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Patients less than 25 years old should be screened once a year for Chlamydia and Gonorrhea, as they have a high incident of causing PID and infertility in women who then in turn suffer from chronic pelvic pain, and dysparunia (painful intercourse).

Another study basically ruled out the cholesterol hypothesis, saying that elderly patients with high LDL levels live just as long or longer than those with low levels.

ME service. He explains that both CBT and GET aim to stabilise a patient at a baseline of activity before gradually trying to improve.

The researchers point out that the pharmacist case managers actively adjusted medication to achieve desired results and suggest this contributed to the beneficial effect.

The FDA has revised the warnings in the drug labels of canagliflozin (Invokana, Invokamet) and dapagliflozin (Farxiga, Xigduo XR) to include information about the risk of acute kidney injury and recommendations to minimize this risk.

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While there is tentative evidence that acupuncture might be effective for some forms of pain relief and nausea, it fails to deliver any medical benefit in any other situations and its underlying concepts are meaningless.

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This phrase is ubiquitous: it appears on the websites of naturopathic medical schools, on materials published by practicing naturopaths, and on lobbying documents to promote the unfettered licensure of naturopaths and to expand eligibility for federal loan repayment programs.

From University of Michigan, Ann Arbor, Michigan; Massachusetts General Hospital, Boston, Massachusetts; Mayo Clinic, Phoenix, Arizona; Duke University School of Medicine, Durham, North Carolina; and Washington University School of Medicine, St.

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The FDA is alerting health care providers and emergency responders that certain lots of AtroPen (atropine), CANA (diazepam), morphine sulfate, and pralidoxime chloride autoinjectors manufactured by Meridian Medical Technologies can be used for up to 1 year beyond the labeled expiration date, which should help mitigate potential shortages of these drugs.

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The Obama administration has dropped its push for age restrictions for access to the Plan B morning-after pill.

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The FDA reviewed the data submitted in the marketing applications used to support approval of Plan B and Plan B One-Step (levonorgestrel), and ella (ulipristal acetate).

HealthDayNews A tiny electronic gadget called a pedometer may encourage more people get up and get moving.

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Using them gives a sense that an effective therapy has been chosen, and the patient may not seek a more effective therapeutic option.

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To receive FDA approval, manufacturers must show that the biosimilar is highly similar to the reference product, omitting minor differences in clinically inactive components.

One strategy that often helps is to learn enough about the cancer to be able to ask questions about its treatment and about what the future may hold.

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FDA-approved label says: "alterations to the endometrium that may affect implantation may also contribute to efficacy.

Vincent Herrin, University of Mississippi Medical Center professor of medicine and adult hematologist and oncologist, said a patients health would not likely be significantly harmed by waiting two weeks for the kind of treatment Mohamed received, though most doctors would try to avoid delays.

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In 1999, a meta-analysis of eight studies of the combined (Yuzpe) regimen concluded that the best point estimate of effectiveness was 74%.

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Sleep problems: are very common, and many different types of physicians see patients with these disorders.

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