Award-winning investigative reporter and author, Katherine Eban has devoted more than a dozen years studying these issue and you can learn what she discovered including how the FDA, politics, substandard foreign drug manufacturing and fraud are at the center of this $115 billion dollar international generic drug industry.
To learn more about these disturbing issues that affect your health and safety, I encourage to watch Katherine’s 16 min. TEDMED talk; A Dose of Reality about Generic Drugs (June, 2020) https://youtu.be/si2M93gZy1E
If you want to learn even more details about this fascinating and distubing story, look for Katherine’s award-winning Book of Lies (just released in paperback) available at your library or favorite bookseller.
Over ninety percent of drugs sold in America are generic.
And, 80% percent of generic prescription drugs are manufactured in India & China along with the Active Pharmaceutical Ingredients (API) that are used in patented brand-name drugs.
Drug manufacturing is one of India’s major industries. They have about 700 Indian drug manufacturing plants that employ tens of thousands of workers.
Foreign-made generics are less regulated and sanctioned by the FDA, even when they have had substantially greater data integrity, sanitary, quality and manufacturing deficiencies.
The FDA’s priority is approving new generic drugs to market faster. In 2019, over 1,200 new generic drugs were approved, while improvements in existing foreign drug manufacturing, safety and data integrity lagged behind.
Neither you, nor your doctor, are likely to know where your generic medications are manufactured and if serious quality and safety deficiencies have been identified by the FDA.
Pharmacies do not necessarily fill your prescription with the same generic manufacturers’ medication each time. They are commonly filled with whatever they have available, especially in mail-order and centralized pharmacy centers.
The FDA approval of generic drugs is substantially less stringent than brand name drugs. And, not all generic prescription drugs are identical for the same conditions. They can differ in the potency of API and the inert ingredients that can result in substantial differences in effectiveness, side-effects and adverse reactions.
The use of generic medications for certain serious medical conditions such as seizure disorders, blood thinners & bipolar disorders can have greater risks due to a narrow therapeutic range for the medication.
If your generic drugs comes in an amber pharmacy vial (compared to an original manufacturer’s bottle), it probably doesn’t include the name and country of where the generic drug was manufactured.
Your fresh and canned food products that you buy and eat include substanially more FDA mandated product label disclosures including the manufacturers’ address and list of ingredients than the FDA regulated generic drugs that you take (on blind faith) for your physical and mental health
Bottle of Lies, 2019 by Katherine Eban
A Guide to Investigating Your Own Drugs, 2019 by Katherine Eban
The High Cost of Cheap Pills, 2019 Bloomberg News
A four-part series following a year-long investigative study of the generic drug industry