Hydrocortisone 1% / Potassium hydroxyquinoline sulfate 0.5% cream
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Therapeutically similar medicines
Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
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SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. BNF code shown is the factual mapping value distributed by NHS Business Services Authority (NHSBSA) in the dm+d supplementary file under OGL v3.0; it is not affiliated with, nor licensed from, the publishers of the British National Formulary. ATC codes from the WHO Collaborating Centre for Drug Statistics Methodology (whocc.no).
Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
1922–2025
Showing the 50 most relevant studies, sorted by most relevant.
Reactions Weekly, 2023
Reactions Weekly, 2024
Reactions Weekly, 2023
Reactions Weekly, 2023
Bimantara Daniswara, Benni Benyamin, Febia Astiawati Sugiarto
Jurnal Medali, 2024
Hamid-Reza Moein, Jarred Kendziorski, Rahul Patel, et al.
Gastrointestinal Endoscopy, 2024
Reactions Weekly, 2025
Mohamad Hossein Nargesi, Kamran Kheiralipour
2025
Jiachuan Wu, Xiaodong Chen
Clinical Gastroenterology, 2024
Ramesh Acharya, Vaishnavi Sabesan, Deepti Pandit, et al.
European Heart Journal. Case Reports, 2025
Abstract Background Hypothyroidism leads to a prolonged QT interval due to modulation of the potassium channel by low circulating T3, leading to a disproportionate lengthening of the action potential. Patients with long QT syndromes (LQTS) have an increased risk of symptomatic ventricular arrhythmias and sudden cardiac death (SCD). Case summary A 40-year-old female with a previous history of congenital LQTS, Type 1 diabetes mellitus, anaemia, and untreated hypothyroidism was brought to the hospital with an abrupt onset of palpitations and disorientation following multiple (>30) automated implantable cardioverter-defibrillator shocks with no identifiable triggers. Emergency medical services telemetry monitoring en route to the hospital revealed torsades de pointes (TdP), following which she received 4 g of magnesium sulfate intravenously and reverted to sinus rhythm. Electrocardiogram revealed sinus rhythm with a prolonged QTc of 515 ms. The laboratory testing revealed high TSH with low T4. The myxoedema coma score was markedly elevated at 40, indicating severe hypothyroidism. The thyroid peroxidase antibody was >600 IU/mL, indicating Hashimoto’s thyroiditis. Echocardiography showed left ventricular ejection fraction of 55%–60% with no wall motion abnormalities. We treated the patient with intravenous hydrocortisone, levothyroxine, and liothyronine. After the treatment, she had no further episodes of torsades, and QTc improved to her baseline of 479 ms. Discussion Hypothyroidism is linked to electrocardiographic abnormalities such as sinus bradycardia, QT interval prolongation, malignant ventricular arrhythmias such as ventricular premature beat, ventricular tachycardia, TdP, and ventricular fibrillation. Assessment of thyroid function is of high value in QT prolongation syndromes to avoid SCD incidence. Thyroid hormone influences ventricular inhomogeneity, and L-thyroxine replacement treatment may minimize malignant ventricular arrhythmia and sudden cardiac death in patients with primary hypothyroidism. Our case highlights the importance of urgent electrolyte replacement and levothyroxine therapy to avoid the risk of ventricular arrhythmias.
Abstract licence: CC BY-NC
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Scientific data (pharmacology, interactions, ADME) is not yet available for this medicine. Clinical sections are sourced from the NHS dm+d database.