COVID-19: NAFDAC approves 14 herbal mixtures clinical trials

0
117

The National Agency for Food and Drug Administration and Control (NAFDAC) has approved the listing of 14 herbal medicines, meaning that they are safe for consumption.

They are to undergo clinical trials before they can be certified efficacious for the treatment of COVID-19.

The Director-General of NAFDAC, Prof Mojisola Adeyeye, made these known yesterday in Abuja, after receiving her first jab of the AstraZeneca vaccine.

She reiterated that the AstraZeneca vaccine is generally safe and that its benefits far outweighs potential risks.

She said: “I believe in herbal medicine. But herbal medicine that is not backed up by research may be effective but we don’t know.

“Especially for COVID-19 vaccine, herbal medicine has to be antiviral. It is not enough that it relieves cold, cough etc., it has to be antiviral.

“We have approved about 14 for listing, meaning they is safe to use, but how efficacious, it is when you do a clinical trial that you will know. Also, it is very costly to do clinical trials.

NAFDAC destroys drugs worth N613 million in Kano

“The government has arranged for a research and development scheme for the health sector. We have many herbal medicines that are going to be used.

“Of course, we would have given them listing, but they will go further for a clinical trial. We are still expecting such. I will not be surprised if we have a herbal medicine that has antiviral against COVID-19.”

Concerning the safety and efficacy of the AstraZeneca vaccine, the NAFDAC boss added: “When we got the application package of this vaccine, we went through it line by line.

“Before we got the application itself, we went through what others had already assessed in their report so that we will be prepared when we start our own. And that was exactly what happened. We have concluded based on the quality, safety and efficacy report.

“For this particular AstraZeneca, over 20,000 people were involved in phase three. Phases 1,2,3 are different based on the number of subjects. When you have over 20,000 people and they say 10 incidences or side effects occurred, statistically and epidemiologically, you categorise as benefit outweigh the risk.

“There is no medicine that doesn’t have side effects, especially when it is going through development. It is whether the benefit outweighs the risk. And the conclusion is that from all indications – quality, safety and efficacy, the benefits outweighed the side effects.

Ooni unveils indigenous medicine to cure virus

“Side effects may be soreness or tenderness in the arm, fever etc. There are few cases of people that have allergies to things that show allergic reactions.

“Everybody that is taking the vaccine must be around for about 45 minutes for the nurse, doctor to watch to make sure that everything is fine. From all indications, it is generally safe.”

She noted that the agency is yet to receive the dossier for Johnson and Johnson COVID-19 vaccine.

LEAVE A REPLY

Please enter your comment!
Please enter your name here

This site uses Akismet to reduce spam. Learn how your comment data is processed.