Reading a Package Insert The Package Insert, also referred to as a "PI," "Prescribing Information" or "Labeling" is prepared by a medication's manufacturer for healthcare professionals who prescribe or dispense prescription medicines. Your pharmacy should have a current Package Insert for any drug that it dispenses. Reading the package insert cannot substitute for a discussion with your doctor, pharmacist or other healthcare professional about any medication you are about to take. The U.S. Food and Drug Administration (FDA) requires prescription drug labeling to contain specific information. Package Insert styles vary from company to company, but generally they must include information under the following section headings and in the order listed. Description This section of a PI contains the following general information: The generic name (sometimes referred to as the scientific or chemical name) and the brand name of the drug Dosage form (for example, capsules, tablets, liquid) and the way it is administered (for example, pill, shot, cream) Pharmacological or therapeutic class (for example, antibiotic, pain reliever, antidepressant) Chemical name and structural formula of the drug Other important chemical or physical information, if appropriate Clinical Pharmacology Clinical pharmacology refers to the properties and actions of the drug or how it works in the body. If the drug's method of action is unknown or if certain information is unavailable, the labeling will contain a statement to that effect. Indications and Usage This section contains information about the treatment of the particular diagnosis or diagnoses for which the FDA has approved the drug. However, drugs can sometimes be prescribed for reasons other than the FDA-approved indications based on currently available clinical data. Ask your doctor, pharmacist or other healthcare professional if you have questions about why a particular drug has been prescribed for you. Contraindications The contraindications section describes situations in which the drug should not be used because the risk of using it clearly outweighs the benefit. If no contraindications are known, this section of the labeling will state "None known." Warnings This section describes serious adverse reactions and potential safety hazards, the limitations they impose on use of the drug, and steps that should be taken if they occur. The FDA may require that notification of any special problems associated with the drug be placed in a prominently displayed box called a "black box." Back to Top Precautions This section of the PI includes precautions for most individuals taking the drug, as well as for specific groups, such as pregnant women, nursing mothers or children. In this section, you will find recommendations for patients to ensure safe and effective use of the drug. For example, there may be precautions about driving when taking the medication or using substances such as other drugs, food or alcohol that may have harmful effects if taken while using the medication. The Precautions section also provides information about lab tests needed to track responses or to identify adverse reactions to the drug or about known interactions with other drugs, foods or ingredients. Adverse Reactions An adverse reaction is an undesirable effect that may be associated with use of a drug. Causes of adverse reactions can include medication errors, such as overdosage, or interactions between different drugs or between drugs and certain foods. This section of the PI lists the adverse reactions that occur with the drug and with other similar or related drugs, if applicable. Drug Abuse and Dependence Here you will find information if the drug is considered to have potential for abuse, dependence or withdrawal. Examples of drugs that may fall into this category are amphetamines and certain pain relievers. Overdosage This section describes the signs, symptoms and laboratory findings associated with an overdosage of the drug, as well as complications that can occur with it. Back to Top Dosage and Administration This section states the usual recommended dose, the usual dosage range and, if appropriate, an upper limit beyond which safety and effectiveness have not been established. Also included in this section is information about the recommended timing between doses, the usual duration of treatment and any modification of dosage needed for special patient populations such as children or people with particular diseases. How Supplied The How Supplied section has information on the dosage forms in which the medication is available. This information generally includes: Strength of the dosage forms, such as 10-milligram tablets Units in which the dosage form is usually available for prescribers (for example, bottles of 100) Information such as shape and color to help identify the dosage forms Special handling and storage conditions Additional Sections The labeling may also contain these additional section headings if appropriate and in compliance with federal regulations: Animal pharmacology. In most cases, the labeling does not need to include this section. Significant animal data necessary for safe and effective use of the drug in humans will usually be included in one or more of the other sections of the labeling. Clinical studies or references. A reference to an important clinical study may appear in any section of the label. 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