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Diovan (Valsartan) - Adverse Event Reports - Hospitalization

 



Index of reports > Cases resulting in hospitalization (294)

     Dyspnoea (34)Blood Lactate Dehydrogenase Increased (27)Hypertension (27)Malaise (26)Dizziness (26)Vomiting (23)Alanine Aminotransferase Increased (20)Haemoglobin Decreased (20)Blood Alkaline Phosphatase Increased (19)Hypotension (18)

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

 Reports 1 - 25 of 294   Next >>

Adverse event in receiving Diovan (Valsartan)

Reported by a pharmacist from Germany on 2007-10-31

Patient:

Adverse reactions / side effects: Porphyria non-Acute

Adverse event resulted in: hospitalization

Suspect drug(s):
Diovan (Valsartan)



Adverse event in 65 year old male receiving Diovan (Valsartan)

Reported by a physician from Japan on 2007-10-31

Patient: 65 year old male, weighing 64.0 kg (140.8 pounds)

Adverse reactions / side effects: Cerebral Infarction, Hemiplegia

Adverse event resulted in: hospitalization

Suspect drug(s):
Diovan (Valsartan)



Adverse event in 75 year old male receiving Diovan (Valsartan)

Reported by a physician from Netherlands on 2007-10-30

Patient: 75 year old male

Adverse reactions / side effects: Circulatory Collapse, Orthostatic Hypotension, Angioplasty

Adverse event resulted in: hospitalization

Suspect drug(s):
Diovan
    Dosage: 320 mg, unk
    Indication: Hypertension
    Start date: 2007-07-01
    End date: 2007-08-07

Diovan
    Dosage: 160 mg, unk
    Start date: 2007-08-08

Other drugs received by patient: Diuretics; Beta Blocking Agents; Plavix; Ascal; Metoprolol; Hydrochlorothiazide; Simvastatin



Adverse event in 87 year old female receiving Diovan (Valsartan)

Reported by a physician from Japan on 2007-10-30

Patient: 87 year old female

Adverse reactions / side effects: Blood Alkaline Phosphatase Increased, Monoplegia, Blood Lactate Dehydrogenase Increased, Lymphopenia, Dysarthria, Blood Creatinine Decreased, Gamma-Glutamyltransferase Increased, Cerebral Infarction, RED Blood Cell Count Decreased, C-Reactive Protein Increased, Oedema Peripheral, Nuclear Magnetic Resonance Imaging Abnormal, Asthenia, White Blood Cell Count Increased

Adverse event resulted in: hospitalization

Suspect drug(s):
Diovan (Valsartan)

Other drugs received by patient: Aspirin; Amlodipine; Aricept; Predonine; Amaryl



Adverse event in 35 year old male receiving Diovan (Valsartan)

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-10-30

Patient: 35 year old male

Adverse reactions / side effects: Blood Alkaline Phosphatase Decreased, Vomiting, Blood Lactate Dehydrogenase Increased, Paralysis, Overdose, Fibrin Increased, Shock, White Blood Cell Count Increased

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Allopurinol
    Dosage: oral
    Administration route: Oral
    Indication: Self Mutilation
    Start date: 2007-08-18
    End date: 2007-08-18

Carvedilol
    Dosage: oral
    Administration route: Oral
    Start date: 2007-08-18
    End date: 2007-08-18

Adalat
    Dosage: oral
    Administration route: Oral
    Start date: 2007-08-18
    End date: 2007-08-18

Diovan
    Dosage: oral
    Administration route: Oral
    Start date: 2007-08-18
    End date: 2007-08-18

Olmesartan Medoxomil
    Dosage: oral
    Administration route: Oral
    Start date: 2007-08-18
    End date: 2007-08-18



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):
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

Bredinin
    Dosage: 150 mg/d
    Administration route: Oral
    Indication: Nephrotic Syndrome

Acecol
    Dosage: 2 mg/d
    Administration route: Oral
    Indication: Nephrotic Syndrome
    End date: 2007-03-01

Diovan
    Dosage: 80 mg/d
    Administration route: Oral
    Indication: Nephrotic Syndrome
    End date: 2007-03-01

Other drugs received by patient: Lipitor; Zyloric



Adverse event in 75 year old male receiving Diovan (Valsartan)

Reported by a physician from Japan on 2007-10-29

Patient: 75 year old male

Adverse reactions / side effects: Nervous System Disorder, Memory Impairment, Extradural Haematoma

Adverse event resulted in: hospitalization

Suspect drug(s):
Diovan (Valsartan)

Other drugs received by patient: Diltiazem HCL; Diart; Lanirapid; Glyburide; Buformin Hydrochloride; Atelec; Actos; Warfarin Sodium



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):
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

Bredinin
    Dosage: 150 mg/d
    Administration route: Oral
    Indication: Nephrotic Syndrome

Acecol
    Dosage: 2 mg/d
    Administration route: Oral
    Indication: Nephrotic Syndrome
    End date: 2007-03-01

Diovan
    Dosage: 80 mg/d
    Administration route: Oral
    Indication: Nephrotic Syndrome
    End date: 2007-03-01

Other drugs received by patient: Lipitor; Zyloric



Adverse event in 73 year old female receiving Diovan (Valsartan)

Reported by a consumer/non-health professional from Argentina on 2007-10-29

Patient: 73 year old female

Adverse reactions / side effects: Abdominal Pain, Dizziness, Gallbladder Disorder, Treatment Noncompliance, Gallbladder Operation

Adverse event resulted in: hospitalization

Suspect drug(s):
Diovan
    Dosage: 80 mg, qd
    Administration route: Oral
    Indication: Hypertension
    Start date: 2007-10-16

Diovan
    Dosage: 80 mg, qd
    Administration route: Oral
    End date: 2007-10-15



Adverse event in 89 year old male receiving Diovan (Valsartan)

Reported by a individual with unspecified qualification from United States on 2007-10-26

Patient: 89 year old male

Adverse reactions / side effects: Haemorrhage, Drug Dispensing Error

Adverse event resulted in: hospitalization

Suspect drug(s):
Coumadin
    Dosage: 4 mg, unk

Diovan

Other drugs received by patient: Proscar; Flomax



Adverse event in 78 year old female receiving Diovan (Valsartan)

Reported by a consumer/non-health professional from Argentina on 2007-10-26

Patient: 78 year old female

Adverse reactions / side effects: Pneumonia

Adverse event resulted in: hospitalization

Suspect drug(s):
Diovan (Valsartan)



Adverse event in 63 year old male receiving Diovan (Valsartan)

Reported by a physician from Japan on 2007-10-25

Patient: 63 year old male, weighing 72.0 kg (158.4 pounds)

Adverse reactions / side effects: Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Hepatic Function Abnormal, Hepatitis Acute, Urticaria, Blood Lactate Dehydrogenase Increased, Alanine Aminotransferase Increased, Jaundice Cholestatic, Leukocytoclastic Vasculitis, Pruritus Generalised, Aspartate Aminotransferase Increased

Adverse event resulted in: hospitalization

Suspect drug(s):
Diovan (Valsartan)

Other drugs received by patient: Aspirin; Famotidine; Tamsulosin Hydrochloride; Apolakete; Bladderon; Melbin; Magnesium Oxide; Prednisolone; Tamsulosin HCL



Adverse event in male receiving Diovan (Valsartan)

Reported by a physician from Japan on 2007-10-25

Patient: male, weighing 60.0 kg (132.0 pounds)

Adverse reactions / side effects: Hyperglycaemia, Ankle Fracture, Asthenia, Loss of Consciousness, Cerebral Haemorrhage

Adverse event resulted in: hospitalization

Suspect drug(s):
Diovan (Valsartan)

Other drugs received by patient: Adalat; Herbessor R; Amaryl; Melbin; Frandol; Warfarin Sodium; Perdipine



Adverse event in 69 year old female receiving Diovan (Valsartan)

Reported by a individual with unspecified qualification from United States on 2007-10-22

Patient: 69 year old female

Adverse reactions / side effects: Heart Rate Increased

Adverse event resulted in: hospitalization

Suspect drug(s):
Diovan
    Dosage: unk, unk

Coreg
    Dosage: 3.25 mg, bid
    Indication: Hypertension
    Start date: 2003-01-01
    End date: 2005-01-01

Coreg
    Dosage: 6.25 mg, bid
    Start date: 2005-01-01
    End date: 2007-09-14

Other drugs received by patient: Lorazepam; Clopidogrel Bisulfate; Aspirin; Torsemide; Potassium Chloride; Warfarin; Cetirizine Hydrochloride



Adverse event in 63 year old male receiving Diovan (Valsartan)

Reported by a physician from Japan on 2007-10-22

Patient: 63 year old male

Adverse reactions / side effects: Hypothermia, Bradycardia, Altered State of Consciousness

Adverse event resulted in: hospitalization

Suspect drug(s):
Diovan
    Dosage: 40 mg, unk
    Indication: Hypertension
    Start date: 2003-01-31
    End date: 2006-01-10

Lioresal
    Indication: Spinal Cord Disorder
    Start date: 1999-04-13

Dantrium
    Administration route: Oral
    Indication: Spinal Cord Disorder
    Start date: 1999-04-13

Harnal
    Indication: Spinal Cord Disorder
    Start date: 2007-04-13

Other drugs received by patient: Depas; Ternelin; Atelec



Adverse event in 89 year old female receiving Diovan (Valsartan)

Reported by a physician from Japan on 2007-10-22

Patient: 89 year old female, weighing 42.0 kg (92.4 pounds)

Adverse reactions / side effects: Eyelid Oedema, Atelectasis, Blood Bilirubin Increased, Respiratory Disorder, Hepatic Function Abnormal, Hyperkalaemia, Atrioventricular Block Complete, Sinus Bradycardia, Haematocrit Decreased, Gamma-Glutamyltransferase Increased, RED Blood Cell Count Decreased, Pleural Effusion, Blood Sodium Increased, Sinus Arrest, Blood Creatinine Increased, Blood Glucose Increased, Decreased Appetite, White Blood Cell Count Decreased, Blood Alkaline Phosphatase Increased, Blood Urea Increased, Hypotension, Blood Lactate Dehydrogenase Increased, Alanine Aminotransferase Increased, General Physical Health Deterioration, Blood Potassium Increased, Haemoglobin Decreased, Sick Sinus Syndrome, Cardiac Failure, Cardiac Pacemaker Insertion, Electrocardiogram Abnormal, Aspartate Aminotransferase Increased

Adverse event resulted in: hospitalization

Suspect drug(s):
Diovan
    Dosage: 40 mg/day
    Administration route: Oral
    Indication: Hypertension
    Start date: 2007-07-20
    End date: 2007-08-17

Diltiazem HCL
    Dosage: 100 mg/day
    Administration route: Oral
    Indication: Angina Pectoris
    Start date: 2007-06-15
    End date: 2007-08-17

Aricept
    Dosage: 5mg
    Administration route: Oral
    Start date: 2007-03-16

Other drugs received by patient: Famogast; Urso 250; Trepibutone; Coniel; Nitroderm; Sigmart; Lasix; Doxazosin Mesylate



Adverse event in 71 year old female receiving Diovan (Valsartan)

Reported by a consumer/non-health professional from Brazil on 2007-10-19

Patient: 71 year old female, weighing 70.0 kg (154.0 pounds)

Adverse reactions / side effects: Dysphagia, Therapeutic Procedure, Depression

Adverse event resulted in: hospitalization

Suspect drug(s):
Diovan (Valsartan)

Other drugs received by patient: Gardan TAB; Aropax



Adverse event in 35 year old male receiving Diovan (Valsartan)

Reported by a individual with unspecified qualification from United Kingdom on 2007-10-19

Patient: 35 year old male

Adverse reactions / side effects: Blood Alkaline Phosphatase Decreased, Vomiting, Hypotension, Blood Lactate Dehydrogenase Increased, Paralysis, Gastrointestinal Tube Insertion, Respiratory Rate Decreased, Overdose, Heart Rate Decreased, White Blood Cell Count Increased, Shock, Fibrin Increased

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Diovan
    Dosage: 40mgx 8 tablets
    Administration route: Oral
    Start date: 2007-08-18
    End date: 2007-08-18

Adalat
    Dosage: 40 mg x 40 tablets
    Administration route: Oral
    Start date: 2007-08-18
    End date: 2007-08-18

Allopurinol
    Dosage: 100 mg x 32 tablets
    Administration route: Oral
    Start date: 2007-08-18
    End date: 2007-08-18

Carvedilol
    Dosage: 10 mg x 32 tablets
    Administration route: Oral
    Indication: Self Mutilation
    Start date: 2007-08-18
    End date: 2007-08-18

Olmetec
    Dosage: 20 mg x 74 tablets
    Administration route: Oral
    Start date: 2007-08-18
    End date: 2007-08-18

Other drugs received by patient: Alcohol



Adverse event in 75 year old female receiving Diovan (Valsartan)

Reported by a consumer/non-health professional from Brazil on 2007-10-19

Patient: 75 year old female

Adverse reactions / side effects: Blood Pressure Increased, Cardiac Pacemaker Insertion, Hemiplegia, Tongue Spasm

Adverse event resulted in: hospitalization

Suspect drug(s):
Diovan
    Dosage: 160 mg, unk
    Administration route: Oral
    Start date: 2005-10-01

Diovan Amlo
    Dosage: 160/5 mg
    Administration route: Oral



Adverse event in 43 year old male receiving Diovan (Valsartan)

Reported by a physician from Japan on 2007-10-18

Patient: 43 year old male, weighing 70.0 kg (154.0 pounds)

Adverse reactions / side effects: Rash Generalised, Pyrexia, Drug Rash With Eosinophilia and Systemic Symptoms

Adverse event resulted in: hospitalization

Suspect drug(s):
Tegretol
    Dosage: 200 mg/day
    Administration route: Oral
    Indication: Nerve Injury
    Start date: 2007-08-07
    End date: 2007-08-27

Lipitor
    Dosage: 10 mg/day
    Administration route: Oral
    Start date: 2007-08-26

Ludiomil
    Dosage: 10 mg/day
    Administration route: Oral
    Start date: 2007-08-15
    End date: 2007-08-27

PL Gran.
    Dosage: 3 mg/day
    Administration route: Oral
    Start date: 2007-08-22
    End date: 2007-08-24

PL Gran.
    Dosage: 3 g/day
    Administration route: Oral
    Start date: 2007-08-28
    End date: 2007-08-29

Mexitil
    Dosage: 300 mg/day
    Administration route: Oral
    Indication: Nerve Injury
    Start date: 2007-07-20
    End date: 2007-08-27

Diovan
    Dosage: 20 mg/day
    Administration route: Oral
    Start date: 2007-07-22
    End date: 2007-08-27

Melbin
    Dosage: 500 mg/day
    Administration route: Oral
    Start date: 2007-08-10
    End date: 2007-08-27



Adverse event in 63 year old male receiving Diovan (Valsartan)

Reported by a physician from Japan on 2007-10-18

Patient: 63 year old male, weighing 72.0 kg (158.4 pounds)

Adverse reactions / side effects: Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Hepatic Function Abnormal, Hepatitis Acute, Urticaria, Blood Lactate Dehydrogenase Increased, Alanine Aminotransferase Increased, Jaundice Cholestatic, Leukocytoclastic Vasculitis, Pruritus Generalised, Aspartate Aminotransferase Increased

Adverse event resulted in: hospitalization

Suspect drug(s):
Diovan (Valsartan)

Other drugs received by patient: Aspirin; Famotidine; Tamsulosin Hydrochloride; Apolakete; Bladderon; Melbin; Magnesium Oxide; Prednisolone; Tamsulosin HCL



Adverse event in 43 year old male receiving Diovan (Valsartan)

Reported by a physician from Japan on 2007-10-18

Patient: 43 year old male, weighing 70.0 kg (154.0 pounds)

Adverse reactions / side effects: Rash Generalised, Pyrexia, Drug Rash With Eosinophilia and Systemic Symptoms

Adverse event resulted in: hospitalization

Suspect drug(s):
Tegretol
    Dosage: 200 mg/day
    Administration route: Oral
    Indication: Nerve Injury
    Start date: 2007-08-07
    End date: 2007-08-27

Lipitor
    Dosage: 10 mg/day
    Administration route: Oral
    Start date: 2007-08-26

Ludiomil
    Dosage: 10 mg/day
    Administration route: Oral
    Start date: 2007-08-15
    End date: 2007-08-27

PL Gran.
    Dosage: 3 mg/day
    Administration route: Oral
    Start date: 2007-08-22
    End date: 2007-08-24

PL Gran.
    Dosage: 3 g/day
    Administration route: Oral
    Start date: 2007-08-28
    End date: 2007-08-29

Mexitil
    Dosage: 300 mg/day
    Administration route: Oral
    Indication: Nerve Injury
    Start date: 2007-07-20
    End date: 2007-08-27

Diovan
    Dosage: 20 mg/day
    Administration route: Oral
    Start date: 2007-07-22
    End date: 2007-08-27

Melbin
    Dosage: 500 mg/day
    Administration route: Oral
    Start date: 2007-08-10
    End date: 2007-08-27



Adverse event in 82 year old female receiving Diovan (Valsartan)

Reported by a physician from Japan on 2007-10-18

Patient: 82 year old female

Adverse reactions / side effects: Gastrointestinal Haemorrhage, Anaemia, Faeces Discoloured

Adverse event resulted in: hospitalization

Suspect drug(s):
Diovan
    Dosage: 20 mg/day
    Administration route: Oral
    Indication: Hypertension
    Start date: 2007-09-20
    End date: 2007-09-26

Diovan
    Start date: 2007-09-27
    End date: 2007-10-08

Other drugs received by patient: Amlodipine; Salobel; Magmitt; Tazin; Transamin; Rhythmy; MS Onshippu



Adverse event in 77 year old female receiving Diovan (Valsartan)

Reported by a individual with unspecified qualification from United States on 2007-10-18

Patient: 77 year old female, weighing 67.6 kg (148.7 pounds)

Adverse reactions / side effects: Weight Decreased, Abdominal Pain, Gastrointestinal Haemorrhage, Autoimmune Hepatitis, Blood Albumin Decreased, Bloody Airway Discharge, Oedema Peripheral, Paracentesis, Blood Test Abnormal, Hepatic Cirrhosis, Iron Binding Capacity Total Decreased, Blood Alkaline Phosphatase Increased, Biliary Fibrosis, Bursitis, Tremor, Aspartate Aminotransferase Increased, Cholecystectomy, Portal Hypertension, Jaundice, Acid Fast Stain Positive, Dyslipidaemia, General Physical Condition Abnormal, Brain Natriuretic Peptide Decreased, Blood Thyroid Stimulating Hormone Abnormal, Disease Progression, Hepatitis B Antibody Abnormal, International Normalised Ratio Decreased, Blood Bilirubin Abnormal, Pleural Effusion, Oedema, Abdominal Distension, Gastrooesophageal Reflux Disease, Decreased Appetite, Dyspnoea, Cataract, Vomiting, Alanine Aminotransferase Increased, Biopsy Liver Abnormal, Ascites, Hepatic Enzyme Increased, Hypertension

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Diovan (Valsartan)

Other drugs received by patient: Ranitidine HCL; Allegra; Fosamax; Calcium; Atarax; Ambien; Lasix; Librium; Imuran; Prednisone; Aldactone; Aldactone; Lactulose; Esomeprazole; Stool Softener



Adverse event in 50 year old male receiving Diovan (Valsartan)

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

Patient: 50 year old male

Adverse reactions / side effects: Angioedema, Drug Interaction, Swollen Tongue

Adverse event resulted in: hospitalization

Suspect drug(s):
Diovan
    Dosage: unk, unk
    Start date: 2007-07-01
    End date: 2007-07-25

Avonex
    Dosage: 30mcg, qw



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