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This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Altace (Ramipril). Click on the relevant link below to view a selection of reports according to the event's seriousness level and/or the nature of the side effect / adverse reaction. Or scroll down to view a sample of recent reports further on this page.
Our database includes reports from Jan 2007 to Dec 2007. The information is not vetted and should not be cosidered as verified clinical evidence.
All cases (182)
Cases resulting in a serious event (175)
Cases resulting in death (13)
Cases resulting in life threatening events (18)
Cases resulting in hospitalization (103)
Cases resulting in disability (14)
Cases resulting in other serious reactions (69)
Below is a sample of reports where side effects / adverse reactions may be related to Altace (Ramipril). For a complete list and/or a specific selection of reports, please use the links in the index above.
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 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 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 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 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 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 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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