BIBLIOGRAPHY

Retrospective biostatistical analysis data for establishing safety in the context of monotherapy involving life saving drugs. This Bibliography reveals how the reference paving the way for producing/ writing, an research article, successfully.

SOP of monotherapeutic drugs (Life saving drugs) was well explained in a table column in the article that are lying behind this Bibliography.  It is useful for calculating volume distribution of drugs ingested. 

A Standard Operating Procedure (SOP) for monotherapeutic drugs, especially life-saving drugs, is a detailed, written instruction that outlines the steps to be taken in the handling, storage, preparation, and administration of these medications.

Purpose
The purpose of this SOP is to ensure the safe and effective handling, storage, preparation, and administration of monotherapeutic drugs, especially life-saving drugs.

Scope
This SOP applies to all healthcare professionals involved in the handling, storage, preparation, and administration of monotherapeutic drugs, especially life-saving drugs.

Responsibilities
*Pharmacists: Responsible for ensuring the accuracy and completeness of medication orders, preparing and labeling medications, and providing medication information to healthcare professionals.
*Nurses: Responsible for administering medications to patients, monitoring patients for medication side effects, and reporting any medication errors or concerns.
*Physicians: Responsible for ordering medications, monitoring patient response to medications, and adjusting medication orders as necessary.

Procedure
Handling and Storage:
*Receive and inspect medications*: Verify the accuracy of medication orders, inspect medications for damage or expiration, and store medications in a secure, climate-controlled area.
*Store medications: Store medications in accordance with manufacturer instructions and hospital policy.
*Monitor medication expiration dates: Regularly check medication expiration dates and remove expired medications from stock.

Preparation
*Prepare medications: Prepare medications in accordance with hospital policy and manufacturer instructions.
*Label medications: Label medications with the patient's name, medication name, dose, and administration time.
*Verify medication preparation: Verify the accuracy of medication preparation, including the medication name, dose, and administration time.

Administration
*Administer medications: Administer medications to patients in accordance with hospital policy and manufacturer instructions.
*Monitor patients for medication side effects: Monitor patients for medication side effects and report any concerns to the physician.
*Document medication administration: Document medication administration, including the medication name, dose, and administration time.

Monitoring and Reporting
*Monitor medication errors: Monitor medication errors, including near misses and adverse events.
*Report medication errors: Report medication errors to the physician and hospital administration.
*Review and revise the SOP: Regularly review and revise the SOP to ensure compliance with hospital policy and manufacturer instructions.

Quality Control
*Regularly review medication orders: Regularly review medication orders to ensure accuracy and completeness.
*Conduct regular inventory checks: Conduct regular inventory checks to ensure medications are stored properly and are not expired.
*Monitor medication administration: Monitor medication administration to ensure medications are administered correctly and in a timely manner.

Training and Competency
*Provide training on the SOP: Provide training on the SOP to all healthcare professionals involved in the handling, storage, preparation, and administration of monotherapeutic drugs.
*Assess competency: Assess competency of healthcare professionals in the handling, storage, preparation, and administration of monotherapeutic drugs.
*Provide ongoing education: Provide ongoing education and training to healthcare professionals on the safe handling, storage, preparation, and administration of monotherapeutic drugs.

Revision History
Version 1.0: Initial document creation
Version 1.1: Revised to include additional quality control measures
Version 1.2: Revised to include additional training and competency requirements