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- W2786751570 abstract "Most of the package labels for any drug consist of warnings about toxicity. Toxicity in humans is also known as “adverse events.” But some package labels have special instructions for increasing the dose or decreasing the dose, when special circumstances arise. These special instructions are called the “Dosage and Administration” section of the package label. Instructions on the package label are needed, for example, when there is a need to cut down the dose when there is toxicity or where there is a need to cut down the dose if the patient suffers a condition resulting in renal impairment." @default.
- W2786751570 created "2018-02-23" @default.
- W2786751570 creator A5053626307 @default.
- W2786751570 date "2018-01-01" @default.
- W2786751570 modified "2023-09-28" @default.
- W2786751570 title "Dose Modification and Dose Titration" @default.
- W2786751570 doi "https://doi.org/10.1016/b978-0-12-814647-7.00004-x" @default.
- W2786751570 hasPublicationYear "2018" @default.
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