LACTEC SODIUM CHLORIDE INJECTION 250mL x 20 Bags

LACTEC SODIUM CHLORIDE INJECTION 250mL x 20 Bags

LACTEC SODIUM CHLORIDE INJECTION, known in Japan as ラクテック注, is a Japanese intravenous electrolyte infusion solution manufactured by 株式会社大塚製薬工場 / Otsuka Pharmaceutical Factory, Inc.. This product is supplied as 250mL bags, with 20 bags per case.

ラクテック注 is an L-lactate sodium Ringer’s solution used for the supplementation and correction of extracellular fluid in clinical settings. It is indicated for decreased circulating blood volume, reduced interstitial fluid and correction of metabolic acidosis under medical supervision.

Product Information

• Product Name: LACTEC SODIUM CHLORIDE INJECTION 250mL x 20 Bags
• Japanese Name: ラクテック注
• Chinese Name: ラクテック注氯化鈉生理鹽水 / 乳酸林格氏液
• Common Name: Lactec Injection / Lactated Ringer Solution / L-Lactate Sodium Ringer Solution
• Dosage Form: Injectable infusion solution
• Route: Intravenous drip infusion
• Specification: 250mL x 20 bags / pcs
• Package: 250mL infusion bag, 20 bags per case
• Product Type: Electrolyte infusion / extracellular fluid replacement solution
• Manufacturer: 株式会社大塚製薬工場 / Otsuka Pharmaceutical Factory, Inc.
• Origin: Japan

Key Features

• Japanese intravenous electrolyte infusion solution
• 250mL infusion bag format
• 20 bags per case
• L-lactate sodium Ringer’s solution
• Used for extracellular fluid replacement
• Supports correction of metabolic acidosis in appropriate clinical settings
• For intravenous drip infusion under healthcare professional supervision

Indications

ラクテック注 is used for the following purposes under medical supervision:

• Supplementation and correction of extracellular fluid
• Fluid replacement in decreased circulating blood volume
• Correction of reduced interstitial fluid
• Correction of metabolic acidosis

Dosage and Administration

For adults, the usual dose is administered by intravenous drip infusion. Dosage and infusion rate should be determined by a doctor or qualified healthcare professional based on the patient’s age, symptoms, body weight, clinical condition and fluid-electrolyte status.

• Usual adult dose: 500mL to 1000mL by intravenous drip infusion
• Usual infusion rate: Approximately 300mL to 500mL per hour
• Adjustment: Dose and rate should be adjusted according to age, condition, body weight and medical judgment
• Administration route: Intravenous drip infusion only

This product must be administered only by trained medical professionals or under appropriate healthcare supervision.

Contraindication

Do not administer this product to patients with the following condition unless specifically determined by a healthcare professional:

• Lactic acidosis: Administration may worsen the condition

Special Precautions

Use caution and close monitoring in patients with the following conditions:

• Heart failure: Increased circulating blood volume may worsen symptoms
• Hypertonic dehydration: Electrolyte-containing fluid may worsen symptoms
• Urinary tract obstruction: Impaired excretion of water and electrolytes may worsen the condition
• Renal impairment: Risk of excessive fluid and electrolyte retention
• Severe liver dysfunction: Risk of worsening acid-base balance and lactic acidosis
• Elderly patients: Careful monitoring and dose adjustment may be required
• Pregnancy or breastfeeding: Use only when the expected therapeutic benefit outweighs possible risk
• Pediatric patients: Safety and efficacy may not be fully established

Possible Side Effects

Side effects may occur during or after administration. Medical monitoring is required during infusion.

• Rash
• Urticaria
• Itching or pruritus
• Hypersensitivity reactions
• Pulmonary edema, especially with rapid or excessive administration
• Cerebral edema, especially with rapid or excessive administration
• Peripheral edema, especially with rapid or excessive administration
• Fluid overload
• Electrolyte imbalance

Handling and Administration Notes

• Use only under appropriate aseptic conditions
• Do not use if the bag is damaged, leaking or discolored
• Check solution clarity before administration
• Do not use if visible particles or contamination are present
• Insert needle or spike vertically into the designated port
• Avoid repeated puncture at the same site
• Confirm compatibility before mixing with other medicines
• Avoid administration with incompatible drugs
• Avoid tandem connection if it may cause air embolism risk
• Ensure that no air enters the infusion system
• Use immediately after opening according to medical facility protocol

Important Medical Notice

This product is a medical intravenous infusion solution. It is not a general health supplement and should not be self-administered. It must be used only in appropriate medical settings by or under the supervision of healthcare professionals.

Storage

Store according to the package insert and official labeling. Keep away from direct sunlight, excessive heat and freezing. Keep out of reach of children. Do not use after the expiry date printed on the package.

Disclaimer

This product information is provided for general reference only and does not replace medical advice, diagnosis, treatment, prescription instructions, package insert information, official labeling or local regulatory requirements. Always follow the instructions of a doctor, pharmacist or qualified healthcare professional.