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Topamax (Topiramate) - Adverse Event Reports - Hospitalization - Convulsion

 



Index of reports > Cases resulting in hospitalization (99) > Cases with Convulsion (8)

Below is the selection of adverse event reports related to Topamax (Topiramate) that includes cases resulting in hospitalization where reactions include convulsion.

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

Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-09

Patient: 12 year old male, weighing 22.0 kg (48.4 pounds)

Adverse reactions / side effects: Renal Disorder, Blood Electrolytes Abnormal, Condition Aggravated, Pyrexia, Hypercalcaemia, Convulsion, Urine Electrolytes Abnormal

Adverse event resulted in: hospitalization

Suspect drug(s):
Elaprase (Idursulfase) Concentrate FOR Infusion
    Dosage: 12 mg, 1x/week, iv drip
    Indication: Mucopolysaccharidosis II
    Start date: 2007-01-01

Topamax

Other drugs received by patient: Klonopin; Atrovent; Miralax



Adverse event in female receiving Topamax (Topiramate)

Reported by a consumer/non-health professional from United States on 2007-07-24

Patient: female, weighing 72.6 kg (159.7 pounds)

Adverse reactions / side effects: Body Height Decreased, Cheilitis, Complex Regional Pain Syndrome, Muscular Weakness, Chronic Obstructive Pulmonary Disease, Convulsion, Cystitis Interstitial

Adverse event resulted in: hospitalization

Suspect drug(s):
Duragesic-100
    Indication: Complex Regional Pain Syndrome

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

Other drugs received by patient: Nexium; Hydromorphone HCL; Zoloft; Alprazolam; Temazepam



Adverse event in female receiving Topamax (Topiramate)

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

Patient: female

Adverse reactions / side effects: Agitation, Ocular Hyperaemia, Platelet Count Decreased, Status Epilepticus, Convulsion

Adverse event resulted in: hospitalization

Suspect drug(s):
Topamax
    Administration route: Oral

Topamax
    Administration route: Oral
    Indication: Epilepsy

Other drugs received by patient: Depakote; Nortrel 7 / 7 / 7; Phenobarbital TAB



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

Reported by a consumer/non-health professional from Canada on 2007-05-11

Patient: 44 year old female, weighing 42.6 kg (93.8 pounds)

Adverse reactions / side effects: Choking Sensation, Weight Decreased, Nasopharyngitis, Therapeutic Response Unexpected, Herpes Zoster, Pharyngeal Oedema, Skin Discolouration, Chest Pain, Dizziness, Palmar Erythema, Gastrooesophageal Reflux Disease, Muscle Spasms, RIB Fracture, Swelling Face, Chest Discomfort, Dyspnoea, Pain in Extremity, Muscular Weakness, Hypoaesthesia, Swollen Tongue, Musculoskeletal Chest Pain, Convulsion, Tremor, Anxiety, Burning Sensation, Throat Irritation, Sensory Disturbance, Depressed Level of Consciousness, Cardiovascular Disorder

Adverse event resulted in: hospitalization

Suspect drug(s):
Topamax

Topamax
    Indication: Pain Management

Ciprofloxacin
    Indication: Drug USE FOR Unknown Indication

Forteo
    Indication: Osteoporosis

Other drugs received by patient: Demerol; Tylenol; Ogen; Calcium Chloride; Vitamin D; Vitamin B-12; Miacalcin



Adverse event in 3 year old male receiving Topamax (Topiramate)

Reported by a consumer/non-health professional from United States on 2007-05-07

Patient: 3 year old male

Adverse reactions / side effects: Blood Glucose Decreased, Nuclear Magnetic Resonance Imaging Abnormal, Convulsion

Adverse event resulted in: hospitalization

Suspect drug(s):
Claritin
    Dosage: 5 ml;once;po
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-03-29
    End date: 2007-03-29

Triaminic SRT
    Dosage: 1 df;q6h;po
    Administration route: Oral
    Indication: Nasopharyngitis
    Start date: 2006-11-01
    End date: 2007-03-29

Robitussin / 00048001 /
    Dosage: 5 ml;once;po
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-03-29
    End date: 2007-03-29

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



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 2007-02-01

Patient: male, weighing 40.8 kg (89.8 pounds)

Adverse reactions / side effects: Accident, Diarrhoea, Pancreatitis, Convulsion, Gastroenteritis Viral

Adverse event resulted in: hospitalization

Suspect drug(s):
Topamax
    Administration route: Oral

Topamax
    Administration route: Oral
    Indication: Epilepsy

Other drugs received by patient: Lamictal; Ativan; Dyastat; Clorasap



Adverse event in male receiving Topamax (Topiramate)

Reported by a physician from Germany on 2007-01-11

Patient: male, weighing 55.0 kg (121.0 pounds)

Adverse reactions / side effects: Mantle Cell Lymphoma Stage III, Status Epilepticus, Convulsion

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Topamax
    Dosage: 100 - 0 - 50 mg
    Administration route: Oral
    Start date: 2003-02-01

Topamax
    Administration route: Oral
    Indication: Epilepsy
    Start date: 2003-02-01

Other drugs received by patient: Tegretol; Tegretol; Carbamazepin Retard; Carbamazepin Retard; Carbamazepin Retard

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