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Index of reports
> Cases resulting in a serious event (101)
> Cases with Muscular Weakness (9)
Below is the selection of adverse event reports related to Botox (Botulinum Toxin Type A) that includes cases resulting in a serious event where reactions include muscular weakness.
Adverse event in receiving Botox (Botulinum Toxin Type A)
Reported by a physician from United States on 2007-10-24
Patient:
Adverse reactions / side effects: Abdominal Pain, Oral Intake Reduced, Weight Decreased, Dysphagia, Pneumonia Aspiration, Incorrect Dose Administered, Muscular Weakness, Asthenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Botox
Dosage: 1370 units, single
Indication: Cerebral Palsy
Start date: 2007-09-18
End date: 2007-09-18
Botox
Indication: Muscle Spasticity
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 male receiving Botox (Botulinum Toxin Type A)
Reported by a consumer/non-health professional from Norway on 2007-10-05
Patient: male
Adverse reactions / side effects: Dysphagia, Muscular Weakness
Adverse event resulted in: hospitalization
Suspect drug(s):
Botox (Botulinum Toxin Type A)
Other drugs received by patient: Enalapril Maleate; Enanton Depot SET; Allopur; Hydrochlorothiazide
Adverse event in female receiving Botox (Botulinum Toxin Type A)
Reported by a consumer/non-health professional from United States on 2007-07-25
Patient: female
Adverse reactions / side effects: Trismus, Drooling, Neck Pain, Muscular Weakness, Skin Burning Sensation, Eye Disorder, Muscle Spasms
Suspect drug(s):
Botox
Dosage: unk, single
Indication: Facial Spasm
Start date: 2006-09-07
End date: 2006-09-07
Botox
Dosage: unk, single
Indication: Headache
Start date: 2006-09-22
End date: 2006-09-22
Botox
Dosage: unk, single
Indication: Temporomandibular Joint Syndrome
Start date: 2006-10-06
End date: 2006-10-06
Adverse event in 2 year old female receiving Botox (Botulinum Toxin Type A)
Reported by a consumer/non-health professional from United States on 2007-06-02
Patient: 2 year old female, weighing 14.0 kg (30.8 pounds)
Adverse reactions / side effects: Dysphagia, Gastroenteritis Rotavirus, Muscular Weakness, Eyelid Ptosis, Botulism
Adverse event resulted in: hospitalization
Suspect drug(s):
Botox
Dosage: 160 units, single
Indication: Quadriparesis
Start date: 2007-05-08
End date: 2007-05-08
Botox
Botox
Other drugs received by patient: Keppra
Adverse event in 2 year old female receiving Botox (Botulinum Toxin Type A)
Reported by a consumer/non-health professional from United States on 2007-05-24
Patient: 2 year old female, weighing 14.0 kg (30.8 pounds)
Adverse reactions / side effects: Dysphagia, Muscular Weakness, Eyelid Ptosis, Botulism
Adverse event resulted in: hospitalization
Suspect drug(s):
Botox
Dosage: 160 units, single
Indication: Quadriparesis
Start date: 2007-05-08
End date: 2007-05-08
Botox
Botox
Adverse event in 40 year old female receiving Botox (Botulinum Toxin Type A)
Reported by a physician from South Africa on 2007-02-20
Patient: 40 year old female, weighing 65.0 kg (143.0 pounds)
Adverse reactions / side effects: Back Pain, Guillain-Barre Syndrome, Nausea, Hypotension, Muscular Weakness, Organ Failure, Brain Oedema, Dizziness, Pulmonary Oedema, Cytomegalovirus Infection, Respiratory Arrest, Ventricular Fibrillation, Cardiac Arrest, Muscle Spasms, Lung Injury
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Botox
Dosage: 22 units, single
Indication: Skin Wrinkling
Start date: 2006-07-27
End date: 2006-07-27
Botox
Dosage: 22 units, single
Start date: 2006-10-25
End date: 2006-10-25
Other drugs received by patient: Natrilix / 00340101 /; Diane
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)
Adverse event in 36 year old female receiving Botox (Botulinum Toxin Type A)
Reported by a consumer/non-health professional from United States on 2007-01-17
Patient: 36 year old female
Adverse reactions / side effects: Trismus, Drooling, Neck Pain, Muscular Weakness, Skin Burning Sensation, Eye Disorder, Muscle Spasms
Suspect drug(s):
Botox
Dosage: unk, single
Indication: Facial Spasm
Start date: 2006-09-07
End date: 2006-09-07
Botox
Dosage: unk, single
Start date: 2006-09-22
End date: 2006-09-22
Botox
Dosage: unk, single
Start date: 2006-10-06
End date: 2006-10-06
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