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Zovirax (Acyclovir) - Adverse Event Reports - Disability - Blood Urea Increased

 



Index of reports > Cases resulting in disability (6) > Cases with Blood Urea Increased (1)

Below is the selection of adverse event reports related to Zovirax (Acyclovir) that includes cases resulting in disability where reactions include blood urea increased.

Adverse event in 32 year old female receiving Zovirax (Acyclovir)

Reported by a physician from Japan on 2007-10-10

Patient: 32 year old female, weighing 53.0 kg (116.6 pounds)

Adverse reactions / side effects: Abdominal Pain, Blood Urea Increased, Vomiting, Nausea, Hyperprolactinaemia, Nephritis, Face Oedema, C-Reactive Protein Increased, Blood Potassium Decreased, Abdominal Symptom, Oedema, Urinary Retention, Blood Creatinine Increased, Beta 2 Microglobulin Increased, Azotaemia, White Blood Cell Count Increased

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Valtrex
    Administration route: Oral
    Indication: Herpes Zoster
    Start date: 2007-08-16
    End date: 2007-08-18

Zovirax
    Indication: Herpes Zoster
    Start date: 2007-08-16
    End date: 2007-08-18

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