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Index of reports
> Cases resulting in hospitalization (103)
> Cases with Syncope (8)
Below is the selection of adverse event reports related to Altace (Ramipril) that includes cases resulting in hospitalization where reactions include syncope.
Adverse event in receiving Altace (Ramipril)
Reported by a consumer/non-health professional from United States on 2007-07-30
Patient:
Adverse reactions / side effects: Syncope, Atrial Fibrillation, Blood Potassium Increased, Blood Creatinine Increased
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Altace
Dosage: 10 mg, qd
Administration route: Oral
Indication: Cardiac Failure
Start date: 2006-12-15
End date: 2007-06-20
Atacand
Dosage: 4 mg, qd
Indication: Cardiac Failure
Start date: 2007-04-18
End date: 2007-05-02
Atacand
Dosage: 8 mg, qd
Administration route: Oral
Start date: 2007-05-03
End date: 2007-06-20
Spironolactone
Dosage: 50 mg, qd
Administration route: Oral
Indication: Cardiac Failure
Start date: 2007-01-18
End date: 2007-06-20
Spironolactone
Dosage: 12.5 mg, qd
Administration route: Oral
Start date: 2007-06-21
Other drugs received by patient: Behepan; Zolpidem Tartrate; Imodium / 00384302 /
Adverse event in receiving Altace (Ramipril)
Reported by a physician from Germany on 2007-07-23
Patient:
Adverse reactions / side effects: Atrial Flutter, Tachyarrhythmia, Drug Interaction Potentiation, Atrial Fibrillation, Fall, Syncope, Palpitations, Dizziness, Unevaluable Event, Asthenia, Blood Pressure Decreased, RIB Fracture
Adverse event resulted in: hospitalization
Suspect drug(s):
Altace
Dosage: 5 mg, qd
Administration route: Oral
Start date: 2006-02-01
Seroquel
Dosage: 150 mg, qd
Administration route: Oral
Start date: 2007-02-15
End date: 2007-02-15
Seroquel
Dosage: 300 mg, qd
Administration route: Oral
Start date: 2007-02-16
End date: 2007-02-16
Seroquel
Dosage: 450 mg, qd
Administration route: Oral
Start date: 2007-02-17
End date: 2007-02-17
Seroquel
Dosage: 600 mg, qd
Administration route: Oral
Start date: 2007-02-18
End date: 2007-02-19
Seroquel
Dosage: 300 mg, qd
Administration route: Oral
Start date: 2007-02-20
End date: 2007-02-21
Norvasc
Dosage: 5 mg, qd
Administration route: Oral
Start date: 2007-02-15
End date: 2007-02-17
Other drugs received by patient: Lorazepam; Lorazepam; Pantazol
Adverse event in receiving Altace (Ramipril)
Reported by a physician from United States on 2007-07-17
Patient:
Adverse reactions / side effects: Vomiting, Haemorrhage Intracranial, Hypotension, Mental Status Changes, Neurological Examination Abnormal, Fall, Dysarthria, Skin Laceration, Syncope
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Altace
Warfarin Sodium
Dosage: 3.7 mg, qd
Start date: 2006-09-12
Norvasc
Toprol-XL
Oxycodone HCL
Adverse event in receiving Altace (Ramipril)
Reported by a consumer/non-health professional from United States on 2007-04-18
Patient:
Adverse reactions / side effects: Abdominal Pain, Arterial Haemorrhage, Syncope, Haemorrhage, Hypotension
Adverse event resulted in: hospitalization
Suspect drug(s):
Altace (Ramipril)
Other drugs received by patient: Thyroid Hormones
Adverse event in 65 year old male receiving Altace (Ramipril)
Reported by a consumer/non-health professional from United States on 2007-02-27
Patient: 65 year old male
Adverse reactions / side effects: Syncope, Dizziness, Arrhythmia
Adverse event resulted in: hospitalization
Suspect drug(s):
Coreg
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2006-12-12
Altace
Indication: Drug USE FOR Unknown Indication
End date: 2007-01-07
Adverse event in 65 year old male receiving Altace (Ramipril)
Reported by a consumer/non-health professional from United States on 2007-02-15
Patient: 65 year old male
Adverse reactions / side effects: Syncope, Dizziness, Arrhythmia
Adverse event resulted in: hospitalization
Suspect drug(s):
Coreg
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2006-12-12
Altace
Indication: Drug USE FOR Unknown Indication
End date: 2007-01-07
Adverse event in receiving Altace (Ramipril)
Reported by a consumer/non-health professional from United States on 2007-01-23
Patient:
Adverse reactions / side effects: Syncope, Hypotension, Vertigo, Bradycardia, Headache
Adverse event resulted in: hospitalization
Suspect drug(s):
Altace
Dosage: 2.5 mg, qd
Administration route: Oral
Indication: Hypertension
Start date: 2005-01-01
End date: 2005-07-01
Hydrochlorothiazide
Dosage: 12.5 mg, qd
Administration route: Oral
Start date: 2005-01-01
End date: 2005-07-01
Seloken / 00376902 /
Dosage: unk, qd
Administration route: Oral
Indication: Hypertension
Start date: 2005-01-01
End date: 2005-07-01
Other drugs received by patient: Coumadin; Pradif; Triniplas; Finastid; Polase / 00196901 /
Adverse event in receiving Altace (Ramipril)
Reported by a individual with unspecified qualification from Sweden on 2007-01-16
Patient:
Adverse reactions / side effects: Blood Blister, Pyrexia, Pallor, Polyneuropathy, Fatigue, Skin Discolouration, C-Reactive Protein Increased, Dizziness, Blood Creatinine Increased, Blister, White Blood Cell Count Increased, Vomiting, Blood Urea Increased, Dyspnoea, Atrial Flutter, Nausea, Renal Failure, Syncope, Sepsis, Vasculitis, Blood Pressure Decreased
Adverse event resulted in: hospitalization
Suspect drug(s):
Altace
Dosage: 2.5 mg, bid
Administration route: Oral
Indication: Atrial Fibrillation
End date: 2006-04-25
Altace
Dosage: 5 mg, bid
Administration route: Oral
Start date: 2006-04-26
End date: 2006-06-28
Furix
Dosage: 40 mg, qd
Start date: 2006-04-01
Dalacin
Dosage: 300 mg, bid
Start date: 2006-06-01
Other drugs received by patient: Metoprolol Succinate; Entocort; Isoptin; Behepan; Prednisolone ^pharmacia + Upjohn^; Allopurinol; Spironolakton ^aco^; Imodium
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