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Index of reports
> Cases resulting in life threatening events (2)
Below is the selection of adverse event reports related to Vasotec (Enalapril) that includes cases resulting in life threatening events.
Adverse event in 47 year old female receiving Vasotec (Enalapril)
Reported by a consumer/non-health professional from United States on 2007-03-26
Patient: 47 year old female, weighing 108.0 kg (237.5 pounds)
Adverse reactions / side effects: Therapeutic Response Unexpected With Drug Substitution, Condition Aggravated, Blood Pressure Fluctuation, Hypertension, Pharmaceutical Product Complaint, Trigger Finger
Adverse event resulted in: life threatening event
Suspect drug(s):
Vasotec
Dosage: 10 mg q day po
Administration route: Oral
Indication: Hypertension
Start date: 2007-01-22
End date: 2007-03-08
Vasotec
Indication: Hypertension
Enalapril Maleate
Dosage: df
Indication: Hypertension
Start date: 1999-01-01
Vasotec
Dosage: df
Indication: Hypertension
End date: 2007-01-21
Other drugs received by patient: Tenex; Protonix; Claritin-D; Vitamin E; Vitamin D
Adverse event in 61 year old male receiving Vasotec (Enalapril)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-02-23
Patient: 61 year old male
Adverse reactions / side effects: Upper Limb Fracture, Fall
Adverse event resulted in: life threatening event
Suspect drug(s):
Prinivil
Potassium Chloride
Vasotec
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