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TREATMENT · GLUTATHIONE INJECTION · SAFETY

Glutathione Injection Side Effects, Sulfites and Asthma

Glutathione is a molecule your body makes in every cell, and the injected form is, in itself, about as well tolerated as an injectable gets. The safety story is not about glutathione. It is about what it comes in — the preservatives and stabilizers in some preparations, one family of which is a known trigger in people with asthma — and about a manufacturing history that makes the source of the product matter more than usual. This page covers both, and what to tell us before your first injection.

The main page covers what glutathione is for and the state of the evidence.

See if you're eligibleA short, confidential online assessment. Reviewed by a clinician.
Medically reviewed by Benjamin H. Krasne, M.D. September 16, 2026

What glutathione itself does

Very little, adversely. Across the small trials of intravenous, oral and inhaled glutathione, the effects attributed to the molecule are mild and uncommon: transient nausea, abdominal discomfort, a flushed or warm feeling, and — with the injection — the local reactions that accompany any subcutaneous injection: redness, tenderness, a small bruise or lump where the needle went in, resolving on their own and reduced by rotating the place you inject.

Some people report a sulfur-like smell or taste shortly after injection. Glutathione contains sulfur, and this is harmless, if unpleasant.

Glutathione has not been associated with organ toxicity, drug interactions of consequence, or dependence. Long-term safety data do not exist, because long-term trials do not, and the main page says so.

Sulfites: the preservative question

Some injectable glutathione preparations contain sulfites — sodium metabisulfite or similar — as preservatives and antioxidants that keep the glutathione from degrading in the vial. Sulfites are the same preservatives found in wine, dried fruit and some medications, and for most people they are harmless.

For a minority, they are not. Sulfite sensitivity produces reactions ranging from flushing, hives and wheezing to, rarely, anaphylaxis, and it is markedly more common in people with asthma — particularly those whose asthma is severe or steroid-dependent. The FDA requires a sulfite warning on every injectable drug that contains one for exactly this reason. Separately, inhaled glutathione has provoked bronchospasm in people with asthma in small studies, through a mechanism that may involve the sulfur chemistry of the molecule itself rather than a preservative. Both lines of evidence point the same way: asthma is the history that matters.

What this means in practice: we ask about asthma and about any previous reaction to sulfites — including reactions to wine or dried fruit that involved wheezing or hives — before prescribing. A person with asthma is not automatically excluded, but the clinician will want to know how severe it is, whether it is well controlled, and whether a sulfite-free preparation is available and appropriate. Your clinician can tell you whether the specific product dispensed contains a sulfite; it is on the label and in the pharmacy's documentation, and asking is reasonable.

Why the source matters

Injectable glutathione has a manufacturing history worth knowing about. In 2019 the FDA warned about a batch of glutathione powder distributed to compounding pharmacies that contained high levels of endotoxin — a bacterial by-product that causes fever, chills, nausea and low blood pressure when injected — after several patients became ill. Glutathione is not an FDA-approved drug, so every injectable preparation is compounded, and the quality of what is in the vial is the pharmacy's responsibility rather than a manufacturer's under FDA license.

That is not a reason to avoid it. It is a reason to use a state-licensed pharmacy that tests its products and to know where yours came from — which is the same rule as every compounded product on this site. Your clinician will tell you which pharmacy dispenses your prescription, that it is licensed in your state, and how to obtain the batch documentation for your lot.

What to stop for

A same-day message to your clinician for any of these, and a stop until you have spoken: wheezing, chest tightness or shortness of breath after an injection; hives or a rash spreading beyond the site of the injection; fever or chills within hours of an injection, which may indicate a contaminated product and must be reported; or a reaction at the site that is hot, spreading and increasingly painful over a day or more.

Swelling of the lips, face or throat, or difficulty breathing, is an emergency — call 911 first and tell us afterwards. If you have asthma and carry a rescue inhaler, keep it with you for the first few injections.

What we ask before prescribing

Asthma — how severe, how controlled, what you take for it. Any previous reaction to sulfites, or to any injection. Any history of anaphylaxis to anything. Pregnancy or breastfeeding, for which there is no safety data. And the full medication and supplement list, because although glutathione has no known interactions of consequence, the absence of evidence is not the same as evidence of absence, and we would rather know.

Questions

Frequently asked questions

  • From glutathione itself: mild and uncommon — transient nausea, flushing, a sulfur smell, and local reactions where the needle went in. The more significant risks come from sulfite preservatives in some preparations and from product quality.

  • Sulfite preservatives in some preparations can trigger wheezing or bronchospasm in sulfite-sensitive people, who are disproportionately asthmatic; inhaled glutathione has caused bronchospasm in asthmatics in studies. Tell us if you have asthma.

  • Some preparations do, as preservatives. Your clinician can tell you whether the product dispensed to you contains one; it is on the label and in the pharmacy documentation.

  • The molecule is well tolerated. The safety questions are the preservative, for sulfite-sensitive people, and the quality of the compounded product, which is why the source matters and why we use a licensed, testing pharmacy.

  • In 2019 the FDA warned about glutathione powder contaminated with endotoxin that made patients ill after injection. It is a reason to know where your product comes from, not a reason to avoid glutathione from a reputable pharmacy.

  • Anyone with a previous sulfite reaction, unless a sulfite-free preparation is confirmed; anyone pregnant or breastfeeding; and people with severe or poorly controlled asthma need a specific clinical decision.

Your next step

Where this fits in your plan

The Glutathione Injection page covers the treatment; this page is what to tell us before it. Asthma and sulfite history are on the assessment for the reasons above.

We measure first. Then we act.

References

  1. FDA. Sulfites in drugs — 21 CFR 201.22, warning statement requirements for prescription drugs containing sulfites.
  2. Vally H, Misso NLA, Madan V. Clinical effects of sulfite additives. Clinical & Experimental Allergy 2009;39:1643–1651.
  3. Marrades RM et al. Nebulized glutathione induces bronchoconstriction in patients with mild asthma. American Journal of Respiratory and Critical Care Medicine 1997;156:425–430.
  4. FDA. Alert concerning glutathione for injection from a bulk-ingredient supplier associated with adverse events (2019).
  5. Richie JP et al. Randomized controlled trial of oral glutathione supplementation on body stores of glutathione. European Journal of Nutrition 2015;54:251–263 — tolerability.
  6. Allen J, Bradley RD. Effects of oral glutathione supplementation on systemic oxidative stress biomarkers in human volunteers. Journal of Alternative and Complementary Medicine 2011;17:827–833.

How we write and review our content

ACT 2 Health provides clinician-led care. Treatments are available only to eligible patients following clinical evaluation and within applicable regulations. This content is educational and is not medical advice. Individual results vary.

Compounded medication. Prepared by a licensed compounding pharmacy under a prescription written for you. Compounded medications are not FDA-approved, are not reviewed by the FDA for safety or effectiveness, and are not equivalent to or interchangeable with any branded product. Prescribed only when a licensed provider determines it is medically appropriate.

Care is delivered via telemedicine by healthcare professionals licensed in the state where the patient is located. Services are available only in states where our providers are licensed.

If you have difficulty breathing or swelling of the face or throat after an injection, call 911.

We measure first. Then we act.

Start with a baseline. Then decide about glutathione injection.