Taste buds symptoms and conditions

I am 51 year old woman and have been on Lisinopril 5mg and Bendroflumethiazide 2.5mg for many years now, about 8 (not sure). I got the dry cough to start with and then it vanished, to be replaced with a productive cough. I get, at any time, but thankfully not all the time, a constant need t clear my throat and a wheezing in my breath. I am producing copious amounts of mucus and this is what sets it off. It most often happens after eating or after I have been sedentary for a long time so I get it a lot when in bed. I cough until it all clears away but sometimes I am sick, or I cough myself dizzy and come over all peculiar. It is not a listed side effect but I never had this before. My hair has suddenly thinned, hairdresser told me he has notice a big change in my hair (am menopausal but not through it yet, I suppose my age and meo could be cause of thinning hair). I suffer from terrible stiffness in my feet. Sometimes I can hardly walk as my legs and feet as so fatigued. I will limp upstairs one at a time. Other days I can s[rint up! No regular pattern but I have started using a walking stick often as one ankle is very weak and can give way. Could it be the Lisinopril? I had three day bout of my taste buds going haywire about four years ago but it righted itself. Now I have it again, only not quite so bad. I can taste tea and coffee and savory foodstuff mostly as normal but sweet things either are tasteless or bitter. I don't know if I should go doctors or not. Does anyone else get this constant hacking cough due to excess mucus suddenly being produced. Tenalady are making too much money out of me due to this, lol!

The dermatologist gave me Bactrim to treat acne, I took the first pill in the afternoon and at night time I was vomiting and had fever.The next couple of days the symptoms went away but then they came back with itching, rash and lost my taste buds.I stop the medication and I am hoping that this symptoms go away. I guess I am allergic to this medication.

Prescribed Bactrim for MRSA skin infection on my arm that I picked up at my local gym. Day 1 OK, Day 2 severe headache at the base of my skull. Day 3 continued headache, general nausea, gas. Day 4 I began to develop a low grade fever and dizziness. Almost passed out after walking just a half mile. Still a severe headache, weakness. Day 5 Headache, consistent fever of 103, chills and muscle aches, light hives visible, weakness, unable to sleep. Day 6 early am, couldn't sleep all night, went to the ER with the worst muscle aches and fever I have ever had. Hives now very clear and pronounced all over my torso. I was tested for the flu. Said it was not, but was a viral infection that was attacking my muscles. Muscle breakdown found in both blood and urine samples. ER physician changed medication to Clindamycin HCL. Told to stop Bactrim, but thought what I had was viral, not a reaction to the Bactrim. I continues to feel bad for a couple more days, but hives started to reduce, fever diminished and started to feel halfway human after being off Bactrim for a couple of days. Still not 100%. New med has it's issues too (have to take every 6 hours, can't lay down after taking it) and a nasty taste in mouth and stomach upset, loose stool. After 5 days of new med went back to my doctor. A secondary infection had set up in the Staph area. The fungal infection needed a different med. Now is 4 weeks later, after finishing all meds, still have an infection. Blood cultures taken to see if the infection is the staph or fungal. I have lost 8lb, have no taste buds, loose stool, severe stomach cramps/burning (now taking Activia to put back good bacteria in my stomach...no one told me to do this before!!). If Staph not gone, need IV antibiotic for a month. I am 50 year old female, but note I had taken this in my 30's without any problems. You can develop an allergic reaction to medicines previously OK for you. Beware of Bactrim. It kicked my behind!

Started with fever, then rashes, then swollen face, then rashes all over the body, then no taste buds and did not feel like eating. Very tired all the time. Stopped taking the drug after the 8th day when fever and rashes started to appear. Took lots of water after that to try to flush out of system. After 12 days, taste bud seem to be coming back. Skin has started to become flaky and peeling. More like extremely dry skin. This was an extremely bad reaction and can cause very bad side effects. See you doctor as soon as an allergic reaction starts. Blood tests seem to be necessary to make sure the drug hasn't affected other organs. Good luck to any one who has to go through this reaction.

Like most of you all I am on Topamax 100mg. I am a 27 year old female that has suffered from severe migraines for over 20 years that would last up to 2-3 days and completely debilitated me. I would bleed from my tear ducts from the extreme pressure and I would need to be in a quiet, cold, closed off room to be left alone until the migraine was gone to continue on with my life. It was ruining my life and taking over my day to day routine. I could never really commit to anything without the constant worry in the back of my mind about a possible migraine until I found Topamax. Now on Topamax I went from 4-5 migraines weekly to 1-2 monthly, it is truly amazing, however there is a catch. Although the medication is wonderful and I will never get off of it at the rate of success that I am at, I do have side effects. I have extreme tingling in my extremities, (hands, feet) along with my face. It feels like they are constantly asleep. I also have noticed the poor tasting carbonating drinks along with my taste buds changing with certain foods that I use to be so fond of. I also have a very smokey haze where it almost feels euphoric if I wake up in the middle of the night. I have horrible nightmares of people that I have not seen in or thought of in years, memory loss and spelling issues-all goes away after 3-4 months of uses. I had shortness of breath, however that subsides as well with the use of the medications along with several other side effects. I have lost over 30lbs that is along with diet, so I can't say it is all Topamax. I have noticed little nodules that have been showing up on my hands since I stared taking the medication that I am in ? about I have a call in to my neurologist to see if he has heard of any such thing. Other than that I love the medication, because if not having migraines is one of the side effects-lol I can handle the side effects. I hope that this will help anyone that might have anything similar to what I am going through. If you can shed some light on my nodule situation please let me know. Thanks

started Zpak last week for a lingering sinus infection. I live in an area where the weather changes constantly. Two days after I finished the 5day Zpak I began experiencing horrible and flu-like symptoms and worse. I can hardly breathe out of my nose. Heavy chest congestion. Lots of diarrhea and even blood in the stool one day. Taste buds are gone. Here I am a week after finishing the Zpak feeling HORRIBLE. I'm afraid to go back to the doctor (uninsured) only to be prescribed something else that might bring on more side effects. Right now I'm taking Sudafed PE and hoping that kicks it. I've been on a Zpak before but NEVER had side effects like this. I don't wish this on anyone. and I'm wondering how long the Zpak stays in your system? It is possible to make you sicker? Seems so in my case and many others here.

For Medications.com October 18th
Earlier this past summer I took this drug for ninety two days after I was prescribed this medication when I visited the doctor for a bladder infection and I was told I also had high blood pressure. No tests were done except for a urine test at that time and no follow up tests were done later. This drug not only gave me a slew of other side effects but pushed my simple bladder infection to where I no longer urinated in a normal manner regardless of the amount of fluid I added. Only after discontinuing this drug did normal urination return after a few days.
Allergic reactions were as follows. Severe debilitating stomach cramping resulting in swelling of the abdomen, and all digestive organs. Angioedema. (no pre history of this) Urine flow continued to lessen even with increased fluid intake, resulting in bladder pain and a sensation of bladder being pushed from the body. Lack of energy, flu like symptoms, insomnia, leg cramps, many bouts of rapid heart beat, some lasting for awhile, even after stopping the drug. Lack of appetite and a change in taste buds. I had several bouts of angioedema but thought it was 'something I ate, stress etc', as within a month of my diagnosis, my daughter had an extreme reaction to Ciprofloxin (see floxintoxin under that medication) and anything that was going on with me was put aside. She was debilitated by her drug reaction and was unable to walk etc, so I thought I wasn't handling stress too well as I was getting older. Each bout increased in severity leaving me lying debilitated on the couch for four days, eventually for a full week until luckily by that time my daughter was able to take care of herself and began thoroughly investigating this drug only to discover that Lisinopril was the true cause. The warnings with this drug are not very explanatory and leave so much out that should be for patients to read and digest to make their own health decisions and it takes a lot to dig deeper on the Internet to find the true adverse reactions.
We thought by stopping the drug I would get back to normal quickly and I did with the help of a herb called marshmallow which reduced the swelling after a couple of days. However after I thought I was cured I stopped marshmallow and within a couple of days had another angiodema reaction and I thought it was because there must be traces of this drug left in my system. I then took marshmallow for over two weeks and feeling fine I stopped again. Then another episode hit me with not only the stomach problems but a severe bout of coughing that lasted a couple of hours and trickled into a few days. It was then I began digging on the Internet to find the words I wanted to hear, that this drug caused long term problems. I found it by adding UK after other words and found this and much more.
ACE-INHIBITORS
A particular group of heart pills called ACE-inhibitors (the chemical names end in -pril, e.g. enalapril, lisinopril, ramipril) can occasionally cause urticaria, although they more commonly cause angioedema; about one person in 100 who takes an ACE inhibitor is likely to get this problem.  
The reaction is not caused by true allergy, allergy skin and blood tests do not show it, so why does it happen?  Reactions are thought to occur because an unwanted pharmacological effect of the drug causes the release of compounds similar to those released in an allergic reaction.  The only way of showing that a regular medication is the true cause is by stopping or changing the treatment.
To complicate matters, the angioedema attacks may not start until the individual has been taking the ACE inhibitor for months or even years making it difficult to spot the relationship. Also, attacks may continue for several weeks after the drug has been stopped.
I could not find anyone doing following to patients with adverse reactions and I think that is a very bad problem. We are on our own. I do hope this helps others and if you want copies of all my research let me know.
Now I am hoping there won't be any more bouts but I'm still taking marshmallow and when I think I have the courage I will wean myself off it slowly and watch for signs. Believe me angiodema isn't fun and you can't see it on the outside of the body which makes it difficult to understand.

I was prescribed SMZ/TMP DS 800-160 for a UTI...one pill twice a day. I had been taking it for 2 days. On the 3rd day, I broke out in hives in areas on my chest, sides, back and stomach and the next day started noticing small bumps on my arms and legs, too, that weren't as small and irritating as the hives the day before. Needless to say, I stopped taking it that day, the 4th day. However, it's the 3rd day since I've stopped taking it and I am still itching and skin is still broken out. This medicine had also caused a loss of appetite and altered my taste buds, but the break out is the worst of all and is ongoing, unlike the other side effects which were back to normal shortly after I stopped taking the pills. If anyone else has experienced the skin irritations, how long did it take for it to stop after taking the pills?

My mother was given this drug, Lisinopril, because the doctor decided she had high blood pressure after she went in for a bladder infection (she's had these all her life, every now & then). The doctor also prescribed Nitrofur (please avoid THAT one like the plague - she was on the couch for a week in stomach agony). We didn't put 2 and 2 together on what was really going on until yesterday. She was on Lisinpril for 3 months and every 2-3 weeks had an episode of extreme stomach spasms, bloating and fatigue. These episodes have lasted 3-5 days each, keeping her on the couch in agony. I researched the internet and found out that Lisinopril is made from SNAKE VENOM, can you believe? Turns out lots of people have reactions from this, including coughing. There was one woman who had the exact same things as my mom and wouldn't you know it, stopped using Lisinopril and the episodes went away. Turns out this is an allergic reaction, something they say is rare, BUT I think it depends how long you take it and how sensitive you are. So my mom immediately stopped taking it. What's happening inside is something they call gastrointestinal angioedema (in layman's terms, internal hives). If you experience coughing, the hives are in your throat. If you experience the stomach pains, the hives are all in your intestinal tract and very possible more areas internally. So then I looked up and found an excerpt from "One Earth Herbal Sourcebook" on Google and found the author had experienced something similar, using ayervedic (indian) herbs to fix the problem. I couldn't find where to buy ayervedic herbs, calling Whole Foods Market with no success. Well, all over the world there are healing herbs that do similar things. So I did find 2 that would work. Marshmallow (the herb, not the campfire kind) will help relieve swelling internally. There is another herb called Goldenseal (don't use it if you have very high blood pressure as it can cause a spike) that has antibiotic and anti-inflammatory properties. Anyway, now you know what is going on inside - hives you can't see from snake venom. Take that to the doctors and see what they say. Maybe your just better off like we are to research yourself and find a natural answer from nature. I hope this can help others avoid the hell we've been through.

I have been on 10 mg Lisinopril for 5 weeks. I wake up in the morning with tight joints and sore muscles. My heart races. I feel light headed at times. I have asthma and worst symptom is it is causing me to stay up all night because I suffocate and cough badly if I lie down. I can hear myself wheeze during the day and night and feel like there is fluid around my heart or lungs. My hands and legs feel swollen. My stomach feels raw and I have no desire to eat red meat it just doesn't taste the same. My taste buds have totally changed as any food or drinks doesn't tastes "good" anymore. I'm also on Lopressor for HTN. I am going to stop taking the Lisinopril as I can not deal with the suffocating and wheezing. I get that more than the "cough" the doctor warned me about.

Took z-pak, in March, have lost my taste buds and cannot smell anything,this is going on three months, I don't know what to do, n smell at all, no taste buds at all.

IM trying to figure out if Boniva is causing me to have severe eczema on my hands and feet; palms and soles. I am 58 yrs old and never had this happen before. I began taking Boniva in late Nov 2007. Followed directions carefully. The first week I STARTED TO HAVE the flu like symptoms and fatigue lasted well into january and also seemed to lose a sense OF TASTE FO R FOOD AND DRINK. JAN17TH -FEB 2 GOT AN AWFUL FLU THAT LASTED ABOUT 5 DAYS. 102 FEVER, MUSCLE ACHES, PAIN, JUST AWFUL. THEN MISSED TEN DAYS AT WORK BECAUSE IT TURNED INTO A SERIOUS BRONCHIAL/ UPPER RESPIRATORY INFECTION- I FELT LIKE I HAD WHOOPING COUGH.THE DOC GAVE ME A REALLY STRONG ANTIBIOTIC-( CLARITHROMYCIN ) AND IT TOOK ME UNTIL MID MARCH TO FEEL LIKE MY SELF. NOTE; I HAVE NOT MISSED MORE THAN A DAY OF WORK FOR SICKNESS IN OVER TEN YEARS.)drink. The taste buds seem to have come back but WHEN I TAKE THE BONIVA PILL I FEEL FLU LIKE AGAIN- FOR ABOUT THREE-FIVE DAYS.
ALL OF THIS WAS BAD ENOUGH BUT I CHALKED IT UP TO FLU SEASON ETC' THEN IN MID MARCH I STARTED TO HAVE A TERRIBLE CASE OF ECZEMA ON THE SOLES OF MY FEET AND PALMS OF MY HANDS, IT IS REALLY CHRONIC AND VERY PAINFUL. I HAVE TO SLATHER MY HANDS AND FEET WITH VASELENE EVERY NIGHT .AND HAVE BEEN TAKING PROBIOTICS AND L-LYSINE FOR THE PAST MONTH WHICH DOES SEEMS TO BE HELPING- BUT NOW I'M WONDERING IF THE SKIN CONDITION IS A SIDE EFFECT FROM THE BONIVA? FIRST THOUGHT IT MIGHT BE THE CLARITHROMYCIN. BUT I HAVE A GUT FEELING ITS THE BONIVA/ ANY IDEAS?

I had a cholesterol of 237 and my doc wanted me take Lipitor. So i did for a month and a half. About a month into it, I started noticing that my mind was becoming foggy. So I started to take it at night. But then I noticed after a month that my right leg tingled for 2 days and I had muscle aches in in my shoulder and that my fingers started to feel weak, like I was losing my strength. I called my doctor and told him I cannot take this drug.

He pointed me to a Doctor Caldwell Esselstyn's website. It seems he reversed heart disease on a VEGAN diet. (Fruits, vegetables, grains and beans...NO MEAT, NO FISH, NO CHICKEN, NO DAIRY, NO EGGS... and so reluctantly I tried it. Even after 2 months, i noticed my body changing for the GOOD. I started losing 5 pounds every 3 weeks and my circulation was better, any aches and pains I had disappeared, my arthritis vanished. It is miraculous. Yes the diet is dull, but your taste buds adapt and all the food you used to love, suddenly tastes too salty, too sweet, too oily...I cant even tell you how much my body has improved in such a short time. I also previously had 2 blood pressure pills. Now I am down to one.

For anyone serious about improving their health. TRY A VEGAN DIET for just 3 months. I'm not kidding.

I didn't really have any side effects with Relpax. The most wonderful thing was that it made my headaches go away. Of course my Dr freaked out when she found out that I was taking them on average 3x a week and switched me to Topamax because the frequency of my headaches meant that I had chronic migraines. I HATE Topamax. It gave me a lot of side effects and I still have my headaches. I want my Relpax back!

Diminshed taste buds, everything taste like pus

I started with 60 mg per day for polymyalgia rheumatica and now after two years have weaned myself down to 5 mg per day. I have a side effect that I have not read anyone else having. It has effected my taste buds. Many foods that I loved in the past, have a foreign taste to me. I am 66, male and have tried to drop down to 2 1/2 mg but the pain is too intense to remain at that level, so had to return to 5 mg. I have lots of pain in the feet and especially toes. I can tell that I am getting better and am very anxious to get off of Prednisone.

Taking Topamax for 2 years started out at 25 mgs 3 times a day for a mood stabalizer (bi-polar). Had tingling in hands and feet sometimes in face. Lost waight, pop tasts nasty, sleepy, short term memory loss, slurred speach. Now I take 100mg at bed time have no symptoms except I still am able to controll my eating (had a problem with over eating) no more road rage but I still felf a little depressed and did cry so I was not to stable until Citalopram 10mg at bedtime and Adderall XL 10mg in the morning was added. Now I finally feel like a totaly normal person. No more anxiety, mood swings, crying, paranoia,or any other weird stuff. I feel pretty good. Rarely I get pins and needles in my hands or feet or I forget where I put something.

I have MS and the first high dose steroid treatment (Prednisone) I was on I weighed 115lbs. I just finished my third high dose treatment over the last 2.5 years and now weigh 170lbs. I'm sure this wont be my last treatment either. The other bad side effect is it seems to kill your taste buds and it takes so long for them to go back to normal.

I have only taken the medication for 24 hrs and have noticed a difference. My taste buds are all messed up. Im a chocolote lover and it doesnt even taste right. I can taste the minerals in bottled water which tastes crappy to me - nothing i like tastes like it use to. reading all the posts kind of scares me - can anyone tell me how long it was when you first started to notice the hair loss? Thanks.

i've been taking sulfameth/trimethoprim800/160 for a bad cough n conjestion n in a few days my tongue swell,taste buds gone my mouth is totally dry. the skin on my tomgue seems to b splitting... i quit taking that stuff.

I took a 7-day course of Biaxin and didn't notice anything during that time. Had bronchitis and got better. After the seven days my taste buds disappeared and I cannot taste. My entire mouth is sore, including tongue. My mouth and tongue feel like a very bad tongue burn. I have a lot of metal in my mouth because I have a partial plate and made mostly of metal in the roof of my mouth. So maybe the taste everyone talks about is a metallic taste. But I tell you this, it hurts. I'm just wondering if my taste will return. Has been like this from 7/01 and it is now 13 days later.

I just took this med along with minocycline to treat a staff infection...after about 7 days I started noticing my tongue was very sensitive...like I ate too much hot spicy stuff and my taste buds were sticking up. Also got really itchy skin and not sure if this was because of this but my appetite changed dramatically...I was ravenously hungry every few hours...would actually wake up in the middle of the night and eat whole meals and then got horrible sleep to boot! I have been off of the meds for a day and a half and am starting to see my symptoms subside, but not completely. Was very irritable, tired, hungry and got very bad sleep while taking this. Not excited about ever taking it again, as I think it really messed me up!

200 mg a day since April 2002, dont know if my visual problems have anything to do with Topamax or not. my visual field is effected. Will know more after further testing. Pressure is great. Tremors under both eyes now. Tingling in hands once in awhile now. Nothing like at first. Headaches much better once a month or every two months. Weight loss was great. Keeping it off. taste buds changed. Couldn't taste much at first. Over salted everything. I can drink soda now. Diet soda doesn't taste good at all. I drink juice now. Water it down. Short term memory lost still is a problem.

I haven't seen the weight loss yet, but have had a decrease in my appetite, but I take imitrex for migraines and have to eat through the headache to feel better. I know weird. Very dry mouth and soda's taste weird, but my teeth are very, very sensitive. I expected the weird taste buds but are the sensitive teeth normal? Taking 75 mg at bedtime. I was on birth control pills until this week. too many headaches!

I have been taking omeprazole generic for prilosec for about 3-4 months now and have been experiencing dry mouth and a cracked tongue as well as my taste buds on my tongue are always irratated. Does anyone else have theses symptoms?