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Prednisolone impurities can affect its pharmacological activity by altering the drug's potency, efficacy, bioavailability, and potential for adverse effects.
Yes, impurities in Prednisolone can potentially impact its stability or shelf life.
Impurities in Prednisolone can compromise its quality and safety by potentially altering its pharmacological activity, causing adverse effects, and reducing therapeutic efficacy.
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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