Brand Name

Veltassa

Generic Name
Patiromer
View Brand Information
FDA approval date: October 23, 2015
Classification: Potassium Binder
Form: Powder

What is Veltassa (Patiromer)?

When the heart, kidneys, or certain medications cause potassium levels in the blood to rise too high, the result known as hyperkalemia can be dangerous and even life-threatening. Many patients living with chronic kidney disease or heart failure face this problem, often without warning. Veltassa (patiromer) helps bring potassium back into balance, allowing people to continue vital treatments safely and reduce the risk of serious complications. 

Veltassa is an oral potassium binder approved by the U.S. Food and Drug Administration (FDA) for the treatment of hyperkalemia in adults. It is not a new fad drug; it’s a well-established, scientifically proven therapy that plays a critical role in maintaining healthy potassium levels. Unlike emergency treatments that act quickly to remove potassium in life-threatening cases, Veltassa works more gradually, helping manage potassium levels over time. This allows many patients with chronic kidney or heart conditions to stay on essential medications that might otherwise raise potassium levels. 

What does Veltassa do? 

Veltassa is used to lower high potassium levels (hyperkalemia) in the blood. Potassium is essential for normal muscle and nerve function, including maintaining a steady heartbeat. However, when potassium levels rise too high, it can cause irregular heart rhythms, muscle weakness, and even cardiac arrest. 

People with chronic kidney disease (CKD) or heart failure are particularly at risk because their bodies have trouble removing excess potassium. Additionally, common medications such as ACE inhibitors, ARBs, and certain diuretics, all vital for heart and kidney protection, can increase potassium levels as a side effect. 

By controlling potassium safely, Veltassa helps patients stay on these life-saving therapies without interruption. Clinical studies have shown that Veltassa effectively lowers potassium within a few days and maintains safe levels with ongoing use (NIH, 2024). Patients often experience greater stability and fewer emergency hospital visits for dangerously high potassium levels. 

How does Veltassa work? 

Veltassa’s active ingredient, patiromer, is a non-absorbed polymer that works inside the digestive tract rather than in the bloodstream. It binds to excess potassium ions in the colon and traps them, preventing the body from absorbing them into the blood. The bound potassium is then removed naturally through the stool. 

This process helps gently and steadily lower potassium levels without causing abrupt changes. Because patiromer is not absorbed into the bloodstream, it has minimal systemic side effects and can be safely used in patients with chronic conditions. 

Clinically, this mechanism matters because controlling potassium allows the heart to beat normally and prevents dangerous arrhythmias. It also helps patients continue medications like ACE inhibitors or mineralocorticoid receptor antagonists, which are essential for managing heart failure and kidney disease but can otherwise increase potassium levels. 

Veltassa side effects 

Veltassa is generally well tolerated, but some people may experience side effects, most of which are mild and manageable. 

Common side effects include: 

  • Constipation or mild stomach discomfort 
     
  • Diarrhea or flatulence 
     
  • Nausea or bloating 
     
  • Low magnesium levels (hypomagnesemia) 

Serious but rare side effects include: 

  • Severe constipation or intestinal blockage 
     
  • Signs of low magnesium, such as muscle cramps, fatigue, or irregular heartbeat 
     
  • Allergic reactions (rash, itching, swelling, or breathing difficulty) 

Patients should inform their healthcare provider if they experience persistent digestive symptoms or signs of electrolyte imbalance. Because Veltassa binds potassium in the gut, it can also bind other medications, reducing their effectiveness. To prevent this, doctors usually recommend taking other oral medications at least three hours before or after Veltassa. 

Who should avoid Veltassa: 
It should not be used by patients with severe bowel obstruction or those who have had major bowel surgery that affects digestion. People with known hypersensitivity to patiromer should also avoid it. 

Overall, Veltassa’s safety record is strong, and with appropriate monitoring, side effects are uncommon and typically mild. 

Veltassa dosage 

Veltassa, a powder, is taken orally mixed with water, never dry or heated. Dosage varies based on potassium levels and treatment goals, adjusted by a doctor. It works in the gut, taking hours to days for desired potassium levels, so it’s not for emergency hyperkalemia. 

During treatment, doctors may monitor: 

  • Serum potassium and magnesium levels 
     
  • Kidney function tests 
     
  • Response to concurrent medications (especially those affecting potassium levels) 

For older adults and patients with kidney disease, no dose adjustment is typically needed, but close monitoring helps ensure safe and effective treatment. Patients should also stay hydrated and maintain a consistent diet unless advised otherwise by their doctor. 

Does Veltassa have a generic version? 

As of 2025, Veltassa (patiromer) does not have a generic equivalent approved in the United States. It is available only as the brand-name product manufactured by Vifor Pharma and Relypsa, Inc. However, international versions may exist in other markets. 

Generic patiromer is being developed and may be available after patent expiration, meeting FDA standards. Until then, patients can explore insurance, savings programs, or alternatives like Lokelma for cost or access issues. 

Conclusion 

Veltassa offers a safe, effective, and well-tolerated solution for managing high potassium levels, especially in patients with chronic kidney disease or heart failure. By binding excess potassium in the gut, it helps prevent dangerous complications while allowing patients to remain on vital heart and kidney medications. 

Veltassa gradually improves stability and reduces hospitalizations with regular use. Essential for patients to communicate with their healthcare provider, follow dosing, complete lab tests, and report symptoms. Proper use helps maintain long-term balance, safety, and peace of mind. 

References 

  1. U.S. Food and Drug Administration (FDA). (2024). Veltassa (patiromer) prescribing information. Retrieved from https://www.accessdata.fda.gov 
     
  1. Mayo Clinic. (2024). Patiromer (oral route) drug information. Retrieved from https://www.mayoclinic.org 
     
  1. MedlinePlus. (2024). Patiromer: Uses, side effects, and precautions. National Library of Medicine. Retrieved from https://medlineplus.gov 
     
  1. National Institutes of Health (NIH). (2024). Hyperkalemia management and potassium binders. Retrieved from https://www.nih.gov 

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Brand Information

VELTASSA (patiromer)
1INDICATIONS AND USAGE
Veltassa is indicated for the treatment of hyperkalemia in adults and pediatric patients ages 12 years and older.
Limitation of Use: Veltassa should not be used as an emergency treatment for life-threatening hyperkalemia because of its delayed onset of action
2DOSAGE FORMS AND STRENGTHS
Veltassa is an off-white to light-brown powder for oral suspension packaged in single-use packets containing 1 gram, 8.4 grams, 16.8 grams or 25.2 grams patiromer.
3CONTRAINDICATIONS
Veltassa is contraindicated in patients with a history of a hypersensitivity reaction to Veltassa or any of its components
4ADVERSE REACTIONS
The following adverse reaction is discussed in greater detail elsewhere in the label:
  • Hypomagnesemia
5DRUG INTERACTIONS
Veltassa has the potential to bind some oral co-administered medications, which could decrease their gastrointestinal absorption. Binding of Veltassa to other oral medications not listed in Table 3 below could cause decreased gastrointestinal absorption and loss of efficacy when taken close to the time Veltassa is administered. Administer other oral medications at least 3 hours before or 3 hours after Veltassa
5.1Clinically Important Interaction of Veltassa with Other Drugs
The
Binding by Veltassa may reduce the systemic exposure and decrease the clinical efficacy of the co-administered drugs shown in Table 2. The administration of these drugs (and any drugs not listed in Table 3) should be separated by at least 3 hours from Veltassa.
5.2No Observed Clinically Important Interaction of Veltassa with Other Drugs
The binding of the following drugs to patiromer was evaluated
6OVERDOSAGE
Doses of Veltassa in excess of 50.4 grams per day have not been tested. Excessive doses of Veltassa may result in hypokalemia. Restore serum potassium if hypokalemia occurs.
7DESCRIPTION
Veltassa is a powder for suspension in water for oral administration. The active ingredient is patiromer sorbitex calcium which consists of the active moiety, patiromer, a non-absorbed potassium-binding polymer, and a calcium-sorbitol counterion. Each gram of patiromer is equivalent to a nominal amount of 2 grams of patiromer sorbitex calcium.
The chemical name for patiromer sorbitex calcium is cross-linked polymer of calcium 2-fluoroprop-2-enoate with diethenylbenzene and octa-1,7-diene, combination with D-glucitol.
Patiromer sorbitex calcium is an amorphous, free-flowing powder that is composed of individual spherical beads. Patiromer sorbitex calcium is insoluble in solvents such as water, 0.1 M HCl, n-heptane and methanol. The chemical structure of patiromer sorbitex calcium is presented in Figure 1.
Figure 1: Chemical Structure of Patiromer Sorbitex Calcium
Figure 1
Each packet of Veltassa contains 1 gram, 8.4 grams, 16.8 grams or 25.2 grams of patiromer, the active moiety. The inactive ingredient is xanthan gum.
8PRINCIPAL DISPLAY PANEL - 8.4 g Packet Carton
30 packets
Veltassa
For Oral Suspension
www.veltassa.com
Each packet contains 8.4 grams of patiromer.
Rx only
8.4 g
PRINCIPAL DISPLAY PANEL - 8.4 g Packet Carton
9PRINCIPAL DISPLAY PANEL - 16.8 g Packet Carton
30 packets
Veltassa
For Oral Suspension
www.veltassa.com
Each packet contains 16.8 grams of patiromer.
Rx only
16.8 g
PRINCIPAL DISPLAY PANEL - 16.8 g Packet Carton
10PRINCIPAL DISPLAY PANEL - 25.2 g Packet Carton
30 packets
NDC 53436-252-30
Veltassa®
(patiromer)
For Oral Suspension
www.veltassa.com
Each packet contains 25.2 grams of patiromer.
Rx only
25.2 g
PRINCIPAL DISPLAY PANEL - 25.2 g Packet Carton
11PRINCIPAL DISPLAY PANEL - 1 g Packet Carton
60 packets
Veltassa
For Oral Suspension
www.veltassa.com
Each packet contains 1 gram of patiromer.
Rx only
1 g
PRINCIPAL DISPLAY PANEL - 1 g Packet Carton