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diclofenac (Oxa Gel / diclofenac, topical)

✓ Approved

Actavis · PTGS1 · Small Molecule

What is diclofenac?

diclofenac is a small molecule developed by Actavis. It is approved for therapeutic indications via transdermal.

Drug Profile

Brand NamesOxa Gel, diclofenac, topical
CompanyActavis
Drug ClassSmall Molecule
Molecular TargetPTGS1, PTGS2
RouteTransdermal
StatusApproved

Mechanism of Action

Molecular Targets

diclofenac acts on 2 molecular targets:

PTGS1prostaglandin-endoperoxide synthase 1 (COX3, PCOX1)
PTGS2prostaglandin-endoperoxide synthase 2 (GRIPGHS, hCox-2)
Want deeper analysis?Noah AI can explain complex mechanisms and compare to similar drugs.

Therapeutic Indications

diclofenac is developed for 5 unique indications across 3 therapeutic areas.

Therapeutic AreaConditionPhase
Musculoskeletal and connective tissue disordersMusculoskeletal pain✓ Approved
Musculoskeletal and connective tissue disordersMyositis✓ Approved
Musculoskeletal and connective tissue disordersRheumatoid arthritis✓ Approved
Injury, poisoning and procedural complicationsTraumatic shock✓ Approved
Skin and subcutaneous tissue disordersActinic keratosisPhase III

Related Research Articles

PubMedVestnik otorinolaringologii2026-09-04

[Topical Therapy of Otitis Externa: Potential Use of Combined Preparations].

Baranov K K KK, Kotova E N EN, Vyazmenov E O EO, Titova E V EV et al.

To assess the potential use of a combined topical preparation in the form of ear drops containing chloramphenicol, clotrimazole, beclomethasone dipropionate, and lidocaine in the treatment of patients with acute otitis externa, based on the clinical presentation and characteristics of the microbiological profile. A retrospective analysis of medical records of 168 patients with acute otitis externa over a 5-year period was performed. The study included children older than 6 years and adult patients. All patients underwent otorhinolaryngological examination, culture-based microbiological testing of discharge from the external auditory canal with species identification, CFU/mL counts and analysis of antimicrobial susceptibility data for clinically significant bacterial isolates according to laboratory reports, as well as local therapy with a combined topical preparation in the form of ear drops containing chloramphenicol, clotrimazole, beclomethasone dipropionate, and lidocaine. In cases where inflammation spread to the skin of the auricle, a combined ointment containing chloramphenicol and methyluracil was additionally used. Treatment efficacy was assessed based on the dynamics of subjective symptoms and objective signs of inflammation; tolerability was evaluated according to the presence of adverse events. Statistical analysis included calculation of mean values and proportions. Positive clinical dynamics were observed with the use of the combined topical ear drop preparation in patients with acute otitis externa: therapy resulted in regression of the main symptoms in 96.4% of patients, including reduction of otalgia, edema, hyperemia of the external auditory canal skin, and pathological discharge. Combined topical therapy with an ear drop preparation demonstrated high efficacy and a favorable safety profile in the treatment of acute otitis externa in children older than 6 years and adult patients, providing positive clinical dynamics in 96.4% of patients.

PubMedVestnik otorinolaringologii2026-09-04

[Hormone therapy for stapedoplasty in patients with otosclerosis].

Kryukov A I AI, Garov E V EV, Sidorina N G NG, Zagorskaya E E EE et al.

Surgical treatment of hearing loss due to otosclerosis is characterized by high clinical efficacy and ensures achievement of an air-bone gap of ≤10 dB in 58-97% of patients. However, acute sensorineural hearing loss as a complication of stapedoplasty occurs in 0.2-0.95% of cases after the primary intervention, in 2.9% after revision stapedoplasty and in 4.8% with the obliterating otosclerosis. Intraoperative adverse factors arising during stapedoplasty play the leading role in the development of early cochleovestibular disorders. On the other hand, the use of glucocorticosteroids (GCS) in the surgical management of patients with otosclerosis remains a subject of debate, as the indications for their use, optimal routes of administration, and clinical efficacy still lack sufficient scientific justification. To determine the indications for and evaluate the efficacy of hormonal therapy methods in patients undergoing stapedoplasty for otosclerosis. Between 2020 and 2023, a total of 112 patients with otosclerosis were examined and surgically treated. Among them, 83 were women and 29 were men; the mean age of the patients was 44±10.5 years. The diagnosis was based on data from otomicroscopy, pure-tone audiometry, acoustic impedance audiometry, and computed tomography of the temporal bones, which served to confirm the condition and identify factors that could adversely affect stapedoplasty outcomes. Functional results were assessed using pure-tone audiometry at days 2 and 7, as well as at 3, 6, and 12 months postoperatively. Considering the features of the intraoperative course, the dynamics of air-bone gap closure, and the GCS therapy regimen applied, the patients were divided into three groups. Group 1 consisted of 45 patients who did not receive GCS therapy. Group 2 included 54 patients, subdivided into 2 subgroups: 22 subjects (Group 2a) received topical GCS therapy using bioabsorbable collagen sponges impregnated with the drug and inserted into the round window niche, and 32 subjects (Group 2b) received systemic GCS therapy. The latter was administered due to an adverse intraoperative course to prevent postoperative complications. Group 3 consisted of 13 patients in whom GCS were used both topically and systemically due to adverse intraoperative factors during stapedoplasty and a subsequent increase in bone conduction thresholds detected on day 2 after surgical treatment. The key factors determining the need for GCS therapy were intraoperative features of the stapedoplasty procedure. In particular, intense tissue bleeding and a pronounced vestibular reaction during vestibulotomy (p≤0.001), as well as blood entering the vestibule and the "dry" vestibule phenomenon (p≤0.05), were significant. In addition, the development of cochleovestibular disorders in the postoperative period is associated not with individual factors, but with their combination. An analysis of the efficacy of topical and systemic dexamethasone in the early stages after stapedoplasty was done based on bone conduction threshold dynamics. In contrast to Group 2b, patients in Groups 1 and 2a showed no clinically significant increase in bone conduction thresholds or signs of cochleovestibular disorders. The results obtained in patients of Group 2a may be attributed to prolonged topical GCS exposure during the intraoperative period when using the developed technique. Despite the higher frequency of combined intraoperative complications in patients of Group 3, bone conduction thresholds remained stable in the postoperative period, which is associated with the use of combination GCS therapy. In patients with otosclerosis, glucocorticosteroid therapy is indicated for managing adverse intraoperative factors and elevated bone conduction thresholds after stapedoplasty. In cases of intraoperative adverse factors in the absence of cochleovestibular disorders in the postoperative period, the use of topical glucocorticosteroid therapy by placing a hemostatic sponge soaked in dexamethasone solution into the round window niche using the original technique is sufficient to achieve satisfactory functional outcomes. Combined topical and systemic glucocorticosteroid therapy is advisable for treating postoperative cochleovestibular disorders and preventing further progression of hearing loss.

PubMedClinical case reports2026-09-04

Drug-Induced Skin Lesions of Bilateral Lower Extremities in an Elderly Patient With Poorly Controlled Diabetes.

Chen Jie J, Wang Hua H, Gu Linxuan L, Zhu Xiwen X et al.

This study described a rare case of an 83-year-old man diagnosed with drug-induced skin lesions of bilateral lower extremities after continuous self-administration with clobetasol propionate ointment for eczema. On admission, his skin was paper-thin, peeling, dry, bruising, and swollen on both lower extremities. Topical clobetasol propionate was immediately discontinued. During a 2-week follow-up period, his symptoms had resolved significantly.

PubMedClinical ophthalmology (Auckland, N.Z.)2026-09-04

Adjunctive Cryopreserved Amniotic Membrane for Recalcitrant Keratopathy: Long-Term Outcomes with Maintenance Therapy.

Thomson Robert James RJ, Stevanovic Milanka M, Ciarmiello Gina G, Eden Robert A RA et al.

Shelf-stable, cryopreserved amniotic membrane (AM) has anti-inflammatory and anti-scarring properties and clinically has been shown to promote corneal epithelialization with benefits reported up to 3 months. Herein, we assessed the long-term outcomes after treatment with AM in patients with recalcitrant keratopathy. A single-center, retrospective review was performed of consecutive recalcitrant keratopathy patients that received treatment with shelf-stable cryopreserved AM and had at least 6-month outcomes. Corneal staining, corneal sensitivity, tear osmolarity, symptoms, concomitant treatments, and complications were assessed before treatment and up to last follow-up visit. A total of 33 eyes of 17 subjects that had recalcitrant keratopathy despite use of prior treatment were included in the analysis. After treatment with shelf-stable AM, corneal staining score significantly improved by a mean of 1.34 ± 0.9 at 1 week (p<0.001), 1.04 ± 0.8 at 1 month (p<0.001), 1.13 ± 0.7 at 6 months (p<0.001), 1.17 ± 0.7 at 12 months (p<0.001) and 1.10 ± 0.7 at 15 months (p<0.001). The proportion of subjects with improved corneal staining compared to baseline was 81.8% at 1 week, 72.0% at 1 month, 81.5% at 6 months, 86.2% at 12 months and 90.0% at 15 months. Improvements in corneal sensitivity were also observed, while tear osmolarity remained relatively unchanged. Despite initial improvement, symptoms gradually returned over time, coinciding with increased use of concomitant topical therapies. No complications related to the AM were observed. Recalcitrant keratopathy patients had significantly improved corneal epithelialization within 1 week of treatment with shelf-stable cryopreserved AM, which persisted in the majority of patients for up to 15 months with concomitant topical treatment.

PubMedAllergy2026-09-04

Tape Strip Transcriptomics Reveal Nemolizumab Effects on Pruritus, Hyperplasia, Inflammation, and Extracellular Matrix Markers in Patients With Moderate-to-Severe Atopic Dermatitis.

Liu Daniel D, Duca Ester Del ED, Delaleu Nicolas N, Lau Megan M et al.

Atopic dermatitis (AD) is characterized by pruritus, epidermal hyperplasia, and lichenification that significantly impairs quality of life. Nemolizumab, an anti-IL-31Rα monoclonal antibody, is approved for treating moderate-to-severe AD in patients aged > 12 years. This study investigated nemolizumab's molecular mechanisms using patient samples from the ARCADIA 1 (NCT03985943) and 2 (NCT03989349) trials. Tape-strips were collected from the lesional and non-lesional skin of 71 nemolizumab-treated and 39 placebo-treated patients, all receiving background topical corticosteroids ± topical calcineurin inhibitors, at baseline and after 16 weeks of treatment for bulk RNAseq analysis. Single cell RNAseq was performed on a subset of untreated patients and used as a reference to map bulk RNA-seq DEGs, providing cellular context for treatment-associated transcriptional changes. Bulk RNAseq revealed significant transcriptomic modulation following 16 weeks of nemolizumab treatment (797 downregulated/142 upregulated genes), while placebo-treated patients showed minimal changes. Nemolizumab treatment attenuated expression of pruritus-related genes (e.g., OSMR, TRPV3, HRH1, KLK6/7/9) and genes involved in epidermal hyperplasia and ECM remodeling (e.g., COL1A1/12A1, IGFBP3). Inflammatory pathways were also modulated, with downregulation of Th17- and Th1-related genes (e.g., S100A7/8/9, PI3, MX1, OASL). Pathway-level analysis demonstrated normalization of pruritus and inflammatory gene signatures, including Th2 and Th22 pathways. Subgroup analysis showed that patients with severe baseline pruritus (PPNRS ≥ 7) had higher baseline expression of immune-related genes and experienced greater downregulation following treatment compared to patients with moderate baseline itch. Single-cell mapping of differentially expressed genes suggested enrichment of these genes in keratinocyte, fibroblast, endothelial, and nerve cell subpopulations. Clinically, improvements in EASI and pruritus scores (PPNRS) correlated with decreased expression of fibrosis- and pruritus-associated genes. Our findings provide molecular evidence supporting nemolizumab's therapeutic efficacy across multiple disease domains, including pruritus, inflammation, and epidermal hyperplasia, highlighting its role in AD treatment and management.

PubMedCureus2026-09-04

Difficult Airway Management of a Patient With Sturge-Weber Syndrome: A Case Report.

Hoshi Haruka H, Sugino Shigekazu S, Kamata Kotoe K, Yamauchi Masanori M

Sturge-Weber syndrome is a rare neurocutaneous disorder characterized by vascular malformations of the brain, eyes, and face, which can lead to difficult airway management. A 57-year-old man with Sturge-Weber syndrome presented with an oral hemangioma. Preoperative assessment, including computed tomography, raised concerns about anticipated difficult mask ventilation and tracheal intubation. Based on these findings, awake intubation was planned. After sedation and topical anesthesia, a video laryngoscope was used to visualize the glottis, and the trachea was successfully intubated. General anesthesia was subsequently induced and maintained, and the surgery proceeded without complications. The patient was extubated after confirmation of the absence of oral bleeding or other airway abnormalities. Careful preoperative airway assessment is important in patients with Sturge-Weber syndrome. Awake intubation using a video laryngoscope may be an appropriate option for adult patients with anticipated difficult mask ventilation and tracheal intubation secondary to hemangiomas.

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