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Evista (Raloxifene) - Adverse Event Reports - Hospitalization

 



Index of reports > Cases resulting in hospitalization (129)

     Fall (18)HIP Fracture (12)Deep Vein Thrombosis (11)Pain (8)Dizziness (7)Femur Fracture (6)Drug Ineffective (6)Atrial Fibrillation (6)Cerebral Infarction (6)Myocardial Infarction (6)

Below is the selection of adverse event reports related to Evista (Raloxifene) that includes cases resulting in hospitalization.

 Reports 1 - 25 of 129   Next >>

Adverse event in female receiving Evista (Raloxifene)

Reported by a consumer/non-health professional from United States on 2007-10-24

Patient: female

Adverse reactions / side effects: Dyspnoea, Spinal Fracture, Hypotension, Pain, Blood Blister, Muscular Weakness, Chronic Obstructive Pulmonary Disease, Fall, Skin Discolouration, Hypertension

Adverse event resulted in: hospitalization

Suspect drug(s):
Evista
    Dosage: 60 mg, daily (1/d)
    Start date: 2004-01-01

Forteo
    Indication: Osteoporosis
    Start date: 2007-03-01

Forteo
    Dosage: unk, unk
    Start date: 2007-01-01

Forteo
    Dosage: unk, unk
    Start date: 2007-09-18

Other drugs received by patient: Zantac; Lipitor; Vitamins; Flexeril; Xanax; Lora TAB



Adverse event in 80 year old female receiving Evista (Raloxifene)

Reported by a physician from United States on 2007-10-23

Patient: 80 year old female

Adverse reactions / side effects: Surgery, Lymphoma, Deep Vein Thrombosis

Adverse event resulted in: hospitalization

Suspect drug(s):
Evista (Raloxifene)

Other drugs received by patient: Antihypertensives



Adverse event in female receiving Evista (Raloxifene)

Reported by a consumer/non-health professional from United States on 2007-10-18

Patient: female

Adverse reactions / side effects: Thrombosis, Blood Pressure Increased, Limb Discomfort, Drug Ineffective, Pain in Extremity, Bone Density Decreased, Cerebrovascular Accident

Adverse event resulted in: hospitalization

Suspect drug(s):
Evista (Raloxifene)

Other drugs received by patient: Vitamins NOS; Prilosec; Thyroid TAB



Adverse event in 50 year old female receiving Evista (Raloxifene)

Reported by a physician from United States on 2007-10-17

Patient: 50 year old female

Adverse reactions / side effects: Gastrointestinal Haemorrhage

Adverse event resulted in: hospitalization

Suspect drug(s):
Evista (Raloxifene)



Adverse event in 80 year old female receiving Evista (Raloxifene)

Reported by a physician from United States on 2007-10-16

Patient: 80 year old female

Adverse reactions / side effects: Surgery, Lymphoma, Deep Vein Thrombosis

Adverse event resulted in: hospitalization

Suspect drug(s):
Evista (Raloxifene)

Other drugs received by patient: Antihypertensives



Adverse event in 50 year old female receiving Evista (Raloxifene)

Reported by a physician from United States on 2007-10-16

Patient: 50 year old female

Adverse reactions / side effects: Gastrointestinal Haemorrhage

Adverse event resulted in: hospitalization

Suspect drug(s):
Evista (Raloxifene)



Adverse event in female receiving Evista (Raloxifene)

Reported by a consumer/non-health professional from United States on 2007-10-09

Patient: female

Adverse reactions / side effects: Osteoporosis, Ovarian Cyst

Adverse event resulted in: hospitalization

Suspect drug(s):
Evista (Raloxifene)

Other drugs received by patient: Calcium Carbonate



Adverse event in 72 year old female receiving Evista (Raloxifene)

Reported by a consumer/non-health professional from United States on 2007-10-09

Patient: 72 year old female

Adverse reactions / side effects: HIP Fracture, Osteonecrosis, Cyst, Fall

Adverse event resulted in: hospitalization

Suspect drug(s):
Evista (Raloxifene)

Other drugs received by patient: Calcium Carbonate; Vitamin D; Pamidronate Disodium



Adverse event in 76 year old female receiving Evista (Raloxifene)

Reported by a physician from Germany on 2007-10-09

Patient: 76 year old female, weighing 60.0 kg (132.0 pounds)

Adverse reactions / side effects: Atrial Fibrillation, Sinobronchitis

Adverse event resulted in: hospitalization

Suspect drug(s):
Evista (Raloxifene)

Other drugs received by patient: Losartan Potassium; Norvasc; Calcium



Adverse event in female receiving Evista (Raloxifene)

Reported by a consumer/non-health professional from United States on 2007-10-09

Patient: female

Adverse reactions / side effects: HIP Fracture, Pain

Adverse event resulted in: hospitalization

Suspect drug(s):
Evista (Raloxifene)

Other drugs received by patient: Calcium Carbonate; Ergocalciferol / Calcium Phosp / Calcium SOD Lact



Adverse event in 62 year old female receiving Evista (Raloxifene)

Reported by a physician from France on 2007-10-09

Patient: 62 year old female

Adverse reactions / side effects: Breast Neoplasm

Adverse event resulted in: hospitalization

Suspect drug(s):
Evista (Raloxifene)



Adverse event in 50 year old female receiving Evista (Raloxifene)

Reported by a consumer/non-health professional from United States on 2007-10-05

Patient: 50 year old female, weighing 72.6 kg (159.7 pounds)

Adverse reactions / side effects: Prothrombin Time Abnormal, Haemorrhage, Pain, Feeling Abnormal, International Normalised Ratio Fluctuation, Deep Vein Thrombosis

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Evista (Raloxifene)



Adverse event in 81 year old female receiving Evista (Raloxifene)

Reported by a physician from Japan on 2007-10-03

Patient: 81 year old female, weighing 58.0 kg (127.6 pounds)

Adverse reactions / side effects: Pulmonary Infarction, Deep Vein Thrombosis

Adverse event resulted in: hospitalization

Suspect drug(s):
Evista (Raloxifene)

Other drugs received by patient: Lipitor; Kamag G; Alfarol; Famotidine



Adverse event in female receiving Evista (Raloxifene)

Reported by a physician from United States on 2007-10-03

Patient: female

Adverse reactions / side effects: Thrombosis, Lung Disorder, Venous Thrombosis Limb

Adverse event resulted in: hospitalization

Suspect drug(s):
Evista (Raloxifene)



Adverse event in 74 year old female receiving Evista (Raloxifene)

Reported by a consumer/non-health professional from United States on 2007-10-03

Patient: 74 year old female

Adverse reactions / side effects: Back Pain, Drug Ineffective, Bone Density Decreased

Adverse event resulted in: hospitalization

Suspect drug(s):
Evista (Raloxifene)



Adverse event in 80 year old female receiving Evista (Raloxifene)

Reported by a consumer/non-health professional from United States on 2007-10-02

Patient: 80 year old female

Adverse reactions / side effects: Cervical Vertebral Fracture, Road Traffic Accident, Ankle Fracture

Adverse event resulted in: hospitalization

Suspect drug(s):
Evista

Forteo
    Start date: 2007-02-07

Other drugs received by patient: Calcium with Vitamin D; Multi-Vitamin; Celebrex; Altace; Lexapro; Glucosamine W / Chondroitin



Adverse event in 72 year old female receiving Evista (Raloxifene)

Reported by a physician from United States on 2007-10-02

Patient: 72 year old female

Adverse reactions / side effects: HIP Fracture, Post Procedural Complication, Tibia Fracture, Blood Cholesterol Increased, Blood Triglycerides Increased

Adverse event resulted in: hospitalization

Suspect drug(s):
Evista (Raloxifene)

Other drugs received by patient: Tricor; Zocor; Calcium; Vitamin D; Prevacid



Adverse event in 69 year old female receiving Evista (Raloxifene)

Reported by a physician from Japan on 2007-07-26

Patient: 69 year old female, weighing 49.0 kg (107.8 pounds)

Adverse reactions / side effects: Cerebellar Haemorrhage

Adverse event resulted in: hospitalization

Suspect drug(s):
Evista
    Dosage: 60 mg, daily (1/d)
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2007-04-05
    End date: 2007-04-23

Evista
    Dosage: 60 mg, daily (1/d)
    Administration route: Oral
    Start date: 2007-03-30
    End date: 2007-04-03

Other drugs received by patient: Thyradin S; Thyradin S; Famotidine



Adverse event in 76 year old female receiving Evista (Raloxifene)

Reported by a physician from Japan on 2007-07-25

Patient: 76 year old female

Adverse reactions / side effects: Cerebral Infarction

Adverse event resulted in: hospitalization

Suspect drug(s):
Evista (Raloxifene)

Other drugs received by patient: Rocaltrol; Peon; Kelnac; Seltouch



Adverse event in 80 year old female receiving Evista (Raloxifene)

Reported by a physician from United States on 2007-07-25

Patient: 80 year old female, weighing 54.9 kg (120.7 pounds)

Adverse reactions / side effects: Spinal Fracture, Sepsis, Osteomyelitis, Abscess, Fall

Adverse event resulted in: hospitalization

Suspect drug(s):
Evista
    Dosage: 60 mg, daily (1/d)
    Indication: Osteoporosis
    Start date: 2003-08-01
    End date: 2003-10-01

Forteo
    Dosage: 20 ug, daily (1/d)
    Indication: Osteoporosis
    Start date: 2003-10-15

Other drugs received by patient: Aspirin; Calcium Carbonate; Celebrex; Folic Acid; Diltiazem CD; Hydroxychloroquine Sulfate; Vitamin D; Prednisone; Methotrexate; Multi-Vitamin; Omeprazole; Isordil; Risedronate Sodium



Adverse event in 74 year old female receiving Evista (Raloxifene)

Reported by a physician from France on 2007-07-23

Patient: 74 year old female

Adverse reactions / side effects: Pulmonary Embolism, Scotoma, Deep Vein Thrombosis, Retinal Artery Thrombosis

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Evista (Raloxifene)

Other drugs received by patient: Secalip; Odrik



Adverse event in 70 year old female receiving Evista (Raloxifene)

Reported by a physician from Japan on 2007-07-20

Patient: 70 year old female, weighing 50.0 kg (110.0 pounds)

Adverse reactions / side effects: Dizziness

Adverse event resulted in: hospitalization

Suspect drug(s):
Evista
    Dosage: 60 mg, daily (1/d)
    Administration route: Oral
    Indication: Osteoporosis Postmenopausal
    Start date: 2007-04-29

Evista
    Dosage: 60 mg, daily (1/d)
    Administration route: Oral
    Start date: 2007-04-05



Adverse event in 65 year old female receiving Evista (Raloxifene)

Reported by a physician from France on 2007-07-20

Patient: 65 year old female

Adverse reactions / side effects: Breast Cancer

Adverse event resulted in: hospitalization

Suspect drug(s):
Evista (Raloxifene)



Adverse event in 76 year old female receiving Evista (Raloxifene)

Reported by a physician from Canada on 2007-07-18

Patient: 76 year old female

Adverse reactions / side effects: Compression Fracture

Adverse event resulted in: hospitalization

Suspect drug(s):
Evista

Forteo
    Dosage: 20 ug, daily (1/d)
    Indication: Osteoporosis
    Start date: 2007-06-28

Other drugs received by patient: Lipitor; Altace; Coumadin; Furosemide; Sotalol Hydrochloride



Adverse event in 47 year old female receiving Evista (Raloxifene)

Reported by a physician from United States on 2007-07-11

Patient: 47 year old female, weighing 70.0 kg (154.0 pounds)

Adverse reactions / side effects: Abdominal Pain, Lactose Intolerance, Weight Decreased, Sinus Polyp, Conjunctivitis, Flatulence, Umbilical Hernia Repair, Throat Tightness, Abdominal Discomfort, Myalgia, Dyspepsia, Oesophagitis, Dizziness, Depression, Gastrooesophageal Reflux Disease, Sinusitis, RIB Fracture, Back Pain, Type 2 Diabetes Mellitus, Nausea, Osteomalacia, Foreign Body Trauma, Osteonecrosis, Arthralgia, Diabetic Neuropathy, Diarrhoea, Insomnia, Asthenia, Oral Fungal Infection, Influenza

Adverse event resulted in: hospitalization

Suspect drug(s):
Evista
    Indication: Osteoporosis
    Start date: 2005-03-10

Fosamax
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 1995-11-21
    End date: 1997-10-10

Fosamax
    Administration route: Oral
    Start date: 2003-09-30
    End date: 2005-01-01

Fosamax
    Administration route: Oral
    Start date: 1998-01-01
    End date: 2003-01-01

Fosamax
    Administration route: Oral
    Indication: Osteopenia
    Start date: 1995-11-21
    End date: 1997-10-10

Fosamax
    Administration route: Oral
    Start date: 2003-09-30
    End date: 2005-01-01

Fosamax
    Administration route: Oral
    Start date: 1998-01-01
    End date: 2003-01-01

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



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