Hemp Hound Investigation & FOI Request Reveals Something Very Whiffy … Connecting MHRA, GW Pharma & Skunk..

Yes you read correctly Skunk!

Hemp Houd are on the trail again and all of  this sounds very on the nose..

On 08/02/25 The Hemp Hound Agency submitted a Freedom of Information Request (FOI) to the MHRA with several questions regarding Cannabidiol (CBD) and Cannabis sativa.

This article will go through their response, which was received on 07/03/25.

Before we begin, I want to highlight an article published two years ago by The Hemp Hound Agency, regarding the MHRA’s Yellow Card lists for CBD and Cannabis sativa.

Killing in the name of‘ looked at the absurdity of some of the recorded cases, and questioned the legitimacy of including CBD supplemental products in lists that are meant to record adverse reactions to medicines and vaccines. The MHRA’s FOI response states that the names of products causing reactions do not have to be reported—somewhat concerning, especially given their admission that some reactions could be logged on a ‘guilt by association’ basis.

What’s more, they have stated that the yellow card list was started due to two fatal reactions to Sativex, and that there were two fatalities from herbal cannabis in 2002 when there were no recognised or authorised medicines or vaccines at the time that fitted that description

The questions asked to the MHRA were:

1. The date when ‘Skunk’ was first listed under the Yellow Card Scheme for Cannabis sativa.

2. The date when CBD supplemental products were first recorded under the Yellow Card

Scheme for Cannabis sativa.

3. The date when CBD products were first listed under the Yellow Card Scheme for CBD specifically.

4. Confirmation that the Yellow Card Scheme is primarily intended for recording adverse reactions to licensed medicines and vaccines.

 

Additionally requested:

5. Identification of the product(s) attributed to fatalities recorded under Cannabis sativa in 2002.
6. Identification of the product(s) attributed to fatalities recorded under CBD in 2006.

7. If the reports in requests 5 and 6 are not associated with recognised products, can the MHRA confirm whether the fatalities in question were linked to medical trials?

If full disclosure was not possible for requests 5, 6, and 7, a further request was added for:

8. The reason under FOI exemptions for withholding this information.

9. Any general categorisation of the products (e.g., pharmaceutical, consumer, investigational use).

The full response 

 

Now that you’re prepped, let’s break down the MHRA’s response—but be warned, it’s filled with contradictions and deflections.

Certain questions will be asked, some of which I will answer, whereas others are open to consideration based on available information.

That being said, I encourage discussion on the interpretation and implications of the information provided.

Question 1: The date when ‘Skunk’ was first listed under the Yellow Card Scheme for Cannabis sativa.

Response: The first UK spontaneous suspected adverse drug reaction (ADR) report we received where the suspect drug was reported using the term “skunk” was received on 15/03/2018.

Analysis

Suspected… that would be the first indicator of some reports working on a ‘guilt by association’ basis.

Skunk is a term for illicit high-THC cannabis, not a regulated pharmaceutical product. The only way its presence would make sense is if the medicine in question was actually made from Skunk #1—which, conveniently, happens to be owned by GW Pharmaceuticals.

So it’s completely inappropriate for ‘Skunk’ to be named on a Yellow Card list meant for medicinal cannabis products—unless, of course, the medicine itself was derived from Skunk #1.
But… the date of inclusion? That’s significant.
 
Thoughts:
There was long-standing suspicion that Skunk was listed on the Cannabis sativa list long before 2018. Now that we know when it was included, it only raises more questions.
If all of that doesn’t make you want to read on I don’t know what would

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