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Index of reports
> Cases resulting in life threatening events (18)
> Cases with Renal Failure Acute (4)
Below is the selection of adverse event reports related to Altace (Ramipril) that includes cases resulting in life threatening events where reactions include renal failure acute.
Adverse event in receiving Altace (Ramipril)
Reported by a consumer/non-health professional from Norway on 2007-10-10
Patient:
Adverse reactions / side effects: Hyperkalaemia, Nausea, General Physical Health Deterioration, Acidosis, Abdominal Pain Upper, Blood Glucose Decreased, Dehydration, Renal Failure Acute
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Altace (Ramipril)
Other drugs received by patient: Atrovent; Nexium; Glimepiride; Glucophage; Lipitor; Burinex
Adverse event in receiving Altace (Ramipril)
Reported by a consumer/non-health professional from France on 2007-07-16
Patient:
Adverse reactions / side effects: Hyperkalaemia, Bundle Branch Block Right, Bundle Branch Block Left, Fall, Sinus Bradycardia, Grand MAL Convulsion, Lung Disorder, Malaise, Protein Total Increased, Pulmonary Oedema, Blood Creatinine Increased, Sinoatrial Block, Renal Failure Acute, Anuria
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Altace
Dosage: 2.5 mg, qd
Administration route: Oral
End date: 2007-05-09
Cardensiel
Dosage: 2.5 mg, qd
Administration route: Oral
End date: 2007-05-09
Pravidual
Dosage: 40 mg, qd
Administration route: Oral
End date: 2007-05-09
Other drugs received by patient: Previscan / 00789001 /; Metformin HCL; Lasilix / 00032601 /
Adverse event in 86 year old male receiving Altace (Ramipril)
Reported by a pharmacist from United States on 2007-07-09
Patient: 86 year old male
Adverse reactions / side effects: Endocarditis Bacterial, Post Procedural Complication, Renal Failure Acute
Adverse event resulted in: life threatening event
Suspect drug(s):
Altace
Lisinopril
Adverse event in receiving Altace (Ramipril)
Reported by a consumer/non-health professional from France on 2007-06-21
Patient:
Adverse reactions / side effects: Vomiting, Diarrhoea, General Physical Health Deterioration, Lactic Acidosis, Renal Failure Acute
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Altace
Dosage: 10 mg, qd
Administration route: Oral
End date: 2007-02-27
Glucophage
Dosage: 3000 mg, qd
Administration route: Oral
Indication: Diabetes Mellitus non-Insulin-Dependent
End date: 2007-02-27
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