We have an updated report [Version - 2024] available. Kindly sign up to get the sample of the report.
all report title image

GENERAL ANESTHESIA DRUGS MARKET ANALYSIS

General Anesthesia Drugs Market, By Drug molecule (Desflurane, Isoflurane, Sevoflurane, Propofol, Etomidate, Methohexital, hiopentone, Midazolam, Ketamine), By Route of Administration (Intravenous Anesthesia, Inhalation Anesthesia), By End User (Hospital, Specialty Clinics, Ambulatory Surgical Centers), By Geography (North America, Latin America, Europe, Asia Pacific, Middle East, and Africa)

  • Published In : Aug 2023
  • Code : CMI524
  • Pages :200
  • Formats :
      Excel and PDF
  • Industry : Pharmaceutical

Leading Companies

Key players are making  development of anesthesia drug and regulations of these drugs are emerging economies is also expected to boost demand of general anesthesia drug market in North America region. For instance, in May 2020, Hikma Pharmaceuticals PLC, a multinational generic drug pharmaceutical company, got quick approval from U.S. Food and Drug Administration (FDA) approval for propofol injectable emulsions during the COVID-19 outbreak, as there was surge in the demand for propofol as it was being used to as a sedative for the COVID-19 patients who were ventilated.

In April 2022, GE Healthcare, a U.S.-based multinational healthcare and medical technology company,  received the U.S. Food and Drugs Approval (FDA) pre-market approval (PMA) for its End-tidal (Et) control software for general anesthesia delivery on its Aisys CS2 Anesthesia Delivery System. The device is to have a direct control of the end-tidal concentration that reflects the drug level in the patient’s blood along with that low-flow anesthesia has benefits for hospitals and the environment.

In September 2021, Medical University of Vienna had positive results from Phase IV for ADV6209 which is a new oral Midazolam formulation, on preoperative anxiety and sedation levels in paediatric anaesthesia.

In May 2021, Heron Therapeutics, Inc., a multinational  biotechnology company, announced the U.S. Food and Drug Administration (FDA) approval for ZYNRELEF, which is indicated in adults for soft tissue to produce postsurgical analgesia for up to 72 hours after small-to-medium open abdominal, foot and ankle, and lower extremity total joint arthroplasty surgical procedures.

Need a Custom Report?

We can customize every report - free of charge - including purchasing stand-alone sections or country-level reports

Customize Now
Logo

Credibility and Certifications

ESOMAR
DUNS Registered
Clutch
DMCA Protected

9001:2015

Credibility and Certifications

27001:2022

Credibility and Certifications

EXISTING CLIENTELE

Joining thousands of companies around the world committed to making the Excellent Business Solutions.

View All Our Clients
trusted clients logo
© 2024 Coherent Market Insights Pvt Ltd. All Rights Reserved.