Safety profile of COVID-19 drugs in a real clinical setting.

PURPOSE: The coronavirus disease 2019 (COVID-19) caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus has affected millions all over the world and has been declared pandemic, as of 11 March 2020. In addition to the ongoing research and development of vaccines, there is still a dire need for safe and effective drugs for the control and treatment against the SARS-CoV-2 virus infection. Numerous repurposed drugs are under clinical investigations whose reported adverse events can raise worries about their safety. The aim of this review is to illuminate the associated adverse events related to the drugs used in a real COVID-19 setting along with their relevant mechanism(s).
METHOD: Through a literature search conducted on PubMed and Google Scholar database, various adverse events suspected to be induced by eight drugs, including dexamethasone, hydroxychloroquine, chloroquine, remdesivir, favipiravir, lopinavir/ritonavir, ivermectin, and tocilizumab, administered in COVID-19 patients in clinical practice and studies were identified in 30 case reports, 3 case series, and 10 randomized clinical trials.
RESULTS: Mild, moderate, or severe adverse events of numerous repurposed and investigational drugs caused by various factors and mechanisms were observed. Gastrointestinal side effects such as nausea, abdominal cramps, diarrhea, and vomiting were the most frequently followed by cardiovascular, cutaneous, and hepatic adverse events. Few other rare adverse drug reactions were also observed.
CONCLUSION: In light of their ineffectiveness against COVID-19 as evident in large clinical studies, drugs including hydroxychloroquine, lopinavir/ritonavir, and ivermectin should neither be used routinely nor in clinical studies. While lack of sufficient data, it creates doubt regarding the reliability of chloroquine and favipiravir use in COVID-19 patients. Hence, these two drugs can only be used in clinical studies. In contrast, ample well-conducted studies have approved the use of remdesivir, tocilizumab, and dexamethasone under certain conditions in COVID-19 patients. Consequently, it is significant to establish a strong surveillance system in order to monitor the proper safety and toxicity profile of the potential anti-COVID-19 drugs with good clinical outcomes.

Introduction

The world is experiencing one of its most turbulent times with the outbreak of the coronavirus disease 2019 (COVID-19) pandemic. First identified in Wuhan city of Hubei Province, China, in December 2019, the deadly virus has spread across the countries and affected countless [1]. According to World Health Organization (WHO), as of 14 June 2021, there have been 75,541,600 cases of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infected patients confirmed so far, of which there are 3,798,361 deaths, globally. On 9 June 2021, WHO declared that a total of 2,156,550,767 vaccine doses have been administered [2].Therefore, although society and researchers at large have successfully worked towards the development of several vaccines, there still exists a need to discover safe and effective, potential drug candidates for the treatment of COVID-19, especially for patients exhibiting critical clinical symptoms. One efficient and economic approach to identifying promising therapeutic drugs is drug repurposing, which refers to the repositioning or reprofiling of existing medications against viruses, malaria, cancer, and arthritis for a new indication, in this case for COVID-19 [3]. A convenient method utilizing already available drugs with known mechanism, pharmacokinetic and pharmacodynamic characteristics, efficacy, and toxicity profiles leads to low cost and less time consumption for drug development [3, 4]. However, in urgency for early and immediate effective treatments, less consideration has been given to their safety in terms of its associated adverse events. Though the significant investigation of adverse events is lacking, reports from existing studies suggest gastrointestinal, cardiovascular, dermatological, and liver symptoms to be some of the common adverse drug reactions among many others in patients after receiving antiviral therapy for COVID-19 [5]. Causality assessment to determine the exact cause of effects is a big challenge owing to the interweaving contributing, confounding risk factors, and incomplete data or background of the event [6]. Thus, strengthened surveillance of therapeutics and its potentially harmful adverse effects or pharmacovigilance is the need of the hour for better management of COVID-19 therapies.

Considering the inadequate literature on patient safety outcomes for COVID-19 medications, this review aims to elucidate the recent adverse drug events associated with eight potential drugs used against SARS-CoV-2 infection in COVID-19 patients.

Search strategy

A literature search, up to June 2021, was conducted on PubMed and Google Scholar database for studies on AEs suspected to be induced by drugs used against COVID-19. The following keywords (alone or in combination) were used: “adverse drug reactions,” “adverse effects,” “COVID-19 drugs,” “dexamethasone,” “remdesivir,” “favipiravir,” “hydroxychloroquine,” “chloroquine,” “lopinavir/ritonavir,” “tocilizumab,” “ivermectin,” and “side effect.” Only studies where patients with COVID-19 illness were included. Case reports, case series, and randomized clinical trials published in the English language were taken into account.

Repurposed drugs which have been evaluated as potential treatment options against SARS-CoV-2

The transmission of the SARS-CoV-2 virus via respiratory droplets or aerosols from one person to another takes place while coughing, talking, and sneezing [7]. After transmission, the replication cycle of the SARS-CoV-2 virus inside the host cell can be divided into the following major steps: binding and entry into a host cell, viral replicase transcription, genomic transcription and replication, translation of structural proteins, and assembly and release of the virus.

Repurposing different drug agents targeting these key stages of the SARS-CoV-2 virus life cycle could be an effective and faster approach towards antiviral drug development [8]. Figure 1 depicts the infection life cycle of the SARS-COV-2 virus and effective targets of potential therapeutic drug candidates interfering with the steps of viral replication.

Fig. 1

Step by step (1–12) life cycle of SARS-COV-2 virus infection from the attachment of the virus to ACE-2 receptor of the host cell to release of newly formed virus particles and the various target sites of potential therapeutic drug candidates

Though repurposing of drugs has hastened the drug development process in the most economical approach, however, in the efforts of searching for a potential therapeutic drug, the exact safety and toxicity profiles of drug candidates have been overlooked. Various sources point to the association of several adverse events with different therapeutic agents currently being used or under clinical trials. Some pieces of evidence demonstrate gastrointestinal side effects such as nausea, vomiting, diarrhea, abdominal pain, cardiovascular adverse events like QT interval prolongation, cardiac arrhythmia, dermatological adverse events including skin rash, Stevens-Johnson syndrome, maculopapular eruptions, alopecia, erythema, pruritus, and hyperpigmentation, liver injury, and many other uncommon adverse drug reactions of several repurposed and investigational drugs [9, 10]. Table 1 summarizes the findings on the various AEs caused by COVID-19 medications in patients infected with the SAR-CoV-2 virus, as reported by case reports, case series, and randomized clinical trials.

Table 1

Summary of published literature describing anti-COVID-19 drugs-associated adverse events

Study design	Drug	Number of cases/participants	Age (years)/sex	Dose of therapy	Concomitant therapy/ies	Adverse event(s)	Treatment and outcome	References
Randomized controlled trial	Dexamethasone	2104 patients assigned to dexamethasone	66.9#/766 female 1338 male	6 mg once a day	NR	Hyperglycemia, gastrointestinalhemorrhage, and psychosis	NR	[11]
Case report	Hydroxychloroquine	Case 1	37/female	200 mg once	Ciprofloxacin 500 mg	QT interval prolongation	Metoprolol tartrate 25 mg twice a day, discharged with cardiac rhythm holter to monitor her cardiac electrical activity	[12]
		Case 2	58/male	200 mg twice a day	Azithromycin 500 mg once a day and oseltamivir 75 mg twice a day		Drug discontinuation, stable cardiac condition
		Case 3	24/NR	NR	NR		Drug discontinuation, improvement of the condition
Case series	Hydroxychloroquine	Case 1	75/male	NR	Azithromycin and cefepime	Multiple episodes of non-sustained ventricular tachycardia	Drug discontinuation, resolution of the adverse event	[13]
		Case 2	56/female	NR	Azithromycin and cefepime	Nausea, vomiting, severe abdominal cramps, and unbearable watery diarrhea	Drug discontinuation and supportive care, improvement of symptoms
Case report	Hydroxychloroquine		29/female	400 mg twice a day	Azithromycin and piperacillin–tazobactam	Tenfold increase in transaminases level	Drug discontinuation, level of transaminases returned to near-normal values within 5 days	[14]
Case report	Hydroxychloroquine		84/female	200 mg twice a day	Oral nifedipine 30 mg twice a day and irbesartan 75 mg twice a day	Sinus bradycardia with QTc prolongation	Drug discontinuation, isoproterenol IV at a maximal dose of 10 mcg/min and epinephrine at a maximal dose of 1 mcg/kg/min, QTc interval was normalized	[15]
Case report	Hydroxychloroquine		42/female	200 mg twice a day	Acetaminophen 500 mg every 6 h	Stevens–Johnson syndrome (SJS)	Drug discontinued and therapy changed to lopinavir/ritonavir 400 mg twice a day, loratadine 10 mg twice a day and diphenhydramine 50 mg thrice a day, discharge after 5 days with nonpruritic scalded skin on the distal of upper extremities	[16]
Case report	Hydroxychloroquine		38/male	200 mg twice a day	Ceftriaxone 2 g intravenously every 12 h and lopinavir + ritonavir 400/100 mg tablet twice a day	Involuntary movements involving bilateral, asynchronous, irregular myoclonus of the limbs	Drug discontinuation, discharge with complete resolution of all involuntary movements	[17]
Case report	Hydroxychloroquine		37/female	200 mg twice a day	Lopinavir-ritonavir 200/50 mg/12 h and azithromycin 250 mg/day	DRESS syndrome	NR	[18]
Case report	Hydroxychloroquine		60/female	400 mg starting dose followed by 200 mg twice a day	Amoxicillin–clavulanic acid 1.2 g thrice a day, oseltamivir 75 mg twice a day, lopinavir 400 mg/ritonavir 100 mg twice a day, meropenem 1,000 mg thrice a day, and amoxicillin–clavulanic acid was replaced by meropenem	Right bundle branch block (RBBB) and critically prolonged QTc	Drug discontinuation, normalization of QTc	[19]
Case series	Hydroxychloroquine	Case 1	74/female	NR	Ondansetron, oseltamivir, and azithromycin	QTc prolongation, and several premature ventricular contractions with R-on-T waves	Hydroxychloroquine, ondansetron, and azithromycin discontinuation, improvement of symptoms and eventual discharge from the hospital	[20]
		Case 2	40/female	NR	NR	Nausea, vomiting, diarrhea, and marked sinus bradycardia	Drug discontinuation, improvement of symptoms, and eventual discharge from the hospital
Case report	Hydroxychloroquine		68/male	600 mg, single dose	Piperacillin/tazobactam	Worsening of hemolysis in a patient with G6PD deficiency	NR	[21]
Case report	Hydroxychloroquine		76/male	200 mg thrice a day	Azithromycin, ceftriaxone	Acute general pustular erythema eruption	Death of patient due to pulmonary embolism	[22]
Randomized controlled trial	Hydroxychloroquine	491 participants Assigned to hydroxychloroquine (n = 244) Contributed data to the primary endpoint (n = 212)	41*/123 female 89 male	800 mg (4 tablets) once, then 600 mg (3 tablets) 6 to 8 h later, then 600 mg (3 tablets) once a day for 4 more days (5 days in total)	NR	Upset stomach, nausea, abdominal pain, diarrhea, or vomiting	NR	[23]
Randomized controlled trial	Hydroxychloroquine	150 patients, 75 patients assigned to hydroxychloroquine plus standard of care 70 received	46#/82 male	Loading dose of 1200 mg daily for 3 days followed by a maintenance dose of 800 mg once a day	Antiviral agents, antibiotics, and systemic glucocorticoid therapy	Diarrhea, nausea	NR	[24]
Case report	Hydroxychloroquine		Early 70 s/male	200 mg twice a day	NR	Phospholipidosis, acute kidney injury	Drug discontinuation, death	[25]
Case report	Chloroquine		84/female	500 mg twice a day	Bisoprolol, letrozole, memantine, and apixaban	Extremely prolonged QT interval, torsades de pointes (TdP)	Chloroquine, memantine, letrozole, and bisoprolol discontinuation, treated with intravenous magnesium, potassium, lidocaine, and isoproterenol, resolution of arrhythmias and normalization of QT interval followed by discharge	[26]
Case report	Chloroquine	Case 1	46/male	NR	Vortioxetine, azithromycin	Psychotic symptoms such as visual hallucinations and incoherent speech, with an outburst of odd behavior and repeated attempts to run away from the hospital	COVID-19 medication and vortioxetine discontinuation, amisulpride 100 mg once a day, disappearance of psychotic symptoms	[27]
		Case 2	35/female	NR	Azithromycin	Insomnia, panic attacks, anxiety, a sensation of death and fear, uncontrollable thoughts and distress	Lorazepam 2.5 mg, azithromycin, chloroquine discontinuation, disappearance of anxiety symptoms
Case report	Chloroquine		66/female	Loading dose of 600 mg orally and a maintenance dose of 300 mg twice a day	NR	QTc prolongation, TdP	Drug discontinuation, erythromycin 250 mg twice a day for gastrointestinal motility started and later discontinued, intravenous Mg 2 g, normalization of QTc interval	[28]
Case report	Remdesivir		59/male	Loading dose of 200 mg intravenously followed by 100 mg IV	Convalescent plasma	Sinus bradycardia, elevated ALT	Drug discontinuation, increase in heart rate and discharge	[29]
Case report	Remdesivir	Case 1	26/female	NR	Ceftriaxone, azithromycin, methylprednisolone, and convalescent plasma	Sinus bradycardia, QTc interval prolongation, and T wave abnormality	Drug discontinuation, stable condition	[30]
		Case 2	77/female	NR	Ceftriaxone, azithromycin, and methylprednisolone	Sinus bradycardia	Drug discontinuation, normalization of heart rate
Case report	Remdesivir		64/male	NR	Amiodarone 700 mg	Acute increase in ALT and AST	Drug discontinuation, rapid decrease in ALT and AST levels to normal	[31]
Case report	Remdesivir		54/female	Loading dose of 200 mg and proceeding with 100 mg once a day	NR	Sinus bradycardia	Drug discontinuation, atropine, condition improved	[32]
Case report	Remdesivir		36/male	Loading dose 200 mg on day 1 followed by 100 mg once a day	Ceftriaxone 2 g once a day, vibramycin 100 mg twice a day, dexamethasone 6 mg once a day, and enoxaparin 60 mg twice a day	Sinus bradycardia	Drug discontinuation, atropine, condition improved	[33]
Case series	Remdesivir	Case 1	68/female	Loading dose of 200 mg IV and a maintenance of 100 mg IV every 24 h	Amiodarone	Increase in AST and ALT levels, acute liver failure	Remdesivir and amiodarone discontinuation, continuous infusion of acetylcysteine, decrease in AST and ALT levels and return to stable values	[34]
		Case 2	80/female	200 mg IV loading dose followed by 100 mg IV once day	Dexamethasone 6 mg orally once a day	Acute liver failure	Continuous infusion of acetylcysteine, restoring of normal values, death due to cardiac arrest
Randomized controlled trial	Remdesivir	193 (10-day remdesivir) 191 (5-day remdesivir)	56*/118 male 75 female, 58*/114 male 77 female	200 mg on day 1, followed by 100 mg once a day	Steroids. hydroxychloroquine/chloroquine, lopinavir-ritonavir, tocilizumab, azithromycin	Nausea, diarrhea, hypokalemia, headache	Drug discontinuation	[35]
Case report	Favipiravir		42/male	1,800 mg twice a day on administration day 1 and 800 mg twice a day after	NR	Hyperuricemia, acute gouty arthritis	Nonsteroidal anti-inflammatory drugs (NSAIDs), improvement of pain and swelling and complete recovery	[36]
Case report	Favipiravir		82/male	1,600 mg twice the first day and 800 mg twice the second day	Ceftriaxone	Fever	Drug discontinuation, improvement of fever	[37]
Case report	Favipiravir		73/male	6000 mg on day 1 and 2400 mg/day from day 2	Meropenem, vancomycin, antithrombin III agents, steroids, trimethoprim-sulfamethoxazole, and micafungin	Acute cholestatic liver injury	NR	[38]
Case report	Favipiravir	Case 1	38/male	1600 mg twice a day followed by 600 mg twice a day for 5 days	Hydroxychloroquine 400 mg twice a day followed by 200 mg	Increase in serum creatinine levels	Drug discontinuation, Improvement of renal functions	[39]
		Case 2	51/male	1600 mg twice a day followed by 600 mg twice a day for 5 days	Hydroxychloroquine 400 mg twice a day followed by 200 mg, methylprednisolone 40 mg twice a day, enoxaparin 40 mg once a day	Increase in serum creatinine levels with non-oliguria	Drug discontinuation, improvement of renal functions
Randomized clinical trial	Favipiravir	40 patients	NR	1600 mg twice a day on day 1 followed by 600 mg twice a day or 1800 mg twice a day on day 1 followed by 800 mg twice a day	Antibiotics, anticoagulants, and/or immunosuppressants and symptomatic treatment	Diarrhea, nausea, vomiting, chest pain, and an increase in liver transaminase levels	Drug discontinuation	[40]
Randomized clinical trial	Favipiravir	73 patients	44.5*/21 female 51 male	1800 mg twice a dayloading dose on day 1; 800 mg twice a daymaintenance dose thereafter	NR	Increased blood uric acid, abnormal liver function tests	NR	[41]
Case report	Lopinavir/ritonavir	Case 1	56/female	400/100 mg twice a day	Arbidol, pantoprazole, methylprednisolone, and chloroquine	QTc interval prolongation	Drug discontinuation, potassium chloride 1 g thrice a day, QTc interval decreased and patient discharged	[42]
		Case 2	56/female	400/100 mg twice a day	Arbidol, pantoprazole, and chloroquine	QTc interval prolongation	Drug discontinuation, potassium chloride 1 g thrice a day, QTc interval decreased and patient discharged
Case report	Lopinavir–ritonavir		67/male	400 mg/100 mg twice a day	Intravenous piperacillin–tazobactam 4 g/0.5 g every 8 h	Sick sinus syndrome	Drug discontinuation, resolution of bradycardic episodes	[43]
Case report	Lopinavir–ritonavir		67/male	Lopinavir 4 mg/kg/ritonavir 1 mg/kg 12-hourly was initiated	Propofol IV, fentanyl	Severe bradycardia and hypotension	Drug discontinuation, ephedrine IV 20 mg, atropine 1200 mcg, dopamine IV 5 mcg/kg/min, transcutaneous pacing pads introduced, bradyarrhythmia episodes disappeared, patient recovered	[44]
Case report	Lopinavir–ritonavir (LPV/r)	Case 1	66/male	400 mg/100 mg twice a day	Hydroxychloroquine 200 mg twice a day, lithium 800 mg once a day, duloxetine 120 mg once a day, haloperidol 1 mg twice a day	Serotonin syndrome (SS)	Duloxetine, lithium, haloperidol, and LPV/r discontinuation, improvement of symptoms	[45]
		Case 2	78/male	400 mg/100 mg twice a day	Hydroxychloroquine 200 mg twice a day, interferon beta-1b, tocilizumab, risperidone 1 mg twice a day, morphine 3 mg	Serotonin syndrome (SS)	LPV/r and risperidone discontinuation. Fluid therapy, active cooling. Clonazepam 0.25 mg every 6 h, improvement of symptoms
Randomized controlled trial	Lopinavir/ritonavir	21 patients	52.2#/11 male 10 female	Oral, q12h, 500 mg each time	Methylprednisolone 40 mg once a day and gamma globulin 10 g once a day	Diarrhea, loss of appetite, elevation of ALT	NR	[46]
Randomized controlled trial	Ivermectin	94 patients assessed, 12 treated with ivermectin	26*/5 female 7 male	Oral, 400 mcg/kg, single dose	NR	Dizziness, blurred vision	NR	[47]
Randomized clinical trial	Ivermectin	476 patients enrolled, 275 assigned to ivermectin	38*/163 female 112 male	Oral, 300 μg/kg	NR	Headache, dizziness, diarrhea, nausea, abdominal pain, visual disturbance	Drug discontinuation in 15 patients	[48]
Case report	Tocilizumab (TCZ)		45/male	8 mg/kg	Favipiravir, nafamostat, propofol, and methylprednisolone 1 g once a day	Hypertriglyceridemia	Fenofibrate, stable triglyceride levels	[49]
Case report	Tocilizumab (TCZ)	Case 1	65/male	NR	Lopinavir/ritonavir, ribavirin, hydroxychloroquine, propofol	Hypertriglyceridemia	NR	[50]
		Case 2	43/male	NR	Lopinavir/ritonavir, ribavirin, hydroxychloroquine, propofol	Hypertriglyceridemia	NR
Case report	Tocilizumab		52/male	Two doses of 400 mg (8 mg/kg), with a 12-h break between doses	Ceftriaxone, azithromycin, and methylprednisolone	Acute liver injury	NR	[51]
Case report	Tocilizumab		65/male	Two doses of tocilizumab IV 8 mg/kg administered 12 h apart	Piperacillin-tazobactam	Neutropenia	NR	[52]
Randomized controlled trial	Tocilizumab	34 patients	63.5*/18 male 16 female	First dose 400 mg IV for more than 1 h, second dose given when patient remained febrile for 24 h after first dose	NR	Hepatic function abnormality, leukopenia, and neutropenia	Symptomatic treatment	[53]

Drug discontinuation refers to the withdrawal of the primary anti-COVID-19 drug being reviewed, unless stated otherwise.

ALT indicates alanine aminotransferase; AST, aspartate aminotransferase; IV, intravenous; NR, not reported.

*Median

#Mean

The following sections will illuminate the eight most common anti-COVID-19 drugs, their mechanism of action, and their related adverse events, as found in the published literature.

Dexamethasone

Anti-inflammatory agents like glucocorticoids, such as dexamethasone, have been widely used in the treatment of diseases closely related to SARS-CoV-2 infection, such as SARS, MERS, and influenza. However, earlier, the evidence to support or discourage its use for COVID-19 was lacking.

In a large, open-label randomized controlled RECOVERY trial, 2104 hospitalized patients with COVID-19 were administered either orally or intravenously with 6 mg of dexamethasone once a day for 10 days. The trial provided evidence of reduced 28-day mortality in patients on respiratory support. However, the clinical outcomes related to dexamethasone also included four cases of serious adverse reactions, namely, two reports of hyperglycemia, and one of gastrointestinal hemorrhage, and psychosis each [11].

Hydroxychloroquine

Widely used antimalarials, hydroxychloroquine, and chloroquine with well-established use in autoimmune disorders like rheumatoid arthritis and lupus erythematosus have been repurposed for their potential antiviral activity against SARS-CoV-2 infection [54, 55]. Though large trials conducted in the past year have already revealed the ineffectiveness of hydroxychloroquine in the treatment of COVID-19 and lack of adequate positive data in case of chloroquine has allowed its use for clinical research only.

Belonging to the 4-aminoquinoline class of compounds, both exert anti-inflammatory, immunomodulatory, and antiviral action through a wide array of specific mechanisms [56]. This includes the rise in the endosome and lysosomal pH, interference in endocytic activity, obstruction of sialic acid receptors, blocking of SARS-CoV-2 entry into the host cell by prevention of glycosylation of ACE2 receptors, and control of cytokine storm induced by inflammatory mediators [57], thus inhibiting the entry, replication, and release of the virus from the host organism. Hydroxychloroquine, in addition to possessing better potency against SARS-CoV-2, causes less toxicity as compared to chloroquine [58, 59]. Nonetheless, its administration for treatment of coronavirus disease 2019 is not one without adverse events.

In their article, Zengin et al. [12] presented three case reports indicating the association of hydroxychloroquine therapy with cardiovascular adverse effects. Primarily, its potential to cause serious QT interval prolongation and cardiac arrhythmias. The mechanism suggested to induce such effects was the inhibitory action on the hyperpolarized cardiac channels that resulted in the delay of depolarization rate and eventually decreased heart rate [13]. As shown in several case reports and case series, co-administration of HCQ with QT prolonging medications like azithromycin may increase the risk of cardiac toxicity among many other factors including age, sex, duration of therapy, hepatic or renal failure, and pre-existing cardiovascular disease [13, 20]. In a case report by Asli et al., patient was administrated with lopinavir/ritonavir, another QTc prolonging agent concomitantly with HCQ that might have contributed to the cause of right bundle branch block (RBBB) and severe QTc interval prolongation [19]. Another such case of an 84-year-old woman with history of hypertension, Alzheimer’s disease, and stage 4 chronic kidney disease (CKD) suggested the close relation of HCQ with sinus bradycardia and QTc prolongation. The QTc levels normalized after discontinuation of drug along with intravenous administration of isoproterenol and epinephrine [15]. In most of the studies, patient QTc intervals and symptoms improved soon after discontinuation of the drug. Consequently, it is advocated that a baseline ECG should be defined for patients who are planned to begin treatment with HCQ [12].

One of the most common adverse effects related to HCQ therapy is gastrointestinal disorders, mainly nausea, vomiting, diarrhea, and abdominal pain. As depicted, these are frequent, mild to moderate in nature and usually resolved following their withdrawal from the drug regime [13, 20]. Skipper et al. [23] conducted a randomized, double-blind, placebo-controlled trial in 491 non-hospitalized patients to study the effect of HCQ treatment on disease course for early COVID-19. Of which 212 participants received hydroxychloroquine in the following dose: 800 mg once, followed by 600 mg in 6 to 8 h, then 600 mg daily for 4 more days. It was observed that 43% (92 of 212) of patients receiving HCQ experienced adverse effects in the form of upset stomach, nausea, abdominal pain, diarrhea, or vomiting as opposed to 22% (46 of 211) in the placebo category. Similarly, an open-label, randomized, controlled trial published in May 2020 assessed the safety and efficacy of HCQ with the standard of care on 150 participants with mild or moderate COVID-19. Out of 150 patients, 70 were administrated with hydroxychloroquine for a duration of 2 to 3 weeks at a loading dose of 1200 mg daily, followed by a maintenance dose of 800 mg daily. The common adverse effects reported were diarrhea, vomiting, and nausea where diarrhea occurred in 7 out of 70 patients [24].

Three case reports revealed the association of hydroxychloroquine and its dermatological adverse effects. In the first case report, a 37-year-old woman was diagnosed with drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome having clear clinical manifestations of skin rash, swollen face, and fever. She had been previously treated with hydroxychloroquine for suspected COVID-19. Later, a positive patch test concluded HCQ was the primary cause of DRESS in the patient [18]. The second case report presented a rare case of hydroxychloroquine-induced Stevens-Johnson syndrome (SJS) of a 42-year-old woman. Following the diagnosis of adverse reaction, HCQ was substituted with lopinavir/ritonavir, and the patient was initiated with 10 mg of loratadine twice daily and 50 mg of diphenhydramine thrice daily for treatment. The patient was discharged from the hospital 5 days later [16]. In the third case report by Delaleu et al. [22], a 76-year-old patient manifested acute generalized exanthematous pustular (AGEP) eruptions after treatment with HCQ. The RegiSCAR score obtained for diagnosis was estimated to be 11, indicating a definite case of AGEP.

Four case reports represented other uncommon adverse events associated with the use of hydroxychloroquine. In a case report of a 29-year-old woman with severe COVID-19, hepatotoxicity related to HCQ therapy was reported. There was a tenfold increase in the serum transaminases level in the patient after HCQ administration which decreased following the withdrawal of drug [14].

Interestingly, Fernando et al. reported a case of HCQ-related ADR, where the patient underwent involuntary movements after drug administration. Though the irregular myoclonic movements completely resolved following the discontinuation of the drug, suggesting a causal relationship of HCQ and the ADR. Unlikely in this case, there exists many factors including predisposing factors, co-morbidities, and drug-drug interactions that should also be taken into consideration while determining the cause of an adverse drug reaction [17].

In addition to established data demonstrating the activation of hemolytic crisis due to COVID-19 infection in a glucose-6-phosphate dehydrogenase deficient patients, Beauverd et al. reported that hydroxychloroquine administration can further aggravate the hemolytic state in patients lacking G6PD [21].

In terms of nephrotoxicity, despite the already known long-term effect of HCQ of drug-induced renal phospholipidosis, one case addressed its occurrence with its short-term treatment. Findings in the case displayed isometric vacuolization of the renal tubular epithelium after patient started on HCQ [25].

Chloroquine

Two cases of torsades de pointes (TdP) characterized by excessive QT prolongation (when QTc interval is > 500 ms) even after discontinuation of chloroquine were reported. Szekely et al. [26] described the incidence of multiple episodes of TdP despite the withdrawal of all suspected QT prolonging agents and oral supplementation of potassium. Similar results were observed in a case by Semedo et al. [28] in which patient suffered from TdP after the suspension of chloroquine. Both the cases suggested the long half-life of chloroquine which ranges from approximately 20 to 60 days. Moreover, special emphasis on factors such as female sex, old age, existing cardiac disease, genetic predisposition, baseline QT interval, and drugs that can contribute to the increased risk for drug-induced QT prolongation should be taken into account when treating a patient with chloroquine.

In another case report published on June 2020, the authors introduced the causality of psychiatric adverse effects with chloroquine [27]. Two case reports of a 46-year-old male and 35-year-old female receiving chloroquine were reported. Psychotic symptoms like visual hallucinations, abnormal behavior, and incomprehensible speech in the former and symptoms of anxiety including uncontrollable thoughts, recurrent panic attacks, insomnia, and fear in the latter were observed. Discontinuation of drug and appropriate treatment with antipsychotic and anti-anxiety medication resulted in the disappearance of the symptoms. Although the mechanism of psychiatric adverse effects remains ambiguous, the authors hypothesized the effect of chloroquine on muscarinic, dopaminergic pathways alongside its antagonistic activity on 5-HT3A, 5-HT3B, and GABA receptors and agonistic action on NMDA receptors to be the trigger of such psychiatric symptoms [27].

Remdesivir

Originally synthesized by Gilead Sciences in 2017 (under the name GS-5734) for treatment against the Ebola virus, studies have shown remdesivir, a monophosphoramidate prodrug to be efficacious against various coronaviruses [60, 61]. It is a direct-acting, small molecule nucleotide analog with a broad spectrum of antiviral action [62]. An RNA-dependent RNA-polymerase (RdRp) inhibitor, it prevents viral RNA synthesis due to the resemblance of its active metabolite triphosphate form (RDV-TP) to the natural adenosine triphosphate substrate and competing with it as the main substrate for RdRp [10]. In addition, it reduces the viral RNA production by disturbing the exoribonuclease activity responsible for proofreading of viral RNA, leading to RDV-TP incorporation and delayed chain termination [61, 63]. As of October 22, 2020, FDA approved the use of remdesivir (Veklury) in hospitalized adults and pediatric patients with SARS-CoV-2 infection [64]. Although one of the most promising therapeutic candidates to combat COVID-19 with enough positive studies validating its effect, numerous clinical trials and reported cases have demonstrated its associated use with mild, moderate, to serious adverse effects.

Four case reports suggested the development of cardiac adverse events like sinus bradycardia and QT prolongation in COVID-19 patients under remdesivir therapy where discontinuation of the suspected drug led to the resolution of the symptoms in all five patients [29, 30, 32, 33]. Though patients were also treated with other known cardiotoxic drugs, this further supported the suspicion of remdesivir being the causative agent. Additionally, according to the Naranjo scale, one patient was given a score of 6 implying a “probable” causal relationship between remdesivir and bradycardia [29]. With regard to the first case, one possible reason can be the co-administrated drug, azithromycin, which is a QT prolonging agent. A probable mechanism behind the AE can also be the strong affinity of remdesivir for human mitochondrial RNA-polymerase, causing mitochondrial dysfunction [33]. Another can be the likeness of nucleotide triphosphate derivative, an active remdesivir metabolite to ATP leading to delayed sinoatrial node spontaneous depolarization [65]. Nevertheless, less evidence is available regarding the potential cardiac-related side effects of remdesivir and more research is needed to determine its possible mechanisms of action.

Although the information on remdesivir-induced hepatotoxicity is limited, there is evidence in the form of case reports and case series reporting incidences of increased liver enzymes in patients on remdesivir use. Leegwater et al. [31] recently reported a case of a 64-year-old man who experienced acute increased levels of ALT and AST after starting remdesivir. Remarkably, a quick fall in the ALT and AST levels were observed after immediate cessation of the drug. The authors hypothesized the drug-drug interaction between remdesivir, P-glycoprotein inhibitors as a potential cause of hepatotoxicity in the patient. Another factor for hepatotoxicity can be the temporarily administered 700 mg of amiodarone, given 2 days after the initiation of remdesivir for new onset atrial fibrillation, since many studies depict its potential for hepatotoxicity [66, 67]. So again drug-drug interaction leading to potentiating effect could be the reason for observed hepatotoxicity. Similarly, Carothers and colleagues published a case series of two patients describing the onset of elevated ALT and AST levels followed by acute liver failure after receiving remdesivir treatment for coronavirus disease 2019. In both cases, instant withdrawal of the drug and administration of acetylcysteine restored the ALT and AST levels to normal [34]. Likewise, it is advised by Aleen et al. to consider stopping remdesivir infusions when de novo increase in liver enzymes values is more than tenfold the upper limit of normal [68].

August 2020 published, randomized open-label trial of hospitalized patients with moderate SARS-CoV-2 infection conducted to evaluate the efficacy of remdesivir against standard care at 11 days serves as an example of other adverse events associated with remdesivir. In the trial, the median age was 56 years and patients were randomized in a 1:1:1 ratio to receive a 10-day course, a 5-day course of remdesivir, or standard care. The remdesivir patient group received a loading dose of 200 mg followed by a maintenance dose of 100 mg daily. In comparison, it was found that adverse events such as nausea, hypokalaemia, and headache were more frequent in the remdesivir group as compared to standard care that comprised of more serious adverse events [35]. Hence, more investigation into its safety and clinical profile is required to validate its use in the treatment of COVID-19.

Favipiravir

Favipiravir (or Avigan) is a potential antiviral drug that also acts by blocking the RNA-dependent RNA-polymerase. Developed by Fujifilm Toyama Chemical, a Japanese pharmaceutical company, it was introduced in Japan in 2014 for therapeutic use in pandemic influenza A and B virus-infected patients [69, 70]. Similar to remdesivir, it works against a wide range of viruses such as influenza virus, ebolavirus, flavivirus, arenavirus, and coronavirus. It exhibits antiviral activity after entering into the host human cell [71]. Following entry, favipiravir becomes activated to form favipiravir ribofuranosyl-5ʹ-triphosphate (favipiravir-RTP) after undergoing intracellular phosphoribosylation and phosphorylation. This activated molecule replaces the purine nucleosides and acts as a substrate for the RdRp enzyme further inhibiting the RdRp enzyme and preventing viral RNA strand elongation and protein synthesis. Additionally, lethal mutagenesis as a result of favipiravir-RTP incorporation into nascent RNA is a possible mechanism of action to stop viral infection [69, 71]. In June 2020, Glenmark Pharmaceuticals Ltd received approval from Indian regulatory authorities to manufacture and market oral favipiravir medication under the trade name “FabiFlu” for the use in mild to moderate COVID-19 patients [72]. However, to determine the adverse events safety outcome of favipiravir administration, it is still undergoing many clinical trials and clinical studies to deem its use as completely safe and effective.

Two patients experienced acute kidney injury (AKI) induced by favipiravir as reported by Nasa et al. [39]. Authors observed an increasing trend in serum creatinine levels which returned to baseline value following the cessation of favipiravir, within 5 days.

Kurita et al. [37] reported the first-ever case of an 82-year-old man with COVID-19, diagnosed with fever caused by favipiravir. The diagnosis was made after careful consideration of the clinical course and disappearance of fever, 4 days after withdrawal of the drug. Additionally, the ADR score of 6 on the Naranjo scale indicating “probable” further suggested favipiravir to be the likely cause of the adverse drug reaction.

Another rare case of favipiravir-associated acute cholestatic liver injury in a patient with a previous history of alcoholic hepatitis and compromised hepatic function was published online in December 2020. A high dose of favipiravir and its structural similarity to pyrazinamide with potential for hepatotoxicity, in addition to an already impaired hepatic function, may have precipitated the liver injury. Thus the authors recommended close monitoring of the liver function of patients treated with favipiravir, especially when administrated in high doses and with compromised liver function [38].

A case of increased uric acid levels and acute gouty arthritis after commencement of favipiravir treatment was reported in a patient with SARS-CoV-2 infection. The mechanism behind hyperuricemia could be inhibitory action on urate excretion transporters like organic anion transporter (OAT1) and OAT3, by favipiravir and favipiravir hydroxide, that prompted reduced uric acid secretion from tubules, as well as the increased reabsorption of uric acid via urate transporter by favipiravir hydroxide, altogether leading to a fall in the excretion of uric acid [36].

Similar results were observed in a randomized, comparative, open-label, multicenter, phase 3 clinical trial assessing the efficacy and safety of favipiravir in patients with mild to moderate COVID-19 illness. A loading dose of 1800 mg twice daily on day one followed by a maintenance dose of 800 mg of favipiravir with standard supportive care was administered to 73 patients. Overall, mainly, treatment-related adverse events were reported in 36% of patients (26 of 73). Of which, the most frequent were elevated blood uric acid levels and abnormal liver function tests that amounted to 16.4% and 6.8% of favipiravir-treated patients, respectively [41].

In phase II/III multicenter randomized clinical trial of moderate COVID-19 patients on treatment with favipiravir, the incidence of adverse effects in 17.5% (7 of 40) participants varied among nausea, vomiting, diarrhea, chest pain, and elevated transaminases levels. The majority of the adverse drug reactions were mild to moderate in severity and caused only 2 out of 40 patients to discontinue the drug [40].

Conversely, favipiravir is mostly considered to possess a good overall safety profile with less proportion of low-grade adverse events, having low intensity in severity [73]. Still, inadequate existing data on its positive effect against SARS-CoV-2 virus necessitates its current use for clinical studies only.

Lopinavir/ritonavir

Lopinavir is an HIV type 1 protease inhibitor used in a fixed combination with ritonavir, also a protease inhibitor that increases its plasma half-life via potent inhibition of cytochrome P450 3A4 [74, 75]. Developed by Abbott Laboratories and approved by FDA in 2000, lopinavir/ritonavir (or Kaletra) is used in combination with other antiretroviral drugs for the treatment of human immunodeficiency virus 1 (HIV-1) infection [76]. Besides the existing in vitro studies showing inhibition of SARS-CoV-1 and MERS-CoV by lopinavir/ritonavir combination, ongoing experiments and past shreds of evidence suggest its potential antiviral activity against SARS-CoV-2 [77]. This drug inhibits 3-chymotrypsin-like protease activity and replication by preventing viral polyprotein cleavage, particularly gag-pol precursors, and causing the formation of immature, non-infectious virions [11, 76, 78]. In an evaluation of LOTUS China, a randomized, controlled trial by Doggrell, lopinavir/ritonavir found no favorable effects in severe patients with COVID-19 and instead induced rapid gastrointestinal adverse events. There was no significant reduction in viral RNA loads or duration of viral RNA detectability when compared to standard supportive care alone [75]. The pharmacodynamics of lopinavir/ritonavir may fail to achieve sufficient drug concentrations that can inhibit the SARS-CoV-2 proteases.

Two cases of increased QTc interval by administration of lopinavir/ritonavir combination reported by Zhu et al. [42] provide further evidence on the relation of conduction abnormalities and antiviral drugs. In both cases, cessation of adverse effect causing drug leads to normalized QT intervals and eventual discharge from the hospital. Several independent risk factors such as female sex, drug-drug interaction, concomitant drugs like chloroquine, and electrolyte imbalance already mentioned earlier could have been the cause of QT prolongation in the two patients. Another article documented a case of 67-year-old man with pre-existing ischemic heart disease and QTc interval prolongation that increased his risk for sick sinus syndrome after treatment with lopinavir-ritonavir [43]. Severe episodes of bradyarrhythmias associated with the use of lopinavir-ritonavir were reported in a COVID-19 patient with moderate acute respiratory distress syndrome. The withdrawal of the combination drug leading to the full recovery of the patient further strengthened the causal relationship between the drug and the adverse event [44].

Serotonin syndrome is a potentially life-threatening disorder related to elevated serotonergic activity, and clinical manifestations involving myoclonic movements, tachycardia, diaphoresis, hyperreflexia, hyperthermia, and altered mental state. Serrano et al. [45] observed the earliest cases of lopinavir-ritonavir triggered serotonin syndrome in SARS-CoV-2 infected patients. The concomitancy of ritonavir with selective serotonin (SSRIs) and serotonin-norepinephrine (SNRIs) reuptake inhibitors leading to reduced elimination is the likely cause of the AE. The combination of lopinavir-ritonavir with duloxetine (SNRI), lithium, and risperidone (atypical antipsychotic), morphine in patients 1 and 2, respectively, induced the typical characteristics of serotonin syndrome.

A single center, exploratory randomized, controlled trial studying the efficacy and safety of lopinavir/ritonavir or arbidol in adult hospitalized patients having mild or moderate SARS-CoV-2 infection revealed gastrointestinal adverse effects in 23.8% of patients treated with LPV/r. Of 21 patients on LPV/r, 14.3% (3 of 21), 9.5% (2 of 21), and 4.8% (1 of 21) experienced diarrhea, loss of appetite, and an increase in ALT levels, respectively [46]. While in a retrospective cohort Chinese study, LPV/r in combination with umifenavir demonstrated promising outcomes in patients with COVID-19 [79, 80].

Lopinavir/ritonavir use in COVID-19 reported several adverse effects with two large randomized controlled trials in hospitalized patients with COVID-19 demonstrating no clinical benefit. Therefore, these drugs should not be used in COVID-19 patients.

Ivermectin

Ivermectin (IVM), primarily an anti-helminthic drug, is used for the treatment of plethora of parasitic infections including onchocerchiasis, strongyloidiasis, head lice, scabies, lymphatic filariasis, ascariasis, entrobiasis, rosacea, and trichuriasis. However, apart from its anti-parasitic activity, IVM has also exhibited broad spectrum antiviral characteristics in vitro [81]. It exerts an inhibitory action on RNA replication in several positive, single-stranded RNA viruses such as dengue virus, human immunodeficiency virus 1, influenza virus, and Zika virus as a nuclear transport inhibitor and interferes in the interaction between importin α/β1-mediated nuclear import and integrase protein, crucial for viral infection [82]. While several studies have demonstrated its efficacy in decreasing the mortality rate, reducing the viral load, and improving patient recovery time in individuals with severe COVID-19 [83, 84], large well-conducted clinical trials have concluded its inefficiency in treatment of COVID-19 patients. The common adverse effects related to IVM treatment include headache, dizziness, rash, and nausea.

According to a pilot, double-blind, placebo-controlled, randomized clinical trial conducted by Chaccour et al. [47] to determine the effect of single-dose IVM on mild COVID-19 patients having no risk factors in comparison to placebo, improved clinical outcome and reduced viral load was observed. In ivermectin-treated group, no serious adverse events were reported apart from the common adverse events, namely, dizziness and blurred vision.

A double-blind, randomized clinical trial was held from July 15 to December 21, 2020, on 476 patients to ascertain the efficacy of IVM administration in mild COVID-19 patients. IVM patient group received a dose 300 μg/kg of body weight each day for 5 days continuously. Both solicited and serious adverse events were accounted, though not much significant differences were observed in the frequency of adverse events on comparing IVM-treated group (76.7%) to placebo group (81.3%). The most common adverse events reported in IVM group were headache, dizziness, diarrhea, and nausea accounting for 50.9%, 35.6%, 30.2%, and 24.0% of total AEs, respectively [48].

Nevertheless, human studies involving clinical trials on a larger scale are required to further corroborate its safety and efficacy profile for use against SARS-CoV-2 virus.

Tocilizumab

Tocilizumab, an interleukin-6 receptor antagonist, is a recombinant humanized monoclonal antibody currently being used for the treatment of severe COVID-19, primarily in patients at risk of cytokine storms [85]. Approved by FDA for use in rheumatoid arthritis, juvenile idiopathic arthritis, giant cell arteritis, and chimeric antigen receptor (CAR) T cell therapy-induced cytokine release syndrome (CRS), it exhibits immunomodulatory and anti-inflammatory effects [86, 87]. Its mechanism of action involves disruption in the signal transduction cascade (classical and trans-signalling pathway) by binding with IL-6 receptor and interrupting its interaction with IL-6, thereby decreasing the release of proinflammatory cytokines [87, 88]. In a retrospective observational study comprising of 30 severe or critically ill hospitalized COVID-19 patients under treatment with TCZ, it was observed that TCZ is a potent therapeutic candidate for severe COVID-19 patients characterized by elevated IL-6 levels. It was found to have reduced the disease mortality and clinical course of the patients [89]. Tocilizumab use is associated with many complications. In particular, increased triglycerides, elevated liver enzymes, nausea, neutropenia, headache, dizziness, mouth ulcerations, and upper abdominal pain are some of the frequent adverse effects related to its administration [90].

Nakamura et al. [49] presented a case of 45-year-old male with elevated triglyceride levels following TCZ administration. Notably, only after a short duration of TCQ treatment, a sharp increase in the TG levels was detected. Thus, suggesting the involvement with severe inflammatory response provoked by COVID-19 in the dramatic surge. IL-6 has an essential function in mobilizing free fatty acids through adipocytes and stimulating glucose and free fatty acid uptake from serum by skeletal muscles. Similar findings were observed in two cases where patients exhibited a peak increase in serum TG levels after TCZ treatment for acute severe respiratory distress syndrome (ARDS). The Naranjo Adverse Drug Reaction Probability Scale gave a score of 7, denoting a probable relationship between hypertriglyceridemia and tocilizumab. According to Morrison et al. [50], the effect of TCZ on the metabolic pathways through inhibition of IL-6 receptor can lead to an increase in triglycerides level. Furthermore, the concurrent use of propofol can be another cause contributing to the worsening of hypertriglyceridemia.

Hepatotoxicity is a rare but serious complication associated with TCZ therapy. Muhović et al. [51] observed the first case of drug-induced liver injury induced by TCZ in a patient with severe COVID-19 infection. The authors noted a 40-fold increase in the transaminases level, 24 h after the patient received two doses of TCZ. The causal relationship of DILI by tocilizumab was given a score of 8 points and deemed “probable” as per the Council for International Organizations of Medical Sciences/Roussel Uclaf Causality Assessment Method (CIOMS/RUCAM).

In one case report, TCZ induced severe, persistent neutropenia in a positive COVID-19 patient was detailed. Despite the lack of proper evidence to form a causal relationship between TCQ and severe, prolonged neutropenia, the authors suspected the neutropenic influence of TCZ, in this case, to have been augmented by the concomitant genetic factor [52].

A recent randomized, controlled, open-label, multicenter trial of 65 participants supported similar findings. Among the TCZ-treated patients, common adverse effects observed were abnormal hepatic function (6 of 34), leukopenia (5/34), and neutropenia (3/35). Also, it was established that the observed adverse events either resolved spontaneously or after symptomatic care [53].

In the randomized controlled open-label RECOVERY (Randomised Evaluation of COVID-19 Therapy) clinical trial, originally conducted in UK, the effects of different therapeutics including dexamethasone, tocilizumab, hydroxychloroquine, lopinavir/ritonavir, corticosteroids, or azithromycin were evaluated in hospitalized COVID-19 patients. The large RECOVERY trial, however, did not publish significant safety data and is still under investigation. The trial has also been launched in four other countries including Indonesia, Nepal, Vietnam, and South Africa [91-93].

Substantial clinical trials such as the SOLIDARITY and DisCoVeRy trial accessing the clinical outcomes of repurposed drugs in COVID-19 patients have enormously contributed in determining the safety and efficacy of these drugs against the SARS-CoV-2 virus. Drugs including hydroxychloroquine, lopinavir, and ivermectin are deemed to be inefficient on the basis of overall mortality, duration of hospital stay, and initiation of ventilation, whereas drugs such as remdesivir, tocilizumab, and dexamethasone are recommended to be used for certain conditions owing to few, sufficiently powered, positive studies, indicating their favorable effects. The effective use of chloroquine and favipiravir, however, is yet to be ascertained on account of insufficient data, allowing their use in clinical studies only so far [11, 94, 95].

Limitations

There are several limitations to this review. To begin with, the number of case reports, case series, and random clinical trials describing the relation of adverse effects to antiviral COVID-19 therapy is inadequate. Due to this, the results of this review should be understood cautiously. This may be because only publications in the English language were incorporated and unpublished literature was not investigated. Underreporting of adverse effects may be another reason for less available evidence. Additionally, these are often a subject of bias with the information obtained from them being incomplete, or incorrect, and resulting in selective reporting and possible publication bias.

Conclusion

In conclusion, there are several adverse drug events induced by various repurposed drugs used against COVID-19 disease, as supported by the collected evidence. Although most are self-limiting and mild to moderate in severity, these can be severe or life-threatening events with confounding factors that demand immediate attention either necessitating prompt discontinuation of the suspected drug or administration of counter medication. Large clinical studies, including the SOLIDARITY and DisCoVeRy trials, have demonstrated the ineffectiveness of drugs such as hydroxychloroquine, lopinavir/ritonavir, and ivermectin on the grounds of overall mortality, duration of hospital stay, initiation of ventilation, and dissuading their administration in COVID-19 patients. These drugs should neither be used as routine medication nor in the case of clinical studies. But for drugs including remdesivir, tocilizumab, and dexamethasone, there are enough, sufficiently powered, positive studies that have recommended their use in the case of patients in specific critical conditions or special circumstances [11, 94, 95]. Studies proving the effectiveness of chloroquine or favipiravir, however, are still inconclusive. And since the data is insufficient to form a reliable conclusion, presently, these drugs should be used in clinical studies only.

Clinicians should be careful before administering any drug and consider weighing the risk versus benefits related to its use. And while the majority of the observed reports propose the causal relationship of COVID-19 drugs and their adverse effects as “probable,” there are several other factors that can affect the safety and effectiveness of a drug. Concomitant medications with their own propensity to induce the adverse effects or drug-drug interactions being two such major factors. Furthermore, vigilant drug monitoring and prompt reporting of any adverse effects are recommended for quick counter interventions to be undertaken. Thus, to gain a greater comprehension of adverse events, their mechanisms, and other potential risk factors, more research and clinical studies into drug-adverse event causality relationship and epidemiology are necessary.