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VELTASSA is the #1 covered branded K+ binder1*

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VELTASSA is covered for 97% of Medicare lives

  • No prior authorization needed for 93% of Medicare lives with VELTASSA
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Eligible commercially insured patients may pay as little as $0 for VELTASSA per month for up to 12 months.

  • Instant savings at the pharmacy
  • Most patients will not need a co-pay card or a printed coupon
  • Patients should ask their pharmacy about co-pay assistance
  • Patient registration is not required
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Overall commercial coverage for VELTASSA is 90%

VELTASSA Konnect is here to provide patient assistance

Formulary Status
Medicare Part D PlansStatus
HumanaPreferred - Exclusive
Prime TherapeuticsPreferred - Exclusive
Aetna Medicare AdvantagePreferred - Exclusive
CVS SilverScriptPreferred - Lowest branded co-pay
WellCarePreferred - Lowest branded co-pay
ESIPreferred - Lowest branded co-pay
UnitedHealth GroupCovered
AnthemCovered
CignaCovered
Commercial PlansStatus
CVS Caremark (Aetna)Preferred
Express Scripts National Preferred FormularyPreferred
CignaPreferred
Prime TherapeuticsPreferred
UnitedHealth GroupCovered
OptumRXCovered
Government Plans
Department of Veterans AffairsNational formulary
Tricare - Department of DefenseOn formulary

As of January 2024 and may be subject to change.

Program is for commercially insured patients. Patients enrolled in a government health insurance program such as Medicare Part D, Medicaid, TRICARE, or Veterans Health Administration are not eligible; this is not an exhaustive list of excluded government health plans. Patients may pay as low as $0 for up to 12 months; after that, renewal is required. The patient is responsible for applicable taxes. Annual maximum limits apply. Co-pay program is not insurance. No party may seek reimbursement for any part of the co-pay benefit received under the program. See full Terms and Conditions below.

Source: Source Health Analytics PTD Dispensed Claims (Data as of January 1, 2024).

Please note that plans may have multiple formularies, and they are subject to change by individual plans. Please confirm formulary status, requirements, and coverage information for individual patients directly with the health plan providers.

Co-pay Terms and Conditions

By participating in Vifor Pharma, Inc.’s Co-pay Savings Program (“Co-pay Program”) for VELTASSA, the patient acknowledges that, at the time of usage, they meet the eligibility criteria and comply with the following terms and conditions.

The Co-pay Program is for commercially insured patients. Patients with prescription coverage through any type of federal or state government-funded program are not eligible (e.g., Medicare, Medicaid, TRICARE, Veterans Administration [VA], Mi Salud).

The patient may pay as low as $0 per month for up to a 12-month period, and afterward renewal is required. Annual maximum limits may apply. The Co-pay Program for VELTASSA is not insurance. Vifor Pharma, Inc. reserves the right to rescind, revoke, or amend this program without notice. The patient must use the Co-pay Program for a valid prescription of VELTASSA, and this cannot be combined with any other coupon, trial, savings card, free drug assistance, or other offer.

Patient must live in the United States (including the District of Columbia, Puerto Rico, and the U.S. Virgin Islands). If the patient is enrolled in Veltassa Konnect, patient is required to promptly inform Veltassa Konnect of any change in insurance status during the course of enrollment.

The patient and participating pharmacy are each obligated to inform the insurance plan of any benefit received under the Co-pay Program as required and may not participate if the Co-pay Program conflicts with the plan’s policy. No party may seek reimbursement for any part of the benefit received by patient under the Co-pay Program. The patient is responsible for applicable taxes. Limit one per person; offer is non-transferable and void where prohibited by law or restricted.

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INDICATION

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.

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INDICATION & Important Safety Information

Important Safety Information

VELTASSA is indicated for the treatment of hyperkalemia.

Limitation of Use: VELTASSA should not be used as an emergency treatment for life-threatening hyperkalemia because of its delayed onset of action.

CONTRAINDICATIONS

VELTASSA is contraindicated in patients with a history of a hypersensitivity reaction to VELTASSA or any of its components.

INDICATION

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.

IMPORTANT SAFETY INFORMATION

CONTRAINDICATIONS

VELTASSA is contraindicated in patients with a history of a hypersensitivity reaction to VELTASSA or any of its components.

WARNINGS AND PRECAUTIONS

Worsening of Gastrointestinal Motility: Avoid use of VELTASSA in patients with severe constipation, bowel obstruction or impaction, including abnormal post-operative bowel motility disorders, because VELTASSA may be ineffective and may worsen gastrointestinal conditions. Patients with a history of bowel obstruction or major gastrointestinal surgery, severe gastrointestinal disorders, or swallowing disorders were not included in clinical studies.

Hypomagnesemia: VELTASSA binds to magnesium in the colon, which can lead to hypomagnesemia. In clinical studies, hypomagnesemia was reported as an adverse reaction in 5.3% of adult patients treated with VELTASSA. Approximately 9% of adult patients in clinical trials developed hypomagnesemia with a serum magnesium value < 1.4 mg/dL. Monitor serum magnesium. Consider magnesium supplementation in patients who develop low serum magnesium levels.

MOST COMMON ADVERSE REACTIONS

The most common adverse reactions (incidence ≥  2%) in adult patients treated with VELTASSA were constipation (7.2%), hypomagnesemia (5.3%), diarrhea (4.8%), nausea (2.3%), abdominal discomfort (2.0%) and flatulence (2.0%). Mild to moderate hypersensitivity reactions were reported in 0.3% of adult patients treated with VELTASSA and included edema of the lips.The safety profile of VELTASSA in a study of 14 pediatric patients ages 12 to 17 years was generally similar to that observed in adult patients.

Reference: 1. Data on file (1/23), CSL Vifor, Inc.