The toxicologist agreed that Nitrosamine causes cancer in humans. He said that not all nitrosamines cause harmful health conditions, but when a human being is exposed to other nitrosamine compounds, things become troublesome. The chance of being diagnosed with Cancer elevates when individuals consume these compounds in the form of heavy doses, and that too for a long period of knowing. Many of them don’t even know what is happening, and the chemical spreads the disease to their liver, stomach, and esophagus.
Even the FDA says that on being exposed to Nitrosamine impurities for a long period of time, or way above the recommended intake, then the risk of getting diagnosed with Cancer simply increases in people. But, it also puts forward another insight that if an individual takes a drug containing Nitrosamines according to the prescribed dosage or limits their daily use for 70 years, they are not at risk of becoming a Cancer patient.
How Many Cases Came Into the Limelight?
You might not believe it, but several cases regarding nitrosamine have come into the limelight. In the past, many medicines were reported to contain this chemical. What was the outcome of the discovery? It was the same as what Towa Pharmaceutical Europe is facing, of recalls and soaring levels of scrutiny as the drug regulatory bodies had to become alert and see how these pharmacies manufactured the medicines. Do you recall Valsartan and Losartan, the drugs responsible for lowering blood pressure? The regulatory bodies showed their responsibility of removing more than 12 million bottles from the market in 2018 only because they consisted of a huge number of Nitrosamines.
Which Batch Of Bottles Was Recalled?
To be precise, FDA recalls Duloxetine bottles in lot No. 220128, which was going to get expire in December 2024.
What Should Be Done When Medicines Are Recalled?
Johnson Arbor relaxed the individuals who were taking this anti-depressant, saying that the recall did not include all the formulations. So, the patients are required to read if their prescription is part of the recall or not. If you spot the name, then the FDA recommends continuing it as the medication cannot afford to stop suddenly. Because then you will face headaches, depression, anxiety, and vomiting. Therefore, consult with your doctor about the nearest potential treatment.
Conclusion
We need to be grateful that FDA recalls Duloxetine, otherwise patients using Duloxetine would have been unknowingly inviting Cancer to invade their body. We hope the blog answered all of your questions of why FDA recalls Duloxetine and that you now know what to do when medicine gets recalled.
