Painkillers are a very powerful tool used to reduce or ease different types of pain. Healthcare professionals and different social media programs are constantly warning us about the possible side effects and overdose consequences. Nevertheless, statistics show that the number of painkiller abuse victims increases annually. Acetaminophen is a well-spread painkiller that is used to reduce and ease the pain in many conditions. This component classifies as a miscellaneous analgesic and antipyretic, approved by FDA in 1980.
Femara (letrozole) is an oral, non-steroidal aromatase inhibitor, usually indicated for the treatment of hormonally responsive breast cancer after surgery and radiation. This medication lowers estrogen levels in postmenopausal women, which can slow the growth of certain types of breast tumors. It may be prescribed for women with ovulation problems, or for the ones with unexplained infertility, being used for ovarian stimulation. It also increases pregnancy chances in ovulating women.
Television commercials over-market birth control pills. They typically use multiple psychology tricks in order to increase the percentage of sales, but it has a damaging effect upon consumers. Young women all over the world are exposed to dangerous consequences after using oral contraceptives (Yaz or Yasmine, for example). Failing to adequately warn patients and physicians about an increased risk of serious side effects is a crime, so if you or a loved one suffered from serious health problems while or after taking this drug, consider hiring a personal injury attorney.
WHAT IS DROSPIRENONE?
Drospirenone is a synthetic hormone in birth control pills and postmenopausal hormone replacement. It is used in order to prevent ovulation (the part of the female menstrual cycle, when a mature ovarian follicle discharges an egg), causing
The liability of any or all of the the parties involved in the chain of manufacture of any product for the damage caused by that product is called product liability. The manufacturer of component parts, the assembly manufacturer, the wholesaler or retail store owner can be responsible for product liability.
Negligence is the basis for product liability claims. The concept of negligence was developed under English Law and emerged as an independent cause of action in the 18th century. Negligence is defined as conduct that falls below the standards of behavior established by law for the protection of others against unreasonable risk of harm. It involves the failure to use reasonable care and in some cases, negligence is defined by statute, known as Negligence Per Se. Some acts are considered to be inherently negligent and do not require to prove the negligence was known or intended, when for example a doctor leaves a sponge inside their patient during surgery.
It is well known that U.S. Food and Drug Administration (FDA) is the oldest consumer protection agency in the U.S. Federal Government and it is responsible for protecting public health in the areas of:
- Human and Veterinary Drugs
- Biological Products
- Medical Devices
- Nation’s Food Supply
- Products that emit radiation
Product recall is defined as removal from the market when the company discovers a problem on their own and decides to recall the product or a product is removed by FDA. A correction can be made to the product due to its defects or potential harm. There can be three Classes of recalls. Class I recalls include products that would cause serious adverse health consequences or death. Class II recalls are applied for those products, which use may cause temporary reversible adverse health consequences. Class III recall is a situation in which a product is not likely to cause adverse health consequences.