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Topamax (Topiramate) - Adverse Event Reports - Disability

 



Index of reports > Cases resulting in disability (25)

     Visual Acuity Reduced (7)Eye Pain (5)Angle Closure Glaucoma (4)Cataract (3)Visual Disturbance (3)Psychomotor Skills Impaired (3)Hydrocephalus (3)Foetal Growth Retardation (3)Convulsion (2)Dysarthria (2)

Below is the selection of adverse event reports related to Topamax (Topiramate) that includes cases resulting in disability.

 Reports 1 - 25 of 25   Next >>

Adverse event in male receiving Topamax (Topiramate)

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

Patient: male, weighing 11.7 kg (25.7 pounds)

Adverse reactions / side effects: Childhood Disintegrative Disorder

Adverse event resulted in: disablity

Suspect drug(s):
Topamax
    Administration route: Oral

Topamax
    Dosage: 75 mg in am, 100 mg in pm
    Administration route: Oral

Topamax
    Administration route: Oral

Topamax
    Administration route: Oral

Topamax
    Administration route: Oral
    Indication: Partial Seizures

Other drugs received by patient: Melatonin



Adverse event in 36 year old female receiving Topamax (Topiramate)

Reported by a physician from Australia on 2007-07-17

Patient: 36 year old female

Adverse reactions / side effects: Visual Disturbance, Visual Acuity Reduced, Eye Pain

Adverse event resulted in: disablity

Suspect drug(s):
Topamax (Topiramate)

Other drugs received by patient: Epilim



Adverse event in male receiving Topamax (Topiramate)

Reported by a physician from United Kingdom on 2007-07-13

Patient: male

Adverse reactions / side effects: Cataract

Adverse event resulted in: disablity

Suspect drug(s):
Topamax (Topiramate)

Other drugs received by patient: Oxcarbazepine; Levetiracetam



Adverse event in male receiving Topamax (Topiramate)

Reported by a physician from United Kingdom on 2007-06-29

Patient: male

Adverse reactions / side effects: Cataract

Adverse event resulted in: disablity

Suspect drug(s):
Topamax (Topiramate)



Adverse event in female receiving Topamax (Topiramate)

Reported by a pharmacist from Canada on 2007-06-29

Patient: female

Adverse reactions / side effects: Facial Palsy, Drooling, Cognitive Disorder, Cerebrovascular Accident, Fall, Somnolence, Dysarthria, Balance Disorder, Dizziness, Gait Disturbance, Hemiplegia

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Topamax
    Administration route: Oral
    Indication: Drug Therapy

Topamax
    Administration route: Oral
    Indication: Epilepsy

Other drugs received by patient: Benztropine; Clopixol; Lamotrigine; Clonazepam; Citalopram Hydrobromide



Adverse event in 34 year old female receiving Topamax (Topiramate)

Reported by a physician from United States on 2007-06-25

Patient: 34 year old female, weighing 66.9 kg (147.2 pounds)

Adverse reactions / side effects: Blindness, Angle Closure Glaucoma

Adverse event resulted in: disablity

Suspect drug(s):
Topamax (Topiramate)



Adverse event in 36 year old female receiving Topamax (Topiramate)

Reported by a physician from Australia on 2007-06-04

Patient: 36 year old female

Adverse reactions / side effects: Visual Disturbance, Visual Acuity Reduced, Eye Pain

Adverse event resulted in: disablity

Suspect drug(s):
Topamax (Topiramate)



Adverse event in 45 year old female receiving Topamax (Topiramate)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-31

Patient: 45 year old female, weighing 133.8 kg (294.4 pounds)

Adverse reactions / side effects: Impaired Driving Ability, Migraine, Loss of Employment, Intraocular Pressure Increased, Visual Acuity Reduced, Blindness, Eye Pain

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Topamax (Topiramate)



Adverse event in 42 year old female receiving Topamax (Topiramate)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-23

Patient: 42 year old female, weighing 54.4 kg (119.7 pounds)

Adverse reactions / side effects: Visual Acuity Reduced, Rash

Adverse event resulted in: disablity

Suspect drug(s):
Topamax (Topiramate)



Adverse event in 57 year old male receiving Topamax (Topiramate)

Reported by a individual with unspecified qualification from United States on 2007-05-18

Patient: 57 year old male, weighing 90.7 kg (199.6 pounds)

Adverse reactions / side effects: Bedridden, Weight Decreased, Wheelchair User, Abasia, Parkinsonism, Hyperhidrosis, Erythema, Walking AID User, Dizziness, Dysgraphia, Motion Sickness, Vomiting, Blood Homocysteine Increased, Loss of Control of Legs, Nausea, Ill-Defined Disorder, Dysarthria, Diarrhoea, Activities of Daily Living Impaired, NO Therapeutic Response, Disturbance in Attention, Gait Disturbance

Adverse event resulted in: disablity

Suspect drug(s):
Topamax (Topiramate)



Adverse event in 36 year old female receiving Topamax (Topiramate)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-16

Patient: 36 year old female, weighing 97.5 kg (214.6 pounds)

Adverse reactions / side effects: Myopathy, Angle Closure Glaucoma

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Topamax (Topiramate)



Adverse event in 12 month old male receiving Topamax (Topiramate)

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-05-14

Patient: 12 month old male, weighing 7.7 kg (16.9 pounds)

Adverse reactions / side effects: Bulbar Palsy, Vomiting, Choking

Adverse event resulted in: disablity

Suspect drug(s):
Topamax (Topiramate)



Adverse event in 46 year old male receiving Topamax (Topiramate)

Reported by a physician from United States on 2007-05-07

Patient: 46 year old male, weighing 67.6 kg (148.7 pounds)

Adverse reactions / side effects: Abdominal Distension, Respiratory Distress, Deep Vein Thrombosis

Adverse event resulted in: life threatening event, hospitalization, disablity

Suspect drug(s):
Topamax
    Administration route: Oral

Topamax
    Administration route: Oral

Topamax
    Administration route: Oral

Topamax
    Administration route: Oral
    Indication: Epilepsy

Other drugs received by patient: Dilantin; Keppra; Lovastatin; Enalapril



Adverse event in female receiving Topamax (Topiramate)

Reported by a physician from United States on 2007-03-27

Patient: female, weighing 63.5 kg (139.7 pounds)

Adverse reactions / side effects: Visual Acuity Reduced, Angle Closure Glaucoma

Adverse event resulted in: disablity

Suspect drug(s):
Topamax (Topiramate)

Other drugs received by patient: Zoloft



Adverse event in 40 year old female receiving Topamax (Topiramate)

Reported by a consumer/non-health professional from United States on 2007-03-26

Patient: 40 year old female, weighing 72.6 kg (159.7 pounds)

Adverse reactions / side effects: Paralysis

Adverse event resulted in: disablity

Suspect drug(s):
Topamax (Topiramate)



Adverse event in male receiving Topamax (Topiramate)

Reported by a physician from United States on 2007-03-14

Patient: male, weighing 91.6 kg (201.6 pounds)

Adverse reactions / side effects: Eye Haemorrhage, Nephrolithiasis, Retinal Vein Occlusion

Adverse event resulted in: disablity

Suspect drug(s):
Topamax (Topiramate)



Adverse event in 37 year old male receiving Topamax (Topiramate)

Reported by a consumer/non-health professional from United States on 2007-03-12

Patient: 37 year old male, weighing 99.8 kg (219.5 pounds)

Adverse reactions / side effects: Autonomic Nervous System Imbalance, Cognitive Disorder, Amnesia, Aggression, Convulsion, Mental Impairment, Burning Sensation, Overdose, Sleep Disorder

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Topamax
    Dosage: 100 mg 1- bedtime 1st week; 2 x -2nd week; 3x day 3rd week
    Start date: 2002-01-31

Topamax
    Dosage: 100 mg 1- bedtime 1st week; 2 x -2nd week; 3x day 3rd week
    Start date: 2002-02-13



Adverse event in male receiving Topamax (Topiramate)

Reported by a consumer/non-health professional from United States on 2007-03-12

Patient: male, weighing 136.1 kg (299.4 pounds)

Adverse reactions / side effects: Confusional State, Weight Decreased, Autonomic Nervous System Imbalance, Body Temperature Increased, Pain, Libido Decreased, Headache, Amnesia, Convulsion, Weight Increased, Thinking Abnormal, Anhidrosis, Insomnia, Feeling Jittery, Eye Disorder

Adverse event resulted in: disablity

Suspect drug(s):
Topamax
    Administration route: Oral

Topamax
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Other drugs received by patient: Aspirin; Vitamin CAP; Vicodin; Vicodin; Valium; Valium; Valium; Valium; Hydrocodone; Morphine



Adverse event in receiving Topamax (Topiramate)

Reported by a health professional (non-physician/pharmacist) from Switzerland on 2007-02-07

Patient:

Adverse reactions / side effects: Drug Exposure During Pregnancy, Psychomotor Skills Impaired, Hydrocephalus, Foetal Growth Retardation

Adverse event resulted in: disablity

Suspect drug(s):
Effexor
    Dosage: unknown
    Start date: 2005-01-27
    End date: 2005-02-17

Topamax
    Dosage: unknown
    Start date: 2005-01-27
    End date: 2005-02-17



Adverse event in female receiving Topamax (Topiramate)

Reported by a consumer/non-health professional from United States on 2007-02-07

Patient: female, weighing 77.1 kg (169.6 pounds)

Adverse reactions / side effects: Impaired Driving Ability, Dysgeusia, Visual Acuity Reduced, Vision Blurred, Eye Pain

Adverse event resulted in: disablity

Suspect drug(s):
Topamax (Topiramate)



Adverse event in 2 year old male receiving Topamax (Topiramate)

Reported by a consumer/non-health professional from Canada on 2007-01-31

Patient: 2 year old male, weighing 18.1 kg (39.9 pounds)

Adverse reactions / side effects: Speech Disorder, Visual Disturbance, Hypotonia, Catatonia, Coordination Abnormal, Apallic Syndrome

Adverse event resulted in: disablity

Suspect drug(s):
Topamax (Topiramate)



Adverse event in receiving Topamax (Topiramate)

Reported by a individual with unspecified qualification from Switzerland on 2007-01-19

Patient:

Adverse reactions / side effects: Drug Exposure During Pregnancy, Psychomotor Skills Impaired, Hydrocephalus, Foetal Growth Retardation

Adverse event resulted in: disablity

Suspect drug(s):
Effexor
    Dosage: transplacental
    Start date: 2005-01-27
    End date: 2005-02-17

Topamax
    Dosage: transplacental
    Start date: 2005-01-27
    End date: 2005-02-17



Adverse event in 13 month old receiving Topamax (Topiramate)

Reported by a physician from Switzerland on 2007-01-16

Patient: 13 month old

Adverse reactions / side effects: Psychomotor Skills Impaired, Hydrocephalus, Foetal Growth Retardation

Adverse event resulted in: disablity

Suspect drug(s):
Effexor
    Indication: Drug Exposure During Pregnancy

Topamax
    Indication: Drug Exposure During Pregnancy



Adverse event in 44 year old female receiving Topamax (Topiramate)

Reported by a pharmacist from United States on 2007-01-10

Patient: 44 year old female, weighing 72.6 kg (159.7 pounds)

Adverse reactions / side effects: Drug Ineffective, Ocular Hyperaemia, Visual Acuity Reduced, Myopia, Vision Blurred, Eye Pain

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Topamax (Topiramate)



Adverse event in 19 year old female receiving Topamax (Topiramate)

Reported by a physician from Thailand on 2007-01-09

Patient: 19 year old female

Adverse reactions / side effects: Cataract, Angle Closure Glaucoma

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Topamax (Topiramate)

Other drugs received by patient: Clonazepam; Phenytoin Sodium CAP; Baclofen



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