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<xml><ArticleSet><Article><Journal><PublisherName>Radiance Research Academy</PublisherName><JournalTitle>International Journal of Current Research and Review</JournalTitle><PISSN>2231-2196</PISSN><EISSN>0975-5241</EISSN><Volume>18</Volume><Issue>3</Issue><IssueLanguage>English</IssueLanguage><SpecialIssue>N</SpecialIssue><PubDate><Year>2026</Year><Month>February</Month><Day>15</Day></PubDate></Journal><ArticleType>Healthcare</ArticleType><ArticleTitle>&#xD;
	Therapeutic Potential of Adiantum Capillus-Veneris in Unani and Modern Medicine: A Review&#xD;
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</ArticleTitle><ArticleLanguage>English</ArticleLanguage><FirstPage>01</FirstPage><LastPage>07</LastPage><AuthorList><Author>Samira Khatoon</Author><AuthorLanguage>English</AuthorLanguage><Author> Shavana Fathima</Author><AuthorLanguage>English</AuthorLanguage><Author> Wajeeha Begum</Author><AuthorLanguage>English</AuthorLanguage></AuthorList><Abstract>&#xD;
	Adiantum capillus-veneris (Pare-siavashan in Persian, Maidenhair fern in English), a plant of the Pteridaceae family, a well known medicinal plant in the Unani system of medicine, has been traditionally used for its diuretic, antipyretic, demulcent, emmenagogue, expectorant, and deobstruent properties. Various parts of the plant, including its leaves, roots, and stems, are employed in the treatment of kidney stones, diabetes, thyroid disorders, fungal infections, and respiratory ailments. Recent stud ies have highlighted its rich phytochemical profile, including the presence of triterpenoids, flavonoids, and other bioactive com pounds. Pharmacological investigations have revealed a broad range of activities such as antioxidant, antimicrobial, antifungal, antidiabetic, anti-obesity, wound healing, lithotriptic, and antiandrogenic effects. The plant is also widely used for managing hair related conditions like alopecia and dandruff. However, due to its anti-implantation effect, it is contraindicated during pregnancy. The findings discussed in this review underscore the therapeutic potential of Adiantum capillus-veneris and emphasize the need for further preclinical and clinical research to validate and expand its medicinal applications.&#xD;
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</Abstract><AbstractLanguage>English</AbstractLanguage><Keywords>Adiantum capillus-veneris, Maidenhair fern, Unani, phytochemical, flavonoids, Medicinal Applications.</Keywords><URLs><Abstract>http://ijcrr.com/abstract.php?article_id=4891</Abstract><Fulltext>http://ijcrr.com/article_html.php?did=4891</Fulltext></URLs><References>&#xD;
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</References></Article></ArticleSet><ArticleSet><Article><Journal><PublisherName>Radiance Research Academy</PublisherName><JournalTitle>International Journal of Current Research and Review</JournalTitle><PISSN>2231-2196</PISSN><EISSN>0975-5241</EISSN><Volume>18</Volume><Issue>3</Issue><IssueLanguage>English</IssueLanguage><SpecialIssue>N</SpecialIssue><PubDate><Year>2026</Year><Month>February</Month><Day>15</Day></PubDate></Journal><ArticleType>Healthcare</ArticleType><ArticleTitle>&#xD;
	Regulatory Obligations in Post-Marketing Surveillance: A Mandate for Drug Safety &amp; Compliance&#xD;
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</ArticleTitle><ArticleLanguage>English</ArticleLanguage><FirstPage>08</FirstPage><LastPage>13</LastPage><AuthorList><Author>Shivani S. Lohate</Author><AuthorLanguage>English</AuthorLanguage><Author> Shilpa Pise</Author><AuthorLanguage>English</AuthorLanguage></AuthorList><Abstract>&#xD;
	Clinical trials conducted before drug approval have limitations such as small population size, short duration, controlled settings, and exclusion of vulnerable groups. These constraints prevent the detection of rare, long-term, or population-specific adverse effects. Once a drug enters real-world use, it interacts with diverse patients, comorbidities, and polypharmacy, revealing new risks that require ongoing evaluation. Post-Marketing Surveillance (PMS) ensures continuous monitoring of the benefit&#x2013;risk bal ance of medicines. This manuscript provides an integrated overview of PMS obligations across major global regulatory authorities including CDSCO (India), USFDA (USA), EMA (Europe), PMDA (Japan), and WHO&#x2013;UMC (global). Key pharmacovigilance tools&#x2014;ICSRs, PSURs, PADERs, RMPs, PASS, FAERS, EudraVigilance, VigiBase, and VigiFlow&#x2014;are summarized to highlight their role in safety signal detection. A comparative regulatory analysis outlines similarities and differences in reporting timelines, early monitoring strate gies, and digital submission systems. Real-world case studies, including Rofecoxib (Vioxx) withdrawal due to cardiovascular risks, the bladder cancer signal associ ated with Pioglitazone, Thalidomide-induced teratogenicity, and Diethylene Glycol contamination in Coldrif syrup, illustrate how PMS systems prevent public health tragedies. Study limitations include restricted access to proprietary internal regulatory data bases and reliance on publicly available electronic sources. The discussion emphasizes strengthening ADR reporting culture, greater use of real-world evidence, and applying digital tech nologies like artificial intelligence for faster signal detection. Overall, the manuscript demonstrates that robust PMS systems are essential for ensuring global drug safety, regulatory compliance, and public trust.&#xD;
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</Abstract><AbstractLanguage>English</AbstractLanguage><Keywords>Post-Marketing Surveillance; Pharmacovigilance; Drug Safety; Regulatory Compliance; Adverse Drug Reactions</Keywords><URLs><Abstract>http://ijcrr.com/abstract.php?article_id=4893</Abstract><Fulltext>http://ijcrr.com/article_html.php?did=4893</Fulltext></URLs><References>&#xD;
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