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Index of reports
> Cases resulting in life threatening events (18)
Below is the selection of adverse event reports related to Altace (Ramipril) that includes cases resulting in life threatening events.
Adverse event in receiving Altace (Ramipril)
Reported by a individual with unspecified qualification from United Kingdom on 2007-10-31
Patient:
Adverse reactions / side effects: Renal Failure, Vomiting, Dehydration, Hypotension, Abdominal Distension, Circulatory Collapse, Pancreatitis
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Altace
Dosage: 10 mg, qd
Administration route: Oral
Indication: Hypertension
Clozapine
Administration route: Oral
Simvastatin
Dosage: 40 mg, qd
Administration route: Oral
Indication: Hypercholesterolaemia
Zaponex
Administration route: Oral
Other drugs received by patient: Amisulpride; Atenolol; Aspirin
Adverse event in receiving Altace (Ramipril)
Reported by a consumer/non-health professional from United Kingdom on 2007-10-15
Patient:
Adverse reactions / side effects: Self-Injurious Ideation
Adverse event resulted in: life threatening event
Suspect drug(s):
Altace (Ramipril)
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
Adverse event in receiving Altace (Ramipril)
Reported by a consumer/non-health professional from France on 2007-06-14
Patient:
Adverse reactions / side effects: Alveolitis, Overdose, Interstitial Lung Disease, Haemoptysis, C-Reactive Protein Increased, Body Temperature Increased, Pleurisy, General Physical Health Deterioration, Inflammation
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Altace
Dosage: 10 mg, qd
Administration route: Oral
Start date: 2006-10-01
End date: 2007-03-27
Cordarone / 00133102 /
Dosage: 100 mg, qd
Administration route: Oral
Start date: 2004-07-01
End date: 2007-03-27
Cosopt / 01419801 /
Indication: Glaucoma
End date: 2007-03-27
Crestor
Dosage: 5 mg, qd
Administration route: Oral
Start date: 2006-10-01
End date: 2007-03-27
Detensiel / 00802601 /
Dosage: 10 mg, qd
Administration route: Oral
Start date: 2006-08-03
End date: 2007-03-27
Other drugs received by patient: Mopral / 00661201 /; Previscan / 00789001 /
Adverse event in receiving Altace (Ramipril)
Reported by a consumer/non-health professional from United States on 2007-06-11
Patient:
Adverse reactions / side effects: Hyperkalaemia, Ventricular Tachycardia, Cardiac Arrest
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Altace
Administration route: Oral
Indication: Prophylaxis
Start date: 2002-04-15
Altace
Potassium Acetate
Adverse event in receiving Altace (Ramipril)
Reported by a physician from Argentina on 2007-05-24
Patient:
Adverse reactions / side effects: Aphasia, Ischaemic Stroke, Paralysis
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Altace
Dosage: unk, qd
Administration route: Oral
Indication: Hypertension
Start date: 2007-04-17
End date: 2007-04-01
Felodipine
Dosage: unk, qd
Administration route: Oral
Indication: Hypertension
Start date: 2007-04-17
End date: 2007-04-01
Other drugs received by patient: Acetylsalicylic Acid SRT; Carvedilol; Statin NOS / 00084401 /
Adverse event in receiving Altace (Ramipril)
Reported by a consumer/non-health professional from United Kingdom on 2007-04-30
Patient:
Adverse reactions / side effects: Skin Ulcer, Oedema, Dermatitis Exfoliative, Dermatitis Psoriasiform, Peripheral Ischaemia
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Altace (Ramipril)
Other drugs received by patient: Amitriptyline Hydrochloride; Aspirin; Atorvastatin Calcium; Bendrofluazide; Bendroflumethiazide; Benzydamine Hydrochloride; Doxazosin Mesylate; Fenofibrate; Fluticasone Propionate; Furosemide; Gaviscon; Glyceryl Trinitrate; Isoket Retard; Lansoprazole; Meloxicam; Metformin HCL; Paracetamol; Prednisolone; Prochlorperazine Maleate; Salbutamol; Salmeterol; Temazepam; Tramadol HCL; Tramadol HCL
Adverse event in receiving Altace (Ramipril)
Reported by a consumer/non-health professional from United States on 2007-03-21
Patient:
Adverse reactions / side effects: Atelectasis, Blood Pressure Increased, Angioedema, Tongue Oedema, Tachycardia, Blood PH Decreased, Acidosis, Blood Bicarbonate Decreased, Asphyxia, Pco2 Increased, Face Oedema, Lung Disorder, Pharyngeal Oedema
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Altace
Dosage: 2.5 mg, qd
Administration route: Oral
Indication: Essential Hypertension
Start date: 2005-12-16
End date: 2006-01-01
Altace
Dosage: 5 mg, qd
Administration route: Oral
Start date: 2006-01-01
End date: 2006-12-01
Other drugs received by patient: Estracyt / 00327002 /; Anafranil; Dicetel / 00505101 /; Seresta; Noctamid; Tahor; Mupiderm
Adverse event in receiving Altace (Ramipril)
Reported by a physician from Canada on 2007-03-05
Patient:
Adverse reactions / side effects: Hypertension
Adverse event resulted in: life threatening event
Suspect drug(s):
Adalat
Dosage: 60 mg, qd
Administration route: Oral
Altace
Dosage: 10 mg, qd
Administration route: Oral
Indapamide
Dosage: 2.5 mg, qd
Administration route: Oral
Investigational Drug
Dosage: 45 mg, qd
Administration route: Oral
Indication: Metastatic Malignant Melanoma
Start date: 2006-11-16
End date: 2006-12-06
Metoprolol Succinate
Dosage: 100 mg, qd
Administration route: Oral
Other drugs received by patient: Enteric Aspirin; Glyburide; Lipitor; Metformin HCL
Adverse event in receiving Altace (Ramipril)
Reported by a physician from Canada on 2007-02-23
Patient:
Adverse reactions / side effects: Angioedema, Face Oedema, Pharyngeal Oedema, Dysphonia, Swollen Tongue, Unevaluable Event
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Altace
Dosage: 10 mg, qd
Administration route: Oral
Indication: Blood Pressure
Start date: 2000-01-01
End date: 2006-07-01
Crestor
Dosage: 20 mg, qd
Administration route: Oral
Indication: Blood Cholesterol Increased
Start date: 2001-01-01
End date: 2006-12-03
Other drugs received by patient: Aspirin; Multi-Vitamins; Calcium Citrate W / Vitamin D NOS; Hydrodiuril; Plavix; Adalat; Doxepin HCL; Epipen
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
Adverse event in receiving Altace (Ramipril)
Reported by a consumer/non-health professional from United States on 2007-02-15
Patient:
Adverse reactions / side effects: Suicidal Ideation
Adverse event resulted in: life threatening event
Suspect drug(s):
Altace (Ramipril)
Other drugs received by patient: Dyazide; Zocor; Reactine / 00884301 /
Adverse event in receiving Altace (Ramipril)
Reported by a physician from Canada on 2007-02-01
Patient:
Adverse reactions / side effects: Angioedema, Face Oedema, Pharyngeal Oedema, Dysphonia, Swollen Tongue
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Altace
Dosage: 10 mg, qd
Administration route: Oral
Indication: Blood Pressure
Start date: 2000-01-01
End date: 2006-07-01
Crestor
Dosage: 20 mg, qd
Administration route: Oral
Indication: Blood Cholesterol Increased
Start date: 2001-01-01
End date: 2006-12-03
Other drugs received by patient: Aspirin; Multi-Vitamins; Calcium Citrate W / Vitamin D NOS; Hydrodiuril
Adverse event in receiving Altace (Ramipril)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-01-31
Patient:
Adverse reactions / side effects: Transplant Failure, Kidney Transplant Rejection, Haemodialysis, Therapeutic Response Decreased, Cardio-Respiratory Arrest, Impaired Healing, Aplastic Anaemia, Carnitine Decreased, LEG Amputation, Thrombocytopenia, Leukopenia
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Altace
Dosage: unk, unk
End date: 2006-05-01
Aspirin
Start date: 2004-11-01
End date: 2006-05-01
Clopidogrel Bisulfate
End date: 2006-05-01
Epogen
Dosage: unk, unk
Indication: Dialysis
Epogen
Dosage: 33300 iu, tiw
Start date: 2004-11-05
End date: 2006-05-01
Epogen
Dosage: 20000 iu, tiw
Start date: 2006-12-22
Heparin
End date: 2006-05-01
Quinine
End date: 2006-05-01
Other drugs received by patient: Zolpidem Tartrate; Carvedilol; Vitamins; Insulin; Atorvastatin Calcium; Lorazepam; Prednisone; Sevelamer Hydrochloride; Sinemet; Tums / 00108001 /; Azathioprine; Cyclosporine
Adverse event in 50 year old female receiving Altace (Ramipril)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-01-25
Patient: 50 year old female, weighing 76.7 kg (168.6 pounds)
Adverse reactions / side effects: Hypersensitivity, Chest Pain, Abdominal Pain Upper
Adverse event resulted in: life threatening event
Suspect drug(s):
Altace (Ramipril)
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