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This technical manual provides detailed information on the functionalities, implementation, and management of the Controlled Substances V. 3.0 module used by the Department of Veterans Affairs for
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How to fill out Controlled Substances V. 3.0 Technical Manual

01
Gather necessary information: Patient details, prescriber information, and medication specifics.
02
Open the Controlled Substances V. 3.0 Technical Manual document.
03
Locate the section relevant to the specific controlled substance being documented.
04
Fill out the required fields accurately, including dosage, frequency, and intended use.
05
Review all entries for accuracy to ensure compliance with regulations.
06
Sign and date the document as required.
07
Submit the completed form to the appropriate authority or keep it in the designated records.

Who needs Controlled Substances V. 3.0 Technical Manual?

01
Healthcare providers who prescribe controlled substances.
02
Pharmacists who dispense controlled substances.
03
Regulatory officials overseeing controlled substance compliance.
04
Researchers working with controlled substances in clinical studies.
05
Administrators in healthcare facilities that manage controlled substance inventories.
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People Also Ask about

Controlled Drugs Schedule I — drugs with a high abuse risk. These drugs have NO safe, accepted medical use in the United States. Schedule II — drugs with a high abuse risk, but also have safe and accepted medical uses in the United States. Schedule III, IV, or V — drugs with an abuse risk less than Schedule II.
Schedule V They result in very limited physical or psychological dependence. Examples include cough medicines with codeine, antidiarrheal medications that contain atropine/diphenoxylate, pregabalin, and ezogabine. Despite their low abuse potential, they still need to be managed appropriately and administered with care.
Schedule V drugs have an accepted medical use and a lower potential for dependence or misuse. They're often prescribed for pain, cough, and diarrhea management. Some examples include: diphenoxylate/atropine (Lomotil, Motofen) guaifenesin/codeine (Robitussin AC)
Schedule V drugs are the least likely of the controlled substances to be misused. They result in very limited physical or psychological dependence. Examples include cough medicines with codeine, antidiarrheal medications that contain atropine/diphenoxylate, pregabalin, and ezogabine.
Schedule V Drugs: Examples include cough preparations with less than 200 milligrams of codeine or per 100 milliliters (Robitussin AC), Lomotil, Motofen, Lyrica, and Parepectolin.
Schedule III drugs, substances, or chemicals are defined as drugs with a moderate to low potential for physical and psychological dependence. Examples of Schedule III drugs are: products containing less than 90 milligrams of codeine per dosage unit (Tylenol with codeine), ketamine, anabolic steroids, testosterone.
Medications classified as Schedule III or IV controlled substances may be refilled up to 5 times in a 6-month period.

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Controlled Substances V. 3.0 Technical Manual is a comprehensive guide that outlines the regulatory framework, procedures, and standards related to the handling, reporting, and management of controlled substances.
Entities or individuals who are authorized to handle, administer, or dispense controlled substances, including healthcare providers, pharmacies, and research institutions, are required to file the Controlled Substances V. 3.0 Technical Manual.
To fill out the Controlled Substances V. 3.0 Technical Manual, follow the instructions provided within the manual, ensuring all required sections are completed accurately, using relevant data and adhering to the submission guidelines.
The purpose of the Controlled Substances V. 3.0 Technical Manual is to provide a standardized approach to the management and reporting of controlled substances to ensure compliance with legal and regulatory requirements.
The information that must be reported includes details on the types of controlled substances handled, quantities, storage conditions, record-keeping practices, and any incidents of diversion or discrepancies.
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