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Index of reports
> Cases resulting in life threatening events (8)
Below is the selection of adverse event reports related to Imitrex (Sumatriptan) that includes cases resulting in life threatening events.
Adverse event in 53 year old female receiving Imitrex (Sumatriptan)
Reported by a physician from Canada on 2007-10-04
Patient: 53 year old female, weighing 65.9 kg (145.0 pounds)
Adverse reactions / side effects: Movement Disorder, Chest Discomfort, Hypoaesthesia, Cardiac Disorder, Cardiac Valve Disease, Hypoaesthesia Facial, Chest Pain, Acute Myocardial Infarction
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Imitrex (Sumatriptan)
Other drugs received by patient: Amitriptyline HCL; Rabeprazole Sodium
Adverse event in 55 year old female receiving Imitrex (Sumatriptan)
Reported by a physician from United States on 2007-10-02
Patient: 55 year old female, weighing 77.0 kg (169.4 pounds)
Adverse reactions / side effects: Ventricular Hypokinesia, Hypotension, Akinesia, Electrocardiogram Poor R-Wave Progression, Chest Pain, Arteriosclerosis Coronary Artery, Electrocardiogram ST Segment Elevation, Electrocardiogram T Wave Inversion
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Imitrex (Sumatriptan)
Adverse event in male receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-04-23
Patient: male
Adverse reactions / side effects: Cerebral Haemorrhage
Adverse event resulted in: death, life threatening event
Suspect drug(s):
Imitrex (Sumatriptan)
Other drugs received by patient: NO Concurrent Medication
Adverse event in 40 year old male receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-04-17
Patient: 40 year old male
Adverse reactions / side effects: Chest Pain, Drug Interaction, Arteriospasm Coronary, Electrocardiogram ST Segment Elevation
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Imitrex
Administration route: Oral
Indication: Migraine
Tylenol Cold + FLU
Adverse event in 40 year old male receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-02-19
Patient: 40 year old male
Adverse reactions / side effects: Chest Pain, Drug Interaction, Arteriospasm Coronary, Electrocardiogram ST Segment Elevation
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Imitrex
Administration route: Oral
Indication: Migraine
Tylenol Cold + FLU
Adverse event in female receiving Imitrex (Sumatriptan)
Reported by a pharmacist from United States on 2007-02-15
Patient: female, weighing 68.0 kg (149.7 pounds)
Adverse reactions / side effects: Serotonin Syndrome
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Celexa
Dosage: 80mg 1 tablet qam oral
Administration route: Oral
Indication: Depression
Start date: 2006-12-01
Imitrex
Dosage: 100mg prn for migraine oral
Administration route: Oral
Indication: Migraine
Other drugs received by patient: Estrogen Patches; Topamax; Buspirone HCL; Triamterene and Hydrochlorothiazide
Adverse event in female receiving Imitrex (Sumatriptan)
Reported by a physician from United States on 2007-01-05
Patient: female, weighing 55.0 kg (121.0 pounds)
Adverse reactions / side effects: Coronary Artery Thrombosis, Acute Myocardial Infarction
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Imitrex (Sumatriptan)
Adverse event in 51 year old male receiving Imitrex (Sumatriptan)
Reported by a pharmacist from United States on 2007-01-02
Patient: 51 year old male, weighing 117.9 kg (259.5 pounds)
Adverse reactions / side effects: Hallucination, Auditory
Adverse event resulted in: life threatening event
Suspect drug(s):
Ciprofloxacin
Dosage: 500 mg q12h po
Administration route: Oral
Indication: Prostatitis
Start date: 2006-12-11
End date: 2006-12-29
Imitrex
Dosage: 50 mg prn po
Administration route: Oral
Indication: Migraine
Start date: 2006-12-25
End date: 2006-12-26
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