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Run: Naloxone Distribution and Training Tracking Log

Track every naloxone distribution event, training session, and inventory handoff in one log. Use it to document who was trained, what was dispensed, and what...

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Event and Site Identification

Date on which naloxone was dispensed or training was delivered.
Name of the facility, community site, or event where distribution occurred (e.g., 'Main Street Harm Reduction Center', 'Eastside Fire Station 4').
Classify the setting where distribution took place.
Full name and role of the person conducting the distribution and/or training (e.g., 'Jane Smith, RN – Program Coordinator'). Do not record SSNs or personal IDs here.
Confirm the distributing staff member holds current naloxone administration and overdose response training. Reference: BOP Naloxone Procedures and Protocol (PS 1610.002).

Naloxone Kit Inventory and Dispensing Record

Select the formulation(s) distributed at this event.
Enter the total number of individual naloxone kits (not doses) dispensed at this event. Each kit typically contains 2 doses.
Record all lot numbers for naloxone units dispensed. Required for recall tracking and inventory reconciliation.
Confirm all units dispensed have a valid expiration date at least 3 months from today. Expired product must not be distributed.
Confirm kits include required ancillary items per program protocol.
Record the on-hand kit count after this distribution event for inventory reconciliation.
Indicate whether current on-hand inventory has dropped to or below the program-defined reorder threshold.

Training Delivery Record

Indicate whether structured training (overdose recognition, rescue breathing, naloxone administration, 911 activation) was provided.
Select the primary training delivery method.
Approximate length of the training session delivered.
Select all topics addressed during training.
Total count of persons who received training (may differ from kits dispensed if bystanders or family members trained without receiving a kit).
Confirm whether participants performed a return demonstration of naloxone administration (best practice per CDC evaluation guidance).
Select all languages in which written or verbal training materials were provided.

Recipient Demographics (Aggregate — Where Required by Funder)

IMPORTANT: Enter aggregate (group-level) counts only. Do not enter individual names, dates of birth, Social Security numbers, or other PII. If your program uses individual-level tracking, record that data in your program's secure case management system, not here.
Total number of unique individuals who received at least one naloxone kit.
Select all recipient categories present at this event. Provide counts in the comments field.
Count of individuals receiving a naloxone kit for the first time from your program. Used to measure program reach.
Number of overdose reversals reported by returning recipients since the prior distribution event. Used for program outcome tracking per CDC evaluation guidance.
Count of previously dispensed kits returned as used (naloxone administered) and exchanged for new kits.
Number of individuals referred to substance use treatment, harm reduction services, or other support resources at this event.

Storage, Cold Chain, and Handling Compliance

Record the ambient or refrigerated storage temperature where naloxone was held prior to distribution. Most formulations require storage between 59°F and 77°F (15°C–25°C); verify against manufacturer labeling.
Confirm storage location protects product from light and humidity degradation.
If naloxone was transported to a mobile or off-site distribution event, confirm temperature was maintained within acceptable range during transport. Select N/A if distribution occurred at a fixed site.
Confirm that naloxone inventory is locked or secured when not actively being dispensed, per program security protocol.

Documentation, Reporting, and Sign-Off

Enter the next reporting deadline for which this event data will be submitted.
Confirm that individual-level or aggregate data has been entered into your program's secure data system (e.g., REDCap, PDMP, or funder-specified platform) as required.
Indicate whether any adverse events (e.g., allergic reaction, kit malfunction, security incident) occurred during this distribution event that require incident reporting.
If an adverse event or incident occurred, describe it here. Include date, nature of event, individuals involved (by role only, no PII), and immediate actions taken.
Record any additional observations, barriers encountered, community feedback, or program improvement notes from this distribution event.
Confirm a supervisor or program manager has reviewed this log entry for accuracy and completeness before submission.
Distributing staff member or volunteer signature attesting to the accuracy of this log entry.

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