Dear Editor,

The World Health Organization (WHO) launched the SOLIDARITY trial on 20 March which includes already approved drugs for other diseases repurposed to treat COVID-19 [1]. Mechanisms of action of these drugs are already known as well as their toxicity. We highlight the potential risks of combining drugs with established macular toxicity that are hydroxychloroquine and ritonavir, as actually performed in our Lombardia region, the heart of COVID-19 Italian break-out [2].

Chloroquine and his hydroxylated analog hydroxychloroquine were initially used as antimalarial agents and then extended to rheumatic disorders [3]. Long-term toxicity of chloroquine and hydroxychloroquine has been widely demonstrated, and recommended protocols as the one proposed by the American Academy of Ophthalmology (AAO) are followed worldwide; acute toxicity has also been reported after treatments at standard dosage after just 2 months [4, 5]. Risk factors include a preexisting maculopathy, renal disease, and tamoxifen use. Tamoxifen use increased the risk of toxicity by 5-folds; this drug has a reported retinal toxicity on its own, and therefore, a synergic toxicity has been hypothesized [4].

Ritonavir is an antiviral drug used in the highly active antiretroviral therapy (HAART) against HIV; it acts as a protease inhibitor and also blocks cytochrome P450; thus, it is given in combination with other antivirals, like lopinavir, to boost their effect. Its toxicity has never been investigated in depth, but since the first experimental studies, hypertrophy of the retinal pigmented epithelium (RPE) was reported. Multiple case reports described toxicity for the RPE with a bull’s eye pattern that resembles the one observed with hydroxychloroquine [6].

Therefore, we alert for a possible synergic toxicity for the retina, just like what happens with hydroxychloroquine and tamoxifen and postulate the need for an ophthalmologic follow-up program for these patients.