Pharmacology Quiz Questions And Answers

Bioavailability refers to the extent to which a drug is absorbed into the bloodstream and reaches the general circulation. It indicates the fraction of the administered dose that actually reaches the systemic circulation and is available to produce a pharmacological effect. Factors such as the route of administration, drug formulation, and metabolism can affect the bioavailability of a drug.

Inhalation is the route of administration used for general anesthesia and in cases of asthma. Inhalation involves the intake of substances through the respiratory system, allowing them to directly reach the lungs and be absorbed into the bloodstream. This method is effective for delivering anesthesia gases and medications to induce unconsciousness during surgery. Additionally, inhalation therapy is commonly used for asthma treatment as it allows medications to directly target the airways, providing quick relief and improving respiratory function.

Efficacy refers to the extent or degree to which a drug is able to produce the desired response or effect in a patient. It measures the effectiveness of a drug in achieving its intended purpose and can vary depending on factors such as dosage, administration, and individual patient characteristics. In other words, efficacy indicates how well a drug works in producing the desired therapeutic outcome.

The answer is CV because drugs classified as CV have a low potential for abuse and are subject to state and local regulation. This means that they have a relatively low risk of causing addiction or dependence compared to drugs in other classifications. These drugs can still have some risk of abuse, but they are considered to have a lower potential for abuse compared to drugs in other categories.

The factors listed in the question, such as species, pH of the drug, solubility of the drug, size and shape of the drug molecule, presence or absence of food in the GI tract, and degree of GI motility/disease process, all contribute to the process of drug absorption. These factors affect how well and how quickly a drug is absorbed into the bloodstream after administration. Therefore, the correct answer is absorption.

The therapeutic index refers to the balance between a drug's effectiveness in producing desired results and its potential to cause harmful or toxic effects. It is a measure of the drug's safety and is calculated by dividing the dose that produces toxic effects by the dose that produces therapeutic effects. A higher therapeutic index indicates a safer drug, as it means that the therapeutic dose is significantly lower than the toxic dose.

Schedule II drugs. DVMs cannot get schedule I drugs.

These are all methods used to transform a drug. Oxidation involves the addition of oxygen or removal of hydrogen from a molecule. Reduction involves the addition of hydrogen or removal of oxygen from a molecule. Hydrolysis is the process of breaking down a compound by adding water. Conjugation involves combining a drug molecule with another molecule, such as a sugar or amino acid, to make it more water-soluble and easier for the body to eliminate.

Pharmacodynamics refers to the study of how drugs interact with the body and produce physiological changes. It involves understanding the mechanisms by which drugs exert their effects, such as binding to specific receptors or altering enzyme activity. This field of study helps in determining the therapeutic effects and potential side effects of drugs, as well as optimizing drug dosages and treatment regimens.

FARAD stands for Food Animal Residue Avoidance Databank. This acronym refers to a resource that provides information and guidance on avoiding the presence of residues in food-producing animals. It is a database that assists veterinarians and animal producers in making informed decisions regarding the use of drugs, chemicals, and other substances in food animals to ensure the safety of animal-derived products for human consumption.

The Drug Enforcement Agency (DEA) was established to control the abuse of dangerous drugs through prevention and enforcement.

One liter is equal to 1000 milliliters or 1 quart.

USDA extension service.

Clinical trials are trials conducted on specific target animals to test the effectiveness and safety of a drug. These trials involve administering the drug to the animals and closely monitoring their response and any potential side effects. The purpose of clinical trials is to gather data and evidence on the drug's efficacy and safety profile before it can be approved for use in humans or other animals.

The correct answer is CIV because drugs in this category have a lower potential for abuse compared to drugs in CI, CII, and CIII categories. They may still cause physical or psychological dependence, but to a lesser extent. Examples of CIV drugs include phenobarbital and diazepam.

Agonists are drugs that easily bind with receptors. They activate the receptors and produce a physiological response. This binding can mimic the action of endogenous substances, such as neurotransmitters, and enhance their effects. Agonists have a high affinity for receptors, allowing them to bind easily and effectively. This interaction between agonists and receptors is crucial in pharmacology, as it determines the drug's efficacy and therapeutic effects.

The correct answer is IP, which stands for intraperitoneal. This route of administration involves injecting a substance directly into the peritoneal cavity, which is the space surrounding the organs in the abdomen. It is commonly used in veterinary medicine to euthanize pocket pets, such as hamsters or guinea pigs. The IP route allows for rapid absorption of the euthanasia solution, leading to a quick and painless death for the animal.

Conjugation is the process of adding glucouronic acid to a drug, which increases its water solubility. This chemical modification allows the drug to be more easily excreted from the body, as water-soluble substances can be eliminated through urine. Conjugation is an important metabolic pathway that helps in detoxification and elimination of drugs from the body.

Underdosing refers to administering a lower dose of a medication or substance than what is recommended or necessary. This can lead to ineffective levels, as the desired therapeutic effect may not be achieved. On the other hand, overdosing refers to administering a higher dose than what is recommended or safe. This can result in toxic effects, as the body may not be able to metabolize or eliminate the excess amount of the substance.

A solution is a homogeneous mixture in which a drug is dissolved in a liquid. In a solution, the drug particles are evenly distributed throughout the liquid and do not settle out if left standing. This is because the particles of the drug are small enough to remain dispersed in the liquid and do not have enough mass to settle under the force of gravity. Therefore, a solution is the correct answer for a drug dissolved in a liquid that does not settle out if left standing.

Most drugs are metabolized by the liver, where they are broken down into smaller, more easily excreted molecules. These metabolites are then eliminated from the body through the kidneys, which filter waste products from the blood and excrete them in the form of urine. The liver and kidneys play crucial roles in the body's detoxification process, ensuring that drugs and other toxins are efficiently processed and eliminated.

A chemical name refers to the specific name given to a drug based on its molecular structure. It is often complex and not commonly used in a clinical setting. The chemical name provides a detailed description of the drug's molecular composition, allowing scientists and researchers to identify and study its properties. However, in clinical practice, drugs are typically referred to by their generic or brand names, which are easier to remember and communicate.

The green book is a comprehensive list of all animal drug products that have received approval. It serves as a reference guide for veterinarians, animal owners, and other stakeholders in the veterinary industry. The green book provides essential information about the approved drugs, including their indications, dosages, and withdrawal periods. It ensures that only safe and effective drugs are used in the treatment and management of animal diseases, promoting animal health and welfare.

Enteric coating is a process in which drugs are coated with a substance that prevents stomach acids from dissolving the pill until it reaches the intestines. This is done to protect the drug from being destroyed by the acidic environment of the stomach and to ensure that it is released in the intestines where it can be absorbed effectively. Enteric coating is commonly used for drugs that are sensitive to stomach acids or that need to be released in a specific part of the gastrointestinal tract.

In order for a veterinarian to prescribe medication, a relationship must be established between the veterinarian and the client. This is because the veterinarian needs to have a thorough understanding of the animal's medical history, previous treatments, and current health condition before prescribing any medication. The relationship allows the veterinarian to assess the animal's needs and ensure that the prescribed medication is safe and appropriate for the specific situation. Without a relationship, the veterinarian would not have the necessary information to make an informed decision about medication.

Quantities of drugs found in animal products are referred to as residues. Residues can occur when animals are treated with drugs such as antibiotics or growth promoters, and traces of these drugs can remain in the animal products, such as meat, milk, or eggs. Monitoring and controlling drug residues in animal products is important to ensure food safety and to prevent potential health risks for consumers.

Receipts for purchase or sale of controlled substances must be kept for 2 years. This is because it is important to maintain records of these transactions for a reasonable period of time to ensure compliance with regulations and to provide evidence if needed for auditing or legal purposes. Keeping the receipts for 2 years allows for sufficient time to address any potential issues or inquiries that may arise related to the purchase or sale of controlled substances.

Parenteral refers to the administration of drugs through routes other than the digestive tract, such as injection. This can include intravenous, intramuscular, or subcutaneous injections. The term "parenteral" is used to differentiate from drugs that are taken orally or through other forms of ingestion. By administering drugs parenterally, they can be absorbed more quickly and directly into the bloodstream, allowing for faster onset of action and more precise control of dosage.

If a drug cannot be approved for animals unless under the supervision of a DVM, it is considered a prescription drug. This means that the drug can only be obtained with a written prescription from a veterinarian. This requirement ensures that the drug is used safely and appropriately, as a veterinarian is able to assess the specific needs and conditions of the animal before prescribing the medication.

Preliminary trials are the initial phase of new drug development. They involve testing the drug on microorganisms and possibly utilizing computer models. These trials help researchers assess the drug's efficacy, safety, and potential side effects before moving on to further testing on animals and humans. By conducting preliminary trials, scientists can gather valuable data that will inform the decision to proceed with the development process or make necessary adjustments to the drug formulation.

Implants are solid dosage forms that are injected under the skin and release medication over an extended period of time. These implants are designed to provide a sustained release of medication, allowing for long-term treatment and reducing the need for frequent injections or oral medication. Implants can be made from a variety of materials, including biodegradable polymers, and are commonly used for hormone therapy, contraception, and the treatment of chronic conditions such as diabetes.

Controlled substances are drugs that have the potential for addiction and abuse, both physically and psychologically. These substances are regulated by laws and regulations to ensure their safe and responsible use. The term "controlled" implies that there are specific restrictions and guidelines in place for the production, distribution, and use of these drugs. This helps to prevent misuse, addiction, and the negative consequences associated with their abuse.

The correct answer is "Off label" or "Extralabel" use of a drug. This term refers to the practice of using a drug in a manner that is not specified on the drug's label or approved by regulatory authorities. In this case, the DVM is prescribing a drug approved for use on dogs to be used on a cat, which is not the intended use according to the FDA.

The given correct answer is CI, which stands for Schedule I. Schedule I drugs have a high potential for abuse and have no approved medicinal purpose in the United States. Examples of Schedule I drugs include LSD, heroin, and crack. These drugs are considered to be the most dangerous and harmful substances, with a high risk of addiction and severe health consequences. They are strictly regulated and illegal to possess or distribute.

Elixirs are solutions of drugs that have been dissolved in sweetened alcohol. They are used for drugs that are not easily dissolved in water. Elixirs provide an effective way to administer medications that are not water-soluble, as the alcohol helps to dissolve the drug and make it easier to consume. This formulation is commonly used in pharmaceuticals to create a palatable and stable solution for oral administration.

The DVM's plan for administering medication is commonly referred to as a regimen or treatment protocol. This plan outlines the specific medications, dosages, and schedule for administration to ensure the optimal treatment outcome for the patient. The term "regimen" is often used to describe a systematic and organized approach to medication administration, while "treatment protocol" emphasizes the comprehensive plan for managing a specific condition or illness. Both terms are widely used in veterinary medicine to guide the administration of medications.

The correct answer is "Sustained-release" or "Sustained release" because this form of medication slowly releases small amounts of the drug into the intestinal mucosa over an extended period of time. This allows for a continuous and controlled release of the drug, maintaining therapeutic levels in the body.

Drugs can pass across membranes through various mechanisms. Pinocytosis is a process in which the cell engulfs the drug particles by forming vesicles. Passive absorption occurs when the drug molecules move across the membrane down their concentration gradient. Active transport involves the movement of drugs against their concentration gradient with the help of carrier proteins. These three mechanisms allow drugs to enter or exit cells. Simple diffusion, facilitated diffusion, and phagocytosis are not mentioned in the answer, so they are not relevant to the explanation.

Compounding refers to the process of diluting or combining drugs. It involves customizing medications according to the specific needs of a patient, such as altering the dosage form or removing certain ingredients. Compounding is commonly done by pharmacists to provide personalized medications that are not commercially available or to accommodate patients with unique requirements.

Tinctures are alcohol solutions that are used for topical application. They are commonly used in medicine and herbal remedies to extract the active compounds from plants. The alcohol acts as a solvent, extracting the beneficial properties of the plant material and preserving them in a concentrated form. Tinctures are often applied externally to the skin for various purposes, such as treating skin conditions or providing localized pain relief. They are a popular choice for topical application due to their ability to effectively deliver the active ingredients to the affected area.

Drug levels can be measured in various bodily fluids such as blood, urine, and cerebrospinal fluid. These fluids provide a representative sample of the drug concentration in the body, allowing healthcare professionals to monitor drug levels and adjust dosages if necessary. Measuring drug levels in blood is a common method as it is easily accessible and provides real-time information. Urine analysis can also provide valuable insights into drug metabolism and excretion. Cerebrospinal fluid testing is particularly useful when monitoring drugs that target the central nervous system. Other fluids mentioned such as tears, saliva, nasal discharge, and shmegma may not be commonly used for drug level measurement or may have limited clinical significance.

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The given answer states that the descending order of metric weights is Kg>g>mg>mcg. This means that Kilogram (Kg) is the heaviest unit, followed by Gram (g), Milligram (mg), and Microgram (mcg) in decreasing order.

Drugs need to move from the absorption site into the bloodstream, specifically the plasma, before they can reach the interstitial fluid surrounding the cells. From there, they can then move into the receptor sites of the target cells.

Preclinical trials involve the use of lab animals to determine the safe and effective doses of drugs before they are tested on humans. These trials help researchers understand the potential effects, toxicity, and dosage levels of a drug. By conducting preclinical trials, scientists can gather important data on the drug's efficacy and potential side effects, which is crucial for ensuring the safety and effectiveness of the drug before it progresses to clinical trials in humans.

The development of new drugs is regulated by multiple organizations, including the FDA (Food and Drug Administration), USDA (United States Department of Agriculture), and EPA (Environmental Protection Agency). Each organization plays a specific role in ensuring the safety, efficacy, and environmental impact of new drugs. The FDA primarily focuses on the approval and regulation of pharmaceutical drugs, while the USDA oversees the development of veterinary drugs and regulates the use of drugs in food-producing animals. The EPA, on the other hand, evaluates the environmental impact of drugs and their manufacturing processes. Therefore, all three organizations are involved in regulating the development of new drugs.

The therapeutic index is represented by a ratio between the lethal dose for 50% of the population (LD50) and the effective dose for 50% of the population (ED50). This ratio helps determine the safety and efficacy of a drug, with a higher therapeutic index indicating a wider margin of safety.

The correct answer is "Dosage interval". The dosage interval refers to the time between doses of a medication or treatment. It determines how often the medication should be taken and helps ensure that the appropriate amount of the drug remains in the body for it to be effective. A shorter dosage interval may be necessary for medications that have a shorter half-life or need to be maintained at a constant level in the body. On the other hand, a longer dosage interval may be appropriate for medications that have a longer duration of action or are taken for chronic conditions.

The kidneys use two methods to excrete drugs: glomerular filtrate and tubular secretion. Glomerular filtrate refers to the process in which drugs are filtered out of the blood and into the kidney tubules. Tubular secretion, on the other hand, involves the active transport of drugs from the blood into the kidney tubules. Both processes play a crucial role in eliminating drugs from the body.