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Captopril (Captopril) - Adverse Event Reports - Disability - Asthenia

 



Index of reports > Cases resulting in disability (3) > Cases with Asthenia (2)

Below is the selection of adverse event reports related to Captopril that includes cases resulting in disability where reactions include asthenia.

Adverse event in male receiving Captopril

Reported by a physician from United States on 2007-06-22

Patient: male, weighing 68.0 kg (149.6 pounds)

Adverse reactions / side effects: Blood Pressure Inadequately Controlled, Dizziness, Gait Disturbance, Asthenia

Adverse event resulted in: disablity

Suspect drug(s):
Norvasc
    Administration route: Oral
    Indication: Hypertension

Norvasc
    Administration route: Oral

Lipitor
    Administration route: Oral
    Indication: Blood Cholesterol Increased
    Start date: 2007-04-10

Captopril
    Indication: Hypertension

Lumigan
    Indication: Glaucoma

Other drugs received by patient: COQ-10 ST



Adverse event in male receiving Captopril

Reported by a consumer/non-health professional from United States on 2007-04-24

Patient: male, weighing 68.0 kg (149.6 pounds)

Adverse reactions / side effects: Gait Disturbance, Asthenia

Adverse event resulted in: disablity

Suspect drug(s):
Norvasc
    Administration route: Oral
    Indication: Hypertension

Norvasc
    Administration route: Oral

Lipitor
    Administration route: Oral
    Indication: Blood Cholesterol Increased
    Start date: 2007-04-10

Captopril
    Indication: Hypertension

Lumigan
    Indication: Glaucoma

Other drugs received by patient: COQ-10 ST

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