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Pediatric Pharmacology
Pediatric Pharmacology

... Enhanced during infancy: due to development of cutaneous layers (not fully developed and thinner), level of hydration and cutaneous perfusion of the epidermis in children o Children/infants also have a higher proportion of body surface area to mass Premature infants: enhanced cutaneous absorption ma ...
Side Effects: Predictable, Understandable and
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“What You Need To Know About Prescription Drugs in York County!”

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Neurology Firm NuPathe Gets $15M For Lead Migraine Patch

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... warning to be added to the drug label to highlight this information. Oral viscous lidocaine solution is not approved to treat teething pain, and use in infants and young children can cause serious harm, including death, indicates FDA in a June 2014 Safety Announcement. FDA advises health care provid ...
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Pharmacogenetics and the Promise of Individualized Medical Care

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Paclitaxel

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... Patients rarely develop chronic liver disease after an acute severe DILI. Patients with cholestatic/mixed liver disease were more prone to developing chronic injury (9%), than those with the hepatocellular form ...
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Compounding

Pharmaceutical compounding (done in compounding pharmacies) is the creation of a particular pharmaceutical product to fit the unique need of a patient. To do this, compounding pharmacists combine or process appropriate ingredients using various tools. This may be done for medically necessary reasons, such as to change the form of the medication from a solid pill to a liquid, to avoid a non-essential ingredient that the patient is allergic to, or to obtain the exact dose(s) needed or deemed best of particular active pharmaceutical ingredient(s). It may also be done for more optional reasons, such as adding flavors to a medication or otherwise altering taste or texture. Compounding is most routine in the case of intravenous/parenteral medication, typically by hospital pharmacists, but is also offered by privately owned compounding pharmacies and certain retail pharmacies for various forms of medication. Whether routine or rare, intravenous or oral, etc., when a given drug product is made or modified to have characteristics that are specifically prescribed for an individual patient, it is known as ""traditional"" compounding.Due to the rising cost of compounding and the shortage of drugs, many hospitals have shown a tendency to rely more upon large-scale compounding pharmacies to meet their regular requirement, particularly of sterile-injectable medications. When compounding is done on bulk production of a given formulation rather than patient-specific production, it is known as ""non-traditional"" compounding (which, as discussed below, is arguably not ""compounding"" but rather ""manufacturing""). This development raises concerns about patient safety and makes a case for proper regulatory control and monitoring.
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