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Threshold dose is the minimum dose of drug that triggers minimal detectable biological effect in an animal. [1] At extremely low doses, biological responses are absent for some of the drugs. The increase in dose above threshold dose induces an increase in the percentage of biological responses. [ 2 ]
Depo-Medrol is available as sterile aqueous solution in 20 mg/mL, 40 mg/mL, or 80 mg/mL strengths. [23] Solu-Medrol is the only derivative of methylprednisolone that is approved for intravenous infusion, as the sterile powder is soluble in water and can be mixed with a diluent. Strengths vary from 40 mg to 2 g. [22]
The term dosage form may also sometimes refer only to the pharmaceutical formulation of a drug product's constituent substances, without considering its final configuration as a consumable product (e.g., capsule, patch, etc.). Due to the somewhat ambiguous nature and overlap of these terms within the pharmaceutical industry, caution is ...
VNPT VinaPhone Corporation (Vietnamese: Tổng Công ty Dịch vụ Viễn thông, lit. 'Telecommunications Services Corporation'), [1] [2] also recognized by its brand name VinaPhone (sometimes stylized all owercase or alternatively Vinaphone), is a major mobile network operator in Vietnam and the core subsidiary of the state-owned Vietnam Posts and Telecommunications Group.
President Trump said he will sign an executive order next week ending past efforts from Biden for the federal government to embrace paper straws.
A combination drug or a fixed-dose combination (FDC) is a medicine that includes two or more active ingredients combined in a single dosage form. [1] Terms like "combination drug" or "combination drug product" can be common shorthand for an FDC product (since most combination drug products are currently FDCs), although the latter is more precise if in fact referring to a mass-produced product ...
have a density of approximately 1.2 to 1.5 g cm −3 (approximately that of the drug to be suspended or dissolved) [16] have a vapour pressure of 40 to 80 psig [18] have no toxicity to the patient [16] [18] be non-flammable [16] [18] be able to dissolve common additives (active ingredients should be either fully soluble or fully insoluble) [16]
Tablets may become unstable and the drug may degrade. High barrier packaging (including seals) is necessary but, by itself, is often not enough. Shelf life of a moisture-sensitive drug can be extended by means of desiccants. [11] Several types of dessicants are available; the type and quantity need to be matched to the particular drug and package.