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Botox (Botulinum Toxin Type A) - Adverse Event Reports - Hospitalization

 



Index of reports > Cases resulting in hospitalization (57)

     Dysphagia (18)Eyelid Ptosis (12)Asthenia (12)Botulism (10)Pneumonia Aspiration (8)Lethargy (7)Muscular Weakness (5)Pyrexia (5)Headache (4)Ventricular Fibrillation (3)

Below is the selection of adverse event reports related to Botox (Botulinum Toxin Type A) that includes cases resulting in hospitalization.

 Reports 1 - 25 of 57   Next >>

Adverse event in male receiving Botox (Botulinum Toxin Type A)

Reported by a physician from Japan on 2007-10-24

Patient: male

Adverse reactions / side effects: Nephrolithiasis, Urinary Tract Infection, Benign Prostatic Hyperplasia

Adverse event resulted in: hospitalization

Suspect drug(s):
Botox
    Dosage: unk, single
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-06-26
    End date: 2007-06-26

Botox
    Dosage: unk, single
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-06-26
    End date: 2007-06-26

Botox
    Dosage: unk, single
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-09-18
    End date: 2007-09-18



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 female receiving Botox (Botulinum Toxin Type A)

Reported by a consumer/non-health professional from United States on 2007-10-19

Patient: female

Adverse reactions / side effects: Facial Paresis, Dysphagia, Vomiting, Aspiration, Dehydration, Urinary Tract Infection, Salivary Hypersecretion, Constipation

Adverse event resulted in: hospitalization

Suspect drug(s):
Botox
    Dosage: 25 units, single
    Indication: Drooling
    Start date: 2007-09-12
    End date: 2007-09-12

Botox
    Indication: Mucopolysaccharidosis IV



Adverse event in female receiving Botox (Botulinum Toxin Type A)

Reported by a physician from United States on 2007-10-19

Patient: female

Adverse reactions / side effects: Endocarditis Bacterial, Bacteraemia, Sepsis

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Botox (Botulinum Toxin Type A)



Adverse event in female receiving Botox (Botulinum Toxin Type A)

Reported by a physician from Finland on 2007-10-18

Patient: female

Adverse reactions / side effects: Dysphagia

Adverse event resulted in: hospitalization

Suspect drug(s):
Botox (Botulinum Toxin Type A)



Adverse event in female receiving Botox (Botulinum Toxin Type A)

Reported by a physician from United States on 2007-10-17

Patient: female

Adverse reactions / side effects: Sepsis, Endocarditis

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Botox (Botulinum Toxin Type A)



Adverse event in female receiving Botox (Botulinum Toxin Type A)

Reported by a physician from United States on 2007-10-12

Patient: female

Adverse reactions / side effects: Urinary Tract Infection, Mediastinitis, Chest Pain, Pharyngolaryngeal Pain, Pyrexia, Oesophageal Ulcer

Adverse event resulted in: hospitalization

Suspect drug(s):
Botox (Botulinum Toxin Type A)

Other drugs received by patient: Pethidin; Midazolam HCL; Glyburide; Insulin



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 male receiving Botox (Botulinum Toxin Type A)

Reported by a physician from United States on 2007-10-10

Patient: male, weighing 88.0 kg (193.6 pounds)

Adverse reactions / side effects: Cellulitis, Pain, Oedema

Adverse event resulted in: hospitalization

Suspect drug(s):
Botox
    Dosage: unk, single
    Indication: Muscular Weakness
    Start date: 2007-02-01
    End date: 2007-02-01

Temozolomide
    Dosage: 145 mg, qd
    Administration route: Oral
    Indication: Glioblastoma Multiforme
    Start date: 2006-12-01
    End date: 2007-01-18



Adverse event in female receiving Botox (Botulinum Toxin Type A)

Reported by a physician from Japan on 2007-10-06

Patient: female

Adverse reactions / side effects: Back Pain, Diarrhoea, Injection Site Pain, Meningitis Viral, Skin Tightness

Adverse event resulted in: hospitalization

Suspect drug(s):
Botox (Botulinum Toxin Type A)



Adverse event in 61 year old male receiving Botox (Botulinum Toxin Type A)

Reported by a physician from United States on 2007-10-05

Patient: 61 year old male, weighing 88.0 kg (193.6 pounds)

Adverse reactions / side effects: Blood Urea Increased, Cellulitis, Diabetes Mellitus, Hyperglycaemia, Lymphopenia, Pain, General Physical Health Deterioration, Hyponatraemia, Insomnia, NO Therapeutic Response, Blood Sodium Increased, Hypoalbuminaemia, Depression, Peripheral Motor Neuropathy, Myopathy Steroid

Adverse event resulted in: hospitalization

Suspect drug(s):
Botox
    Dosage: once
    Indication: Muscular Weakness
    Start date: 2007-02-01
    End date: 2007-02-01

Temozolomide
    Dosage: po
    Administration route: Oral
    Indication: Glioblastoma Multiforme
    Start date: 2006-12-01
    End date: 2007-01-18



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 2007-07-31

Patient: female

Adverse reactions / side effects: Migraine, Drug Ineffective

Adverse event resulted in: hospitalization

Suspect drug(s):
Botox (Botulinum Toxin Type A)



Adverse event in female receiving Botox (Botulinum Toxin Type A)

Reported by a physician from United States on 2007-07-30

Patient: female

Adverse reactions / side effects: Dysphagia, Hepatic Failure, Rash

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Botox (Botulinum Toxin Type A)



Adverse event in male receiving Botox (Botulinum Toxin Type A)

Reported by a physician from United States on 2007-07-24

Patient: male

Adverse reactions / side effects: Rash Generalised, Chills, Pyrexia, Somnolence, Asthenia

Adverse event resulted in: hospitalization

Suspect drug(s):
Botox (Botulinum Toxin Type A)



Adverse event in male receiving Botox (Botulinum Toxin Type A)

Reported by a consumer/non-health professional from United States on 2007-07-13

Patient: male, weighing 20.0 kg (44.0 pounds)

Adverse reactions / side effects: Pneumonia Aspiration, Dysphagia, Eyelid Ptosis, Asthenia, Botulism, Lethargy

Adverse event resulted in: hospitalization

Suspect drug(s):
Botox
    Dosage: 600 units, single
    Indication: Muscle Spasticity
    Start date: 2007-04-23
    End date: 2007-04-23

Botox

Botox

Other drugs received by patient: Sinemet; Depakote; Leucovorin Calcium



Adverse event in female receiving Botox (Botulinum Toxin Type A)

Reported by a physician from United States on 2007-06-22

Patient: female

Adverse reactions / side effects: Mass, Blood Blister, Musculoskeletal Stiffness, Headache, Swollen Tongue, Throat Tightness

Adverse event resulted in: hospitalization

Suspect drug(s):
Botox
    Dosage: 350 units, single
    Indication: Torticollis
    Start date: 2006-12-01
    End date: 2006-12-01

Botox
    Dosage: 350 units, single
    Start date: 2007-03-12
    End date: 2007-03-12



Adverse event in male receiving Botox (Botulinum Toxin Type A)

Reported by a consumer/non-health professional from United States on 2007-06-22

Patient: male, weighing 20.0 kg (44.0 pounds)

Adverse reactions / side effects: Pneumonia Aspiration, Dysphagia, Eyelid Ptosis, Asthenia, Botulism, Lethargy

Adverse event resulted in: hospitalization

Suspect drug(s):
Botox
    Dosage: 600 units, single
    Indication: Muscle Spasticity
    Start date: 2007-04-23
    End date: 2007-04-23

Botox

Botox

Other drugs received by patient: Sinemet; Depakote; Leucovorin Calcium



Adverse event in receiving Botox (Botulinum Toxin Type A)

Reported by a consumer/non-health professional from United States on 2007-06-21

Patient:

Adverse reactions / side effects: Mechanical Ventilation

Adverse event resulted in: hospitalization

Suspect drug(s):
Botox (Botulinum Toxin Type A)



Adverse event in male receiving Botox (Botulinum Toxin Type A)

Reported by a consumer/non-health professional from United States on 2007-06-15

Patient: male, weighing 20.0 kg (44.0 pounds)

Adverse reactions / side effects: Pneumonia Aspiration, Dysphagia, Eyelid Ptosis, Asthenia, Botulism, Lethargy

Adverse event resulted in: hospitalization

Suspect drug(s):
Botox
    Dosage: 600 units, single
    Indication: Muscle Spasticity
    Start date: 2007-04-23
    End date: 2007-04-23

Botox

Botox

Other drugs received by patient: Sinemet; Depakote; Leucovorin Calcium



Adverse event in male receiving Botox (Botulinum Toxin Type A)

Reported by a consumer/non-health professional from United States on 2007-06-14

Patient: male, weighing 20.0 kg (44.0 pounds)

Adverse reactions / side effects: Pneumonia Aspiration, Dysphagia, Eyelid Ptosis, Asthenia, Botulism, Lethargy

Adverse event resulted in: hospitalization

Suspect drug(s):
Botox
    Dosage: 600 units, single
    Indication: Muscle Spasticity
    Start date: 2007-04-23
    End date: 2007-04-23

Botox

Botox

Other drugs received by patient: Sinemet; Depakote; Leucovorin Calcium



Adverse event in male receiving Botox (Botulinum Toxin Type A)

Reported by a consumer/non-health professional from Canada on 2007-06-14

Patient: male

Adverse reactions / side effects: Migraine, Vision Blurred, Pyrexia, Asthenia

Adverse event resulted in: hospitalization

Suspect drug(s):
Botox (Botulinum Toxin Type A)

Other drugs received by patient: Lorazepam



Adverse event in male receiving Botox (Botulinum Toxin Type A)

Reported by a physician from Germany on 2007-06-14

Patient: male

Adverse reactions / side effects: Epilepsy

Adverse event resulted in: hospitalization

Suspect drug(s):
Botox (Botulinum Toxin Type A)



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 male receiving Botox (Botulinum Toxin Type A)

Reported by a consumer/non-health professional from Canada on 2007-06-08

Patient: male

Adverse reactions / side effects: Migraine, Vision Blurred, Pyrexia, Asthenia

Adverse event resulted in: hospitalization

Suspect drug(s):
Botox (Botulinum Toxin Type A)

Other drugs received by patient: Lorazepam



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