Sulodexide Possibly Benefits Chronic Tinnitus

It may be a wild and borderline theory, but what if big pharma companies are sabotaging these drugs and trials because these compounds all have expired patents on them? Who wants a cheap a easily produced generic drug that may work? Not the Big Pharma for sure...
If any "Big Pharma" company had a drug that helps with tinnitus they would have marketed it as such decades ago, they aren't sitting on their patents.
 
Just because things don't work out the way we hoped doesn't mean some nasty unfeeling entity has to have conspired to deny us. It seems society has become sort of stunted and we too easily bond over these sorts of easy explanations and not enough people are willing to push-back on them.
Sure, I try to stay as reasonable as possible but everything is about money. If it is simply not viable, there is not a single pharma company that would poke it with a ten foot stick.

They play with risk/reward during research but their motif is first and foremost always be profit. They don't do it for anyone's well being. Of course I'm talking about the legal entities, there are a lot of dedicated scientist who really want to make a change.

So following this logic it's quite logical they would let a trial die like this, that might undermine their x million dollar research investment.
 
If any "Big Pharma" company had a drug that helps with tinnitus they would have marketed it as such decades ago, they aren't sitting on their patents.
They aren't (well, they actually have to until a new drug is cleared for the market), but they won't help these cheap potential remedies either. That would make their expensively researched, developed and tested future medicines redundant.

A patent for a drug is granted for 20 years. It starts from the moment they file the documents for a new chemical compound. After that, the clock is ticking and it's usually takes years (at best 7-8 years) for a new drug to hit the market. So they usually have half the time to reap the financial rewards before the novel drug becomes free for all and any other company can produce a generic version of it.
 
They aren't (well, they actually have to until a new drug is cleared for the market), but they won't help these cheap potential remedies either. That would make their expensively researched, developed and tested future medicines redundant.

A patent for a drug is granted for 20 years. It starts from the moment they file the documents for a new chemical compound. After that, the clock is ticking and it's usually takes years (at best 7-8 years) for a new drug to hit the market. So they usually have half the time to reap the financial rewards before the novel drug becomes free for all and any other company can produce a generic version of it.
Having patent protection is not always the sole underlying reason for the business decision. You're also simplifying the drug development / approval process considerably.

This drug is already being sold in many countries for non-tinnitus related underlying conditions. Many of the countries that it is sold in do not offer near the protective rights of the patent holder as the US and EU. Clearance from the FDA and similar bodies in developed countries is equally as important to protecting distribution of a new drug to that market as a patent. However, as we know on this forum, clinical trials require significant resources. Generics are a risk, but still need to pass through an approval process by the FDA or similar regulatory body. In the case of a prescription being required, the doctor can also be a factor in determining if the patient should be prescribed the on-brand version or generic.
 
Having patent protection is not always the sole underlying reason for the business decision. You're also simplifying the drug development / approval process considerably.

This drug is already being sold in many countries for non-tinnitus related underlying conditions. Many of the countries that it is sold in do not offer near the protective rights of the patent holder as the US and EU. Clearance from the FDA and similar bodies in developed countries is equally as important to protecting distribution of a new drug to that market as a patent. However, as we know on this forum, clinical trials require significant resources. Generics are a risk, but still need to pass through an approval process by the FDA or similar regulatory body. In the case of a prescription being required, the doctor can also be a factor in determining if the patient should be prescribed the on-brand version or generic.
Thanks for the clarification. Yes, I did simplify as I'm not an expert in the medical field, but with a little expertise in intellectual property. With a common sense it's obvious that it's always about profit, at least for the legal entities.

Of course generic drugs are a risk for the innovator companies as they cut way below their prices. Maybe that's bad for the company but good for the patients as these drugs cost a fraction of the original. I'm also not aware how these things actually happen, but my guess is big pharma companies have huge lobbying activity in what is being prescribed.

Brand drugs have a time window to milk the heck out of the market with a novel drug, as they can sell it for whatever they think of.

About regulations and FDA, it's basically a shitshow at this point. The scandal with the new drug for Alzheimer's is a perfect example. It is a drug originally developed in China. What goes behind the closed doors of these regulatory boards is a mystery, but heavily tinted with politics, business, and corruption.
 
I was in Mexico just before the pandemic hit and bought a couple boxes of Sulodexide just before I left. You don't need a prescription and it's super inexpensive (less than $10 for a box). It comes in blister pack of 50 small solid pills listed at 250 LRU (Lipid) or 25 mg.

I had forgotten about them. I started taking them 3 days ago in the AM and I have to say, my tinnitus has been lower these last 3 days I should have waited longer to post but I'm moving (again) and didn't want to forget.

The box says "Vessel Due F, Sulodexida Capsula 250 LRU Caja con 50 capsulas". It's distributed by AlphaSigma S.P.A. in Mexico City but on the back of the box it says it's made in Italy.
 
I was in Mexico just before the pandemic hit and bought a couple boxes of Sulodexide just before I left. You don't need a prescription and it's super inexpensive (less than $10 for a box). It comes in blister pack of 50 small solid pills listed at 250 LRU (Lipid) or 25 mg.

I had forgotten about them. I started taking them 3 days ago in the AM and I have to say, my tinnitus has been lower these last 3 days I should have waited longer to post but I'm moving (again) and didn't want to forget.

The box says "Vessel Due F, Sulodexida Capsula 250 LRU Caja con 50 capsulas". It's distributed by AlphaSigma S.P.A. in Mexico City but on the back of the box it says it's made in Italy.
Nice. Can you do us all a favor and maybe keep a log rating your tinnitus (loudness, annoyance, etc) while on and off the drug? Maybe take it for a week straight, then take a couple weeks off, then take it again. It would be nice to see some actual data from someone using this... otherwise we end up with vague "I think it works" or "It doesn't work" which isn't really very meaningful.
 
I was in Mexico just before the pandemic hit and bought a couple boxes of Sulodexide just before I left. You don't need a prescription and it's super inexpensive (less than $10 for a box). It comes in blister pack of 50 small solid pills listed at 250 LRU (Lipid) or 25 mg.

I had forgotten about them. I started taking them 3 days ago in the AM and I have to say, my tinnitus has been lower these last 3 days I should have waited longer to post but I'm moving (again) and didn't want to forget.

The box says "Vessel Due F, Sulodexida Capsula 250 LRU Caja con 50 capsulas". It's distributed by AlphaSigma S.P.A. in Mexico City but on the back of the box it says it's made in Italy.
Do you know if I would legally be able to take this across the US border if I drive down to Tijuana?
 
Dear all,

I have read Tinnitus Talk a lot and I write you for the first time because I have just bought capsules of Sulodexide. Fortunately, I am on holiday in Spain. It is very easy to get it here at a "low" cost (€13/$10). The brand I got is Aterina. The dosage available is 15 mg. There are 60 capsules in a box.

FYI, my tinnitus appeared following a concert. So my condition is linked to a sound trauma. I have hearing loss from the 8 kHz as far as I remember.

I took 2 capsules this morning. I will take two more capsules this evening with Melatonin.

I will let you know.
 
The box says "Vessel Due F, Sulodexida Capsula 250 LRU Caja con 50 capsulas". It's distributed by AlphaSigma S.P.A. in Mexico City but on the back of the box it says it's made in Italy.
I found a few instances of Italian doctors on online forums suggesting Vessel (Sulodexide) as treatment attempt for idiopathic tinnitus.
 
Dear all,

I have read Tinnitus Talk a lot and I write you for the first time because I have just bought capsules of Sulodexide. Fortunately, I am on holiday in Spain. It is very easy to get it here at a "low" cost (€13/$10). The brand I got is Aterina. The dosage available is 15 mg. There are 60 capsules in a box.

FYI, my tinnitus appeared following a concert. So my condition is linked to a sound trauma. I have hearing loss from the 8 kHz as far as I remember.

I took 2 capsules this morning. I will take two more capsules this evening with Melatonin.

I will let you know.
If you are planning to take the drug for a while, can you keep a journal of your tinnitus each day you're on the drug and/or off the drug. Rate things like loudness, annoyance, etc of the tinnitus. This will help members get a better gauge of the effectiveness of the drug.
 
I found a few instances of Italian doctors on online forums suggesting Vessel (Sulodexide) as treatment attempt for idiopathic tinnitus.
Vessel is prescribed quite often in Italy when vascular issues are thought to be the cause of tinnitus. I tried it myself for a couple of months, with no effect; my tinnitus has no vascular origin though.
 
If you are planning to take the drug for a while, can you keep a journal of your tinnitus each day you're on the drug and/or off the drug. Rate things like loudness, annoyance, etc of the tinnitus. This will help members get a better gauge of the effectiveness of the drug.
Sure, I will keep a journal up to date. I will also check for the side effects...
 
Interesting. I will look into that. I live in Spain and will go out to my local drugstore ASAP.

What is the recommended amount of Melatonin to be taken with Sulodexide?
 
Interesting. I will look into that. I live in Spain and will go out to my local drugstore ASAP.

What is the recommended amount of Melatonin to be taken with Sulodexide?
Can you try it for a week without Melatonin and then with staggered mg of Melatonin (ie: 1 week with 5 mg, 10 mg, 15 mg? I'm not sure there's a documented amount, so there may be some trial.

As I've asked from others, can you keep a journal of your tinnitus while on Sulodexide, with / without Melatonin, and when not on the drug? Track tinnitus loudness and annoyance with a rating.
 
Can you try it for a week without Melatonin and then with staggered mg of Melatonin (ie: 1 week with 5 mg, 10 mg, 15 mg? I'm not sure there's a documented amount, so there may be some trial.

As I've asked from others, can you keep a journal of your tinnitus while on Sulodexide, with / without Melatonin, and when not on the drug? Track tinnitus loudness and annoyance with a rating.
This is "citizen science" in action! Science conducted by the people, for the people. Although for this to be truly scientific and objective we need accuracy and more participants. I wish I could obtain the drug and partake. Thank you to all who do end up experimenting with this and reporting back.
 
This is "citizen science" in action! Science conducted by the people, for the people. Although for this to be truly scientific and objective we need accuracy and more participants. I wish I could obtain the drug and partake. Thank you to all who do end up experimenting with this and reporting back.
I will eventually try this if other things on my list do not help. Keeping a log is difficult for me though as I'm very forgetful, which has gotten even worse since my tinnitus worsened.
 
Hello. Just to let you know, Sulodexide has had no effect on me after 30 days of taking the capsules on a daily basis (neither bad effect nor good on my tinnitus). No side effects either. I have a journal up to date as discussed... Nothing interesting to share... But I will copy it if it makes sense...
 
Hello. Just to let you know, Sulodexide has had no effect on me after 30 days of taking the capsules on a daily basis (neither bad effect nor good on my tinnitus). No side effects either. I have a journal up to date as discussed... Nothing interesting to share... But I will copy it if it makes sense...
Really sad. Would you try to add 3 mg Melatonin before the sleep as in the study?
 
Really sad. Would you try to add 3 mg Melatonin before the sleep as in the study?
Good point! I reproduced the study. I took the Melatonin as well...

I think it cannot help tinnitus induced by hearing loss like me. It should be more effective for people impacted by blood pressure for instance.
 
This is from Wikipedia, under uses for the drug.

"Clinically, sulodexide is used for the prophylaxis and treatment of thromboembolic diseases; however, recent research has also demonstrated the beneficial effects of sulodexide in animal models of reperfusion injury and the treatment of diabetic nephropathy. In combination with Melatonin, sulodexide has been shown to be a viable treatment option for patients suffering from central or sensorineural tinnitus."

Sounds like it's worth a try, also looks like there is no risk of interaction with other drugs, and also very minimal transient GI side effects.
 
I have been taking Sulodexide (aka Vessel Due F) that I bought in Mexico. I'm also taking Melatonin at night under my tongue.

They DO help with my tinnitus. I'm back in the USA and running out of Sulodexide, so I have been looking around for some online source. I used to be in California so driving to TJ isn't a big deal, but now I'm in Hawaii so I'm looking for an online source.

Long story short, I am 70, and I've been having a new incidence of joint pain in my hands, feet and one shoulder. Well, I just found out this is a possible side effect of Heparin (which Sulodexide basically seems to be in oral form). I imagine most of you are younger and the joint pain thing will not be an issue. I assumed it was arthritis.

Anyway, I'm going to cold turkey my remaining month's stash of Sulodexide and see what happens. If the tinnitus comes back much worse, I'll have to decide. Worst case, put up with the joint pain and fly to Mexico and buy a ****load of the stuff. Best case, the tinnitus doesn't get any worse and the joint pain goes away.

Anyway, here's some more data for you'all trying to deal with tinnitus. But the Sulodexide/Melatonin combo definitely has helped me a lot.
 
I have been taking Sulodexide (aka Vessel Due F) that I bought in Mexico. I'm also taking Melatonin at night under my tongue.

They DO help with my tinnitus. I'm back in the USA and running out of Sulodexide, so I have been looking around for some online source. I used to be in California so driving to TJ isn't a big deal, but now I'm in Hawaii so I'm looking for an online source.

Long story short, I am 70, and I've been having a new incidence of joint pain in my hands, feet and one shoulder. Well, I just found out this is a possible side effect of Heparin (which Sulodexide basically seems to be in oral form). I imagine most of you are younger and the joint pain thing will not be an issue. I assumed it was arthritis.

Anyway, I'm going to cold turkey my remaining month's stash of Sulodexide and see what happens. If the tinnitus comes back much worse, I'll have to decide. Worst case, put up with the joint pain and fly to Mexico and buy a ****load of the stuff. Best case, the tinnitus doesn't get any worse and the joint pain goes away.

Anyway, here's some more data for you'all trying to deal with tinnitus. But the Sulodexide/Melatonin combo definitely has helped me a lot.
Thanks for the update. I hope to try Sulodexide.
 
So I made the round trip to Spain and bought a box of Sulodexide (Aterina, 15 mg per capsule).

I took 2 capsules per day over the past week, along with 3.8 mg of Melatonin in the evening for sleep. (I did not want to take Melatonin in the morning so as not to get sleepy during the day).

So far the result is inconclusive. It may have an effect and I felt really good during the week overall, the best I've felt since my tinnitus onset back in May. Also it was the first week without any problems sleeping, which I really thought was impossible just 2 months ago. Nothing that can't be attributed to habituation however, which has slowly been kicking in over the past 2 months.

My tinnitus already fluctuates a lot. I don't think in terms of "spikes" but rather "high" and "low" periods, half of the time being high and the other half low. This week the proportion was reduced to about 25% high and 75% low, so that was encouraging. Sadly, I wouldn't go as far as call it a definitive reduction in volume yet. I'm not saying there's no reduction, just that if there is, it is only a statistical improvement. No unmistakable suppression.

I was confident I would have some effect on me because my tinnitus briefly takes a pulsatile aspect when transitioning between high and low periods, which I took it as a sign that it somehow reacts to changes in blood aspect / blood pressure. I will try not taking it the next week and see if that changes anything. After that I may try taking it again, this time raising the daily dose to match the trial dosage more closely.

In short, I feel like it may help but it may be placebo effect. It's certainly not a magic pill and spikes are still there.
 
Update: After a 1 week pause, I've been taking Sulodexide again for the last 3 days. Tinnitus has been high the whole time regardless. I'm starting to think the respite I had during my first week with Sulodexide may have been a coincidence. (Part of my normal tinnitus cycle.)

I'll try to double the dosage (to 2x30 mg + 6 mg melatonin) next week. At this point I'm doubtful it'll have any effect.
 
I gave up on it after a month - I kept a careful log and saw no noticeable effect. Moral of the story for me is that if there was a drug that made a real difference, we'd all know about it by now. I've got a few leftover boxes of Sulodexide if anyone else wants to give it a try, but honestly I couldn't recommend it based on my experience.
 
A question to folks that already bought it. I live in Canada, where this is not sold.
I am about to travel to Germany, where this is not available either. However, it is widely available in plenty of other EU countries, which may make it easier for me to purchase it. If not for the prescription requirement.

I saw someone saying in a different post that they were able to purchase it OTC in Spain. However, I called some pharmacies in Spain, and they mentioned that a prescription was required.

Are there some countries that are more lax regarding Sulodexide prescriptions there?
I can't get my doctor to prescribe something that is not even regulated here. At the same time, it would be hard for me to get a prescription with a random doctor abroad.
 

Log in or register to get the full forum benefits!

Register

Register on Tinnitus Talk for free!

Register Now