Propofol injectable emulsion is an intravenous general anesthetic and sedation drug indicated for: Induction of General Anesthesia for Patients Greater than or Equal to 3 Years of Age, Maintenance of General Anesthesia for Patients Greater than or Equal to 2 Months of Age, Initiation and Maintenance of Monitored Anesthesia Care (MAC) Sedation in Adult Patients, Sedation for Adult Patients in Combination with Regional Anesthesia, Intensive Care Unit (ICU) Sedation of Intubated, Mechanically Ventilated Adult Patients.
From the U.S. FDA-approved label for Propofol. Full label: DailyMed.
Propofol injectable emulsion is an intravenous general anesthetic and sedation drug indicated for: Induction of General Anesthesia for Patients Greater than or Equal to 3 Years of Age, Maintenance of General Anesthesia for Patients Greater than or Equal to 2 Months of Age, Initiation and Maintenance of Monitored Anesthesia Care (MAC) Sedation in Adult Patients, Sedation for Adult Patients in Combination with Regional Anesthesia, Intensive Care Unit (ICU) Sedation of Intubated, Mechanically Ventilated Adult Patients.
From the U.S. FDA-approved label for Propofol. Full label: DailyMed.
See Full Prescribing Information for detailed dosing instructions. 2.1 Important Dosage and Administration Information Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration whenever solution and container permit. Shake well before use.
Directions from the U.S. FDA-approved label for Propofol — your doctor or pharmacist may advise differently.
Propofol injectable emulsion is contraindicated in patients with a known hypersensitivity to propofol or any of propofol injectable emulsion components. Propofol injectable emulsion is contraindicated in patients with a history of anaphylaxis to eggs, egg products, soybeans or soy products. Known hypersensitivity to propofol, egg or soybean
Excerpt from the U.S. FDA-approved label for Propofol. Talk to a pharmacist or doctor before use.
Hypersensitivity Reactions: Serious and sometimes fatal reactions Microbial Contamination: Strict aseptic technique must be maintained during handling. Propofol injectable emulsion vials are never to be accessed more than once or used on more than one person. Administration should commence promptly and be completed within 12 hours after the vial has been opened. Discard unused drug product. Do not use if contamination is suspected Cardiovascular Depression: Cases of bradycardia, asystole, and cardiac arrest have been reported.
Warnings and precautions excerpt from the U.S. FDA-approved label for Propofol — not a complete list. Talk to a pharmacist or doctor before use.
The following serious or otherwise important adverse reactions are discussed elsewhere in the labeling: Hypersensitivity reaction, Hypotension and/or bradycardia, Propofol Infusion Syndrome In the description below, rates of the more common events represent US/Canadian clinical study results. Less frequent events are also derived from publications and marketing experience in over 8 million patients;
Excerpt from the U.S. FDA-approved label for Propofol — not a complete list. Talk to a pharmacist or doctor about side effects.
5 brands · 4 makers in the NepalDoc catalog — see the full Propofol guide →
Store at 20°C to 25°C (68°F to 77°F).. Do not freeze. Shake well before use.
Storage information from the U.S. FDA-approved label for Propofol.
What is PROPOVAN?
PROPOVAN 1% AMP is a Propofol medicine made by Baxter Healthcare. It comes as 1% AMP.
What is the generic name of PROPOVAN?
The generic name of PROPOVAN is Propofol.
Which brands of Propofol are available in Nepal?
5 brands of Propofol are listed in the NepalDoc catalog, from 4 makers — including Neorof Injection, PROVIVE 1% Injection, Rapifol 10mg Injection, Rapifol 50mg Injection.
What are the side effects of Propofol?
The following serious or otherwise important adverse reactions are discussed elsewhere in the labeling: Hypersensitivity reaction, Hypotension and/or bradycardia, Propofol Infusion Syndrome In the description below, rates of the more common events represent US/Canadian clinical study results.
This page is information only and is not medical advice. Medicine details come from the sources listed above and may change — always confirm the medicine, strength and dose with a pharmacist or doctor before use. A catalog listing does not guarantee that a medicine is in stock at any pharmacy.
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