Dental work symptoms and conditions

Metallic taste, loss of taste: A few weeks after beginning my once/month Boniva dosage, I lost my full sense of taste. I now continuously have a sort of metallic taste in my mouth, a combination of salty/bitter tastes, and have lost the 'sweet' tastebuds. Further on the back of the tongue I still have some taste, but it is not what it was before. It's a personal loss, as I used to have very sensitive taste buds, this loss handicaps my ability to cook well, and I had been a very good home cook. I still retain a full sense of smell.

I have been on Boniva for about a year and a half, my doctor says she's never heard of anyone losing taste sensations as a side effect of this medication. I'm too concerned about possible osteoporosis, as I have osteopenia, to discontinue the drug for this alone. Has anyone experienced this side effect, is it permanent, or does it disappear if the drug is discontinued?

Hi, I am a 47 year old female and have been on Coumadin since Nov 1997 after developing several DVT's after surgery for a broken kneecap. Coumadin makes me feel like crap and the only time i have felt good in the last 11 years is when i have come off the medication for dental work or surgery. Some of my side effects are cold chills and cannot warm up, upset stomach, retaining fluid, heavy periods, added weight and my fat looks flabby even though i work out 4 times a week, lethargy, a very heavy neck on occasions and the list goes on and on. My coumadin has become very sensitive to what i put in my mouth. With "nutrients" added to so many foods i find i am now reading labels more than ever. The worst "nutrient" is Omega-3. This can cause bruising and bleeding without any help from Coumadin. Several deaths have been reported in the Australian media. I believe there is research being conducted in Norway using Kiwifruit as an alternative to Warfarin. I hope this is so and they are successful soon.

I got off Diovan because of diminished energy, drowsiness, and all-around lack of ability to focus after several years on it. I didn't realize it was the Diovan until I got off it and got on a weight loss med: Phentermine. I felt like I was 20 again. But that was short-lived of course because you can only take that stuff for 90 days, max. Diovan was bad for me. Then the Doc prescribed Lisinopril and I was on that for a couple of months until a week ago. I'd been suffering with a dry cough for a week when I told the Doc about the side effect and I've been off Lisinopril for 7 days. The cough is still but slowly going away. Bouts of coughing are no longer every hour on the hour but about 2-3 times a day and still all night long. I'm off of any BP meds now and my BP is 150/90, same as it was on both Lisinopril and Diovan. Apparently it takes a while for the Lisinopril coughing spells to go away.

I had septocaine for 2 minor fillings in feb 2008. It took me until nov after seeing a number of dental and medical professionals to be diagnosed with trigeminal neuropathic pain in the V2 region. I'm still in a lot of pain with no relief in site. I can't sleep, I can barely eat because all my teeth shifted from the poor dental work and I can't concentrate on anything. This drug ruined my life.

After being injected with lidocaine during a root canal procedure, the vision in one of my eyes was beyond distorted (the side they were working on). I had 3 injections prior to prep the tooth which is located upper right near the wisdom tooth. An hour into the procedure, I began to feel the doctor working on the tooth. So I wouldn't experience major pain, he then injected me one more time in the roof of my mouth. Within seconds, I noticed my vision was in that eye was beyond blurry. It was like I was seeing cross eyed, but my eyes were not physically crossed and my vision was distorted beyond belief. This totally freaked me out and lasted for a few hours until the lidocaine wore off. I have had a few root canals and dental work over the course of the years, but they used carbocaine instead, because I get too jittery with regular novacaine. Therefore no epi. What makes matters worse, is that they were unable to finish the root canal procedure, because it freaked me out so bad and my vision was messed up, that I was sent to the ER. I was told that he must have hit an optic nerve during the injection which most likely caused this situation and they were categorizing it as a possible allergic reaction, but again feel as though it was just the optic nerve that the lidocaine traveled to. Now I have to finish the rest of the root canal a week from now and will be having another dentist perform it. I'm so frightened that this will happen again. I honestly thought that my vision wouldn't be restored back to normal. Has anyone ever experienced anything like this?

Thanks.

I am a healthy 58 yr old woman. On May 20 2008, I went to the dentist to have two small fillings done. At the time of the shot I experienced what felt as though I had received an electrical jolt because the shot hit my nerve. This jolt radiated down to my ovaries. I complained to the dentist instantly. Right after the visit I started noticing that my hair was thinning. On June 17, 2008 at my normal hair appointment I commented to the beautician that my hair was thinning. On June 27, 2008 at the second visit to the dentist I experience the same problem from the shot and again told the dentist of problem. By July 18th I noticed some extreme hair loss in two locations on my scalp. I pointed out my hair loss condition to the Dermatologist at the Cleveland Clinic on July 18, 2008 he referred me to a hair loss specialist. On September 2, 2008 I meet the specialist she stated that the hair loss was caused by some extreme stress to my system. I told her about the dental work and my reaction to the injection. She said that could have been the catalyst that started this problem. The doctor said if there is some "shock to the system", as many as 70% of the scalp hairs are then shed in large numbers about 1 to 2 months after the "shock". This sudden increase in hair loss, usually described as the hair coming out in handfuls is called acute telogen effluvium. Has anyone else had a similar experience?

I had 2 surgeries at once last week and was prescribed Meprozine 1-2 capsules every 4-6 hours. The first 4 days I took 2 at a time and within 20 minutes my pain was gone, I felt relaxed and a little drowsy and was able to nap, which I needed for at least the first two days after my surgery. Twice in 4 days, one of my legs twitched and once my arm twitched. After the first 4 days, I would take only 1 as needed, usually in the evening after I has been up all day and was in a little pain. I had slight dizziness when I first stood up the first day only when I would get up to go to the bathroom. Other than that, I had no nausea, and I have to eat something before I take any medication, no stomach pains, no allergic reactions (I am allergic to medications with codeine in it), no depression, no emotional swings (in fact, if I wasn't sleeping, I was so relaxed that I was able communicate normally, laugh, make my normal jokes, etc.), I did not hallucinate or see things. I was also on an antibiotic, which my pharmacist said would make me very thirsty so I attributed my dry mouth to that. Last year, I was prescribed several different strong pain medications for severe chronic headaches and they did nothing. I would recommend Meprozine for short term relief for pain management. I do know someone who got addicted to Meprozine after taking it everyday for several months because a doctor kept prescribing it to her, so it is definitely only to be used for short term use. If I ever have to have surgery again, dental work, or need something for pain management, I will be asking my doctor for a one time prescription for Meprozine.

Yes dry eyes, blurry vision, stomach lining problems I now need reading glasses. I had to take ibuprofen for dental work & migraines for about 5 weeks straight 400-600 mg every 7 hours. Getting very sluggish and slow like my liver is congested again.Happened before on other meds. Had to take liver/colon herbs to bring my liver levels back down to normal....thank god for those herbs! I got them from Rene Ponder.

I discovered I had endometriosis in March 2000 at which time I had surgery to remove what was there, then the gyn followed up with the Depo-Lupron shots for six months. To help with the hot flashes, mood swings etc. My doctor put me on a very low dose of Estrogen which helped. I was having fertility issues before this and when I finished up the shots and the time had ran out and still had no period, my doctor put me on fertility drugs to give my body a jump start, and in April 2001 we found out we were pregnant, during which time my teeth started deteriating and by the time I have my second and last child in March 2003, I had to have major dental work done. I blame the lupron shot for this issue, apparently my calcium level dropped. I told my gyn about it and he said he had never heard of any such thing before as a side affect of the drug. I pretty muched laughed in his face and told him to advise future patients to increase the calcium while on the drug. Then recently I discovered like a lot of you that there are some really serious side affects from Lupron. Since this after having my last child I went on the Depo Prevera shot for 6 months, gained unsightly weight, so I got off of that and got my tubes tied in 2004, then by March of 2006 I knew my endometriosis was back full fledge and in June 2006 I had to have a hysterectomy. My only long term affects from the Lupron and Prevera shots is still trying to lose some of the weight and living in pain during every meal but due to the extreme affect it took on my teeth, I can not afford even with insurance to get all the work needed done!!!! If I had to do it over again, I would have had the surgery and then worked on getting pregnant immediately, because long term..... It isnt worth the "preventative" HaHaHa!!!!

I have had severe gum pain which is radiating in to my jaw from a septocaine injection I got 2 weeks ago for dental work. It felt as though I had received an electrical jolt or a hot poker when I got the shot. Have been in misery ever since. Still have a large ulcer type sore on my gum where the needle hit. Please, never give this drug to anyone else. It has been a nightmare for me.

I have been on pred for 2 years off and on for Temporal Arteritis that the doctors at long last have decided that I don't have. They started me out on 60 mm and now they are taking me off at 1mm every other week. I am down to 11mm now. I have experienced all the side effects except the acne and problems with periods. I gained 40 pounds and have such bad pains in my lower back that I can't stay on my feet for long. And I'm always hungry though I try to control it. My main withdrawal symptom is extreme itching from my neck to my wrists and thighs. especially where there is any pressure on the body such as waist bands etc. I tried to get off it once but it was at a faster rate and that is when the itching started. I will gladly put up with the itching as long as I can get off this "Satans curse" of a medicine. I also have jerking in my hands and a general feeling of shakiness. I was glad to read that someone else had painful sensitive teeth I didn't know it was connected to the pred. I too wonder if I will be able to lose all this weight after I'm off the pred. I do know that the moon face goes away because it did the one time I came off the pred then had to get back on it. I also have weakness in my thighs and arms. and my arms are always getting big ugly bruises or torn skin on them to the point that I have to wear long sleeves in hot weather.feel free to email me with your story. Especially if you are off of it so I can have some idea what might happen to me