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Index of reports
> Cases resulting in life threatening events (91)
> Cases with Pyrexia (17)
Below is the selection of adverse event reports related to Lamictal (Lamotrigine) that includes cases resulting in life threatening events where reactions include pyrexia.
Adverse event in 26 year old female receiving Lamictal (Lamotrigine)
Reported by a consumer/non-health professional from United States on 2007-10-19
Patient: 26 year old female, weighing 46.8 kg (103.0 pounds)
Adverse reactions / side effects: Back Pain, Confusional State, Abdominal Pain, Jaundice, Vomiting, Nausea, Drug Hypersensitivity, Pyrexia, Erythema, Hepatitis, Hepatic Enzyme Increased, Abdominal Pain Upper, Postnasal Drip, Fatigue, Hepatotoxicity, Upper Respiratory Tract Infection, Anorexia
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Lamictal (Lamotrigine)
Other drugs received by patient: Carbamazepine; Keppra; Prevacid
Adverse event in 61 year old female receiving Lamictal (Lamotrigine)
Reported by a consumer/non-health professional from United States on 2007-10-16
Patient: 61 year old female
Adverse reactions / side effects: Lymphadenopathy, Hepatic Cyst, Chills, Hepatic Failure, Rash, Headache, Pyrexia
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Lamictal (Lamotrigine)
Other drugs received by patient: Seroquel
Adverse event in 41 year old male receiving Lamictal (Lamotrigine)
Reported by a consumer/non-health professional from United States on 2007-10-09
Patient: 41 year old male
Adverse reactions / side effects: Pneumonia, Rash, Pyrexia
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Lamictal (Lamotrigine)
Other drugs received by patient: Campral; Lexapro; Lyrica
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 15 year old female receiving Lamictal (Lamotrigine)
Reported by a consumer/non-health professional from United States on 2007-07-24
Patient: 15 year old female
Adverse reactions / side effects: Gallbladder Enlargement, Hypersensitivity, Mouth Ulceration, Pain, Pyrexia, Treatment Noncompliance, Drug Toxicity, Multi-Organ Failure, Eye Disorder, Vomiting, Nausea, Rash, Hepatic Enzyme Increased, Eating Disorder, Rash Macular, Rocky Mountain Spotted Fever, Renal Failure, Eye Swelling, Asthenia, Infection
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Lamictal (Lamotrigine)
Other drugs received by patient: Adderall XR 10
Adverse event in 47 year old female receiving Lamictal (Lamotrigine)
Reported by a consumer/non-health professional from United States on 2007-07-19
Patient: 47 year old female
Adverse reactions / side effects: LIP Swelling, Lymphadenopathy, Hypoventilation, Eye Discharge, Urticaria, Chapped Lips, Pyrexia, Erythema, Pharyngeal Oedema, Auricular Swelling, Burns Third Degree, Skin Lesion, Open Wound, Blister, Candidiasis, Swelling Face, LIP DRY, Rash, Swelling, Eye Swelling
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Lamictal (Lamotrigine)
Other drugs received by patient: Revlimid; Concurrent Medications
Adverse event in 47 year old female receiving Lamictal (Lamotrigine)
Reported by a consumer/non-health professional from United States on 2007-07-12
Patient: 47 year old female
Adverse reactions / side effects: Hypoventilation, Eye Discharge, Rash, Pyrexia, Skin Lesion, Swelling, Eye Swelling, Candidiasis
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Lamictal (Lamotrigine)
Other drugs received by patient: Revlimid; Concurrent Medications
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 26 year old female receiving Lamictal (Lamotrigine)
Reported by a consumer/non-health professional from Italy on 2007-04-26
Patient: 26 year old female
Adverse reactions / side effects: Lymphadenopathy, Arthralgia, Pyrexia, Drug Rash With Eosinophilia and Systemic Symptoms, Leukocytosis, Rash Pruritic
Adverse event resulted in: life threatening event
Suspect drug(s):
Lamictal (Lamotrigine)
Other drugs received by patient: Escitalopram
Adverse event in 52 year old male receiving Lamictal (Lamotrigine)
Reported by a physician from France on 2007-04-04
Patient: 52 year old male
Adverse reactions / side effects: Drug Eruption, Pruritus, Chills, LIP Oedema, Pyrexia, Eosinophilia, Convulsion, Rash Morbilliform, Cough
Adverse event resulted in: life threatening event
Suspect drug(s):
Ciprofloxacin HCL
Administration route: Oral
Indication: Unevaluable Event
Start date: 2005-09-25
End date: 2005-09-30
Imovane
Dosage: total daily dose: 7.5 mg
Administration route: Oral
Indication: Unevaluable Event
Start date: 2005-01-01
End date: 2005-08-01
Imovane
Dosage: total daily dose: 7.5 mg
Administration route: Oral
Start date: 2005-09-22
End date: 2005-10-03
Lamictal
Administration route: Oral
Indication: Traumatic Brain Injury
Start date: 2005-09-01
End date: 2005-09-13
Lamictal
Administration route: Oral
Start date: 2005-09-07
End date: 2005-09-01
Lamictal
Administration route: Oral
Start date: 2005-09-01
End date: 2005-09-01
Lamictal
Administration route: Oral
Start date: 2005-09-13
End date: 2005-10-03
Depakene
Dosage: total daily dose: 2000 mg unit dose: 500 mg
Administration route: Oral
Indication: Traumatic Brain Injury
End date: 2005-09-11
Stablon
Administration route: Oral
Indication: Unevaluable Event
Xenetix
Indication: Prophylaxis
Start date: 2005-09-20
End date: 2005-09-20
Xenetix
Start date: 2005-10-03
End date: 2005-10-03
Other drugs received by patient: Fosamax; Orocal D3
Adverse event in 52 year old male receiving Lamictal (Lamotrigine)
Reported by a consumer/non-health professional from France on 2007-04-02
Patient: 52 year old male
Adverse reactions / side effects: Hypersensitivity, LIP Disorder, Pruritus, Skin Exfoliation, Chills, Pyrexia, LIP Oedema, Cheilitis, Tongue Disorder, Oedema, Rash Morbilliform, Gastrooesophageal Reflux Disease, Oxygen Saturation Decreased, Cough, Dysphagia, Eosinophilia, Rash Maculo-Papular
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Lamictal
Administration route: Oral
Indication: Head Injury
Start date: 2005-09-07
End date: 2005-10-03
Clamoxyl
Indication: Sputum Purulent
Start date: 2005-10-12
End date: 2005-10-14
Imovane
Dosage: 7.5mg per day
Administration route: Oral
End date: 2005-10-03
Ciprofloxacin HCL
Administration route: Oral
Indication: Head Injury
Start date: 2005-09-25
End date: 2005-09-30
Depakene
Dosage: 1000mg twice per day
Administration route: Oral
Indication: Head Injury
End date: 2005-09-11
Stablon
Administration route: Oral
Iobitridol
Dosage: 120ml per day
Start date: 2005-10-03
End date: 2005-10-03
Other drugs received by patient: Fosamax; Orocal
Adverse event in 28 year old female receiving Lamictal (Lamotrigine)
Reported by a individual with unspecified qualification from United States on 2007-02-06
Patient: 28 year old female, weighing 81.6 kg (179.6 pounds)
Adverse reactions / side effects: Pain, Swollen Tongue, Pyrexia, Rash, Oral Soft Tissue Disorder
Adverse event resulted in: life threatening event, disablity
Suspect drug(s):
Lamictal (Lamotrigine)
Adverse event in 52 year old male receiving Lamictal (Lamotrigine)
Reported by a physician from France on 2007-01-30
Patient: 52 year old male
Adverse reactions / side effects: Drug Eruption, Pruritus, Chills, LIP Oedema, Pyrexia, Eosinophilia, Convulsion, Rash Morbilliform, Cough
Adverse event resulted in: life threatening event
Suspect drug(s):
Ciprofloxacin
Administration route: Oral
Indication: Unevaluable Event
Start date: 2005-09-25
End date: 2005-09-30
Imovane
Dosage: total daily dose: 7.5 mg
Administration route: Oral
Indication: Unevaluable Event
Start date: 2005-01-01
End date: 2005-08-01
Imovane
Dosage: total daily dose: 7.5 mg
Administration route: Oral
Start date: 2005-09-22
End date: 2005-10-03
Lamictal
Administration route: Oral
Indication: Traumatic Brain Injury
Start date: 2005-09-01
End date: 2005-09-13
Lamictal
Administration route: Oral
Start date: 2005-09-07
End date: 2005-09-01
Lamictal
Administration route: Oral
Start date: 2005-09-01
End date: 2005-09-01
Lamictal
Administration route: Oral
Start date: 2005-09-13
End date: 2005-10-03
Depakene
Dosage: total daily dose: 2000 mg unit dose: 500 mg
Administration route: Oral
Indication: Traumatic Brain Injury
End date: 2005-09-11
Stablon
Administration route: Oral
Indication: Unevaluable Event
Xenetix
Indication: Prophylaxis
Start date: 2005-09-20
End date: 2005-09-20
Xenetix
Start date: 2005-10-03
End date: 2005-10-03
Other drugs received by patient: Fosamax; Orocal D3
Adverse event in 52 year old male receiving Lamictal (Lamotrigine)
Reported by a consumer/non-health professional from France on 2007-01-29
Patient: 52 year old male
Adverse reactions / side effects: Hypersensitivity, LIP Disorder, Pruritus, Skin Exfoliation, Chills, Pyrexia, LIP Oedema, Cheilitis, Tongue Disorder, Oedema, Rash Morbilliform, Gastrooesophageal Reflux Disease, Oxygen Saturation Decreased, Cough, Dysphagia, Eosinophilia, Rash Maculo-Papular
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Lamictal
Administration route: Oral
Indication: Head Injury
Start date: 2005-09-07
End date: 2005-10-03
Clamoxyl
Indication: Sputum Purulent
Start date: 2005-10-12
End date: 2005-10-14
Imovane
Dosage: 7.5mg per day
Administration route: Oral
End date: 2005-10-03
Ciprofloxacin
Administration route: Oral
Indication: Head Injury
Start date: 2005-09-25
End date: 2005-09-30
Depakene
Dosage: 1000mg twice per day
Administration route: Oral
Indication: Head Injury
End date: 2005-09-11
Stablon
Administration route: Oral
Iobitridol
Dosage: 120ml per day
Start date: 2005-10-03
End date: 2005-10-03
Other drugs received by patient: Fosamax; Orocal
Adverse event in 37 year old female receiving Lamictal (Lamotrigine)
Reported by a consumer/non-health professional from United States on 2007-01-09
Patient: 37 year old female
Adverse reactions / side effects: Blood Ethanol Increased, Overdose, Coma, Pyrexia, Convulsion
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Lamictal (Lamotrigine)
Other drugs received by patient: Cymbalta
Adverse event in 27 year old female receiving Lamictal (Lamotrigine)
Reported by a consumer/non-health professional from United States on 2007-01-04
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, Lactic Acidosis, Acidosis, Pyrexia, Pericardial Effusion, Acute Respiratory Distress Syndrome, Myocarditis, Fungus Urine Test Positive, Pneumonia, Chest Discomfort, Urine Output Decreased, Anaemia, Tremor, Occult Blood Positive, Flushing, Atelectasis, Hypersensitivity, Chills, Generalised Oedema, Fungaemia, Pleural Effusion, Stevens-Johnson Syndrome, Intestinal Ischaemia, Dyspnoea, International Normalised Ratio Increased, Hepatic Enzyme Increased, Ascites, Mucosal Erosion, Haematochezia, 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 84 year old female receiving Lamictal (Lamotrigine)
Reported by a consumer/non-health professional from United States on 2007-01-04
Patient: 84 year old female
Adverse reactions / side effects: Hypersensitivity, Urinary Tract Infection, Toxic Epidermal Necrolysis, Rash, Purpura, Pyrexia, Herpes Zoster, Malaise, Liver Function Test Abnormal
Adverse event resulted in: death, life threatening event, hospitalization, disablity
Suspect drug(s):
Lamictal (Lamotrigine)
Other drugs received by patient: Lipitor; Ultram; Epidural
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