Different color symptoms and conditions

I am 33 years old with borderline HBP, but otherwise healthy. I have been on lisinopril for about 2 years. I thought it was a miracle drug as well lowering my BP (110-120/75-80) with no side effects. The pill's appearance changed about 6 or 7 months ago and now is the faint yellow pill that says Watson 408 on them. They did not used to say that, and they used to be a different color. I immediately noticed side effects. For the past 9 months I have gotten stress tests, wore an event monitor for a month, corotid artery scan, been to the ER about 5 times, had bloodwork done etc...
My symptoms have been:
1. When at work the room looks darker, I am a programmer and it's like someone turned down the dimmer switch and I strain to see the screen
2. I have been suffering palpitations and the sharp stabbing pains on my left side and right side of my chest
3. Most recently I have developed headaches and just this week I went to the ER b/c I got dizzy and disoriented at work. The ER said it was a spell of Vertigo.

I never even considered that it could be the lisinopril, I guess that seems pretty silly but I thought that if that was it my doc would have told me. Instead they tried to put me on Lexapro and Zoloft and even gave me some Xanax. Tomorrow I have another doc appointment and will suggest to her (yeah she is pretty hot - looks like Angelina Jolie) that it is the lisinopril. I am going to insist that I get off of it. I will post what happens. Thanks to all of you for the valuable information.
God Bless.

I have been on Levoxyl for over 10 years with no problem. When I picked up my refill two weeks ago the pharmacist said that the pill may be a different color but it's just that the company that was making Levoxyl sold it to another company and is now making it. Within a week I was very itchy, then I started getting hives at night and waking up with them in the morning. I also developed severe heartburn. I feel very full and cannot lie down at night. I also can't eat very much at one time because of the heartburn/reflux. My family doctor advised I call my endo which I did. She advised me that she has had patients all week that are having problems with Levoxyl that never had them before. She took me off the Levoxyl and put me on Synthroid. I will start that tomorrow morning and hope I will get some relief soon. The pharmacist said I wasn't the only one going off the 'new' Levoxyl, others have been in all week exchanging their prescriptions as well. Has anyone else had this same situation?

Stomach cramps, night sweats which stopped when I forgot to take them on a long weekend away.

I get HEADACHES that don't go away. I know this a listed side-efect, but I was given this inhaler the last time I got Bronchitis. The name Albuterol was in the name of the inhaler so I assumed it was like other inhalers I was given when I would get bad Bronchitis (turns out it was Albuteral Sulfate HFA). The Bronchitis I get, happens at least once every 2 years and on down years mabe twice a year or twice every 15 months. I don't smoke, rarely drink, have no medical conditions (including Asthma), and I'm in the fitness industry, so I'm in great shape, eat a damn good diet, etc.. But nothing can overcome, either bad luck or bad genes or certain physical weaknesses. Not sure which it is that makes me so susceptible to Bronchitis, but I have to deal with it quite often it seems. It happens the same way each time - Beginning with a sore throat & stuffy head (no headache just horribly stuffed up) then after 3-5 days the sore thoat goes away and it moves down into my chest to a cough, then in about 48hrs it turns into full-blown Bronchitis where I can't breathe w/o wheezing and eventually coughing - nights are the worst.
So I go to my doctor and am prescribed antibiotics, sometimes narcotic cough syrup (yum) and an inhaler. It was ALWAYS just Albuterol in th past ( I know it was different because there was no 'Sulfate' or 'HFA' in the name and the inhaler looked different (color, length, even the horrible aftertaste it gave - but I knew it worked). With this Albuterol Sulfate HFA inhaler, yes it has a different color, packaging, length etc.. and all together which I would chalk up to no big deal (I'm not a M.D. or Pharmacist, so maybe it's a different company making the same medication). But the addition of 'Sulfate on the end of the name and the missing horrible aftertaste (which I miss only because the previous Albuterol inhalers I recieved worked great and I felt better in hours despite the wretched taste), let me suspect I was given a new inhaler medication. Well I got all better in about 5 days (about 3 more than t usually takes me) and it turns out I was given a different medication because the government seems to think my previous inhaler was for only those with certain medical conditions, was often abused(? news to me, why would somne abuse something that tastes so bad - I guess it got them feeling high - I don't know or care to),
Anyway, this inhaler was also responsible for TERRIBLE HEADACHES ( and I was already sick with a sever cough, congestion, a little fever, sore throat, and lots of yellowish mucus(sorry for the description),. I sure as hell didn't need a horrible headache to follow that, and these would only appear after I used the inhaler (it took me a couple days to figure this out), and they'sd stick around for about 12 hrs. I didn't want to take anymore advil or tylenol than I already was considering the rest of the medicine I was already taking.
So apparently my M.D. could've prescribed me the old Albuterol (I think), but for some reason the government put restrictins on it's distribution, either that or he was very scared to prescribe it. And this was coming from a M.D. who at the same time prescribed 300ml of Vicodin Tuss cough syrup. I know the horror stories of Vicodin, and I didn't even come close to sing all that cough syrup.
I just can't help but wonder why the previous Albuterol inhaler that helped so well over the years suddenly has a problem with the AMA or DEA or one of those agencies. This was the same type of inaler that worked well for my Bronchitis - and I'm sure thousands of other patients - over the past several years.) Again, I usually get it once a year, and go to the same M.D. who prescribes me the same Antibiotic, Cough syrup, and inhaler).
Whatever the case, I plan on politely asking my M.D. the next time I'm in there, but I've read quite a bit about Albuterol's sudden problems with dispensing now that this SulfateHFA has come along.
Well... WARNING: It will give you HORRIBLE HEADACHES and according to the post above me, it might even give you BRONCHITIS!!! The same stuff I was prescibed it to get rid of. This is just a microchosim of a microchosim of what is wrong with our government - in particular the Health Care industry. Find something that works.... might as well get rid of it, because a few bad apples are spoiling the bunch.
Imagine what would happen if they stopped using Morphine or Morphine derivitive pankillers just because there is a huge segment of this country's society abusing them? Don't get me wrong, painkiler abuse has become an epidemic in this country and a cousn of mine blew his head off after getting hooked to Oxycontin after severe back surgery, and when the Dr. wouldn't give him anymore for his pain, he went to the streets - a few months later he committed suicide and left behind a wife a baby boy. All due to getting what the Dr's and specialists told him was surgery ( he was a farmer and manual labor, including bending over, was something he did for years - but he had a wife and family to support)on his lower back that was absolutely necessary, and he was told it would give him a pain free life from then on and he could return to work. So I understand when companies are scared of drug abuse, or use for other than what wa intended. And for the record I'm so happy Oxycontin got their pants sued off for millions of dollars(and on a side note Rudy Guiliani, who wants to be outr next President, lobbyed on behalf of Purdue Pharma (makes of Oxycontin) for lenancy before the criminal sentance came down. And that supposed 'Great Leader' Guliani, knew full well of the misleading info that Purdue gave to Doctors about Oxycontn being a 'safe alternative' to addictive painkillers, and he knew how Purdue spent millions promoting Oxycontn's 'almost non-existant potential for abuse,' even after all these overdoses, addictions, and suicides that have been blamed on the drug. Yet due to his stake in the stock and his close position with Purdue's CEOs, even after everything, after Oxy's horror stories and addiction potential was fully known, and after thousands have either died or become addicted to this drug, and even after Purdue Pharma was found GUILTY in a Criminal Caseof misleading the Public(including Doctors) in the abusive potential of what has become one of the most abused drug in decades, Oxycontin, Rudy Guliani still got up in front of a judge in court to ask for leniency in his punishment of Purdue Pharma.
But is Albuterol Oxycontin - I don't think so.
If you are prescibes Albuterol Sulfate HFA - ask for something else, the side effects can hurt an already bad situation and there is already a different inhaler out there with Albuterol that works like a charm. And it certainly isn't addictive as a dirivite of morphine and heroin - like Oxycontin.

I have been taking lisinopril for about four months and my doctor increased my meds to 20mg from 10mg. Everything was fine except the tiredness so I take it at night before bed or I could not stay awake during the day. Then I wole up with numb feet one morning and just thought it was nothing as i get swelling when the weather gets warm. well the numbness is still there two weeks later. It is very uncomfortable and is moving up my legs and my arms and legs feel very tired and weak. Last night I counted the pills remaining from the last prescription refill and sure enough the amount left coinsides with the last refill, which by the way is a different manufacturer because the pills are a different color, shape and size. I went to the doctor this week and am waiting for the blood test results. I should know today. I am active and walk five days a week and work out at the Y three times a week. Has anyone else had funny feet problems?

I have been on synthroid for 18 months. I have always been 120 lbs. Now weigh 136. Way to much for me. My eyes feel like there is sand in them all the time. My hair is thinning, am tired all the time, my finger joints & toe joints ache, have a change in the skin on the front of my legs (skin apprears thicker & a different color, with nodules in a few places around the area), my throat feels thick. Yet my MD says my TC4's are right where they should be.