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Carbamazepine (Carbamazepine) - Adverse Event Reports - Disability

 



Index of reports > Cases resulting in disability (16)

     Dysmorphism (4)Renal Dysplasia (4)Renal Hypertrophy (4)Drug Exposure During Pregnancy (4)Renal Impairment Neonatal (3)Prominent Epicanthal Folds (3)Condition Aggravated (3)Hypertelorism of Orbit (3)Congenital Anomaly (3)Congenital Cystic Kidney Disease (3)

Below is the selection of adverse event reports related to Carbamazepine that includes cases resulting in disability.

Adverse event in 32 year old female receiving Carbamazepine

Reported by a individual with unspecified qualification from Brazil on 2007-10-15

Patient: 32 year old female

Adverse reactions / side effects: Cholestasis, Condition Aggravated, Depression, Hepatitis, Stevens-Johnson Syndrome

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Copaxone
    Dosage: 20 mg (20 mg, 1-2) subcutaneous, 20 mg (20 mg, 1 in 1 d), subcutaneous
    Indication: Multiple Sclerosis
    Start date: 2005-09-29
    End date: 2005-10-17

Copaxone
    Dosage: 20 mg (20 mg, 1-2) subcutaneous, 20 mg (20 mg, 1 in 1 d), subcutaneous
    Indication: Multiple Sclerosis
    Start date: 2005-10-31

Interferon Beta
    Dosage: double blind: 250 or 500 microgram
    Indication: Relapsing-Remitting Multiple Sclerosis
    Start date: 2005-07-25
    End date: 2005-09-22

Phenytoin
    Dosage: 1 gram (1 gram, 1 in 1 d) intravenous (not otherwise specified)
    Indication: Convulsion
    Start date: 2005-09-16
    End date: 2005-09-16

Phenytoin
    Dosage: 300 mg (300 mg, 1 in 1 d); oral, 300 mg (300 mg, 1 in 1 d); oral
    Administration route: Oral
    Start date: 2005-09-17
    End date: 2005-09-18

Phenytoin
    Dosage: 300 mg (300 mg, 1 in 1 d); oral, 300 mg (300 mg, 1 in 1 d); oral
    Administration route: Oral
    Start date: 2005-09-20
    End date: 2005-09-21

Fluoxetine
    Dosage: 20 mg (20 mg, 1 in 1 d); oral
    Administration route: Oral
    Indication: Depression
    Start date: 2005-06-27
    End date: 2005-09-02

Chlorpromazine
    Dosage: 50 mg (50 mg, 1 in 1 d); intravenous (not otherwise specified)
    Indication: Depression
    Start date: 2005-09-21
    End date: 2005-09-26

Carbamazepine
    Dosage: 800 mg (400 mg, 2 in 1 d); oral
    Administration route: Oral
    Indication: Convulsion
    Start date: 2005-09-22
    End date: 2005-10-17

Amitriptyline HCL
    Dosage: 50 mg, (50 mg, 1 in 1 d); oral
    Administration route: Oral
    Indication: Depression
    Start date: 2005-09-27
    End date: 2005-10-12

Other drugs received by patient: Diane; Captopril; Diazepam; Belacodid; Prednisone; Diclofenac; Sertraline; Clonazepam; Ibuprofen; Paracetamol; Dimenhydrinate; Dipyron; Tramadol HCL; Metoclopramide; Ranitidine HCL; Sodium Chloride



Adverse event in 32 year old female receiving Carbamazepine

Reported by a individual with unspecified qualification from Brazil on 2007-10-01

Patient: 32 year old female

Adverse reactions / side effects: Hepatic Enzyme Abnormal, Hepatic Function Abnormal, Pyoderma, Cholestasis, Hepatitis, Septic Shock, Stevens-Johnson Syndrome

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Copaxone
    Dosage: 20 mg (20 mg, 1 in 1 d)
    Indication: Multiple Sclerosis
    Start date: 2005-09-29
    End date: 2005-10-22

Phenytoin
    Dosage: 1 gram (1 gram, 1 in 1 d) intravenous (not otherwise specified); 300 mg (300 mg, 1 in 1 d) oral
    Indication: Convulsion
    Start date: 2005-09-16
    End date: 2005-09-16

Phenytoin
    Dosage: 1 gram (1 gram, 1 in 1 d) intravenous (not otherwise specified); 300 mg (300 mg, 1 in 1 d) oral
    Indication: Convulsion
    Start date: 2005-09-17
    End date: 2005-09-18

Phenytoin
    Dosage: 1 gram (1 gram, 1 in 1 d) intravenous (not otherwise specified); 300 mg (300 mg, 1 in 1 d) oral
    Indication: Convulsion
    Start date: 2005-09-20
    End date: 2005-09-21

Fluoxetine
    Dosage: 20 mg (20 mg, 1 in 1 d)
    Administration route: Oral
    Indication: Depression
    Start date: 2005-06-27
    End date: 2005-09-02

Chlorpromazine
    Dosage: 50 (50 mg, 1 in 1 d) intravenous (not otherwise specified)
    Indication: Depression
    Start date: 2005-09-21
    End date: 2005-09-26

Carbamazepine
    Dosage: 800 mg (400 mg, 2 in 1 d)
    Administration route: Oral
    Indication: Convulsion
    Start date: 2005-09-22
    End date: 2005-10-17

Amitriptyline HCL
    Dosage: 50 mg (50 mg, 1 in 1 d)
    Administration route: Oral
    Indication: Depression
    Start date: 2005-09-27
    End date: 2005-10-12

Other drugs received by patient: Diane; Captopril; Diazepam; Belacodid; Prednisone; Diclofenac Sodium; Sertraline; Clonazepam; Ibuprofen; Paracetamol; Dimenhydrinate; Dipyron; Tramadol HCL; Metoclopramide; Ranitidine HCL; Sodium Chloride



Adverse event in 7 year old female receiving Carbamazepine

Reported by a individual with unspecified qualification from United States on 2007-07-27

Patient: 7 year old female

Adverse reactions / side effects: Irritability, Muscle Spasticity, Somnolence, Pharmaceutical Product Complaint, Oxygen Saturation Decreased, Lethargy

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

Suspect drug(s):
Carbamazepine

Other drugs received by patient: Risperdal; Topamax; Chloral Hydrate (Chloral Hydrate); Valium; Omnicef



Adverse event in 62 year old female receiving Carbamazepine

Reported by a individual with unspecified qualification from United Kingdom on 2007-07-27

Patient: 62 year old female, weighing 145.0 kg (319.0 pounds)

Adverse reactions / side effects: Vomiting, Loss of Consciousness, Mobility Decreased

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Carbamazepine

Other drugs received by patient: Citalopram Hydrobromide; Levetiracetam; Rosuvastatin



Adverse event in male receiving Carbamazepine

Reported by a health professional (non-physician/pharmacist) from France on 2007-07-05

Patient: male, weighing 1.6 kg (3.5 pounds)

Adverse reactions / side effects: Cleft LIP, Micrognathia

Adverse event resulted in: disablity

Suspect drug(s):
Rivotril
    End date: 2007-01-31

Carbamazepine
    End date: 2007-01-31

Epitomax
    End date: 2007-01-31

DI-Hydan
    End date: 2007-01-31

Other drugs received by patient: Depakene



Adverse event in receiving Carbamazepine

Reported by a individual with unspecified qualification from Italy on 2007-06-29

Patient:

Adverse reactions / side effects: Congenital Nose Malformation, Congenital Renal Cyst, Dysmorphism, Drug Exposure During Pregnancy, Prominent Epicanthal Folds, Hypertelorism of Orbit, Renal Dysplasia, Renal Hypertrophy

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

Suspect drug(s):
Carbamazepine
    Dosage: oral
    Administration route: Oral
    Indication: Epilepsy

Phenobarbital TAB
    Dosage: oral
    Administration route: Oral
    Indication: Epilepsy



Adverse event in receiving Carbamazepine

Reported by a individual with unspecified qualification from Italy on 2007-06-29

Patient:

Adverse reactions / side effects: Pelvic Mass, Dysmorphism, LIP Disorder, Renal Impairment Neonatal, Prominent Epicanthal Folds, Renal Dysplasia, Renal Hypertrophy, Drug Exposure During Pregnancy, Congenital Anomaly, Congenital Cystic Kidney Disease

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

Suspect drug(s):
Carbamazepine
    Dosage: oral
    Administration route: Oral
    Indication: Epilepsy

Phenobarbital TAB
    Dosage: oral
    Administration route: Oral
    Indication: Epilepsy



Adverse event in receiving Carbamazepine

Reported by a individual with unspecified qualification from Italy on 2007-06-29

Patient:

Adverse reactions / side effects: Dysmorphism, Renal Impairment Neonatal, Hypertelorism of Orbit, Renal Dysplasia, Renal Hypertrophy, Drug Exposure During Pregnancy, Congenital Anomaly, Congenital Cystic Kidney Disease

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Carbamazepine
    Indication: Epilepsy

Phenobarbital TAB
    Indication: Epilepsy



Adverse event in receiving Carbamazepine

Reported by a individual with unspecified qualification from Italy on 2007-06-29

Patient:

Adverse reactions / side effects: Dysmorphism, Renal Impairment Neonatal, Prominent Epicanthal Folds, Hypertelorism of Orbit, Renal Dysplasia, Renal Hypertrophy, Drug Exposure During Pregnancy, Congenital Anomaly, Congenital Cystic Kidney Disease

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

Suspect drug(s):
Carbamazepine
    Dosage: oral
    Administration route: Oral
    Indication: Epilepsy

Phenobarbital TAB
    Dosage: oral
    Administration route: Oral
    Indication: Epilepsy



Adverse event in male receiving Carbamazepine

Reported by a health professional (non-physician/pharmacist) from France on 2007-06-22

Patient: male, weighing 1.6 kg (3.5 pounds)

Adverse reactions / side effects: Cleft LIP, Premature Baby, Micrognathia, Pierre Robin Syndrome, Foetal Growth Retardation

Adverse event resulted in: disablity

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

DI-Hydan
    Indication: Drug Exposure During Pregnancy

Rivotril
    Indication: Drug Exposure During Pregnancy

Carbamazepine
    Indication: Drug Exposure During Pregnancy

Other drugs received by patient: Depakene



Adverse event in 60 year old female receiving Carbamazepine

Reported by a individual with unspecified qualification from United States on 2007-05-31

Patient: 60 year old female

Adverse reactions / side effects: Bipolar Disorder, Mental Disorder, Condition Aggravated, Convulsion

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Carbamazepine

Other drugs received by patient: Lithium Carbonate; Risperdal; Prozac



Adverse event in 60 year old female receiving Carbamazepine

Reported by a individual with unspecified qualification from United States on 2007-04-30

Patient: 60 year old female

Adverse reactions / side effects: Impaired Driving Ability, Mental Disability, Condition Aggravated, Convulsion

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Carbamazepine



Adverse event in 30 year old female receiving Carbamazepine

Reported by a individual with unspecified qualification from Turkey on 2007-03-30

Patient: 30 year old female

Adverse reactions / side effects: Balance Disorder, Dizziness, Hyponatraemia, Sinusitis, Lethargy

Adverse event resulted in: disablity

Suspect drug(s):
Carbamazepine
    Dosage: 200mg, bid, oral
    Administration route: Oral
    Indication: Epilepsy

Clarithromycin
    Dosage: 500mg, bid, oral
    Administration route: Oral
    Indication: Sinusitis



Adverse event in female receiving Carbamazepine

Reported by a physician from Germany on 2007-03-16

Patient: female, weighing 51.0 kg (112.2 pounds)

Adverse reactions / side effects: Anticonvulsant Drug Level Above Therapeutic, Anticonvulsant Drug Level Below Therapeutic

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Keppra
    Dosage: 1 g 3/d;po
    Administration route: Oral
    Start date: 2006-10-01

Valproic Acid
    Dosage: 500 mg 6/d;po
    Administration route: Oral

Carbamazepine
    Dosage: 400 mg;po
    Administration route: Oral
    Start date: 2007-02-07
    End date: 2007-02-27



Adverse event in 80 year old female receiving Carbamazepine

Reported by a health professional (non-physician/pharmacist) from Norway on 2007-01-19

Patient: 80 year old female

Adverse reactions / side effects: Paraplegia, Spinal Epidural Haemorrhage, Drug Interaction

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Zocor

Diclofenac Sodium
    Administration route: Oral

Levothyroxine Sodium
    Administration route: Oral

Warfarin Sodium
    Administration route: Oral
    Indication: Atrial Fibrillation
    End date: 2006-11-30

Acetaminophen
    Administration route: Oral

Carbamazepine
    Administration route: Oral

Other drugs received by patient: Morphine Hydrochloride; Gabapentin



Adverse event in 80 year old female receiving Carbamazepine

Reported by a health professional (non-physician/pharmacist) from Norway on 2007-01-16

Patient: 80 year old female

Adverse reactions / side effects: Paraplegia, Spinal Epidural Haemorrhage, Drug Interaction

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Zocor

Diclofenac Sodium
    Administration route: Oral

Levothyroxine Sodium
    Administration route: Oral

Warfarin Sodium
    Administration route: Oral
    Indication: Atrial Fibrillation
    End date: 2006-11-30

Acetaminophen
    Administration route: Oral

Carbamazepine
    Administration route: Oral

Other drugs received by patient: Morphine Hydrochloride; Gabapentin

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