Fildena CT 100 (often referred to as Fildena Chewable 100 mg) is a version of Fildena that comes in a chewable tablet form, making it easier for people who may have difficulty swallowing regular tablets. It contains the same active ingredient as regular Fildena—Sildenafil Citrate—which is used to treat erectile dysfunction (ED). Like other medications, Fildena CT 100 has been safety reviewed by health authorities for several important reasons. Health authorities around the world, including the U.S. Food and Drug Administration (FDA), the European Medicines Agency (EMA), and national health organizations, carry out these reviews to ensure that the drug is effective, safe, and suitable for public use. Reasons for Health Authorities Reviewing Fildena CT 100: 1. Ensuring Safety and Efficacy: Sildenafil citrate, the active ingredient in Fildena CT 100, has been thoroughly studied and tested for its safety and effectiveness in treating erectile dysfunction. Health authorities like the FDA and EMA require that all drugs, including generics like Fildena, undergo rigorous clinical trials to evaluate: The effectiveness in treating the intended condition (e.g., ED). The safety profile, including potential side effects and drug interactions. These trials ensure that the drug works as intended and that its benefits outweigh any risks when used appropriately. 2. Regulation of Generic Drugs: Fildena CT 100 is a generic form of Viagra (sildenafil citrate). Generic medications are held to the same rigorous standards as brand-name drugs. Health authorities review and approve generic drugs to ensure they have the same active ingredient, dosage, and effectiveness as the brand-name versions, but at a lower cost. Bioequivalence: Fildena CT 100 must be shown to be bioequivalent to the branded sildenafil, meaning it should be absorbed into the body at the same rate and produce the same therapeutic effect as Viagra. 3. Quality Control and Manufacturing Standards: Manufacturing facilities that produce Fildena CT 100 must comply with Good Manufacturing Practices (GMP), a set of regulations enforced by health authorities worldwide. These regulations ensure that the drug is produced in a controlled environment, with strict quality standards, to guarantee that every pill is safe and consistent in its ingredients and potency. Regular inspections and audits by health authorities help ensure that these standards are maintained.