A Pharmacovigilance Study of Adverse Drugreactions Report Forms in Dic Of Svcp, Tirupati

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Mallikarjuna B.P
B.Vinod Kumar Naik


Pharmacovigilance is an important and necessary component of clinical research. Both clinical trial safety and post-marketing surveillance pharmacovigilance are critical throughout the product lifecycle.Pharmacovigilance is defined as "the pharmacological science relating to the detection, assessment, comprehension, and prevention of adverse effects of medicines." In India, pharmacovigilance is still in its infancy, Pharmacovigilance monitors any adverse drug effects.Improve public health and safety in the use of medications.Contribute to the assessment of medicine's benefit, harm, effectiveness, and risk, encouraging safe, rational, and effective use.ADR (Adverse drug reaction) is a noxious and unintended response to a drug that occurs at doses normally used in man for disease prevention, diagnosis, or therapy, or for the modification of physiological function.

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K.Mounika, Mallikarjuna B.P, A.Supriya, B.Vinod Kumar Naik, M.Pavithra, P.Gowthamuni, R.Poojitha, & R.Radhika. (2023). A Pharmacovigilance Study of Adverse Drugreactions Report Forms in Dic Of Svcp, Tirupati. Journal of Coastal Life Medicine, 11(2), 1471–1480. Retrieved from https://www.jclmm.com/index.php/journal/article/view/1183


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