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The People's Pharmacy

Show 1167: Will a Tick Bite Make You Allergic to Meat?

The People's Pharmacy

Joe and Terry Graedon

Health & Fitness, Medicine, Kids & Family, Alternative Health

4.5934 Ratings

🗓️ 30 May 2019

⏱️ 59 minutes

🧾️ Download transcript

Summary

For some years, emergency doctors and allergists were puzzled by people who started having extremely serious allergic reactions in the middle of the night, a long time after they had eaten or drunk anything or had any contact with obvious allergens. Smart sleuthing from our guest and his colleagues determined that a tick bite can […]

Transcript

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0:00.0

I'm Joe Gradyton and I'm Terry Grady. Welcome to this podcast of the People's Pharmacy.

0:06.1

You can find previous podcasts and more information on a range of health topics at people's Pharmacy.com.

0:15.0

Could a tech bite make you allergic to burgers, bratwurst, and barbecue?

0:20.0

How can Alpha Gal allergy affect you or your friends?

0:23.7

This is the People's Pharmacy with Terry and Joe Grayden. For years, emergency doctors were puzzled by people who started having severe allergic reactions in the middle of the night, hours after they'd gone to bed.

0:43.0

No bug bites, no unusual activities.

0:46.0

Just a terrible reaction.

0:48.0

How did allergists ever figure out what was going on?

0:51.0

Alpha-gal allergy to red meat is not the only consequence of a tick bite.

0:55.6

There's Lyme disease, eryliciosis, and Rocky Mountain spotted fever to name just a few.

1:01.3

Coming up on the People's Pharmacy, your calls and questions about alpha gal, insect stings, and other allergies.

1:08.0

First, the news studies

1:15.0

to news.

1:18.0

two news studies question the value of FDA's accelerated approval process for new cancer drugs.

1:25.0

People with cancer are often enthusiastic about the latest purported advance

1:30.0

that might offer them a better quality of life and improve longevity.

1:34.0

Drug companies are also eager to bring their new and pricey cancer medications to market

1:40.0

as quickly as possible. Since 1992, the FDA has permitted drug manufacturers to use the

1:47.4

accelerated approval pathway for their new cancer medicines. Instead of

1:52.0

proving that the drug prolongs life, all the company has to

1:55.8

show is that it improves some measure of the disease process. This might be tumor shrinkage,

2:01.6

response rate, or time to tumor progression.

...

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