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Safety Data Sheet SDS created:29920201 Identification of substance and manufacturer Axon catalogue ID 3174 Product name Obeticholic acid IUPAC name (4R)4[(3R,5S,6R,7R,8S,9S,10S,13R,14S,17R)6Ethyl3,7dihydroxy10,13dimethyl2,3,4,5,6,7,8,9,11,12,14,15,16,17tetradecahydro1HCAS
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Identify the relevant sections needed for completion, such as chemical properties, hazard identification, and handling precautions.
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Healthcare professionals prescribing obeticholic acid.
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Pharmaceutical companies developing similar medications.
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Regulatory agencies assessing the safety profile of the drug.
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Patients considering treatment with obeticholic acid.
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Obeticholic acid int-747 safety data refers to the clinical trial data and post-marketing surveillance information collected to assess the safety and tolerability of obeticholic acid in patients. This may include adverse event reports, laboratory test results, and other relevant clinical information.
Manufacturers, sponsors of clinical trials, and any organizations involved in the development or marketing of obeticholic acid are required to file safety data. This includes pharmaceutical companies and any regulatory bodies overseeing drug safety.
To fill out obeticholic acid int-747 safety data, one should collect relevant patient data, document any adverse events, complete the required forms with accurate details, and submit to the designated regulatory authority following their guidelines.
The purpose of obeticholic acid int-747 safety data is to monitor the safety profile of the drug in real-world use, identify any potential risks or side effects, and ensure that the benefits of the drug outweigh its risks.
Safety data must typically include details about adverse events, patient demographics, dosage information, concomitant medications, and any laboratory results that are relevant to assessing the drug's safety.
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