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Diovan (Valsartan) - Adverse Event Reports - Life Threatening Events - White Blood Cell Count Increased

 



Index of reports > Cases resulting in life threatening events (51) > Cases with White Blood Cell Count Increased (12)

Below is the selection of adverse event reports related to Diovan (Valsartan) that includes cases resulting in life threatening events where reactions include white blood cell count increased.

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 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 35 year old male receiving Diovan (Valsartan)

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-10-09

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):
Artist
    Dosage: 320mg per day
    Administration route: Oral
    Indication: Self Mutilation
    Start date: 2007-08-18
    End date: 2007-08-18

Allopurinol
    Dosage: 32000mg per day
    Administration route: Oral
    Indication: Self Mutilation
    Start date: 2007-08-18
    End date: 2007-08-18

Olmetec
    Dosage: 1480mg per day
    Administration route: Oral
    Indication: Self Mutilation
    Start date: 2007-08-18
    End date: 2007-08-18

Adalat
    Dosage: 1920mg per day
    Administration route: Oral
    Indication: Self Mutilation
    Start date: 2007-08-18
    End date: 2007-08-18

Diovan
    Dosage: 320mg per day
    Administration route: Oral
    Indication: Self Mutilation
    Start date: 2007-08-18
    End date: 2007-08-18



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

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-10-09

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):
Artist
    Dosage: 320mg per day
    Administration route: Oral
    Indication: Self Mutilation
    Start date: 2007-08-18
    End date: 2007-08-18

Allopurinol
    Dosage: 32000mg per day
    Administration route: Oral
    Indication: Self Mutilation
    Start date: 2007-08-18
    End date: 2007-08-18

Olmetec
    Dosage: 1480mg per day
    Administration route: Oral
    Indication: Self Mutilation
    Start date: 2007-08-18
    End date: 2007-08-18

Adalat
    Dosage: 1920mg per day
    Administration route: Oral
    Indication: Self Mutilation
    Start date: 2007-08-18
    End date: 2007-08-18

Diovan
    Dosage: 320mg per day
    Administration route: Oral
    Indication: Self Mutilation
    Start date: 2007-08-18
    End date: 2007-08-18



Adverse event in 79 year old male receiving Diovan (Valsartan)

Reported by a physician from Japan on 2007-07-09

Patient: 79 year old male

Adverse reactions / side effects: Blood Bilirubin Increased, Pyrexia, Liver Disorder, Malaise, Haematocrit Decreased, RED Blood Cell Count Decreased, Gamma-Glutamyltransferase Increased, White Blood Cell Count Increased, Blood Glucose Increased, Lymphocyte Count Decreased, Blood Alkaline Phosphatase Increased, Blood Urea Increased, Pneumonia, Blood Lactate Dehydrogenase Increased, Alanine Aminotransferase Increased, Urine Output Decreased, Haemoglobin Decreased, Aspartate Aminotransferase Increased, Platelet Count Decreased

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Diovan (Valsartan)

Other drugs received by patient: Lendormin; Pariet; Norvasc; Rinderon; Aspirin; Clarithromycin; Rizaben



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

Reported by a individual with unspecified qualification from Japan on 2007-07-02

Patient: 82 year old female, weighing 56.0 kg (123.2 pounds)

Adverse reactions / side effects: Hyperkalaemia, Feeling Cold, Blood Pressure Inadequately Controlled, Sinus Arrest, Blood Creatinine Increased, White Blood Cell Count Increased, Renal Failure Acute, Ventricular Extrasystoles, Blood Urea Increased, Muscular Weakness, Blood Potassium Increased, Blood Bicarbonate Decreased, Computerised Tomogram Abnormal, Tremor, Haemodialysis, Haemoglobin Decreased, Anorexia, Renal Hypertension, Electrocardiogram Abnormal, Bradycardia, Gait Disturbance, Blood Pressure Decreased, Asthenia

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Diovan
    Dosage: 80 mg, qd
    Administration route: Oral
    Indication: Hypertension
    Start date: 2002-12-01

Diovan
    Start date: 2002-12-12
    End date: 2003-01-06

Trandolapril
    Administration route: Oral
    Indication: Hypertension
    Start date: 1982-01-01

Spironolactone
    Dosage: unk, unk
    Administration route: Oral
    Indication: Hypertension
    Start date: 2002-11-01

Odrik
    Dosage: 2 mg/day
    Administration route: Oral
    Indication: Hypertension
    Start date: 1997-11-06
    End date: 2003-01-06

Aldactone
    Dosage: 25 mg/day
    Administration route: Oral
    Indication: Hypertension
    Start date: 2002-11-18
    End date: 2003-01-06

Landel
    Dosage: 60 mg/day
    Administration route: Oral
    Indication: Hypertension
    Start date: 2001-02-27
    End date: 2003-01-06

Landel
    Dosage: 20 mg/day
    Administration route: Oral
    Start date: 2003-01-10

Salobel
    Dosage: 100 mg/day
    Administration route: Oral
    Indication: Hyperuricaemia
    Start date: 1997-02-25
    End date: 2003-01-06

Pimenol
    Dosage: 100 mg/day
    Administration route: Oral
    Indication: Ventricular Arrhythmia
    Start date: 1997-11-06
    End date: 2003-01-06



Adverse event in 51 year old male receiving Diovan (Valsartan)

Reported by a physician from Japan on 2007-06-19

Patient: 51 year old male

Adverse reactions / side effects: Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Toxic Epidermal Necrolysis, Varicella, Mycoplasma Infection, Staphylococcal Infection, NO Therapeutic Response, Hypoalbuminaemia, Dermatitis Exfoliative, White Blood Cell Count Increased, Infection

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Zonisamide
    Dosage: 200 mg, 2 in 1 d, oral
    Administration route: Oral
    Indication: Cerebral Haemorrhage
    Start date: 2007-01-04
    End date: 2007-02-07

Diovan
    Dosage: 1 dosage forms, 1 in 1 d, oral
    Administration route: Oral
    Indication: Hypertension
    Start date: 2006-12-31
    End date: 2007-03-17

Other drugs received by patient: Lansoprazole; NI (Magnesium Oxide); Pursennid (Sennoside) (Senna Leaf)



Adverse event in 51 year old male receiving Diovan (Valsartan)

Reported by a physician from Japan on 2007-05-14

Patient: 51 year old male

Adverse reactions / side effects: Drug Eruption, Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Toxic Epidermal Necrolysis, Pyrexia, White Blood Cell Count Increased

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Zonisamide
    Dosage: 200 mg, 2 in 1 d, oral
    Administration route: Oral
    Indication: Cerebral Haemorrhage
    Start date: 2007-01-04
    End date: 2007-02-07

Diovan
    Dosage: 1 in 1 d, oral
    Administration route: Oral
    Indication: Hypertension
    Start date: 2006-12-31
    End date: 2007-03-17

Other drugs received by patient: Lansoprazole; (Magnesium Oxide) (Magnesium Oxide); Pursennid (Sennoside) (Senna Leaf)



Adverse event in 76 year old male receiving Diovan (Valsartan)

Reported by a pharmacist from Japan on 2007-03-05

Patient: 76 year old male

Adverse reactions / side effects: Choking Sensation, PO2 Decreased, Interstitial Lung Disease, C-Reactive Protein Increased, Palpitations, Tracheostomy, Blood Bicarbonate Increased, Cell Marker Increased, Acute Respiratory Failure, White Blood Cell Count Increased, Oxygen Saturation Decreased, Blood Alkaline Phosphatase Increased, Dyspnoea, Blood Lactate Dehydrogenase Increased, Lung Disorder, Hypertension, Inflammation

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

Suspect drug(s):
Diovan (Valsartan)

Other drugs received by patient: Adalat; Actos; Lasix



Adverse event in 76 year old male receiving Diovan (Valsartan)

Reported by a pharmacist from Japan on 2007-02-27

Patient: 76 year old male

Adverse reactions / side effects: Choking Sensation, PO2 Decreased, Interstitial Lung Disease, C-Reactive Protein Increased, Palpitations, Tracheostomy, Blood Bicarbonate Increased, Cell Marker Increased, Acute Respiratory Failure, White Blood Cell Count Increased, Oxygen Saturation Decreased, Blood Alkaline Phosphatase Increased, Dyspnoea, Blood Lactate Dehydrogenase Increased, Lung Disorder, Hypertension, Inflammation

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

Suspect drug(s):
Diovan (Valsartan)

Other drugs received by patient: Adalat; Actos; Lasix



Adverse event in 76 year old male receiving Diovan (Valsartan)

Reported by a pharmacist from Japan on 2007-02-19

Patient: 76 year old male

Adverse reactions / side effects: Choking Sensation, PO2 Decreased, Interstitial Lung Disease, C-Reactive Protein Increased, Palpitations, Tracheostomy, Blood Bicarbonate Increased, Acute Respiratory Failure, Cell Marker Increased, Oxygen Saturation Decreased, White Blood Cell Count Increased, Blood Alkaline Phosphatase Increased, Dyspnoea, Blood Lactate Dehydrogenase Increased, Lung Disorder, Hypertension, Inflammation

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

Suspect drug(s):
Adalat
    Dosage: 40 mg/ day
    Administration route: Oral
    Indication: Hypertension
    Start date: 2005-08-29
    End date: 2006-10-16

Actos
    Dosage: 15 mg/day
    Administration route: Oral
    Indication: Diabetes Mellitus
    Start date: 2005-08-29
    End date: 2006-10-16

Lasix
    Dosage: 20 mg/day
    Administration route: Oral
    Indication: Hypertension
    Start date: 2005-08-29
    End date: 2006-10-16

Diovan
    Dosage: 80 mg, tid
    Administration route: Oral
    Indication: Hypertension
    Start date: 2005-08-25
    End date: 2006-10-16



Adverse event in 76 year old male receiving Diovan (Valsartan)

Reported by a physician from Japan on 2007-02-12

Patient: 76 year old male

Adverse reactions / side effects: Choking Sensation, PO2 Decreased, Palpitations, Interstitial Lung Disease, Tracheostomy, Blood Bicarbonate Increased, Cell Marker Increased, Acute Respiratory Failure, White Blood Cell Count Increased, Oxygen Saturation Decreased, Blood Alkaline Phosphatase Increased, Dyspnoea, Blood Lactate Dehydrogenase Increased, Lung Disorder, Hypertension, Inflammation

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

Suspect drug(s):
Diovan (Valsartan)

Other drugs received by patient: Adalat; Actos; Lasix

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