Dear Editor,Different cutaneous manifestations of coronavirus disease 2019 (COVID‐19) has been reported, some of which are due to the adverse effects of the medications. Favipiravir, a broad spectrum antiviral, effective against RNA viruses including influenza and Ebola, is one of the current medications approved for the treatment of Covid‐19.Favipiravir selectively inhibits the RNA‐dependent RNA polymerase by acting as a guanine analog. It transforms into active phosphoribosylated form in cells, causing chain termination, slowing viral RNA synthesis and lethal mutagenesis.
Despite the lack of double‐blind randomized controlled studies regarding its effects on severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2), favipiravir has been employed in patients in our country among with Russia, China and India.
It is prescribed to all patients with a positive Reverse Transcriptase Polymerase Chain Reaction (PCR) test. Favipiravir is effective on COVID‐19 only at high doses.
Current treatment scheme consists of 1600 mg bid on the first day followed by 600 mg bid po reaching a total dose of 8000 mg in Turkey. Lungs, kidneys, spleen, and brain are main targets for Favipiravir.
No cutaneous side effect of favipiravir has been reported.The main purpose of the Wood's lamp examination is to enhance the visibility of some substances by using their fluorescence properties. Fluorescence may occur due to certain substances like elastin, collagen, melanin precursors found naturally in the skin or external factors like drugs. Drug metabolites or excipients may accumulate in the skin and cause fluorescence. Yellow fluorescence is observed in both lunula and nails after oral tetracycline and yellow‐green fluorescence on the nails is seen due to quinacrine hydrochloride.We aimed to present the fluorescence of the nails and hair of our five patients, four of whom received only oral favipiravir treatment and paracetamol for COVID‐19 (Table 1). It was observed that the fluorescent parts of the nails were proportionally elongated with the drug initiation time. While fluorescence was seen in the middle portion of nail plates in Case 1, it was seen half portion of the nail plates near the proximal nail folds in Case 2 and 3. Greenish fluorescence was seen in the lunula and nail plate portion near proximal nail fold in Case 4 who used the drug recently. Green fluorescence was also observed on the hair of the four patients. No fluorescence was observed on the nails and hair of Case 5 who did not have favipiravir but had paracetamol (Figures 1, 2, 3, 4). This suggests that the fluorescence formation in the nails is due to favipiravir use.
TABLE 1
The demographic properties and clinical findings of the patients
Case
Age
Gender
BMI kg/m2
Symptoms
Days passeda
Total dose of favipiravir
Fluorescence on nails
Fluorescence on hair
1
27
Female
19.8
None
54
8000 mg
The middle portion of the nail plate and no fluorescence on the proximal and distal part of the nail plate.
Yes
2
42
Female
32.8
Loss of taste and smellHeadacheNausea vomitingDiarrhea
36
8000 mg
One half of the nail plate beginning from the proximal nail fold
Yes
3
51
Female
27.9
CoughBack painWeaknessLoss of taste and smell
30
8000 mg
One half of the nail plate beginning from the proximal nail fold
Yes
4
30
Female
26.6
Nausea vomitingHeadache
17
5600 mgb
The portion of the nail plate near to the proximal nail fold and lunula.
Yes
5
29
Male
34.7
None
17
None
No
No
Days passed after PCR positivity on Wood's examination day.
Quitted the drug because of nausea.
FIGURE 1
Fluorescence on the nail and hair on Case 1. Fluorescence is seen on the middle portion of the nail plates and no fluorescence on the proximal and distal part of the nail plates
FIGURE 2
A,B, Fluorescence on the nail and hair on Case 2. C,D, Fluorescence on the nail and hair on Case 3. Fluorescence is seen on one half of the nail plate beginning from the proximal nail fold
FIGURE 3
Fluorescence on the nail and hair on Case 4. Fluorescence is seen on the portion of the nail plate near to the proximal nail fold and lunula
FIGURE 4
The nail and hair of Case 5. No fluorescence is seen
The demographic properties and clinical findings of the patientsDays passed after PCR positivity on Wood's examination day.Quitted the drug because of nausea.Fluorescence on the nail and hair on Case 1. Fluorescence is seen on the middle portion of the nail plates and no fluorescence on the proximal and distal part of the nail platesA,B, Fluorescence on the nail and hair on Case 2. C,D, Fluorescence on the nail and hair on Case 3. Fluorescence is seen on one half of the nail plate beginning from the proximal nail foldFluorescence on the nail and hair on Case 4. Fluorescence is seen on the portion of the nail plate near to the proximal nail fold and lunulaThe nail and hair of Case 5. No fluorescence is seenThe fluorescence appearance seen in human hair and nails due to favipiravir use has not been reported. In fact, it is a mystery whether the fluorescent substance is mainly caused by the drug metabolites or by the ingredients such as titanium dioxide, yellow ferric oxide in the tablet. The drug's active phosphorylated metabolite was shown in human plasma and its concentration and fluorescence intensity had shown a linear relationship.
Systemically taken metals like titanium create temporary concentrations in blood/body fluids, but have continuity in the the skin appendages like nails and hair which could show the past exposure.
,
The phosphorylated metabolite or the ingredients may explain the fluorescence being present only in the proximal part of the nail plate in patients with recent drug use and the fluorescence retention of the ½ portion of the nail plate in the patients who used the drug a month ago.Considering that the substance accumulated in the tissues like hair and nails with a high dose of favipiravir, it may be necessary to be careful in accumulation in the other tissues. Since it is known that the drug distributes in the kidney, lungs, spleen and brain, and titanium dioxide in organs such as the liver and spleen more, caution should be taken in patients with comorbidities such as liver and kidney dysfunction.
Authors: Suzanne J F Kaptein; Sofie Jacobs; Lana Langendries; Laura Seldeslachts; Sebastiaan Ter Horst; Laurens Liesenborghs; Bart Hens; Valentijn Vergote; Elisabeth Heylen; Karine Barthelemy; Elke Maas; Carolien De Keyzer; Lindsey Bervoets; Jasper Rymenants; Tina Van Buyten; Xin Zhang; Rana Abdelnabi; Juanita Pang; Rachel Williams; Hendrik Jan Thibaut; Kai Dallmeier; Robbert Boudewijns; Jens Wouters; Patrick Augustijns; Nick Verougstraete; Christopher Cawthorne; Judith Breuer; Caroline Solas; Birgit Weynand; Pieter Annaert; Isabel Spriet; Greetje Vande Velde; Johan Neyts; Joana Rocha-Pereira; Leen Delang Journal: Proc Natl Acad Sci U S A Date: 2020-10-09 Impact factor: 11.205
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