Intestines symptoms and conditions

was give coumadin in November, and by April my stomach hurt so bad I couldn't stand the pain. i hac a colonoscopy, and sigmoidoscopy. This doc couldn't find anything wrong. Made another appointment, ad just had the colonscopy, and sigmoid again. I have ulcers in my stomach, and the upper part of my intestines.

I know it has to be the coumadin.

Hi. I just had a laproscopy done 3 weeks ago for endometriosis. I am 26 yrs old and have been dealing with this pain for almost 2 yrs now and it is the worst pain in my entire life. My doctor is now suggesting Lupron because even after the laproscopy the endometriosis was level 4 and had bonded to my intestines and literally trapped my ovaries and uterus against the lining of my stomach. The pain was a 15 to say the least and the past 3 mos it had landed me in the E.R. Finally the docs figured it out. I started my period 2 weeks after the surgery and the pain was still pretty bad. An 8. Now I am seriously considering Lupron. My health is on the line and this pain is not right. At this point I am considering a hysterectomy if Lupron does not work. Any help suggestions please? Monday I follow up with the Dr.

I was diagnosed with pneumonia on July 6 and prescribed Levaquin 500 mg for 10 days. I took my last pill tonight and could not understand the pain in my right hip, red eyes which I suspect comes from the insomnia I have been experiencing since July 10. I am still having difficulty sleeping and tonight I feel extremely tire with discomfort in the back and shoulders. I wish I had read these comments earlier, I would have discontinue using this drug. I have not experience any depression, but lack of appetite, stomach pain and upset stomach. I have had intermittent diarrhea. How long will it take for this drug to get out of my system.

My precious daughter, Trinity, aged 5, had UTI symptoms, and I took her to urgent care on 7/1/09...she took her first dose at 3pm on 7/1, and about 4.5 hrs. later said her head hurt on the top of her head (almost has NEVER complained of her head hurting her whole life!). Then, today, 7/2, she has been having lots of eye discomfort and pain and has red eyes (poss. from fever?), and the most striking symptom after taking sulfamethoxazole-Trimethoprim DS is that she says she feels VERY sick and has been about to cry and just looks at me pleadingly and says her stomach hurts. Also, she cannot eat much. She says she wants to eat, but she can't. She has felt like she wants to throw up, but hasn't yet. ATTENTION: Go to http://www.remedy-bladder-infection.com/children.html and you can use a NATURAL URIBIOTIC derived from fruit that the e.coli is attracted to, binds to it, and then is detached from your urinary tract walls, and can be washed out by your urine. I will NOT be giving her anymore of this, as I know it wipes out the beneficial AND the bad bacteria from her intestines, and 80% of the immune system is in the intestines! I was just afraid cause she was so sick, and I thought these antibiotics were the best thing to use...I just tonight found the sight about the URIBIOTICS! Try those! I will protect my daughter from this!

I got my IUD a yr ago in March 2008. The only contraception that had the least side effects for me was the Depo shot, but my doctor said I shouldn't use it too long consecutively. He suggested the Mirena. I had my doubts because of the stories I heard. But I personally knew two women who had got it, and had no real problems. So I took a chance. I went in, the first time the doctor couldn't put it in cause I was moving, it felt like strong contractions when he tried putting it in, so he gave me muscle relaxer for next time. But that didn't work and a procedure that says takes minutes, took an hour and half way through I told the doctor to stop because I was having contracting pains. He said no turning back it was almost in place. It finally got placed, and I bled so heavily for weeks non-stop and went through numerous pads each day and I went to the doctor two weeks after and said I wanted out, he promised symptoms would subside, to give it three months. So I did, and came back wanting it out, he said give it another three months. So I did and just stuck with having periods 19 days apart for two weeks long. I was always Pmsing, always bleeding until I switched docs this year and asked my new doctor to remove it. This thing has ruined me. I had two surgeries to get it out. First was a DNC, and the doctor wasn't sure she got it all out, because the ultrasound I received did not show anything. She was concerned that it may have perforated my uterus and went outside. So I got an XRAY which showed it was in my stomach just sitting there, not near the bladder cause it could have caused damage. So she scheduled a laproscopy surgery with a small incision but told me to prepare for the worse in case she couldnt get it that way .Sure enough, the worse was inevitable and she had to cut me open, they found the IUD stuck to my incision and my uterus and intestines were stuck to my abdominal wall. I am now recovering for six weeks and terrified of any other birth control.

On April 21, 2009 I was given Avelox for a sinus infection that I have been fighting since September. I has nausea ,vomiting, hurting all over, headaches, burning pain down my neck, my intestines feel like they want to come out, my kidney s feel like they are trying to rip out my back, i am weak, having crazy dreams, acid reflux, craving salt....i was given a ten day supply ...I took nine. I had no idea that all of this was from Avelox until I found this website I feel like I could just die. When will I get better and how long will the symptoms last I have not taken any since April 29,2009 Can anyone give me answers!!!!!!!!!

PERFORATED MY UTERUS --- The placement of the Mirena was extremely painful. I could barely drive afterwards. I was sure that something was wrong, but the doctor assured me that everything was fine. I breastfed my son for a year (I had it placed 6 weeks post-partem) which is why I had it placed in the first place. It was considered safe for breastfeeding mothers (please research side-effects of the active hormone it releases on infants. We now know why our 13 month old has had respiratory issues since he was 5 months old). Over the year, I had radial stabbing pains up my back and down my legs. It hurt during sex. At my year check up, I asked the doctor to remove it, but he could not find the strings to remove it. After an x-ray confirmed that it was still in my abdomen, he scheduled a hystoscope to find it and remove it (he assumed that it was still in my uterus). During the procedure, he could not find the Mirena in my uterus and had to perform emergency laparoscopic surgery to remove it from MY ABDOMEN. It had PERFORATED MY UTERUS. My husband and I now know of 4 women that this has happened to just by telling people our story. WE LIVE IN A SMALL TOWN!!!! THE NEGATIVE SIDE EFFECTS ARE UNDER REPORTED!!! PLEASE INFORM YOURSELF BEFORE GETTING THIS DEVICE.

I have been on the nuvaring for almost 3 years.
The first year was great! I hated taking a pill everyday, so at first i opted for the Depo, which was great for a year, but i really didn't trust it and not having periods made me uneasy.

The nuvaring seemed like a blessing! I had no trouble for the first year and a half. I recommended it to all my friends. I didn't have any side effects, and I loved the convenience!

However, now i am experiencing some serious side effects, and thanks to this website I realize I am not the only one. I have two concerns that i link to the BC: depression and no sex drive. Some days I just want to lay in bed, and sleep. I do not want to leave the house, or see anyone. I have told my BF (of 3 years) that i just need some "me time". I am fatigued and show many symptoms of depression.
I am only 24 years old, and i have NO sex drive. It has taken a tole on the relationship with my boyfriend. Many nights i try to get in bed before him, so i can appear asleep. There have been so many nights where i would tell him "i'm sick", "i have cramps"... sooo many excuses. When we do have sex it is usually forced, and i do it because i haven't in a week!

This past year I have also had digestive problems, which seemed to have appeared out of no where. Im not sure if I blame them on the nuvaring, but I've noticed a few other people have mentioned it as well.

My daughter is 16 and was given Levaquin 500 for a sinus infection. While on the medication she was tired but not much else in the side effect category. Now here we are 4 weeks later and she has acute abdomen pain, extreme fatigue,nausea, a headache, and she has lost 21 lbs in 2 weeks. I took her to the doctor and they ran a cbc, chem 12, urinalysis, and an electrolyte panel. All came back negative. Basically my perfectly healthy little girl is suffering from this. I went back and looked at the Levaquin packet because I know it can sometimes take a few weeks AFTER medications are stopped for side effects to show themselves and of course, all her symptoms are listed.

My Mirena has actually gone through my uterus wall and attached to my intestines, after experiencing server cramping (worst than labor) and going back and forth to the doctor they couldn't find the Mirena and had to x-ray to discover it was in my intestines, this explained the excoriating pain i had as i am sure it is quite a big task for the Mirena to work its way through my uterus wall!. I was going to get it removed but the specialist said that it was more risky to take out than leave in. I used to get sever migraines until they found out the mirena was no longer in my uterus so i had to go back on the pill and this has stopped the migraines, however i am constantly still experiencing headaches, lower back pain, server anxiety, panic attacks, tiredness, feel sick and unwell a lot of the time. After discovering this site I am so getting this thing removed and hopefully will be able to get back to my normal self.

Hi
They gave me this antibiotic for kidney infection , I was medically evacuated to Baghdad ER, infection is clearing but am bloated, thirsty, belching worsen as I had Acid reflux surgery, part of the day I feel better and part very tired, worse am in a war zone and I need to be alert but can`t, medicine was given by the DR. Er, military Dr am sleepy tired, gas ,tightness in chest , fast heart beat ,unable to sleep though tired but took Tylenol and slept 2 night ago I have to walk in the middle of the night out of my chu to release gas and bloating , I still have 2 doses , 7 days of hell, also I have diarrhea some and pain in my lower back , am 44, healthy, I pray it clears out ,I do not like the crap is causing me, as am flying home back to the US to be seen by urologist,digestive disease specialist so my R&R will be with Doctors. worse I spent my birthday in the ER with IV and all kinds of tests hope all u guys feel better. Thanks T.

ent into cardiac arrest while being given carboplatin ,Had to be resusatated,was put on a ventilator my left eye and my hands and my tongue and my lips swelled twice their normal size,was in icu for 2 days and in isolation for 2 days due to this carboplatin ,I had to be resusatated twice in a short time period.I have anal carcinoma and it has metastasized to my intestines and liver.

I have Crohn's disease and have been on birth control since before my diagnosis. I use to have flare-ups of the disease every now and then (I was on Mircette). Then last year, I was put on Nortrel and my disease started acting WAY up. I was put on the NuvaRing two months ago and I am having even more flare-ups now. Is there anyone who has a digestive disease and have had their symptoms worsen with the NuvaRing?

Only on it for 1 month so far and already having issues. I apparently have the worst case of endometriosis all my doctors have seen, including a cancer specialist that had to do all my surgeries because of the severity. Granted, I am only 31 years old and have had a full hysterectomy. So, after 3 surgeries I am still having severe abdominal pain and bleeding (don't know where that is coming from since I don't have a uterus anymore) so they said try Lupron and I finally gave in. Now I started getting such severe pain in my lower back that I can't stand for longer than 15 minutes and terrible side aches. I started getting headaches (which I already take pills for for years now),and have gotten the hot flashes as well. What are we to do ladies? I am so sick of complaining to the doctors about pain. You feel as if you are a big cry baby. What are my options here and does this ever stop?

Hey ladies! I am not shocked to hear all of this! I had the Mirena placed in me on July,10,2008. It is now October 27th, 2008. Almost 4 months with this in me and i feel like crap! I mean, i thought my headaches were from lack of sleep or something. Im cramping all the time, I have had sharp pains in either right or left side of my stomach but never both sides at the same time. I broke out with acne on my arms UGH and i have never had acne on my body. When i have a period, they are heavy, i fill the toilet up with blood, i fill up a pad in NO time, it lasts a lil over a week, and i have had meat like substances (looks like intestines, or chewed up hamburger *sorry*), and dime & nickle sized clots pass out of me! I have a picture of it and dated time of the passings. When i called a nurse about the passing of the meat and clots, all she had to tell me was "take a pregnancy test and if negative, then take Motrin tablets and see if that helps" WHAT?! I have noticed im a lot angrier now. Its not a pretty sight. =/ I have 1 child, my son (22mths old). I haven't noticed weight gain, maybe at the beginning but i figured it was bloating. When i talked to a different nurse about all of this a while ago, she had thought the mirena had fallen out!!!!!!!!!!!!!!!!!!!!!!!!!!! Uhm noone told me about this happening!!!!! All i heard was the best about it and not the worst! I havent taken a pregnancy test yet, im so scared to! I cant afford another little one right now! =/ I am going to weigh this out one more month, because they did tell me it takes 3 months to adjust. So after another month, by December, if its still the same. Im removing it.

Why does Singulair cause these symptoms? I am going to give my explanation which is only a HYPOTHESIS. This should not be categorized as any thing but an educated guess. This is not backed by scientific research because nobody will do any research that would appear to anger
Merck even if people are suffering in the thousands.

1. The original research that preceded the development of Singulair (montelukast) seemed to focus on the theory that asthma was caused by an unusual immune response to certain pathological stimulus. There are many references to the observation that a high percentage of asthma sufferers are people whose asthma is caused by fungus. Many people suffer from asthma and are told that they are allergic to dust mites. Dust mites can live only because the fungus aspergillus pre-digests the
food source that dust mites can then absorb. Other sources of fungus occur in the home due to dampness or problems with wood rot.

2. The body's immune system fights certain categories of pathogens such as bacteria and fungus by creating nitric oxide which kills them at the site where they try to enter the body. The mast cell is the immune cell that is responsible for the production of nitric oxide. Mast cells are found in the skin, airways, intestines etc. The mast cell is capable of many different types of biochemical functions that are designed to signal other cells or other chemical responses. When the mast cell knows that pathogens
are present and nitric oxide is NOT produced, then it signals other immune cells to be sent to the site of the infection. Thus in the case of asthma, it is known that excessive numbers of eosinophils appear in the airways and these cells create inflammation.

3. Singulair was developed for asthma and later allowed to be prescribed for other reasons. I believe that montelukast probably creates a source of nitric oxide that prevents the mast cell from signalling for other immune cells to arrive at the source of infection. I arrived at that conclusion from studying the chemical structure of montelukast, the chemical structure of the gene cysLT1 receptor, and the chemical structure of the cell wall of fungus which would be what the mast cell uses to determine "what to do in order to kill the fungus."

The researchers who invented montelukast first had to clone the gene-cysLT1 receptor meaning that they had to be able to identify the gene and replicate it. Then by trial and error they had a find a "chemical"
that would bind (connect chemically) to the cysLT1 receptor. The theory would be that montelukast would take the place of the fungus or other pathogen and thus prevent the gene from reacting to produce the
responses that the sick patient with asthma produced. Merck says in the literature that montelukast binds with the cysLT1 receptor in order to prevent the mast cell from signalling the eosinophils to arrive in excessive
numbers that cause inflammation. I believe that montelukast is also causing the production of an amount of nitric oxide that is actually killing the pathogens that are present. For one thing, I would think that it
would be dangerous to incapacitate the immune system in that way without providing a way to kill the pathogens. I don't believe that the asthma response is just allergies to something like dust. Pollen from trees and flowers is loaded with fungus spores.

4. IF, IF, IF, montelukast does actually produce nitric oxide, then it does so by binding with the gene. Any place in the body where a molecule of montelukast encounters the cysLT1 receptor (a gene) then the corresponding molecules of nitric oxide are produced before the liver enzymes break the montelukast molecules up. Nitric oxide is TOXIC and
INFLAMMATORY. So let's look at the symptoms in regard to the location of the cysLT1 receptors. The location of these symptoms would not be places in the body where the mast cells normally encounter fungus or bacteria. The cysLT1 also has other functions in that it communicates with the cysLT2 receptors. Obviously, nitric oxide
should not be produced in these locations because of the signalling effect of nitric oxide on other physiological functions.

a. intestinal pain - the cysLT1 receptors are located in the small intestines
b. leg pain actually caused by vasculitis - cysLT1 receptors are found inside blood vessels- consistent with the fact that montelukast causes
Churg-Strauss
c. some people who didn't have asthma develop asthma - the cysLT1 receptors are in the airways
d. nightmares, depression, neurological damage - when montelukast penetrates the blood brain barrier probably due to unusual conditions of blood pH or electrolyte imbalance then nitric oxide in the brain causes neuron damage and excitoxicity

5. Why do some patients not experience side effects? Probably because genetically they are completely compatible with the model that researchers created when they cloned the cysLT1 receptor gene. I didn't not find any information about whether researchers knew that there are many different variations of this gene.

6. IF, my theory is even close to being correct, then why doesn't Merck do anything about researching these side effects. Maybe because nobody in the company knows how this drug works but the researchers who created it. All of the Merck literature is very vague about any biochemical information.

Again, this is just speculation and hypothesis. I have made an attempt to put this in simplistic language and therefore sacrifice scientific accuracy. But, I think that you will get the point.

SINGULAIR IS VERY DANGEROUS TO PATIENTS WHO EXPERIENCE NEGATIVE SIDE EFFECTS. DOCTORS SHOULD JUST REALIZE THAT
THOSE PATIENTS ARE NOT COMPATIBLE WITH THE MODEL FOR THE DRUG.

I had my mirena put in at the beginning of march for the one reason that my husband and I didn't want to use condoms anymore. I really enjoyed sex with no stress or mess of condoms or remembering pills..WHAT I DID NOT ENJOY was the 3 months of bed rest I had to go through starting from the second I had that F%@$#NG THING INSERTED. I wish the doctor would have shot me in the face instead. It started with the absolute WORST pain I have ever felt, exactly like all of you were saying. Im not a fainter..but I seriously came close. They wouldn't let me leave the clinic I was in such horrible pain after. My body turned white, I started sweating profusely and all I saw was black for a good half hour. It felt like they stabbed a knife through my uteris. That pain lasted a good 3 months and I didn't want to go through all that for nothing just to take it out, ya know? So I bared threw it. I gained WEIGHT THAT COULD NOT LOSE!! AT ALL!!!! I walked miles for no reason because it did nothing...and Im normally able to drop 5 pounds at the drop of a hat..this weight was freegin concreted to my stomach. I also have never had acne a day in my life and until I got it put in, now I am Miss Pizza face. Nothing works, not even proactive and its even all over my chest. And twice- I ducked down bending my body to go under a rope and something happened, I think the mirena scrapped the walls of my uterus because my whole stomach/ uterus felt exactly like mush. It hurt so bad I thought my intestines flipped upside down, I even went to the ER the first time it happened. WELL..yesterday, I had it taken out. I got fed up of being an acne faced fatty just for better sex. NOT WORTH IT. oh and periods? Yeah, I like 2 and a half week long periods and cramps that paralyze my legs. I feel 100 times better now already, I know my face will go back to normal and if I want to take a bite of anything, I don't have to worry about being bloated as if I just ate a thanksgiving meal (which by the way..I boated like a hot air balloon when I ate ANYTHING and EVERYTHING on the damn mirena!!!!). GOOD F&&^@KING RIDDANCE. and I am all in on a fatty lawsuit against this sh*t too..

Oh My Gosh - as I sit here with abdominal cramps typing my experience - I can see the light at the end of the tunnel. I started taking Lisinopril in late April 2008. On May 2 I had severe abdominal cramps and massive vomiting for 8 hours. Finally got myself to ER after I sent my family on to our vacation (I joined 2 days later). The ER attributed it to food poisoning. Lo and behold, I had another "attack" on May 9th. Back to ER I went (my husband witnessed my attack and insisted I go). They took X-rays and MRI - found intestinal inflammation but didn't know why. My internest send me to gastro dr. Third attack hit on June 5th and gastro doctor sent me to major hospital ER. They, too, did MRI & blood work. Looked at gall bladder, pancreas, stomach, intestines, etc. They found intestinal inflammation. Gastro Dr. took more blood and did more test (CT, MRI, Colonoscopy, Endoscopy). He couldn't find anything so he sent me to rheumatologist. She did add'l blood work and genetic testing. She though I had an auto-immune disorder - like Mediterranean Familial Fever! Please...! But all her tests came back negative. She too had no answers, only treatment for symptoms - Colchicine and Prednisone. Yuk. After having my 8th debilitating attack yesterday (since May), I've had enough. I went to the Web and found this wonderful site - along with some others with helpful info. I don't have confirmation that the lisinopril is causing this - but it sure sounds like it. I am a 49 yr old female and I've had no "life changing" events in my life (except for this nastiness) and have been on no other meds. I find it interesting that out of all the doctors I've seen - and all knew of the lisinopril - that none suspected this as a side effect.

My 1 year old son got into my box of chocolate Ex-Lax and ate about 3 or 4 pieces. Called Poison Control and they didn't have any suggestions except to keep him hydrated. I put him to bed that night, he was still in a diaper, and he had a bowel movement during the night. In the morning his butt had huge blisters where his stool had laid. The senna in the Ex-Lax caused severe chemical burns. He had to be admitted to the burn center at Akron Children's hospital. Most people aren't aware of how dangerous this product is because adults wipe after using the bathroom, but imagine what this chemical in Ex-Lax is doing to the inside of your stomach, intestines, and colon. I would like to make people aware of the seriousness of this drug, especially parents whose kids, like mine, will eat anything chocolate. I always assumed Ex-Lax was so safe, as they even claim on their box and that it would just cause you to use the bathroom without harm(as obviously even the Poison Control Center doesn't know the dangers), but Ex-Lax is very dangerous!

In 1999, Ex-Lax company changed the main ingredient to senna because the old main ingredient caused cancer. Ex-Lax and other senna-containing product companies don't want people to know about this. It's not even labeled on their box or website! They definitely know about it because I have called the Novartis Company and they have also had many other similar incidences. Please pass on.

V. Donaldson

My experience has been alright with Mirena...

I'm 18 years old. I got it inserted on January 17, 2008. The first day I had horrid cramps, and would get pretty bad cramps randomly for the first month or so.

I spotted and got break-through bleeding for about 3 months or so afterwards, and then my cycle started steadying out some. My period became lighter with minimal cramps, but it didn't become shorter. Finally after about 6 months my period was back in order. I now have lighter bleeding with minimal cramps, but the amount of time my period takes has not changed any. My period has always lasted around 8 days and these light periods I'm having also last around 8 days (maybe longer), but I LOVE the fact that it has virtually gotten rid of my cramps. I used to get awful cramps that would put me in a cold sweat on the floor with nausea and feeling faint and all that stuff. My period also used to be very heavy the first few days.

As for side effects... I've never had a weight problem and it didn't lower or make me gain weight. I've always had a history of anxiety and depression so I can't really say if it has aggravated either of those disorders. I sometimes get problems with my stomach and intestines (usually just mild to moderate cramping, mild to moderate nausea, and sometimes constipation), but my anxiety has always given me GI trouble.

So, to summarize my experience... I had about 3 months of irregular light bleeding on top of regular, and sometimes heavier, periods. After about 3 months my body gradually regulated itself back to no virtually no spotting or break-through bleeding and I now have a regular monthly period again in which I experience pretty much no pain, lighter bleeding, but how long my period lasts is still the same.

All in all I'm doing alright with the IUD. The most annoying side effects are the possible GI side effects and just generally adjusting to it with the spotting, break-through bleeding, etc. It can take up to a year for your body to fully adjust to Mirena though, so I'm going to wait at least a year before I decide if I want to keep it or not. But so far my experience has been alright. I would like to see my periods be shortened and a little more predictable (they usually are predictable, but sometimes they last longer than my period used to last), but that's about it. :)

I am actually very relieved and excited to see that there is a connection between erythromycin and depression. I had taken erythromycin for years for acne. I found a strange correlation between taking the drug and feeling depressed. I asked both my doctor and pharmacist about this, and they both responded as if I were both crazy and stupid. "Of course not," was the reply. So I continued to take it.
I began taking it again about a week ago, and have found that I've been slipping into a very dark depressive state. This time I am very aware of what is going on around me, since I stopped taking my anti-depression medication last February (under the care of a physician and a psychiatrist) I am noting the same 'darkness' that I felt in previous times with erythromycin. A general 'nothing matters, might as well die' sort of attitude, as well as irritability and a strong desire to isolate. I started researching this morning on the internet, and I have found several links now. There have been studies that have shown a direct correlation between erythromycin use and depression.
Okay, now, here's the kicker: the erythromycin I've been taking is topical. It's a 2% solution, suspended in alcohol. I've been slathering it on my face three or four times a day. Apparently it doesn't matter if it is absorbed through the skin or through the stomach/intestines. Erythromycin causes depression in me. I don't care what my face looks like. I'm going to stop taking it.

I took 2 pills before dinner and my stomach was great after the meal, no gas whatsoever. Intestines felt great, but I noticed I was very uncomfortable on the couch, restless. Feeling was similar to RLS, restless leg syndrome, but all over my body. Lasted about 2 hours then feeling went away.

I finished a 5 day course of 1000 mg a day over a month ago. About a week afterward, I started having sharp pinging pains in the "bend" areas of where my colon is. Painful gas and bowel movements, and blood in the bowl. (not in stool) Also have had gum pain and mouth ulcers. My intestines feel blistered. I'll be ok a couple of days when eliminating, then suddenly a bowel movement will be followed by bright red blood and tissue. Very scary. I am taking Acidophilus, trying to eat carefully and drink only water, nothing harsh or citrusy. I have pain on the left side of my gut mostly. Under ribs, at waist and very low left side. I'm afraid, but then, this is a harsh drug and I do not have fever, have not dropped weight, lost appetite, or felt weak. I just feel like my insides are shredding and ulcerated. I will NEVER take this again. It's odd, because I have taken it before, for much long than this. I refused to take the last 2 doses the former time, because it literally tasted like fertilizer smells when i would belch after a pill. Vicious drug. I am watching myself and my issues, and hoping I don't have to have further treatment and that I have not totally ruined my colon beyond repair.

I had horrible, horrible pains in my intestines from taking metronidazole 500 mg 1 pill 2 times daily. i felt like i was going to die and so far the pain has lasted for an hour. I have taken this before and it did the same thing. It’s a horrible drug. You’re better off using natural things such as garlic pills and apple cider vinegar baths.

I was diagnosed with severe sinusitis a week ago, and my doctor prescribed omnicef for me since I was allergic to PENICILLIN. After the first day on Omnicef, I felt fine, perhaps a little better. As days continued to pass, however, I began to get some horrible reactions. They started out mild, and now (after taking it for the seventh day) I have major tongue and gland swelling in addition to a horrible headache and weakness. I've felt close to fainting several times throughout the past several days. I went through a random bout of depression a couple days ago, too, and there was no reason why. I feel more irritable, but I've been attempting to control it. I haven't lashed out wrongly at my loved ones yet, but I've come pretty close. I have some pain in my lower abdomen (where the intestines are located) as well, but only when I walk in a quick manner. No diarrhea, yet, but I think that's because I normally have digestion problems (constipation). Some of the joints in my hands are acting funny. They aren't as strong as usual, and they've been going numb/cold more often, causing their movements to be a little slower/stalled.

I'm seventeen, and when my mom contacted the doctor yesterday, the doctor said that "these aren't allergies/side effects" of this medication, and that I need to continue taking them. So I took them again yesterday (the seventh day), and that's when the swelling of the tongue and glands in my throat took place. When my mom called today and notified the doctor of that issue, the doctor said that..oh, how was that worded... That "it's the first time I've had this reaction" (while on this medication), and that it isn't caused by that medication but from something else. I'm sorry, but I'm not taking any other medications, and I haven't eaten anything strange/new that would cause me these difficulties. It's definitely the medication.

I'm done with this medication. After doing research on it this morning, I've learned that at least ten percent of those allergic to penicillin is also allergic to omnicef, and I'm allergic to penicillin. Why my doctor is being so stubborn about these reactions, I don't know. I guess this is just an example of a doctor who isn't well-educated and sticks ONLY to the side-effects/allergic reactions listed on the prescription bottle. If problems persist, my mom will take me to another doctor. For now, I'm going to stick to the Neti pod and nasal spray to try to rid me of my sinusitis. Maybe it'll work out alright and my problems from this medication will go away quickly. I'm sick of being sick all summer.