Index of reports
> Cases with Femur Fracture (16)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Evista (Raloxifene) where reactions include femur fracture. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Evista side effects in
Reported by a consumer/non-health professional from United States on 2012-07-10
Patient:
Reactions: Femur Fracture, Breast Cancer in Situ, Chronic Obstructive Pulmonary Disease, Fall, Breast Cyst, Breast Hyperplasia, Fibula Fracture, Injury, Hypercalciuria, LOW Turnover Osteopathy, Mitral Valve Prolapse, Lung Neoplasm, Breast Mass, Granuloma, Ankle Fracture, Rhinitis Allergic, Bone Neoplasm Malignant, Lung Disorder, Procedural Vomiting, Procedural Nausea, Sleep Apnoea Syndrome, Face Injury
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Evista
Indication: Bone Disorder
Start date: 2008-01-01
Fosamax
Dosage: 70 mg, qw
Administration route: Oral
Start date: 2002-01-31
End date: 2010-01-01
Fosamax
Administration route: Oral
Indication: Osteopenia
Start date: 2000-10-01
End date: 2009-09-01
Fosamax
Dosage: 10 mg, unk
Administration route: Oral
Indication: Osteoporosis
Start date: 2000-10-01
End date: 2001-12-17
Other drugs received by patient: Calcium (Unspecified); Vitamin D (Unspecified); MK-9278
Possible Evista side effects in female
Reported by a consumer/non-health professional from United States on 2012-06-25
Patient: female, weighing 55.8 kg (122.7 pounds)
Reactions: Femur Fracture, Contusion, Blood Calcium Increased, Blood Triglycerides Increased, Intentional Drug Misuse, Fall, Abdominal Discomfort, Fatigue, Malaise, Dizziness, Blood Cholesterol Increased, Vomiting, Retching, Nausea, Urinary Tract Infection, Cholelithiasis, HIP Fracture, Heart Rate Increased
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Evista
Dosage: unk, unknown
Forteo
Dosage: 20 ug, qd
Indication: Osteoporosis
Start date: 2011-04-01
End date: 2011-04-05
Forteo
Dosage: 20 ug, qd
Forteo
Dosage: 20 ug, qd
Forteo
Dosage: 20 ug, qd
Start date: 2011-04-11
Forteo
Dosage: 20 ug, qd
Forteo
Dosage: 20 ug, qd
Other drugs received by patient: Pseudoephedrine HCL; Calcium W / Vitamin D NOS; Pravachol; Cortisone Acetate; Proair HFA; Excedrin (Migraine); Tylenol (Caplet); Spiriva; Claritin
Possible Evista side effects in 92 year old female
Reported by a physician from United States on 2012-05-11
Patient: 92 year old female
Reactions: Vaginal Prolapse, Vitamin D Deficiency, Joint Instability, Femur Fracture, Flatulence, Chronic Obstructive Pulmonary Disease, Iron Deficiency Anaemia, Carotid Artery Occlusion, Ingrowing Nail, Sinus Congestion, LOW Turnover Osteopathy, White Blood Cell Count Increased, Intervertebral Disc Protrusion, Dysphagia, Pneumonia, Anaemia, Drug Intolerance, Sinus Operation, Inguinal Hernia, Glaucoma, Pain, Myelodysplastic Syndrome, Cystocele, Overdose, Road Traffic Accident, Fibrocystic Breast Disease, Gastrooesophageal Reflux Disease, Blood Iron Increased, Tooth Fracture, Blood Urea Increased, Urinary Tract Infection, Nephrogenic Anaemia, Blood Potassium Increased, Carotid Artery Stenosis, Syncope, Hypothyroidism, Hypertension
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Actonel
Administration route: Oral
Indication: Osteoporosis
Start date: 2005-08-13
End date: 2005-11-01
Actonel
Administration route: Oral
Start date: 2006-04-12
End date: 2006-04-20
Actonel
Administration route: Oral
Start date: 2004-09-28
End date: 2004-11-01
Alendronate Sodium
Administration route: Oral
Start date: 2008-08-02
End date: 2009-03-13
Alendronate Sodium
Administration route: Oral
Indication: Osteoporosis
Start date: 2008-06-07
End date: 2008-08-01
Evista
Administration route: Oral
Indication: Osteoporosis
Start date: 2005-10-27
Fosamax
Administration route: Oral
Indication: Osteoporosis
Start date: 2001-03-13
End date: 2004-09-28
Fosamax
Administration route: Oral
Start date: 1999-01-01
End date: 2001-03-13
Fosamax
Administration route: Oral
Start date: 2001-03-08
Fosamax
Administration route: Oral
Start date: 2005-07-13
End date: 2010-01-11
Possible Evista side effects in female
Reported by a consumer/non-health professional from United States on 2012-05-02
Patient: female
Reactions: Femur Fracture, Drug Ineffective, Pain in Extremity, Fall, HIP Fracture, Ecchymosis, Oedema Peripheral, Transfusion, Mobility Decreased
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Evista
Other drugs received by patient: Prolia; Magnesium; Synthroid; Antihypertensives; Vitamin TAB; Calcium; Analgesics; Fish OIL
Possible Evista side effects in female
Reported by a consumer/non-health professional from United States on 2012-04-17
Patient: female
Reactions: Body Height Decreased, Femur Fracture, Wrist Fracture, Lower Limb Fracture
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Evista
Other drugs received by patient: Lovastatin; Meloxicam; Calcium Carbonate; Lecithin; Gabapentin; Vitamin D; Antacids, Other Combinations
Possible Evista side effects in 65 year old female
Reported by a physician from United States on 2012-04-11
Patient: 65 year old female
Reactions: Weight Decreased, Femur Fracture, Urinary Incontinence, Diverticulitis, Sciatica, Clostridium Difficile Colitis, Pyrexia, Nocturia, Fracture, Iron Deficiency Anaemia, Musculoskeletal Disorder, Tracheitis, Anaemia Postoperative, Pneumonia, Cerumen Impaction, Vulvovaginal Candidiasis, Type V Hyperlipidaemia, Bunion, Bone Pain, Adverse Drug Reaction, Fall, Constipation, Fatigue, Interstitial Lung Disease, Aortic Arteriosclerosis, Intervertebral Disc Degeneration, Injury, Sinusitis, Pharyngitis, Decreased Appetite, Vomiting, Mixed Incontinence, Diarrhoea, Pseudomembranous Colitis, Lung Infiltration, Leukocytosis, Hypertension
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Alendronate Sodium
Administration route: Oral
Start date: 2008-03-23
End date: 2010-01-08
Evista
Administration route: Oral
Indication: Osteoporosis
Fosamax
Administration route: Oral
End date: 2010-01-08
Fosamax
Administration route: Oral
Fosamax
Administration route: Oral
Indication: Osteopenia
Start date: 1999-01-01
End date: 2009-01-01
Fosamax
Administration route: Oral
Indication: Osteoporosis
Start date: 1999-01-01
End date: 2009-01-01
Fosamax
Administration route: Oral
End date: 2010-01-08
Fosamax
Administration route: Oral
Fosamax Plus D
Administration route: Oral
Start date: 2006-10-18
End date: 2007-09-17
Other drugs received by patient: Omega-3 Marine Triglycerides; Vitamin E; Selective Estrogen Receptor Modulator (Unspecified); Viactiv Soft Calcium Chews; Citracal; Vitamins (Unspecified); Lovaza; Vitamin D (Unspecified)
Possible Evista side effects in female
Reported by a consumer/non-health professional from United States on 2012-03-29
Patient: female
Reactions: HIP Fracture, Femur Fracture, Pain in Extremity, Oedema Peripheral, Ecchymosis, Transfusion, Fall
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Evista
Other drugs received by patient: Calcium Carbonate; Antihypertensives; Synthroid; Vitamin TAB; Fish OIL; Magnesium; Analgesics
Possible Evista side effects in female
Reported by a consumer/non-health professional from United States on 2012-03-23
Patient: female, weighing 55.8 kg (122.7 pounds)
Reactions: Contusion, Femur Fracture, Blood Triglycerides Increased, Blood Calcium Increased, Intentional Drug Misuse, Fall, Abdominal Discomfort, Fatigue, Malaise, Dizziness, Blood Cholesterol Increased, Vomiting, Nausea, Retching, Urinary Tract Infection, HIP Fracture, Heart Rate Increased
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Evista
Dosage: unk, unknown
Forteo
Dosage: 20 ug, qd
Start date: 2011-04-11
Forteo
Dosage: 20 ug, qd
Forteo
Dosage: 20 ug, qd
Forteo
Dosage: 20 ug, qd
Indication: Osteoporosis
Start date: 2011-04-01
End date: 2011-04-05
Forteo
Dosage: 20 ug, qd
Forteo
Dosage: 20 ug, qd
Other drugs received by patient: Cortisone Acetate; Calcium W / Vitamin D NOS; Excedrin (Migraine); Tylenol (Caplet); Pseudoephedrine HCL; Claritin; Proair HFA; Pravachol; Spiriva
Possible Evista side effects in female
Reported by a consumer/non-health professional from United States on 2012-03-21
Patient: female
Reactions: Body Height Decreased, Femur Fracture, HIP Arthroplasty, Wrist Fracture, Knee Arthroplasty, Lower Limb Fracture
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Evista
Other drugs received by patient: Lovastatin; Calcium Carbonate; Vitamin D; Lecithin; Antacids, Other Combinations; Gabapentin; Meloxicam
Possible Evista side effects in 65 year old female
Reported by a physician from United States on 2012-03-12
Patient: 65 year old female
Reactions: Weight Decreased, Femur Fracture, Sciatica, Diverticulitis, Urinary Incontinence, Clostridium Difficile Colitis, Nocturia, Pyrexia, Fracture, Iron Deficiency Anaemia, Musculoskeletal Disorder, Tracheitis, Anaemia Postoperative, Pneumonia, Cerumen Impaction, Vulvovaginal Candidiasis, Type V Hyperlipidaemia, Bunion, Bone Pain, Adverse Drug Reaction, Fall, Constipation, Fatigue, Interstitial Lung Disease, Aortic Arteriosclerosis, Intervertebral Disc Degeneration, Sinusitis, Pharyngitis, Decreased Appetite, Vomiting, Mixed Incontinence, Diarrhoea, Pseudomembranous Colitis, Leukocytosis, Hypertension, Lung Infiltration
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Alendronate Sodium
Administration route: Oral
Evista
Administration route: Oral
Indication: Osteoporosis
Fosamax
Administration route: Oral
Indication: Osteopenia
Start date: 1999-01-01
End date: 2009-01-01
Fosamax
Administration route: Oral
Fosamax
Administration route: Oral
End date: 2010-01-08
Fosamax
Administration route: Oral
End date: 2010-01-08
Fosamax
Administration route: Oral
Fosamax
Administration route: Oral
Indication: Osteoporosis
Start date: 1999-01-01
End date: 2009-01-01
Fosamax Plus D
Administration route: Oral
Other drugs received by patient: Selective Estrogen Receptor Modulator (Unspecified); Lovaza; Viactiv Soft Calcium Chews; Vitamin D (Unspecified); Omega-3 Marine Triglycerides; Vitamin E; Vitamins (Unspecified); Citracal
Possible Evista side effects in 65 year old female
Reported by a physician from United States on 2012-01-25
Patient: 65 year old female
Reactions: Weight Decreased, Femur Fracture, Diverticulitis, Adverse Drug Reaction, Bone Pain, Sciatica, Nocturia, Pyrexia, Fall, Fatigue, Interstitial Lung Disease, Iron Deficiency Anaemia, Fracture, Aortic Arteriosclerosis, Intervertebral Disc Degeneration, Sinusitis, Tracheitis, Decreased Appetite, Pharyngitis, Vomiting, Pneumonia, Cerumen Impaction, Vulvovaginal Candidiasis, Mixed Incontinence, Diarrhoea, Type V Hyperlipidaemia, Pseudomembranous Colitis, Hypertension
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Alendronate Sodium
Administration route: Oral
Evista
Administration route: Oral
Indication: Osteoporosis
Fosamax
Administration route: Oral
Indication: Osteoporosis
Start date: 1999-01-01
End date: 2009-01-01
Fosamax
Administration route: Oral
End date: 2010-01-08
Fosamax
Administration route: Oral
Fosamax
Administration route: Oral
End date: 2010-01-08
Fosamax
Administration route: Oral
Fosamax
Administration route: Oral
Indication: Osteopenia
Start date: 1999-01-01
End date: 2009-01-01
Fosamax Plus D
Administration route: Oral
Other drugs received by patient: Selective Estrogen Receptor Modulator (Unspecified); Viactiv Soft Calcium Chews; Vitamin D (Unspecified); Citracal; Omega-3 Marine Triglycerides; Vitamins (Unspecified); Lovaza; Vitamin E
Possible Evista side effects in female
Reported by a health professional (non-physician/pharmacist) from United States on 2011-12-20
Patient: female
Reactions: Femur Fracture
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Actonel
Administration route: Oral
Indication: Osteoporosis
Start date: 2003-11-03
End date: 2006-04-20
Boniva
Administration route: Oral
Indication: Osteoporosis
Start date: 2006-04-20
Evista
Administration route: Oral
Indication: Osteopenia
Start date: 2003-11-03
End date: 2003-11-03
Premarin
Indication: Product Used FOR Unknown Indication
Other drugs received by patient: Lyrica; Potassium Chloride; Metoprolol Tartrate; Lanoxin; Coumadin; Lasix
Possible Evista side effects in 47 year old female
Reported by a physician from United States on 2011-11-28
Patient: 47 year old female, weighing 57.0 kg (125.4 pounds)
Reactions: Femur Fracture, Breast Cancer in Situ, Fall, Chronic Obstructive Pulmonary Disease, Breast Cyst, Breast Hyperplasia, Injury, Fibula Fracture, Hypercalciuria, LOW Turnover Osteopathy, Mitral Valve Prolapse, Lung Neoplasm, Breast Mass, Granuloma, Ankle Fracture, Lung Disorder, Rhinitis Allergic, Bone Neoplasm Malignant, Procedural Vomiting, Procedural Nausea, Sleep Apnoea Syndrome, Face Injury
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Evista
Indication: Bone Disorder
Start date: 2008-01-01
Fosamax
Administration route: Oral
Start date: 2002-01-31
End date: 2010-01-01
Fosamax
Administration route: Oral
Indication: Osteopenia
Start date: 2000-10-01
End date: 2001-12-01
Fosamax
Administration route: Oral
Indication: Osteoporosis
Start date: 2000-10-01
End date: 2001-12-01
Fosamax
Administration route: Oral
Start date: 2000-10-01
End date: 2009-09-01
Fosamax
Administration route: Oral
Start date: 2000-10-01
End date: 2009-09-01
Fosamax
Administration route: Oral
Start date: 2002-01-31
End date: 2010-01-01
Other drugs received by patient: Vitamin D (Unspecified); Vitamins (Unspecified); Calcium (Unspecified)
Possible Evista side effects in 65 year old female
Reported by a physician from United States on 2011-11-14
Patient: 65 year old female
Reactions: Weight Decreased, Femur Fracture, Bone Pain, Diverticulitis, Adverse Drug Reaction, Sciatica, Nocturia, Pyrexia, Fall, Fatigue, Iron Deficiency Anaemia, Fracture, Intervertebral Disc Degeneration, Sinusitis, Tracheitis, Pharyngitis, Decreased Appetite, Vomiting, Cerumen Impaction, Vulvovaginal Candidiasis, Mixed Incontinence, Diarrhoea, Type V Hyperlipidaemia, Pseudomembranous Colitis, Hypertension
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Alendronate Sodium
Administration route: Oral
Evista
Administration route: Oral
Indication: Osteoporosis
Fosamax
Administration route: Oral
End date: 2010-01-08
Fosamax
Administration route: Oral
Indication: Osteopenia
Start date: 1999-01-01
End date: 2009-01-01
Fosamax
Administration route: Oral
Indication: Osteoporosis
Start date: 1999-01-01
End date: 2009-01-01
Fosamax
Administration route: Oral
End date: 2010-01-08
Fosamax
Administration route: Oral
Fosamax
Administration route: Oral
Fosamax Plus D
Administration route: Oral
Other drugs received by patient: Lovaza; Vitamins (Unspecified); Citracal; Omega-3 Marine Triglycerides; Viactiv Soft Calcium Chews; Vitamin D (Unspecified); Vitamin E; Selective Estrogen Receptor Modulator (Unspecified)
Possible Evista side effects in female
Reported by a consumer/non-health professional from United States on 2011-10-17
Patient: female
Reactions: Contusion, Femur Fracture, Blood Calcium Increased, Blood Triglycerides Increased, Intentional Drug Misuse, Fall, Abdominal Discomfort, Malaise, Fatigue, Dizziness, Blood Cholesterol Increased, Vomiting, Nausea, Retching, Urinary Tract Infection, HIP Fracture, Heart Rate Increased, Swelling
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Evista
Dosage: unk, unknown
Forteo
Dosage: 20 ug, qd
Indication: Osteoporosis
Start date: 2011-04-04
End date: 2011-04-05
Forteo
Dosage: 20 ug, qd
Forteo
Dosage: 20 ug, qd
Forteo
Dosage: 20 ug, qd
Forteo
Dosage: 20 ug, qd
Start date: 2011-04-11
Other drugs received by patient: Cortisone Acetate
Possible Evista side effects in 92 year old female
Reported by a physician from United States on 2011-10-06
Patient: 92 year old female
Reactions: Vitamin D Deficiency, Vaginal Prolapse, Joint Instability, Femur Fracture, Flatulence, Chronic Obstructive Pulmonary Disease, Iron Deficiency Anaemia, Carotid Artery Occlusion, Ingrowing Nail, Sinus Congestion, LOW Turnover Osteopathy, Intervertebral Disc Protrusion, Dysphagia, Pneumonia, Drug Intolerance, Anaemia, Sinus Operation, Inguinal Hernia, Glaucoma, Pain, Myelodysplastic Syndrome, Cystocele, Fibrocystic Breast Disease, Road Traffic Accident, Overdose, Gastrooesophageal Reflux Disease, Blood Iron Increased, Tooth Fracture, Blood Urea Increased, Nephrogenic Anaemia, Blood Potassium Increased, Osteoarthritis, Carotid Artery Stenosis, Blood Pressure, Hypothyroidism
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Actonel
Administration route: Oral
Indication: Osteoporosis
Start date: 2005-08-13
End date: 2005-11-01
Actonel
Administration route: Oral
Start date: 2006-04-12
End date: 2006-04-20
Actonel
Administration route: Oral
Start date: 2004-09-28
End date: 2004-11-01
Alendronate Sodium
Administration route: Oral
Start date: 2008-08-02
End date: 2009-03-13
Alendronate Sodium
Administration route: Oral
Indication: Osteoporosis
Start date: 2008-06-07
End date: 2008-08-01
Evista
Administration route: Oral
Indication: Osteoporosis
Start date: 2005-10-27
Fosamax
Administration route: Oral
Start date: 2001-03-08
Fosamax
Administration route: Oral
Indication: Osteoporosis
Start date: 2001-03-13
End date: 2004-09-28
Fosamax
Administration route: Oral
Start date: 2005-07-13
End date: 2010-01-11
Fosamax
Administration route: Oral
Start date: 1999-01-01
End date: 2001-03-13
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