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Index of reports
> Cases resulting in hospitalization (301)
> Cases with Stevens-Johnson Syndrome (52)
Below is the selection of adverse event reports related to Lamictal (Lamotrigine) that includes cases resulting in hospitalization where reactions include stevens-johnson syndrome.
Reports 1 - 25 of 52 Next >>
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 female receiving Lamictal (Lamotrigine)
Reported by a individual with unspecified qualification from United States on 2007-10-05
Patient: female, weighing 56.9 kg (125.1 pounds)
Adverse reactions / side effects: Drug Clearance Decreased, Thrombocytopenia, Generalised Oedema, Stevens-Johnson Syndrome
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Lamictal
Dosage: 100 mg bid po
Administration route: Oral
Indication: Convulsion
Start date: 2007-09-13
Lamictal
Dosage: 100 mg bid po
Administration route: Oral
Indication: Convulsion
Start date: 2007-10-01
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 female receiving Lamictal (Lamotrigine)
Reported by a consumer/non-health professional from United States on 2007-10-02
Patient: female
Adverse reactions / side effects: Pyrexia, Organ Failure, Stevens-Johnson Syndrome, Influenza Like Illness
Adverse event resulted in: death, hospitalization
Suspect drug(s):
FLU Vaccine
Indication: Prophylaxis
Lamictal
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Adverse event in 51 year old female receiving Lamictal (Lamotrigine)
Reported by a consumer/non-health professional from United States on 2007-07-19
Patient: 51 year old female
Adverse reactions / side effects: Lymphadenopathy, Hypersensitivity, Pain, Scab, Urticaria, Pyrexia, Swollen Tongue, Anxiety, Pharyngeal Oedema, Tongue Disorder, Oedema Peripheral, Vision Blurred, Bronchospasm, Stevens-Johnson Syndrome, Blister
Adverse event resulted in: hospitalization
Suspect drug(s):
Lamictal (Lamotrigine)
Other drugs received by patient: NO Concurrent Medication
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 62 year old male receiving Lamictal (Lamotrigine)
Reported by a pharmacist from United States on 2007-07-10
Patient: 62 year old male, weighing 80.5 kg (177.1 pounds)
Adverse reactions / side effects: 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 64 year old female receiving Lamictal (Lamotrigine)
Reported by a consumer/non-health professional from Italy on 2007-07-02
Patient: 64 year old female
Adverse reactions / side effects: Death, Sepsis, Pyrexia, Erythema, Stevens-Johnson Syndrome, Blister
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Lamictal (Lamotrigine)
Other drugs received by patient: Duloxetine; Lormetazepam
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 53 year old male receiving Lamictal (Lamotrigine)
Reported by a physician from United States on 2007-06-27
Patient: 53 year old male
Adverse reactions / side effects: 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 2007-06-21
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 51 year old female receiving Lamictal (Lamotrigine)
Reported by a consumer/non-health professional from France on 2007-06-18
Patient: 51 year old female
Adverse reactions / side effects: Dysphagia, Oral Mucosal Eruption, Respiratory Distress, Erythema, Vaginal Ulceration, Urinary Tract Disorder, Face Oedema, Skin Lesion, Rash Maculo-Papular, Stevens-Johnson Syndrome, Pharyngitis
Adverse event resulted in: hospitalization
Suspect drug(s):
Lamictal (Lamotrigine)
Other drugs received by patient: Depakene; Triflucan; Zeclar; Pariet; Maxilase; Medrol; Diffu-K; Magnogene; Sterdex; Daktarin; Lomexin
Adverse event in female receiving Lamictal (Lamotrigine)
Reported by a consumer/non-health professional from United States on 2007-06-14
Patient: female
Adverse reactions / side effects: Rash, Pyrexia, Stevens-Johnson Syndrome, Scar
Adverse event resulted in: hospitalization
Suspect drug(s):
Lamictal (Lamotrigine)
Other drugs received by patient: Zoloft
Adverse event in 17 year old female receiving Lamictal (Lamotrigine)
Reported by a physician from United States on 2007-06-11
Patient: 17 year old female, weighing 54.4 kg (119.7 pounds)
Adverse reactions / side effects: Headache, Facial Pain, Streptococcal Infection, White Blood Cells Urine Positive, Dysuria, RED Blood Cells Urine Positive, Rash Maculo-Papular, Stevens-Johnson Syndrome
Adverse event resulted in: hospitalization
Suspect drug(s):
Provigil
Dosage: 300 mg qam oral
Administration route: Oral
Indication: Attention Deficit / Hyperactivity Disorder
Start date: 2005-10-18
End date: 2005-12-02
Provigil
Dosage: 100 mg qd oral
Administration route: Oral
Indication: Attention Deficit / Hyperactivity Disorder
Start date: 2006-01-13
End date: 2006-01-13
Lamictal
Dosage: 150 mg qd oral
Administration route: Oral
Indication: Bipolar Disorder
Start date: 2005-10-18
Lamictal
Dosage: 300 mg bid oral
Administration route: Oral
Indication: Bipolar Disorder
Start date: 2005-11-30
End date: 2005-12-03
Other drugs received by patient: Abilify. Mfr: Otusaka Pharmaceutical Co., Ltd.; Spironolactone
Adverse event in 36 year old male receiving Lamictal (Lamotrigine)
Reported by a physician from United States on 2007-06-08
Patient: 36 year old male
Adverse reactions / side effects: LIP Swelling, Oral Mucosal Blistering, Rash Pruritic, Oedema Peripheral, Blindness, Conjunctival Scar, Pharyngitis, Stevens-Johnson Syndrome
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Zithromax
Lamictal
Administration route: Oral
Indication: Bipolar Disorder
Start date: 2006-10-23
End date: 2006-11-21
Omnicef
Indication: Pharyngitis
Medrol
Vicodin
Other drugs received by patient: Sertraline Hydrochloride; Mometasone Furoate; Sumatriptan Succinate; Hydrochlorothiazide
Adverse event in 51 year old female receiving Lamictal (Lamotrigine)
Reported by a lawyer from United States on 2007-06-07
Patient: 51 year old female
Adverse reactions / side effects: Lymphadenopathy, Hypersensitivity, Pain, Scab, Urticaria, Pyrexia, Swollen Tongue, Anxiety, Pharyngeal Oedema, Tongue Disorder, Oedema Peripheral, Vision Blurred, Bronchospasm, Stevens-Johnson Syndrome, Blister
Adverse event resulted in: hospitalization
Suspect drug(s):
Lamictal (Lamotrigine)
Other drugs received by patient: NO Concurrent Medication
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 51 year old female receiving Lamictal (Lamotrigine)
Reported by a lawyer from United States on 2007-05-18
Patient: 51 year old female
Adverse reactions / side effects: Lymphadenopathy, Scab, Pain, Swollen Tongue, Pyrexia, Anxiety, Pharyngeal Oedema, Tongue Disorder, Oedema Peripheral, Vision Blurred, Blister, Stevens-Johnson Syndrome
Adverse event resulted in: hospitalization
Suspect drug(s):
Lamictal (Lamotrigine)
Other drugs received by patient: NO Concurrent Medication
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 51 year old female receiving Lamictal (Lamotrigine)
Reported by a lawyer from United States on 2007-04-27
Patient: 51 year old female
Adverse reactions / side effects: Lymphadenopathy, Scab, Pain, Swollen Tongue, Pyrexia, Anxiety, Pharyngeal Oedema, Tongue Disorder, Oedema Peripheral, Vision Blurred, Blister, Stevens-Johnson Syndrome
Adverse event resulted in: hospitalization
Suspect drug(s):
Lamictal (Lamotrigine)
Other drugs received by patient: NO Concurrent Medication
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 36 year old female receiving Lamictal (Lamotrigine)
Reported by a physician from United States on 2007-04-25
Patient: 36 year old female
Adverse reactions / side effects: Skin Graft, Toxic Epidermal Necrolysis, Rash, Stevens-Johnson Syndrome
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Lamictal (Lamotrigine)
Other drugs received by patient: Hydroxyzine
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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