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Global Statistics

All countries
695,781,740
Confirmed
Updated on September 26, 2023 9:04 pm
All countries
627,110,498
Recovered
Updated on September 26, 2023 9:04 pm
All countries
6,919,573
Deaths
Updated on September 26, 2023 9:04 pm

Global Statistics

All countries
695,781,740
Confirmed
Updated on September 26, 2023 9:04 pm
All countries
627,110,498
Recovered
Updated on September 26, 2023 9:04 pm
All countries
6,919,573
Deaths
Updated on September 26, 2023 9:04 pm

New Risk Factor for COVID-19: Baldness?

Publisher’s Platform: Radical transparency? What I am asking the FDA to do Is not radical at all

Robert F. Kennedy Jr. has rightly made “radical transparency” the motto of his Department of Health and Human Services. HHS even has a page by that name. I think it is a good motto, and I want to help Secretary Kennedy and Acting FDA Commissioner Kyle Diamantas deliver on it in food safety, with two citizen petitions

Reports of infants choking result in FDA warning about Once Upon a Time snacks

Published: October 30, 2026, 10:16 pm Several reports of children choking have led to an FDA warning against Once Upon A Time snacks. The warning covers all flavors, quantities, lots and dates of Once Upon A Farm Tractor Wheels Organic, Toddler Soft-Baked Bars. The FDA has received several reports that describe infants ages 1.5 to

FDA Approves Tildrakizumab for Psoriatic Arthritis in Adults

The FDA has cleared the interleukin (IL)-23 inhibitor tildrakizumab (Ilumya) for the treatment of active psoriatic arthritis (PsA) in adults. Sun Pharma announced the approval on October 30. “As an IL-23 inhibitor administered exclusively by a healthcare provider, Ilumya is now an option for adults with active psoriatic arthritis who are unable to self-administer treatment

Medicare Drug Plans Are Hiking Premiums While Trump Claims Victory on Medicine Prices

Millions of Medicare enrollees who buy stand-alone prescription drug plans will see their average monthly premiums rise by 50% in 2027, a new analysis finds. But enrollees can avoid the average increase — from $34 a month to $51 — by switching to lower-cost plans during the program’s open enrollment period, which runs through Dec.

Here’s What Congress Might Do on Healthcare After the Midterms

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(Newser)
–
Research already has suggested that men face a greater risk of severe illness and death from COVID-19. Now, scientists say male pattern baldness might actually be a risk factor, reports the Telegraph. “We really think that baldness is a perfect predictor of severity,” says Brown University’s Carlos Wambier, lead author of two small studies in Spain. The first study of 41 men admitted to Spanish hospitals with COVID-19 found 71% had male pattern baldness, which is estimated to affect 31% to 53% of white men. The second study of 122 men admitted to three Madrid hospitals with COVID-19 found 79% had male pattern baldness, reports Science. As male pattern baldness is linked to dihydrotestosterone—an androgen, or so-called “male” sex hormone—the thought is that androgens may boost the virus’ ability to penetrate cells.

There is other evidence in support of this theory. For instance, a study of 42,000 men with prostate cancer in Veneto, Italy, found patients on androgen-deprivation therapy—drugs that reduce levels of androgens that fuel prostate cancer cells—were significantly less likely to fall ill, be hospitalized, or die of COVID-19 than men with prostate cancer who were not taking the drugs. These results are replicated in a second, still-unpublished study, whose author believes “androgen deprivation may limit those severe outcomes,” per Science. A US trial is already underway to see if drugs that treat male pattern baldness (by blocking the conversion of testosterone to dihydrotestosterone) are effective at treating COVID-19. Another study of 200 veterans in Los Angeles, Seattle, and New York will analyze the effect of prostate cancer drugs, per the Telegraph. (Read more coronavirus stories.)

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Hot Topics

Publisher’s Platform: Radical transparency? What I am asking the FDA to do Is not radical at all

Robert F. Kennedy Jr. has rightly made “radical transparency” the motto of his Department of Health and Human Services. HHS even has a page by that name. I think it is a good motto, and I want to help Secretary Kennedy and Acting FDA Commissioner Kyle Diamantas deliver on it in food safety, with two citizen petitions

Reports of infants choking result in FDA warning about Once Upon a Time snacks

Published: October 30, 2026, 10:16 pm Several reports of children choking have led to an FDA warning against Once Upon A Time snacks. The warning covers all flavors, quantities, lots and dates of Once Upon A Farm Tractor Wheels Organic, Toddler Soft-Baked Bars. The FDA has received several reports that describe infants ages 1.5 to

FDA Approves Tildrakizumab for Psoriatic Arthritis in Adults

The FDA has cleared the interleukin (IL)-23 inhibitor tildrakizumab (Ilumya) for the treatment of active psoriatic arthritis (PsA) in adults. Sun Pharma announced the approval on October 30. “As an IL-23 inhibitor administered exclusively by a healthcare provider, Ilumya is now an option for adults with active psoriatic arthritis who are unable to self-administer treatment

Related Articles

Publisher’s Platform: Radical transparency? What I am asking the FDA to do Is not radical at all

Robert F. Kennedy Jr. has rightly made “radical transparency” the motto of his Department of Health and Human Services. HHS even has a page by that name. I think it is a good motto, and I want to help Secretary Kennedy and Acting FDA Commissioner Kyle Diamantas deliver on it in food safety, with two citizen petitions

Reports of infants choking result in FDA warning about Once Upon a Time snacks

Published: October 30, 2026, 10:16 pm Several reports of children choking have led to an FDA warning against Once Upon A Time snacks. The warning covers all flavors, quantities, lots and dates of Once Upon A Farm Tractor Wheels Organic, Toddler Soft-Baked Bars. The FDA has received several reports that describe infants ages 1.5 to

FDA Approves Tildrakizumab for Psoriatic Arthritis in Adults

The FDA has cleared the interleukin (IL)-23 inhibitor tildrakizumab (Ilumya) for the treatment of active psoriatic arthritis (PsA) in adults. Sun Pharma announced the approval on October 30. “As an IL-23 inhibitor administered exclusively by a healthcare provider, Ilumya is now an option for adults with active psoriatic arthritis who are unable to self-administer treatment