I will also address why the majority of new parents practice intermittent bedsharing despite governmental and
medical warnings against it.
Not exact matches
Experts have been
warning for some time that our antibiotic use is unsustainable and now the UK's chief
medical officer, Dame Sally Davies, is calling for urgent action worldwide
against what she is calling «a catastrophic threat.»
«While originally targeting individuals, these plans have gained some momentum as a substitute to an employer - sponsored group
medical plan,» wrote one analysis,
warning against the risks employers take on with such programs, which do not guarantee coverage.
There are reports from the Journal of the American
Medical Association that
warn specifically
against parents using newer «smart» baby monitors that sync to their smart phone, to
warn if their baby stops breathing.
More worryingly, nursing mothers are forced to allow overnight contact for babies as young as 8 months old, despite all the health
warnings and
medical professionals advising
against it, including La Leche League (LLL) International.
Or that the American
Medical Association and several other health groups also
warned against its use in cattle.
The
medical community has long
warned against overusing antibiotics in farm animals because of the potential threat to human health.
After all, nearly all major
medical organizations
warn against bedsharing, on the grounds that it increases the chances of Sudden Infant Death Syndrome (SIDS).
The FDA
warns against having ultrasounds for fun (as opposed to for
medical reasons), since such three - dimensional imaging machines use higher power than the typical ultrasound machines at your doctor's office.
Respondents in this year's survey pointed to five main causes of the field's less than favorable reputation: drug and product recalls such as the withdrawal of Avandia; safety issues such as the discovery of problems with raw material from China used in
medical products; scandals, including evidence that pharmaceutical companies have failed to release data from trials whose results cast doubts on their drugs» safety and efficacy; lawsuits brought
against companies that failed to
warn patients of problems with their products; and ethical issues such as kickbacks for physicians promoting specific medications.
Dr. Martin Blaser MD of New York University's Langone
Medical Center who writes in the August 2011 edition of Nature,
warns against harming the beneficial microbes in the gut:
«For years,
medical groups have
warned against custom - compounded hormones.
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Warns It Will Increase Missile Range If Threatened By Europe Iran Factions Use Earthquake Relief Effort to Pursue Power Struggle Hezbollah, on the rise in Lebanon, fends off Saudi Arabia Lebanon's Hariri takes critical line on Hezbollah Lebanese Druze leader urges Saudis, Iranians to talk White House reiterates support for Saudi, Gulf allies
against «Iran aggression» Aid Workers And
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A product liability case
against a pharmaceutical or
medical device manufacturer may be appropriate if the manufacturer failed to
warn the public about inherent dangers in a drug, hid information about serious drug implications from the FDA, failed to follow marketing protocol, or allowed a product to be introduced to the market when the manufacturer knew or should have known of the product's potential danger.
Specifically, a party injured as a result of a defective
medical product may seek damages
against the manufacturer based on theories of a breach of a promise, express or implied, negligence, or strict product liability, including a failure to
warn users of dangers.
When a doctor fails to provide
warnings of complications that could occur after a particular
medical procedure and you are injured, then you may be eligible to pursue a claim
against the physician.
The Drug and
Medical Device Product Liability Deskbook includes: detailed coverage of: warning - related claims and defenses; other information - based theories; strict liability; FDA - related per se liability; preemption of common law tort claims by the Food, Drug & Cosmetic Act and FDA regulations; class actions in drug and medical device litigation; theories of liability asserted against entities other than manufacturers; practical issues involving litigation management; the use of expert witnesses; and many other important
Medical Device Product Liability Deskbook includes: detailed coverage of:
warning - related claims and defenses; other information - based theories; strict liability; FDA - related per se liability; preemption of common law tort claims by the Food, Drug & Cosmetic Act and FDA regulations; class actions in drug and
medical device litigation; theories of liability asserted against entities other than manufacturers; practical issues involving litigation management; the use of expert witnesses; and many other important
medical device litigation; theories of liability asserted
against entities other than manufacturers; practical issues involving litigation management; the use of expert witnesses; and many other important topics.
The New York
Medical Malpractice Law Blog: «The true impact of this case is, of course, that similarly situated victims of inadequate drug
warnings will now be able to initiate actions
against the drug maker in state court.