The stability of a drug is the ability of the drug to maintain its chemical, physical, therapeutic and toxicological properties throughout its shelf life. Often times environmental and other unexplainable factors affect the stability of drugs by causing degradation of either the active ingredient of the drug product or the excipients, reducing the bioavailability of the drug or changing the physical appearance of the drug.
Drug Stability refers to the capacity of a drug substance or product to remain within established specifications of identity, strength quality, and purity in a specified period of time.factors that affect drug stability include temperature condition, moisture, light, microbes, packaging materials, transportation, components of drug composition and the nature of the active ingredient.
What do you mean by "the self life of drug with stability", be more specific
Which drug can receive the effects of anaphylaxis
Stability data of drugs refers to information about how a drug's quality and effectiveness may change over time due to various factors such as temperature, light, humidity, and packaging. This data helps determine the drug's shelf-life and storage conditions to ensure its safety and efficacy. It includes results from stability testing studies conducted under various conditions to assess the drug's degradation profile.
how do we separate the effects of specific and non specific drug effects
what are the effects of the drug silvia
shelf life
The fin
Temperature can affect the viscosity, volatility, and stability of an API. Higher temperatures can decrease viscosity and increase volatility, potentially affecting the delivery and performance of the drug. Temperature extremes can also degrade the API, affecting its potency and safety.
The term for the body's reaction to a drug is "drug response" or "drug reaction". This can include a variety of effects, such as therapeutic benefits or side effects.
what is telebrix and the side effects.
Context?