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Cozaar (Losartan) - Adverse Event Reports - Life Threatening Events

 



Index of reports > Cases resulting in life threatening events (27)

     Chest Pain (4)Renal Failure Acute (4)Dyspnoea (3)Atrial Fibrillation (3)Metastases TO Lymph Nodes (3)Neuroendocrine Carcinoma of THE Skin (3)Cardiac Failure Congestive (3)Coronary Artery Disease (2)Hypoglycaemic Coma (2)Toxic Skin Eruption (2)

Below is the selection of adverse event reports related to Cozaar (Losartan) that includes cases resulting in life threatening events.

 Reports 1 - 25 of 27   Next >>

Adverse event in 66 year old female receiving Cozaar (Losartan)

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

Patient: 66 year old female

Adverse reactions / side effects: Subarachnoid Haemorrhage

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Cozaar
    Administration route: Oral
    Indication: Hypertension
    Start date: 2006-11-01
    End date: 2007-01-23

Cozaar
    Administration route: Oral
    Start date: 2007-01-24

Other drugs received by patient: Rosuvastatin Calcium; Paroxetine Hydrochloride



Adverse event in 56 year old female receiving Cozaar (Losartan)

Reported by a physician from Norway on 2007-10-24

Patient: 56 year old female

Adverse reactions / side effects: Dyspnoea, Hyponatraemia, Obstructive Airways Disorder, Generalised Oedema

Adverse event resulted in: life threatening event

Suspect drug(s):
Ibux
    Indication: Arthralgia
    Start date: 2007-08-01

Naproxen
    Administration route: Oral
    Indication: Arthralgia

Cozaar
    Dosage: 1 df, qd
    Administration route: Oral
    Indication: Hypertension

Diural
    Dosage: 40 mg, qd
    Administration route: Oral
    Indication: Oedema
    Start date: 2007-08-28

Brexidol
    Administration route: Oral
    Indication: Arthralgia

Voltaren
    Dosage: 50 mg, tid
    Administration route: Oral
    Indication: Arthralgia
    Start date: 2007-08-01

Other drugs received by patient: Pinex Forte; Doxylin; Vival; Noni Juice; Pinex; Fenazon-Koffein



Adverse event in 17 year old male receiving Cozaar (Losartan)

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

Patient: 17 year old male, weighing 77.6 kg (170.6 pounds)

Adverse reactions / side effects: Movement Disorder, Dyspnoea, Abasia, Hypoaesthesia, Fall, Convulsion, Pulse Absent, Unevaluable Event, Cardiac Arrest, Asthenia

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Cozaar (Losartan)



Adverse event in 64 year old female receiving Cozaar (Losartan)

Reported by a physician from Japan on 2007-10-01

Patient: 64 year old female, weighing 44.0 kg (96.8 pounds)

Adverse reactions / side effects: Hepatic Function Abnormal, Blood Creatine Phosphokinase Increased, Pericarditis, Platelet Count Decreased

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Cozaar
    Administration route: Oral
    End date: 2007-07-19

Cilostazol
    Administration route: Oral
    End date: 2007-07-19

Adalat
    Administration route: Oral
    End date: 2007-07-19

Renagel
    Administration route: Oral
    End date: 2007-07-19

Caltan
    Administration route: Oral
    End date: 2007-07-19

Other drugs received by patient: [therapy Unspecified]; Predonine; Predonine; Predonine



Adverse event in 78 year old female receiving Cozaar (Losartan)

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

Patient: 78 year old female

Adverse reactions / side effects: Hypoglycaemic Coma

Adverse event resulted in: life threatening event

Suspect drug(s):
Cozaar (Losartan)

Other drugs received by patient: Amaryl; Basen; Melbin; Lasix; Aldactone; Amlodipine; Depas; Guanabenz Acetate; Ticlopidine Hydrochloride; Halcion; Levoglutamide and Sodium Gualenate; Magnesium Oxide; Loxonin; Mucosta; Myonal; Prodif



Adverse event in 78 year old female receiving Cozaar (Losartan)

Reported by a physician from Japan on 2007-07-19

Patient: 78 year old female

Adverse reactions / side effects: Hypoglycaemic Coma

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Cozaar (Losartan)

Other drugs received by patient: Amaryl; Basen; Melbin; Lasix; Aldactone; Amlodipine; Depas; Guanabenz Acetate; Ticlopidine Hydrochloride; Halcion; Levoglutamide and Sodium Gualenate; Magnesium Oxide; Loxonin; Mucosta; Myonal; Prodif



Adverse event in 88 year old female receiving Cozaar (Losartan)

Reported by a physician from Japan on 2007-07-13

Patient: 88 year old female, weighing 42.0 kg (92.4 pounds)

Adverse reactions / side effects: Renal Failure Acute, Toxic Skin Eruption

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Cozaar
    Administration route: Oral
    Indication: Cardiac Failure Chronic
    Start date: 2007-06-01
    End date: 2007-06-03

Cozaar
    Administration route: Oral
    Indication: Mitral Valve Incompetence
    Start date: 2007-06-01
    End date: 2007-06-03

Allopurinol
    Administration route: Oral
    Indication: Hyperuricaemia
    Start date: 2007-05-29
    End date: 2007-06-03

Pepcid RPD
    Administration route: Oral
    Indication: Gastritis
    End date: 2007-06-03

Other drugs received by patient: Aricept; Natrix; Aldactone; Pletal; Lasix; Levofloxacin



Adverse event in 88 year old female receiving Cozaar (Losartan)

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

Patient: 88 year old female, weighing 42.0 kg (92.4 pounds)

Adverse reactions / side effects: Renal Failure Acute, Toxic Skin Eruption

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Cozaar
    Administration route: Oral
    Indication: Cardiac Failure Chronic
    Start date: 2007-06-01
    End date: 2007-06-03

Cozaar
    Administration route: Oral
    Indication: Mitral Valve Incompetence
    Start date: 2007-06-01
    End date: 2007-06-03

Allopurinol
    Administration route: Oral
    Indication: Hyperuricaemia
    Start date: 2007-05-29
    End date: 2007-06-03

Pepcid RPD
    Administration route: Oral
    Indication: Gastritis
    End date: 2007-06-03

Other drugs received by patient: Aricept; Natrix; Aldactone; Pletal; Lasix; Levofloxacin



Adverse event in 80 year old male receiving Cozaar (Losartan)

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-07-05

Patient: 80 year old male

Adverse reactions / side effects: Haemoglobin Decreased, Malaise, C-Reactive Protein Increased, Alpha-1 Acid Glycoprotein Increased, RED Blood Cell Sedimentation Rate Increased

Adverse event resulted in: life threatening event, disablity

Suspect drug(s):
Cozaar (Losartan)

Other drugs received by patient: Simvastatin; Simvastatin



Adverse event in 76 year old male receiving Cozaar (Losartan)

Reported by a individual with unspecified qualification from Philippines on 2007-06-15

Patient: 76 year old male

Adverse reactions / side effects: Oral Intake Reduced, Gastrointestinal Haemorrhage, Hepatic Failure, Pyrexia, Multi-Organ Failure, Hepatic Encephalopathy, Cyanosis, Chest Pain, Ischaemic Hepatitis, Cardiac Failure Congestive, Respiratory Rate Increased, Hypotension, General Physical Health Deterioration, Atrial Fibrillation, Blood Glucose Decreased, Sepsis, Heart Rate Increased, Central Nervous System Infection

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

Suspect drug(s):
Cozaar (Losartan)

Other drugs received by patient: Furosemide; Isosorbide Mononitrate



Adverse event in 46 year old female receiving Cozaar (Losartan)

Reported by a physician from United States on 2007-05-24

Patient: 46 year old female, weighing 95.3 kg (209.6 pounds)

Adverse reactions / side effects: Anaphylactic Reaction

Adverse event resulted in: life threatening event, disablity

Suspect drug(s):
Amlodipine
    Dosage: 1 tab daily po
    Administration route: Oral
    Indication: Hypertension
    Start date: 2007-05-07
    End date: 2007-05-07

Cozaar
    Dosage: 1 tab daily po
    Administration route: Oral
    Indication: Hypertension



Adverse event in 80 year old female receiving Cozaar (Losartan)

Reported by a individual with unspecified qualification from Brazil on 2007-04-24

Patient: 80 year old female

Adverse reactions / side effects: Neuroendocrine Carcinoma of THE Skin, Metastases TO Lymph Nodes

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Cozaar (Losartan)

Other drugs received by patient: Amlodipine Besylate; Carvedilol; Digoxin; Furosemide; Pantoprazole



Adverse event in 80 year old female receiving Cozaar (Losartan)

Reported by a individual with unspecified qualification from Brazil on 2007-04-09

Patient: 80 year old female

Adverse reactions / side effects: Neuroendocrine Carcinoma of THE Skin, Metastases TO Lymph Nodes

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Cozaar (Losartan)

Other drugs received by patient: Amlodipine Besylate; Carvedilol; Digoxin; Furosemide; Pantoprazole



Adverse event in 80 year old female receiving Cozaar (Losartan)

Reported by a individual with unspecified qualification from Brazil on 2007-04-03

Patient: 80 year old female

Adverse reactions / side effects: Neuroendocrine Carcinoma of THE Skin, Metastases TO Lymph Nodes

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Cozaar (Losartan)

Other drugs received by patient: Amlodipine; Carvedilol; Digoxin; Furosemide; Pantoprazole



Adverse event in male receiving Cozaar (Losartan)

Reported by a individual with unspecified qualification on 2007-04-02

Patient: male, weighing 3.2 kg (7.2 pounds)

Adverse reactions / side effects: Sacral Hypoplasia, Urinoma, Multiple Congenital Abnormalities, Renal Aplasia, Ventricular Septal Defect, Anal Atresia, Heart Disease Congenital

Adverse event resulted in: life threatening event, disablity

Suspect drug(s):
Lasilix / 00032601 /
    Indication: Drug USE FOR Unknown Indication

Cozaar
    Administration route: Oral
    Indication: Cardiomyopathy

Digoxin
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication



Adverse event in male receiving Cozaar (Losartan)

Reported by a health professional (non-physician/pharmacist) from France on 2007-03-29

Patient: male, weighing 3.0 kg (6.6 pounds)

Adverse reactions / side effects: Oligohydramnios, Hypertrophic Cardiomyopathy, Urinoma, Multiple Congenital Abnormalities, Ventricular Septal Defect, Spine Malformation, Anorectal Disorder, Renal Aplasia, Anal Atresia

Adverse event resulted in: life threatening event

Suspect drug(s):
Cozaar
    Indication: Congestive Cardiomyopathy

Furosemide
    Indication: Congestive Cardiomyopathy

Digoxin
    Indication: Congestive Cardiomyopathy



Adverse event in 81 year old female receiving Cozaar (Losartan)

Reported by a physician from Belgium on 2007-03-22

Patient: 81 year old female

Adverse reactions / side effects: Atrial Fibrillation, Cardiac Failure Congestive

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Cozaar
    Administration route: Oral
    Indication: Hypertension
    Start date: 2005-03-24

Sotalol Hydrochloride
    Administration route: Oral
    Start date: 2000-04-03
    End date: 2006-07-13

Propafenone Hydrochloride
    Administration route: Oral
    Start date: 2000-04-03
    End date: 2006-07-13

Other drugs received by patient: Nebivolol Hydrochloride; Lercanidipine Hydrochloride; Otilonium Bromide; Alendronate Sodium; Bromazepam



Adverse event in 86 year old female receiving Cozaar (Losartan)

Reported by a physician from Japan on 2007-03-16

Patient: 86 year old female

Adverse reactions / side effects: Hyperkalaemia

Adverse event resulted in: death, life threatening event

Suspect drug(s):
Cozaar
    Administration route: Oral
    Indication: Hypertension
    Start date: 2006-08-03
    End date: 2007-02-07

Aldactone
    Administration route: Oral
    Indication: Cardiac Failure
    Start date: 2004-04-07
    End date: 2007-02-07

Other drugs received by patient: Lasix; Takepron; Lendormin; Zolpidem Tartrate; Pursennid; Argamate Jelly



Adverse event in 60 year old male receiving Cozaar (Losartan)

Reported by a physician from Canada on 2007-03-15

Patient: 60 year old male

Adverse reactions / side effects: Chest Pain, Coronary Artery Disease

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Cozaar
    Administration route: Oral
    Indication: Hypertension
    Start date: 2006-02-25
    End date: 2006-04-23

Cozaar
    Administration route: Oral
    Start date: 2006-04-24
    End date: 2006-05-22

Cozaar
    Administration route: Oral
    Start date: 2006-05-23
    End date: 2007-02-17

Hyzaar
    Administration route: Oral
    Indication: Hypertension
    Start date: 2006-05-23
    End date: 2007-02-17

Other drugs received by patient: Micardis; Adalat; Lipidil; Rhinalar



Adverse event in 60 year old male receiving Cozaar (Losartan)

Reported by a physician from Canada on 2007-03-14

Patient: 60 year old male

Adverse reactions / side effects: Chest Pain, Coronary Artery Disease

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Cozaar
    Administration route: Oral
    Indication: Hypertension
    Start date: 2006-02-25
    End date: 2006-04-23

Cozaar
    Administration route: Oral
    Start date: 2006-04-24
    End date: 2006-05-22

Cozaar
    Administration route: Oral
    Start date: 2006-05-23
    End date: 2007-02-17

Hyzaar
    Administration route: Oral
    Indication: Hypertension
    Start date: 2006-05-23
    End date: 2007-02-17

Other drugs received by patient: Micardis; Adalat; Lipidil; Rhinalar



Adverse event in 86 year old female receiving Cozaar (Losartan)

Reported by a physician from Japan on 2007-03-09

Patient: 86 year old female

Adverse reactions / side effects: Hyperkalaemia

Adverse event resulted in: death, life threatening event

Suspect drug(s):
Cozaar
    Administration route: Oral
    Indication: Hypertension
    Start date: 2006-08-03
    End date: 2007-02-07

Aldactone
    Administration route: Oral
    Indication: Cardiac Failure
    Start date: 2004-04-07
    End date: 2007-02-07

Other drugs received by patient: Pursennid; Argamate Jelly; Lasix; Takepron; Lendormin; Zolpidem Tartrate



Adverse event in 49 year old male receiving Cozaar (Losartan)

Reported by a physician from United States on 2007-02-23

Patient: 49 year old male

Adverse reactions / side effects: Rhabdomyolysis, Renal Failure Acute

Adverse event resulted in: life threatening event

Suspect drug(s):
Cozaar (Losartan)

Other drugs received by patient: Lisinopril; Glucophage



Adverse event in 72 year old male receiving Cozaar (Losartan)

Reported by a physician from Belgium on 2007-02-16

Patient: 72 year old male

Adverse reactions / side effects: Ventricular Hypertrophy, Atrial Fibrillation, Cardiac Failure Congestive

Adverse event resulted in: life threatening event, disablity

Suspect drug(s):
Cozaar (Losartan)

Other drugs received by patient: Sotalol HCL; Lasix; Pravastatin Sodium



Adverse event in 81 year old male receiving Cozaar (Losartan)

Reported by a individual with unspecified qualification from Taiwan, Province of China on 2007-02-12

Patient: 81 year old male

Adverse reactions / side effects: Cardiac Enzymes Increased, Chest Pain, Urosepsis, Catheter Site Pain, Septic Shock, Renal Failure Acute

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

Suspect drug(s):
Cozaar (Losartan)

Other drugs received by patient: Carvedilol; Clopidogrel Bisulfate; Furosemide; Glimepiride; Isosorbide Dinitrate



Adverse event in 68 year old female receiving Cozaar (Losartan)

Reported by a physician from Canada on 2007-02-05

Patient: 68 year old female

Adverse reactions / side effects: Cerebrovascular Accident, Cerebral Haemorrhage

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

Suspect drug(s):
Cozaar
    Administration route: Oral
    Indication: Hypertension
    Start date: 2006-09-19
    End date: 2006-11-13

Cozaar
    Administration route: Oral
    Start date: 2006-11-14
    End date: 2006-12-13

Cozaar
    Administration route: Oral
    Start date: 2006-12-14
    End date: 2007-01-29

Other drugs received by patient: Hyzaar; Atorvastatin Calcium; Risedronate Sodium; Calcium (Unspecified) and Vitamin D (Unspecified); Vitamins (Unspecified)



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