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  2. Electronic prescribing - Wikipedia

    en.wikipedia.org/wiki/Electronic_prescribing

    Physicians, physician assistants, nurse practitioners and other prescribers will be able to use the system either through their existing electronic medical record or through a standalone application. Health Canada included supporting better prescribing practices, including e-prescribing, as part of its Action on Opioid Misuse plan.

  3. The latest eye medicine to be recalled: 715,000 bottles of ...

    www.aol.com/latest-eye-medicine-recalled-715...

    The FDA posting of the recall says Teva’s pulling Clear Eyes, Once Daily, Eye Allergy Itch Relief drops for a failed impurities test. This covers the 715,682 bottles in lot Nos. 114349 ...

  4. CDC warns not to use these eye drops after 3 deaths, eyeball ...

    www.aol.com/cdc-warns-not-eye-drops-154738245.html

    The CDC says not to use EzriCare or Delsam Pharma's Artificial Tears as they've been linked to a drug-resistant strain of bacteria, which has led to 3 deaths.

  5. Physicians' Desk Reference - Wikipedia

    en.wikipedia.org/wiki/Physicians'_Desk_Reference

    The Physicians' Desk Reference (PDR), renamed Prescriber's Digital Reference after its physical publication was discontinued, is a compilation of manufacturers' prescribing information (package insert) on prescription drugs, updated regularly and published by ConnectiveRx. [citation needed]

  6. 2 medications from 1 manufacturer recalled for a failure that ...

    www.aol.com/2-medications-1-manufacturer...

    American Health Packaging on behalf of BluePoint Laboratories recalled 21 batches of the same capsules, also made by Glenmark and also in 100-count (NDC No. 68001-396-00) and 500-count (NDC No ...

  7. FDA recall policies - Wikipedia

    en.wikipedia.org/wiki/FDA_recall_policies

    FDA's role under the guidelines is to monitor company recalls and assess the adequacy of a firm's action. After a recall is completed, FDA makes sure that the product is destroyed or suitably reconditioned and investigates why the product was defective. Generally, FDA accepts reports and other necessary recall information submitted by e-mail.

  8. Over 27 Eye Drops Have Been Recalled: What You Need to Know - AOL

    www.aol.com/eye-drop-recall-know-113000380.html

    Eye drops are being recalled due to a rare bacterium found in artificial tears. Find a list of recalled drops in 2023. Plus, eye infection symptoms.

  9. Electronic health records in the United States - Wikipedia

    en.wikipedia.org/wiki/Electronic_health_records...

    Federal and state governments, insurance companies and other large medical institutions are heavily promoting the adoption of electronic health records.The US Congress included a formula of both incentives (up to $44,000 per physician under Medicare, or up to $65,000 over six years under Medicaid) and penalties (i.e. decreased Medicare and Medicaid reimbursements to doctors who fail to use ...