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Index of reports
> Cases resulting in a serious event (67)
Below is the selection of adverse event reports related to Imitrex (Sumatriptan) that includes cases resulting in a serious event.
Reports 1 - 25 of 67 Next >>
Adverse event in 37 year old female receiving Imitrex (Sumatriptan)
Reported by a individual with unspecified qualification from United States on 2007-10-31
Patient: 37 year old female
Adverse reactions / side effects: Nasal Discomfort, Cranial Nerve Disorder, Vision Blurred, Ear Pain, Lacrimation Increased, Infection
Adverse event resulted in: hospitalization
Suspect drug(s):
Imitrex (Sumatriptan)
Adverse event in 54 year old female receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-10-16
Patient: 54 year old female, weighing 68.0 kg (149.7 pounds)
Adverse reactions / side effects: Drug Ineffective, Drug Hypersensitivity, Headache, Swollen Tongue, Ill-Defined Disorder, Pharyngeal Oedema, Hallucinations, Mixed, Insomnia, Thyroid Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Rozerem
Dosage: 8 mg, qhs, per oral; 8 mg, qhs, per oral; 8 mg, qhs, per oral
Administration route: Oral
Indication: Insomnia
Start date: 2007-09-01
End date: 2007-09-01
Rozerem
Dosage: 8 mg, qhs, per oral; 8 mg, qhs, per oral; 8 mg, qhs, per oral
Administration route: Oral
Indication: Insomnia
Start date: 2007-08-01
Rozerem
Dosage: 8 mg, qhs, per oral; 8 mg, qhs, per oral; 8 mg, qhs, per oral
Administration route: Oral
Indication: Insomnia
Start date: 2007-09-01
Ambien CR
Dosage: qhs, per oral
Administration route: Oral
Indication: Insomnia
Start date: 2006-01-01
End date: 2007-09-01
Imitrex
Dosage: 50 mg, as required, per oral; 50 mg, as required, per oral
Administration route: Oral
Indication: Headache
Start date: 2003-01-01
End date: 2007-09-01
Imitrex
Dosage: 50 mg, as required, per oral; 50 mg, as required, per oral
Administration route: Oral
Indication: Headache
Start date: 2007-09-01
Unknown Sleep Medication (All Other Therapeutic Products)
Indication: Sleep Disorder Therapy
Start date: 2007-08-01
End date: 2007-08-01
Other drugs received by patient: Vicodin; Flexeril; Unknown Anti-Inflammatory (All Other Therapeutic Products); Unknown Anti-Depressant (Antidepressants)
Adverse event in 48 year old female receiving Imitrex (Sumatriptan)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-09
Patient: 48 year old female, weighing 90.7 kg (199.6 pounds)
Adverse reactions / side effects: Weight Increased, Transient Ischaemic Attack, Cardiac Failure Congestive, Paraesthesia
Adverse event resulted in: hospitalization
Suspect drug(s):
Opana ER
Dosage: 120 mg; bid
Indication: Back Pain
Start date: 2006-06-01
Opana ER
Dosage: 120 mg; bid
Indication: Fibromyalgia
Start date: 2006-06-01
Imitrex
Dosage: 100 mg; prn; po
Administration route: Oral
Indication: Migraine
Start date: 2000-01-01
Imitrex
Dosage: prn; nas
Indication: Migraine
Start date: 2000-01-01
Other drugs received by patient: Hydromorphone HCL; Trazodone HCL; Cymbalta; Zanaflex; Prevacid; Synthroid; Aspirin
Adverse event in 54 year old female receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-10-09
Patient: 54 year old female, weighing 68.0 kg (149.7 pounds)
Adverse reactions / side effects: Drug Ineffective, Drug Hypersensitivity, Headache, Swollen Tongue, Ill-Defined Disorder, Pharyngeal Oedema, Hallucinations, Mixed, Insomnia, Thyroid Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Rozerem
Dosage: 8 mg, qhs, per oral; 8 mg, qhs, per oral; 8 mg, qhs, per oral
Administration route: Oral
Indication: Insomnia
Start date: 2007-09-01
End date: 2007-09-01
Rozerem
Dosage: 8 mg, qhs, per oral; 8 mg, qhs, per oral; 8 mg, qhs, per oral
Administration route: Oral
Indication: Insomnia
Start date: 2007-08-01
Rozerem
Dosage: 8 mg, qhs, per oral; 8 mg, qhs, per oral; 8 mg, qhs, per oral
Administration route: Oral
Indication: Insomnia
Start date: 2007-09-01
Ambien CR
Dosage: qhs, per oral
Administration route: Oral
Indication: Insomnia
Start date: 2006-01-01
End date: 2007-09-01
Imitrex
Dosage: 50 mg, as required, per oral; 50 mg, as required, oral; 50 mg, as required, per oral
Administration route: Oral
Indication: Headache
Start date: 2003-01-01
End date: 2007-09-01
Imitrex
Dosage: 50 mg, as required, per oral; 50 mg, as required, oral; 50 mg, as required, per oral
Administration route: Oral
Indication: Headache
Start date: 2007-09-01
Unknown Sleep Medication (All Other Therapeutic Products)
Indication: Sleep Disorder Therapy
Start date: 2007-08-01
End date: 2007-08-01
Other drugs received by patient: Vicodin; Flexeril; Unknown Anti-Inflammatory (All Other Therapeutic Products); Unknown Anti-Depressant (Antidepressants)
Adverse event in 55 year old male receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-10-08
Patient: 55 year old male
Adverse reactions / side effects: Glare, Photopsia, Blindness
Suspect drug(s):
Imitrex (Sumatriptan)
Other drugs received by patient: Canasa; Migraine Drug (Unspecified); Ibuprofen
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 53 year old female receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from Canada on 2007-10-02
Patient: 53 year old female
Adverse reactions / side effects: Movement Disorder, Cardiac Valve Disease, Chest Discomfort, Chest Pain, Hypoaesthesia Facial, Hypoaesthesia, Cardiac Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Imitrex (Sumatriptan)
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 23 year old female receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-07-30
Patient: 23 year old female
Adverse reactions / side effects: Dizziness Postural, Convulsion
Suspect drug(s):
Imitrex (Sumatriptan)
Other drugs received by patient: Phenytoin
Adverse event in female receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-07-30
Patient: female
Adverse reactions / side effects: Upper Limb Fracture, Fall
Suspect drug(s):
Wellbutrin SR
Dosage: 150mg unknown
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Imitrex
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Bactroban
Administration route: Topical
Indication: Drug USE FOR Unknown Indication
Adverse event in 55 year old female receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-07-30
Patient: 55 year old female
Adverse reactions / side effects: Hypersensitivity
Suspect drug(s):
Imitrex (Sumatriptan)
Other drugs received by patient: Concurrent Medications
Adverse event in 21 year old female receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-07-30
Patient: 21 year old female
Adverse reactions / side effects: Chest Pain, Electrocardiogram Change
Adverse event resulted in: hospitalization
Suspect drug(s):
Imitrex (Sumatriptan)
Adverse event in 50 year old female receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-07-30
Patient: 50 year old female
Adverse reactions / side effects: Myocardial Infarction
Adverse event resulted in: hospitalization
Suspect drug(s):
Imitrex (Sumatriptan)
Other drugs received by patient: Hormone; Blood Pressure Medication
Adverse event in female receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-07-27
Patient: female
Adverse reactions / side effects: Upper Limb Fracture, Fall
Suspect drug(s):
Wellbutrin SR
Dosage: 150mg unknown
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Imitrex
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Bactroban
Administration route: Topical
Indication: Drug USE FOR Unknown Indication
Adverse event in 44 year old female receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-07-26
Patient: 44 year old female
Adverse reactions / side effects: Migraine, Expired Drug Administered, Pharmaceutical Product Complaint, Device Malfunction
Suspect drug(s):
Imitrex (Sumatriptan)
Other drugs received by patient: Celexa; Lyrica; Celebrex; Zanaflex; Nortriptyline HCL; Advil Liqui-Gels; Vicodin; Xanax; Prednisone; Calcium Salt + Vitamin B; Multi-Vitamin; Crystalline VIT B12 INJ
Adverse event in 49 year old male receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-07-20
Patient: 49 year old male
Adverse reactions / side effects: Agitation, Irritability, Yawning, Nausea, Panic Reaction
Adverse event resulted in: disablity
Suspect drug(s):
Imitrex (Sumatriptan)
Other drugs received by patient: Zocor; Magnesium Tablet; Petadolex
Adverse event in female receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-07-12
Patient: female
Adverse reactions / side effects: Arteriospasm Coronary, Cardiomyopathy
Adverse event resulted in: hospitalization
Suspect drug(s):
Amerge
Administration route: Oral
Indication: Migraine
Imitrex
Administration route: Oral
Indication: Migraine
Axert
Indication: Migraine
Frova
Relpax
Adverse event in female receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-06-28
Patient: female
Adverse reactions / side effects: Arteriospasm Coronary, Cardiomyopathy
Adverse event resulted in: hospitalization
Suspect drug(s):
Amerge
Administration route: Oral
Indication: Migraine
Imitrex
Administration route: Oral
Indication: Migraine
Frova
Relpax
Adverse event in 55 year old male receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-06-28
Patient: 55 year old male
Adverse reactions / side effects: Optic Neuropathy
Adverse event resulted in: disablity
Suspect drug(s):
Imitrex (Sumatriptan)
Other drugs received by patient: Ibuprofen; Testosterone
Adverse event in 36 year old female receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-06-19
Patient: 36 year old female, weighing 132.0 kg (290.4 pounds)
Adverse reactions / side effects: Incorrect Route of Drug Administration, Nausea, Feeling Hot, Paraesthesia
Adverse event resulted in: hospitalization
Suspect drug(s):
Imitrex (Sumatriptan)
Other drugs received by patient: Effexor; Fluoxetine; Seroquel; Alprazolam; Rozerem
Adverse event in male receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-06-14
Patient: male
Adverse reactions / side effects: Visual Disturbance, Drug Ineffective, Drug Abuser, Pharmaceutical Product Complaint, Epistaxis
Suspect drug(s):
Imitrex
Dosage: 20mg per day
Indication: Migraine
End date: 2006-11-01
Imitrex
Administration route: Oral
Start date: 2000-01-01
Imitrex
Other drugs received by patient: Inderal; Colace; Sinemet; Requip; Indocin; Chlorpheniramine Maleate; Lisinopril; Verapamil; Lovastatin; Detrol; Prevacid; Asthma Medication; Neurontin; Depakote; Baclofen; Prozac; Axert
Adverse event in female receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-06-08
Patient: female
Adverse reactions / side effects: Drug Ineffective
Adverse event resulted in: hospitalization
Suspect drug(s):
Imitrex (Sumatriptan)
Other drugs received by patient: Toprol-XL
Adverse event in female receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-06-08
Patient: female
Adverse reactions / side effects: Intracranial Aneurysm
Suspect drug(s):
Imitrex (Sumatriptan)
Adverse event in 26 year old female receiving Imitrex (Sumatriptan)
Reported by a pharmacist from United States on 2007-05-22
Patient: 26 year old female
Adverse reactions / side effects: Movement Disorder, Tinnitus, Vomiting, Headache, Cerebrovascular Accident, Paraesthesia, Diplopia, Dysarthria, Haematocrit Decreased, Facial Paresis, Dizziness, Vertigo, Coordination Abnormal
Adverse event resulted in: hospitalization
Suspect drug(s):
Yasmin
Dosage: 1 tablet daily oral
Administration route: Oral
Indication: Contraception
Imitrex
Indication: Migraine
Adverse event in receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-05-22
Patient:
Adverse reactions / side effects: Rectal Haemorrhage
Suspect drug(s):
Imitrex (Sumatriptan)
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