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Tegretol-XR (Carbamazepine) - Disability - Suspected Cause - Side Effect Reports

 
 



Index of reports > Disability (7)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Tegretol-XR (Carbamazepine) disability. The selected reports were submitted to the FDA during the sample period of about a year.

Possible Tegretol-XR side effects in female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-07-27

Patient: female

Reactions: Nausea, Head Injury, Thirst, Joint Injury, Fall, Dysstasia, Balance Disorder, Dizziness, Vision Blurred, Lethargy

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Tegretol-XR



Possible Tegretol-XR side effects in 37 year old male

Reported by a pharmacist from Portugal on 2012-06-27

Patient: 37 year old male

Reactions: Blindness

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Tegretol-XR



Possible Tegretol-XR side effects in female

Reported by a health professional (non-physician/pharmacist) from Netherlands on 2012-05-31

Patient: female, weighing 75.0 kg (165.0 pounds)

Reactions: Daydreaming, Disturbance in Attention, Mental Retardation, Somnolence, Aggression

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Tegretol-XR
    Dosage: 100-200 mg
    Indication: Epilepsy
    Start date: 1975-03-01

Depakene
    Dosage: 600-750 mg
    Indication: Epilepsy
    Start date: 1975-03-01

Lamictal
    Dosage: 75-100 mg
    Indication: Epilepsy
    Start date: 1975-03-01

Other drugs received by patient: Diazepam; Transipeg; Naproxen



Possible Tegretol-XR side effects in female

Reported by a health professional (non-physician/pharmacist) from France on 2012-05-03

Patient: female

Reactions: Abdominal Pain, Hepatic Function Abnormal, Pruritus, Intraventricular Haemorrhage, Cholestasis, Hepatic Lesion, Coma, Pyrexia, Serum Ferritin Increased, Cerebral Haemorrhage, Death, Periportal Sinus Dilatation, Hepatorenal Syndrome, Diarrhoea Haemorrhagic, Cholangitis, Intracranial Pressure Increased, Blood Creatinine Increased, Anuria, Vomiting, Hypertensive Crisis, Renal Failure, Dilatation Intrahepatic Duct Acquired, Renal Tubular Necrosis

Adverse event resulted in: death, disablity

Drug(s) suspected as cause:
Ketoprofen
    Dosage: 200 mg, qd
    Administration route: Oral
    Start date: 2011-05-26
    End date: 2011-06-11

Xarelto
    Dosage: 10 mg, qd
    Administration route: Oral
    Start date: 2011-05-30

Bisoprolol Fumarate and Hydrochlorothiazide
    Dosage: 2.5/6.25 mg
    Administration route: Oral
    Start date: 2011-06-03
    End date: 2011-06-16

Tegretol-XR
    Dosage: 200 mg, qd
    Administration route: Oral
    End date: 2011-06-16

Bisoprolol Fumarate and Hydrochlorothiazide
    Dosage: 2.5/6.25 mg
    Administration route: Oral

Other drugs received by patient: Acetaminophen W / Codeine; Bisoprolol Fumarate; Rabeprazole Sodium; Wytens / SPA /; Rabeprazole Sodium; Levothyroxine Sodium; Nexium; Renitec / NET /; Bisoprolol Fumarate; Ursolvan



Possible Tegretol-XR side effects in male

Reported by a consumer/non-health professional from Ecuador on 2012-02-03

Patient: male

Reactions: Head Injury, Haemorrhage Intracranial, Fall, Convulsion

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Tegretol-XR



Possible Tegretol-XR side effects in female

Reported by a individual with unspecified qualification from Ecuador on 2011-12-16

Patient: female

Reactions: Tendon Rupture, Fall

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Tegretol-XR

Other drugs received by patient: Blaqueta



Possible Tegretol-XR side effects in 48 year old male

Reported by a physician from Belgium on 2011-10-11

Patient: 48 year old male

Reactions: Drug Interaction, Complex Partial Seizures

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Tegretol-XR

Other drugs received by patient possibly interacting with the suspect drug:
Naprosyn
    Dosage: unk ukn, unk
    Indication: Arthropathy
    Start date: 2011-07-02
    End date: 2011-07-05

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