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The edition · Clinical Pharmacology

One week of rifampicin cut long-acting rilpivirine levels by 83%, below target

A measured case shows how fast enzyme induction strips a depot antiretroviral and how fast it recovers; low-dose apixaban on dialysis had no major bleeds in a small clinic series; and FDA recorded label supplements for abrocitinib and toripalimab.

The edition in brief

A Dutch case report measured plasma levels in a man on long-acting cabotegravir and rilpivirine every eight weeks who needed seven days of rifampicin. With oral dolutegravir-based bridging in place, cabotegravir fell 57% and rilpivirine 83%, below its target trough, then recovered within a week of stopping rifampicin as the depot continued to release drug; viral load stayed undetectable. The fall in rilpivirine exceeded model predictions. A UK tertiary clinic series of 88 patients on dialysis found no major bleeds with apixaban 2.5 mg twice daily against 7.3% with vitamin K antagonists, with more strokes on apixaban (7.1 vs 1.1 per 100 patient-years); neither difference was significant, and nearly all apixaban anti-Xa troughs were within the general population range. FDA's database records supplemental approvals for abrocitinib on 2 September and toripalimab on 31 August; the records do not state what changed. A commentary argues that adverse drug reaction forms should capture withdrawal reactions, to support safer deprescribing.

In this edition
01
Clinical update

Rifampicin cut long-acting rilpivirine by 83% in a week, then levels recovered

If rifampicin cannot be avoided in a patient on long-acting cabotegravir and rilpivirine, give full oral antiretroviral cover and monitor levels and viral load.

2 min · British journal of clinical pharmacologyRead →
Primary outcome
Plasma cabotegravir and rilpivirine concentrations during 7 days of rifampicin
Effect
Cabotegravir -57% (to 0.90 mg/L); rilpivirine -83% (to 0.022 mg/L, below 0.032 target)
02Regulatory

FDA records a supplemental approval for abrocitinib

FDA recorded supplemental approvals for abrocitinib and toripalimab; read the revised labels before changing practice, as the records do not say what changed.

1 minRead →
03Research

Low-dose apixaban on dialysis: no major bleeds, but more strokes, in a small series

Low-dose apixaban may be a second-line option on dialysis when a vitamin K antagonist is unsuitable, ideally with anti-Xa monitoring; this series is too small to show it is safer.

2 min · British journal of clinical pharmacologyRead →
04Pearl

Rifampicin induction takes about two weeks to come and to go

Allow about two weeks for rifampicin induction to wear off, and adjust induced drugs over that period after the last dose.

1 minRead →
05Practice changer

Report withdrawal reactions as adverse drug reactions when deprescribing

When deprescribing, report withdrawal and rebound reactions to your pharmacovigilance programme with the taper details, and warn patients what to expect.

1 min · Clinical pharmacology and therapeuticsRead →

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