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Electrolyte Supplement (Potassium)/Discontinued

MICRO-K LS

MICRO-K LS

Clinical safety rating

caution

Comprehensive clinical and safety monograph for MICRO-K LS (MICRO-K LS).


Mechanism of Action

Potassium supplement; replaces intracellular potassium, essential for nerve conduction, muscle contraction, and acid-base balance.

What the body does with it

MetabolismNot metabolized; excreted primarily via kidneys.
ExcretionRenal: ~90% as KCl (proportional to intake). Biliary/fecal: <10%.
Half-lifeNot applicable (K+ is an electrolyte, not eliminated by first-order kinetics). Clinical context: Serum K+ decline follows redistribution and excretion with a half-life of ~2-4 hours after IV bolus.
Protein bindingNone (K+ is free ion).
Volume of Distribution0.35 L/kg (approximate total body water; distributes primarily in extracellular fluid).
BioavailabilityOral: ~80-100% for microencapsulated KCl (MICRO-K), but can be incomplete due to slower release.
Onset of ActionOral: 30-60 minutes for serum K+ increase. IV: Immediate.
Duration of ActionOral: Maintains K+ levels for 6-12 hours (dose-dependent). IV: Effect sustained only during infusion.
Molecular Weight74.55

Classification & Brands

Dosing & administration

10-20 mEq (as potassium chloride) orally twice daily; maximum 100 mEq/day.

Dosage formFOR SUSPENSION, EXTENDED RELEASE
Renal impairmentGFR 50-90 mL/min: no adjustment. GFR 30-49 mL/min: reduce dose by 25-50%. GFR <30 mL/min: avoid use or reduce dose by 50-75% with close monitoring.
Liver impairmentChild-Pugh A: no adjustment. Child-Pugh B: reduce dose by 25-50%. Child-Pugh C: avoid use or reduce dose by 50%.
Pediatric use1-3 mEq/kg/day orally in 2-4 divided doses; maximum 1 mEq/kg per dose and 100 mEq/day.
Geriatric useInitiate at lower end of dosing range (10-20 mEq/day); monitor renal function and serum potassium frequently; adjust based on renal function.

Use during pregnancy

1st trimesterPotassium chloride is generally avoided in the first trimester unless necessary for maternal benefit, as hypokalemia can be harmful. There are no well-controlled studies, but no significant teratogenicity has been reported.
2nd trimesterUse with caution during the second trimester. Potassium supplementation should be based on maternal need, with monitoring of serum potassium levels.
3rd trimesterUse with caution during the third trimester. Hypokalemia may be associated with adverse pregnancy outcomes; however, excessive potassium can cause maternal hyperkalemia, which may affect the fetus. Close monitoring is required.

Clinical note

Comprehensive clinical and safety monograph for MICRO-K LS (MICRO-K LS).

Placental transferPotassium readily crosses the placenta. Fetal serum potassium levels are approximately 0.5 mEq/L higher than maternal levels due to active transport.
BreastfeedingPotassium chloride passes into breast milk in small amounts. It is considered compatible with breastfeeding as it is a normal milk component; however, the potential for infant electrolyte imbalance should be considered, especially with high maternal doses.
Lactation RatingL1 (Compatible)
Teratogenic RiskMICRO-K LS (potassium chloride) is not associated with teratogenicity. No fetal risks have been reported in any trimester. Use during pregnancy is considered safe when indicated.
Fetal MonitoringMonitor serum potassium levels periodically, especially in renal impairment or concomitant medications affecting potassium. No specific fetal monitoring required.
Fertility EffectsNo known effects on fertility. Potassium chloride is a normal electrolyte; therapeutic use does not impair reproductive function.

Warnings & precautions

■ FDA Black Box Warning

No black box warning.

Side Effect Profile

Serious Effects

Absolute Contraindications

Hyperkalemia (serum potassium >5.5 mEq/L)Severe renal impairment (creatinine clearance <30 mL/min)Untreated Addison's diseaseAcute dehydrationExtensive tissue breakdown (e.g., severe burns, crush injuries)

Clinical Precautions

PrecautionsRisk of hyperkalemia especially in renal impairment, Use with caution in cardiac disease, GI irritation or ulceration with oral forms, Slow release formulations may cause GI lesions
Food/DietaryAvoid excessive intake of potassium-rich foods (e.g., bananas, oranges, potatoes, spinach, avocados, dried fruits, salt substitutes containing potassium chloride). Do not take with alcohol as it may increase GI irritation. Grapefruit juice has no significant interaction, but large amounts of any food high in potassium should be avoided.

Clinical Tips & Counseling

Clinical PearlsMICRO-K LS contains potassium chloride microencapsulated granules for sustained release. Avoid in patients with severe renal impairment (CrCl <30 mL/min), untreated Addison's disease, or hyperkalemia. Use with caution in patients with cardiac disease or concurrent use of ACE inhibitors, ARBs, or potassium-sparing diuretics. Do not crush or chew capsules; administer with a full glass of water to prevent GI mucosal damage. Monitor serum potassium regularly, especially in elderly and diabetic patients.
Patient AdviceTake this medication exactly as prescribed, preferably with meals or a full glass of water. · Do not crush, chew, or break the capsules; swallow them whole. · Avoid foods high in potassium (e.g., bananas, oranges, tomatoes, salt substitutes) unless directed by your doctor. · Contact your doctor immediately if you experience muscle weakness, irregular heartbeat, numbness/tingling, or dark/tarry stools. · Store at room temperature away from moisture and heat.

MICRO-K LS Interactions

Loading safety data…

This overview is compiled from peer-reviewed clinical sources and FDA labeling. It's here to support — not replace — clinical judgment. Always verify dosing against your institution's current protocols before prescribing.

On this page

Mechanism of ActionDosing & administrationUse during pregnancyWarnings & precautionsDrug interactions

Compare with

KAON CLKAON CL-10MICRO-KMICRO-K 10

External sources

DailyMed (NIH) PubMed OpenFDA