For intravenous use only.Subcutaneous or intramuscular injection may cause severe necrosis and sloughing.
WARNING: This product contains aluminum that may be toxic. Aluminum may reach toxic levels with prolonged parenteral administration if kidney function is impaired. Premature neonates are particularly at risk because their kidneys are immature, and they require large amounts of calcium and phosphate solutions, which contain aluminum.
Research indicates that patients with impaired kidney function, including premature neonates, 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.
Calcium Gluconate Injection, USP is used to treat conditions arising from calcium deficiencies such as hypocalcemic tetany, hypocalcemia related to hypoparathyroidism and hypocalcemia due to rapid growth or pregnancy. It is also used in the treatment of black widow spider bites to relieve muscle cramping and as an adjunct in the treatment of rickets, osteomalacia, lead colic and magnesium sulfate overdosage. Calcium gluconate has also been employed to decrease capillary permeability in allergic conditions, nonthrombocytopenic purpura and exudative dermatoses such as dermatitis herpetiformis and for pruritus of eruptions caused by certain drugs. In hyperkalemia, calcium gluconate may aid in antagonizing the cardiac toxicity, provided the patient is not receiving digitalis therapy.
Calcium Gluconate Injection, USP is a sterile, nonpyrogenic, supersaturated solution of calcium gluconate for intravenous use only.
Each mL contains: Calcium gluconate 94 mg; calcium saccharate (tetrahydrate) 4.5 mg; water for injection q.s. Hydrochloric acid and/or sodium hydroxide may have been added for pH adjustment (6.0 to 8.2).
Calcium saccharate provides 6% of the total calcium and stabilizes the supersaturated solution of calcium gluconate.
Each 10 mL of the injection provides 93 mg elemental calcium (Ca++) equivalent to 1 g of calcium gluconate.
The dose is dependent on the requirements of the individual patient. Intravenous calcium gluconate injection must be administered slowly.
Adults—500 mg to 2 g (5 to 20 mL)
Pediatric patients—200 to 500 mg (2 to 5 mL)
Infants—Not more than 200 mg (not more than 2 mL)
Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.
The dose is dependent on the requirements of the individual patient. Intravenous calcium gluconate injection must be administered slowly.
Adults—500 mg to 2 g (5 to 20 mL)
Pediatric patients—200 to 500 mg (2 to 5 mL)
Infants—Not more than 200 mg (not more than 2 mL)
Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.
The dose is dependent on the requirements of the individual patient. Intravenous calcium gluconate injection must be administered slowly.
Usual Dosage
Adults—500 mg to 2 g (5 to 20 mL)
Pediatric patients—200 to 500 mg (2 to 5 mL)
Infants—Not more than 200 mg (not more than 2 mL)
Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.
Usual Dosage
Adults—500 mg to 2 g (5 to 20 mL)
Pediatric patients—200 to 500 mg (2 to 5 mL)
Infants—Not more than 200 mg (not more than 2 mL)
Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.
Cattle: 250 mL to 500 mL. Administer intravenously or intraperitoneally. Solution should be warmed to body temperature and administered slowly.
This product is sterile in unopened container. It contains no preservative. Use entire contents when first opened. Discard any unused portion. Handle under aseptic conditions. If there is no apparent improvement in the animal's condition within 24 hours, consult a veterinarian.
Cattle: 250 to 500 mL Administer intravenously or intraperitoneally. Solution should be warmed to body temperature and administered slowly. This product is sterile in unopened container. It contains no preservative. Use entire contents when first opened. It should be handled under strict aseptic conditions. If there is no apparent improvement in the animal's condition within 24 hours, consult a veterinarian.
DOSAGE AND ADMINISTRATION: Cattle: 250 mL to 500 mL. Administer intravenously or intraperitoneally. Solution should be warmed to body temperature and administered slowly.
This product is sterile in unopened container. It contains no preservative. Use entire contents when first opened. Discard any unused portion. Handle under aseptic conditions. If there is no apparent improvement in the animal's condition within 24 hours, consult a veterinarian.
Administer intravenously, intraperitoneally or subcutaneously. If given subcutaneously, divide dosage among several injection sites and massage to aid in absorption.
Solution should be warmed to body temperature and administered slowly. This product is sterile in unopened container. It contains no preservative. Use entire contents when first opened. It should be handled under aseptic conditions.
Calcium Gluconate should be administered intravenously either directly or by infusion. The dose is dependent upon the individual requirements of the patient. Calcium Gluconate may also be administered by intermittent infusion at a rate not exceeding 200 mg/min, or by continuous infusion.
DIRECTIONS FOR DISPENSING FROM 100 mL PHARMACY BULK PACKAGE - NOT FOR DIRECT INFUSION.
The 100 mL Pharmacy Bulk Package is for use in a Pharmacy Admixture Service only. The 100 mL Pharmacy Bulk Package should be suspended (inverted) by its IV hang label in a laminar flow hood or biological safety cabinet. Prior to entering a Pharmacy Bulk Package remove the flip-off seal and cleanse the rubber closure with a suitable antiseptic agent. Entry into the Pharmacy Bulk Package must be made with a sterile transfer set or other sterile dispensing device and the contents dispensed in aliquots using aseptic technique. Use of a syringe needle is not recommended as it may cause leakage. ANY UNUSED PORTION MUST BE DISCARDED
WITHIN 4 HOURS AFTER INITIAL ENTRY. The date and the time initially opened should be recorded in the space provided on the Pharmacy Bulk Package label.
USUAL DOSAGE:
Adults: 500 mg - 2 grams (5-20 mL)
Children: 200-500 mg (2-5 mL)
Infants: not more than 200 mg (not more than 2 mL)
Calcium Gluconate | General Injectables & Vaccines, Inc.
Calcium Gluconate should be administered intravenously either directly or by infusion. The dose is dependent upon the individual requirements of the patient. Calcium Gluconate may also be administered by intermittent infusion at a rate not exceeding 200 mg/min, or by continuous infusion.
DIRECTIONS FOR DISPENSING FROM 100 mL PHARMACY BULK PACKAGE - NOT FOR DIRECT INFUSION.
The 100 mL Pharmacy Bulk Package is for use in a Pharmacy Admixture Service only. The 100 mL Pharmacy Bulk Package should be suspended (inverted) by its IV hang label in a laminar flow hood or biological safety cabinet. Prior to entering a Pharmacy Bulk Package remove the flip-off seal and cleanse the rubber closure with a suitable antiseptic agent. Entry into the Pharmacy Bulk Package must be made with a sterile transfer set or other sterile dispensing device and the contents dispensed in aliquots using aseptic technique. Use of a syringe needle is not recommended as it may cause leakage. ANY UNUSED PORTION MUST BE DISCARDED WITHIN 4 HOURS AFTER INITIAL ENTRY. The date and the time initially opened should be recorded in the space provided on the Pharmacy Bulk Package label.
USUAL DOSAGE:
Adults: 500 mg - 2 grams (5-20mL)
Children: 200-500 mg (2-5 mL)
Infants: not more than 200 mg (not more than 2 mL)
The dose is dependent on the requirements of the individual patient. Intravenous calcium gluconate injection must be administered slowly.
Usual Dosage
Adults—500 mg to 2 g (5 to 20 mL)
Pediatric patients—200 to 500 mg (2 to 5 mL)
Infants—Not more than 200 mg (not more than 2 mL)
Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.
Usual Dosage
Adults—500 mg to 2 g (5 to 20 mL)
Pediatric patients—200 to 500 mg (2 to 5 mL)
Infants—Not more than 200 mg (not more than 2 mL)
Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.
For use as a dietary supplement in adults, take 1 to 16 tablets per day, in divided doses, preferably 1 to 2 hours after meals, or as directed by a physician.
Do not use if printed foil under cap is broken of missing.
Keep bottle tightly closed. Store in a cool, dry place, out of reach of children. In case of overdose, get medical help or contact a Poison Control Center immediately.
As with any supplement, if you are pregnant or nursing a baby, contact your healthcare professional.
Questions or Comments?
Call 1-800-962-8364
You may also report serious side effects to this phone number.
The dose is dependent on the requirements of the individual patient. Intravenous calcium gluconate injection must be administered slowly.
Usual Dosage
Adults—500 mg to 2 g (5 to 20 mL)
Pediatric patients—200 to 500 mg (2 to 5 mL)
Infants—Not more than 200 mg (not more than 2 mL)
Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.
Usual Dosage
Adults—500 mg to 2 g (5 to 20 mL)
Pediatric patients—200 to 500 mg (2 to 5 mL)
Infants—Not more than 200 mg (not more than 2 mL)
Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.
Calcium Gluconate | Bimeda, Inc., Division Of Cross Vetpharm Group
DOSAGE AND ADMINISTRATION:
Cattle: 250 mL to 500 mL. Administer intravenously or intraperitoneally. Solution should be warmed to body temperature and administered slowly. This product is sterile in unopened container. It contains no preservative. Use entire contents when first opened. Discard any unused portion. Handle under aseptic conditions.
If there is no apparent improvement in the animal's condition within 24 hours, consult a veterinarian.
Administer intravenously. Solution should be warmed to body temperature and administered slowly. This product is sterile in unopened container. It contains no preservative. Use entire contents when first opened. It should be handled under aseptic conditions. If there is no apparent improvement in the animal's condition within 24 hours; consult a veterinarian.
Administer intravenously. Solution should be warmed to body temperature and administered slowly. This product is sterile in unopened container. It contains no preservative. Use entire contents when first opened. It should be handled under aseptic conditions. If there is no apparent improvement in the animal's condition within 24 hours; consult a veterinarian.
Solution should be warmed to body temperature and administered slowly. This product is sterile in unopened container. It contains no preservative. Use entire contents when first opened. It should be handled under aseptic conditions. If there is no apparent improvement in the animal's condition within 24 hours, consult a veterinarian.
Administer intravenously or intraperitoneally. Solution should be warmed to body temperature and administered slowly. This product is sterile in unopened container. It contains no preservative. Use entire contents when first opened. it should be handled under aseptic conditions. If there is no apparent improvement in the animal's condition within 24 hours, consult a veterinarian.
Cattle: 250 to 500 mL Administer intravenously, intraperitoneally or subcutaneously. If given subcutaneously, divide dosage among several injection sites and massage to aid in absorption. Solution should be warmed to body temperature and administered slowly. This product is sterile in unopened container. It contains no preservative. Use entire contents when first opened. It should be handled under aseptic conditions. If there is no apparent improvement in the animal's condition within 24 hours, consult a vetrinarian.
Calcium Gluconate | General Injectables & Vaccines, Inc
The dose is dependent on the requirements of the individual patient. Intravenous calcium gluconate injection must be administered slowly.
Usual Dosage
Adults-500 mg to 2 g (5 to 20 mL)
Pediatric Patients-200 to 500 mg (2 to 5 mL)
Infants-Not more than 200 mg (not more than 2 mL)
Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.
•
this product does not contain directions or complete warnings for adult use
•
do not give more than directed (see overdose warning)
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shake well before using
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mL = milliliter
•
find right dose on chart. If possible, use weight to dose; otherwise, use age.
•
push air out of syringe. Insert syringe tip into bottle opening.
•
flip bottle upside down. Pull yellow part of syringe to the first dose line and then push product back into bottle.
•
pull yellow part of syringe until it reaches and stays at the correct dose
•
dispense liquid slowly into child’s mouth, toward inner cheek
•
repeat dose every 4 hours while symptoms last
•
do not give more than 5 times in 24 hours
•
replace cap tightly to maintain child resistance
Dosing Chart
Weight (lb)
Age (yr)
Dose (mL)*
under 24
under 2 years
ask a doctor
24-35
2-3 years
5 mL
* or as directed by a doctor
Attention: use only enclosed syringe specifically designed for use with this product. Do not use any other dosing device.