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Index of reports
> Cases resulting in disability (19)
Below is the selection of adverse event reports related to Diovan (Valsartan) that includes cases resulting in disability.
Adverse event in 10 year old male receiving Diovan (Valsartan)
Reported by a individual with unspecified qualification from Japan on 2007-10-29
Patient: 10 year old male, weighing 60.0 kg (132.0 pounds)
Adverse reactions / side effects: Blood Urea Increased, Headache, Superior Sagittal Sinus Thrombosis, Nephrotic Syndrome, Convulsion, Cerebral Infarction, Dehydration, Proteinuria, Oliguria, Oedema, Blood Creatinine Increased, Acute Prerenal Failure, Anuria, Influenza
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Acecol
Dosage: 2 mg/d
Administration route: Oral
Indication: Nephrotic Syndrome
End date: 2007-03-01
Bredinin
Dosage: 150 mg/d
Administration route: Oral
Indication: Nephrotic Syndrome
Diovan
Dosage: 80 mg/d
Administration route: Oral
Indication: Nephrotic Syndrome
End date: 2007-03-01
Neoral
Dosage: 140 mg/d
Administration route: Oral
Indication: Nephrotic Syndrome
End date: 2007-03-19
Predonine
Dosage: 40 mg/d
Administration route: Oral
Indication: Nephrotic Syndrome
Other drugs received by patient: Lipitor; Zyloric
Adverse event in 10 year old male receiving Diovan (Valsartan)
Reported by a individual with unspecified qualification from Japan on 2007-10-29
Patient: 10 year old male, weighing 60.0 kg (132.0 pounds)
Adverse reactions / side effects: Blood Urea Increased, Headache, Superior Sagittal Sinus Thrombosis, Nephrotic Syndrome, Convulsion, Cerebral Infarction, Dehydration, Proteinuria, Oliguria, Oedema, Blood Creatinine Increased, Acute Prerenal Failure, Anuria, Influenza
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Acecol
Dosage: 2 mg/d
Administration route: Oral
Indication: Nephrotic Syndrome
End date: 2007-03-01
Bredinin
Dosage: 150 mg/d
Administration route: Oral
Indication: Nephrotic Syndrome
Diovan
Dosage: 80 mg/d
Administration route: Oral
Indication: Nephrotic Syndrome
End date: 2007-03-01
Neoral
Dosage: 140 mg/d
Administration route: Oral
Indication: Nephrotic Syndrome
End date: 2007-03-19
Predonine
Dosage: 40 mg/d
Administration route: Oral
Indication: Nephrotic Syndrome
Other drugs received by patient: Lipitor; Zyloric
Adverse event in 39 year old female receiving Diovan (Valsartan)
Reported by a physician from United States on 2007-10-15
Patient: 39 year old female
Adverse reactions / side effects: Visual Acuity Reduced
Adverse event resulted in: disablity
Suspect drug(s):
Diovan (Valsartan)
Adverse event in female receiving Diovan (Valsartan)
Reported by a physician from Netherlands on 2007-10-09
Patient: female
Adverse reactions / side effects: Chronic Sinusitis, Deafness, Sinusitis, Eustachian Tube Disorder
Adverse event resulted in: disablity
Suspect drug(s):
Diovan
Dosage: 160 mg/day
Administration route: Oral
Indication: Hypertension
Start date: 2006-09-01
Diovan
Dosage: 80 mg/day
Administration route: Oral
Other drugs received by patient: Lipitor; Aspirin and Dipyridamole
Adverse event in 68 year old male receiving Diovan (Valsartan)
Reported by a pharmacist from Japan on 2007-07-27
Patient: 68 year old male, weighing 48.0 kg (105.6 pounds)
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Intubation, Blood Albumin Decreased, X-RAY Abnormal, Haematocrit Decreased, C-Reactive Protein Increased, Gamma-Glutamyltransferase Increased, RED Blood Cell Count Decreased, Interstitial Lung Disease, Blood Sodium Increased, Blood Creatinine Increased, Oxygen Saturation Decreased, White Blood Cell Count Increased, Blood Urea Increased, Blood Lactate Dehydrogenase Increased, Alanine Aminotransferase Increased, Blood Chloride Increased, Life Support, Protein Total Decreased, Albumin Globulin Ratio Decreased, Computerised Tomogram Abnormal, Mean Cell Volume Abnormal, Haemoglobin Decreased, Aspartate Aminotransferase Increased, Cell Marker, Platelet Count Decreased
Adverse event resulted in: disablity
Suspect drug(s):
Amiodarone HCL
Dosage: 400 mg/day
Administration route: Oral
Start date: 2007-04-24
End date: 2007-06-04
Diovan
Dosage: 80 mg, bid
Administration route: Oral
Indication: Hypertension
Start date: 2007-05-16
End date: 2007-05-16
Diovan
Dosage: 160 mg, bid
Administration route: Oral
Start date: 2007-05-17
End date: 2007-06-07
Adverse event in 68 year old male receiving Diovan (Valsartan)
Reported by a pharmacist from Japan on 2007-07-26
Patient: 68 year old male, weighing 48.0 kg (105.6 pounds)
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Intubation, Blood Albumin Decreased, X-RAY Abnormal, Blood Albumin Increased, Haematocrit Decreased, C-Reactive Protein Increased, Gamma-Glutamyltransferase Increased, Interstitial Lung Disease, RED Blood Cell Count Decreased, Blood Sodium Increased, Blood Creatinine Increased, Oxygen Saturation Decreased, White Blood Cell Count Increased, Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Blood Chloride Increased, Life Support, Protein Total Decreased, Computerised Tomogram Abnormal, Mean Cell Volume Abnormal, Haemoglobin Decreased, Aspartate Aminotransferase Increased, Cell Marker, Platelet Count Decreased
Adverse event resulted in: disablity
Suspect drug(s):
Amiodarone HCL
Dosage: 400 mg/day
Administration route: Oral
Start date: 2007-04-24
End date: 2007-06-04
Diovan
Dosage: 80 mg, bid
Administration route: Oral
Indication: Hypertension
Start date: 2007-05-16
End date: 2007-05-16
Diovan
Dosage: 160 mg, bid
Administration route: Oral
Start date: 2007-05-17
End date: 2007-06-07
Adverse event in 75 year old female receiving Diovan (Valsartan)
Reported by a physician from Canada on 2007-07-19
Patient: 75 year old female
Adverse reactions / side effects: Fatigue, Activities of Daily Living Impaired, Muscular Weakness
Adverse event resulted in: disablity
Suspect drug(s):
Diovan (Valsartan)
Other drugs received by patient: Lipitor; Metoprolol Tartrate
Adverse event in 56 year old female receiving Diovan (Valsartan)
Reported by a individual with unspecified qualification from United States on 2007-07-17
Patient: 56 year old female
Adverse reactions / side effects: Dyspnoea, Chest Discomfort, Pain in Extremity, Skin Exfoliation, Abasia, DRY Skin, Stress, Hyperhidrosis, Arthralgia, Thyroidectomy, Insomnia, Alopecia, Thyroid Disorder, Gait Disturbance, Arthritis
Adverse event resulted in: life threatening event, disablity
Suspect drug(s):
Diovan (Valsartan)
Other drugs received by patient: Fluoxetine
Adverse event in 75 year old female receiving Diovan (Valsartan)
Reported by a individual with unspecified qualification from Canada on 2007-07-16
Patient: 75 year old female
Adverse reactions / side effects: Fatigue, Activities of Daily Living Impaired, Muscular Weakness
Adverse event resulted in: disablity
Suspect drug(s):
Diovan (Valsartan)
Adverse event in 68 year old male receiving Diovan (Valsartan)
Reported by a pharmacist from Japan on 2007-07-06
Patient: 68 year old male, weighing 48.0 kg (105.6 pounds)
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Intubation, Blood Albumin Decreased, X-RAY Abnormal, Blood Albumin Increased, Haematocrit Decreased, C-Reactive Protein Increased, Gamma-Glutamyltransferase Increased, Interstitial Lung Disease, RED Blood Cell Count Decreased, Blood Sodium Increased, Blood Creatinine Increased, Oxygen Saturation Decreased, White Blood Cell Count Increased, Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Blood Chloride Increased, Life Support, Protein Total Decreased, Computerised Tomogram Abnormal, Mean Cell Volume Abnormal, Haemoglobin Decreased, Aspartate Aminotransferase Increased, Cell Marker, Platelet Count Decreased
Adverse event resulted in: disablity
Suspect drug(s):
Amiodarone HCL
Dosage: unk, unk
Administration route: Oral
Start date: 2007-04-24
End date: 2007-06-04
Diovan
Dosage: 80 mg, bid
Administration route: Oral
Indication: Hypertension
Start date: 2007-05-16
End date: 2007-05-16
Diovan
Dosage: 160 mg, bid
Administration route: Oral
Start date: 2007-05-17
End date: 2007-06-07
Adverse event in 68 year old male receiving Diovan (Valsartan)
Reported by a pharmacist from Japan on 2007-07-06
Patient: 68 year old male, weighing 48.0 kg (105.6 pounds)
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Intubation, Blood Albumin Decreased, X-RAY Abnormal, Blood Albumin Increased, Haematocrit Decreased, C-Reactive Protein Increased, Gamma-Glutamyltransferase Increased, Interstitial Lung Disease, RED Blood Cell Count Decreased, Blood Sodium Increased, Blood Creatinine Increased, Oxygen Saturation Decreased, White Blood Cell Count Increased, Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Blood Chloride Increased, Life Support, Protein Total Decreased, Computerised Tomogram Abnormal, Mean Cell Volume Abnormal, Haemoglobin Decreased, Aspartate Aminotransferase Increased, Cell Marker, Platelet Count Decreased
Adverse event resulted in: disablity
Suspect drug(s):
Amiodarone HCL
Dosage: unk, unk
Administration route: Oral
Start date: 2007-04-24
End date: 2007-06-04
Diovan
Dosage: 80 mg, bid
Administration route: Oral
Indication: Hypertension
Start date: 2007-05-16
End date: 2007-05-16
Diovan
Dosage: 160 mg, bid
Administration route: Oral
Start date: 2007-05-17
End date: 2007-06-07
Adverse event in 82 year old male receiving Diovan (Valsartan)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-20
Patient: 82 year old male, weighing 88.9 kg (195.6 pounds)
Adverse reactions / side effects: Metastatic Neoplasm, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Aspartate Aminotransferase Increased, Alanine Aminotransferase Increased, Bile Duct Cancer
Adverse event resulted in: death, disablity
Suspect drug(s):
Diovan (Valsartan)
Other drugs received by patient: Lasix; Vitamin B-12; Aspirin; Alopurinol
Adverse event in 59 year old male receiving Diovan (Valsartan)
Reported by a consumer/non-health professional from United States on 2007-04-17
Patient: 59 year old male, weighing 115.7 kg (254.5 pounds)
Adverse reactions / side effects: Myalgia, Back Pain, Arthralgia, Impaired Work Ability, Chest Pain, Muscle Tightness, Exercise Tolerance Decreased
Adverse event resulted in: disablity
Suspect drug(s):
Diovan (Valsartan)
Other drugs received by patient: Wellbutrin; Concerta
Adverse event in 73 year old female receiving Diovan (Valsartan)
Reported by a physician from United States on 2007-04-13
Patient: 73 year old female
Adverse reactions / side effects: Antinuclear Antibody Positive, Pruritus, Systemic Lupus Erythematosus Rash, Complement Factor C3 Increased
Adverse event resulted in: disablity
Suspect drug(s):
Diovan
End date: 2007-02-01
Hydrochlorothiazide
End date: 2007-02-01
Zetia
Administration route: Oral
Indication: Blood Cholesterol Increased
Start date: 2007-01-01
Other drugs received by patient: Simvastatin; Prevacid; Toprol-XL; Aspirin
Adverse event in 69 year old male receiving Diovan (Valsartan)
Reported by a individual with unspecified qualification from United States on 2007-04-05
Patient: 69 year old male, weighing 88.4 kg (194.6 pounds)
Adverse reactions / side effects: Surgery, Fatigue, Neoplasm Malignant, Pollakiuria, Renal Cell Carcinoma Stage Unspecified, Gait Disturbance, Hypertension, Lung Infiltration, Metastases TO Lung, Decreased Appetite
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Diovan (Valsartan)
Other drugs received by patient: Indocin
Adverse event in 69 year old male receiving Diovan (Valsartan)
Reported by a individual with unspecified qualification from United States on 2007-03-28
Patient: 69 year old male, weighing 88.4 kg (194.6 pounds)
Adverse reactions / side effects: Surgery, Fatigue, Neoplasm Malignant, Pollakiuria, Renal Cell Carcinoma Stage Unspecified, Gait Disturbance, Hypertension, Lung Infiltration, Metastases TO Lung, Decreased Appetite
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Diovan (Valsartan)
Other drugs received by patient: Indocin
Adverse event in 41 year old female receiving Diovan (Valsartan)
Reported by a physician from Japan on 2007-02-13
Patient: 41 year old female, weighing 63.0 kg (138.6 pounds)
Adverse reactions / side effects: Hemiplegia, Putamen Haemorrhage
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Diovan
Dosage: 80 mg, qd
Administration route: Oral
Start date: 2002-12-19
Warfarin Sodium
Dosage: 4mg
Administration route: Oral
Indication: Systemic Lupus Erythematosus
Start date: 2002-10-31
Warfarin Sodium
Dosage: 3mg
Administration route: Oral
End date: 2005-08-01
Warfarin Sodium
Dosage: 2mg
Administration route: Oral
Start date: 2005-10-06
Other drugs received by patient: Neoral; Prednisolone; Gaster D
Adverse event in 56 year old female receiving Diovan (Valsartan)
Reported by a physician from Japan on 2007-02-12
Patient: 56 year old female
Adverse reactions / side effects: Respiratory Disorder, Headache, Subarachnoid Haemorrhage, Cerebral Decompression, Ventriculo-Peritoneal Shunt, Depressed Level of Consciousness, Intra-Cerebral Aneurysm Operation, Hemiplegia
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Diovan (Valsartan)
Other drugs received by patient: Perdipine; Thyradin S; Mevalotin
Adverse event in 55 year old female receiving Diovan (Valsartan)
Reported by a physician from Austria on 2007-01-31
Patient: 55 year old female
Adverse reactions / side effects: Haemarthrosis
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Diovan (Valsartan)
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