GUAIFENESIN INJECTION | |
| Vedco Product No.: | |
| ANADA 200-230, Approved by FDA | |
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| Material Safety Data Sheet | |
| Active Ingredients: | 50 mg per mL Guaifenesin, 3 - lo-Methoxyphenoxyl -1,2-propanediol, is a white to slightly gray, crystalline powder having a bitter taste. It may have a slight characteristic odor. Each mL of the injection contains: 50 mg guaifenesin, 50 mg dextrose (anhydrous), 20 mg propylene glycol), ~O mg dimethylacetamide (parenteral grade), 0.75 mg edetate disodium, water for injection q.s. |
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| Indications: | For intravenous use as a skeletal muscle relaxant for horses. ACTIONS: Guaifenesin is a guaiacol derivative closely related to mephenesin. The propanediol derivatives are central-acting skeletal muscle relaxants which selectively depress transmission of nerve impulses at the internuncial neurons of the spinal cord, brainstem, and subcortical regions of the brain. Propanediol derivatives have a wide margin of safety, the toxic dose is three times greater than the recommended dose. Respiration is not severely depressed, and the function of the diaphragm is uninterrupted. Tidal volume is slightly decreased and minute volume remains normal. In addition to skeletal muscle, the pharyngeal and laryngeal muscles are sufficiently relaxed for easier surgical intubation procedures. At the beginning of relaxation, there is a slight fall in blood pressure, however, throughout the relaxation period the heart function is unchanged. There is a slight increase in gastrointestinal activity. There is no apparent impairment of lung and kidney functions. With the recommended administration and dosage of Guaifenesin Injection, induction is usually smooth and rapid (two to four minutes) providing a duration of action between 15 to 25 minutes. A slightly transient hemolysis occurs at a 5% concentration. Higher concentrations cause intravascular hemolysis. The 5% dextrose minimizes the hemolytic action of Guaifenesin alone and reduces the tendency to form thrombi at the intravenous injection site. Guaifenesin appears safe when administered to pregnant mares and in human studies did not pass the placental barrier. Metabolism and excretion of guaifenesin not well understood. Oxidation products are excreted in the urine as a glycuronimide. |
| Precautions: | Avoid perivascular leakage to prevent local tissue irritation. If used for prolonged periods, such as in tetanus, serum hemoglobin levels should be monitored. Oxygen or sustained artificial respiration facilities should be available when the drug is employed. Additional care should be employed when administering the drug to anemic or hypovolemic animals with cardiac or respiratory problems. Extreme care should be exercised at all times in handling this product to prevent the introduction of microbial contamination. DOSAGE AND ADMINISTRATION For intravenous use only. Administer rapidly with a positive pressure system or gravity flow using a 12 to 14 gauge needle at the dose rate of 1 mL/pound of body weight. From a standing position the patient will begin to relax and gradually fall when approximately 1/2 the total dose has been given. Continue the remaining calculated dose for complete relaxation. Average duration of muscle relaxation is 10-25 minutes. For continued relaxation time, additional Guaifenesin Injection may be administered as determined by the veterinarian at a rate necessary to achieve the desired plane of relaxation. Recovery is usually smooth and uneventful with the horse regaining an upright position usually within 45 minutes after the medication is discontinued. FOR INTRAVENOUS USE IN HORSES ONLY |
| Warning: | Not to be used in horses intended for food. Store between 2° and 30°C (36° and 86°F). Do not freeze. Destroy partially used vials. PRECAUTIONS: Avoid perivascular leakage to prevent local tissue irritation. If used for prolonged periods, such as in tetanus, serum hemoglobin levels should be monitored. Oxygen or sustained artificial respiration facilities should be available when the drug is employed. Additional care should be employed when administering the drug to anemic or hypovolemic animals with cardiac or respiratory problems. Extreme care should be exercised at all times in handling this product to prevent the introduction of microbial contamination. DOSAGE AND ADMINISTRATION For intravenous use only. Administer rapidly with a positive pressure system or gravity flow using a 12 to 14 gauge needle at the dose rate of 1 mL/pound of body weight. From a standing position the patient will begin to relax and gradually fall when approximately 1/2 the total dose has been given. Continue the remaining calculated dose for complete relaxation. Average duration of muscle relaxation is 10-25 minutes. For continued relaxation time, additional Guaifenesin Injection may be administered as determined by the veterinarian at a rate necessary to achieve the desired plane of relaxation. Recovery is usually smooth and uneventful with the horse regaining an upright position usually within 45 minutes after the medication is discontinued. FOR INTRAVENOUS USE IN HORSES ONLY CAUTIONs: Federal law restricts this drug to use by or on the order of a licensed veterinarian. warnings: |
| Presentation & Packaging: | 1,000 mL sterile, single dose plastic vial. |
Material Safety Data Sheet | |
VEDCO GUAIFENESIN INJECTION | |
| Section 1: General Information | |
| Manufacturer: Phoenix Scientific Inc. Address: 3915 S. 48Th Street Terrace St. Joseph MO 64503 Emergency Telephone Number: 816-364-3777 or 816-253-9341 Trade name and synonyms: Guaifenesin Injection Chemical name and synonyms: Guaifenesin Injection Chemical Family: Veterinary Expectorant Formula: N/A | |
| Section 2: Ingredients | |
| N/A | |
| Section 3: Physical Data | |
| Boiling Point (*F): 102°C Vapor Pressure (mm Hg): N/A Vapor density (air=1):N/A Solubility in water: Miscible Appearance and odor: Clear, Practically colorless solution with characteristic odor of Guaifenesin Specific Gravity(h20=1): 1.1 Percent volatile by volume(%) N/A Evaporation rate: N/A | |
| Section 4: Fire and Explosion Data | |
| Flash Point (method used): N/A Flammable Limits: N/A Extinguishing media: As appropriate for surrounding material Unusual fire and explosion hazards: None Special Fire Fighting Procedures: None | |
| Section 5: Health Hazard | |
| Threshold limit value: N/A Effects of overexposure Nausea, vomiting, shortness of breath Emergency First Aid Procedures Contact nearest poison control center. Eyes: Flush eyes with water for 15 minutes. Seek medical attention if irritation persists. Skin: Wash with soap and water. Seek medical attention if irritation persists. Inhalation: Remove victim to fresh air. Apply artificial respiration if needed. Ingestion: Induce vomiting if victim is conscious. (Never induce vomiting in an unconscious person). Seek medical attention if adverse reactions occur. | |
| Section 6: Reactivity Data | |
| Stability: Stable(xx)Unstable ( ) Incompatibility( materials to avoid): None Hazardous Decomposition Products: None Hazardous polymerization: Will occur ( )will not occur(xx) Conditions to avoid: N/A | |
| Section 7: Spill or Leak Procedures | |
| Steps to be taken in case material is released or spilled: Flush to drain using plenty of water. Waste disposal method: As per local, state and federal regulations. | |
| Section 8: Special Protection Information | |
| Respiratory protection Ventilation: None normally required. Protective gloves: If desired. Eye Protection: Safety goggles. Other protective equipment: Special protective equipment not normally needed. | |
| Note | |
| The information contained in this material safety data sheet is provided in good faith and is accurate to the best of our knowledge. However, the manufacturer assumes no warranties expressed or implied. Users of these products are advised to verify that the information is suitable to their particular purposes prior to their use of them. | |