Dyspnoea Exertional, Skin Ulcer, Wound Drainage, Lymphoedema, Pain in JAW, Scoliosis, Squamous Cell Carcinoma, Multiple Fractures, Cystitis, Anxiety, Osteoarthritis, Diarrhoea, Neoplasm Malignant, Spinal Osteoarthritis, Tooth Disorder, Infection, Infusion Site Extravasation

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Administration route: Oral
    Start date: 2001-10-12
    End date: 2001-12-01

Fosamax
    Administration route: Oral
    Start date: 2001-10-12
    End date: 2001-12-01

Fosamax
    Administration route: Oral
    Indication: Osteopenia
    Start date: 1997-01-01
    End date: 2007-01-01

Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1997-01-01
    End date: 2007-01-01

Fosamax Plus D
    Administration route: Oral
    Indication: Osteoporosis

Fosamax Plus D
    Administration route: Oral
    Indication: Osteopenia

Other drugs received by patient: Calcium (Unspecified)



Possible Fosamax Plus D side effects in 55 year old female

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

Patient: 55 year old female, weighing 54.0 kg (118.8 pounds)

Reactions: Blood Creatine Phosphokinase Increased, Uterine Polyp, Pruritus Allergic, Oesophagitis, Palpitations, Postmenopausal Haemorrhage, Upper Motor Neurone Lesion, Back Disorder, LOW Turnover Osteopathy, Hypotension, Lumbar Radiculopathy, Coronary Artery Disease, Osteopenia, Diverticulum, Limb Injury, Increased Tendency To Bruise, Angiopathy, Dermatitis Allergic, Osteoporosis, Fall, Kyphosis, Computerised Tomogram Coronary Artery Abnormal, Hypercholesterolaemia, Dermatitis Contact, Exostosis, Extremity Contracture, Haemorrhoids, Muscular Weakness, Joint Dislocation, Fibroma, Mitral Valve Incompetence, Gait Disturbance, Foot Deformity, Femur Fracture, Osteochondroma, Herpes Zoster, Food Allergy, Uterine Leiomyoma, Nodule, Muscle Spasms, Intervertebral Disc Protrusion, Cardiac Murmur, Hiatus Hernia, Pain in Extremity, Anaemia, Insomnia, Stress Fracture, Grief Reaction, Fracture Nonunion, Constipation, Myalgia, Fatigue, Intervertebral Disc Disorder, Intervertebral Disc Degeneration, Dizziness, Gastrooesophageal Reflux Disease, Scoliosis, Spondylolisthesis, Nausea, Urinary Tract Infection, Drug Hypersensitivity, Varicose Vein, Osteoarthritis, Hyperlipidaemia, Bronchitis, Arthritis, Deep Vein Thrombosis

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Administration route: Oral
    Start date: 2004-11-16
    End date: 2008-08-01

Fosamax
    Administration route: Oral
    Indication: Prophylaxis
    Start date: 1996-09-01

Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1996-09-01

Fosamax
    Administration route: Oral
    Start date: 2004-11-16
    End date: 2008-08-01

Fosamax Plus D
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2005-12-01
    End date: 2008-12-01

Other drugs received by patient: Premarin; Provera; Synthroid



Possible Fosamax Plus D side effects in 45 year old female

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

Patient: 45 year old female, weighing 82.0 kg (180.4 pounds)

Reactions: Weight Decreased, Femur Fracture, Adverse Drug Reaction, Pain, Headache, Muscle Tightness, Fatigue, Blood Cholesterol Increased, Rotator Cuff Syndrome, Hypermetropia, Depression, Gastrooesophageal Reflux Disease, Tendonitis, Wound Drainage, Cough, Pain in JAW, Muscle Spasms, LOW Turnover Osteopathy, Haematoma, Back Pain, Pain in Extremity, Muscular Weakness, Rhinorrhoea, Exercise Tolerance Decreased, Iliotibial Band Syndrome, Device Failure, Respiratory Tract Congestion, Sleep Apnoea Syndrome, DRY Eye, Device Breakage

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Administration route: Oral
    Indication: Osteopenia
    Start date: 1998-01-01
    End date: 2007-12-01

Fosamax Plus D
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2007-12-12
    End date: 2008-10-30



Possible Fosamax Plus D side effects in 51 year old female

Reported by a physician from United States on 2012-06-28

Patient: 51 year old female, weighing 55.0 kg (121.0 pounds)

Reactions: Asthma, Femur Fracture, Tinnitus, Diabetes Mellitus, Lipids Increased, Dermatitis, Upper Respiratory Tract Infection, Cardiovascular Deconditioning, Ingrowing Nail, Vertebral Foraminal Stenosis, Stress Urinary Incontinence, LOW Turnover Osteopathy, Cough, Haematoma, Intervertebral Disc Protrusion, Pneumonia, Hypotension, Anaemia, Coronary Artery Disease, Cardiomyopathy, Hepatic Steatosis, Myopathy, Gastrointestinal Disorder, Compression Fracture, Vitamin D Decreased, Nervous System Disorder, Stress Fracture, Dermal Cyst, Spinal Column Stenosis, Rectal Polyp, Osteoporosis, Wheezing, Conjunctivitis, Constipation, Laryngitis, Atrioventricular Block Second Degree, Foot Fracture, Weight Increased, Hypercholesterolaemia, Neuropathy Peripheral, Fatigue, Liver Function Test Abnormal, Intervertebral Disc Degeneration, Myocardial Infarction, Gastrooesophageal Reflux Disease, Migraine, Urinary Tract Infection, Haemorrhoids, Muscular Weakness, Cystitis, Osteoarthritis, Haematochezia, Hypophosphataemia, Atrophic Vulvovaginitis, Arthralgia, Hypothyroidism, Gait Disturbance, Bronchitis, Hypertension

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Alendronate Sodium
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2009-05-23
    End date: 2010-06-01

Alendronate Sodium
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2009-05-23
    End date: 2010-06-01

Fosamax
    Administration route: Oral
    Indication: Osteopenia
    Start date: 1999-04-05
    End date: 2010-03-01

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

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

Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1999-04-05
    End date: 2010-03-01

Fosamax Plus D
    Administration route: Oral
    Start date: 2007-01-01
    End date: 2009-05-22

Fosamax Plus D
    Administration route: Oral
    Indication: Osteoporosis



Possible Fosamax Plus D side effects in 67 year old female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-06-27

Patient: 67 year old female, weighing 109.0 kg (239.8 pounds)

Reactions: Asthma, Foot Deformity, Femur Fracture, Diabetes Mellitus, Wound Haematoma, Bundle Branch Block Right, Visual Acuity Reduced, Nocturia, Eczema, Seroma, Dermatitis, Iron Deficiency Anaemia, Dyspepsia, Adverse Event, Bone Density Decreased, Post Procedural Haemorrhage, Clostridial Infection, Stress Urinary Incontinence, Anaemia Postoperative, Nervousness, Back Pain, Cellulitis, Pain in Extremity, Wound Dehiscence, Device Difficult To Use, Anaemia, Coronary Artery Disease, Micturition Urgency, Synovial Disorder, Staphylococcal Infection, Swelling, Electrocardiogram Abnormal, Osteoporosis, Adverse Drug Reaction, Pain, Fall, Gastritis, Weight Increased, Hypoacusis, Dyspnoea Exertional, Rotator Cuff Syndrome, Depression, Lymphoedema, Exostosis, Cataract, Fracture Malunion, Breast Disorder, Squamous Cell Carcinoma, Skin Disorder, Muscular Weakness, Multiple Fractures, Device Failure, Osteoarthritis, Impaired Healing, Neoplasm Malignant, Hypothyroidism, Blood Disorder, Gait Disturbance, Tooth Disorder, Gravitational Oedema, Infection

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Administration route: Oral
    Indication: Osteopenia
    Start date: 1997-01-01
    End date: 2007-01-01

Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1997-01-01
    End date: 2007-01-01

Fosamax Plus D
    Administration route: Oral
    Indication: Osteoporosis

Fosamax Plus D
    Administration route: Oral
    Indication: Osteopenia

Other drugs received by patient: Calcium (Unspecified)



Possible Fosamax Plus D side effects in 63 year old female

Reported by a physician from United States on 2012-06-25

Patient: 63 year old female, weighing 59.0 kg (129.8 pounds)

Reactions: Foot Deformity, Bunion, Femur Fracture, Hyperkeratosis, Hypertrophy, Adverse Drug Reaction, Neoplasm, Fall, Lumbar Spinal Stenosis, Nephrolithiasis, Spinal Compression Fracture, Peroneal Nerve Palsy, Oedema Peripheral, Intervertebral Disc Degeneration, Gastrooesophageal Reflux Disease, Intervertebral Disc Protrusion, Back Pain, Pain in Extremity, Nausea, Haematuria, Drug Hypersensitivity, Urinary Tract Infection, Muscular Weakness, Onychomycosis, Cystitis, Radius Fracture, Paraesthesia, Intervertebral Disc Space Narrowing, Arthralgia, Visual Impairment, Essential Hypertension, Scar

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Alendronate Sodium
    Indication: Osteoporosis
    Start date: 2008-07-01
    End date: 2010-08-01

Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2001-09-01
    End date: 2010-09-01

Fosamax Plus D
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2001-09-01
    End date: 2010-09-01

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



Possible Fosamax Plus D side effects in 67 year old female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-06-22

Patient: 67 year old female, weighing 109.0 kg (239.8 pounds)

Reactions: Asthma, Foot Deformity, Femur Fracture, Diabetes Mellitus, Wound Haematoma, Visual Acuity Reduced, Bundle Branch Block Right, Nocturia, Eczema, Seroma, Iron Deficiency Anaemia, Dyspepsia, Dermatitis, Adverse Event, Bone Density Decreased, Stress Urinary Incontinence, Post Procedural Haemorrhage, Clostridial Infection, Nervousness, Anaemia Postoperative, Back Pain, Cellulitis, Pain in Extremity, Wound Dehiscence, Anaemia, Device Difficult To Use, Coronary Artery Disease, Synovial Disorder, Micturition Urgency, HIP Fracture, Staphylococcal Infection, Swelling, Electrocardiogram Abnormal, Osteoporosis, Pain, Adverse Drug Reaction, Fall, Gastritis, Weight Increased, Hypoacusis, Dyspnoea Exertional, Rotator Cuff Syndrome, Depression, Lymphoedema, Exostosis, Fracture Malunion, Cataract, Squamous Cell Carcinoma, Breast Disorder, Skin Disorder, Muscular Weakness, Multiple Fractures, Osteoarthritis, Device Failure, Neoplasm Malignant, Impaired Healing, Hypothyroidism, Blood Disorder, Gait Disturbance, Tooth Disorder, Gravitational Oedema, Infection

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Administration route: Oral
    Indication: Osteopenia
    Start date: 1997-01-01
    End date: 2007-01-01

Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1997-01-01
    End date: 2007-01-01

Fosamax Plus D
    Administration route: Oral
    Indication: Osteoporosis

Fosamax Plus D
    Administration route: Oral
    Indication: Osteopenia

Other drugs received by patient: Calcium (Unspecified)



Possible Fosamax Plus D side effects in 61 year old female

Reported by a physician from United States on 2012-06-20

Patient: 61 year old female

Reactions: Femur Fracture, Blood Creatine Phosphokinase Increased, Goitre, Sciatica, Joint Stiffness, Arthropathy, Fracture Displacement, Stress Urinary Incontinence, Open Wound, LOW Turnover Osteopathy, Muscle Spasms, Back Pain, Intervertebral Disc Protrusion, Pain in Extremity, Fracture Delayed Union, Pubis Fracture, Laceration, Blood Creatine Phosphokinase MB Increased, HIP Fracture, Emotional Distress, Limb Injury, Benign Neoplasm of Thyroid Gland, Pseudarthrosis, Dyslipidaemia, Fall, Fracture Nonunion, Cystocele, Hypokalaemia, Fatigue, Intervertebral Disc Degeneration, Depression, Gastrooesophageal Reflux Disease, Blood Glucose Increased, Abdominal Pain Lower, Vomiting, Nausea, Urinary Tract Infection, Muscular Weakness, Onychomycosis, Hyperlipidaemia, Rectocele, Osteoarthritis, Anxiety, Arthralgia, Diarrhoea, Gait Disturbance, Hypertension

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Fosamax
    Administration route: Oral
    Indication: Osteopenia
    Start date: 1998-01-01
    End date: 2005-04-01

Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1998-01-01
    End date: 2005-04-01

Fosamax
    Administration route: Oral
    Start date: 2008-02-06
    End date: 2009-10-10

Fosamax
    Administration route: Oral
    Start date: 2008-02-06
    End date: 2009-10-10

Fosamax Plus D
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2005-05-01
    End date: 2009-02-25

Fosamax Plus D
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2005-05-01
    End date: 2009-02-25



Possible Fosamax Plus D side effects in 51 year old female

Reported by a physician from United States on 2012-06-15

Patient: 51 year old female, weighing 55.0 kg (121.0 pounds)

Reactions: Tinnitus, Diabetes Mellitus, Dermatitis, Upper Respiratory Tract Infection, Multiple Injuries, Vertebral Foraminal Stenosis, LOW Turnover Osteopathy, Hypotension, Coronary Artery Disease, Lumbar Radiculopathy, Cardiomyopathy, Hepatic Steatosis, Tonsillar Disorder, Emotional Distress, Activities of Daily Living Impaired, Compression Fracture, Gastrointestinal Disorder, Osteoporosis, Wheezing, Hypercholesterolaemia, Foot Fracture, Liver Function Test Abnormal, Depression, Bone Disorder, Myocardial Infarction, Haemorrhoids, Muscular Weakness, Cardiogenic Shock, Haematochezia, Atrophic Vulvovaginitis, Hypophosphataemia, Arthralgia, Hypothyroidism, Gait Disturbance, Bone Fragmentation, Asthma, Femur Fracture, Lipids Increased, Cardiovascular Deconditioning, Ingrowing Nail, Stress Urinary Incontinence, Haematoma, Cough, Intervertebral Disc Protrusion, Pneumonia, Anaemia, Haemorrhagic Anaemia, Myopathy, Osteosclerosis, Vitamin D Decreased, Dermal Cyst, Stress Fracture, Nervous System Disorder, Spinal Column Stenosis, Rectal Polyp, Conjunctivitis, Fear, Bone Pain, Pain, Constipation, Atrioventricular Block Second Degree, Laryngitis, Weight Increased, Fatigue, Neuropathy Peripheral, Intervertebral Disc Degeneration, Gastrooesophageal Reflux Disease, Migraine, Urinary Tract Infection, Cystitis, Anxiety, Bronchitis, Hypertension

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Alendronate Sodium
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2009-05-23
    End date: 2010-06-01

Alendronate Sodium
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2009-05-23
    End date: 2010-06-01

Fosamax
    Administration route: Oral
    Indication: Osteopenia
    Start date: 1999-04-05
    End date: 2010-03-01

Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1999-04-05
    End date: 2010-03-01

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

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

Fosamax Plus D
    Administration route: Oral
    Start date: 2007-01-01
    End date: 2009-05-22

Fosamax Plus D
    Administration route: Oral
    Indication: Osteoporosis



Possible Fosamax Plus D side effects in 67 year old female

Reported by a physician from United States on 2012-06-14

Patient: 67 year old female, weighing 67.0 kg (147.4 pounds)

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

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2004-01-01
    End date: 2005-12-19

Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2004-01-01
    End date: 2005-12-19

Fosamax Plus D
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2006-02-18
    End date: 2009-12-17

Fosamax Plus D
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2006-02-18
    End date: 2009-12-17

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



Possible Fosamax Plus D side effects in 50 year old female

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

Patient: 50 year old female

Reactions: Femur Fracture, Fear, Muscular Weakness, Synovial Disorder, Fall, Anxiety, Poor Quality Sleep, Compression Fracture, Depression, Gait Disturbance, Hypertension, LOW Turnover Osteopathy, Infection

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2001-01-01
    End date: 2009-01-01

Fosamax
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2001-01-01
    End date: 2009-01-01

Fosamax Plus D
    Administration route: Oral
    Indication: Osteopenia
    Start date: 2006-07-05
    End date: 2009-01-26

Other drugs received by patient: Ascorbic Acid; Calcium (Unspecified); Vitamins (Unspecified); Corticosteroids (Unspecified)



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