Thiamine (Vitamin B1)
Thiamine (Vitamin B1) is an injectable form of vitamin B1 used to treat or prevent serious thiamine deficiency and its complications.
🧬 Where this information comes from Click to expand
The clinical label records used on this page are FDA-filed Structured Product Labeling (SPL) retrieved through openFDA. We identified 1 clinical label set within the page’s selected clinical scope after exact ingredient or ingredient-combination matching and applicable route/form matching. Forms, routes, brands, labelers, strengths, and NDC product-record counts are built separately from matching FDA National Drug Code Directory records. The linked DailyMed document is a representative official source for verification, not the page’s only clinical source. View the linked label on DailyMed →
Thiamine injection is vitamin B1, which the body needs to burn carbohydrates and clear certain acids, given into a muscle or vein as the standard hospital treatment for dangerous deficiency, including beriberi, Wernicke’s encephalopathy (a serious brain disorder from low B1) and related heart failure. Most people tolerate it well, noticing at most warmth, itching, sweating or a sore muscle injection site. The danger is anaphylaxis, a severe allergic reaction that has been fatal even after earlier uneventful doses, which is why it is given only where emergency care is on hand. The boxed warning adds that its aluminum can reach toxic levels with weak kidneys, especially in premature newborns.
Clinical pearls
- Once the acute phase passes, the doctor often switches to thiamine by mouth or a multivitamin plus a balanced diet.
- If you are on IV sugar (dextrose) fluids and at risk of deficiency, thiamine may be added to prevent depletion.
- Past drug allergies or a prior thiamine reaction call for a skin test first, though a clean result cannot fully rule out anaphylaxis.
- Severe vomiting in pregnancy can cause B1-related nerve problems, and these injections may be used under close medical supervision.
Patient information guide A plain-language walkthrough of Thiamine (Vitamin B<sub>1</sub>), written from its FDA label.
What Thiamine (Vitamin B<sub>1</sub>) is used for
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Thiamine hydrochloride injection is used to rapidly restore vitamin B1 levels when deficiency is severe or oral intake isn't possible. Main conditions it treats include:
- Beriberi — both "dry" beriberi (affecting the nervous system) and "wet" beriberi (affecting the heart and circulation)
- Wernicke's encephalopathy / Wernicke-Korsakoff syndrome — a serious brain disorder caused by thiamine deficiency, often linked to alcohol use or poor nutrition
- Infantile beriberi — thiamine deficiency in infants, including cases with acute collapse
- Neuritis of pregnancy — nerve problems during pregnancy when vomiting prevents adequate oral intake
- Heart failure from thiamine deficiency — cardiovascular disease directly caused by low B1 levels
- Prevention of heart failure in patients receiving IV dextrose — used when patients with borderline thiamine levels are getting glucose through an IV
- Established thiamine deficiency with inability to eat — for patients who cannot take thiamine by mouth due to severe nausea, vomiting, anorexia, or malabsorption
How Thiamine (Vitamin B<sub>1</sub>) works
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Thiamine (vitamin B1) is essential for energy production. Once in the body, it combines with ATP (adenosine triphosphate, the body's main energy molecule) to form thiamine pyrophosphate — the active coenzyme form. This coenzyme is critical for breaking down carbohydrates, specifically for a step called decarboxylation of pyruvic acid and other alpha-keto acids. Without enough thiamine, pyruvic acid builds up in the blood — a key sign of B1 deficiency — and cells, especially in the brain and heart, can't generate energy properly.
Because the body needs more thiamine when carbohydrate intake is higher, people eating a high-carbohydrate diet or receiving IV dextrose are at greater risk of depleting their thiamine stores quickly. The body can become depleted after roughly three weeks without any thiamine intake.
Thiamine (Vitamin B<sub>1</sub>) dosage
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Thiamine hydrochloride injection is given by a healthcare professional — either into a muscle (IM) or into a vein (IV), depending on the condition and its severity. Wet beriberi with heart failure is treated as a cardiac emergency and requires slow IV administration. For other forms of deficiency, IM injections are typically given multiple times a day for a period of weeks.
- IV administration must be done slowly and with caution — rapid IV infusion increases the risk of a severe reaction
- Once the acute phase improves, a doctor may switch to an oral multivitamin with thiamine taken daily for about a month to fully replenish body stores
- Correcting diet — eating a balanced, nutritious diet — is an important part of full recovery
Follow your prescriber's instructions carefully, and do not adjust the dose or schedule on your own.
Dosing details from the FDA-approved label
From the Thiamine (Vitamin B<sub>1</sub>) prescribing information (“Dosage and Administration”). Doses are set by your prescriber for your product, condition, kidney function and age — never change a dose on your own.
In the treatment of beriberi, 10 to 20 mg of thiamine hydrochloride are given IM three times daily for as long as two weeks.
Read the label’s full dosing text
DOSAGE AND ADMINISTRATION: “Wet” beriberi with myocardial failure must be treated as an emergency cardiac condition, and thiamine must be administered slowly by the IV route in this situation (see WARNINGS ). In the treatment of beriberi, 10 to 20 mg of thiamine hydrochloride are given IM three times daily for as long as two weeks. (See WARNINGS regarding repeated injections of thiamine.) An oral therapeutic multivitamin preparation containing 5 to 10 mg thiamine, administered daily for one month, is recommended to achieve body tissue saturation. Infantile beriberi that is mild may respond to oral therapy, but if collapse occurs, doses of 25 mg may cautiously be given IV. Poor dietary habits should be corrected and an abundant and well-balanced dietary intake should be prescribed. Patients with neuritis of pregnancy in whom vomiting is severe enough to preclude adequate oral therapy should receive 5 to 10 mg of thiamine hydrochloride IM daily. In the treatment of Wernicke-Korsakoff syndrome, thiamine hydrochloride has been administered IV in an initial dose of 100 mg, followed by IM doses of 50 to 100 mg daily until the patient is consuming a regular, balanced diet. (See WARNINGS regarding repeated injections of thiamine.) Patients with marginal thiamine status to whom dextrose is being administered should receive 100 mg thiamine hydrochloride in each of the first few liters of IV fluid to avoid precipitating heart failure. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.
Read the full Dosage and Administration section on DailyMed →
Thiamine (Vitamin B<sub>1</sub>) side effects
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Most people tolerate thiamine injections well, but some reactions can occur:
Common side effects
- Feeling of warmth
- Itching (pruritus) or hives (urticaria)
- Sweating
- Nausea
- Weakness
- Restlessness
- Tenderness or firmness at the injection site (with IM use)
- Tenderness or a firm lump at the IM injection site
When to get medical help
- Call 911 or get emergency help immediately if you develop tightness of the throat, swelling of the face or throat (angioneurotic edema), bluish skin color (cyanosis), or difficulty breathing — these are signs of a severe allergic (anaphylactic) reaction
- Seek emergency care for sudden collapse or loss of consciousness after an injection
- Tell your care team right away if you notice signs of fluid in the lungs (pulmonary edema), such as severe shortness of breath
- If you have kidney problems or are a premature infant, alert your care team — aluminum in this product can build up to toxic levels in these situations
Rarely, a severe and potentially fatal allergic reaction (anaphylaxis) can occur — with symptoms like throat tightening, bluish skin (cyanosis), swelling, fluid in the lungs, or collapse. Get emergency help immediately if any of these develop after an injection.
Thiamine (Vitamin B<sub>1</sub>) warnings and precautions
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- Anaphylaxis risk: Serious, life-threatening allergic reactions have been reported — including deaths — especially with repeated injections. Thiamine must always be administered where emergency treatment (epinephrine, oxygen, airway support) is immediately available.
- Allergy testing before injection: If you have a history of drug allergies or have reacted to thiamine before, a small test dose should be given under the skin first and watched for 30 minutes before a full dose is given. Even a negative skin test does not fully rule out a reaction.
- Aluminum toxicity: This product contains aluminum. In patients with kidney problems — especially premature newborns — aluminum can accumulate and cause toxicity affecting the brain and bones.
- Wet beriberi emergency: If beriberi has caused heart failure, this is a cardiac emergency. IV thiamine must be given very slowly and under close medical supervision.
Thiamine (Vitamin B<sub>1</sub>) interactions
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The FDA label for this product does not list specific drug, food, or supplement interactions.
Not a complete list. The label covers the interactions the manufacturer studied or reported, and our own interaction database does not cover every medicine either. Bring your full medication list, including vitamins and herbal products, to your pharmacist.
Before taking Thiamine (Vitamin B<sub>1</sub>)
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- Allergy to thiamine: Do not use this product if you have a known allergy to thiamine or any ingredient in the formulation.
- Kidney problems: Tell your care team if you have impaired kidney function — aluminum in this product can build up and become toxic when the kidneys can't clear it properly.
- Premature newborns: This population is at especially high risk for aluminum toxicity because their kidneys are not yet mature.
- History of drug allergies: Let your doctor know if you've had allergic reactions to medications before — a skin test should be performed first.
- Pregnancy with severe vomiting: If you're pregnant and can't keep food or oral vitamins down, talk to your doctor — injection may be appropriate but requires medical oversight.
Thiamine (Vitamin B<sub>1</sub>) overdose
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Single parenteral (injected) doses given in research have not caused toxic effects. However, the body can only use a limited amount of thiamine at a time — once tissues are saturated, the rest is excreted in the urine. If intake is pushed even higher, thiamine appears unchanged in the urine, meaning the excess simply passes out of the body.
What Thiamine (Vitamin B<sub>1</sub>) does in the body
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Thiamine is essential for carbohydrate metabolism — specifically, it helps break down pyruvic acid and alpha-keto acids in the blood. When thiamine is deficient, pyruvic acid builds up, which can be measured in the blood as a marker of deficiency. The heart and nervous system are particularly sensitive to this buildup, which is why deficiency causes both neurological and cardiovascular problems. Restoring thiamine reverses these metabolic disruptions.
How your body processes Thiamine (Vitamin B<sub>1</sub>)
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Thiamine is a water-soluble vitamin absorbed throughout the body, with the highest concentrations found in the liver, brain, kidneys, and heart. After an IM injection, absorption is rapid and complete. The body stores thiamine up to two to three times normal levels when intake is plentiful, but stores become depleted if intake is insufficient — full depletion can occur in about three weeks without any thiamine. Because it's water-soluble, any excess thiamine is quickly excreted in the urine, first as a breakdown product called pyrimidine and then as unchanged thiamine as levels rise further.
How to store Thiamine (Vitamin B<sub>1</sub>)
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Store at 20° to 25°C (68° to 77° F) . PROTECT FROM LIGHT.
Written from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →
Thiamine (Vitamin B<sub>1</sub>): pharmacist answers to common questions
Quick, plain-English answers to the questions patients ask most about Thiamine (Vitamin B<sub>1</sub>) — the kind of thing our pharmacy team would talk through with you at the counter.
Why am I getting a vitamin B1 shot instead of just taking a pill?
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What should I watch out for after getting the injection?
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Is it possible to get too much thiamine from these injections?
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I've had thiamine shots before without any problems — do I still need to worry about a reaction?
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I have kidney problems. Is this injection safe for me?
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Once I'm feeling better, do I need to keep getting shots?
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Is Thiamine (Vitamin B<sub>1</sub>) available over the counter?
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When was Thiamine (Vitamin B<sub>1</sub>) first available?
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Answers drafted from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →
More about Thiamine (Vitamin B<sub>1</sub>) on HelloPharmacist
Thiamine (Vitamin B<sub>1</sub>) on the U.S. market: products, makers and brands
How Thiamine (Vitamin B<sub>1</sub>) appears in the FDA’s National Drug Code Directory — including its dosage forms, strengths, brand names, manufacturers, and FDA-listed product records. These are directory records, not sales or prescription volume.
The FDA lists Thiamine (Vitamin B<sub>1</sub>) products; the earliest marketing or approval year on record is 1947.
How widely Thiamine (Vitamin B<sub>1</sub>) is used (Medicaid data)
A general measure of how commonly Thiamine (Vitamin B<sub>1</sub>) is prescribed, based on Medicaid — one of the largest public drug programs. The figure below is prescriptions filled in Q1–Q4 2025, summed across every form and brand of the drug.
Think of this as a proxy for how widely Thiamine (Vitamin B<sub>1</sub>) is used, drawn from freely available public data. Medicaid is just one program — these numbers don’t include Medicare, other government coverage, or commercial and cash-pay prescriptions, so real-world use is higher than what’s shown here.
How commonly is Thiamine (Vitamin B<sub>1</sub>) prescribed? Of the 1,601 medications we measure, Thiamine (Vitamin B<sub>1</sub>) ranks #741 by Medicaid prescriptions — more than 54% of them.
Utilization by Thiamine (Vitamin B<sub>1</sub>) product
Pick a product to see its own Medicaid numbers. Each chip is one clinical product — a specific strength & dosage form as defined by RxNorm — with brand-name and generic versions combined.
thiamine hydrochloride 100 MG/ML Injectable Solution
Summed across the 12 of 45 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 313324
Shares are of the Medicaid prescriptions shown here. Product grouping follows RxNorm (the National Library of Medicine’s drug terminology), so “one product” means one strength & dosage form regardless of manufacturer. Dollar figures are gross Medicaid reimbursement before mandatory rebates — rebates (often large, especially for brand-name drugs) are confidential, so actual net cost to Medicaid is lower than shown.
Source: Medicaid State Drug Utilization Data (CMS), aggregated by generic ingredient — summed across every NDC (all brands, strengths, salt forms and dosage forms) of Thiamine (Vitamin B<sub>1</sub>), and across all states and both fee-for-service and managed-care claims. A general popularity signal; it excludes Medicare, commercial insurance and cash prescriptions, so it is not total U.S. use. Based on the 12 of 45 listed Thiamine (Vitamin B<sub>1</sub>) NDCs with Medicaid activity.
Thiamine (Vitamin B<sub>1</sub>) side effects reported to the FDA (FAERS)
After a medicine reaches the market, patients, doctors and drugmakers can send the FDA reports of problems they think may be linked to it. Here’s what’s been reported for Thiamine (Vitamin B<sub>1</sub>) — a signal of what to watch for, not proof the drug caused it.
Source: openFDA, from the FDA Adverse Event Reporting System (FAERS). These are voluntary reports — they don’t prove the drug caused the effect, and counts reflect how often something was reported, not how often it actually happens. Reports also often name the very problem the medicine is taken for — a common reason to file one is that the drug didn’t help — so for a pain reliever you may see “pain” high on the list; that points to why the report was filed, not to the drug causing the symptom. This counts every report that lists Thiamine (Vitamin B<sub>1</sub>) in any role, so the total runs higher than the FDA’s official dashboard, which counts only cases where the drug is the suspect. For the authoritative figures, see the FDA FAERS Public Dashboard. Always talk to your pharmacist or doctor.
Thiamine (Vitamin B<sub>1</sub>) FDA approval history
How Thiamine (Vitamin B<sub>1</sub>) went from FDA review to the pharmacy shelf — the key milestones in its regulatory journey.
Source: Drugs@FDA.
Thiamine (Vitamin B<sub>1</sub>) recall history
A recall is when a specific batch of a medicine is pulled from the market — usually a manufacturing issue, not a problem with the drug itself. Class I is most serious, Class III least.
The FDA’s enforcement reports list no Thiamine recalls since July 2021.
✅No Thiamine recalls on record since July 2021Source: FDA enforcement (recall) reports, via openFDA; our copy was last updated Sep 24, 2026.
RxNorm Concept Web — From Ingredient to Every Form and Strength
This page starts with one exact multiple-ingredient concept (MIN). The branches below show its dose-form concepts (SCDF), then the available clinical drug and strength concepts (SCD). A product with a different ingredient combination belongs on a different page.
RxCUI 10454 3 dose forms · 7 strengths
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Dose form (SCDF) Injectable Solution RxCUI 370492No current FDA listingClinical drug / strength (SCD) hydrochloride 100 MG/MLRxCUI 313324hydrochloride 500 MG/MLRxCUI 2001441 -
Dose form (SCDF) Oral Capsule RxCUI 374091No current FDA listingClinical drug / strength (SCD) 100 MGRxCUI 247886 -
Dose form (SCDF) Oral Tablet RxCUI 374093No current FDA listingClinical drug / strength (SCD) 50 MGRxCUI 150921100 MGRxCUI 313323250 MGRxCUI 313326500 MGRxCUI 212470
Look up RxCUI 10454 in the RxCUI Atlas →
RxNorm is the U.S. National Library of Medicine’s normalized drug vocabulary. Its concept hierarchy can include forms that are not currently marketed; the status on each branch compares that concept with current FDA listings. RxCUIs identify vocabulary concepts, not individual packages or manufacturers.
Thiamine (Vitamin B<sub>1</sub>) supply and shortage status
Whether Thiamine (Vitamin B<sub>1</sub>) is in short supply in the U.S. right now, plus any shortage history the FDA has on record. A shortage usually reflects a manufacturing or demand issue — not a safety problem with the drug.
Source: openFDA, from the FDA Drug Shortages database.
Thiamine (Vitamin B<sub>1</sub>) drug class (RxNorm)
Thiamine (Vitamin B<sub>1</sub>) belongs to the Vitamin B1, plain class.
Classified by RxNorm RxClass — the U.S. National Library of Medicine's standardized drug-classification service (Established Pharmacologic Class from the FDA, the ATC drug family from the WHO, and mechanism of action). Reference only, not medical advice.
Sources for this Thiamine (Vitamin B<sub>1</sub>) page
Core label, product, RxNorm, safety, and utilization data on this page come from the sources identified below. AI-written, editorial, and licensed sections are labeled separately.
How this page is built
HelloPharmacist combines public FDA and NLM records and does not author the underlying clinical facts. The plain-language sections are written with AI from the FDA-approved label text and reviewed by our pharmacy team before publication. Fresenius Kabi USA, LLC is the representative DailyMed label linked for verification and dates. This is general education, not medical advice: always talk to your doctor or pharmacist about your own medicines. How we build and review drug pages →