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

 



Index of reports > Cases resulting in life threatening events (27) > Cases with Dyspnoea (3)

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

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