Medical studies symptoms and conditions

Started Lisinopril eight weeks ago and took it for three weeks. I suffered the consistent cough. However the worst was the altered taste. It is worse than just metallic, it is bitter and food taste can change mid-meal. The problem started after the first week taking the medication and has not gone away even though I am five weeks since the last dose. I am concerned as to how long it takes this side effect to go away.

I get these painful cramps in both legs the back of my legs above my
calf muscles. They always come after midnight when I am asleep. i
get up and I have to walk 30 minutes or more until they stop,and for
two days my legs are sore.

I just got a very condescending private message from a doctor on this site who said that while my articles from Europe are very helpful that I don't know what I am talking about and that I could mislead the public. Then I see how many parents and patients got a condescending attitude from their own doctors.

Well the public has been mislead but it is not my fault. I don't see any experts in this field stepping up to the plate to acknowledge that these side effects exist, have been reported by authorities in other countries, and that these experts are interested in learning why they are happening. This is an extremely widely prescribed medication that involves the lives of millions.

Merck's research director was quoted as saying that they know of no mechanisms by which these side effects could be related to psychiatric adverse drug reactions. That was a flat out LIE. So what if I quoted you a research article from China that was very complicated and yes, could possibly be misinterpreted by somebody? I just needed to give you an example. The only expert so far that had the guts to give you a truthful statement was Dr. J. Douglas Bremner. Thankfully, he corrected a misunderstanding about saying that it was "unclear."

I hope that we will all hang in there and something will be said by somebody, anybody on this site that will make the FDA listen and investigate Singulair (montelukast) all the way back to the very original studies done in test tubes not on people. And, then take a new look at it from the standpoint of what we now know about human genetics. I guess I will keep repeating myself about one size does not fit all.

I would also PRAY that all clinical studies on Singulair (montelukast) would be suspended until the FDA decides why these side effects occur. And that they would issue a statement to doctors to make conservative decisions regarding treatment with Singulair until the results of the investigation have been reported.

I hope that nobody thinks that I am trying to mislead anyone. The answers are either unknown or being hidden by Merck. How would I know the answers? I don't work for Merck. How many other people are out there trying to translate articles in foreign languages to see what's going on? American doctors are calling Merck and being assured that there is nothing to these claims.

I wonder how many experts there are that just don't want to be another Jeffrey Wigand or don't know what is wrong?

I know that I am ranting but somebody should do it.

This is all very interesting, but it's all anecdotal! Can you PROVE that Singulair is responsible for all this stuff?

What other meds are you all taking? In what doses? Under what conditions? Do you have a family history of ? Are you under stress? Or are at least SOME of you just hypochondriacs who, reading this stuff, say to yourself, "Say, I get headaches -- sure, it's gotta be the Singulair!" C'mon, now -- hair loss?!

I've been taking Singulair for over 10 months, and if I'd been as damaged as you all, I think I'd know it.

Without rigourous medical studies to show what is REALLY going on, you lot are just gossipping.

This site is obviously trolling for a class-action suit.