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Coronavirus (COVID-19) Update: April 30, 2021

For Speedy Launch:

The U.S. Meals and Drug Administration at this time introduced the next actions taken in its ongoing response effort to the COVID-19 pandemic:

  • On April 28, the FDA permitted an abbreviated new drug software (ANDA) for 23.4% Sodium Chloride Injection USP, 120 mEq/30 mL (4 mEq/mL) single dose vial, indicated as an additive in parenteral (injection) fluid remedy to be used in sufferers who’ve particular issues of sodium electrolyte consumption or excretion (to replenish sodium in sufferers with uncommon fluid and electrolyte wants). Unwanted effects embrace edema (fluid retention) and medical signs resembling these of congestive coronary heart failure. 
  • On April 28, the FDA up to date the EUA Approved Serology Check Efficiency web page on the FDA’s web site.The FDA offered info on the anticipated predictive worth of approved serology exams which have submitted efficiency information with SARS-CoV-2 antibody prevalence assumptions starting from 5% to 50%. These estimates could assist well being care suppliers interpret these antibody take a look at outcomes for his or her sufferers.  Moreover, the up to date internet web page clarifies the usage of serology exams when assessing a affected person’s adaptive immune response.
  • On April 29, the FDA permitted an ANDA for Morphine Sulfate Injection USP, 30 mg/30 mL (1 mg/1 mL) Single-dose (preservative-free Affected person Managed Analgesia [PCA] vial), indicated for the administration of ache extreme sufficient to require use of an opioid analgesic by PCA and for which different therapies are insufficient. Unwanted effects embrace respiratory melancholy, respiratory arrest, circulatory melancholy, shock, and cardiac arrest. The FDA acknowledges the elevated demand for sure merchandise in the course of the COVID-19 public well being emergency, and we stay dedicated to facilitating entry to medical merchandise to assist handle crucial wants of the American public.
  • On April 30, the FDA revoked the emergency use authorization (EUA) of the Battelle CCDS Important Care Decontamination System, which was approved to be used in decontaminating appropriate N95 respirators for multiple-user reuse by healthcare personnel. The FDA revoked the EUA in response to Battelle’s request for voluntary withdrawal of the authorization. In response to altering buyer wants, as of March 31, 2021, Battelle has ceased all Battelle CCDS decontamination web site operations and advertising and marketing actions. As a reminder, decontaminated respirators and respirators which have undergone bioburden discount ought to be used solely when there are inadequate provides of recent filtering facepiece respirators (FFRs) or any new respirators. Furthermore, earlier this month, the FDA issued a letter to well being care suppliers recommending transitioning from use of decontaminated disposable respirators.
  • Testing updates:
    • As of at this time, 369 exams and pattern assortment gadgets are approved by the FDA underneath emergency use authorizations (EUAs). These embrace 270 molecular exams and pattern assortment gadgets, 76 antibody and different immune response exams, and 23 antigen exams. There are 49 molecular authorizations and one antibody authorization that can be utilized with home-collected samples. There’s one molecular prescription at-home take a look at, two antigen prescription at-home exams, 4 over-the-counter (OTC) at-home antigen exams, and two OTC molecular exams.
    • The FDA has approved 8 antigen exams and a couple of molecular exams for serial screening packages. The FDA has additionally approved 477 revisions to EUA authorizations.

Associated Info



The FDA, an company throughout the U.S. Division of Well being and Human Providers, protects the general public well being by assuring the security, effectiveness, and safety of human and veterinary medication, vaccines and different organic merchandise for human use, and medical gadgets. The company is also chargeable for the security and safety of our nation’s meals provide, cosmetics, dietary dietary supplements, merchandise that give off digital radiation, and for regulating tobacco merchandise.


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