Sometimes it takes millions to convince the world of something. In other cases, everything could be pushed over the edge by just one instance. The latter is the case when the Food and Drug Administration’s decision to finally oblige pharmaceutical companies to put warning signs on their contraceptive patches is discussed. While there have been patients and doctors who have tried to achieve this over the years, only one case of a very real risk of death was required to finally get the FDA to do what many would have done from the start

The problem arises from the risk of some synthetic compounds that hormone-based contraceptive methods that get into the body can cause blood clots. These blood clots, specifically known as venous thromboembolism (VTEs), can be dangerous for people because they can cause harm if they get into the lungs. These clots, an extremely rare side effect of contraceptive hormones, are known to cause highly lethal pulmonary embolism. As mentioned earlier, VTEs are among the rarest, if not the rarest, possible side effects of the pill and the patch. For many years, the risk to the pill was considered so small and insignificant that it was largely ignored by the world. However, for these many years it has been assumed that this is a wrong assumption for the patch.

The old suspicion that the contraceptive patch releases hormones more directly into the body, which increases the risk of side effects. was recently confirmed. In particular, the blood clots in question have given rise to great concern over the years. Women groups and affected medical professionals have identified the potential effects of the increased hormones and increased risk of VTEs in the patches and have tried to convince the FDA to issue orders to issue a warning. However, the FDA has managed to maintain its original decision that until recently the risks to the patch were as small as the risks to the pill. In addition to a prominent incident, a scientific study also served as the final confirmation that the FDA needed to finally take note. Some of the more extreme elements welcomed the FDA regulation, but consider it more cautious to ban contraceptive patches from the US market.

In their defense, pharmaceutical companies stated that the risks of using the patches are drastically outplayed. They claim that the patches pose no increased risk to healthy women; At least not more than the pill. However, they openly admitted that certain lifestyle, genetic, and health factors could come into play to increase the risk of side effects, including the formation of VTEs. According to a number of pharmaceutical companies, these factors can include things like smoking, alcoholism, history of substance abuse, hormonal imbalances, and genetic abnormalities that affect the blood. They also mentioned that patients do not have to use the patches and that they have numerous alternatives to contraception.

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