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Ultram (Tramadol) - Adverse Event Reports - Serious Event - Convulsion

 



Index of reports > Cases resulting in a serious event (48) > Cases with Convulsion (6)

Below is the selection of adverse event reports related to Ultram (Tramadol) that includes cases resulting in a serious event where reactions include convulsion.

Adverse event in female receiving Ultram (Tramadol)

Reported by a consumer/non-health professional from United States on 2007-10-09

Patient: female

Adverse reactions / side effects: Convulsion

Suspect drug(s):
Ultram ER
    Dosage: 1 in 1 day, oral
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Ultram
    Dosage: 1 in 1 d, oral
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication



Adverse event in female receiving Ultram (Tramadol)

Reported by a physician from United States on 2007-06-19

Patient: female, weighing 64.9 kg (142.7 pounds)

Adverse reactions / side effects: Accident, Hypoglycaemia, Analgesic Drug Level, Convulsion

Suspect drug(s):
Ultram
    Administration route: Oral

Ultram
    Dosage: 50mg every 4 hours as needed, up to 8 tablets per day
    Administration route: Oral
    Indication: Fibromyalgia

Other drugs received by patient: Suboxone; Ativan



Adverse event in male receiving Ultram (Tramadol)

Reported by a consumer/non-health professional from United States on 2007-06-07

Patient: male, weighing 68.0 kg (149.7 pounds)

Adverse reactions / side effects: Overdose, Drug Withdrawal Syndrome, Self-Medication, Convulsion

Suspect drug(s):
Ultram (Tramadol)

Other drugs received by patient: Effexor; Effexor; Neurontin



Adverse event in 57 year old female receiving Ultram (Tramadol)

Reported by a individual with unspecified qualification from United States on 2007-05-25

Patient: 57 year old female

Adverse reactions / side effects: Pneumonia Aspiration, Unresponsive TO Stimuli, Tricuspid Valve Incompetence, Somnolence, Foaming AT Mouth, Cyanosis, Sputum Culture Positive, Multiple Drug Overdose, Apnoea, Blood Glucose Increased, Blood Urea Increased, Blood Pressure Systolic Increased, Haemophilus Infection, Blood Chloride Increased, Troponin Increased, Streptococcal Infection, Aggression, Convulsion, Heart Rate Increased, Mitral Valve Incompetence

Adverse event resulted in: hospitalization

Suspect drug(s):
Soma (Carisoprodol, Usp) 350mg
    Dosage: 87 tablets (350 mg tablets), oral
    Administration route: Oral
    Start date: 2003-06-01
    End date: 2003-06-01

Motrin
    Dosage: 71 tablets (800 mg tablets), oral
    Administration route: Oral
    Start date: 2003-06-01
    End date: 2003-06-01

Buspar
    Dosage: 33 tablets (5 mg tablets), oral
    Administration route: Oral
    Start date: 2003-06-01
    End date: 2003-06-01

Ultram
    Dosage: 100 tablets, oral
    Administration route: Oral
    Start date: 2003-06-01
    End date: 2003-06-01

Lorazepam
    Dosage: 28 tablets (30mg tablets), oral
    Administration route: Oral
    Start date: 2003-06-01
    End date: 2003-06-01

Other drugs received by patient: Claritin; Neurontin; Celexa; Phenazopyridine HCL TAB; Dalmane; Potassium Chloride



Adverse event in 44 year old male receiving Ultram (Tramadol)

Reported by a consumer/non-health professional from United States on 2007-04-26

Patient: 44 year old male, weighing 81.6 kg (179.6 pounds)

Adverse reactions / side effects: Weight Decreased, Convulsion

Suspect drug(s):
Ultram
    Dosage: 50 mg, oral
    Administration route: Oral
    Indication: Pain

Generic Tramadol (Tramadol Hydrochloride) Unspecified
    Indication: Back Pain

Other drugs received by patient: Unknown Antidepressant (Antidepressants)



Adverse event in 41 year old female receiving Ultram (Tramadol)

Reported by a pharmacist from United States on 2007-03-02

Patient: 41 year old female, weighing 41.0 kg (90.2 pounds)

Adverse reactions / side effects: Pneumonia Aspiration, Incorrect Dose Administered, Atrial Fibrillation, Mental Status Changes, Convulsion

Adverse event resulted in: hospitalization

Suspect drug(s):
Ultram
    Dosage: 1-2 -50mg- tablets q4-6 prn pain po (duration 1x; all at once)
    Administration route: Oral
    Indication: Pain

Wellbutrin
    Dosage: po (duration: 1x; not patient's med)
    Administration route: Oral
    Indication: Self-Medication

Other drugs received by patient: Tramadol HCL; Fluoxetine

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