
Thursday, July 28, 2016
Thursday, July 21, 2016
Sanders, Other Lawmakers Urge FDA Approval of Generic Crestor
Two months ago, AstraZeneca
gained approval for the use of Crestor in children suffering from homozygous
familial hypercholesterolemia (HoFH) and, under the Orphan Drug Act (ODA), the
drug then qualified for extended market exclusivity for the treatment of this
new condition. With the impending loss of patent protection for Crestor’s
common use in adults, AstraZeneca has filed a lawsuit accusing the FDA of
illegally interpreting a federal law that will allow generic medications to
exclude indications for HoFH on their labels. Without the ruling, generic
manufacturers would be required to include HoFH dosing and instructions on
their labels, therefore violating the exclusivity granted by the ODA and
extending AstraZeneca’s market hold. Bernie Sanders, along with several other
lawmakers, are petitioning the FDA to approve the generics and offer a lower
cost alternative to consumers.
Read the Stat News article on it here.
Read the Stat News article on it here.
Friday, July 1, 2016
[Podcast from 2 Docs Talk] Direct-To-Consumer Marketing - Letting the Fox Guard The Henhouse
Summary: Direct-to-consumer drug
marketing has, historically, been a controversial topic. In 2002, Merck spent
$160 million on a marketing campaign for the new pain medication, Vioxx. Later,
the drug was found to increase the risk of stroke and heart attacks and was
being used, largely, by individuals who were well-suited for alternative drugs
(like ibuprofen). In addition to the increased potential for misuse, many ad
claims are misleading for consumers: A reported “significant” increase in
length of life for patients on a treatment for lung cancer is actually three
months. As pressure builds to regulate, or even halt, these advertising
practices, the pharmaceutical industry has a proposed solution. They recommend
giving the FDA approval rights for all prescription drug ads prior to their
release, funded by manufacturers through a per ad ‘user fee.’ This approach is
already used for drug approvals, with manufacturers funding over half of the
FDA’s budget; prior to the implementation of these fees in 1993, drug company
investment accounted for less than 10% of funds received by the FDA. Opponents
of the measure are concerned how the impact of additional pharma industry
funding will jeopardize the ultimate efficacy of the FDA’s practices.
Here the podcast from 2 Docs Talk here.
Here the podcast from 2 Docs Talk here.
Wednesday, June 22, 2016
'Cross Protection' Occurs Between Bacterial Strains
Scientists recently
discovered a mutually beneficial relationship occurring between bacterial
strains: cross protection. In a new study, researchers grew two types of E.
coli, each resistant to a different antibiotic, in the same test tube. The environment
also contained the two antibiotics to which the strains were resistant. Instead
of being eliminated, both bacteria deactivated “their” antibiotic, providing protection
for the other strain. While not occurring in this study, experts suspect that, over
time, this stable environment could lead to the exchange of resistance genes –
making both strains of bacteria resistant to both antibiotics.
Listen to Scientific American's podcast about it here.
Listen to Scientific American's podcast about it here.
Friday, May 27, 2016
Wednesday, May 25, 2016
GlaxoSmithKline CEO On Why Drugs Cost So Much
Sir Andrew Witty, the CEO
of Britain’s GlaxoSmithKline (GSK), the sixth largest pharmaceutical company in
the world, discusses the current period of ‘extreme challenge’ in the industry
and acknowledges the disconnect between the global push for affordable
healthcare and the current cost of needed medications. Specifically, he points
to the U.S.’s lack of transparency requirements as a major driver for the
issues that our country is facing today – an inability to determine the actual
price of a drug makes it impossible to determine a realistic cost-benefit
analysis for the system. Ultimately, he suggests, the system needs to balance
cost, value and innovation to ensure shareholders remain invested and patients
have access to the drugs they need.
Hear the podcast on it here.
Hear the podcast on it here.
Thursday, April 28, 2016
New 'Scarier' Zika Warnings in the U.S.
The CDC recently released a
broader range of Zika-related complications beyond microcephaly, including
stillbirth, placenta damage, prematurity, etc., as well as potential links to
additional non-pregnancy conditions. In this comprehensive discussion about the
existing and anticipated impact of the virus, experts explain the developing
understanding of transmission, effects and prevention. Although there is
evidence that the disease is not in the continental US (beyond those that
traveled to infected countries), experts estimate the range of the carrier
mosquito to include parts of at least 30 states – with an additional potential
carrier type extending as far north as Minnesota. Combined with the difficult
of containment, due to the uniqueness of the mosquito (including breeding,
biting habits, etc.), experts suspect that an outbreak in the United States
would be the “public health version of [Hurricane] Katrina.”
Listen to the podcast about it from On Point with Tom Ashbrook.
Listen to the podcast about it from On Point with Tom Ashbrook.
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