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Index of reports
> Cases resulting in a serious event (175)
Below is the selection of adverse event reports related to Altace (Ramipril) that includes cases resulting in a serious event.
Reports 1 - 25 of 175 Next >>
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
Simvastatin
Dosage: 40 mg, qd
Administration route: Oral
Indication: Hypercholesterolaemia
Clozapine
Administration route: Oral
Zaponex
Administration route: Oral
Other drugs received by patient: Amisulpride; Atenolol; Aspirin
Adverse event in male receiving Altace (Ramipril)
Reported by a consumer/non-health professional from United States on 2007-10-24
Patient: male
Adverse reactions / side effects: Tooth Fracture
Suspect drug(s):
Altace
Administration route: Oral
Indication: Cardiac Pacemaker Insertion
Start date: 2006-02-17
Plavix
Administration route: Oral
Indication: Cardiac Pacemaker Insertion
Start date: 2006-02-17
End date: 2006-06-05
Other drugs received by patient: Aspirin; Coreg
Adverse event in receiving Altace (Ramipril)
Reported by a consumer/non-health professional from United States on 2007-10-23
Patient:
Adverse reactions / side effects: Macular Degeneration
Suspect drug(s):
Altace (Ramipril)
Adverse event in receiving Altace (Ramipril)
Reported by a physician from Argentina on 2007-10-23
Patient:
Adverse reactions / side effects: Productive Cough, Syncope, Fall, Lung Infiltration, Face Injury, Infection
Suspect drug(s):
Altace
Indication: Hypertension
Start date: 2007-07-19
Felodipine
Indication: Hypertension
Start date: 2007-07-19
Other drugs received by patient: Clarithromycin
Adverse event in receiving Altace (Ramipril)
Reported by a pharmacist from Germany on 2007-10-22
Patient:
Adverse reactions / side effects: Drug Exposure During Pregnancy, Congenital Anomaly
Suspect drug(s):
Altace (Ramipril)
Adverse event in receiving Altace (Ramipril)
Reported by a consumer/non-health professional from France on 2007-10-22
Patient:
Adverse reactions / side effects: Cryptogenic Organising Pneumonia, Dyspnoea, Eosinophilic Pneumonia, Bronchomalacia, Asthenia, Cough
Adverse event resulted in: hospitalization
Suspect drug(s):
Altace
Dosage: 5 mg, qd
Administration route: Oral
Indication: Hypertension
Start date: 2006-11-15
End date: 2007-01-15
Tenormin
Dosage: 1 u, qd
Administration route: Oral
Start date: 2006-11-15
End date: 2007-06-13
Kardegic / 00002703 /
Dosage: 160 mg, qd
Administration route: Oral
Indication: Prophylaxis
Start date: 2006-11-15
Tahor
Dosage: 80 mg, qd
Administration route: Oral
Start date: 2006-11-15
Plavix
Dosage: 75 mg, qd
Administration route: Oral
Indication: Prophylaxis
Start date: 2006-11-15
End date: 2007-01-15
Adverse event in receiving Altace (Ramipril)
Reported by a consumer/non-health professional from United States on 2007-10-22
Patient:
Adverse reactions / side effects: Cardiac Failure
Adverse event resulted in: hospitalization
Suspect drug(s):
Altace
Dosage: 5 mg, qd
Administration route: Oral
Indication: Cardiac Failure
Start date: 2007-07-10
Metoprolol Succinate
Dosage: 100 mg, qd
Administration route: Oral
Indication: Cardiac Failure
Start date: 2007-07-10
Other drugs received by patient: Trombyl; Simvastatin
Adverse event in 59 year old male receiving Altace (Ramipril)
Reported by a health professional (non-physician/pharmacist) from Canada on 2007-10-19
Patient: 59 year old male
Adverse reactions / side effects: Angioedema, Face Oedema, Dysphonia, Tongue Oedema, Cardiac Disorder
Suspect drug(s):
Crestor
Administration route: Oral
Altace
Administration route: Oral
Other drugs received by patient: Adalat CC; Aspirin; Calcium; Vitamin D; Multi-Vitamins; Doxepin Hydrochloride; Hydrodiuril; Plavix
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 2007-10-18
Patient:
Adverse reactions / side effects: HIP Fracture, Fall, Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Altace
Dosage: 1.25 mg, qd
Administration route: Oral
Indication: Hypertension
End date: 2007-06-18
Burinex
Dosage: 5 mg, qd
Administration route: Oral
Indication: Cardiac Failure
End date: 2007-06-18
Adverse event in receiving Altace (Ramipril)
Reported by a consumer/non-health professional from France on 2007-10-17
Patient:
Adverse reactions / side effects: Drug Exposure During Pregnancy, Ventricular Septal Defect
Suspect drug(s):
Altace
Dosage: 2.5 mg, qd
Administration route: Oral
Indication: Hypertension
End date: 2007-01-01
Levemir
Dosage: 90 iu, qd
Indication: Diabetes Mellitus
End date: 2007-01-01
Adverse event in receiving Altace (Ramipril)
Reported by a consumer/non-health professional from France on 2007-10-17
Patient:
Adverse reactions / side effects: Hypotension, Rectal Haemorrhage, Gastric Ulcer
Adverse event resulted in: hospitalization
Suspect drug(s):
Altace
Dosage: 1 u, qd
Administration route: Oral
Indication: Hypertension
Lasix
Dosage: 40 mg, qd
Administration route: Oral
Indication: Cardiac Failure
Previscan / 00789001 /
Dosage: 25 mg, qd
Administration route: Oral
Indication: Thrombosis
End date: 2006-10-13
Previscan / 00789001 /
Start date: 2006-10-15
Aldactone
Dosage: 1 u film-coated tablet
Administration route: Oral
Indication: Cardiac Failure
Elisor
Dosage: 1 u tablet,qd
Administration route: Oral
Indication: Hypercholesterolaemia
Adverse event in receiving Altace (Ramipril)
Reported by a consumer/non-health professional from United States on 2007-10-17
Patient:
Adverse reactions / side effects: Blood Pressure Increased, Malaise, Diarrhoea, Dyspepsia, Dizziness, Asthenia
Suspect drug(s):
Altace
Dosage: 6.25 mg, qd
Administration route: Oral
Indication: Blood Pressure
Start date: 2007-09-17
End date: 2007-09-18
Altace
Dosage: 7.5 mg, qd
Administration route: Oral
Altace
Dosage: 5 mg, qd
Administration route: Oral
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 France on 2007-10-15
Patient:
Adverse reactions / side effects: Blood Alkaline Phosphatase Increased, Jaundice, Scratch, Pruritus, Alanine Aminotransferase Increased, Impetigo, Glomerulonephritis Membranous, Hepatitis Cholestatic, Gamma-Glutamyltransferase Increased, Aspartate Aminotransferase Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Altace
Dosage: unk, qd
Administration route: Oral
Start date: 2006-06-15
End date: 2007-06-10
Chloraminophene
Dosage: 12 mg, qd
Administration route: Oral
Indication: Glomerulonephritis
Start date: 2007-02-15
End date: 2007-03-15
Tahor
Dosage: 20 mg, unk
Administration route: Oral
Start date: 2006-06-15
End date: 2007-06-10
Effexor / 01233802 /
Dosage: unk, qd
Start date: 2006-06-15
End date: 2007-06-10
Other drugs received by patient: Aldactone; Lasix; Levothyrox
Adverse event in receiving Altace (Ramipril)
Reported by a physician from Russian Federation on 2007-10-11
Patient:
Adverse reactions / side effects: Pain in Extremity, Intermittent Claudication
Adverse event resulted in: hospitalization
Suspect drug(s):
Altace (Ramipril)
Other drugs received by patient: Crestor
Adverse event in receiving Altace (Ramipril)
Reported by a consumer/non-health professional from United Kingdom on 2007-10-10
Patient:
Adverse reactions / side effects: Dysphagia, Oropharyngeal Swelling, Rhinitis
Suspect drug(s):
Altace (Ramipril)
Other drugs received by patient: Adcal-D3; Aspirin; Atenolol; Atenolol; Glyceryl Trinitrate; Prednisolone; Rabeprazole Sodium; Simvastatin; Strontium Ranelate
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 United Kingdom on 2007-10-09
Patient:
Adverse reactions / side effects: Drug Interaction, Somnolence
Suspect drug(s):
Altace
Dosage: 10 mg, qd
Administration route: Oral
Indication: Blood Pressure Increased
Start date: 2007-06-26
Amlodipine
Dosage: 5 mg, qd
Administration route: Oral
Indication: Blood Pressure Increased
Start date: 2007-08-17
End date: 2007-09-06
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
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
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
Other drugs received by patient: Atorvastatin Calcium; Aspirin
Adverse event in receiving Altace (Ramipril)
Reported by a consumer/non-health professional from France on 2007-10-05
Patient:
Adverse reactions / side effects: Phlebitis, Pulmonary Embolism, Deep Vein Thrombosis
Adverse event resulted in: hospitalization
Suspect drug(s):
Altace
Dosage: 1.25 mg, qd
Administration route: Oral
Indication: Nephrotic Syndrome
Lasix
Dosage: unk, qd
Administration route: Oral
Indication: Nephrotic Syndrome
Thalidomide
Dosage: 200 mg, qd
Administration route: Oral
Indication: Multiple Myeloma
Aldactone
Dosage: 75 mg, qd
Administration route: Oral
Indication: Nephrotic Syndrome
Other drugs received by patient: Alkeran; Dexamethasone 0.5mg TAB; Previscan / 00789001 /
Adverse event in receiving Altace (Ramipril)
Reported by a physician from Ireland on 2007-10-05
Patient:
Adverse reactions / side effects: Skin Exfoliation
Suspect drug(s):
Altace (Ramipril)
Other drugs received by patient: Epanutin / 00017402 /; Tegretol; Lipitor
Adverse event in receiving Altace (Ramipril)
Reported by a consumer/non-health professional from Belgium on 2007-10-04
Patient:
Adverse reactions / side effects: Epididymitis, Vasculitis, Diffuse Vasculitis, Purpura, Lung Infiltration
Suspect drug(s):
Altace (Ramipril)
Adverse event in receiving Altace (Ramipril)
Reported by a physician from Argentina on 2007-10-04
Patient:
Adverse reactions / side effects: Syncope, Fall, Cough, Face Injury
Suspect drug(s):
Altace
Indication: Hypertension
Start date: 2007-07-19
Felodipine
Indication: Hypertension
Start date: 2007-07-19
Other drugs received by patient: Clarithromycin
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):
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
Asacol
Administration route: Oral
Indication: Inflammatory Bowel Disease
Start date: 2007-05-01
Altace
Administration route: Oral
Indication: Thrombosis Prophylaxis
Start date: 2007-05-01
Other drugs received by patient: Aspirin; Lipitor
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