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CASE REPORT |
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Year : 2021 | Volume
: 35
| Issue : 2 | Page : 103-105 |
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A case report of urticaria as a rare side effect of favipiravir in a patient with COVID-19
Amit Kumar1, Ankita Gupta2
1 Department of Respiratory Medicine, Max Shalimar Bagh, Delhi, India 2 Department of Respiratory Medicine, University College of Medical Sciences, GTB Hospital, Delhi, India
Date of Submission | 11-Jan-2021 |
Date of Acceptance | 10-Jan-2022 |
Date of Web Publication | 08-Jul-2022 |
Correspondence Address: Dr. Ankita Gupta C-40, East Krishna Nagar, Delhi - 110 051 India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/ijaai.ijaai_5_21
COVID-19 pandemic has been caused by severe acute respiratory syndrome coronavirus 2 which has caused worldwide health concerns. A 48-year-old female suffering from COVID-19 was started on favipiravir (FPV) along with other drugs. Within 12 h of initiation of FPV, the patient developed urticaria all over the body. She was given stat dose of injection dexamethasone and injection avil. Symptoms resolved within 3 days. Urticaria is a rare side effect of FPV but requires vigilant monitoring in the treatment of COVID-19 patients.
Keywords: COVID-19, favipiravir, urticaria
How to cite this article: Kumar A, Gupta A. A case report of urticaria as a rare side effect of favipiravir in a patient with COVID-19. Indian J Allergy Asthma Immunol 2021;35:103-5 |
How to cite this URL: Kumar A, Gupta A. A case report of urticaria as a rare side effect of favipiravir in a patient with COVID-19. Indian J Allergy Asthma Immunol [serial online] 2021 [cited 2022 Aug 8];35:103-5. Available from: https://www.ijaai.in/text.asp?2021/35/2/103/350081 |
Introduction | |  |
The new coronavirus, severe acute respiratory syndrome coronavirus 2, is associated with a wide variety of cutaneous manifestations. Although new skin manifestations caused by COVID-19 are continuously being described, other cutaneous entities should also be considered in the differential diagnoses, including adverse cutaneous reactions to drugs used in the treatment of COVID-19 infections.[1] Favipiravir (FPV), an antiviral drug, is currently being considered for the treatment of COVID-19, and no adverse cutaneous events have been reported to date.[2]
Case Report | |  |
We hereby present a case of a 48-year-old previously healthy married female with two children presented to the emergency department with a 1-day history of bilateral eyelid swelling and a generalized pruritic rash, all starting simultaneously. The rash started on the back and subsequently spread to her face and extremities within hours. She denied similar previous presentations or history of allergies. She did not report a history of smoking or alcohol consumption and also denied family history of allergies. Before the symptoms occurred, she had a 3-day history of mild, nonproductive cough with low-grade fever with a history of COVID-19 contact in the family, for which she did online consultation and was advised nasopharyngeal swab test for SARS-CoV-2 using a reverse transcriptase-polymerase chain reaction (RT-PCR) assay. COVID RT-PCR report came to be positive. She was advised home isolation and with her consent was started from day 1 on tablet azithromycin 500 mg once a day for 5 days, tablet ivermectin 12 mg 1 tablet once a day for 3 days, tablet zinc 50 mg once a day, capsule Vitamin C 1000 mg once a day, and tablet paracetamol 500 mg sos. From day 4, she was started on FPV orally (1800 mg twice daily [day 1], followed by 800 mg twice daily [days 2–14]). Within 3 h of ingestion of FPV, she noticed rashes all over the body, for which she presented to the emergency.
Vital signs on admission were as follows: temperature 37.4°C, blood pressure 118/67 mm Hg, respiratory rate 22/min, and oxygen saturation 97% on room air. Erythematous generalized urticarial rash was noted, more prominent on the face and extremities, where it was reddish, itchy, painful maculopapular lesions to start with followed by patches sparing the palms and soles. Dermographism was not detected. Eyelids were swollen with rashes around the eyes as shown in [Figure 1]. No other skin abnormalities were found. There were no wheezes or crackles on chest examination.
Laboratory investigation results were within normal limits. FPV was withheld and the rest of the treatment was continued as above. Urticaria was treated with stat dose of injection dexamethasone 8 mg and injection avil followed by injection dexamethasone 4 mg once a day and oral fexofenadine 180 mg once a day.
During hospitalization, the patient remained vitally and hemodynamically stable and did not require oxygen support. Urticaria resolved within 3 days, and fexofenadine and dexamethasone were discontinued. FPV re-challenge was not attempted. Fever resolved within 5 days, whereas the cough persisted for another 10 days. There was no recurrence of urticaria, and the patient was discharged in accordance with posthospitalization protocol for patient discharged with a positive COVID-19 PCR test result.
Discussion | |  |
Most antiviral agents used for COVID-19 act either by inhibiting RNA-dependent RNA polymerase (remdesivir [GS-5734)) or proteases (lopinavir/ritonavir [LPV/r], FPV, ribavirin, and darunavir). Remdesivir and FPV are considered to be the most effective agents and are mostly used in combination with other COVID-19 medications such as hydroxychloroquine.[2],[3],[4],[5]
Drug hypersensitivity reactions to ribavirin, darunavir, LPV/r, remdesivir, and oseltamivir are rarely reported, whereas no drug hypersensitivity reactions to FPV and umifenovir are known at present.[6],[7],[8],[9]
In the study by Agrawal et al, they concluded that hyperuricemia and elevation in transaminases as the most frequent adverse effects and observed that the frequency of hypersensitivity rash and eczema/pruritus was 0.5%–<1% and <0.5%, respectively.[10]
Hypersensitivity reactions appear to be a rare side effect of FPV, but it should be used cautiously in COVID-19 patients with proper informing about its side effects, and further evaluation is required with large sample size to study the side effects profile of FPV in COVID-19 patients.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
References | |  |
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[Figure 1]
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