|
Index of reports
> Cases resulting in disability (2)
Below is the selection of adverse event reports related to Vasotec (Enalapril) that includes cases resulting in disability.
Adverse event in male receiving Vasotec (Enalapril)
Reported by a individual with unspecified qualification from United States on 2007-07-06
Patient: male, weighing 104.3 kg (229.5 pounds)
Adverse reactions / side effects: Dyspnoea, Hypoglycaemia, Irritability, Malaise, Disease Recurrence, Sinus Headache, Heart Rate Increased, Tension, Asthenia, Pharmaceutical Product Complaint
Adverse event resulted in: disablity
Suspect drug(s):
Vasotec
Dosage: (20 mg bid oral)
Administration route: Oral
Indication: Blood Pressure Increased
Start date: 2007-06-13
End date: 2007-06-15
Vasotec
Dosage: (df)
End date: 2007-06-12
Vasotec
Dosage: (20 mg bid oral)
Administration route: Oral
Indication: Blood Pressure Increased
Start date: 2007-06-13
End date: 2007-06-16
Vasotec
Dosage: (df)
Start date: 2007-06-01
Adverse event in 44 year old female receiving Vasotec (Enalapril)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-02-20
Patient: 44 year old female
Adverse reactions / side effects: Night Sweats, Nasopharyngitis, Pyrexia, Postnasal Drip, Oedema Peripheral, Dizziness, Depression, Cough, Swelling Face, Hypotension, Amnesia, Flushing, Rhinitis Allergic, Mental Disorder, Vision Blurred, Libido Increased, Feeling Abnormal
Adverse event resulted in: disablity
Suspect drug(s):
Vasotec (Enalapril)
Other drugs received by patient: Procardia; Other Unspecified Medication
|
