Evaluation of Evidence

ISBN-13: 9786200321121 / Angielski / Miękka / 240 str.

Venkata Rama Rao Nallani; Rama Rao Nadendla

Opis

Once a drug is marketed, it leaves the secure and protected scientific environment of clinical trials and is free for consumption by the general public. At this point, most medicines will only have been tested for short-term safety and efficacy on a limited number of carefully selected individuals. A person with drug toxicity has accumulated too much of medication in the bloodstream. Hence, the need of Pharmacovigilance arises which includes, securing the early detection of new adverse reactions or patients subgroups of exceptional sensitivity; and introducing certain measures in order to manage such risks. The field of Patients drug safety has been receiving a great deal of attention since adverse drug reactions are recognized as hazards of drug therapy. In addition, adverse drug reactions have a major impact on public health by imposing a considerable economic burden on patients, societyand the already stretched health care system.

O autorze

Nallani, Venkata Rama RaoDr. Venkata Rama Rao Nallani is working as Professor & HOD, Dept. of Pharmacy Practice, Chalapathi Institute of Pharmaceutical Sciences, Guntur since 2011. His awards & Achievements : Received Best Clinical Services Award on 15 August 2021 on 75 th Independence Day in Govt. General Hospital, Guntur. Received Best Blood donor Provider in GGH.