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Lamictal (Lamotrigine) - Adverse Event Reports - Disability - Skin Lesion

 



Index of reports > Cases resulting in disability (81) > Cases with Skin Lesion (4)

Below is the selection of adverse event reports related to Lamictal (Lamotrigine) that includes cases resulting in disability where reactions include skin lesion.

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 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 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)

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