Інструмент 777ua Nano Banana 2, що працює на основі штучного інтелекту Gemini, призначений для створення зображень та редагування фотографій.

Курс «ШІ для бізнесу» від Google допоможе швидко інтегрувати штучний інтелект у власну справу, зокрема для масштабування. У програмі також правильне написання промптів — створення контенту за допомогою ШІ, розвиток критичного мислення.

Drug Labels Inadequate article featured image showing tons of orange pill bottles with white labels and caps

Drug Labels Inadequate

Product liability lawsuits may be filed against manufacturers when their drug labels are inadequate. Sometimes the U.S. Food and Drug Administration catches the error and sends a warning letter, demands a label change, or mandates a recall. Federal action is not necessary to initiate a claim, however. One need only demonstrate that harm was caused…

Metformin Recall

Metformin Recalls Ordered Based on Cancer-Causing Impurities

There has been a recall of the widely-prescribed diabetes medication metformin by at least one drug maker due to high levels of a cancer-causing agent known as N-Nitrosodimethylamine (NDMA). The U.S. Food and Drug Administration (FDA) stated that it is in contact with five pharmaceutical manufacturers about recalling their extended-release versions of the popular diabetes drug. Laboratory…

Elmiron Lawsuit Claims Vision Loss featured image showing a gavel slamming on top of multi colored drugs in the form of pills

Elmiron Lawsuit Claims Vision Loss

All medications come with potential side effects, but consumers have a right to know about possible risks so that they can make informed decisions about their health. When manufacturers fail to disclose side effects or mislead the medical community or public at large, they may be held responsible under theories of product liability. This is…

Zantac Update: FDA Recalls All Ranitidine From Market

Zantac Update: FDA Recalls All Ranitidine From Market

On Wednesday, April 1, 2020, the U.S. Food and Drug Administration requested that manufacturers recall all prescription and OTC ranitidine drugs from the market immediately. The agency has determined that an impurity increases over time, particularly in warm storage temperatures, resulting in unacceptable exposure to the carcinogen NDMA. While some samples tested did not contain…