NDC 0338-0202 Clinimix E

Leucine, Phenylalanine, Lysine, Methionine, Isoleucine, Valine, Histidine, Threonine, Tryptophan, Alanine, Glycine, Arginine, Proline, Serine, Tyrosine, Sodium Acetate, Dibasic Potassium Phosphate, Magnesium Chloride, Sodium Chloride, Calcium Chloride, Dextrose

NDC Product Code 0338-0202

NDC CODE: 0338-0202

Proprietary Name: Clinimix E What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Leucine, Phenylalanine, Lysine, Methionine, Isoleucine, Valine, Histidine, Threonine, Tryptophan, Alanine, Glycine, Arginine, Proline, Serine, Tyrosine, Sodium Acetate, Dibasic Potassium Phosphate, Magnesium Chloride, Sodium Chloride, Calcium Chloride, Dextrose What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • Drug uses not available
  • Drug uses not available
  • Drug uses not available
  • This product is used to treat dryness inside the nose (nasal passages). It helps add moisture inside the nose to dissolve and soften thick or crusty mucus. In babies and young children with stuffy noses who cannot blow their noses, using this product helps to make the mucus easier to remove with a nasal bulb syringe. This helps relieve stuffiness and makes breathing easier. This product contains a purified gentle salt solution (also called saline or sodium chloride solution). It does not contain any medication.
  • Drug uses not available
  • Drug uses not available

NDC Code Structure

  • 0338 - Baxter Healthcare Corporation

NDC 0338-0202-06

Package Description: 6 BAG in 1 CARTON > 1000 mL in 1 BAG (0338-0202-01)

NDC Product Information

Clinimix E with NDC 0338-0202 is a a human prescription drug product labeled by Baxter Healthcare Corporation. The generic name of Clinimix E is leucine, phenylalanine, lysine, methionine, isoleucine, valine, histidine, threonine, tryptophan, alanine, glycine, arginine, proline, serine, tyrosine, sodium acetate, dibasic potassium phosphate, magnesium chloride, sodium chloride, calcium chloride, dextrose. The product's dosage form is injection and is administered via intravenous form.

Labeler Name: Baxter Healthcare Corporation

Dosage Form: Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.

Product Type: Human Prescription Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Clinimix E Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • LEUCINE 584 mg/100mL
  • PHENYLALANINE 448 mg/100mL
  • LYSINE 464 mg/100mL
  • METHIONINE 320 mg/100mL
  • ISOLEUCINE 480 mg/100mL
  • VALINE 464 mg/100mL
  • HISTIDINE 384 mg/100mL
  • THREONINE 336 mg/100mL
  • TRYPTOPHAN 144 mg/100mL
  • ALANINE 1656 mg/100mL
  • GLYCINE 824 mg/100mL
  • ARGININE 920 mg/100mL
  • PROLINE 544 mg/100mL
  • SERINE 400 mg/100mL
  • TYROSINE 32 mg/100mL
  • SODIUM ACETATE 340 mg/100mL
  • POTASSIUM PHOSPHATE, DIBASIC 261 mg/100mL
  • MAGNESIUM CHLORIDE 51 mg/100mL
  • SODIUM CHLORIDE 205 mg/100mL
  • CALCIUM CHLORIDE 33 mg/100mL
  • DEXTROSE 14 g/100mL

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Intravenous - Administration within or into a vein or veins.
  • Intravenous - Administration within or into a vein or veins.

Pharmacological Class(es)

What is a Pharmacological Class?
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

  • Amino Acid - [EPC] (Established Pharmacologic Class)
  • Amino Acids - [CS]
  • Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
  • Magnesium Ion Exchange Activity - [MoA] (Mechanism of Action)
  • Osmotic Laxative - [EPC] (Established Pharmacologic Class)
  • Osmotic Activity - [MoA] (Mechanism of Action)
  • Inhibition Small Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Increased Large Intestinal Motility - [PE] (Physiologic Effect)
  • Stimulation Large Intestine Fluid/Electrolyte Secretion - [PE] (Physiologic Effect)
  • Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Osmotic Laxative - [EPC] (Established Pharmacologic Class)
  • Increased Large Intestinal Motility - [PE] (Physiologic Effect)
  • Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Osmotic Activity - [MoA] (Mechanism of Action)
  • Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
  • Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
  • Calcium - [CS]
  • Cations -
  • Divalent - [CS]

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Baxter Healthcare Corporation
Labeler Code: 0338
FDA Application Number: NDA020678 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: NDA - A product marketed under an approved New Drug Application. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 09-21-2020 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Clinimix E Product Label Images

Clinimix E Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

1 Indications And Usage

CLINIMIX E is indicated as a source of calories, protein, and electrolytes for patients requiring parenteral nutrition when oral or enteral nutrition is not possible, insufficient, or contraindicated. CLINIMIX E may be used to treat negative nitrogen balance in patients.

2.1 Preparation Prior To Administration

  • •Tear protective foil overwrap across top at slit and remove solution container. Small amounts of moisture may be found on the solution container from water permeating from inside the container. The amount of permeated water is insufficient to affect the solution significantly. If larger amounts of water are found, the container should be checked for tears or leaks. •Inspect the bag prior to activation. Some opacity of the plastic due to moisture absorption during the sterilization process may be observed. This is normal and does not affect the solution quality or safety. The opacity will diminish gradually. Evaluate the following:oIf the outlet or additive port protectors are damaged, detached, or not present, discard container as solution path sterility may be impaired.oCheck to ensure seal between chambers is intact, solutions are contained in separate chambers, and the content of the individual chambers is clear, colorless or slightly yellow. Discard if the seal is broken or if the solution is bright yellow or yellowish brown.oCheck for minute leaks by separately squeezing each chamber. If external leaks or leakage between the chambers are found, discard solution as sterility or stability may be impaired. •Lipids and/or additives can be introduced to the container after opening seal between chambers. Because additives may be incompatible, evaluate all additions to the plastic container for compatibility. Activate chambers of bag prior to introduction of additives. Mix thoroughly when additives have been introduced. Supplemental medication may be added with a 19 to 22 gauge needle through the medication port. •Calcium and phosphate ratios must be considered. Excess addition of calcium and phosphate, especially in the form of mineral salts, may result in the formation of calcium phosphate precipitates [see Warnings and Precautions (5.1)]. •Inspect the bag to ensure precipitates have not formed during the mixing or addition of additives. A slight yellow color does not alter the quality and efficacy of this product. If lipid has been added, ensure the emulsion has not separated. Separation of the emulsion can be visibly identified by a yellowish streaking or the accumulation of yellowish droplets in the mixed emulsion. Discard the admixture if any of the above are observed.

2.2 Important Administration Instructions

  • •Set the vent to the closed position on a vented intravenous administration set to prevent air embolism. •Use a dedicated line without any connections to avoid air embolism. •CLINIMIX E is for intravenous infusion only into a central or peripheral vein. The choice of a central or peripheral venous route should depend on the osmolarity of the final infusate. Solutions with osmolarity of 900 mOsm/L or greater must be infused through a central catheter [see Warnings and Precautions (5.7)]. oFor central vein infusion only: CLINIMIX E 2.75/10, 4.25/10, 4.25/25, 5/15, 5/20, 5/25oFor central or peripheral vein infusion: CLINIMIX E 2.75/5 and 4.25/5 •The solution should be inspected for precipitates before admixing, after admixing, and again before administration. •Use a 0.22 micron filter for administration of CLINIMIX E. If a lipid is also administered, use a 1.2 micron filter. •If lipid emulsion is added, do not use administration sets and lines that contain di-2-ethylhexyl phthalate (DEHP). Administration sets that contain polyvinyl chloride (PVC) components have DEHP as a plasticizer. •Ceftriaxone must not be administered simultaneously with calcium-containing intravenous solutions such as CLINIMIX E via a Y-site. However, in patients other than neonates, ceftriaxone and CLINIMIX E may be administered sequentially if the infusion lines are thoroughly flushed between infusions with a compatible fluid [see Contraindications (4), Warnings and Precautions (5.2)].

2.3 Instructions For Use

  • 1.Open by tearing protective foil overwrap across top at slit and remove solution container.2.Lay the bag onto a flat surface. Grasp the container firmly on each side of the top of the bag (Figure 1).3.Starting from the top squeeze and roll bag to open seal between chambers until the peel-seal is completely broken as shown in Figure 2.4.If the seal has not been separated completely flip the bag over and repeat process.5.Mix the contents thoroughly by inverting the bag upside down to ensure a homogenous admixture (Figure 3). 6.Once the bag is mixed, check for leaks.7.Make additions (if prescribed).  Because additives may be incompatible, evaluate all additions to the bag for compatibility and stability of the resulting preparation. Consult with pharmacist, if available. Questions about compatibility may be directed to Baxter. If it is deemed advisable to introduce additives, use aseptic technique. For information on adding lipid emulsions see Dosage and Administration (2.4). a.Prepare medication port.b.Using syringe with 19 to 22 gauge needle, puncture resealable medication port and inject.c. Mix solution and medication thoroughly (Figure 3). For high density medication (high specific gravity), such as potassium chloride, squeeze ports while ports are upright and mix thoroughly.8.Inspect final solution for discoloration and particulate matter. Check for leaks.9.Spike and hang bag.a.Suspend container from eyelet support.b.Twist off protector from outlet port at bottom of container (Figure 4).c.Attach administration set. Refer to complete directions accompanying set.For single dose only. Discard unused portion.Figures 1 – 4:Instructions on StorageStorage After Removal of Overwrap: Once removed from the protective foil overwrap, mixed (peel seal activated) or unmixed (peel seal intact), CLINIMIX E Injection solutions may be stored under refrigeration for up to 9 days.Storage Once any Additive is Added:Use promptly after mixing. Any storage with additives should be under refrigeration and limited to a brief period of time, less than 24 hours. After removal from refrigeration, use promptly and complete the infusion within 24 hours. Any remaining mixture must be discarded.

2.4 Preparation And Addition Of Lipid Emulsion

  • 1. Prior to adding lipid emulsion, mix amino acid and dextrose injection as shown in Figures 1-3. 2. Prepare lipid emulsion transfer set following instructions provided. 3. Attach transfer set to lipid emulsion container using aseptic technique. 4. Twist off protector on the additive port of the container. 5. Attach the transfer set to the exposed additive port. 6. Open clamp on transfer set. 7. After completing transfer, use appropriate plastic clamp or metal ferrule to seal off additive port tube. 8. Remove transfer set. 9. Mix contents of container thoroughly. Inspect final solution for discoloration and particulate matter. Check for leaks.Storage Once Lipids are Added: Use promptly after mixing. Any storage with additives should be under refrigeration and limited to a brief period of time, no longer than 24 hours. After removal from refrigeration, use promptly and complete the infusion within 24 hours. Any mixture remaining must be discarded.

2.5 Dosing Considerations

  • •The dosage of CLINIMIX E should be individualized based on the patient’s clinical condition (ability to adequately metabolize amino acids and dextrose), body weight and nutritional/fluid requirements, as well as additional energy given orally/enterally to the patient. Prior to initiating CLINIMIX E the following patient information should be reviewed: review of all medications, gastrointestinal function and laboratory data such as electrolytes (including magnesium, calcium, and phosphorus), glucose, urea/creatinine, liver panel, complete blood count and triglyceride level (if adding lipid emulsion). Refer to the complete prescribing information of lipid emulsion for dosing information. •CLINIMIX E formulations have varying concentrations of protein, carbohydrate and a standard concentration of electrolytes; thus infusion rates to achieve requirements will vary. Protein, caloric, fluid and electrolyte requirements all need to be taken into consideration when determining individual patient dosage needs. •The dosage selection is based only on the recommended protein requirements. The maximum dextrose infusion rates and calorie and fluid requirements must also be considered when determining the clinically appropriate infusion rate for patients. •CLINIMIX E meets the total nutritional requirements for protein and dextrose in stable patients, and can be individualized to meet specific needs with the addition of nutrients. •Total daily fluid requirements can be met beyond the volume of amino acids solution by supplementing with non-carbohydrate or carbohydrate-containing electrolyte solutions. In many patients, provision of adequate calories in the form of hypertonic dextrose may require the administration of exogenous insulin to prevent hyperglycemia and glycosuria. •Prior to administration of CLINIMIX E correct severe fluid, electrolyte and acid-base disorders. •Monitor levels of serum potassium during therapy. It may be necessary to add additional potassium to the CLINIMIX E admixture. •Lipid emulsion administration should be considered with prolonged use (more than 5 days) of CLINIMIX E in order to prevent essential fatty acid deficiency (EFAD). Serum lipids should be monitored for evidence of EFAD in patients maintained on fat-free parenteral nutrition. See prescribing information of lipid emulsion. •The flow rate should be increased gradually. The flow rate must be adjusted taking into account the dose being administered, the daily volume intake, and the duration of the infusion.
  • The recommended daily nutritional requirements for protein and dextrose compared to the amount of nutrition provided by CLINIMIX E are shown in Table 1.  As indicated on an individual basis, maintenance vitamins, additional electrolytes, trace elements and other components (including lipids) should be administered as required to prevent deficiencies and complications from developing. The maximum infusion rates in adult patients are show in Table 2.In addition to meeting protein needs, the administration rate should be governed, especially during the first few day of therapy, by the patient’s tolerance to dextrose. Daily intake of amino acids and dextrose should be increased gradually to the maximum required dose as indicated by frequent determinations of blood glucose levels.Table 1: Nutritional Comparison – Adult PatientsRecommended Nutritional Requirements1Recommended Clinimix E Adult DosageStable PatientsCritically Ill PatientsDo not use in patients with conditions that are contraindicated [see Contraindications (4)].Clinimix E 2.75/5Clinimix E 2.75/10Clinimix E 4.25/5Clinimix E 4.25/10Clinimix E 4.25/25Clinimix E 5/15Clinimix E 5/20Clinimix E 5/25Fluid (mL/kg/day)30 to 40Minimum needed to deliver adequate nutrition29 to 4029 to 4019 to 4019 to 4019 to 4016 to 4016 to 4016 to 40ProteinProtein is provided as amino acids. When infused intravenously amino acids are metabolized and utilized as the building blocks of protein.(g/kg/day)(Nitrogen g/kg/day)0.8 to 1(0.13 to 0.16)1.5 to 2 (0.24 to 0.32)0.8 to 1.1(0.13 to 0.18)0.8 to 1.1(0.13 to 0.18)0.8 to 1.7(0.13 to 0.27)0.8 to 1.7(0.13 to 0.27)0.8 to 1.7(0.13 to 0.27)0.8 to 2(0.13 to 0.32)0.8 to 2(0.13 to 0.32)0.8 to 2(0.13 to 0.32)Dextrose (g/kg/day)≤10≤5.81.45 to 22.9 to 40.95 to 21.9 to 44.75 to 102.4 to 63.2 to 84 to 10Table 2: Maximum Infusion Rate in Adult PatientsMaximum Infusion Rates in Adults PatientsClinimix E 2.75/5Clinimix E 2.75/10Clinimix E 4.25/5Clinimix E 4.25/10Clinimix E 4.25/25Clinimix E 5/15Clinimix E 5/20Clinimix E 5/25Maximum Infusion Rate (mL/kg/hour)3.62.52.42.411.671.251Corresponding infusion rateAmino Acid (g/kg/hour)0.1Rate limiting factor0.070.10.10.040.080.060.05Dextrose (g/kg/hour)0.180.250.120.240.250.250.250.25

2.7 Dosage Modifications In Patients With Renal Impairment

Prior to administration, correct severe fluid or electrolyte imbalances. Closely monitor serum electrolyte levels and adjust the volume of CLINIMIX E administered as required [see Warnings and Precautions (5.11)].Patients with renal impairment not needing dialysis require 0.6 to 0.8 g of protein/kg/day. Serum electrolyte levels should be closely monitored. Patients on hemodialysis or continuous renal replacement therapy should receive 1.2 to 1.8 g of protein/kg/day up to a maximum of 2.5 g of protein/kg/day based on nutritional status and estimated protein losses.2 The CLINIMIX E dosage can be adjusted based on the severity of renal impairment, supplementing protein as indicated. If required, additional amino acids may be added to the CLINIMIX E bag or infused separately. Compatibility of additions should be evaluated by a pharmacist and questions may be directed to Baxter.

  • The dosage and constant infusion rate of intravenous dextrose must be selected with caution in pediatric patients, particularly neonates and low weight infants, because of the increased risk of hyperglycemia/hypoglycemia [see Use in Specific Populations (8.4)]. Frequent monitoring of serum glucose concentrations is required when dextrose is prescribed to pediatric patients, particularly neonates and low birth weight infants. The infusion rate and volume should be determined by the consulting physician experienced in pediatric intravenous fluid therapy. In pediatric patients, CLINIMIX E is dosed on the basis of protein provided as amino acids. The recommended dosage, by age group is provided in Tables 3 - 6. Infusion rates are based on protein and do not take carbohydrates, fluid or electrolytes into consideration.This product does not contain the amino acids cysteine and taurine, considered conditionally essential for neonates and infants. If possible, these amino acids should be added to this product if used in this pediatric population.Table 3: Preterm and Term Infants Less than 1 Month of AgeRecommended Nutritional Requirements1Recommended Clinimix E Dosage in Preterm and Term Infants Less than 1 Month of AgeClinimix E 2.75/5Clinimix E 2.75/10Clinimix E 4.25/5Clinimix E 4.25/10Clinimix E 4.25/25Clinimix E 5/15Clinimix E 5/20Clinimix E 5/25Infusion Rate Range (mL/kg/hr)4.5 to 64.5 to 62.9 to 3.92.9 to 3.92.9 to 3.32.5 to 3.32.5 to 3.32.5 to 3.3Fluid (mL/kg/day)100 to 150108 to 144108 to 14470 to 9470 to 9470 to 7960 to 7960 to 7960 to 79ProteinProtein is provided as amino acids. When infused intravenously amino acids are metabolized and utilized as the building blocks of protein.(g/kg/day)(Nitrogen g/kg/day)3 to 4(0.48 to 0.64)3 to 4(0.48 to 0.64)3 to 4(0.48 to 0.64)3 to 4(0.48 to 0.64)3 to 4(0.48 to 0.64)3 to 3.4(0.48 to 0.54)3 to 4(0.48 to 0.64)3 to 4(0.48 to 0.64)3 to 4(0.48 to 0.64)Dextrose (g/kg/day)7 to 205.4 to 7.210.8 to 14.43.5 to 4.77 to 9.417.5 to 19.89 to 11.912 to 15.815 to 19.81.Protein is provided as amino acids. When infused intravenously amino acids are metabolized and utilized as the building blocks of protein.Table 4: Pediatric Patients 1 Month to Less than 1 Year of AgeRecommended Nutritional Requirements1Recommended Clinimix E Dosage in Pediatric Patients 1 Month to Less than 1 Year of AgeClinimix E 2.75/5Clinimix E 2.75/10Clinimix E 4.25/5Clinimix E 4.25/10Clinimix E 4.25/25Clinimix E 5/15Clinimix E 5/20Clinimix E 5/25Infusion Rate Range (mL/kg/hr)3 to 4.53 to 4.52 to 2.92 to 2.92 to 2.91.7 to 2.51.7 to 2.51.7 to 2.5Fluid (mL/kg/day)100 mL/kg for the first 10 kg + 50 mL/kg for the second 10 kg.72 to 10872 to 10848 to 7048 to 7048 to 7041 to 6041 to 6041 to 60ProteinProtein is provided as amino acids. When infused intravenously amino acids are metabolized and utilized as the building blocks of protein.(g/kg/day)(Nitrogen g/kg/day)2 to 3(0.32 to 0.48)2 to 3(0.32 to 0.48)2 to 3(0.32 to 0.48)2 to 3(0.32 to 0.48)2 to 3(0.32 to 0.48)2 to 3(0.32 to 0.48)2 to 3(0.32 to 0.48)2 to 3(0.32 to 0.48)2 to 3(0.32 to 0.48)Dextrose (g/kg/day)7 to 203.6 to 5.47.2 to 10.82.4 to 3.54.8 to 712 to 17.56.1 to 98.2 to 1210.2 to 15Table 5: Pediatric Patients 1 Year to Less than 11 Years of AgeRecommended Nutritional Requirements1Recommended Clinimix E Dosage in Pediatric Patients 1 Year to Less than 11 Years of AgeClinimix E 2.75/5Clinimix E 2.75/10Clinimix E 4.25/5Clinimix E 4.25/10Clinimix E 4.25/25Clinimix E 5/15Clinimix E 5/20Clinimix E 5/25Infusion Rate Range (mL/kg/hr)1.5 to 31.5 to 31 to 21 to 21 to 20.8 to 1.70.8 to 1.70.8 to 1.7Fluid (mL/kg/day)100 mL/kg for the first 10 kg + 50 mL/kg for the second 10 kg + 20 mL/kg for weight > 20 kg 36 to 7236 to 7224 to 4824 to 4824 to 4819 to 4119 to 4119 to 41ProteinProtein is provided as amino acids. When infused intravenously amino acids are metabolized and utilized as the building blocks of protein.(g/kg/day)(Nitrogen g/kg/day)1 to 2(0.16 to 0.32)1 to 2(0.16 to 0.32)1 to 2(0.16 to 0.32)1 to 2(0.16 to 0.32)1 to 2(0.16 to 0.32)1 to 2(0.16 to 0.32)1 to 2(0.16 to 0.32)1 to 2(0.16 to 0.32)1 to 2(0.16 to 0.32)Dextrose (g/kg/day)7 to 141.8 to 3.63.6 to 7.21.2 to 2.42.4 to 4.86 to 122.9 to 6.13.8 to 8.24.8 to 10.2Table 6: Pediatric Patients 11 Years to 17 Years of AgeRecommended Nutritional Requirements1Recommended Clinimix E Dosage in Pediatric Patients 11 Years to 17 Years of AgeClinimix E 2.75/5Clinimix E 2.75/10Clinimix E 4.25/5Clinimix E 4.25/10Clinimix E 4.25/25Clinimix E 5/15Clinimix E 5/20Clinimix E 5/25Infusion Rate Range (mL/kg/hr)1.2 to 2.31.2 to 2.30.8 to 1.50.8 to 1.50.8 to 1.50.7 to 1.30.7 to 1.30.7 to 1.3Fluid (mL/kg/day)100 mL/kg for the first 10 kg + 50 mL/kg for the second 10 kg + 20 mL/kg for weight > 20 kg 29 to 5529 to 5519 to 3619 to 3619 to 3617 to 3117 to 3117 to 31ProteinProtein is provided as amino acids. When infused intravenously amino acids are metabolized and utilized as the building blocks of protein.(g/kg/day)(Nitrogen g/kg/day)0.8 to 1.5(0.13 to 0.24)0.8 to 1.5(0.13 to 0.24)0.8 to 1.5(0.13 to 0.24)0.8 to 1.5(0.13 to 0.24)0.8 to 1.5(0.13 to 0.24)0.8 to 1.5(0.13 to 0.24)0.8 to 1.5(0.13 to 0.24)0.8 to 1.5(0.13 to 0.24)0.8 to 1.5(0.13 to 0.24)Dextrose (g/kg/day)5 to 91.4 to 2.82.9 to 5.51 to 1.81.9 to 3.64.8 to 92.5 to 4.73.4 to 6.24.2 to 7.8

2.9 Discontinuation Of Clinimix E

To reduce the risk of hypoglycemia after discontinuation, a gradual decrease in flow rate in the last hour of infusion should be considered.

3 Dosage Forms And Strengths

  • CLINIMIX E injection is available in 1000 mL and 2000 mL dual chamber bags. The individual chambers contain essential and nonessential amino acids with electrolytes and dextrose with calcium. Table 7 describes the individual components of CLINIMIX E.Table 7 INGREDIENTS PER 100mL OF CLINIMIX EStrength of CLINIMIX ECLINIMIX E 2.75/5 sulfite‑free(2.75% Amino Acid in 5% Dextrose) InjectionCLINIMIX E 2.75/10 sulfite‑free(2.75% Amino Acid in 10% Dextrose) InjectionCLINIMIX E 4.25/5 sulfite‑free(4.25% Amino Acid in 5% Dextrose) InjectionCLINIMIX E 4.25/10 sulfite‑free(4.25% Amino Acid in 10% Dextrose) InjectionCLINIMIX E 4.25/25 sulfite‑free(4.25% Amino Acid in 25% Dextrose) InjectionCLINIMIX E 5/15 sulfite‑free(5% Amino Acid in 15% Dextrose) InjectionCLINIMIX E 5/20 sulfite‑free(5% Amino Acid in 20% Dextrose) InjectionCLINIMIX E 5/25 sulfite‑free(5% Amino Acid in 25% Dextrose) InjectionDextrose Hydrous, USP (g/100 mL)51051025152025Amino Acids (g/100 mL)2.752.754.254.254.25555Total Nitrogen (mg/100 mL)454454702702702826826826 Essential Amino Acids (mg/100 mL)Leucine 201201311311311365365365Isoleucine 165165255255255300300300Valine 160160247247247290290290Lysine (added as the hydrochloride salt) 159159247247247290290290Phenylalanine 154154238238238280280280Histidine 132132204204204240240240Threonine 116116179179179210210210Methionine 110110170170170200200200Tryptophan5050777777909090 Nonessential Amino Acids(mg/100 mL)Alanine 570570880880880103510351035Arginine 316316489489489575575575Glycine 283283438438438515515515Proline 187187289289289340340340Serine 138138213213213250250250Tyrosine1111171717202020 Electrolytes(mg/100 mL)Sodium Acetate Trihydrate, USP 217217297297297340340340Dibasic Potassium Phosphate, USP261261261261261261261261Sodium Chloride, USP 112112777777595959Magnesium Chloride, USP 5151515151515151Calcium Chloride Dihydrate, USP 3333333333333333Electrolyte Profile (mEq/L)Balanced by ions from amino acids.Sodium3535353535353535Potassium3030303030303030Magnesium55555555Calcium4.5(2.2 mmol/L)4.5(2.2 mmol/L)4.5(2.2 mmol/L)4.5(2.2 mmol/L)4.5(2.2 mmol/L)4.5(2.2 mmol/L)4.5(2.2 mmol/L)4.5(2.2 mmol/L)AcetateDerived from glacial acetic acid (for pH adjustment) and sodium acetate.5151707070808080ChlorideContributed by calcium chloride, lysine hydrochloride, magnesium chloride, and sodium chloride.3939393939393939Phosphate (as HPO4)30(15 mmol/L)30(15 mmol/L)30(15 mmol/L)30(15 mmol/L)30(15 mmol/L)30(15 mmol/L)30(15 mmol/L)30(15 mmol/L)pHpH of sulfite-free amino acid injection with electrolytes in the outlet port chamber was adjusted with glacial acetic acid.(Range)6.0 (4.5 to 7.0)6.0(4.5 to 7.0)6.0(4.5 to 7.0)6.0(4.5 to 7.0)6.0(4.5 to 7.0)6.0(4.5 to 7.0)6.0(4.5 to 7.0)6.0(4.5 to 7.0)Osmolarity (mOsmol/L) (calc)66592081510701825139516501900Caloric Content (kcal/L)From Dextrose170340170340850510680850From Amino Acids110110170170170200200200TOTAL (Dextrose and Amino Acids)28045034051010207108801050

4 Contraindications

  • The use of CLINIMIX E is contraindicated in: •Neonates (less than 28 days of age) receiving concomitant treatment with ceftriaxone, even if separate infusion lines are used, due to the risk of fatal ceftriaxone calcium salt precipitation in the neonate’s bloodstream [see Warnings and Precautions (5.2), Use in Specific Populations (8.4)]. •Patients with known hypersensitivity to one or more amino acids or dextrose [see Warnings and Precautions (5.3)]. •Patients with inborn errors of amino acid metabolism due to risk of severe metabolic and neurologic complications. •Patients with pulmonary edema or acidosis due to low cardiac output.

5.1 Pulmonary Embolism Due To Pulmonary Vascular Precipitates

Pulmonary vascular precipitates causing pulmonary vascular emboli and pulmonary distress have been reported in patients receiving parenteral nutrition. In some cases, fatal outcomes due to pulmonary embolism have occurred. Patients, especially those with hypophosphatemia, may require the addition of phosphate. To prevent hypocalcemia, calcium supplementation should always accompany phosphate administration. Excessive addition of calcium and phosphate increases the risk of the formation of calcium phosphate precipitates. Precipitates have been reported even in the absence of phosphate salt in the solution. Precipitation following passage through an in-line filter and suspected in vivo precipitate formation has also been reported. If signs of pulmonary distress occur, stop the infusion and initiate a medical evaluation. In addition to inspection of the solution [see Dosage and Administration (2.1, 2.2, 2.3, 2.4)], the infusion set and catheter should also periodically be checked for precipitates.

5.2 Precipitation With Ceftriaxone

Precipitation of ceftriaxone-calcium can occur when ceftriaxone is mixed with calcium-containing parenteral nutrition solutions, such as CLINIMIX E, in the same intravenous administration line. Do not administer ceftriaxone simultaneously with CLINIMIX E via a Y-site. Deaths have occurred in neonates (less than 28 days of age) who received concomitant intravenous calcium-containing solutions with ceftriaxone resulting from calcium-ceftriaxone precipitates in the lungs and kidneys, even when separate infusion lines were used. CLINIMIX E is contraindicated in neonates receiving ceftriaxone [see Contraindications (4),Use in Specific Populations (8.4)].In patients older than 28 days (including adults), ceftriaxone and CLINIMIX E may be administered sequentially if the infusion lines are thoroughly flushed between infusions with a compatible fluid.

5.3 Hypersensitivity Reactions

Hypersensitivity/infusion reactions including anaphylaxis have been reported with CLINIMIX E. Stop infusion immediately and treat patient accordingly if any signs or symptoms of a hypersensitivity reaction develop. Signs or symptoms may include: hypotension, hypertension, peripheral cyanosis, tachycardia, dyspnea, vomiting, nausea, urticaria, rash, pruritus, erythema, hyperhidrosis, pyrexia, and chills.

5.4 Risk Of Infections

Patients who require parenteral nutrition are at high risk of infections because the nutritional components of these solutions can support microbial growth. Infection and sepsis may also occur as a result of the use of intravenous catheters to administer parenteral nutrition.The risk of infection is increased in patients with malnutrition-associated immunosuppression, hyperglycemia exacerbated by dextrose infusion, long-term use and poor maintenance of intravenous catheters, or immunosuppressive effects of other concomitant conditions, drugs, or other components of the parenteral formulation (e.g., lipid emulsion). To decrease the risk of infection, ensure aseptic technique in catheter placement and maintenance, as well as aseptic technique in the preparation and administration of the nutritional formula. Monitor for signs and symptoms (including fever and chills) of early infections, including laboratory test results (including leukocytosis and hyperglycemia) and frequent checks of the parenteral access device and insertion site for edema, redness and discharge.

5.5 Refeeding Syndrome

Refeeding severely undernourished patients may result in refeeding syndrome, characterized by the intracellular shift of potassium, phosphorus, and magnesium as the patient becomes anabolic. Thiamine deficiency and fluid retention may also develop. To prevent these complications, monitor severely undernourished patients and slowly increase nutrient intakes.

5.6 Hyperglycemia Or Hyperosmolar Hyperglycemic State

When using CLINIMIX E in patients with diabetes mellitus, impaired glucose tolerance may worsen hyperglycemia. Administration of dextrose at a rate exceeding the patient’s utilization rate may lead to hyperglycemia, coma, and death. Patients with underlying confusion and renal impairment who receive dextrose infusions, may be at greater risk of developing hyperosmolar hyperglycemic state. Monitor blood glucose levels and treat hyperglycemia to maintain optimum levels while administering CLINIMIX E. Insulin may be administered or adjusted to maintain optimal blood glucose levels during CLINIMIX E administration.

5.7 Vein Damage And Thrombosis

Solutions with osmolarity of 900 mOsm/L or greater must be infused through a central catheter. CLINIMIX E solutions containing more than 5% dextrose have an osmolarity greater than or equal to 900 mOsm/L. CLINIMIX E 2.75/10, 4.25/10, 4.25/25, 5/15, 5/20, and 5/25 are indicated for administration into a central vein only, such as the superior vena cava [see Dosage and Administration (2.2)]. The infusion of hypertonic nutrient injections into a peripheral vein may result in vein irritation, vein damage, and/or thrombosis.CLINIMIX E 2.75/5 and 4.25/5 are indicated for peripheral administration, or may be infused into a central vein [see Dosage and Administration (2.2)]. The primary complication of peripheral access is venous thrombophlebitis, which manifests as pain, erythema, tenderness or a palpable cord. Remove the catheter as soon as possible, if thrombophlebitis develops.

5.8 Hepatobiliary Disorders

Hepatobiliary disorders are known to develop in some patients without preexisting liver disease who receive parenteral nutrition, including cholecystitis, cholelithiasis, cholestasis, hepatic steatosis, fibrosis and cirrhosis, possibly leading to hepatic failure. The etiology of these disorders is thought to be multifactorial and may differ between patients. Increase in blood ammonia levels and hyperammonemia may occur in patients receiving amino acid solutions. In some patients this may indicate hepatic insufficiency or the presence of an inborn error of amino acid metabolism [see Contraindications (4)].Monitor liver function parameters and ammonia levels. Patients developing signs of hepatobiliary disorders should be assessed early by a clinician knowledgeable in liver diseases in order to identify possible causative and contributory factors, and possible therapeutic and prophylactic interventions.

5.9 Aluminum Toxicity

CLINIMIX E contains no more than 25 mcg/L of aluminum. However, with prolonged parenteral administration in patients with renal impairment, the aluminum contained in CLINIMX E may reach toxic levels. Preterm infants are at a greater risk because their kidneys are immature, and they require large amounts of calcium and phosphate solutions, which contain aluminum.Patients with renal impairment, including preterm infants, who receive parenteral levels of aluminum at greater than 4 to 5 mcg/kg/day, accumulate aluminum at levels associated with central nervous system and bone toxicity. Tissue loading may occur at even lower rates of administration.

5.10 Risk Of Parenteral Nutrition Associated Liver Disease

Parenteral Nutrition Associated Liver Disease (PNALD) has been reported in patients who receive parenteral nutrition for extended periods of time, especially preterm infants, and can present as cholestasis or steatohepatitis. The exact etiology is unknown and is likely multifactorial. If CLINIMIX E treated patients develop liver test abnormalities consider discontinuation or dosage reduction.

5.11 Electrolyte Imbalance And Fluid Overload

Patients with renal impairment, such as pre-renal azotemia, renal obstruction, and protein-losing nephropathy may be at increased risk of electrolyte and fluid volume imbalance. Patients with cardiac insufficiency due to left ventricular systolic dysfunction are susceptible to excess fluid accumulation. Use CLINIMIX E with caution in patients with cardiac insufficiency or renal impairment. CLINIMIX E dosage may require adjustment with specific attention to fluid, protein, and electrolyte content in these patients.Monitor renal function parameters. Patients developing signs of renal impairment should be assessed early by a clinician knowledgeable in renal disease in order to determine the appropriate CLINIMIX E dosage and other treatment options.

5.12 Monitoring/Laboratory Tests

Monitor fluid and electrolyte status, serum osmolarity, blood glucose, liver and kidney function, blood count and coagulation parameters throughout treatment. In situations of severely elevated electrolyte levels, stop CLINIMIX E until levels have been corrected.

6 Adverse Reactions

  • The following serious adverse reactions are discussed in greater detail in other sections of the prescribing information. •Pulmonary embolism due to pulmonary vascular precipitates [see Warnings and Precautions (5.1)] •Death in neonates due to calcium-ceftriaxone precipitates [see Warnings and Precautions (5.2)] •Hypersensitivity reactions [see Warnings and Precautions (5.3)] •Risk of Infections [see Warnings and Precautions (5.4)] •Refeeding syndrome [see Warnings and Precautions (5.5)] •Hyperglycemia or hyperosmolar hyperglycemic state [see Warnings and Precautions (5.6)] •Vein damage and thrombosis [see Warnings and Precautions (5.7)] •Hepatobiliary disorders [see Warnings and Precautions (5.8)] •Parenteral Nutrition Associated Liver Disease (PNALD) [see Warnings and Precautions (5.10)] •Electrolyte imbalance and fluid overload [see Warnings and Precautions (5.11)]The following adverse reactions from voluntary reports or clinical studies have been reported with CLINIMIX E. Because many of these reactions were reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure. •Diuresis •Extravasation •Glycosuria •Hyperglycemia •Hyperosmolar coma

7.1 Drugs That Can Cause Hyperkalemia

Because of its potassium content, CLINIMIX E should be administered with caution in patients treated with agents or products that can cause hyperkalemia or increase the risk of hyperkalemia, such as potassium sparing diuretics (amiloride, spironolactone, triamterene), with ACE inhibitors, angiotensin II receptor antagonists, or the immunosuppressants tacrolimus and cyclosporine.

Risk Summary

There are no adequate or well-controlled studies in pregnant women with CLINIMIX E. Additionally, animal reproduction studies have not been conducted with amino acids and electrolytes and dextrose. It is not known whether CLINIMIX E can cause fetal harm when administered to a pregnant woman.The estimated background risk of major birth defects and miscarriage for the indicated population is unknown. However, the estimated background risk in the U.S. general population of major birth defects is 2 to 4% and of miscarriage is 15 to 20% of clinically recognized pregnancies.

It is not known whether CLINIMIX E is present in human milk. There are no data on the effects of CLINIMIX E on the breastfed infant or on milk production. The developmental and health benefits of breastfeeding should be considered along with the mother’s clinical need for CLINIMIX E and any potential adverse effects on the breastfed child from CLINIMIX E or from the underlying maternal condition.

Clinical Considerations

Disease-Associated Maternal and/or Embryo-Fetal RiskBased on clinical practice guidelines, parenteral nutrition should be considered in cases of severe maternal malnutrition where nutritional requirements cannot be fulfilled by the enteral route because of the risks to the fetus associated with severe malnutrition, such as preterm delivery, low birth weight, intrauterine growth restriction, congenital malformations and perinatal mortality.

8.4 Pediatric Use

Safety and effectiveness of CLINIMIX E in pediatric patients have not been established by adequate and well-controlled studies. Use of dextrose, amino acid infusions and electrolytes in pediatric patients is based on clinical practice [see Dosage and Administration (2.8)].Deaths have occurred in neonates (less than 28 days of age) who received concomitant intravenous calcium-containing solutions with ceftriaxone resulting from calcium-ceftriaxone precipitates in the lungs and kidneys, even when separate infusion lines were used. CLINIMIX E is contraindicated in neonates receiving ceftriaxone [see Contraindications (4), Warnings and Precautions (5.2)].Newborns, especially those born premature and with low birth weight, are at increased risk of developing hypo – or hyperglycemia and therefore need close monitoring during treatment with intravenous glucose solutions to ensure adequate glycemic control in order to avoid potential long term adverse effects. Hypoglycemia in the newborn can cause prolonged seizures, coma and brain damage. Hyperglycemia has been associated with intraventricular hemorrhage, late onset bacterial and fungal infection, retinopathy of prematurity, necrotizing enterocolitis, bronchopulmonary dysplasia, prolonged length of hospital stay, and death. Plasma electrolyte concentrations should be closely monitored in the pediatric population as this population may have impaired ability to regulate fluids and electrolytes.Because of immature renal function, preterm infants receiving prolonged treatment with CLINIMIX E, may be at risk of aluminum toxicity [see Warnings and Precautions (5.9)].Patients, including pediatric patients, may be at risk for Parenteral Nutrition Associated Liver Disease (PNALD) [see Warnings and Precautions (5.10)].Hyperammonemia is of special significance in infants (birth to two years). This reaction appears to be related to a deficiency of the urea cycle amino acids of genetic or product origin. It is essential that blood ammonia be measured frequently in infants [see Warnings and Precautions (5.8)].

8.5 Geriatric Use

Clinical studies of CLINIMIX E did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from other younger subjects. Other reported clinical experience has not identified differences in responses between the elderly and younger patients. In general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or drug therapy.

10 Overdosage

An increased infusion rate of CLINIMIX E can cause hyperglycemia, hyperosmolality, and adverse effects on water and electrolyte balance [see Warnings and Precautions (5.6, 5.11)].Severe hyperglycemia and severe dilutional hyponatremia, and their complications, can be fatal.Discontinue infusion and institute appropriate corrective measures in the event of overhydration or solute overload during therapy, with particular attention to respiratory and cardiovascular systems.For current information on the management of poisoning or overdosage, contact the National Poison Control Center at 1-800-222-1222 or www.poison.org.

11 Description

CLINIMIX E sulfite-free (amino acids with electrolytes in dextrose with calcium) injection for intravenous use consists of sterile, nonpyrogenic, hypertonic solutions in a dual chamber container.The outlet port chamber contains essential and nonessential amino acids with electrolytes. The formulas for the individual electrolytes and amino acids are provided in Table 8.Table 8: Formulas for Electrolytes and Amino AcidsElectrolytesSodium AcetateC2H3NaO2•3H2OPotassium Phosphate, dibasicK2HPO4Magnesium ChlorideMgCl2•6H2OSodium ChlorideNaClEssential Amino AcidsLeucine(CH3)2 CHCH2CH (NH2) COOHIsoleucineCH3CH2CH (CH3) CH (NH2) COOHValine(CH3)2 CHCH (NH2) COOHLysine (added as the hydrochloride salt)H2N (CH2)4 CH (NH2) COOHPhenylalanine(C6H5) CH2 CH (NH2) COOHHistadine(C3H3N2) CH2CH (NH2) COOHThreonineCH3CH (OH) CH (NH2) COOMethionineCH3S (CH2)2 CH (NH2) COOHTryptophan(C8H6N) CH2 CH (NH2) COOHNonessential Amino AcidsAlanineCH3CH (NH2) COOHArginineH2NC (NH) NH (CH2)3 CH (NH2) COOHGlycineH2NCH2COOHProline[(CH2)3 NH CH] COOHSerineHOCH2CH (NH2) COOHTyrosine[C6H4 (OH)] CH2CH (NH2) COOHThe injection port chamber contains dextrose with calcium. The formula for Calcium Chloride is: CaCl2•2H2O. Dextrose, USP, is chemically designated D-glucose, monohydrate (C6H12O6 • H2O) and has the following structure:Dextrose is derived from corn.See Table 7 for composition, pH, osmolarity, ionic concentration and caloric content of the admixed product [see Dosage Forms and Strengths (3)].The dual chamber container is a lipid-compatible plastic container (PL 2401 Plastic). CLINIMIX E contains no more than 25 mcg/L of aluminum.

12.1 Mechanism Of Action

CLINIMIX E is used as a supplement of nutrition in patients, providing macronutrients (amino acids and dextrose) and micronutrients (electrolytes) parenterally.The amino acids provide the structural units that make up proteins and are used to synthesize proteins and other biomolecules or are oxidized to urea and carbon dioxide as a source of energy.The administered dextrose is oxidized to carbon dioxide and water, yielding energy.

12.3 Pharmacokinetics

The disposition of infused amino acids, dextrose, and electrolytes are essentially the same as those absorbed from food.

15 References

  • 1.Ayers Phil, et al. A.S.P.E.N. Parenteral Nutrition Handbook, 2nd ed. 2014, pg. 123.2.Mueller CM ed. The A.S.P.E.N. Nutrition Support Core Curriculum, 2nd ed. 2012. Chapter 29. Wolk R, Foulks C. Renal Disease, pg. 500.

16 How Supplied/Storage And Handling

  • CLINIMIX E (amino acids with electrolytes in dextrose with calcium) injection (sulfite-free) is available in 1000 mL and 2000 mL volumes (See Table 9).Table 9: CLINIMIX E Formulations After mixing, the product represents 1000 mL Code and NDC Number 2000 mL Code and NDC Number CLINIMIX E 2.75/5 sulfite-free (2.75% Amino Acid with Electrolytes in 5% Dextrose with Calcium) Injection Code 2B7735NDC 0338-1142-03 Code 2B7713NDC 0338-1107-04 CLINIMIX E 2.75/10 sulfite-free (2.75% Amino Acid with Electrolytes in 10% Dextrose with Calcium) Injection Code 2B7736NDC 0338-1143-03 Code 2B7714NDC 0338-1109-04 CLINIMIX E 4.25/5 sulfite-free (4.25% Amino Acid with Electrolytes in 5% Dextrose with Calcium) Injection Code 2B7737NDC 0338-1144-03 Code 2B7716NDC 0338-1113-04 CLINIMIX E 4.25/10 sulfite-free (4.25% Amino Acid with Electrolytes in 10% Dextrose with Calcium) Injection Code 2B7738NDC 0338-1145-03 Code 2B7717NDC 0338-1115-04 CLINIMIX E 4.25/25 sulfite-free (4.25% Amino Acid with Electrolytes in 25% Dextrose with Calcium) Injection Code 2B7739NDC 0338-1146-03 Code 2B7719NDC 0338-1119-04 CLINIMIX E 5/15 sulfite-free (5% Amino Acid with Electrolytes in 15% Dextrose with Calcium) Injection Code 2B7740NDC 0338-1147-03 Code 2B7721NDC 0338-1123-04 CLINIMIX E 5/20 sulfite-free (5% Amino Acid with Electrolytes in 20% Dextrose with Calcium) Injection Code 2B7741NDC 0338-1148-03 Code 2B7722NDC 0338-1125-04 CLINIMIX E 5/25 sulfite-free (5% Amino Acid with Electrolytes in 25% Dextrose with Calcium) Injection Code 2B7742NDC 0338-1149-03 Code 2B7723NDC 0338-1127-04Minimize exposure of CLINIMIX E to heat and avoid excessive heat. Protect from freezing. Store CLINIMIX E at room temperature (25°C/77°F) (may briefly store at up to 40°C/104°F). Refrigerated storage is limited to 9 days once the protective foil overwrap has been opened.Do not use if the protective foil overwrap has been previously opened or damaged.For storage of admixed solutions seeDosage and Administration (2.3, 2.4).

17 Patient Counseling Information

  • Inform patients, caregivers, or home healthcare providers of the following risks of CLINIMIX E: •Pulmonary embolism due to pulmonary vascular precipitates [see Warnings and Precautions (5.1)] •Death in neonates due to calcium-ceftriaxone precipitates [see Warnings and Precautions (5.2)] •Hypersensitivity reactions [see Warnings and Precautions (5.3)] •Risk of Infections [see Warnings and Precautions (5.4)] •Refeeding syndrome [see Warnings and Precautions (5.5)] •Hyperglycemia or hyperosmolar hyperglycemic state [see Warnings and Precautions (5.6)] •Vein damage and thrombosis [see Warnings and Precautions (5.7)] •Hepatobiliary disorders [see Warnings and Precautions (5.8)] •Aluminum toxicity [see Warnings and Precautions (5.9)] •Parenteral Nutrition Associated Liver Disease (PNALD) [see Warnings and Precautions (5.10)] •Electrolyte imbalance and fluid overload [see Warnings and Precautions (5.11)] Baxter Healthcare CorporationDeerfield, IL 60015 USAPrinted in USA Baxter and Clinimix E are trademarks of Baxter International Inc. 07-19-77-170

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