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Index of reports
> Cases resulting in disability (18)
> Cases with Dyspnoea (3)
Below is the selection of adverse event reports related to Cozaar (Losartan) that includes cases resulting in disability where reactions include dyspnoea.
Adverse event in 81 year old female receiving Cozaar (Losartan)
Reported by a individual with unspecified qualification from United Kingdom on 2007-06-28
Patient: 81 year old female
Adverse reactions / side effects: Polymyalgia Rheumatica, Dyspnoea, Blood Pressure Systolic Increased, Hypotension, Pyrexia, Renal Impairment, Basal Cell Carcinoma, Dizziness, Inflammation
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Cozaar (Losartan)
Other drugs received by patient: Acetaminophen; Aspirin; Bisoprolol; Codeine Phosphate; Furosemide; Levothyroxine Sodium; Omeprazole; Risedronate Sodium; Senna; Simvastatin; Spironolactone
Adverse event in 72 year old male receiving Cozaar (Losartan)
Reported by a individual with unspecified qualification from United Kingdom on 2007-06-05
Patient: 72 year old male
Adverse reactions / side effects: Dyspnoea, Dilatation Ventricular, Headache, Loss of Consciousness, Ventricular Tachycardia, Ventricular Dysfunction, Left Atrial Dilatation, Dizziness, Scar
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Cozaar
Dosage: po
Administration route: Oral
Indication: Cardiac Failure Congestive
Start date: 2003-10-03
End date: 2007-03-22
Cozaar
Dosage: po
Administration route: Oral
Indication: Cardiac Failure Congestive
Start date: 2007-03-24
Other drugs received by patient: Acetaminophen; Albuterol; Amoxicillin; Aspirin; Beclomethasone Dipropionate; Esomeprazole Magnesium; Ferrousso4; Furosemide; Isosorbide Mononitrate; Nitroglycerin; Simvastatin; Spironolactone
Adverse event in male receiving Cozaar (Losartan)
Reported by a individual with unspecified qualification from United Kingdom on 2007-01-17
Patient: male, weighing 62.0 kg (136.4 pounds)
Adverse reactions / side effects: Dyspnoea, Blood Pressure Systolic Increased, Drug Ineffective, Pain in Extremity, Drug Interaction, Eye Pain, Osteoarthritis, Ventricular Dysfunction, NO Therapeutic Response, Musculoskeletal Stiffness
Adverse event resulted in: disablity
Suspect drug(s):
Allopurinol
Indication: Gout
Cozaar
Dosage: 25 mg, qd, oral
Administration route: Oral
Indication: Ventricular Dysfunction
Start date: 2006-05-19
End date: 2006-08-09
Other drugs received by patient: Aspirin; Lanoxin; Perindopril Erbumine; Ramipril
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