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Index of reports
> Cases resulting in other serious reactions (54)
> Cases with Dyspnoea (5)
Below is the selection of adverse event reports related to Botox (Botulinum Toxin Type A) that includes cases resulting in other serious reactions where reactions include dyspnoea.
Adverse event in male receiving Botox (Botulinum Toxin Type A)
Reported by a physician from United States on 2007-10-11
Patient: male, weighing 86.2 kg (189.6 pounds)
Adverse reactions / side effects: Blood Pressure Increased, Dysphagia, Dyspnoea, Pain in Extremity, Headache, Muscle Spasticity, Mantle Cell Lymphoma, Anxiety, Dysarthria, Malaise, Fatigue, Dysphonia, Neck Pain, Dizziness
Adverse event resulted in: hospitalization
Suspect drug(s):
Botox
Dosage: 400 units, single
Indication: Pain
Start date: 2007-02-06
End date: 2007-02-06
Botox
Indication: Dystonia
Other drugs received by patient: Celebrex; Tylenol W / Codeine NO. 3
Adverse event in female receiving Botox (Botulinum Toxin Type A)
Reported by a consumer/non-health professional from Sweden on 2007-06-29
Patient: female
Adverse reactions / side effects: LIP Swelling, Dyspnoea, Oedema Mouth
Suspect drug(s):
Botox
Dosage: unk, unk
Indication: Drug USE FOR Unknown Indication
Start date: 2007-03-14
End date: 2007-03-14
Botox
Start date: 2007-03-22
End date: 2007-03-22
Adverse event in female receiving Botox (Botulinum Toxin Type A)
Reported by a consumer/non-health professional from Sweden on 2007-06-26
Patient: female
Adverse reactions / side effects: LIP Swelling, Dyspnoea, Oedema Mouth
Suspect drug(s):
Botox
Dosage: unk, unk
Indication: Drug USE FOR Unknown Indication
Start date: 2007-03-14
End date: 2007-03-14
Botox
Start date: 2007-03-22
End date: 2007-03-22
Adverse event in 9 year old male receiving Botox (Botulinum Toxin Type A)
Reported by a consumer/non-health professional from Australia on 2007-06-12
Patient: 9 year old male
Adverse reactions / side effects: Dysphagia, Dyspnoea, Pneumonia, Vomiting, Stridor, Laryngeal Obstruction, Obstructive Airways Disorder, Haematemesis
Adverse event resulted in: hospitalization
Suspect drug(s):
Botox
Dosage: 400 units, unk
Indication: Cerebral Palsy
Start date: 2004-07-01
End date: 2004-07-01
Botox
Dosage: 400 units, unk
Start date: 2005-01-01
End date: 2005-01-01
Botox
Dosage: 400 units, unk
Start date: 2005-08-01
End date: 2005-08-01
Botox
Dosage: 400 units, unk
Start date: 2005-12-01
End date: 2005-12-01
Adverse event in 60 year old male receiving Botox (Botulinum Toxin Type A)
Reported by a consumer/non-health professional from United States on 2007-05-31
Patient: 60 year old male, weighing 86.2 kg (189.6 pounds)
Adverse reactions / side effects: Dyspnoea, Dysphagia, Paralysis, Vocal Cord Paralysis, Headache, Botulism, Speech Disorder, Muscle Strain, Fatigue, Dysphonia, Oesophageal Disorder, Heart Rate Increased, Vasodilatation, Tracheal Disorder, Asthenia
Adverse event resulted in: life threatening event
Suspect drug(s):
Botox
Dosage: 400 units one time im
Indication: Muscle Spasms
Start date: 2007-02-06
End date: 2007-02-06
Botox
Dosage: 400 units one time im
Indication: Musculoskeletal Pain
Start date: 2007-02-06
End date: 2007-02-06
Botox
Dosage: 400 units one time im
Indication: Neck Pain
Start date: 2007-02-06
End date: 2007-02-06
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