→Appendix 1: tenofovir disoproxil
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▶Common or very common Abdominal distension. flatulence
▶Uncommon Proximal renal tubulopathy
▶Rare or very rare Acute tubular necrosis. hepatic disorders
. nephritis. nephrogenic diabetes insipidus. renal
impairment
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Manufacturer advises caution in
decompensated hepatic disease (limited information
available).
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Dose adjustments Granules: 132 mg once daily if eGFR
30–50 mL/minute/1.73 m2; 66 mg once daily if eGFR
20–30 mL/minute/1.73 m2; 33 mg once daily if eGFR
10–20 mL/minute/1.73 m2.
Tablets: 245 mg every 2 days if eGFR
30–50 mL/minute/1.73 m2; 245 mg every 3–4 days if eGFR
10–30 mL/minute/1.73 m2.
Monitoring Monitor renal function—interrupt treatment if
further deterioration.
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▶Test renal function and serum phosphate before
treatment, then every 4 weeks (more frequently if at
increased risk of renal impairment) for 1 year and then
every 3 months, interrupt treatment if renal function
deteriorates or serum phosphate decreases.
▶When treating chronic hepatitis B with tenofovir, monitor
liver function tests every 3 months and viral markers for
hepatitis B every 3–6 months during treatment (continue
monitoring for at least 1 year after discontinuation—
recurrent hepatitis may occur on discontinuation).
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