What Is Hush Money and What Is the Big Deal?
The Hush money meaning can be explained as the money that is given to an individual so that he/she keeps quiet about a particular incident or activity. The word is usually followed by scandal, misconduct, or sensitive information that may hurt a reputation, career, or business. Hush money involves a fundamental pillar of secrecy; that is, money is given in lieu of silence.
Paying hush money is not necessarily a crime but in many cases, it may involve legitimate and critical legal and ethical concerns. Where the money is paid to hush up crime, then it may amount to obstruction of justice or conspiracy. Ethically, hush money may lead to the culture of silence, where victims or whistleblowers are less likely to emerge.
Numerous high-profile hush money cases have come to the public eye, particularly those of celebrities, politicians, and corporations. The most notorious one could be the hush money payments, which are associated with political campaigns. Such cases frequently attract media coverage and usually lead to legal repercussions, especially when campaign finance or corporate governance rules are violated.
There are many reasons why people take hush money. It could be because of fear of retaliation, the need for privacy or the feeling that they will not succeed in a legal battle. The payout may be considered an easier or less injurious solution compared to a long court process or being the subject of media attention.
Hush money can also be employed in the workplace to hush up complaints of harassment, discrimination or other wrongdoings. Employers can also give out severance package or non-disclosure agreements (NDA) in consideration of silence. Such agreements are legally acceptable but may be controversial, particularly when they facilitate the repetition of offense by influential persons.
In the past few years, there have been enactments of laws and regulations to curb the use of hush money in given circumstances. In some states, it is now prohibited by law to insist upon NDAs which would interfere with an employee reporting harassment or abuse. Governments and courts are taking a closer look at these payments and the purpose of such payments.
There is an increase in the awareness of the people regarding the cases of hush money, particularly, with the emergence of social media and independent journalism. Citizens are better informed and intolerant of any attempt to purchase silence especially when the vulnerable members of the society are targeted. Hush money can be a dangerous move because transparency and accountability are becoming important values in society.
The hush money is an ambivalent and tricky issue. Although it might appear as a remedy to dealing with scandals or reputation safeguard, it can boomerang in legal, ethical, and social circles. Being aware of its implications, individuals and organizations may make decisions that are better and more transparent.
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FDA Grants Priority Review for Zoliflodacin New Drug Application for the Treatment of Uncomplicated Gonorrhea and Assigns Target PDUFA Date of December 15, 2025
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The U.S. FDA has granted zoliflodacin a Qualified Infectious Disease Product (QIDP) designation. This designation allows it to benefit from FDA Priority Review, and Extended Market Exclusivity. Entasis Therapeutics, Inc., the legal NDA holder and affiliate of Innoviva Specialty Therapeutics, Inc., retains the commercial rights for zoliflodacin in the major markets in North America, Europe, and Asia-Pacific. GARDP retains the right to register and commercialize the product in more than three-quarters of the world's countries, including all low-income countries, most middle-income countries, and several high-income countries. GARDP is committed to working with its partners and local health authorities in markets where zoliflodacin receives regulatory approval to help remove access barriers to ensure treatment is available to address unmet medical needs while ensuring appropriate and sustainable use. About Uncomplicated Gonorrhea With more than 82 million new gonorrhea infections occurring globally each year, gonorrhea is the second most common bacterial sexually transmitted infection (STI), affecting both men and women, which, if left untreated, can result in serious and permanent health consequences. With the rise and spread of drug-resistant infections, the World Health Organization (WHO) has identified antimicrobial resistance (AMR) as one of the ten most critical global threats to public health. The bacterium Neisseria gonorrhoeae, which causes gonorrhea, has progressively developed resistance to most classes of antibiotics used to treat these infections, including ceftriaxone, a widely used intramuscular injection that was first made available in 1984. About Zoliflodacin Zoliflodacin is an investigational first-in-class antibacterial that is administered in a single oral dose for the treatment of uncomplicated gonorrhea. The oral route of administration simplifies treatment by providing a convenient option for patients unable to receive an intramuscular injection. Zoliflodacin has a unique mechanism of action, inhibiting a crucial bacterial enzyme called type II topoisomerase, which is essential for bacterial function and reproduction. In in vitro studies, zoliflodacin demonstrated activity against multidrug-resistant strains of Neisseria gonorrhoeae, including those resistant to ceftriaxone and azithromycin, with no cross-resistance to other antibiotics. In a pivotal Phase 3 clinical trial, zoliflodacin demonstrated non-inferiority in achieving microbiological cure at the urogenital site of infection with a single oral dose of zoliflodacin compared to a treatment regimen of a single intramuscular injection of 500mg ceftriaxone followed by 1g of oral azithromycin. The Phase 3 study found that zoliflodacin was generally well-tolerated, with no serious adverse events or deaths reported during the trial. About GARDP The Global Antibiotic Research & Development Partnership (GARDP) is a not-for-profit global health organization driven to protect people from the rise and spread of drug-resistant infections, one of the biggest threats to us all. By forging the public and private partnerships that matter, we develop and make accessible antibiotic treatments for people who need them. Vital support for our work comes from the governments of Canada, Germany, Japan, Monaco, the Netherlands, Switzerland, the United Kingdom, the Canton of Geneva, the European Union, as well as the Gates Foundation, Global Health EDCTP3, GSK, the RIGHT Foundation, the South African Medical Research Council (SAMRC) and Wellcome. About Innoviva Innoviva is a diversified holding company with a core royalties portfolio, a leading critical care and infectious disease platform known as Innoviva Specialty Therapeutics ('IST'), and a portfolio of strategic investments in healthcare assets. Innoviva's royalty portfolio includes respiratory assets partnered with Glaxo Group Limited ('GSK'). Innoviva is entitled to receive royalties from GSK on sales of RELVAR ® /BREO ® ELLIPTA ® and ANORO ® ELLIPTA ®. Innoviva's other innovative healthcare assets include infectious disease and critical care assets stemming from acquisitions of Entasis Therapeutics, including XACDURO ® (sulbactam for injection; durlobactam for injection), co-packaged for intravenous use approved for the treatment of adults with hospital-acquired bacterial pneumonia and ventilator-associated bacterial pneumonia caused by susceptible strains of Acinetobacter baumannii-calcoaceticus complex and the investigational zoliflodacin currently being developed for the treatment of uncomplicated gonorrhea, and La Jolla Pharmaceutical Company, including GIAPREZA ® (angiotensin II), approved to increase blood pressure in adults with septic or other distributive shock and XERAVA ® (eravacycline) for the treatment of complicated intra-abdominal infections in adults. Innoviva also markets ZEVTERA® (ceftobiprole), an advanced-generation cephalosporin antibiotic, in the U.S. through an exclusive license from Basilea Pharmaceutica International Ltd, Allschwil. For more information about Innoviva, go to For information about Innoviva Specialty Therapeutics, go to ANORO ®, RELVAR ® and BREO ® are trademarks of the GSK group of companies. ZEVTERA ® is a trademark of Basilea Pharmaceutica Ltd, Allschwil.
