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Index of reports
> Cases resulting in disability (4)
> Cases with Somnolence (1)
Below is the selection of adverse event reports related to Botox (Botulinum Toxin Type A) that includes cases resulting in disability where reactions include somnolence.
Adverse event in female receiving Botox (Botulinum Toxin Type A)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-24
Patient: female
Adverse reactions / side effects: Vomiting, Middle Ear Effusion, Pyrexia, Amnesia, Hyperhidrosis, Somnolence, Paraesthesia, Fatigue, Malaise, Arthralgia, Joint Swelling, Cough
Adverse event resulted in: disablity
Suspect drug(s):
Botox
Dosage: 300 units, single
Indication: Cluster Headache
Start date: 2006-12-21
End date: 2006-12-21
Botox
Dosage: unk, single
Start date: 2006-08-01
End date: 2006-08-01
Other drugs received by patient: Maxalt; Lyrica; Topamax; Lidocaine
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