Results 271 to 280 of about 3,107,552 (340)
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On Therapeutic Equivalency and the Antisubstitution Laws

JAMA: The Journal of the American Medical Association, 1973
The comparative bioavailability of a drug in similarly formulated preparations is becoming a subject of considerable interest and importance to the physician. Drugs usually are not administered as pure compounds but are combined with materials such as binders, excipients, lubricants, preservatives, or other substances generally considered to be ...
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[The concept of therapeutic equivalence].

Medizinische Klinik (Munich, Germany : 1983), 1997
Usually, it is the purpose of a clinical trial to demonstrate the superiority of a (new) treatment in comparison to another treatment with regard to a well-defined criterion of efficacy. However, other aspects rather than improved efficacy might be regarded as advantages of a new therapy, i.e.
S, Lange, J, Windeler
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Generic Drugs

Drug Safety, 1996
For economic reasons, the use of generic substitution is increasingly being supported by health authorities. Potentially, this may be problematic for drugs with a narrow therapeutic window if quality control and/or bioequivalence is not optimal. Many developing countries do not have the resources or expertise to carry out appropriate quality control ...
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Biologic Availability and Therapeutic Equivalence

The Journal of Clinical Pharmacology, 1976
J D, Arnold, J, Sicé
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Therapeutic equivalents in clinical practice.

International journal of fertility and women's medicine, 2001
With increasing debate over the rising expenses of health care, a variety of cost-saving measures has been attempted over the years. Use of primary care physicians as "gate keepers," reduction in the length of hospital stays, and pushing women toward vaginal birth after Cesarean section have all been utilized despite on going issues with patient ...
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Integrative oncology: Addressing the global challenges of cancer prevention and treatment

Ca-A Cancer Journal for Clinicians, 2022
Jun J Mao,, Msce   +2 more
exaly  

Therapeutic equivalence of mesalamine products.

Reviews in gastroenterological disorders, 2004
No bioequivalence studies have been conducted for mesalamine because of differences in formulation. Based on U.S. Food and Drug Administration definitions for bioequivalence, none of these drugs can be classified as bioequivalent or therapeutically equivalent.
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