Drug Facts
Composition & Profile
Identifiers & Packaging
HOW SUPPLIED Potassium Chloride Injection in flexible plastic containers is available as follows: NDC No. Potassium per container 0409–7074–26 10 mEq/100 mL 0990-7074-26 10 mEq/100 mL 0409–7075–14 10 mEq/50 mL 0990-7075-14 10 mEq/50 mL 0409–7075–26 20 mEq/100 mL 0990-7075-26 20 mEq/100 mL 0409–7077–14 20 mEq/50 mL 0990-7077-14 20 mEq/50 mL 0409–7077–26 40 mEq/100 mL 0990-7077-26 40 mEq/100 mL ICU Medical is transitioning NDC codes from "0409" to a "0990" labeler code. Both NDC codes are expected to be in the market for a period of time. Store at 20 to 25°C (68 to 77°F). [See USP Controlled Room Temperature.] Revised: June, 2018 EN-4654 ICU Medical, Inc., Lake Forest, Illinois, 60045, USA; PRINCIPAL DISPLAY PANEL - 100 mL Bag Label For Use Only With A Calibrated Infusion Device Highly Concentrated 100 mEq/L 100 mL NDC 0990-7074-26 POTASSIUM CHLORIDE Inj. 10 mEq EACH 100 mL CONTAINS POTASSIUM CHLORIDE 745 mg IN WATER FOR INJECTION. ELECTROLYTES PER 1000 mL: POTASSIUM 100 mEq; CHLORIDE 100 mEq. 200 mOsmol/LITER (CALC.) pH 5.8 (4.0 to 8.0) DO NOT ADD SUPPLEMENTARY MEDICATION. WHENEVER POSSIBLE USE CENTRAL ROUTE. SINGLE-DOSE CONTAINER. FOR I.V. USE. USUAL DOSAGE: SEE INSERT. STERILE, NONPYROGENIC. USE ONLY IF SOLUTION IS CLEAR AND CONTAINER IS UNDAMAGED. MUST NOT BE USED IN SERIES CONNECTIONS. Rx ONLY 3 V CONTAINS DEHP ICU Medical, Inc., Lake Forest, Illinois, 60045, USA icumedical IM-4339 PRINCIPAL DISPLAY PANEL - 100 mL Bag Label; PRINCIPAL DISPLAY PANEL - 100 mL Bag Pouch Label TO OPEN – TEAR AT NOTCH NDC 0990-7074-26 For use only with a calibrated infusion device. HIGHLY CONCENTRATED 100 mEq/L POTASSIUM CHLORIDE Inj. 10 mEq Total in 100 mL Each 100 mL contains potassium chloride 745 mg in water for injection. Electrolytes per 1000 mL: potassium 100 mEq; chloride 100 mEq. 200 mOsmol/liter (CALC.) pH 5.8 (4.0 to 8.0) DO NOT ADD SUPPLEMENTARY MEDICATION. WHENEVER POSSIBLE USE CENTRAL ROUTE. Single-dose container. For I.V. use. Usual dosage: See insert. Sterile, nonpyrogenic. Use only if solution is clear. After removing the overwrap, check for minute leaks by squeezing container firmly. If leaks are found, discard unit as sterility may be impaired. Must not be used in series connections. The overwrap is a moisture barrier. Do not remove unit from overwrap until ready for use. Use unit promptly when pouch is opened. Store at 20 to 25°C (68 to 77°F). [See USP Controlled Room Temperature.] Protect from freezing. See insert. Rx only 7 OTHER F WR-0529 ICU Medical, Inc., Lake Forest, Illinois, 60045, USA icumedical PRINCIPAL DISPLAY PANEL - 100 mL Bag Pouch Label; PRINCIPAL DISPLAY PANEL - 50 mL Bag Label - IM-4340 For Use Only With A Calibrated Infusion Device Highly Concentrated 200 mEq/L 50 mL NDC 0990-7075-14 POTASSIUM CHLORIDE Inj. 10 mEq EACH 100 mL CONTAINS POTASSIUM CHLORIDE 1490 mg IN WATER FOR INJECTION. ELECTROLYTES PER 1000 mL: POTASSIUM 200 mEq; CHLORIDE 200 mEq. 400 mOsmol/LITER (CALC.) pH 5.8 (4.0 to 8.0) DO NOT ADD SUPPLEMENTARY MEDICATION. WHENEVER POSSIBLE USE CENTRAL ROUTE. SINGLE-DOSE CONTAINER. USUAL DOSAGE: SEE INSERT. FOR I.V. USE. STERILE, NONPYROGENIC. USE ONLY IF SOLUTION IS CLEAR AND CONTAINER IS UNDAMAGED. MUST NOT BE USED IN SERIES CONNECTIONS. Rx ONLY 3 V CONTAINS DEHP icumedical IM-4340 ICU Medical, Inc., Lake Forest, Illinois, 60045, USA PRINCIPAL DISPLAY PANEL - 50 mL Bag Label - IM-4340; PRINCIPAL DISPLAY PANEL - 50 mL Bag Pouch Label - WR-0530 TO OPEN – TEAR AT NOTCH NDC 0990-7075-14 For use only with a calibrated infusion device. HIGHLY CONCENTRATED 200 mEq/L POTASSIUM CHLORIDE Inj. 10 mEq Total in 50 mL Each 100 mL contains potassium chloride 1490 mg in water for injection. Electrolytes per 1000 mL: potassium 200 mEq; chloride 200 mEq. 400 mOsmol/liter (CALC.) pH 5.8 (4.0 to 8.0) DO NOT ADD SUPPLEMENTARY MEDICATION. WHENEVER POSSIBLE USE CENTRAL ROUTE. Single-dose container. For I.V. use. Usual dosage: See insert. Sterile, nonpyrogenic. Use only if solution is clear. After removing the overwrap, check for minute leaks by squeezing container firmly. If leaks are found, discard unit as sterility may be impaired. Must not be used in series connections. The overwrap is a moisture barrier. Do not remove unit from overwrap until ready for use. Use unit promptly when pouch is opened. Store at 20 to 25°C (68 to 77°F). [See USP Controlled Room Temperature.] Protect from freezing. See insert. Rx only 7 OTHER F WR-0530 ICU Medical, Inc., Lake Forest, Illinois, 60045, USA icumedical PRINCIPAL DISPLAY PANEL - 50 mL Bag Pouch Label - WR-0530; PRINCIPAL DISPLAY PANEL - 50 mL Bag Label - IM-4342 For Use Only With A Calibrated Infusion Device Highly Concentrated 400 mEq/L 50 mL NDC 0990-7077-14 POTASSIUM CHLORIDE Inj. 20 mEq EACH 50 mL CONTAINS POTASSIUM CHLORIDE 1.49 g IN WATER FOR INJECTION. ELECTROLYTES PER 1000 mL: POTASSIUM 400 mEq; CHLORIDE 400 mEq. 799 mOsmol/LITER (CALC.) pH 5.8 (4.0 to 8.0) HYPERTONIC – MAY CAUSE VEIN DAMAGE. DO NOT ADD SUPPLEMENTARY MEDICATION. WHENEVER POSSIBLE USE CENTRAL ROUTE. DISCONTINUE INFUSION IF ADVERSE REACTION OCCURS. SINGLE-DOSE CONTAINER. FOR I.V. USE. USUAL DOSAGE: SEE INSERT. STERILE, NONPYROGENIC. USE ONLY IF SOLUTION IS CLEAR AND CONTAINER IS UNDAMAGED. MUST NOT BE USED IN SERIES CONNECTIONS. Rx ONLY 3 V CONTAINS DEHP ICU Medical, Inc., Lake Forest, Illinois, 60045, USA IM-4342 icumedical PRINCIPAL DISPLAY PANEL - 50 mL Bag Label - IM-4342; PRINCIPAL DISPLAY PANEL - 50 mL Bag Pouch Label - WR-0536 TO OPEN – TEAR AT NOTCH NDC 0990-7077-14 For use only with a calibrated infusion device. HIGHLY CONCENTRATED 20 mEq POTASSIUM CHLORIDE Inj. 400 mEq/L Total in 50 mL Each 50 mL contains potassium chloride 1.49 g in water for injection. Electrolytes per 1000 mL: potassium 400 mEq; chloride 400 mEq. 799 mOsmol/liter (CALC.) pH 5.8 (4.0 to 8.0) Hypertonic – may cause vein damage. DO NOT ADD SUPPLEMENTARY MEDICATION. WHENEVER POSSIBLE USE CENTRAL ROUTE. Discontinue infusion if adverse reaction occurs. Single-dose container. For I.V. use. Usual dosage: See insert. Sterile, nonpyrogenic. Use only if solution is clear. After removing the overwrap, check for minute leaks by squeezing container firmly. If leaks are found, discard unit as sterility may be impaired. Must not be used in series connections. The overwrap is a moisture barrier. Do not remove unit from overwrap until ready for use. Use unit promptly when pouch is opened. Store at 20 to 25°C (68 to 77°F). [See USP Controlled Room Temperature.] Protect from freezing. See insert. Rx only 7 OTHER F WR-0536 ICU Medical, Inc., Lake Forest, Illinois, 60045, USA icumedical PRINCIPAL DISPLAY PANEL - 50 mL Bag Pouch Label - WR-0536
- HOW SUPPLIED Potassium Chloride Injection in flexible plastic containers is available as follows: NDC No. Potassium per container 0409–7074–26 10 mEq/100 mL 0990-7074-26 10 mEq/100 mL 0409–7075–14 10 mEq/50 mL 0990-7075-14 10 mEq/50 mL 0409–7075–26 20 mEq/100 mL 0990-7075-26 20 mEq/100 mL 0409–7077–14 20 mEq/50 mL 0990-7077-14 20 mEq/50 mL 0409–7077–26 40 mEq/100 mL 0990-7077-26 40 mEq/100 mL ICU Medical is transitioning NDC codes from "0409" to a "0990" labeler code. Both NDC codes are expected to be in the market for a period of time. Store at 20 to 25°C (68 to 77°F). [See USP Controlled Room Temperature.] Revised: June, 2018 EN-4654 ICU Medical, Inc., Lake Forest, Illinois, 60045, USA
- PRINCIPAL DISPLAY PANEL - 100 mL Bag Label For Use Only With A Calibrated Infusion Device Highly Concentrated 100 mEq/L 100 mL NDC 0990-7074-26 POTASSIUM CHLORIDE Inj. 10 mEq EACH 100 mL CONTAINS POTASSIUM CHLORIDE 745 mg IN WATER FOR INJECTION. ELECTROLYTES PER 1000 mL: POTASSIUM 100 mEq; CHLORIDE 100 mEq. 200 mOsmol/LITER (CALC.) pH 5.8 (4.0 to 8.0) DO NOT ADD SUPPLEMENTARY MEDICATION. WHENEVER POSSIBLE USE CENTRAL ROUTE. SINGLE-DOSE CONTAINER. FOR I.V. USE. USUAL DOSAGE: SEE INSERT. STERILE, NONPYROGENIC. USE ONLY IF SOLUTION IS CLEAR AND CONTAINER IS UNDAMAGED. MUST NOT BE USED IN SERIES CONNECTIONS. Rx ONLY 3 V CONTAINS DEHP ICU Medical, Inc., Lake Forest, Illinois, 60045, USA icumedical IM-4339 PRINCIPAL DISPLAY PANEL - 100 mL Bag Label
- PRINCIPAL DISPLAY PANEL - 100 mL Bag Pouch Label TO OPEN – TEAR AT NOTCH NDC 0990-7074-26 For use only with a calibrated infusion device. HIGHLY CONCENTRATED 100 mEq/L POTASSIUM CHLORIDE Inj. 10 mEq Total in 100 mL Each 100 mL contains potassium chloride 745 mg in water for injection. Electrolytes per 1000 mL: potassium 100 mEq; chloride 100 mEq. 200 mOsmol/liter (CALC.) pH 5.8 (4.0 to 8.0) DO NOT ADD SUPPLEMENTARY MEDICATION. WHENEVER POSSIBLE USE CENTRAL ROUTE. Single-dose container. For I.V. use. Usual dosage: See insert. Sterile, nonpyrogenic. Use only if solution is clear. After removing the overwrap, check for minute leaks by squeezing container firmly. If leaks are found, discard unit as sterility may be impaired. Must not be used in series connections. The overwrap is a moisture barrier. Do not remove unit from overwrap until ready for use. Use unit promptly when pouch is opened. Store at 20 to 25°C (68 to 77°F). [See USP Controlled Room Temperature.] Protect from freezing. See insert. Rx only 7 OTHER F WR-0529 ICU Medical, Inc., Lake Forest, Illinois, 60045, USA icumedical PRINCIPAL DISPLAY PANEL - 100 mL Bag Pouch Label
- PRINCIPAL DISPLAY PANEL - 50 mL Bag Label - IM-4340 For Use Only With A Calibrated Infusion Device Highly Concentrated 200 mEq/L 50 mL NDC 0990-7075-14 POTASSIUM CHLORIDE Inj. 10 mEq EACH 100 mL CONTAINS POTASSIUM CHLORIDE 1490 mg IN WATER FOR INJECTION. ELECTROLYTES PER 1000 mL: POTASSIUM 200 mEq; CHLORIDE 200 mEq. 400 mOsmol/LITER (CALC.) pH 5.8 (4.0 to 8.0) DO NOT ADD SUPPLEMENTARY MEDICATION. WHENEVER POSSIBLE USE CENTRAL ROUTE. SINGLE-DOSE CONTAINER. USUAL DOSAGE: SEE INSERT. FOR I.V. USE. STERILE, NONPYROGENIC. USE ONLY IF SOLUTION IS CLEAR AND CONTAINER IS UNDAMAGED. MUST NOT BE USED IN SERIES CONNECTIONS. Rx ONLY 3 V CONTAINS DEHP icumedical IM-4340 ICU Medical, Inc., Lake Forest, Illinois, 60045, USA PRINCIPAL DISPLAY PANEL - 50 mL Bag Label - IM-4340
- PRINCIPAL DISPLAY PANEL - 50 mL Bag Pouch Label - WR-0530 TO OPEN – TEAR AT NOTCH NDC 0990-7075-14 For use only with a calibrated infusion device. HIGHLY CONCENTRATED 200 mEq/L POTASSIUM CHLORIDE Inj. 10 mEq Total in 50 mL Each 100 mL contains potassium chloride 1490 mg in water for injection. Electrolytes per 1000 mL: potassium 200 mEq; chloride 200 mEq. 400 mOsmol/liter (CALC.) pH 5.8 (4.0 to 8.0) DO NOT ADD SUPPLEMENTARY MEDICATION. WHENEVER POSSIBLE USE CENTRAL ROUTE. Single-dose container. For I.V. use. Usual dosage: See insert. Sterile, nonpyrogenic. Use only if solution is clear. After removing the overwrap, check for minute leaks by squeezing container firmly. If leaks are found, discard unit as sterility may be impaired. Must not be used in series connections. The overwrap is a moisture barrier. Do not remove unit from overwrap until ready for use. Use unit promptly when pouch is opened. Store at 20 to 25°C (68 to 77°F). [See USP Controlled Room Temperature.] Protect from freezing. See insert. Rx only 7 OTHER F WR-0530 ICU Medical, Inc., Lake Forest, Illinois, 60045, USA icumedical PRINCIPAL DISPLAY PANEL - 50 mL Bag Pouch Label - WR-0530
- PRINCIPAL DISPLAY PANEL - 50 mL Bag Label - IM-4342 For Use Only With A Calibrated Infusion Device Highly Concentrated 400 mEq/L 50 mL NDC 0990-7077-14 POTASSIUM CHLORIDE Inj. 20 mEq EACH 50 mL CONTAINS POTASSIUM CHLORIDE 1.49 g IN WATER FOR INJECTION. ELECTROLYTES PER 1000 mL: POTASSIUM 400 mEq; CHLORIDE 400 mEq. 799 mOsmol/LITER (CALC.) pH 5.8 (4.0 to 8.0) HYPERTONIC – MAY CAUSE VEIN DAMAGE. DO NOT ADD SUPPLEMENTARY MEDICATION. WHENEVER POSSIBLE USE CENTRAL ROUTE. DISCONTINUE INFUSION IF ADVERSE REACTION OCCURS. SINGLE-DOSE CONTAINER. FOR I.V. USE. USUAL DOSAGE: SEE INSERT. STERILE, NONPYROGENIC. USE ONLY IF SOLUTION IS CLEAR AND CONTAINER IS UNDAMAGED. MUST NOT BE USED IN SERIES CONNECTIONS. Rx ONLY 3 V CONTAINS DEHP ICU Medical, Inc., Lake Forest, Illinois, 60045, USA IM-4342 icumedical PRINCIPAL DISPLAY PANEL - 50 mL Bag Label - IM-4342
- PRINCIPAL DISPLAY PANEL - 50 mL Bag Pouch Label - WR-0536 TO OPEN – TEAR AT NOTCH NDC 0990-7077-14 For use only with a calibrated infusion device. HIGHLY CONCENTRATED 20 mEq POTASSIUM CHLORIDE Inj. 400 mEq/L Total in 50 mL Each 50 mL contains potassium chloride 1.49 g in water for injection. Electrolytes per 1000 mL: potassium 400 mEq; chloride 400 mEq. 799 mOsmol/liter (CALC.) pH 5.8 (4.0 to 8.0) Hypertonic – may cause vein damage. DO NOT ADD SUPPLEMENTARY MEDICATION. WHENEVER POSSIBLE USE CENTRAL ROUTE. Discontinue infusion if adverse reaction occurs. Single-dose container. For I.V. use. Usual dosage: See insert. Sterile, nonpyrogenic. Use only if solution is clear. After removing the overwrap, check for minute leaks by squeezing container firmly. If leaks are found, discard unit as sterility may be impaired. Must not be used in series connections. The overwrap is a moisture barrier. Do not remove unit from overwrap until ready for use. Use unit promptly when pouch is opened. Store at 20 to 25°C (68 to 77°F). [See USP Controlled Room Temperature.] Protect from freezing. See insert. Rx only 7 OTHER F WR-0536 ICU Medical, Inc., Lake Forest, Illinois, 60045, USA icumedical PRINCIPAL DISPLAY PANEL - 50 mL Bag Pouch Label - WR-0536
Overview
This Potassium Chloride Injection is a sterile, nonpyrogenic, highly concentrated, ready-to-use solution of Potassium Chloride, USP in Water for Injection, USP for electrolyte replenishment in a single dose container for intravenous administration. It contains no antimicrobial agents. Potassium Chloride Injection mEq Potassium/ Container Composition (g/L) Potassium Chloride, USP (KCl) Osmolarity* (mOsmol/L) (calc) pH Ionic Concentration (mEq/L) Potassium Chloride 10 mEq/100 mL 7.45 200 5.8 (4.0 to 8.0) 100 100 10 mEq/50 mL 20 mEq/100 mL 14.9 400 5.8 (4.0 to 8.0) 200 200 20 mEq/50 mL 40 mEq/100 mL 29.8 799 5.8 (4.0 to 8.0) 400 400 *Normal physiologic osmolarity range is approximately 280 to 310 mOsmol/L. Administration of substantially hypertonic solutions (≥600 mOsmol/L) may cause vein damage. This flexible plastic container is fabricated from a specially formulated polyvinylchloride. Exposure to temperatures above 25°C (77°F) during transport and storage will lead to minor losses in moisture content. Higher temperatures lead to greater losses. It is unlikely that these minor losses will lead to clinically significant changes within the expiration period. The amount of water that can permeate from inside the container into the overwrap is insufficient to affect the solution significantly. Solutions in contact with the plastic container may leach out certain of its chemical components from the plastic in very small amounts; however, biological testing was supportive of the safety of the plastic container materials.
Indications & Usage
Potassium Chloride Injection is indicated in the treatment of potassium deficiency states when oral replacement is not feasible. THIS HIGHLY CONCENTRATED, READY-TO-USE POTASSIUM CHLORIDE INJECTION IS INTENDED FOR THE MAINTENANCE OF SERUM K + LEVELS AND FOR POTASSIUM SUPPLEMENTATION IN FLUID RESTRICTED PATIENTS WHO CANNOT ACCOMMODATE ADDITIONAL VOLUMES OF FLUID ASSOCIATED WITH POTASSIUM SOLUTIONS OF LOWER CONCENTRATION. When using these products, these patients should be on continuous cardiac monitoring and frequent testing for serum potassium concentration and acid-base balance.
Dosage & Administration
The dose and rate of administration are dependent upon the specific condition of each patient. Administer intravenously only with a calibrated infusion device at a slow, controlled rate. Because pain associated with peripheral infusion of Potassium Chloride solution has been reported, whenever possible, administration via central route is recommended for thorough dilution by the blood stream and avoidance of extravasation. Highest concentrations (300 and 400 mEq/L) should be exclusively administered via central route. Recommended administration rates should not usually exceed 10 mEq/hour or 200 mEq for a 24-hour period if the serum potassium level is greater than 2.5 mEq/liter. In urgent cases where the serum potassium level is less than 2 mEq/liter or where severe hypokalemia is a threat (serum potassium level less than 2 mEq/liter and electrocardiographic changes and/or muscle paralysis), rates up to 40 mEq/hour or 400 mEq over a 24-hour period can be administered very carefully when guided by continuous monitoring of the EKG and frequent serum K + determinations to avoid hyperkalemia and cardiac arrest. Parenteral drug products should be inspected visually for particulate matter and discoloration, whenever solution and container permit. Use of a final filter is recommended during administration of all parenteral solutions where possible. Do not add supplementary medication. Preparation for Administration (Use aseptic technique) Close flow control clamp of administration set. Remove cover from outlet port at bottom of container. Insert piercing pin of administration set into port with a twisting motion until the set is firmly seated. NOTE: See full directions on administration set carton. Suspend container from hanger. Squeeze and release drip chamber to establish proper fluid level in chamber. Open flow control clamp and clear air from set. Close clamp. Attach set to venipuncture device. If device is not indwelling, prime and make venipuncture. Regulate rate of administration with flow control clamp. WARNING: Do not use flexible container in series connections. Do not add supplementary medication. Such use could result in air embolism due to residual air being drawn from the primary container before administration of the fluid from the secondary container is completed.
Warnings & Precautions
WARNINGS THIS HIGHLY CONCENTRATED, READY-TO-USE POTASSIUM CHLORIDE INJECTION IS INTENDED FOR THE MAINTENANCE OF SERUM K + LEVELS AND FOR POTASSIUM SUPPLEMENTATION IN FLUID RESTRICTED PATIENTS WHO CANNOT ACCOMMODATE ADDITIONAL VOLUMES OF FLUID ASSOCIATED WITH POTASSIUM SOLUTIONS OF LOWER CONCENTRATION. TO AVOID POTASSIUM INTOXICATION, DO NOT INFUSE THESE SOLUTIONS RAPIDLY. PATIENTS REQUIRING HIGHLY CONCENTRATED SOLUTIONS SHOULD BE KEPT ON CONTINUOUS CARDIAC MONITORING AND UNDERGO FREQUENT TESTING FOR SERUM POTASSIUM AND ACID-BASE BALANCE, ESPECIALLY IF THEY RECEIVE DIGITALIS. In patients with renal insufficiency, administration of potassium chloride may cause potassium intoxication and life-threatening hyperkalemia. Administer intravenously only with a calibrated infusion device at a slow, controlled rate. ( See DOSAGE AND ADMINISTRATION .) Because pain associated with peripheral infusion of Potassium Chloride solution has been reported, whenever possible administration via a central route is recommended for thorough dilution by the blood stream and avoidance of extravasation. Highest concentrations (300 and 400 mEq/L) should be exclusively administered via central route. The administration of intravenous solutions can cause fluid and/or solute overload resulting in dilution of serum electrolyte concentrations, overhydration, congested states or pulmonary edema. The risk of dilutional states is inversely proportional to the electrolyte concentration. The risk of solute overload causing congested states with peripheral and pulmonary edema is directly proportional to the electrolyte concentration.
Boxed Warning
Highly Concentrated
Contraindications
Potassium Chloride Injection is contraindicated in diseases where high potassium levels may be encountered, and in patients with hyperkalemia, renal failure and in conditions in which potassium retention is present.
Adverse Reactions
Potassium intoxication with mild or severe hyperkalemia has been reported. The signs and symptoms of intoxication include paresthesia of the extremities, areflexia, muscular or respiratory paralysis, mental confusion, weakness, hypotension, cardiac arrhythmia, heart block, electrographic abnormalities and cardiac arrest. EKG abnormalities serve as a clinical reflection of the seriousness of changes in serum potassium concentrations: peaked T waves and prolonged P-R intervals usually occur with modest elevations above the upper limit of normal potassium concentrations; P waves disappear, the QRS complex widens, and eventual asystole usually occurs with higher elevations. Reactions which may occur because of the solution or the technique of administration include febrile response, infection at the site of injection, venous thrombosis or phlebitis extending from the site of injection, extravasation and hypervolemia. Infusion of highly concentrated potassium chloride solutions may cause local pain and vein irritation. (See WARNINGS ). Reactions reported with the use of potassium-containing solutions include nausea, vomiting, and abdominal pain and diarrhea. If an adverse reaction does occur, discontinue the infusion, evaluate the patient, institute appropriate therapeutic countermeasures and save the remainder of the fluid for examination if deemed necessary.
Similar Drugs
Related medications based on brand, generic name, substance, active ingredients.