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Lamictal (Lamotrigine) - Adverse Event Reports - Other Serious Reactions - Stevens-Johnson Syndrome

 



Index of reports > Cases resulting in other serious reactions (472) > Cases with Stevens-Johnson Syndrome (46)

Below is the selection of adverse event reports related to Lamictal (Lamotrigine) that includes cases resulting in other serious reactions where reactions include stevens-johnson syndrome.

 Reports 1 - 25 of 46   Next >>

Adverse event in male receiving Lamictal (Lamotrigine)

Reported by a physician from United States on 2007-10-17

Patient: male

Adverse reactions / side effects: Rash, Stevens-Johnson Syndrome

Suspect drug(s):
Concerta
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Lamictal
    Indication: Drug USE FOR Unknown Indication

Other drugs received by patient: Risperdal



Adverse event in 21 year old female receiving Lamictal (Lamotrigine)

Reported by a consumer/non-health professional from United States on 2007-10-16

Patient: 21 year old female, weighing 61.8 kg (136.0 pounds)

Adverse reactions / side effects: Skin Exfoliation, Urinary Tract Infection, Ocular Hyperaemia, Pain, Pharmaceutical Product Complaint, Rash Vesicular, Stevens-Johnson Syndrome

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Lamictal (Lamotrigine)

Other drugs received by patient: Iron



Adverse event in 27 year old female receiving Lamictal (Lamotrigine)

Reported by a consumer/non-health professional from United States on 2007-10-02

Patient: 27 year old female, weighing 54.5 kg (119.9 pounds)

Adverse reactions / side effects: Systemic Candida, Abdominal Pain, Disseminated Intravascular Coagulation, Hepatic Failure, Acidosis, Lactic Acidosis, Pyrexia, Pericardial Effusion, Acute Respiratory Distress Syndrome, Myocarditis, Fungus Urine Test Positive, Pneumonia, Chest Discomfort, Urine Output Decreased, Anaemia, Drug Rash With Eosinophilia and Systemic Symptoms, Occult Blood Positive, Tremor, Flushing, Atelectasis, Chills, Generalised Oedema, Fungaemia, Pleural Effusion, Stevens-Johnson Syndrome, Intestinal Ischaemia, Dyspnoea, International Normalised Ratio Increased, Organ Failure, Hepatic Enzyme Increased, Ascites, Haematochezia, Mucosal Erosion, Renal Failure, Respiratory Failure, Sinus Tachycardia

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

Suspect drug(s):
Lamictal (Lamotrigine)

Other drugs received by patient: Lexapro; Oral Contraceptives; Valtrex; FLU Vaccine



Adverse event in 19 year old female receiving Lamictal (Lamotrigine)

Reported by a consumer/non-health professional from United States on 2007-07-12

Patient: 19 year old female, weighing 59.0 kg (129.7 pounds)

Adverse reactions / side effects: Fatigue, Lymphadenopathy, Toxic Epidermal Necrolysis, Drug Interaction, Onychomadesis, Stevens-Johnson Syndrome

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Lamictal (Lamotrigine)



Adverse event in female receiving Lamictal (Lamotrigine)

Reported by a consumer/non-health professional from United States on 2007-07-10

Patient: female

Adverse reactions / side effects: Multi-Organ Failure, Wheelchair User, Dysphagia, Skin Exfoliation, Abasia, Stevens-Johnson Syndrome

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

Suspect drug(s):
Lamictal (Lamotrigine)

Other drugs received by patient: NO Concurrent Medication



Adverse event in 49 year old female receiving Lamictal (Lamotrigine)

Reported by a individual with unspecified qualification from United States on 2007-07-09

Patient: 49 year old female

Adverse reactions / side effects: Pruritus, Bone Pain, Drug Hypersensitivity, Pain of Skin, Erythema, Peripheral Sensory Neuropathy, Exercise Tolerance Decreased, Hepatic Enzyme Increased, Burning Sensation, Speech Disorder, Fatigue, Food Allergy, Nervous System Disorder, Mobility Decreased, Stevens-Johnson Syndrome

Suspect drug(s):
Bactrim
    Dosage: unk, oral
    Administration route: Oral
    Start date: 2007-02-15

Pegasys
    Start date: 2006-05-15
    End date: 2007-03-09

Ribavirin
    Start date: 2006-05-15
    End date: 2007-03-09

Lamictal

Trileptal

Effexor



Adverse event in female receiving Lamictal (Lamotrigine)

Reported by a physician from United States on 2007-07-09

Patient: female

Adverse reactions / side effects: Neuropathy, Fatigue, Food Allergy, Bone Pain, Nervous System Disorder, Stevens-Johnson Syndrome

Suspect drug(s):
Effexor
    Dosage: 150 mg, frequency unknown

Effexor
    Dosage: 300 mg, frequency unknown

Trileptal
    Dosage: unknown

Bactrim
    Dosage: unknown
    Start date: 2007-02-15

Lamictal
    Dosage: unknown

Pegasys
    Dosage: unknown
    Start date: 2006-05-15
    End date: 2007-03-09

Ribavirin
    Dosage: unknown
    Start date: 2006-05-15
    End date: 2007-03-09



Adverse event in 49 year old female receiving Lamictal (Lamotrigine)

Reported by a individual with unspecified qualification from United States on 2007-07-06

Patient: 49 year old female

Adverse reactions / side effects: Neuropathy, Pruritus, Pain, Bone Pain, Drug Hypersensitivity, Skin Burning Sensation, Palmar-Plantar Erythrodysaesthesia Syndrome, Erythema, Hepatic Enzyme Increased, Speech Disorder, Fatigue, Hypokinesia, Food Allergy, Gastric Bypass, Presyncope, Nervous System Disorder, Asthenia, Stevens-Johnson Syndrome

Suspect drug(s):
Trileptal

Pegasys
    Start date: 2006-05-15
    End date: 2007-03-09

Ribavirin
    Start date: 2006-05-15
    End date: 2007-03-09

Bactrim
    Start date: 2007-02-15

Lamictal

Effexor
    Dosage: 300 mg, unk

Effexor
    Dosage: 150mg, unk



Adverse event in 44 year old female receiving Lamictal (Lamotrigine)

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

Patient: 44 year old female

Adverse reactions / side effects: Pyrexia, Stevens-Johnson Syndrome, Scar

Suspect drug(s):
Lamictal (Lamotrigine)

Other drugs received by patient: Cymbalta



Adverse event in 35 year old female receiving Lamictal (Lamotrigine)

Reported by a health professional (non-physician/pharmacist) from Taiwan, Province of China on 2007-07-05

Patient: 35 year old female

Adverse reactions / side effects: Drug Ineffective, Stevens-Johnson Syndrome

Suspect drug(s):
Aripiprazole
    Dosage: dose incr to 30mg/d after 1 month on 10mg/d
    Indication: Schizophrenia

Lamictal
    Dosage: initial dose 12.5mg/d incr to 25mg/d in second week
    Indication: Schizophrenia



Adverse event in 24 year old female receiving Lamictal (Lamotrigine)

Reported by a health professional (non-physician/pharmacist) from Taiwan, Province of China on 2007-06-29

Patient: 24 year old female

Adverse reactions / side effects: Drug Ineffective, Stevens-Johnson Syndrome

Suspect drug(s):
Aripiprazole
    Dosage: titrated to 30mg/day after 1 month.

Lamictal
    Dosage: increaesed to 25/mg/d in the second week.



Adverse event in 46 year old male receiving Lamictal (Lamotrigine)

Reported by a consumer/non-health professional from United States on 2007-06-29

Patient: 46 year old male, weighing 55.5 kg (122.1 pounds)

Adverse reactions / side effects: Vomiting, Eye Discharge, Conjunctivitis, Tongue Ulceration, Gingival Hypertrophy, Convulsion, Diarrhoea, Dizziness, Stevens-Johnson Syndrome, Cough

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Lamictal (Lamotrigine)

Other drugs received by patient: Qvar 40; Albuterol; Singulair



Adverse event in 49 year old female receiving Lamictal (Lamotrigine)

Reported by a consumer/non-health professional from United States on 2007-06-28

Patient: 49 year old female

Adverse reactions / side effects: Movement Disorder, Pruritus, Bone Pain, Erythema, Speech Disorder, Fatigue, Neuropathy Peripheral, Food Allergy, Stevens-Johnson Syndrome, Pain of Skin, Drug Hypersensitivity, Palmar-Plantar Erythrodysaesthesia Syndrome, Hepatic Enzyme Increased, Burning Sensation, Presyncope, Swelling, Nervous System Disorder, Asthenia

Suspect drug(s):
Lamictal
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Pegasys
    Indication: Drug USE FOR Unknown Indication
    Start date: 2006-05-15
    End date: 2007-03-09

Ribavirin
    Indication: Drug USE FOR Unknown Indication
    Start date: 2006-05-15
    End date: 2007-03-09

Bactrim
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-02-15

Trileptal
    Indication: Drug USE FOR Unknown Indication

Effexor
    Indication: Drug USE FOR Unknown Indication



Adverse event in female receiving Lamictal (Lamotrigine)

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

Patient: female

Adverse reactions / side effects: Oral Mucosal Blistering, Blood Blister, Pyrexia, Rash, Stevens-Johnson Syndrome

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Lamictal (Lamotrigine)



Adverse event in 55 year old male receiving Lamictal (Lamotrigine)

Reported by a physician from United States on 2007-06-12

Patient: 55 year old male

Adverse reactions / side effects: Pruritus, Burns Second Degree, Skin Exfoliation, Pain, Stevens-Johnson Syndrome

Suspect drug(s):
Lamictal (Lamotrigine)

Other drugs received by patient: Nsaids



Adverse event in 41 year old female receiving Lamictal (Lamotrigine)

Reported by a consumer/non-health professional from United States on 2007-06-11

Patient: 41 year old female

Adverse reactions / side effects: Lymphadenopathy, Fatigue, Oral Pain, Pharyngolaryngeal Pain, Rash, Stevens-Johnson Syndrome

Suspect drug(s):
Lamictal (Lamotrigine)

Other drugs received by patient: Allegra; Biaxin; Topamax; Albuterol



Adverse event in 55 year old female receiving Lamictal (Lamotrigine)

Reported by a consumer/non-health professional from United States on 2007-06-05

Patient: 55 year old female, weighing 85.0 kg (187.0 pounds)

Adverse reactions / side effects: Malaise, Pyrexia, Stevens-Johnson Syndrome, Hepatic Enzyme Increased

Adverse event resulted in: disablity

Suspect drug(s):
Lamictal (Lamotrigine)

Other drugs received by patient: Maxalt; Neurontin



Adverse event in 7 year old male receiving Lamictal (Lamotrigine)

Reported by a consumer/non-health professional from United States on 2007-05-31

Patient: 7 year old male

Adverse reactions / side effects: Skin Lesion, Stevens-Johnson Syndrome

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Lamictal (Lamotrigine)

Other drugs received by patient: Adderall 10; Klonopin; Guaifenesin



Adverse event in male receiving Lamictal (Lamotrigine)

Reported by a physician from United States on 2007-05-29

Patient: male

Adverse reactions / side effects: Burns Second Degree, Skin Exfoliation, Stevens-Johnson Syndrome

Suspect drug(s):
Lamictal (Lamotrigine)



Adverse event in 26 year old female receiving Lamictal (Lamotrigine)

Reported by a consumer/non-health professional from United States on 2007-05-16

Patient: 26 year old female, weighing 61.4 kg (135.1 pounds)

Adverse reactions / side effects: Malaise, Dyspnoea, Drug Hypersensitivity, Pharyngolaryngeal Pain, Drug Administration Error, Toxic Epidermal Necrolysis, Pharyngitis Streptococcal, Asthenia, Stevens-Johnson Syndrome

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

Suspect drug(s):
Lamictal
    Administration route: Oral
    Indication: Bipolar Disorder
    Start date: 2006-12-19

Penicillin

Other drugs received by patient: Trazodone HCL



Adverse event in 33 year old female receiving Lamictal (Lamotrigine)

Reported by a consumer/non-health professional from United States on 2007-05-15

Patient: 33 year old female, weighing 54.1 kg (119.0 pounds)

Adverse reactions / side effects: Skin Exfoliation, Toxic Epidermal Necrolysis, Pulmonary Embolism, Hepatic Failure, Epilepsy, Electroencephalogram Abnormal, Renal Failure, Skin Lesion, Rash Vesicular, Mucous Membrane Disorder, Stevens-Johnson Syndrome

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

Suspect drug(s):
Lamictal (Lamotrigine)



Adverse event in male receiving Lamictal (Lamotrigine)

Reported by a consumer/non-health professional from United States on 2007-05-15

Patient: male

Adverse reactions / side effects: Burns Second Degree, Skin Exfoliation, Stevens-Johnson Syndrome

Suspect drug(s):
Lamictal (Lamotrigine)



Adverse event in male receiving Lamictal (Lamotrigine)

Reported by a consumer/non-health professional from United States on 2007-04-27

Patient: male

Adverse reactions / side effects: Rash, Stevens-Johnson Syndrome

Suspect drug(s):
Lamictal (Lamotrigine)

Other drugs received by patient: Cymbalta; Zyprexa



Adverse event in 43 year old female receiving Lamictal (Lamotrigine)

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

Patient: 43 year old female, weighing 68.0 kg (149.7 pounds)

Adverse reactions / side effects: Drug Hypersensitivity, Impaired Work Ability, Pharyngitis Streptococcal, Asthenia, Haemorrhoidal Haemorrhage, Scarlet Fever, Stevens-Johnson Syndrome

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Lamictal
    Dosage: 25 mg daily oral
    Administration route: Oral
    Indication: Anxiety
    Start date: 2007-03-19
    End date: 2007-03-29

Lamictal
    Dosage: 25 mg daily oral
    Administration route: Oral
    Indication: Mood Swings
    Start date: 2007-03-19
    End date: 2007-03-29

Other drugs received by patient: Pexeva



Adverse event in 59 year old male receiving Lamictal (Lamotrigine)

Reported by a consumer/non-health professional from Argentina on 2007-04-20

Patient: 59 year old male

Adverse reactions / side effects: Multi-Organ Failure, Intestinal Perforation, Sepsis, Pharyngeal Lesion, Stevens-Johnson Syndrome, Oral Soft Tissue Disorder, Infection

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

Suspect drug(s):
Lamictal (Lamotrigine)

Other drugs received by patient: Fluoxetine; Aspirin



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