Order: ceftriaxone 2 g in 100 mL of 0.9% NaCI (normal saline solution) over 30 minutes

Available: Macro drip set: 15 gtt/mL

Calculate the IV flow rate in gtt/min.

A) 600 g
This is incorrect because it represents the quantity 600 grams, which is a significantly larger amount than "six hundredth." The phrase "six hundredth" refers to six out of 100, or 0.06 in decimal form. In the metric system, 600 grams would indicate a much higher quantity, far from what is requested. Therefore, this option does not fit the definition of "six hundredth."

B) 0.06 g
The term "six hundredth" refers to six parts out of one hundred, which is mathematically expressed as 0.06. In the metric system, it is common to represent small quantities of mass, such as grams, in decimal form. The number 0.06 is precisely six hundredths, and the proper representation for this in terms of grams is 0.06 g. This is the correct scientific notation for the given quantity, as it accurately reflects six hundredths of a gram.

C) 0.006 g
This is incorrect because 0.006 grams represents six thousandths, not six hundredths. In decimal notation, six thousandths would be represented as 0.006, which is one order of magnitude smaller than six hundredths. The difference between 0.006 and 0.06 is significant. While both numbers are small, 0.006 would refer to an even smaller quantity than 0.06, which is not in line with the intended meaning of "six hundredth."

D) 0.6 g
While 0.6 grams may appear similar at first glance, it represents six-tenths (6/10), not six hundredths (6/100). The number 0.6 is much larger than 0.06, and it would be used to indicate a weight that is 60% of a gram, not a small fraction like six hundredths.

A) Drug Enforcement Administration (DEA)
The DEA is primarily responsible for enforcing the controlled substances laws and regulations, including monitoring the manufacturing and distribution of drugs that are classified as controlled substances. While the DEA plays an important role in regulating drugs, particularly those that have a high potential for abuse, it is not the primary authority on drug standards or approval processes.

B) Food and Drug Administration (FDA)
The FDA is the primary authority responsible for drug standards in the United States. The FDA regulates the safety, efficacy, and quality of pharmaceutical drugs, vaccines, biologics, and medical devices. It is responsible for approving new medications, ensuring they meet rigorous standards for safety and effectiveness before they are made available to the public. The FDA also monitors drugs after they are approved, requiring post-market surveillance and, if necessary, issuing recalls or safety warnings.

C) Centers for Disease Control and Prevention (CDC)
The CDC is focused on public health and disease prevention rather than the regulation of drugs. The CDC plays an important role in providing guidelines for the treatment and prevention of diseases, offering recommendations for vaccination schedules, and conducting epidemiological research.

D) National Institutes of Health (NIH)
The NIH is a leading medical research organization that conducts and funds biomedical research. While the NIH plays a crucial role in advancing scientific knowledge and supporting the development of new treatments, it does not have the authority to regulate or set standards for drugs.