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Fla. Ct. of Appeal Refuses to Force Mayo Clinic to Treat Covid Patient with Ivermectin, etc.

Drug & Device Law

Mayo Clinic , 2022 Fla. 27, 2022), and its reasoning is crystalline and straightforward. Against the authority of the Mayo Clinic and other reputable sources, the plaintiffs relied on the testimony of a single doctor. The doctor testifying for the plaintiffs was licensed in Florida, but with no board certifications.

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The BFDs – The Ten Best Prescription Drug/Medical Device Decisions of 2023

Drug & Device Law

2023) (remote trial testimony cannot be compelled beyond Rule 45’s 100-mile limit on subpoenas) ( here ); Carson v. They excluded bogus expert testimony under Fed. As a matter of science, the purported link was imaginary, as discussed at great length in one of the many excellent Zantac ( 2022+4 ) MDL opinions. Bonta , 85 F.4th

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Unimpressed Learned Intermediaries Defeat Warning Causation

Drug & Device Law

The law presumes that licensed doctors know what they are doing. Somatics, LLC , 2022 WL 989469 (9th Cir. April 1, 2022) (the companion case to this ). The prescriber’s] testimony, however, does not establish that he would have altered his prescribing conduct. These propositions were employed recently in Himes v.

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S.D. Texas Trims Back Mesh Plaintiff Regulatory Expert Opinions

Drug & Device Law

Texas March 2, 2022)— is a veritable mixed bag. The issue in Robinson was the admissibility of testimony by the plaintiff’s regulatory expert. So much for judicial gate-keeping, Inadequate Warnings to Doctors. How does such testimony meet the relevance requirement of Fed. The “mesh case of the week” — Robinson v.

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Wisconsin Court of Appeals Reverses Injunction Forcing Ivermectin Use

Drug & Device Law

We’ve been writing for a while about cases rejecting someone’s insistence that a doctor prescribe ivermectin for Covid-19, even when that doctor (or hospital) thinks such use of ivermectin is not appropriate medical care – is, in fact, horsebleep. ?. Aurora Healthcare , 2022 WL 1657559 (Wisc. The appellate court was unimpressed.

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The Medical Device Labeling Exception for “Commonly Known” Hazards

Drug & Device Law

That requirement comes with an exception: Provided, however , That such information may be omitted from the dispensing package if, but only if, the article is a device for which directions, hazards, warnings, and other information are commonly known to practitioners licensed by law to use the device. 2022 WL 970681 (N.D. Bard, Inc. ,