drug administration - определение. Что такое drug administration
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Что (кто) такое drug administration - определение

SUBSTANCE USED TO DIAGNOSE, CURE, TREAT, OR PREVENT DISEASE
Pharmaceutical; Pharmaceuticals; Medications; Blockbuster drug; Medicines; Medicaments; Medicated; Medical drug; Medical drugs; Medicinal drug; Medicinal product; Meds; Use of drugs to treat disease; Blockbuster Drugs; Blockbuster medicine; Medicament; Pharmaceutical drugs; Pharmaceutical products; Q8h; Administration (medicine); Drug administration; Medicine administration; Pharmaceutical preparation; Medical preparation; Pharmacologic agents; Pharmacologic agent; Therapeutic agents; Therapeutic agent; Name brand drugs; Name brand drug; History of pharmaceutical drugs; Gastrointestinal medication; Pharmaceutical agents; Pharmaceutical agent; Gamot; Pharmaceutical drug; Medication drugs; Medication drug; Controversies surrounding pharmaceutical drugs
  • A medication is a [[prescription drug]] used to treat a disease.

Ophthalmic drug administration         
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  • Figure 6.0 - Cornea epithelium
  • Figure 8.0 - Dry eye syndrome complications
  • Figure 7.0 - Glaucoma complications
  • Figure 5.0 - Example of zero-order release kinetics (y = % of drug released from contact lens; x = time (days))
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  • Figure 3.0 - Molecular imprinting technique
  • Figure 4.0 - Example of a nanoparticle
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ADMINISTRATION OF A DRUG THROUGH THE EYES
Ophthalmic administration
Ophthalmic drug administration is the administration of a drug to the eyes, most typically as an eye drop formulation. Topical formulations are used to combat a multitude of diseased states of the eye.
FDA         
  • FDA scientist prepares blood donation samples for testing.
  • Medical Officer Alexander Fleming, M. D., examines a portion of a 240-volume new drug application around the late 1980s. Applications grew considerably after the efficacy mandate under the 1962 Drug Amendments.
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  • FDA lab at Building 64 in Silver Spring, Maryland
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  • [[Harvey W. Wiley]], chief advocate of the Food and Drug Act
  • Jefferson, Arkansas]] is the headquarters of the National Center for Toxicological Research.
  • Jamaica, Queens, New York Regional Office - USFDA
AGENCY OF THE US DEPARTMENT OF HEALTH AND HUMAN SERVICES
FDA; United States Food and Drug Administration; US Food and Drug Administration; Product licensing application; Food and drug administration; Bureau of Chemistry; USFDA; Fda; Food & Drug Administration; Food and Drug Adminstration; ODE IV; American Food and Drug Administration; US FDA; FDA approval; FDA drug approval & regulation; U.S. Food & Drug Administration; U.S. Food and Drug Administration; The Food and Drug Administration (FDA or USFDA); Food and Drug Administration (FDA or USFDA); FDA Regulation; Food and Drug Administration (United States); USA Food and Drug Administration; United States Food And Drug Administration; U S Food and Drug Administration; Food and Drugs Administration; Pediatric exclusivity; Food and Drug Administration (US); Food, Drug, and Insecticide Administration; Taha Kass-Hout; United States Food & Drug Administration; USA FDA; U. S. Food and Drug Administration; United states food and drug administration; Federal Drug Administration; U.S. FDA; US food and drug administration; The Real Cost; Fda.gov; Food and Drugs Authority
FORTRAN Design Aid (Reference: FORTRAN)
FDA         
  • FDA scientist prepares blood donation samples for testing.
  • Medical Officer Alexander Fleming, M. D., examines a portion of a 240-volume new drug application around the late 1980s. Applications grew considerably after the efficacy mandate under the 1962 Drug Amendments.
  • alt=
  • alt=
  • FDA lab at Building 64 in Silver Spring, Maryland
  • alt=
  • [[Harvey W. Wiley]], chief advocate of the Food and Drug Act
  • Jefferson, Arkansas]] is the headquarters of the National Center for Toxicological Research.
  • Jamaica, Queens, New York Regional Office - USFDA
AGENCY OF THE US DEPARTMENT OF HEALTH AND HUMAN SERVICES
FDA; United States Food and Drug Administration; US Food and Drug Administration; Product licensing application; Food and drug administration; Bureau of Chemistry; USFDA; Fda; Food & Drug Administration; Food and Drug Adminstration; ODE IV; American Food and Drug Administration; US FDA; FDA approval; FDA drug approval & regulation; U.S. Food & Drug Administration; U.S. Food and Drug Administration; The Food and Drug Administration (FDA or USFDA); Food and Drug Administration (FDA or USFDA); FDA Regulation; Food and Drug Administration (United States); USA Food and Drug Administration; United States Food And Drug Administration; U S Food and Drug Administration; Food and Drugs Administration; Pediatric exclusivity; Food and Drug Administration (US); Food, Drug, and Insecticide Administration; Taha Kass-Hout; United States Food & Drug Administration; USA FDA; U. S. Food and Drug Administration; United states food and drug administration; Federal Drug Administration; U.S. FDA; US food and drug administration; The Real Cost; Fda.gov; Food and Drugs Authority
¦ abbreviation (in the US) Food and Drug Administration.

Википедия

Medication

A medication (also called medicament, medicine, pharmaceutical drug, medicinal drug or simply drug) is a drug used to diagnose, cure, treat, or prevent disease. Drug therapy (pharmacotherapy) is an important part of the medical field and relies on the science of pharmacology for continual advancement and on pharmacy for appropriate management.

Drugs are classified in multiple ways. One of the key divisions is by level of control, which distinguishes prescription drugs (those that a pharmacist dispenses only on the order of a physician, physician assistant, or qualified nurse) from over-the-counter drugs (those that consumers can order for themselves). Another key distinction is between traditional small molecule drugs, usually derived from chemical synthesis, and biopharmaceuticals, which include recombinant proteins, vaccines, blood products used therapeutically (such as IVIG), gene therapy, monoclonal antibodies and cell therapy (for instance, stem cell therapies). Other ways to classify medicines are by mode of action, route of administration, biological system affected, or therapeutic effects. An elaborate and widely used classification system is the Anatomical Therapeutic Chemical Classification System. The World Health Organization keeps a list of essential medicines.

Drug discovery and drug development are complex and expensive endeavors undertaken by pharmaceutical companies, academic scientists, and governments. As a result of this complex path from discovery to commercialization, partnering has become a standard practice for advancing drug candidates through development pipelines. Governments generally regulate what drugs can be marketed, how drugs are marketed, and in some jurisdictions, drug pricing. Controversies have arisen over drug pricing and disposal of used drugs.

Примеры употребления для drug administration
1. Food and Drug Administration are also investigating.
2. Food and Drug Administration, Kommersant reported.
3. The Food and Drug Administration is investigating.
4. Food and Drug Administration, Andrew von Eschenbach.
5. Food and Drug Administration approval of its concept.