What are the benefits and side effects of NAD+ (Nicotinamide adenine dinucleotide) drips?

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Last updated: November 9, 2025View editorial policy

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NAD+ Drips: Benefits and Side Effects

NAD+ infusions are not recommended for therapeutic use outside of research protocols, as there are no FDA-approved injectable NAD+ products, no clinical practice guidelines supporting their use for any medical condition, and insufficient evidence of clinical benefit. 1, 2

Current Regulatory and Clinical Status

Injectable NAD+ lacks any guideline support or regulatory approval:

  • No FDA-approved injectable NAD+ products exist for clinical use in the United States 2
  • Injectable NAD+ is not found in any current clinical practice guidelines for treatment of any condition 2
  • The American Academy of Physical Medicine and Rehabilitation does not recommend NAD patches due to lack of clinical evidence 1
  • FDA labeling for intravenous NAD lists only cosmetic uses, not therapeutic medical indications 1

Claimed Benefits (Lacking Clinical Evidence)

While NAD+ plays essential roles in cellular function, the evidence for benefits from IV administration is absent:

  • NAD+ is involved in over 400 enzymatic reactions including energy metabolism, DNA repair, gene expression, and stress responses 2, 3
  • Oral NAD+ precursors (nicotinamide riboside) have shown some promise in raising NAD+ levels and potentially reducing blood pressure and arterial stiffness in middle-aged and older adults 4
  • Oral NADH supplementation has been associated with improvements in quality of life, decreased anxiety, and reduced maximum heart rate in some studies 5
  • However, these benefits are from oral precursors, not IV NAD+, and the pharmacokinetics of IV administration remain unknown 2

Side Effects and Safety Concerns

Injectable NAD+ carries significant risks without proven benefit:

Immediate Risks of IV Administration

  • Infection risk from improper sterile technique 2
  • Potential for hypersensitivity reactions 2
  • Unknown pharmacokinetics when administered parenterally 2
  • No standardized dosing protocols exist 2

Known Side Effects from NAD+ Precursors

  • High doses of nicotinic acid can cause flushing, nausea, vomiting, liver toxicity, blurred vision, and impaired glucose tolerance 1
  • Common side effects associated with NAD supplementation include muscle pain, nervous disorders, fatigue, sleep disturbance, and headaches 5
  • Patch delivery systems may cause local skin reactions 1

Theoretical Long-Term Risks

  • Accumulation of potentially toxic metabolites 6
  • Possible tumorigenesis concerns 6
  • Potential promotion of cellular senescence 6
  • NAD(P)H oxidase activity has been implicated in anthracycline-induced cardiotoxicity, raising concerns about NAD supplementation in certain contexts 7

Evidence-Based Alternative Approach

For patients seeking NAD+ benefits, recommend the following algorithm:

First-Line: Dietary Sources

  • Recommend dietary sources of niacin including meat, poultry, fish (especially red fish like tuna and salmon), nuts, legumes, and fortified packaged foods 1, 3
  • Adult males require 16 mg/day and adult females 14 mg/day of niacin 3

Second-Line: Oral Supplementation (If Deficiency Suspected)

  • Measure blood or tissue NAD+ levels if pellagra symptoms present (diarrhea, dermatitis, dementia) 1
  • If deficiency confirmed, use oral nicotinic acid (15-20 mg/day) or nicotinamide (300 mg/day) 1
  • The upper limit for nicotinamide is approximately 900 mg/day for adults 2, 3
  • The upper limit for free nicotinic acid is only 10 mg/day due to flushing effects 1, 3

For Parenteral Nutrition (Only When GI Tract Non-Functional)

  • Parenteral nutrition should provide at least 40 mg of niacin per day 1, 3
  • The oral/enteral route should be used whenever the gastrointestinal tract is functional 1

Critical Clinical Pitfall

The most important caveat is that injectable NAD+ administration falls outside standard medical practice and bypasses normal protective barriers. 2 Despite marketing claims, there is no high-quality evidence supporting therapeutic benefits of IV NAD+, and the practice carries unnecessary risks. Oral NAD+ precursors (nicotinamide riboside, nicotinamide mononucleotide) are better studied, safer, and represent the only evidence-based approach to augmenting NAD+ levels. 4, 5, 8

References

Guideline

NAD Infusion in Humans: Current Evidence

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

NAD+ Injectable Administration: Safety and Regulatory Status

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

NAD+ Supplementation Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Evaluation of safety and effectiveness of NAD in different clinical conditions: a systematic review.

American journal of physiology. Endocrinology and metabolism, 2024

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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