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Prednisolone
References
FAQ's
References
- Fried, Josef; Thoma, Richard W., Synthesis of steroids, Olin Mathieson Chemical Corp., US2793164A, May 21, 1957 ()
- Loo, J. C. K.; Butterfield, A. G.; Moffatt, J.; Jordan, N.Loo, J. C. K.; Butterfield, A. G.; Moffatt, J.; Jordan, N., Analysis of prednisolone in plasma by high-performance liquid chromatography,Journal of Chromatography, Biomedical Applications, Volume: 143 Issue: 3, Pages: 275-80, 1977
Frequently Asked Questions
How do Prednisolone impurities impact its pharmacological activity?
Prednisolone impurities can affect its pharmacological activity by altering the drug's potency, efficacy, bioavailability, and potential for adverse effects.
Can Prednisolone impurities impact its stability or shelf life?
Yes, impurities in Prednisolone can potentially impact its stability or shelf life.
How do Prednisolone impurities affect the quality and safety of the drug?
Impurities in Prednisolone can compromise its quality and safety by potentially altering its pharmacological activity, causing adverse effects, and reducing therapeutic efficacy.
What are the temperature conditions required to store Prednisolone impurities?
Prednisolone impurities are stored preferably at a regulated room temperature of 2-8°C or as specified on the Certificate of Analysis (CoA).
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