NAD+ Intake Form Template

NAD+ (Nicotinamide Adenine Dinucleotide) is a critical coenzyme involved in cellular energy production, DNA repair, and sirtuin activation. It is administered via IV infusion, IM injection, or subcutaneous injection through compounding pharmacies for chronic fatigue, cognitive decline, anti-aging, and addiction recovery support. This intake form documents energy and cognitive symptoms and screens for contraindications including allergy and cancer history.

4 sections
17 fields
HIPAA-ready
2 citations

Free Template

NAD+ Intake Form

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Your Practice Name

NAD+ Intake Form

Preview
1

General Patient Information

Please provide your personal information.

First Name

Jane

Last Name

Smith

Date of Birth

Can you confirm you are 18 years or older?

Height

e.g. 5'8"

Weight

e.g. 170 lbs

2

Medical History

Please answer all questions as accurately as possible. Your provider will review this information.

Are you actively taking any medications? If so, please list them.

List all current medications, dosages, and frequencies

Do you have any medication allergies? If so, please list them.

List all known drug allergies and reactions

Are you currently being treated or have you been treated for any medical conditions? If so, please list them.

List all current and past medical conditions

Have you had any past surgeries? If so, please list them.

List all surgeries and approximate dates

What is/was your sex assigned at birth?

Male

Emergency contact name and phone number

Name — (555) 000-0000

Mailing address

123 Main St, City, State, ZIP

Any other questions or concerns?

Optional — share anything else you'd like your provider to know

3

Symptoms

Select all symptoms that currently apply to you.

Which of the following symptoms are you experiencing?
4

Contraindications

Select all conditions that currently apply to you.

Do any of the following apply to you?

Preview only. Your live form will include your branding and e-signature capture.

Submit

Compliance & Regulatory Notes

Review these notes before deploying this form in your practice.

NAD+ for IV/IM use must be compounded by a licensed 503A or 503B pharmacy. Verify pharmacy licensure and purity documentation. See FDA: https://www.fda.gov/drugs/human-drug-compounding

IV NAD+ infusions can cause transient side effects including flushing, nausea, and chest tightness. Patients should be monitored during infusion.

Due to NAD+ role in cellular metabolism and sirtuin activation, use in active cancer patients requires specialist evaluation. See FSMB: https://www.fsmb.org

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  • Automated refill management
  • E-signatures and HIPAA audit trail
  • 50-state provider network included
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Sources & References

  1. FDA Human Drug Compounding Guidance
  2. NIH - NAD+ Metabolism and Aging

Frequently Asked Questions

What are the benefits of IV NAD+ therapy?

IV NAD+ delivers the coenzyme directly into the bloodstream, bypassing GI absorption limitations. It is used for energy restoration, cognitive clarity, cellular repair support, and addiction recovery protocols.

Is NAD+ therapy FDA-approved?

NAD+ is not FDA-approved for the clinical indications listed above. It is compounded and administered off-label. Patients must provide informed consent acknowledging the investigational nature of the therapy.