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Index of reports
> Cases resulting in a serious event (227)
> Cases with Dyspnoea (11)
Below is the selection of adverse event reports related to Cozaar (Losartan) that includes cases resulting in a serious event where reactions include dyspnoea.
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):
Brexidol
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
Ibux
Indication: Arthralgia
Start date: 2007-08-01
Naproxen
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 25 year old male receiving Cozaar (Losartan)
Reported by a physician from United States on 2007-07-20
Patient: 25 year old male
Adverse reactions / side effects: Dyspnoea, Cardiac Failure
Suspect drug(s):
Cozaar (Losartan)
Adverse event in receiving Cozaar (Losartan)
Reported by a physician from United States on 2007-07-20
Patient:
Adverse reactions / side effects: Dyspnoea, Cardiac Failure, Exercise Tolerance Decreased
Suspect drug(s):
Cozaar (Losartan)
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 34 year old male receiving Cozaar (Losartan)
Reported by a physician from United States on 2007-05-23
Patient: 34 year old male, weighing 86.0 kg (189.2 pounds)
Adverse reactions / side effects: Dyspnoea, Urticaria, Dehydration, Rash
Suspect drug(s):
Cozaar (Losartan)
Other drugs received by patient: Ambien
Adverse event in male receiving Cozaar (Losartan)
Reported by a physician from United States on 2007-05-08
Patient: male, weighing 86.0 kg (189.2 pounds)
Adverse reactions / side effects: Dyspnoea, Urticaria, Dehydration, Rash
Suspect drug(s):
Cozaar (Losartan)
Other drugs received by patient: Ambien
Adverse event in receiving Cozaar (Losartan)
Reported by a consumer/non-health professional from France on 2007-02-05
Patient:
Adverse reactions / side effects: Pulmonary Hypertension, Right Ventricular Failure, Dyspnoea, Hypotension, Electromechanical Dissociation, Renal Failure, Cyanosis, Hypoxia, Hypertension, Shock, Venous Occlusion
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Altace
Dosage: 10 mg, qd
Administration route: Oral
Cellcept
Dosage: 1000 mg, qd
Administration route: Oral
Start date: 2005-07-16
End date: 2006-12-09
Cozaar
Dosage: 1 u, qd
Administration route: Oral
Detensiel / 00802601 /
Dosage: 10 mg, qd
Administration route: Oral
Lercan
Dosage: 1 u, qd
Administration route: Oral
End date: 2006-12-09
Rapamune
Dosage: 4 mg, qd
Administration route: Oral
End date: 2006-12-09
Other drugs received by patient: Luteran
Adverse event in 77 year old male receiving Cozaar (Losartan)
Reported by a health professional (non-physician/pharmacist) from Germany on 2007-01-26
Patient: 77 year old male, weighing 95.0 kg (209.0 pounds)
Adverse reactions / side effects: Chest Discomfort, Dyspnoea, Atrial Flutter
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Cozaar
Administration route: Oral
Indication: Hypertension
Start date: 2001-01-01
Sildenafil Citrate
Administration route: Oral
Indication: Pulmonary Hypertension
Start date: 2006-09-13
End date: 2006-09-15
Other drugs received by patient: Nebivolol Hydrochloride; Nebivolol Hydrochloride
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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