Classification Of Drugs and Categories

Classification Of Drugs and Categories

Edited By Shivani Poonia | Updated on Jul 02, 2025 07:48 PM IST

Drugs are part and parcel of our lives; they have a very important role in maintaining our health, treating illnesses, and improving our well-being. From simple painkillers like aspirin to take away a headache to the very complex chemotherapeutic agents in fighting an innumerable number of cancer patients, drugs have become an integral part of the armamentarium of modern medicine. However, with such vast numbers of drugs, it becomes important to understand how they are actually categorized and what these classifications do.

This Story also Contains
  1. Basics of Drugs Classification
  2. Classification of Drugs
  3. Types of Drug Classifications
  4. Need for Classification of Drugs
  5. Some Solved Examples
  6. Summary
Classification Of Drugs and Categories
Classification Of Drugs and Categories

Basics of Drugs Classification

Drug classification—this is the grouping of the arrangement of drugs according to established features: the structure, mechanism of action, therapeutic effect, and pharmacological features. It is the science approach to make it easier for proper understanding by practitioners, researchers, and policymakers on different drugs and features, predictions, and possibilities for interaction, for reasoned use.

One of the most broadly applied classifications, for example, is the Anatomical Therapeutic Chemical classification developed by WHO. This class categorizes drugs based on their target organ or system and their therapeutic, pharmacological, and chemical properties. An example is cardiovascular disease drugs, classified under the "C" group, which then further classifies the nervous system drugs as part of the "N" group.

All medicines are drugs but all drugs are not medicines. A drug may be habit-forming, causing addiction while a medicine is safe to use and does not cause addiction. Drugs may be a single chemical substance or a combination of two or more different substances. An ideal drug should satisfy the following requirements:

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  • When administered to the ailing individual or host, its action should be localized at the site where it is desired to act. In actual practice, there is no drug that behaves in this manner.
  • It should act on a system with efficiency and safety.
  • It should have minimum side effects.
  • It should not injure host tissues or physiological processes.
  • The cells should not acquire resistance to the drug after some time.

Classification of Drugs

Drugs may be classified in a number of different ways. Some of these are mentioned below:

1. On the basis of pharmacological effect:

This classification is based on the pharmacological effect of the drugs. It is useful for doctors because it provides them with the whole range of drugs available for the treatment of a particular disease or infection. For example, analgesics have pain pain-killing effect while antiseptics kill or arrest the growth of microorganisms.

2. On the basis of drug action:

It is based on the action of a drug on a particular biochemical process. For example, all antihistamines inhibit the action of histamine which causes inflammation in the body. There are various ways in which the action of histamines can be blocked.

3. On the basis of chemical structure:

It is based on the chemical structure of the drug because drugs have common structural features and often have similar pharmacological activity. For example, sulphonamides having common structural features as given below are mostly antibacterial.

Types of Drug Classifications

There are many ways in which drugs may be classified. On these grounds, different drug types can also be seen divided by:

1. Chemical classification: Categorization of the drugs based on their chemical structure; that is to say, alkaloids, steroids, or phenothiazines would be exemplary.

2. Therapeutic classification: Drugs may also be classified on the basis of their class of therapy, such as analgesics—pain relievers, antibiotics, and antidepressants.

3. Pharmacological classification: Based on mechanism of action, for example, alpha-blockers, beta-blockers, or proton pump inhibitors.

4. Adverse effect classification: Based on the type of side effects the drug can cause, like drugs causing sedation or drugs acting on the cardiovascular system.

Need for Classification of Drugs

1. Better safety of patients: Relationship complexities between different drugs aid the health professional in predicting and dealing with probable drug interactions, thereby reducing the occurrence of side effects.

2. Faster drug development: Drug classification will help in rapidly identifying potential drug candidates by showing similarities to that of existing drugs.

3. Effectual treatment planning: Drug classification by the health professional helps in the selection of the most appropriate drug to an individual's malady and, at the same time, takes into account the special requirements of the patient.

4. Compliance with regulatory bodies: The classification of drugs allows the regulating bodies, like the Food and Drug Administration (FDA) or European Medicines Agency (EMA), to control which drugs ensure their safe and effective use.

Some Solved Examples

Example 1:

Matching Drugs with Their Therapeutic Actions

Question:
Match the following drugs with their therapeutic actions:

(i) Ranitidine
(ii) Nardil (Phenelzine)
(iii) Chloramphenicol
(iv) Dimethane (Brompheniramine)

(a) Antidepressant
(b) Antibiotic
(c) Antihistamine
(d) Antacid
(e) Analgesic

Solution:
(i) Ranitidine $\longrightarrow$ (d) Antacid
(ii) Nardil (Phenelzine) $\longrightarrow$ (a) Antidepressant
(iii) Chloramphenicol $\longrightarrow$ (b) Antibiotic
(iv) Dimethane (Brompheniramine) $\longrightarrow$ (c) Antihistamine

Hence, the answer is option (2).

Example 2:

Deficiency of Nor-Adrenaline

Question:
If a person is suffering from a deficiency of noradrenaline, what kind of drug can be suggested?

1) Anti-inflammatory
2) Antidepressant
3) Antihistamine
4) Analgesic

Solution:
Noradrenaline is a neurotransmitter. If nor-adrenaline is low, a person may suffer from depression. Hence, an antidepressant drug is suggested.
Therefore, the answer is option (2).

Example 3:

Drugs Used for Therapeutic Purposes

Question:
Drugs that are used for therapeutic purposes are generally called?

1) Enzymes
2) Receptors
3) Chemical Messengers
4) Medicines

Solution:
Medicines are drugs that are used for therapeutic purposes like diagnosis, prevention, and treatment of diseases.
Hence, the answer is option (4).

Example 4:

Classification of Drugs for Medicinal Chemists

Question:
The most useful classification of drugs for medicinal chemists is:

1) On the basis of chemical structure
2) On the basis of drug action
3) On the basis of molecular target
4) On the basis of pharmacological effect

Solution:
One of the methods of classification of drugs is based on molecular targets. Drugs possessing some common structural features may have the same mechanism of action on targets. The classification based on molecular targets is the most useful classification for medicinal chemists.
Hence, the answer is option (3).

Example 5:

Identifying Drug Molecule Structure

Question:
The structure shown below is of which well-known drug molecule?

1) Ranitidine
2) Seldane
3) Cimetidine
4) Codeine

Solution:
The given structure is of Cimetidine, which is a well-known drug molecule.
Hence, the answer is option (3).

Summary

By their very nature, the classifying of drugs represents the cornerstone of pharmacology and medicine. It structures the understanding and the probable usages of the different medicines. When one learns about the various classifications of drugs, one can only appreciate the complexity and importance of this area and how the usage of drugs could be assured to be safe and effective for one's health.

Frequently Asked Questions (FAQs)

1. What is the difference between pharmacodynamics and pharmacokinetics in drug classification?
Pharmacodynamics refers to what the drug does to the body, including its mechanism of action and effects. Pharmacokinetics describes what the body does to the drug, including absorption, distribution, metabolism, and excretion. Both are crucial in understanding and classifying drug behavior.
2. What distinguishes prodrugs from active drugs?
Prodrugs are inactive compounds that are metabolized in the body to produce the active drug. Active drugs are already in their effective form when administered. Prodrugs can offer advantages like improved absorption, targeted delivery, or reduced side effects.
3. What distinguishes agonists from antagonists in receptor-based drug actions?
Agonists bind to receptors and activate them, mimicking the action of natural substances in the body. Antagonists bind to receptors without activating them, blocking the action of natural substances or other drugs. This fundamental difference determines their effects on body systems.
4. What is the key difference between synthetic and semi-synthetic drugs?
Synthetic drugs are entirely artificially created in laboratories. Semi-synthetic drugs start with a naturally occurring compound that is then chemically modified. This distinction affects production methods, costs, and sometimes the properties of the final drug.
5. What is the primary purpose of classifying drugs into different categories?
The main purpose of drug classification is to group medications based on their chemical structure, mechanism of action, or therapeutic effects. This helps in understanding how drugs work, predicting their effects, and guiding their appropriate use in medical treatments.
6. Why are some drugs classified as "controlled substances"?
Drugs are classified as controlled substances when they have a high potential for abuse, addiction, or severe side effects. This classification allows for stricter regulation of their manufacture, distribution, and use to prevent misuse while ensuring availability for legitimate medical purposes.
7. How do diuretics work, and why are they classified separately from other medications?
Diuretics increase urine production and excretion, helping the body eliminate excess water and salt. They're classified separately because their primary action is on kidney function, affecting fluid balance in the body, which is distinct from other drug categories that target specific organs or systems.
8. What distinguishes psychoactive drugs from other drug categories?
Psychoactive drugs primarily affect the central nervous system, altering brain function and resulting in changes in perception, mood, consciousness, or behavior. This sets them apart from drugs that primarily target other body systems or have localized effects.
9. How do antihistamines differ in their first-generation and second-generation forms?
First-generation antihistamines can cross the blood-brain barrier, causing drowsiness and other central nervous system effects. Second-generation antihistamines are designed to have limited ability to cross this barrier, reducing these side effects while still effectively treating allergy symptoms.
10. How do analgesics differ from anesthetics?
Analgesics are pain-relieving drugs that don't cause loss of consciousness, while anesthetics are drugs that induce a state of unconsciousness or loss of sensation. Analgesics target pain receptors, whereas anesthetics affect the central nervous system more broadly.
11. What distinguishes narcotic analgesics from non-narcotic analgesics?
Narcotic analgesics, also known as opioids, are derived from opium or synthetic alternatives and work by binding to specific opioid receptors in the brain. They are more potent but have a higher risk of addiction. Non-narcotic analgesics, like acetaminophen or ibuprofen, work through different mechanisms and have lower addiction potential.
12. How do antibiotics differ from antivirals in their mechanism of action?
Antibiotics target and kill bacteria or inhibit their growth, often by interfering with cell wall synthesis or protein production. Antivirals, on the other hand, work by interfering with viral replication processes within host cells, as viruses cannot reproduce on their own.
13. What is the difference between broad-spectrum and narrow-spectrum antibiotics?
Broad-spectrum antibiotics are effective against a wide range of bacterial types, both gram-positive and gram-negative. Narrow-spectrum antibiotics target specific types of bacteria. Broad-spectrum antibiotics are used when the infecting organism is unknown, while narrow-spectrum antibiotics are preferred when the specific pathogen is identified to reduce antibiotic resistance.
14. What is the key difference between antiseptics and disinfectants?
Antiseptics are chemical agents used on living tissues to prevent or stop the growth of microorganisms, while disinfectants are similar substances used on non-living surfaces. Antiseptics are generally milder to avoid harming living cells, while disinfectants can be stronger.
15. How do antacids differ from proton pump inhibitors in treating acid reflux?
Antacids work by neutralizing stomach acid directly, providing quick but temporary relief. Proton pump inhibitors (PPIs) reduce acid production by blocking the proton pumps in stomach cells, offering longer-lasting relief but taking longer to start working.
16. How do ACE inhibitors and beta-blockers differ in their approach to treating hypertension?
ACE (Angiotensin-Converting Enzyme) inhibitors lower blood pressure by preventing the formation of angiotensin II, a hormone that narrows blood vessels. Beta-blockers work by blocking the effects of adrenaline on the heart, slowing heart rate and reducing the force of heart contractions.
17. How do statins differ from other cholesterol-lowering medications?
Statins work by inhibiting an enzyme (HMG-CoA reductase) involved in cholesterol production in the liver. Other cholesterol-lowering medications may work by different mechanisms, such as blocking cholesterol absorption in the intestines (like ezetimibe) or binding bile acids (like cholestyramine).
18. How do antiemetics differ in their mechanisms of action?
Antiemetics prevent nausea and vomiting through various mechanisms. Some block serotonin receptors in the gut and brain (like ondansetron), others block dopamine receptors (like metoclopramide), and some affect the vestibular system (like antihistamines). The choice depends on the cause of nausea.
19. What is the difference between antipyretics and anti-inflammatory drugs?
Antipyretics specifically reduce fever by affecting the body's temperature regulation in the hypothalamus. Anti-inflammatory drugs reduce inflammation throughout the body. Some drugs, like ibuprofen, have both antipyretic and anti-inflammatory properties.
20. What distinguishes local anesthetics from general anesthetics?
Local anesthetics block nerve signals in a specific area of the body without affecting consciousness. General anesthetics induce a state of unconsciousness, affecting the entire body and central nervous system.
21. What is the key difference between stimulants and depressants in their effects on the central nervous system?
Stimulants increase activity in the central nervous system, leading to heightened alertness, increased energy, and elevated mood. Depressants, conversely, slow down central nervous system activity, resulting in relaxation, reduced anxiety, and sometimes drowsiness.
22. How do antipsychotics differ from antidepressants in their primary targets and effects?
Antipsychotics primarily target dopamine receptors to manage symptoms of psychosis like hallucinations and delusions. Antidepressants typically target serotonin, norepinephrine, or both to alleviate symptoms of depression and anxiety.
23. What distinguishes immunosuppressants from other drug categories?
Immunosuppressants are unique in that they deliberately weaken the immune system. They're used to prevent organ rejection in transplant patients or to treat autoimmune diseases by reducing the body's immune response, unlike most drugs which aim to boost or support normal body functions.
24. How do bronchodilators differ from corticosteroids in treating asthma?
Bronchodilators provide quick relief by relaxing and opening constricted airways, allowing easier breathing. Corticosteroids reduce inflammation in the airways over time, preventing asthma symptoms and attacks. Bronchodilators offer immediate relief, while corticosteroids provide long-term control.
25. What is the difference between anticoagulants and antiplatelet drugs?
Anticoagulants, often called blood thinners, work by interfering with the clotting process itself, often by inhibiting clotting factors. Antiplatelet drugs specifically prevent platelets from sticking together and forming clots. Both reduce clot formation but through different mechanisms.
26. How do osmotic laxatives differ from stimulant laxatives?
Osmotic laxatives work by drawing water into the intestines, softening stool and making it easier to pass. Stimulant laxatives increase intestinal contractions to move stool through the colon more quickly. Osmotic laxatives are generally gentler and can be used more regularly.
27. What distinguishes antifungal drugs from antibacterial drugs?
Antifungal drugs target structures or processes specific to fungal cells, such as ergosterol in cell membranes. Antibacterial drugs target bacterial structures or processes, like cell wall synthesis or protein production. This specificity allows each to combat different types of infections.
28. How do alpha-blockers differ from beta-blockers in their mechanism and use?
Alpha-blockers relax certain muscles and help small blood vessels remain open by blocking the hormone norepinephrine. Beta-blockers slow the heart rate and reduce blood pressure by blocking the effects of epinephrine. While both can treat hypertension, they have different additional uses and side effect profiles.
29. What is the key difference between SSRIs and SNRIs in treating depression?
Selective Serotonin Reuptake Inhibitors (SSRIs) primarily increase serotonin levels in the brain. Serotonin-Norepinephrine Reuptake Inhibitors (SNRIs) increase both serotonin and norepinephrine levels. SNRIs may be more effective for some patients, particularly those with additional symptoms like pain.
30. What distinguishes antispasmodics from muscle relaxants?
Antispasmodics specifically target smooth muscle in the digestive tract to relieve cramping and spasms. Muscle relaxants typically affect skeletal muscle, reducing tension and spasms in the musculoskeletal system. Their sites of action and uses are distinct despite both affecting muscle activity.
31. How do vasodilators differ from vasoconstrictors in their effects on blood vessels?
Vasodilators widen blood vessels, reducing blood pressure and increasing blood flow. Vasoconstrictors narrow blood vessels, which can increase blood pressure and reduce blood flow to specific areas. They have opposite effects and are used for different medical purposes.
32. What is the difference between first-line and second-line drugs in disease treatment?
First-line drugs are the initial, preferred treatment for a condition due to their proven efficacy and safety profile. Second-line drugs are used when first-line treatments are ineffective, not tolerated, or contraindicated. The classification helps guide treatment decisions and manage risks.
33. How do anticholinergics differ from cholinergics in their effects on the nervous system?
Anticholinergics block the neurotransmitter acetylcholine, reducing nerve impulses. This can relax smooth muscles and reduce bodily secretions. Cholinergics, conversely, mimic or enhance the effects of acetylcholine, increasing nerve impulses. They have opposite effects on various body systems.
34. What distinguishes biologics from traditional small-molecule drugs?
Biologics are large, complex molecules derived from living organisms, often proteins. Small-molecule drugs are chemically synthesized and have a well-defined structure. Biologics are more targeted in their effects but more complex to manufacture and administer, often requiring injection or infusion.
35. How do antiarrhythmic drugs differ in their classification and mechanisms?
Antiarrhythmic drugs are classified into four main classes based on their effects on cardiac ion channels. Class I affects sodium channels, Class II are beta-blockers, Class III affect potassium channels, and Class IV are calcium channel blockers. Each class targets different aspects of heart rhythm regulation.
36. How do anticonvulsants differ from anxiolytics, despite both affecting the central nervous system?
Anticonvulsants primarily prevent or reduce the severity of seizures by stabilizing electrical activity in the brain. Anxiolytics reduce anxiety by enhancing the effect of GABA, a calming neurotransmitter. While both affect the CNS, their primary targets and uses are distinct.
37. How do monoclonal antibodies differ from traditional drug therapies?
Monoclonal antibodies are highly specific, engineered proteins that target particular molecules in the body. Traditional drug therapies often have broader effects. Monoclonal antibodies can offer more targeted treatment with potentially fewer side effects, especially in areas like cancer and autoimmune diseases.
38. What is the key difference between enteric-coated and immediate-release drug formulations?
Enteric-coated formulations have a special coating that prevents the drug from being released in the stomach, instead releasing it in the intestines. Immediate-release formulations dissolve quickly after ingestion. Enteric coating can protect the drug from stomach acid or reduce stomach irritation.
39. How do enzyme inhibitors differ from enzyme inducers in drug interactions?
Enzyme inhibitors slow down the metabolism of other drugs by blocking enzymes, potentially increasing their concentration and effects. Enzyme inducers speed up drug metabolism by increasing enzyme production, potentially decreasing the concentration and effects of other drugs.
40. What distinguishes orphan drugs from mainstream pharmaceuticals?
Orphan drugs are developed specifically to treat rare diseases affecting a small percentage of the population. Mainstream pharmaceuticals target more common conditions. Orphan drugs often have different development, approval, and marketing processes due to the smaller patient population.
41. How do selective and non-selective beta-blockers differ in their effects?
Selective beta-blockers primarily affect β1 receptors found in the heart, while non-selective beta-blockers affect both β1 and β2 receptors found in the heart, lungs, and other tissues. Selective beta-blockers may have fewer side effects on the respiratory system.
42. What is the difference between pharmacological and physiological classification of drugs?
Pharmacological classification groups drugs based on their chemical structure or mechanism of action. Physiological classification groups drugs based on the body system or function they primarily affect. Both systems are useful for understanding drug effects and guiding treatment choices.
43. How do extended-release formulations differ from immediate-release in terms of drug delivery?
Extended-release formulations are designed to release the drug slowly over time, maintaining a steady concentration in the body. Immediate-release formulations release the drug quickly for rapid absorption. Extended-release can improve compliance by reducing dosing frequency and may reduce side effects.
44. How do NSAIDs differ from COX-2 inhibitors in their mechanism and side effects?
Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) inhibit both COX-1 and COX-2 enzymes, reducing inflammation but potentially causing gastrointestinal side effects. COX-2 inhibitors specifically target the COX-2 enzyme, offering anti-inflammatory effects with reduced gastrointestinal risks.
45. What is the difference between empiric and targeted antimicrobial therapy?
Empiric antimicrobial therapy involves using broad-spectrum antibiotics based on likely pathogens before identifying the specific cause of infection. Targeted therapy uses specific antibiotics chosen based on identified pathogens and their susceptibilities. Empiric therapy is initial, while targeted is more precise.
46. How do photosensitizing drugs differ from other medications in terms of side effects?
Photosensitizing drugs increase sensitivity to sunlight, potentially causing skin reactions when exposed to UV radiation. This unique side effect is not common to most other medications and requires specific precautions like avoiding sun exposure or using sunscreen.
47. What distinguishes chemopreventive agents from traditional chemotherapy drugs?
Chemopreventive agents are used to prevent the development or progression of cancer in high-risk individuals. Traditional chemotherapy drugs are used to treat existing cancer. Chemopreventives often have a better safety profile for long-term use compared to more potent chemotherapy drugs.
48. How do gastroprotective drugs differ in their mechanisms of action?
Gastroprotective drugs work through various mechanisms. Proton pump inhibitors reduce acid production, H2 blockers reduce histamine's effect on acid secretion, and mucosal protectants form a physical barrier on the stomach lining. Each type offers protection through a different approach.
49. How do nootropics differ from traditional cognitive enhancers or stimulants?
Nootropics are substances claimed to enhance cognitive function, particularly executive functions, memory, creativity, or motivation, often with minimal side effects. Traditional cognitive enhancers or stimulants may have more pronounced effects but also carry higher risks of side effects or dependency.

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