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Kaletra (Lopinavir / Ritonavir) - Toxic Epidermal Necrolysis - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with Toxic Epidermal Necrolysis ()

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Kaletra (Lopinavir / Ritonavir) where reactions include toxic epidermal necrolysis. The selected reports were submitted to the FDA during the sample period of about a year.

Possible Kaletra side effects in male

Reported by a physician from France on 2012-01-13

Patient: male

Reactions: Confusional State, Blood Creatine Phosphokinase Increased, Dreamy State, Quality of Life Decreased, Coma, Corneal Disorder, Eye Infection, Abdominal Pain Upper, Overdose, Bronchial Disorder, Hypoxia, Oral Mucosa Erosion, Stevens-Johnson Syndrome, Renal Disorder, Toxic Epidermal Necrolysis, Cardiogenic Shock, Odynophagia, Nosocomial Infection, Eye Pain, Anxiety, Lung Disorder, Dysuria, Pharyngeal Erosion, DRY Eye

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

Drug(s) suspected as cause:
Kaletra
    Dosage: 200/50mg
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2008-02-05
    End date: 2008-03-06

Truvada
    Dosage: 200mg/245mg
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2008-02-05
    End date: 2008-03-06

Other drugs received by patient: Primperan TAB; Magnesium Hydroxide TAB; Alprazolam; Raltegravir; Gaviscon; PPI; Maraviroc; Enfuvirtide; Acetaminophen; Aspirin



Possible Kaletra side effects in male

Reported by a physician from France on 2011-12-16

Patient: male

Reactions: Confusional State, Blood Creatine Phosphokinase Increased, Dreamy State, Quality of Life Decreased, Coma, Corneal Disorder, Eye Infection, Abdominal Pain Upper, Overdose, Bronchial Disorder, Hypoxia, Oral Mucosa Erosion, Stevens-Johnson Syndrome, Renal Disorder, Toxic Epidermal Necrolysis, Nosocomial Infection, Odynophagia, Cardiogenic Shock, Eye Pain, Anxiety, Lung Disorder, Dysuria, Pharyngeal Erosion, DRY Eye

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

Drug(s) suspected as cause:
Kaletra
    Dosage: 200/50mg (unit dose)
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2008-02-05
    End date: 2008-02-28

Truvada
    Dosage: 200mg/245mg (unit dose)
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2008-02-05
    End date: 2008-02-28

Other drugs received by patient: Raltegravir; Maraviroc; Primperan TAB; Magnesium Hydroxide TAB; Aspirin; PPI; Enfuvirtide; Gaviscon; Acetaminophen



Possible Kaletra side effects in male

Reported by a lawyer from France on 2011-12-05

Patient: male

Reactions: Confusional State, Blood Creatine Phosphokinase Increased, Dreamy State, Quality of Life Decreased, Coma, Corneal Disorder, Eye Infection, Abdominal Pain Upper, Overdose, Bronchial Disorder, Hypoxia, Oral Mucosa Erosion, Stevens-Johnson Syndrome, Renal Disorder, Toxic Epidermal Necrolysis, Nosocomial Infection, Odynophagia, Cardiogenic Shock, Eye Pain, Anxiety, Lung Disorder, Dysuria, Pharyngeal Erosion, DRY Eye

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

Drug(s) suspected as cause:
Kaletra
    Dosage: 200/50mg (unit dose)
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2008-02-05
    End date: 2008-02-28

Truvada
    Dosage: 200mg/245mg (unit dose)
    Administration route: Oral
    Indication: HIV Infection
    Start date: 2008-02-05
    End date: 2008-02-28

Other drugs received by patient: Maraviroc; Enfuvirtide; Magnesium Hydroxide TAB; Aspirin; PPI; Gaviscon; Raltegravir; Acetaminophen; Primperan TAB

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