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Zometa (Zoledronic Acid) - Life Threatening Events - Suspected Cause - Side Effect Reports

 
 



Index of reports > Life Threatening Events (50)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Zometa (Zoledronic Acid) life threatening events. The selected reports were submitted to the FDA during the sample period of about a year.

 Reports 1 - 30 of 50   Next >>

Possible Zometa side effects in female

Reported by a physician from France on 2012-08-27

Patient: female

Reactions: Confusional State, Acute Pulmonary Oedema, Agitation, Renal Failure Acute

Adverse event resulted in: death, life threatening event

Drug(s) suspected as cause:
Acetaminophen
    Administration route: Oral
    End date: 2012-07-26

Aspirin
    Administration route: Oral

Atorvastatin
    Administration route: Oral

Bisoprolol Fumarate
    Dosage: 2.5 mg in the morning and 1.25 mg in the evening
    Administration route: Oral
    End date: 2012-07-27

Cymbalta
    Administration route: Oral
    End date: 2012-07-26

Duragesic-100
    End date: 2012-07-26

Lercanidipine
    Administration route: Oral
    End date: 2012-07-26

Lyrica
    Administration route: Oral
    End date: 2012-07-26

Nexium
    Administration route: Oral

Nitroglycerin
    End date: 2012-07-26

Plavix
    Administration route: Oral

Ramipril
    Administration route: Oral
    End date: 2012-07-26

Zometa
    Start date: 2012-07-19
    End date: 2012-07-19



Possible Zometa side effects in 61 year old female

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

Patient: 61 year old female

Reactions: Agitation, Confusional State, Acute Pulmonary Oedema, Metastatic Pain, Hypercalcaemia, Renal Failure Acute

Adverse event resulted in: death, life threatening event, hospitalization

Drug(s) suspected as cause:
Acetaminophen
    Dosage: 1 g, 1x/day
    Administration route: Oral
    End date: 2012-07-26

Aspirin
    Dosage: 75 mg, 1x/day
    Administration route: Oral

Atorvastatin
    Dosage: 10 mg, 1x/day
    Administration route: Oral

Bisoprolol Fumarate
    Dosage: 3.75 mg, 1x/day
    Administration route: Oral
    End date: 2012-07-27

Cymbalta
    Dosage: 60 mg, 1x/day
    Administration route: Oral
    End date: 2012-07-26

Duragesic-100
    Dosage: 50 mg, 1x/day
    End date: 2012-07-26

Lercanidipine
    Dosage: 10 mg, 1x/day
    Administration route: Oral
    End date: 2012-07-26

Lyrica
    Dosage: 75 mg, 2x/day
    Administration route: Oral
    End date: 2012-07-26

Nexium
    Dosage: 20 mg, 1x/day
    Administration route: Oral

Nitroglycerin
    Dosage: 5 mg, 1x/day
    End date: 2012-07-26

Plavix
    Dosage: 75 mg, 1x/day
    Administration route: Oral

Ramipril
    Dosage: 10 mg, 1x/day
    Administration route: Oral
    End date: 2012-07-26

Zometa
    Dosage: 4 mg, single
    Indication: Hypercalcaemia
    Start date: 2012-07-19
    End date: 2012-07-19



Possible Zometa side effects in 61 year old female

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

Patient: 61 year old female

Reactions: Confusional State, Agitation, Renal Failure Acute

Adverse event resulted in: death, life threatening event

Drug(s) suspected as cause:
Acetaminophen
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    End date: 2012-07-26

Aspirin
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication

Atorvastatin
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication

Bisoprolol Fumarate
    Dosage: 2.5-0-1.25
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    End date: 2012-07-27

Cymbalta
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    End date: 2012-07-26

Duragesic-100
    Indication: Product Used FOR Unknown Indication
    End date: 2012-07-26

Lercanidipine
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    End date: 2012-07-26

Lyrica
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    End date: 2012-07-26

Nexium
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication

Nitroglycerin
    Indication: Product Used FOR Unknown Indication
    End date: 2012-07-27

Plavix
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication

Ramipril
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    End date: 2012-07-26

Zometa
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-07-19
    End date: 2012-07-19



Possible Zometa side effects in female

Reported by a physician from France on 2012-08-24

Patient: female

Reactions: Confusional State, Nephrolithiasis, Acute Pulmonary Oedema, Agitation, Dyspnoea, Hypercalcaemia, Renal Failure Acute

Adverse event resulted in: death, life threatening event

Drug(s) suspected as cause:
Acetaminophen
    Dosage: 1 mg, unk
    End date: 2012-07-26

Aspirin
    Dosage: 75 mg, unk

Atorvastatin
    Dosage: 10 mg, qd

Bisoprolol Fumarate
    Dosage: 3.75 mg, daily (2.5 mg in the morning and 1.25 mg in the evening)
    End date: 2012-07-27

Cymbalta
    Dosage: 60 mg, qd
    End date: 2012-07-26

Duragesic-100
    Dosage: 50 ug, daily
    End date: 2012-07-26

Lercanidipine
    Dosage: 10 mg, qd
    End date: 2012-07-26

Lyrica
    Dosage: 75 mg, bid
    End date: 2012-07-26

Nexium
    Dosage: 20 mg, qd
    End date: 2012-07-26

Nitroglycerin
    Dosage: 5 mg, daily
    End date: 2012-07-27

Plavix
    Dosage: 75 mg, qd
    End date: 2012-07-26

Ramipril
    Dosage: 10 mg, qd
    End date: 2012-07-26

Zometa
    Dosage: 4 mg, in 15 min
    Indication: Hypercalcaemia
    Start date: 2012-07-19



Possible Zometa side effects in female

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

Patient: female

Reactions: Agitation, Confusional State, Renal Failure Acute

Adverse event resulted in: death, life threatening event

Drug(s) suspected as cause:
Acetaminophen
    Administration route: Oral
    End date: 2012-07-26

Aspirin
    Administration route: Oral

Atorvastatin
    Administration route: Oral

Bisoprolol Fumarate
    Administration route: Oral
    End date: 2012-07-27

Cymbalta
    Administration route: Oral
    End date: 2012-07-26

Duragesic-100
    End date: 2012-07-26

Lercanidipine
    Administration route: Oral
    End date: 2012-07-26

Lyrica
    Administration route: Oral
    End date: 2012-07-26

Nexium
    Administration route: Oral

Nitroglycerin
    End date: 2012-07-27

Plavix
    Administration route: Oral

Ramipril
    Administration route: Oral
    End date: 2012-07-26

Zometa
    Start date: 2012-07-19
    End date: 2012-07-19



Possible Zometa side effects in female

Reported by a physician from France on 2012-08-24

Patient: female

Reactions: Agitation, Confusional State, Acute Pulmonary Oedema, Nephrolithiasis, Dyspnoea, Hypercalcaemia, Renal Failure Acute

Adverse event resulted in: death, life threatening event

Drug(s) suspected as cause:
Acetaminophen
    Dosage: 1 mg, unk
    End date: 2012-07-26

Aspirin
    Dosage: 75 mg, unk

Atorvastatin
    Dosage: 10 mg, qd

Bisoprolol Fumarate
    Dosage: 3.75 mg, daily (2.5 mg in the morning and 1.25 mg in the evening)
    End date: 2012-07-27

Cymbalta
    Dosage: 60 mg, qd
    End date: 2012-07-26

Duragesic-100
    Dosage: 50 ug, daily
    End date: 2012-07-26

Lercanidipine
    Dosage: 10 mg, qd
    End date: 2012-07-26

Lyrica
    Dosage: 75 mg, bid
    End date: 2012-07-26

Nexium
    Dosage: 20 mg, qd
    End date: 2012-07-26

Nitroglycerin
    Dosage: 5 mg, daily
    End date: 2012-07-27

Plavix
    Dosage: 75 mg, qd
    End date: 2012-07-26

Ramipril
    Dosage: 10 mg, qd
    End date: 2012-07-26

Zometa
    Dosage: 4 mg, in 15 min
    Indication: Hypercalcaemia
    Start date: 2012-07-19



Possible Zometa side effects in female

Reported by a physician from France on 2012-08-24

Patient: female

Reactions: Nephrolithiasis, Agitation, Confusional State, Acute Pulmonary Oedema, Dyspnoea, Hypercalcaemia, Renal Failure Acute

Adverse event resulted in: death, life threatening event

Drug(s) suspected as cause:
Acetaminophen
    Dosage: 1 mg, unk
    End date: 2012-07-26

Aspirin
    Dosage: 75 mg, unk

Atorvastatin
    Dosage: 10 mg, qd

Bisoprolol Fumarate
    Dosage: 3.75 mg, daily (2.5 mg in the morning and 1.25 mg in the evening)
    End date: 2012-07-27

Cymbalta
    Dosage: 60 mg, qd
    End date: 2012-07-26

Duragesic-100
    Dosage: 50 ug, daily
    End date: 2012-07-26

Lercanidipine
    Dosage: 10 mg, qd
    End date: 2012-07-26

Lyrica
    Dosage: 75 mg, bid
    End date: 2012-07-26

Nexium
    Dosage: 20 mg, qd
    End date: 2012-07-26

Nitroglycerin
    Dosage: 5 mg, daily
    End date: 2012-07-27

Plavix
    Dosage: 75 mg, qd
    End date: 2012-07-26

Ramipril
    Dosage: 10 mg, qd
    End date: 2012-07-26

Zometa
    Dosage: 4 mg, in 15 min
    Indication: Hypercalcaemia
    Start date: 2012-07-19



Possible Zometa side effects in male

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

Patient: male

Reactions: Neoplasm Malignant, Muscular Weakness, Biliary Tract Disorder, Liver Disorder

Adverse event resulted in: life threatening event

Drug(s) suspected as cause:
Zometa
    Dosage: 4 mg/100 ml once per 84 days
    Start date: 2012-05-14

Zometa
    Dosage: 4 mg/100 ml once per 84 days
    Start date: 2012-07-30

Zometa
    Dosage: 4 mg/100 ml once per 84 days
    Indication: Prostate Cancer Metastatic
    Start date: 2012-02-10

Other drugs received by patient: Selokeen; Tramadol HCL; Casodex; Acetaminophen; Leuprolide Acetate



Possible Zometa side effects in 92 year old male

Reported by a physician from Japan on 2012-08-09

Patient: 92 year old male, weighing 41.0 kg (90.2 pounds)

Reactions: Overdose, Fatigue, Anaemia, Hypocalcaemia, Renal Failure Acute

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Zometa

Other drugs received by patient: Sulpiride; Leuprolide Acetate; Kremezin; Famotidine



Possible Zometa side effects in 80 year old male

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

Patient: 80 year old male

Reactions: Tooth Loss, Exposed Bone in JAW, Hepatic Neoplasm Malignant, Pain, Periodontitis, Periodontal Infection, Tenderness, Pain in JAW, Aphagia, Fistula, Osteitis, Oral Mucosal Erythema, Osteonecrosis of JAW, Neoplasm Malignant, Poor Personal Hygiene, Swelling, Gingival Infection

Adverse event resulted in: death, life threatening event, hospitalization, disablity

Drug(s) suspected as cause:
Zometa



Possible Zometa side effects in male

Reported by a health professional (non-physician/pharmacist) from Netherlands on 2012-08-02

Patient: male

Reactions: Neoplasm Malignant, Muscular Weakness, Biliary Tract Disorder, Liver Disorder

Adverse event resulted in: life threatening event

Drug(s) suspected as cause:
Zometa
    Dosage: 4 mg/100 ml once per 84 days
    Start date: 2012-07-30

Zometa
    Dosage: 4 mg/100 ml once per 84 days
    Start date: 2012-05-14

Zometa
    Dosage: 4 mg/100 ml once per 84 days
    Indication: Prostate Cancer Metastatic
    Start date: 2012-02-29



Possible Zometa side effects in 80 year old male

Reported by a health professional (non-physician/pharmacist) from Japan on 2012-07-30

Patient: 80 year old male

Reactions: Tooth Loss, Fistula, Exposed Bone in JAW, Hepatic Neoplasm Malignant, Osteitis, Periodontitis, Osteonecrosis of JAW, Neoplasm Malignant, Hypophagia, Pain in JAW

Adverse event resulted in: death, life threatening event, hospitalization, disablity

Drug(s) suspected as cause:
Zometa



Possible Zometa side effects in male

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

Patient: male

Reactions: Hyperkalaemia, Pancreatic Carcinoma, Dehydration, Renal Tubular Necrosis, Fall, Melaena, Renal Failure Acute

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Zometa

Other drugs received by patient: Lasix



Possible Zometa side effects in male

Reported by a consumer/non-health professional from Netherlands on 2012-07-12

Patient: male

Reactions: Pneumonia, Terminal State

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Zometa
    Dosage: 4 mg/100 ml solution for iv infusion 1x per 21 days
    Start date: 2012-01-04

Zometa
    Dosage: 4 mg/100 ml solution for iv infusion 1x per 21 days
    Start date: 2012-05-08

Zometa
    Dosage: 4 mg/100 ml solution for iv infusion 1x per 21 days
    Indication: Metastases To Bone

Zometa
    Dosage: 4 mg/100 ml solution for iv infusion 1x per 21 days
    Start date: 2012-03-28



Possible Zometa side effects in 70 year old female

Reported by a physician from Spain on 2012-07-12

Patient: 70 year old female

Reactions: Hypocalcaemia

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Zometa
    Dosage: 3 mg, unk

Zometa
    Dosage: 4 mg, unk
    Start date: 2011-12-16

Zometa
    Dosage: 4 mg, unk
    End date: 2012-06-20



Possible Zometa side effects in 91 year old male

Reported by a physician from Japan on 2012-07-10

Patient: 91 year old male

Reactions: Overdose, Fatigue, Anaemia, Hypocalcaemia, Renal Failure Acute

Adverse event resulted in: life threatening event

Drug(s) suspected as cause:
Zometa



Possible Zometa side effects in male

Reported by a consumer/non-health professional from Netherlands on 2012-07-05

Patient: male

Reactions: Pneumonia, Terminal State

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Zometa
    Dosage: 4 mg/100 ml solution for iv infusion 1x per 21 days
    Start date: 2012-03-28

Zometa
    Dosage: 4 mg/100 ml solution for iv infusion 1x per 21 days
    Indication: Metastases To Bone

Zometa
    Dosage: 4 mg/100 ml solution for iv infusion 1x per 21 days
    Start date: 2012-01-04



Possible Zometa side effects in 67 year old female

Reported by a physician from Spain on 2012-06-08

Patient: 67 year old female

Reactions: HIP Fracture

Adverse event resulted in: life threatening event, disablity

Drug(s) suspected as cause:
Zometa
    Dosage: unk
    End date: 2011-12-01

Zometa
    Dosage: unk
    Indication: Metastases To Bone
    Start date: 2009-04-01



Possible Zometa side effects in 67 year old female

Reported by a health professional (non-physician/pharmacist) from Spain on 2012-06-07

Patient: 67 year old female

Reactions: HIP Fracture

Adverse event resulted in: life threatening event

Drug(s) suspected as cause:
Zometa



Possible Zometa side effects in 63 year old female

Reported by a physician from Japan on 2012-06-05

Patient: 63 year old female

Reactions: Blood Alkaline Phosphatase Increased, Hepatic Function Abnormal, Gamma-Glutamyltransferase Increased, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Pyrexia

Adverse event resulted in: life threatening event

Drug(s) suspected as cause:
Femara
    Dosage: 2.5 mg, daily
    Administration route: Oral
    Indication: Breast Cancer
    Start date: 2011-11-29
    End date: 2011-11-30

Loxonin
    Dosage: 60 mg, daily
    Administration route: Oral
    Start date: 2011-11-29
    End date: 2011-11-30

Zometa
    Dosage: 4 mg, unk
    Indication: Metastases To Bone
    Start date: 2011-11-30



Possible Zometa side effects in 63 year old female

Reported by a physician from Japan on 2012-06-03

Patient: 63 year old female

Reactions: Hepatic Function Abnormal, Pyrexia

Adverse event resulted in: life threatening event

Drug(s) suspected as cause:
Femara
    Dosage: 2.5 mg, daily
    Administration route: Oral
    Indication: Breast Cancer
    Start date: 2011-11-29
    End date: 2011-11-30

Loxonin
    Dosage: 60 mg, daily
    Administration route: Oral
    Start date: 2011-11-29
    End date: 2011-11-30

Zometa
    Dosage: 4 mg, unk
    Indication: Metastases To Bone
    Start date: 2011-11-30



Possible Zometa side effects in 67 year old female

Reported by a health professional (non-physician/pharmacist) from Spain on 2012-05-25

Patient: 67 year old female

Reactions: HIP Fracture

Adverse event resulted in: life threatening event

Drug(s) suspected as cause:
Zometa



Possible Zometa side effects in female

Reported by a physician from United States on 2012-05-24

Patient: female, weighing 79.8 kg (175.6 pounds)

Reactions: Blepharitis, Cardiomegaly, Malnutrition, Pancytopenia, Musculoskeletal Discomfort, Ataxia, Bursitis, Osteopenia, Staphylococcal Infection, Rosacea, Vision Blurred, Actinomycosis, Essential Hypertension, Seborrhoeic Keratosis, Osteoporosis, Mental Status Changes, Fall, Bone Disorder, Exostosis, Dyspnoea, Cataract, Gastrointestinal Toxicity, Arrhythmia, Acquired Diaphragmatic Eventration, Arthralgia, Hypothyroidism, Gait Disturbance, Asthenia, Depressed Mood, Weight Decreased, Gastrointestinal Haemorrhage, Herpes Zoster, Colonic Polyp, Spinal Compression Fracture, Tongue Disorder, Tendonitis, Pneumonia, Cellulitis, Pain in Extremity, Supraventricular Tachycardia, Renal Cyst, Peritonitis, Fungal Infection, Colitis, Septic Shock, Atelectasis, Constipation, Bone Erosion, Neuropathy Peripheral, Skin Ulcer, Basal Cell Carcinoma, Skin Bacterial Infection, Pleural Effusion, Gastrooesophageal Reflux Disease, Pain in JAW, Polyp, Bone Lesion, Squamous Cell Carcinoma, Urinary Tract Infection, Cystitis Noninfective, Deformity, Plantar Fasciitis, Ileus Paralytic, Osteoarthritis, Anxiety, Panic Attack, Renal Failure, Neoplasm Malignant, Respiratory Failure, Diarrhoea, Osteonecrosis of JAW, Bronchitis, Spinal Osteoarthritis, Atrophy, Meningioma, Infection

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Aredia
    Dosage: unk ukn, qmo

Zometa
    Dosage: unk ukn, unk

Other drugs received by patient: Alkeran; Altabax; Cleocin Hydrochloride; Multi-Vitamins; Prednisone TAB; Extra Strength Tylenol; Synthroid; Dexamethasone; Velcade; Prednisone TAB; Cymbalta; Lisinopril; Chemotherapeutics NOS; Coumadin; Revlimid



Possible Zometa side effects in female

Reported by a physician from France on 2012-04-23

Patient: female, weighing 56.0 kg (123.2 pounds)

Reactions: Confusional State, Renal Tubular Disorder, Metabolic Acidosis, Dyspnoea, Hyperkalaemia, Urine Output Decreased, Oedema Peripheral, Renal Tubular Necrosis, Anuria, Renal Failure Acute

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Zometa
    Dosage: 4 mg, every 21 days
    Indication: Metastases To Bone
    Start date: 2010-01-01

Zometa
    Dosage: 4 mg, every 28 days
    Start date: 2011-09-01

Zometa
    Dosage: 3 mg
    Start date: 2012-01-01

Other drugs received by patient: Lasix; Faslodex; Potassium Chloride; Tramadol HCL



Possible Zometa side effects in male

Reported by a physician from Japan on 2012-04-10

Patient: male

Reactions: Atelectasis, Haemoglobin Decreased, Pneumonia, Neoplasm Malignant, Neoplasm Progression

Adverse event resulted in: death, life threatening event

Drug(s) suspected as cause:
Afinitor
    Dosage: 10 mg, daily
    Administration route: Oral
    Indication: Metastatic Renal Cell Carcinoma
    Start date: 2011-01-31
    End date: 2011-09-17

Zometa
    Dosage: unk ukn, unk
    End date: 2011-05-19

Zometa
    Dosage: unk ukn, unk
    Indication: Metastatic Renal Cell Carcinoma
    Start date: 2011-02-08
    End date: 2011-05-19

Other drugs received by patient: Oxycontin; Paxil; Zolpidem; Lyrica; Risperdal; Rohypnol; Rabeprazole Sodium; Acetylol; Myser; Meloxicam; Amitriptyline HCL; Clonazepam



Possible Zometa side effects in male

Reported by a physician from Japan on 2012-04-10

Patient: male

Reactions: Haemoglobin Decreased, Atelectasis, Pneumonia, Neoplasm Malignant, Neoplasm Progression

Adverse event resulted in: death, life threatening event

Drug(s) suspected as cause:
Afinitor
    Dosage: 10 mg, daily
    Administration route: Oral
    Indication: Metastatic Renal Cell Carcinoma
    Start date: 2011-01-31
    End date: 2011-09-17

Zometa
    Dosage: unk ukn, unk
    End date: 2011-05-19

Zometa
    Dosage: unk ukn, unk
    Indication: Metastatic Renal Cell Carcinoma
    Start date: 2011-02-08
    End date: 2011-05-19

Other drugs received by patient: Zolpidem; Oxycontin; Lyrica; Risperdal; Myser; Amitriptyline HCL; Paxil; Rohypnol; Rabeprazole Sodium; Meloxicam; Clonazepam; Acetylol



Possible Zometa side effects in male

Reported by a health professional (non-physician/pharmacist) from Canada on 2012-03-28

Patient: male

Reactions: Blood Pressure Increased, Back Pain, Dyspnoea, Musculoskeletal Chest Pain, Torsade DE Pointes, Heart Rate Decreased, Prostatic Specific Antigen Increased, Prostate Cancer Metastatic, Atrioventricular Block, Circulatory Collapse, Cardiac Arrest, Myocardial Infarction

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Zometa



Possible Zometa side effects in male

Reported by a health professional (non-physician/pharmacist) from Netherlands on 2012-03-16

Patient: male

Reactions: Cervical Vertebral Fracture, Drug Ineffective, Muscular Weakness, Paralysis, General Physical Health Deterioration, Neoplasm Progression, Death, Neoplasm Malignant, Terminal State

Adverse event resulted in: death, life threatening event, hospitalization

Drug(s) suspected as cause:
Zometa

Other drugs received by patient: Dexamethasone Sodium Phosphate; Sutent; Oxycontin; Fentanyl; Methadone HCL; Diclofenac Sodium; Oxybutynin; Paroxetine HCL; Temazepam; Molexol; Instanyl; Acetaminophen; Omeprazole; Metoclopramide



Possible Zometa side effects in male

Reported by a pharmacist from Japan on 2012-03-14

Patient: male, weighing 58.0 kg (127.6 pounds)

Reactions: Blood Alkaline Phosphatase Increased, Urine Output Decreased, Haematuria, Neoplasm Progression, Hepatic Failure, Hyperhidrosis, Anxiety, Neoplasm Malignant, Heart Rate Increased, Depressed Level of Consciousness, Apnoea, Blood Pressure Decreased, Oxygen Saturation Decreased

Adverse event resulted in: death, life threatening event

Drug(s) suspected as cause:
Zometa

Other drugs received by patient: Sodium Chloride Solution; Prochlorperazine; Morphine; Famotidine; Vitamedin Capsule; Ascorbic Acid; Intralipid 10%; Flurbiprofen; Veen D; TPN Electrolytes IN Plastic Container



Possible Zometa side effects in male

Reported by a physician from France on 2012-02-24

Patient: male, weighing 76.5 kg (168.3 pounds)

Reactions: Metabolic Acidosis, Urinary Tract Infection, Hypocalcaemia, Klebsiella Test Positive, Convulsion

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Docetaxel
    Dosage: 140 mg, daily
    Indication: Prostate Cancer
    Start date: 2011-02-16
    End date: 2011-03-09

Lenalidomide
    Dosage: 25 mg, daily
    Administration route: Oral
    Indication: Prostate Cancer
    Start date: 2011-02-16
    End date: 2011-03-09

Prednisone TAB
    Dosage: 10 mg, daily
    Indication: Prostate Cancer
    Start date: 2011-02-16
    End date: 2011-03-09

Zometa
    Dosage: 3.3 mg, qmo
    Indication: Bone Lesion
    Start date: 2010-11-01

Other drugs received by patient: Furosemide; Zoladex; Innohep; Zoladex; Colchicine; UN-Alfa; Atorvastatin; Atenolol; Nexium; Amlodipine; Fosinopril Sodium; Lantus; Allopurinol; UN-Alfa



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