Urgent recall of blood pressure medications over fear pills can cause irregular heart beat, cardiac arrest
What prompted the recall of blood pressure medications?
The recall of blood pressure medications was prompted by the discovery that certain batches of potassium chloride extended-release capsules may not properly dissolve when ingested by patients. This could potentially lead to high potassium levels in the blood, or hyperkalemia, which can cause an irregular heartbeat and even cardiac arrest. The recall was initiated by Glenmark Pharmaceuticals and American Health Packaging as a precautionary measure.
What potential health risk does the pill's failed dissolution pose?
The failed dissolution of the potassium chloride extended release capsules can cause high potassium levels in the blood, also known as hyperkalemia3. Hyperkalemia may lead to an irregular heartbeat, which can result in cardiac arrest2. Patients using the medication for high blood pressure management and prevention of heart or kidney failure are at risk.
How many batches of Potassium Chloride were recalled?
Glenmark Pharmaceuticals voluntarily recalled 114 batches of Potassium Chloride Extended-Release Capsules, USP (750 mg) 10 mEq K. The recall was due to failed dissolution, which could lead to hyperkalemia and potentially cause irregular heartbeat, cardiac arrest, and other adverse events5.