Agree 100%. I can totally see why people that aren't at all into pharmacology or knowledgeable about hormones could buy into the "permanent fin ED" fearmongering but it's a little silly for us. Like you said there's tons of things in the PED world that can fuck up libido, but no one ever claims deca dick is permanent.
Fin is a "toxic ass drug" now? Really? What exactly makes it so toxic? It's one of the most well tolerated drugs out there. Side effects are reported in less than 2% of participants in some studies, around 6% in others. And the side effects that are reported are honestly not serious and may also simply be psychosomatic or caused by other factors.
"Pharmaceutical loving ass" my friend you are literally on a website devoted to injecting constituted chinese powder into your ass.
You don’t know the history of that poster. He’s an infection on steroids forums. He doesn’t use gear. He doesn’t lift. He uses ChatGPT to give medical advice to PED users. He’s been banned multiple times from Meso for racism and harassing sources. And now that infection is here on SST trying the same shit.
Now, back to fin/dut. While most of these studies used higher doses and the drugs were used for long periods of time, the risks still exist. If you are not susceptible to male pattern baldness the risks are not worth it.
5α-dihydrotestosterone (5α-DHT) is the most potent natural androgen. 5α-DHT elicits a multitude of physiological actions, in a host of tissues, including prostate, seminal vesicles, hair follicles, skin, kidney, and lacrimal and meibomian glands. ...
pmc.ncbi.nlm.nih.gov
“Although many clinical studies claimed that finasteride and dutasteride ‘are safe and tolerable’ [
7], new emerging evidence suggests that finasteride and dutasteride induce metabolic dysfunction, such as hyperglycemia [
16], IR [
13,
16], liver fat accumulation [
12,
14], liver steatosis and liver fibrosis [
12,
14], and T2DM [
17]. It should be noted that many reported clinical trials failed to incorporate specific measures of metabolic dysfunction (
e.g., liver lipid accumulation; hyperglycemia, IR) as primary or secondary end points, in order to evaluate the effects of these drugs on metabolic dysfunction [
9,
10].”
“But 25 people interviewed by CBC/Radio Canada during a six-month investigation of finasteride's side-effects tell a different story. They say the drug caused sexual, psychological and physical side-effects for them that have lasted months if not years after they ceased taking the drug.”
5α-dihydrotestosterone (5α-DHT) is the most potent natural androgen. 5α-DHT elicits a multitude of physiological actions, in a host of tissues, including prostate, seminal vesicles, hair follicles, skin, kidney, and lacrimal and meibomian glands. However, the physiological role of 5α-DHT in...
pubmed.ncbi.nlm.nih.gov
“This treatment may result in development of non-alcoholic fatty liver diseases (NAFLD), insulin resistance (IR), type 2 diabetes (T2DM), dry eye disease, potential kidney dysfunction, among other metabolic dysfunctions. We suggest that long-term use of finasteride and dutasteride may be associated with health risks including NAFLD, IR, T2DM, dry eye disease and potential kidney disease.