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Index of reports
> Cases resulting in disability (4)
Below is the selection of adverse event reports related to Botox (Botulinum Toxin Type A) that includes cases resulting in disability.
Adverse event in male receiving Botox (Botulinum Toxin Type A)
Reported by a consumer/non-health professional from Denmark on 2007-10-18
Patient: male
Adverse reactions / side effects: Myalgia, Incorrect Route of Drug Administration, Activities of Daily Living Impaired, Muscular Weakness
Adverse event resulted in: disablity
Suspect drug(s):
Botox (Botulinum Toxin Type A)
Other drugs received by patient: Lyrica
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
Adverse event in receiving Botox (Botulinum Toxin Type A)
Reported by a pharmacist from United States on 2007-05-21
Patient:
Adverse reactions / side effects: Therapeutic Product Contamination, Pharmaceutical Product Complaint, Botulism
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Botox (Botulinum Toxin Type A)
Adverse event in female receiving Botox (Botulinum Toxin Type A)
Reported by a consumer/non-health professional from United States on 2007-02-15
Patient: female, weighing 54.0 kg (118.8 pounds)
Adverse reactions / side effects: Muscle Atrophy, Pain, Skin Disorder, Muscular Weakness, Paralysis, Myalgia, Injection Site Reaction, Mastication Disorder
Adverse event resulted in: disablity
Suspect drug(s):
Botox (Botulinum Toxin Type A)
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