F40 Cabergoline .25mg x 25 TABLETS

Description

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Cabergoline 0.25mg – 25 Tablets, Anti-Prolactin by F40

Cabergoline is highly regarded among athletes using anabolic steroids and performance-enhancing drugs for its effectiveness in reducing the risk of prolactin-induced side effects. Extensive research has shown that Cabergoline effectively lowers prolactin levels, addressing conditions and side effects associated with elevated prolactin. This drug is particularly useful in treating hyperprolactinemia and its symptoms. Moreover, Cabergoline has been proven beneficial in treating sexual dysfunction caused by excess prolactin—a common issue with certain anabolic steroids like Trenbolone and Deca Durabolin. The use of Cabergoline can also shorten recovery times and enhance the frequency of erections between orgasms. Beyond these benefits, this performance-enhancing drug is known to improve all aspects of sexual function and libido. Cabergoline is also effective in managing estrogenic side effects such as oily skin, acne, gynecomastia, and bloating and can help in treating galactorrhea and sexual dysfunction.

Side Effects

Cabergoline may cause side effects in individuals sensitive to the active ingredient or those who exceed the recommended dosage. Excessive use can lead to a sharp decline in prolactin levels, causing decreased appetite, insomnia, dizziness, constipation, nausea, skin rashes, difficulty breathing, mood swings, swelling in the limbs, and low blood pressure. It’s important to monitor your prolactin levels before initiating treatment with Cabergoline.

Administration and Dosage

In sports applications, Cabergoline is typically administered following a protocol of 0.25 mg taken once every four days. If prolactin levels are notably elevated, the dosage may be adjusted to 0.25 mg taken every other day until prolactin levels normalize, after which the dosage can revert to the standard regimen. In addition to its primary benefits, Cabergoline can also help mitigate adverse reactions such as facial swelling and excess fluid retention in muscle tissues during a steroid cycle.