What Is Medication: Types, Forms & How Drugs Work

Medically reviewed | Last reviewed: | Evidence level: 1A
Medications are substances used to prevent, diagnose, treat, or cure diseases and medical conditions. They contain active ingredients that produce therapeutic effects and inactive ingredients (excipients) that help with manufacturing, stability, and delivery. Before any medication can be sold, it must be approved by regulatory agencies like the FDA, EMA, or WHO that verify its safety, quality, and effectiveness.
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Written and reviewed by iMedic Medical Editorial Team | Specialists in pharmacology and clinical medicine

📊 Quick facts about medications

Generic savings
30-80% less
than brand-name
Drug forms
10+ types
oral, injection, topical
WHO Essential
500+ drugs
on essential list
Approval time
10-15 years
from discovery to market
Patent duration
20 years
before generic allowed
ATC Classification
WHO System
Anatomical Therapeutic

💡 The most important things you need to know

  • Generic drugs are equally effective: They contain the same active ingredients in the same amounts as brand-name medications but cost 30-80% less
  • Medications work through four processes: Absorption, distribution, metabolism, and excretion (ADME) determine how drugs affect your body
  • Form affects absorption: Injections work fastest, while extended-release tablets provide steady levels over time
  • Always read the label: Check dosage, frequency, interactions, and storage requirements before taking any medication
  • Complete the full course: Especially for antibiotics - stopping early can lead to treatment failure and resistance
  • Store properly: Most medications need cool, dry storage away from sunlight; some require refrigeration
  • Check expiration dates: Expired medications may lose effectiveness or become potentially harmful

What Is Medication and How Does It Work?

Medication (also called medicine or drugs) refers to substances used to prevent, diagnose, treat, or cure diseases. Every medication contains one or more active ingredients that produce therapeutic effects, plus inactive ingredients (excipients) that help with manufacturing, stability, taste, and delivery to the body.

Understanding what medication is and how it works is fundamental to managing your health effectively. When you take a medication, whether it's a simple pain reliever or a complex prescription drug, you're introducing a carefully designed chemical compound into your body that interacts with specific biological targets to produce a desired therapeutic effect.

The journey from a natural remedy to modern pharmaceuticals spans thousands of years. Ancient civilizations used plants, minerals, and animal products to treat ailments - many of which we now understand contain pharmacologically active compounds. Today's medications are the result of rigorous scientific research, clinical trials, and regulatory oversight that ensure they are safe, effective, and of consistent quality.

Every medication must be approved by regulatory agencies before it can be sold. In the United States, this is the Food and Drug Administration (FDA). In Europe, it's the European Medicines Agency (EMA). Globally, the World Health Organization (WHO) provides guidelines and maintains the Essential Medicines List. These agencies evaluate manufacturers' data on a drug's effectiveness, potential side effects, and manufacturing quality before granting approval.

Active Ingredients vs. Inactive Ingredients

Every medication contains two types of components that work together to deliver treatment effectively. Understanding this distinction helps you make informed decisions about your medications and identify potential allergens or sensitivities.

Active ingredients (also called active pharmaceutical ingredients or APIs) are the compounds that produce the medication's therapeutic effect. For example, in a standard pain reliever, ibuprofen or acetaminophen is the active ingredient that reduces pain and inflammation. The active ingredient is what your doctor prescribes and what determines the drug's classification.

Inactive ingredients (excipients) don't directly treat your condition but serve essential functions. These include binders that hold tablets together, fillers that make pills large enough to handle, coatings that protect the drug or make it easier to swallow, colors for identification, and preservatives for stability. Common excipients include lactose, starch, cellulose, talc, and various dyes.

Important for people with allergies:

If you have allergies or sensitivities to certain substances, check both active and inactive ingredients. The full ingredient list is found on the package or in the package insert (the information leaflet that comes with your medication). Common allergens in medications include lactose, gluten, certain dyes, and preservatives.

How Medications Are Regulated

The regulatory process for medications is one of the most rigorous in any industry, designed to protect public health while ensuring access to effective treatments. Before a drug can reach patients, it must pass through multiple stages of testing and review.

Drug development typically takes 10 to 15 years from initial discovery to market approval. This includes laboratory research, animal studies, and three phases of human clinical trials involving thousands of participants. The entire process can cost over $2 billion per successfully approved drug.

Regulatory agencies like the FDA and EMA continuously monitor medications even after approval through post-marketing surveillance. This ongoing oversight has led to the withdrawal of drugs that showed unexpected safety issues in larger populations or over longer periods of use.

What Are the Different Types of Medication?

Medications are categorized into several types based on their origin and patent status: original (brand-name) drugs, generic drugs, biosimilars, parallel-imported drugs, and licensed drugs. Each type undergoes regulatory review to ensure safety and effectiveness, though they may differ in price and availability.

Understanding the different types of medication helps you make informed decisions about your treatment options and potentially save money without sacrificing quality. The pharmaceutical market offers several categories of drugs, each with distinct characteristics, benefits, and considerations.

Original (Brand-Name) Medications

When a pharmaceutical company develops a new drug, it receives patent protection for a set number of years - typically 20 years from the date of patent filing. During this time, only the patent holder can manufacture and sell the drug under its brand name. This exclusivity period allows companies to recoup their substantial research and development investments.

Original medications often carry higher prices because the manufacturer must recover the costs of years of research, clinical trials, marketing, and the many unsuccessful drug candidates that never reached the market. The brand name is chosen by the company and is different from the drug's generic (scientific) name.

For example, Lipitor is the brand name for atorvastatin, a cholesterol-lowering medication. The brand name "Lipitor" is a trademark of Pfizer, while "atorvastatin" is the drug's international nonproprietary name (INN) used worldwide.

Generic Medications

Once a drug's patent expires, other manufacturers can produce and sell copies called generic medications. These drugs contain the same active ingredient(s) in the same amounts as the original but are typically sold at 30-80% lower prices because the manufacturer doesn't bear the original research and development costs.

Generic drugs must meet the same quality, safety, and efficacy standards as brand-name drugs. Regulatory agencies require that generics demonstrate bioequivalence - meaning they deliver the same amount of active ingredient into the bloodstream at the same rate as the original drug.

While generics contain identical active ingredients, they may differ from the original in their inactive ingredients, appearance (color, shape, size), and packaging. These differences don't affect the medication's effectiveness. Generic drug names often combine the active ingredient's name with the manufacturer's name (e.g., "Atorvastatin Teva").

Key differences between brand-name and generic medications
Feature Brand-Name Drug Generic Drug
Active ingredient Original formulation Identical to original
Quality standards FDA/EMA approved Same FDA/EMA standards
Price Higher (covers R&D) 30-80% lower
Appearance Trademarked design May differ in color/shape

Biosimilars

Biosimilars are medications highly similar to already-approved biological medicines (biologics), but they are fundamentally different from generic drugs. While generics are chemically synthesized and can be made identical to the original, biosimilars are produced from living cells and may have minor structural differences that don't affect safety or efficacy.

Biological medicines are complex, large-molecule drugs derived from living organisms. They include insulin, monoclonal antibodies, and vaccines. Because of their complexity, biosimilars cannot be exact copies of the reference biologic, but they must demonstrate no clinically meaningful differences in safety, purity, and potency.

Biosimilars undergo more extensive testing than generic drugs but typically cost 15-35% less than the original biologic. They've significantly increased access to expensive treatments for conditions like rheumatoid arthritis, cancer, and inflammatory bowel disease.

Parallel-Imported Medications

Parallel importation occurs when medications are legally purchased in one country and then imported to another where prices are higher. This practice takes advantage of price differences between markets in different countries and can offer cost savings to healthcare systems and patients.

Parallel-imported drugs are genuine, approved medications - not counterfeits. However, they must be repackaged to meet the importing country's labeling and language requirements. Regulatory agencies verify that the repackaging process maintains the drug's quality and that the patient receives the same medication they would from the original manufacturer.

Licensed Medications

Licensed medications are drugs that aren't approved for sale in a particular country but can be legally obtained through special permission. Healthcare providers can request a license from regulatory authorities when a patient needs a medication that's approved in another country but not domestically available.

This pathway is typically used when no suitable alternative exists in the home market, or when a specific patient cannot tolerate the locally available options. The prescribing physician must justify why the patient needs this particular medication, and the pharmacy applies for the import license.

What Are the Different Forms of Medication?

Medications come in over 10 different forms including tablets, capsules, liquids, injections, patches, creams, inhalers, suppositories, eye drops, ear drops, and nasal sprays. The form affects how quickly the drug works, how much reaches the bloodstream, and how convenient it is to use.

The form in which a medication is delivered - known as its dosage form or formulation - is carefully chosen based on the drug's properties, the condition being treated, and patient factors like age and ability to swallow pills. Different forms provide different advantages in terms of onset of action, duration of effect, and ease of use.

Sometimes the same medication is available in multiple forms, allowing doctors to choose the most appropriate option for each patient. For example, if you have difficulty swallowing tablets, your doctor might prescribe a liquid form of the same drug.

Oral Medications (Taken by Mouth)

Oral medications are the most common and convenient form, accounting for about 80% of all pharmaceutical products. They travel through the digestive system, are absorbed primarily in the small intestine, and then enter the bloodstream to reach their target sites.

  • Tablets: Solid, compressed doses that may be scored for splitting. Can be immediate-release or extended-release (providing gradual medication release over hours)
  • Capsules: Medication enclosed in a dissolvable shell, either hard (for powder/granules) or soft (for liquids/oils). Often easier to swallow than tablets
  • Liquids: Solutions (drug fully dissolved), suspensions (drug particles suspended - shake before use), or syrups. Ideal for children or those who can't swallow pills
  • Chewable tablets: Designed to be chewed before swallowing; common for antacids and children's medications
  • Sublingual/buccal: Dissolve under the tongue or between cheek and gum for rapid absorption directly into bloodstream

The oral route has limitations: some drugs are destroyed by stomach acid or liver metabolism before reaching the bloodstream (called "first-pass effect"), and absorption can be affected by food, other medications, or digestive conditions.

Injectable Medications

Injections deliver medication directly into body tissues, bypassing the digestive system for faster, more predictable absorption. Different injection sites offer different advantages:

  • Subcutaneous (under the skin): Common for insulin, blood thinners, and some vaccines. Slower absorption than intramuscular
  • Intramuscular (into muscle): Used for vaccines, antibiotics, and hormones. Larger volumes possible than subcutaneous
  • Intravenous (into vein): Fastest onset; medication enters bloodstream immediately. Used in hospitals for emergencies and when precise dosing is critical

Topical Medications (Applied to Skin or Mucous Membranes)

Topical medications are applied directly where they're needed, minimizing effects on the rest of the body. They come in various forms including creams, ointments, gels, lotions, and patches.

Transdermal patches deserve special mention - they deliver medication through the skin into the bloodstream at a controlled rate over hours or days. Examples include nicotine patches for smoking cessation, pain medication patches, and hormone replacement therapy patches.

Inhaled Medications

Inhaled medications are breathed in through the mouth or nose, delivering drugs directly to the lungs or nasal passages. This route is essential for respiratory conditions and offers rapid absorption into the bloodstream through the lung's extensive blood vessel network.

Inhaler types include metered-dose inhalers (MDIs), dry powder inhalers (DPIs), and nebulizers (which convert liquid medication into a fine mist). Proper inhaler technique is crucial for effectiveness - ask your pharmacist or healthcare provider to demonstrate correct use.

Other Medication Forms

  • Eye drops and ointments: Treat conditions in and around the eye; minimal systemic absorption
  • Ear drops: Treat ear infections and earwax buildup
  • Nasal sprays: Treat congestion, allergies, or deliver systemic medications (some migraine treatments, flu vaccines)
  • Rectal suppositories: Insert into the rectum; useful when oral route isn't possible or for local treatment
  • Vaginal medications: Creams, tablets, or rings for local treatment of infections or hormone delivery

How Do Medications Work in the Body?

Medications work through four main processes called ADME: Absorption (entering the bloodstream), Distribution (traveling to target tissues), Metabolism (being processed, mainly by the liver), and Excretion (leaving the body, mainly through kidneys). The active ingredient then interacts with specific biological targets to produce therapeutic effects.

Understanding how your body processes medications helps explain why dosing schedules matter, why some drugs must be taken with food while others require an empty stomach, and why certain combinations of medications can be dangerous.

Absorption: How Drugs Enter Your System

Absorption is the process by which a medication moves from its site of administration into the bloodstream. The rate and extent of absorption depend on the drug's chemical properties, the dosage form, and patient factors.

For oral medications, absorption primarily occurs in the small intestine, where the large surface area and good blood supply facilitate drug uptake. Factors affecting oral absorption include stomach acidity, presence of food, intestinal motility, and the drug's solubility. Some medications work best on an empty stomach, while others require food to enhance absorption or reduce stomach irritation.

Bioavailability describes what percentage of the administered dose reaches the systemic circulation. Intravenous medications have 100% bioavailability by definition. Oral medications often have lower bioavailability due to incomplete absorption and first-pass metabolism in the liver.

Distribution: Where Drugs Travel

Once in the bloodstream, medications distribute throughout the body. Some drugs bind to blood proteins, creating a reservoir that's released gradually. Others quickly leave the bloodstream to concentrate in specific tissues.

Drug distribution is affected by blood flow to different organs, the drug's ability to cross cell membranes, and protein binding. The blood-brain barrier selectively limits which substances can reach the brain, which is why some medications for brain conditions must be specifically designed to cross this barrier.

Metabolism: How Drugs Are Processed

The liver is the primary site of drug metabolism, using enzymes (especially the cytochrome P450 family) to chemically modify medications. Metabolism typically makes drugs more water-soluble so they can be eliminated by the kidneys, and often converts active drugs to inactive forms.

However, some medications are prodrugs - inactive compounds that the liver converts into active forms. The speed of metabolism varies between individuals based on genetics, age, liver function, and other medications being taken. This is why drug interactions can occur - one medication may speed up or slow down another's metabolism.

Excretion: How Drugs Leave Your Body

Excretion is the final removal of medications and their metabolites from the body. The kidneys are the primary route of excretion, filtering drugs from the blood into urine. Other routes include the liver (into bile and then feces), lungs (for volatile substances), and skin (through sweat).

The half-life of a drug - the time it takes for blood concentration to decrease by half - determines dosing frequency. Short half-life drugs need more frequent dosing, while long half-life drugs may be taken once daily or even less often.

Important warning about kidney and liver function:

Patients with impaired kidney or liver function may process medications differently. Doses often need to be adjusted to prevent drug accumulation and toxicity. Always inform your healthcare provider about any kidney or liver conditions, and have regular monitoring if you take medications long-term.

How Should You Take Medications Safely?

Take medications exactly as prescribed: read the label carefully, follow timing instructions (with or without food), use the correct dose, complete the full course, and store properly. Never share prescription medications, and inform your healthcare provider about all medications and supplements you take to avoid dangerous interactions.

Taking medications safely involves more than just swallowing a pill. Proper medication use maximizes therapeutic benefits while minimizing risks of side effects, interactions, and treatment failure.

Reading and Understanding Medication Labels

Every medication comes with labeling that provides essential information. For prescription drugs, this includes the drug name, dosage, frequency, special instructions, prescriber's name, and pharmacy contact information. Over-the-counter medications have standardized "Drug Facts" labels.

Pay attention to:

  • Dosage: The amount of medication per dose (e.g., 500 mg)
  • Frequency: How often to take it (e.g., twice daily, every 8 hours)
  • Duration: How long to continue treatment
  • Timing: With or without food, time of day
  • Warnings: Activities to avoid (e.g., driving), substances to avoid (e.g., alcohol)
  • Storage: Temperature requirements, keep away from children
  • Expiration date: Don't use medications past this date

Timing and Food Interactions

When you take a medication relative to meals can significantly affect its absorption and effectiveness. Follow these general guidelines unless your specific medication requires otherwise:

  • "On an empty stomach": Take 1 hour before or 2 hours after eating for optimal absorption
  • "With food": Take during or immediately after a meal to enhance absorption or reduce stomach upset
  • "At bedtime": Some medications cause drowsiness or work best during sleep
  • "Morning": Some medications affect sleep patterns or align with body rhythms

Certain foods can interact with specific medications. Grapefruit and grapefruit juice, for example, can affect the metabolism of many drugs. Dairy products can reduce absorption of some antibiotics. Always ask your pharmacist about food interactions.

Completing the Full Course

For some medications, especially antibiotics, completing the entire prescribed course is crucial even if you feel better before it's finished. Stopping early can allow bacteria to survive and develop resistance, potentially causing a harder-to-treat infection.

However, for some medications, this rule doesn't apply. Pain relievers, for instance, are typically taken as needed. Your prescribing instructions will clarify whether to take the medication for a specific duration or only when symptoms are present.

Proper Storage

Medications can degrade if stored improperly, becoming less effective or potentially harmful. General storage guidelines include:

  • Room temperature (15-25°C/59-77°F): Most medications unless otherwise specified
  • Refrigerated (2-8°C/36-46°F): Some antibiotics, insulin, certain biologics
  • Protected from light: Some medications degrade when exposed to light
  • Dry conditions: Avoid storing medications in bathrooms where humidity is high
  • Original containers: Keep medications in their original packaging with child-resistant caps

What About Supplements and Natural Products?

Dietary supplements (vitamins, minerals, herbs) are regulated as foods, not drugs, and don't require pre-market safety approval. While some supplements have proven benefits, they can interact with medications and may not contain what their labels claim. Always inform your healthcare provider about supplements you take.

The distinction between medications and supplements is important for understanding what you're putting in your body. While medications undergo rigorous testing and approval processes, supplements face different regulatory standards.

Dietary Supplements

Dietary supplements include vitamins, minerals, proteins, fatty acids, fiber, herbs, and plant extracts. They are classified as foods, not drugs, which means manufacturers don't need to prove safety or effectiveness before selling them. The regulatory agencies can only act against unsafe products after they reach the market.

Supplements are labeled "dietary supplement" and often carry disclaimers stating they haven't been evaluated by regulatory agencies and aren't intended to diagnose, treat, cure, or prevent any disease.

Herbal and Natural Medicines

Herbal medicines (botanical products) and natural medicines contain substances from plants, animals, or microorganisms. Many modern medications were originally derived from natural sources - aspirin from willow bark, digoxin from foxglove, morphine from poppies.

In some countries, traditional herbal medicines have formal registration pathways that require demonstration of quality and traditional use, though not the same level of clinical evidence as pharmaceutical drugs.

Important about supplements and medications:

Natural doesn't mean safe. Herbal products can have powerful effects and interact with prescription medications. St. John's Wort, for example, can reduce the effectiveness of birth control pills, blood thinners, and many other drugs. Always tell your healthcare provider about ALL products you take, including supplements and herbal remedies.

Medical Devices

Medical devices are products used in healthcare that work through physical means rather than pharmacological action. They range from simple products like bandages and thermometers to complex equipment like pacemakers and MRI machines.

Products you might find in pharmacies include blood glucose meters, blood pressure monitors, pregnancy tests, lice combs, and condoms. These must meet specific safety standards and are marked with regulatory approval symbols (like the CE mark in Europe).

What Are Important Medication Safety Considerations?

Medication safety involves avoiding dangerous interactions, recognizing side effects, preventing medication errors, and knowing when to seek medical help. Key precautions include maintaining a current medication list, using one pharmacy, reading labels carefully, and never sharing prescription medications.

Every medication carries some risk of side effects and interactions. Understanding these risks and knowing how to minimize them is essential for safe medication use.

Drug Interactions

Drug interactions occur when one substance affects how another works. This can result in increased effects (potentially dangerous), decreased effects (treatment failure), or new side effects. Interactions can occur between:

  • Drug-drug: Two or more medications affecting each other
  • Drug-food: Foods affecting medication absorption or metabolism
  • Drug-supplement: Vitamins, herbs, or supplements affecting medications
  • Drug-condition: Medical conditions affecting how medications work

Side Effects

All medications can cause side effects - unwanted effects that occur alongside the intended therapeutic effect. Side effects range from mild and temporary (like nausea or headache) to serious and potentially life-threatening (like severe allergic reactions or organ damage).

Common side effects are usually listed on the medication label or package insert. Less common but serious side effects are also documented. Contact your healthcare provider if you experience unexpected or concerning symptoms after starting a new medication.

Special Populations

Certain groups require special consideration when taking medications:

  • Pregnant and breastfeeding: Many drugs can affect the fetus or pass into breast milk. Always consult a healthcare provider before taking any medication during pregnancy or while breastfeeding
  • Children: Dosages must be adjusted for weight and age. Not all medications are approved for pediatric use
  • Elderly: Age-related changes in metabolism and kidney function often require dose adjustments. Older adults are more susceptible to side effects and interactions
  • Kidney or liver disease: These organs process most medications, so impairment requires careful dose adjustment

Frequently asked questions about medications

Medical References and Sources

This article is based on current medical research and international guidelines. All claims are supported by scientific evidence from peer-reviewed sources.

  1. World Health Organization (2023). "WHO Model List of Essential Medicines - 23rd List." WHO Essential Medicines The WHO's core list of medications needed for basic health systems.
  2. U.S. Food and Drug Administration (2024). "Generic Drug Facts." FDA Generic Drugs FDA guidance on generic drug quality and equivalence standards.
  3. European Medicines Agency (2024). "Biosimilars in the EU: Information Guide for Healthcare Professionals." EMA Biosimilars European guidelines on biosimilar medications.
  4. Institute for Safe Medication Practices (2024). "Safe Medication Practices Guidelines." ISMP Resources for medication error prevention and safe use.
  5. Brunton, L.L., et al. (2023). "Goodman & Gilman's: The Pharmacological Basis of Therapeutics, 14th Edition." McGraw-Hill Education. Authoritative textbook on pharmacology and therapeutics.
  6. National Institute for Health and Care Excellence (2024). "Medicines Guidance and Guidelines." NICE Guidelines Evidence-based guidance for medication use in clinical practice.

Evidence grading: This article uses the GRADE framework (Grading of Recommendations Assessment, Development and Evaluation) for evidence-based medicine. Information is based on established pharmacological principles, regulatory agency guidelines, and peer-reviewed medical literature.

iMedic Medical Editorial Team

Specialists in pharmacology and clinical medicine

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