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Index of reports
> Cases resulting in other serious reactions (69)
> Cases with Oedema Peripheral (6)
Below is the selection of adverse event reports related to Altace (Ramipril) that includes cases resulting in other serious reactions where reactions include oedema peripheral.
Adverse event in receiving Altace (Ramipril)
Reported by a consumer/non-health professional from United Kingdom on 2007-10-18
Patient:
Adverse reactions / side effects: Tinnitus, Arthralgia, Oedema Peripheral, Feeling of Body Temperature Change, Paraesthesia
Suspect drug(s):
Altace (Ramipril)
Other drugs received by patient: Istin; Ranitidine HCL
Adverse event in receiving Altace (Ramipril)
Reported by a consumer/non-health professional from United States on 2007-10-05
Patient:
Adverse reactions / side effects: Inappropriate Schedule of Drug Administration, Headache, Disorientation, Hypoaesthesia, Amnesia, Dyspnoea Exertional, Chest Pain, Oedema Peripheral, Hypoaesthesia Facial, Disturbance in Attention
Suspect drug(s):
Altace
Dosage: 5 mg, qd
Administration route: Oral
Start date: 2007-05-01
Asacol
Dosage: 400 mg, bid
Administration route: Oral
Indication: Inflammatory Bowel Disease
Start date: 2007-05-01
Nexium
Dosage: 40 mg, qd
Administration route: Oral
Indication: Reflux Oesophagitis
Start date: 2007-05-01
Plavix
Dosage: 75 mg, qd
Administration route: Oral
Start date: 2005-09-01
End date: 2007-04-01
Plavix
Dosage: 75 mg, qd
Administration route: Oral
Start date: 2007-04-01
Other drugs received by patient: Atorvastatin Calcium; Aspirin
Adverse event in 526 month old male receiving Altace (Ramipril)
Reported by a consumer/non-health professional from United States on 2007-10-02
Patient: 526 month old male, weighing 122.5 kg (269.5 pounds)
Adverse reactions / side effects: Headache, Disorientation, Hypoaesthesia, Accidental Overdose, Amnesia, Dyspnoea Exertional, Chest Pain, Oedema Peripheral, Disturbance in Attention
Suspect drug(s):
Altace
Administration route: Oral
Indication: Thrombosis Prophylaxis
Start date: 2007-05-01
Asacol
Administration route: Oral
Indication: Inflammatory Bowel Disease
Start date: 2007-05-01
Nexium
Administration route: Oral
Indication: Gastrooesophageal Reflux Disease
Start date: 2007-05-01
Plavix
Administration route: Oral
Indication: Ischaemic Heart Disease Prophylaxis
Start date: 2005-09-01
End date: 2007-04-01
Plavix
Administration route: Oral
Start date: 2007-04-01
Other drugs received by patient: Aspirin; Lipitor
Adverse event in receiving Altace (Ramipril)
Reported by a consumer/non-health professional from France on 2007-06-13
Patient:
Adverse reactions / side effects: Eosinophilic Fasciitis, Pain in Extremity, Urticaria, Skin Disorder, Eosinophilia, Synovial Cyst, Myalgia, C-Reactive Protein Increased, Oedema Peripheral, Oedema, Carpal Tunnel Syndrome, Hypergammaglobulinaemia, Inflammation
Suspect drug(s):
Altace (Ramipril)
Adverse event in receiving Altace (Ramipril)
Reported by a consumer/non-health professional from France on 2007-06-05
Patient:
Adverse reactions / side effects: Eosinophilic Fasciitis, Pain in Extremity, Urticaria, Skin Disorder, Eosinophilia, Synovial Cyst, Myalgia, C-Reactive Protein Increased, Oedema Peripheral, Oedema, Carpal Tunnel Syndrome, Hypergammaglobulinaemia, Inflammation
Suspect drug(s):
Altace (Ramipril)
Adverse event in receiving Altace (Ramipril)
Reported by a physician from United Kingdom on 2007-02-20
Patient:
Adverse reactions / side effects: Rhabdomyolysis, Sensory Loss, Lactic Acidosis, Pallor, Partial Seizures, Overdose, Cardio-Respiratory Arrest, Oedema Peripheral, Tachypnoea, Apnoea, Abdominal Pain Lower, Vomiting, Metabolic Acidosis, Pain in Extremity, Hypotension, Compartment Syndrome, Body Temperature Decreased, Blood Lactic Acid Increased, Renal Impairment, Diarrhoea, Dehydration, LEG Amputation
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Alcohol / 00002101 /
Dosage: 500 ml over 4 hours
Altace
Dosage: 35 mg, single
Metformin
Dosage: 56 g, single
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