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PYROLATE 0.2MG/ML
PYROLATE 0.2MG/ML
PYROLATE 0.2MG/ML
PYROLATE 0.2MG/ML
PYROLATE 0.2MG/ML
PYROLATE 0.2MG/ML
PYROLATE 0.2MG/ML
PYROLATE 0.2MG/ML
PYROLATE 0.2MG/ML
PYROLATE 0.2MG/ML
PYROLATE 0.2MG/ML
PYROLATE 0.2MG/ML

PYROLATE 0.2MG/ML

Price 11.4 INR/ Unit

MOQ : 50 Units

PYROLATE 0.2MG/ML Specification

  • Pacakaging (Quantity Per Box)
  • 5 ampoules
  • Origin of Medicine
  • Allopathic
  • Life Span
  • 24 MONTHS
  • Dosage Form
  • Injection
  • Salt Composition
  • Glycopyrrolate 0.2mg/ml
  • Indication
  • Reduction of secretions, reversal of neuromuscular blockade, prevention of bradycardia during anesthesia
  • Drug Type
  • Other
  • Ingredients
  • PYROLATE INJECTION - Glycopyrrolate Injection I.P. Brand: PYROLATE Injection Content: Glycopyrrolate I.P. 0.2 mg / ml Company / Manufacturer: Neon Laboratories Ltd Pack: 1 ml Ampoule Category: Anticholinergic Agent / Antimuscarinic Drug Product Description PYROLATE Injection contains Glycopyrrolate, a synthetic quaternary ammonium anticholinergic agent formulated for parenteral administration. It is extensively utilized in pre-anesthetic medication, operating rooms, and intensive care settings to reduce salivary, tracheobronchial, and pharyngeal secretions before surgery. This sterile injectable medication also helps block cardiac vagal inhibitory reflexes during anesthesia induction and intubation, and protects against the adverse muscarinic side effects triggered by neuromuscular blockade reversal agents. Key Uses Pre-anesthetic medication to reduce salivary, tracheobronchial, and pharyngeal secretions before surgeries Protection against cardiac vagal inhibitory reflexes during anesthesia induction and intubation Prevention of peripheral muscarinic side effects induced by cholinergic drugs like neostigmine Adjunctive therapy in gastric ulcer management where reduction of gastric secretions is needed How It Works Glycopyrrolate works by competitively blocking the action of acetylcholine at postganglionic muscarinic receptors found in smooth muscle, cardiac muscle, and exocrine glands. As a quaternary ammonium compound, it does not easily cross the blood-brain barrier, which minimizes central nervous system side effects like sedation or confusion. By inhibiting these muscarinic receptors, it efficiently decreases body secretions, reduces gastric acidity, and prevents bradycardia or slow heart rate drops during anesthesia. Directions for Use Administer via intramuscular or intravenous injection routes based on clinical requirements Visually inspect the sterile fluid inside the glass ampoule for any particulate matter or discoloration before drawing Can be mixed in the same syringe with specific pre-anesthetic medications as per institutional protocols Must be prepared and administered exclusively by an anesthesiologist, clinician, or trained healthcare professional Key Features High-potency antimuscarinic action that provides prolonged reduction of airway secretions Quaternary structure ensures highly targeted peripheral action with minimal risk of central drowsiness Formulated in a stable, clear solution format packed in convenient single-use sterile glass ampoules Processed and certified under stringent quality control standards by Neon Laboratories Ltd Important Safety Notes Storage Temperature: Store below 30 C in a cool, dry place. Protect from direct light and do not freeze. Contraindicated in patients with glaucoma, mechanical urinary tract obstruction, or intestinal obstruction Exercise extreme caution in patients with coronary artery disease, rapid heart rates, or high blood pressure Schedule H Prescription Drug: Strictly intended for hospital institutional trade and supply to verified buyers with drug licenses
  • Physical Form
  • Other
  • Function
  • Other
  • Recommended For
  • As directed by the physician
  • Dosage
  • Dosage as prescribed by the physician
  • Dosage Guidelines
  • Intravenous or intramuscular use
  • Quantity
  • 50 Boxes
  • Storage Instructions
  • Store below 25 C. Protect from light. Do not freeze.
  • Marketed By
  • Samarth Life Sciences Pvt. Ltd.
  • Strength
  • 0.2MG/ML
  • Regulatory Status
  • Rx Only
  • Molecule
  • Glycopyrrolate Injection
  • Therapeutic Class
  • Antimuscarinic agent
  • Common Side Effects
  • Dry mouth, blurred vision, tachycardia, urinary retention
  • Brand Name
  • PYROLATE
  • Appearance
  • Clear, colorless solution
  • Route of Administration
  • IV / IM
  • Shelf Life
  • 24 months from the date of manufacture
 

PYROLATE 0.2MG/ML Trade Information

  • Minimum Order Quantity
  • 50 Units
  • Supply Ability
  • 1000 Units Per Month
  • Delivery Time
  • 7 Days
  • Sample Available
  • No
 

About PYROLATE 0.2MG/ML

BRAND NAME : PYROLATE 0.2MG/ML
CONTENT : GLYCOPYRROLATE INJECTION I.P
COMPANY NAME : NEON
PACKING : 10X5 AMPOULES OF 1ML
RATE : 11.01
MRP : 16.12

Given rate is negotiable for bulk quantity.


Key Benefits and Indications

PYROLATE 0.2MG/ML effectively reduces oral, respiratory, and gastrointestinal secretions. It helps prevent bradycardia during anesthesia and supports the reversal of neuromuscular blockade, making it valuable in surgical and critical care settings. This antimuscarinic agent ensures smoother perioperative management and enhances patient safety under anesthesia.


How to Use PYROLATE Safely

PYROLATE should be administered only as directed by a qualified healthcare professional, either intravenously or intramuscularly. Dosage and frequency depend on the physician's assessment of your health condition and treatment goals. It is important to follow all medical advice and never self-administer or adjust the prescribed regimen.


Storage and Handling Recommendations

To maintain potency, PYROLATE must be stored below 25C, kept away from light, and never frozen. Each ampoule is designed for single-use, reducing contamination risks. Check the expiry date before use (24 months shelf life from manufacture), and always consult your healthcare provider for guidance regarding disposal or handling queries.

FAQ's of PYROLATE 0.2MG/ML:


Q: How should PYROLATE 0.2MG/ML be administered?

A: PYROLATE 0.2MG/ML should be given only by a healthcare professional, using either intravenous (IV) or intramuscular (IM) injection, as directed by a physician.

Q: What are the primary uses of PYROLATE?

A: PYROLATE is primarily indicated for reducing secretions, preventing bradycardia during anesthesia, and aiding in the reversal of neuromuscular blockade in medical and surgical procedures.

Q: When is the appropriate time to use PYROLATE?

A: PYROLATE is given before or during anesthesia, or as part of the recovery from certain procedures, following your doctor's instructions based on your specific medical situation.

Q: Where should I store PYROLATE ampoules?

A: You should store PYROLATE below 25C, away from light, and do not freeze the ampoules. Always keep the medication out of reach of children.

Q: What are the common side effects of PYROLATE?

A: Common side effects include dry mouth, blurred vision, rapid heartbeat (tachycardia), and difficulty urinating. Contact your healthcare provider if side effects are persistent or concerning.

Q: What is the process for receiving PYROLATE treatment?

A: After prescription, your healthcare provider will administer PYROLATE by injection. The dosage and schedule are tailored individually, and you will be closely monitored during and after treatment for safety.

Q: What benefits does PYROLATE offer during surgical procedures?

A: PYROLATE minimizes oral and respiratory secretions, helps maintain stable heart rates during anesthesia, and assists in the safe reversal of muscle relaxants, contributing to improved patient comfort and safety.

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