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Index of reports
> Cases resulting in a serious event (67)
> Cases with Headache (7)
Below is the selection of adverse event reports related to Imitrex (Sumatriptan) that includes cases resulting in a serious event where reactions include headache.
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 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 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 2007-05-16
Patient:
Adverse reactions / side effects: Drug Ineffective, Headache, Convulsion
Suspect drug(s):
Imitrex (Sumatriptan)
Adverse event in 44 year old female receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-02-19
Patient: 44 year old female, weighing 78.6 kg (172.9 pounds)
Adverse reactions / side effects: Nausea, Injection Site Pain, Headache, Injection Site Swelling
Adverse event resulted in: disablity
Suspect drug(s):
Imitrex (Sumatriptan)
Other drugs received by patient: Unknown
Adverse event in 44 year old female receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-02-05
Patient: 44 year old female
Adverse reactions / side effects: Nausea, Headache
Adverse event resulted in: disablity
Suspect drug(s):
Imitrex (Sumatriptan)
Other drugs received by patient: Unknown
Adverse event in female receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-01-18
Patient: female
Adverse reactions / side effects: Headache, Pharmaceutical Product Complaint, Blindness, Accidental Exposure
Suspect drug(s):
Imitrex (Sumatriptan)
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