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Index of reports
> All cases (159)
> Cases with Headache (13)
Below is the selection of adverse event reports related to Imitrex (Sumatriptan) that includes all cases where reactions include headache.
Adverse event in female receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-10-30
Patient: female
Adverse reactions / side effects: Headache
Suspect drug(s):
Imitrex (Sumatriptan)
Adverse event in 52 year old female receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-10-30
Patient: 52 year old female
Adverse reactions / side effects: Headache, Somnolence
Suspect drug(s):
Imitrex (Sumatriptan)
Other drugs received by patient: Singulair; Claritin; Flonase; Blood Pressure Medication; Estrogens; Butalbital; Tylenol (Caplet); Midrin
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 49 year old female receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-07-30
Patient: 49 year old female
Adverse reactions / side effects: Headache
Suspect drug(s):
Imitrex (Sumatriptan)
Other drugs received by patient: Prozac
Adverse event in 56 year old female receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-07-30
Patient: 56 year old female
Adverse reactions / side effects: Wrong Technique in Drug Usage Process, Headache, Pharmaceutical Product Complaint
Suspect drug(s):
Imitrex (Sumatriptan)
Adverse event in receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-07-30
Patient:
Adverse reactions / side effects: Pain, Headache
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 2007-05-16
Patient:
Adverse reactions / side effects: Drug Ineffective, Headache, Convulsion
Suspect drug(s):
Imitrex (Sumatriptan)
Adverse event in 37 year old female receiving Imitrex (Sumatriptan)
Reported by a consumer/non-health professional from United States on 2007-02-28
Patient: 37 year old female
Adverse reactions / side effects: Headache, Pharmaceutical Product Complaint
Suspect drug(s):
Imitrex (Sumatriptan)
Other drugs received by patient: NO Concurrent Medication
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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