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Celebrex Begins Resource in Answers
How long do I take Celebrex before it starts working? I just began to take this medicine today.I'm wondering how long it will be before I can notice any difference in arthritis pain?

GeeeOhhh replied: "I took Celebrex for my shoulder and i noticed that after about 4 or 5 days i had better movement with it, with less pain. Im sure its different in everyone though. Hope you feel better soon."

hiten_lakra replied: "click this link for answer: "

How soon I can I begin drinking alcohol after stopping Celebrex? My doctor prescribed me Celebrex for my sciatic nerve but after researching all of it's negative side effects I have decided not to continue taking it. I have only taken 2 100mg tablets (one day's worth of the medicine) and am not planning to take any more. I have a friend's birthday tommorow and am wondering if I will be able to drink at it? It will have been slightly over 24 hours from the last dose. How long does it take to get out of my system? I'm not concerned about tracing, I am just worried about the stomach bleeding.

Carlos replied: "It will be traceable for longer, though it will not be metabolizing in 24 hours -- you're safe."

Will my sciatica ever end? In Jan 2005 I had spinal fusion surgery to correct Spondylothesis of my L5 vertebrae. They fused my L5 to my sacrum. Prior to the fusion, I had several flare-ups of pain in my lower back, but never down my leg. 2 months after the surgery, terrible pain began shooting down the back of my right leg down to my calf. The pain is so bad sometimes it brings me to tears. I have tried many therapies including chiropractic, acupuncture, physical therapy, naprapathy, water therapy, massage, intense stretching, celebrex, mobic, robaxin, skellaxin, seriods, ice, heat, in other words, everything I can think of! This has been going on for a year and 3 months. Can anyone offer any hope?

medicgvd replied: "You can try looking here it offers some home remedies that you may find helpful. Good luck to you."

hushnowjustplayit replied: "Been there done that... Are you on muscle relaxers? Pain killers? What does the surgeon who did the surgery say? Perhaps you should seek another opinion. If it's any comfort, mine did go away. I've had twinges now and then and once it stopped me for almost two weeks, but it's been years now. My heart just goes out to you. My prayers are with you. Please search for a physician that will help you and don't give up until you find one. Pain like that is just beyond words and no one should suffer like that in this day and age. My hopes are that you soon find relief. May God bless you and comfort you."

JustMe replied: "Here's a testimony from an individual who says - After riding over 12 hours on a bus, my sciatica flared up as a result of inflammation. After using Joint & Muscle Pain Cream and Pain Relief Complex, the pain completed disappeared. They said, this is incredible, because inflammation that puts pressure on the sciatica causes excruciating pain to radiate down your entire leg. These products are wonderful. It might be worth looking into."

what is a sure fire way to get my doctor to increase my percocet dosage??:)? i have been on percocet 7.5 325 for ten months now for a herniated disc i have told my doctor on countless ocassions that i am no longer getting the same relief. that i used to when i first began taken .percocet. all he does is give me celebrex/lyrica. which doesent do sh*t. i know what im feeling and what kind of pain i am expericing.but its always the same song and dance. all he says is i really dont want to raise your dosage.we will see next month.any help will be appreciated

alpla replied: "He's doing what is reasonable and what 99% of doctors would do. What you need is definitive treatment as surgery."

Johnny Boy replied: "u junkie!!! if i tell u how to get more percs then u gotta mail some to me as payment!!"

Sashaleana replied: "Just be careful when you stop taking painkillers, your body is probably already dependant on it. Withdrawal is EXTREMELY uncomfortable!! It is very easy to find a doctor that will increase the dose. If yours won't, change doctors. I do not recommend buying it illegally (off of the internet or from a street dealer), you don't always get what you ask for. I use to go to the emergency room, they give out prescriptions like candy. I didn't even have pain, just withdrawal from stopping opiates because I was addicted. ~Best of luck~"

meowzie replied: "Ask for a referral to a chronic pain specialist. Doctors are very leery of giving narcotics and often are too cautious in my opinion. I saw a chronic pain specialist for my fibromyalgia and arthritis. I couldn't even function I was so bad and no one would help me. They put me on methadone for pain and although I had to pee in a cup once a month, it was worth it! I was only on it for four months and was able to taper down after participating in an intensive chronic pain program. However, if you really want relief and surgery is not an option, definitely go to a chronic pain specialist. They also have other pain control methods that I know have helped people with chronic back problems. There are pain pumps, shots and all sorts of things. Seriously, get a referral. Your doctor won't up your dosage, its time to see a specialist. I hope you get relief soon. Michelle PS: I don't know where you live, however I'm including a link to the clinic I went to here in Minnesota. There should be a pain clinic by you. This link can give you some information on the different pain relief options. I have also listed a couple others that can help you find a doctor/clinic near you"

*J replied: "its not that youre not getting the same relief anymore, i think what youmeant to say is that youre not getting the same high anymore. you clearly have a drug problem, otherwise you wouldnt be on here asking how to raise your dosage. if your pain was that extreme, your doctor would know and you probably wouldnt be on those weak perks, youd be on somethin much stronger(good thing youre not) count your blessings that hes not raising your dose, hes seeing through your lies. try not to do anymore tommorow... or the next day. its too late since youve been on them for 10 months.. youre going to have realy bad withdrawals but at least its not from a higher dose of percocet. youre so immature because many are faced with addiction, and you are too, you just dont know it yet... you show all the signs of addict behavior. lying, exagerating, denial. get on suboxone for opiod abuse treatment and it will help with your pain too. but i bet you wouldnt be open to it cuz you think you dont have a problem."

Women's problems...kind of icky...? Some background first. I have one child, she is three. About a year after I had her, I had the Mirena IUD system put it. Two years went by with no problems whatsoever. Within the past couple months, however, I have been having (after over a year of no periods) very heavy flow with lots of clotting. It first began about a month and a half ago, and then after two weeks, it stopped. A couple weeks later, I started to have really bad cramping, and a really bad, almost skunky smell. I'm monogamous (married), and we are pretty clean people, so I thought the smell may just be a run of the mill bacterial. However, the cramping started to get worse, and I began to have a very thick whitish-green discharge. One night, after cramps so bad I was in tears, I quit stalling and made an apointment. The doctor said my IUD was in place and looked just fine. She said that I did have a minor bacterial infection, and that the cramping was probably a cyst. She sent my home with some antibiotic meds and some celebrex for the cramping. I started my antibiotic, but decided against the celebrex as the cramping had subsided almost completely by that time. About the same time I started to take the antibiotics, which is a gel that is inserted with a tube, I started to have a weird "period." The blood is a mix of bright fresh blood and old brown blood. There is no longer any odor, but with the blood, there are some clots, and a substance that looks like ground beef or something similar. It's reddish-brown, and is doesn't look like the clotted blood that is accompanying it. It's solid, and in bits and pieces. I have also started to cramp again. I had something similar to this after the birth of my daughter. Frightened, I took a pregnancy test, and it was negative. My question now is, has this happened to anyone before? With or without the IUD? Does anyone have any idea what this could be? We are wanting to have children, so a hysterectomy would be a last resort, really. I am calling my doctor tommorrow to have everything checked out again.

Elizabeth C replied: "Without IUD. I'd had it my entire teenage life.But I can't call it normal, mainly because I've only heard people talk about here on yahoo! Answers. But I thought I'd let you know you aren't alone when it comes to this. I hope things clear up soon:)"

jc replied: "over a year and half with no periods??? yeah i think that is your body trying to get rid of all that stuff... not having a period every month cannot be healthy... maybe you should consider changing your type of birth control that might help....."

Wendy S replied: "First, take a deep breath and relax. For the past three years I have had the same trouble. It first started as just some extra painful cramps then it proceeded to some extra days with my period. I thought ok it has to be starting the change of life early. This went on for a year, I just keep telling myself that it was normal. Went to the doctor they told me not to worry, and put me on bithcontrol to which I did not need because my husband was fixed. The said that would regulate me. In stead it gave me leg cramps and mad my moods very hard to handle and did not regulate me. Another year and things just go a lot worse. The bleeding was flowing so much the I would hate the thought of standing up for fear that I would have a royal mess. The cramps intensified and now I had my perion for 2wks at a time. Life was just bad. I felt dirty and I felt that everyone around me could smell what I smelled. I ended up wearing a pad everyday that I worked for fear of getting. I know longer knew when I would have my period. My poor husband was lucky to have sex once a month. I tried to have sex during it but I felt dirty and it was such a mess. It even got to a point where I told my husband that I am not able to be a wife and you can leave me if you want. This year was the last straw. The bleeding was non-stop clotting the size of golf balls, constantly soiled bedding. I even had one day at work that I went through all my supplies headed home and bleed through all my clothing. That was it. I doubled up so bad in pain went to the doctor and ended up at the hospital because they thought it was my appendix's. But what it was I started my cycle again and that is how bad the pms was. Hormones so uncontrolable. One minute happy, next crying for no reason and finally so mad I could have killed. I had some tests done they found cysts, enlarged uterus. I went to my ob-gyn and he did a scope. Which I chose to be put out for and HIGHLY recommend that. Even if they say it's nothing tell them I would feel better if I had it in a hospital or surgery center. Less stress on you and no pain you have been through enough. Trust me I am no wimp to pain I love getting tatoos, but no matter how they do it you feel the needles and the cliping they do for testing. It cam back that I had precancer cells and I could take hormones but there was no definate answer that it would stop and that the cells would not change. It went constant visits to the doctor. Or have a hysterectomy. I chose the surgery. I just had it do on 8/22/08 and it was laperscopi and vaginal. I was in the hospital 1 day and honestly feeling pretty good. The first few days I won't lie I was sore. But I have done everything I have been told to do and I go back in on 9/4 to have stitches checked then again in 6 wks. I will not be able to work until 6 wks but that is ok. I can keep you posted. Personally if you are not planning on more children this is really the only way for it to stop. It took me a long time as you can see to make that choice. It took not having a fun life anymore to do this. Before the surgery I was in constant pain and bleeding, always feeling run down because I became anemic and continually catching every bug going a round. I am not completely healed, but I can tell you that I no longer have the rash from the pads, I sleep through the night not worring if I will have a mess in the morning. I do not have the constant discharge and I feel CLEAN. I have even started wanting my husband to sit and just touch me. I can't wait to be able to be a wife again P.S. Life can be fun again"

I just don't understand? Why would a doctor question me whether I have a pain somewhere or not - especially if I have total health coverage and he is getting his money? I was having bad back pain, my orthopeadic surgeon and my general doctor more or less questioned it was as bad as I was telling them. For 4 years, I was given physical thearpy (which made it absolutely worse - and I told them so), I was given celebrex (which worked for a couple of months), I was given Mobic (which didn't work to well at all). I was in agony - serious agony, and eventually was told there was nothing to be done. I finally got in touch with a pain specialist who gave me a series of epidural injections. This is the first time I've had no pain in 4 years. Why wasn't I given this option to begin with? The first 2 doctors are not idiots - they are tops in the field - but I always felt they thought I was lying. Even if I was - why would they care?

Bored Enough To Be Here replied: "They aren't just in it for the money, they are liable for treating you, medicating you, and for setting physical demand limitations for employment purposes. They have to be sure of the condition before doing those things."

sandman replied: "They're trying to tell if your drug-seeking.And the epidurals are the last stage before surgery"

flutterby replied: "A lot of doctors question a patient and the severity of their pain/injury when they go in. The first reason is that they want a diagnosis and another reason is that they want to make sure you are actually hurting and not just looking for a Rx. It's not surprising that they wanted to know about your pain but the fact that you felt like you were on trial for hurting just isn't right. Especially when what you needed were some injections or something just to stop the pain. Most of the time doctors get cautious when you ask for pain killer or something specific, but if you were just trying to resolve the issue, no matter what the treatment was then they shouldn't have made you feel like you were doing something wrong."

momwithabat replied: "To avoid malpractice suits docs have to have a physical reason to prescribe procedures.......you can thank insurance companies for this by the way. You have to meet certain criteria to have insurance pay for meds and procedures. It's not the doctors....it's the insurance company that cares. Blame them for setting guidelines for the doctors. Insurance companies don't WANT to have to pay."

Mae F replied: "They care if you're lying because they care about their patients. There has been so much overmedicading lately. Sounds like they were just being cautious. I'm so happy to hear you're feeling better now!"

dances_with_unicorns1955 replied: "If they thought you were angling to get narcotics, they could have been reluctant to acknowlege your pain and prescribe what they THOUGHT you were trying to get. While an unscrupulous doctor won't care about anything but money, a doctor with reasonable ethics will not be willing to prescribe narcotic medication for someone if they're not comfortable with the person's need. That being said, the fact that you presented as being in pain means that they should have done SOMETHING. To tell you that nothing could be done is irresponsible; no matter what their suspicions, they have the responibility to ensure that you are not in pain if they are able to prevent it. More than anything, if you don't know what a doctor is thinking, then ASK. They don't read minds, and if you think that they think you're lying, then ASK why they won't prescribe you something. Communication is obviously important, but sometimes it has to be the patient who initiates it if the doctor is trying to simply be polite. If you don't get the communication you want after that, it's time to find a new doctor!"

Nurse Susan replied: "Many doctors are under-educated in pain management. If they can't see the problem, it must not exist. Thankfully, this is being taught in more medical schools now; and pain specialists now are available. They care because they don't want to go before the medical board, accused of distributing [ writing false prescriptions for] narcotics."

Anon Chicago replied: "It could be for a whole bunch of reasons. Sometimes all doctors have to go on is diagnostic testing, what they can observe. It's possible that your expression of pain and complaints did not mirror the doctor's perception of what was going on, based on their exam, knowledge, etc. That does happen frequently, where patients can be in terrible pain but their doctors are like, "Your tests show nothing of the kind." So in other words, it may not be that they're doubting you but that they simply don't know how to treat what they can't actually see or find on a diagnostic test. Another reason may be your insurance or the way the doctor handles referrals, etc., through his office. I used to have an HMO and they would make doctors do the most conservative care forever, before moving on to other things (like the injections you received, which are considered more invasive). It's possible the doctors didn't want to leap into the more invasive measures and sometimes physical therapy can help for back pain, so they figured they'd give it a shot. I'm glad you found something that worked - you may want to check out a chiropractor too. They're not quacks, they really do help with back problems and other issues. I have been seeing one with great results and so have my family members. Either way if you don't trust that this doctor takes your pain seriously, then get a new doctor. There are plenty of them. Being the best in his field doesn't mean he's the best for YOU."

ronk replied: "doctors always are suspicious of back pain b/c they cannot measure it well especially without tests like emg's"

pxnanc replied: "Protecting their reputations by not giving addictive narcotics--see that's not really a solution anyway. Malpractice is sky high and they have heard every rationalization in the book. I will only take Ultram,an opiate-like painkiller that is not a narcotic. I actually can keep my pain at bay without the addiction problem. Pain management places are more flexible and take more time with the patient. It also tells them that you seriously have pain because you're there."

Bob A replied: "YOUR DOCTORS ARE AFRAID OF THE D.E.A. (DRUG ENFORCEMENT AGENCY) DOCTORS WHO WRITE TOO MANY SCRIPTS FOR CERTAIN PAIN MEDS BRING ATTENTION TO THEMSELVES AND PUT THIER LICENSES IN JEOPARDY. A DOCTOR WOULD RATHER LEAVE YOU IN PAIN THEN TAKE A CHANCE ON LOSING HIS LICENSE. THIS IS WHY ONLY THOSE DOCTORS WHO DEAL ONLY WITH PAIN PATIENTS AND CAN ESTABLISH LONG TERM HISTORIES AND TREATMENT PLANS TAKE THE CHANCE TO TREAT YOU WITH THE CORRECT MEDICATIONS."

charmel5496 replied: "sometimes people need to advocate for themselves and take charge of their own problem....why would you wait 4 years to seek other treatment...if they are idiots as you say why keep going back to them....sad to say but there are people weho do fake things just to get meds and such and doctors have been under the gun about issues like this....also whatever insurance may not have covered certain things,like an epidural untill more traditional treatment was done most doctors are not pain management specialists. back pain is a very tricky thing to prove...unless there is an obvious problem that shows on an x-ray,mri etc anyone can go in and say their back hurts and get meds,be put on dbl etc etc every narcotic prescription written has a doctors dea number on it and gets recorded and since people do doctor shop to get meds from multiple docs there is alot of abuse and some doctors are not about to risk their licenses to write scripts that can be used in an abusive manner,which is within their right....the doctor does not have to write you a script...thats why people need to advocate and find pain specialists or whatever other services they need you can thank the people who have abused the system and the ones who file frivolous lawsuits for these changes in procedure"

Should I go to the ER for pain relief due to Fibromyalgia? I am newly diagnosed with Fibromyalgia after months of unreolsving pain and fatigue. My primary care physician prescribed Celebrex for pain 2 weeks ago. It has not helped at all. Currently my Primary care physician is closed. I called my rheumatologist who told me to begin taking the Cymbalta he gave me, and to expect relief in 3-6 weeks. I cannot sleep and am having trouble walking and dressing due to pain, I simply cannot wait 3-6 weeks. The rheumatologist told me he could do nothing else. I am not finding relief in Tylenol and cannot take other OTC pain meds due to a stomach condition. I am going out of my mind with pain, stress, distress, worry and lack of sleep. I called my pyschologist and left a message with her. I HAVE to work today till 9 pm. Would the ER be a good idea after work? I am just beside myself, crying at work, and a mess. I don't know what I want them to do, I feel like the doctors are relutant to treat my pain because so many people abuse pain meds. But I've never been prescribed anything aside from when I had surgery. Any suggestions will be greatfully accepted.

Kung Fu replied: "If you can afford it and are open to it Hypnosis and Acupuncture work wonders."

Donna <>< replied: "I have fibromyalgia also and have had for more years than I can count. Many doctors have the opinion still that it is controllable with stress relief or relaxation. I had a doctor that put me on Vicodins and Morphine (which I got addicted to). The last one took me off both and wouldn't give anything to me except Naproxen, which doesn't work. I have been to the ER for pain relief and gotten Vicodins, they work, but I used them very sparingly because they caused very bad constipation. So mostly I have to deal with the pain, which I've seen is worse right before it rains or the weather gets cold. One medication that they do have for it now is Lyrica, which I can't take. But when I did take it, at least the pain was less. Also I was put on Cymbalta, which helped some but then I got put on an anti-depressant called Zoloft and can't take them together. There is a website that might give you suggestions to try. "

justmeinthisworld replied: "I doubt the Er will help--they won't even treat me for unrelated conditions sinc ei have fibro-but if you have time and money-try it-a small percentage of time--teh doc actually cares- but be prepared to flee if they become abusive. as soon as possible--ask about lyrica--it works faster and is in teh ani seizure class----there have been some reports of trmadol helping--it is an opiate--but not a 'controlled substance' you need some new docs--i hav ben trying to fin a competant 1 for 8 years Celebrex is CONTRAINDICATED for fms-it is an NSAID and tehre is no inflmaation-so it generally does not help at all--- and if you just have cymbalta-that may or may not work-and teh doc says tehre is nothing else--he is an idiot"

Sinus surgery complications/odd nasal problems...? I had nasal allergies since I was at least 11, I am now 26. About 5 yrs ago I began to have very bad nose bleeds after using nasal spray for a week. My nose has never been the same. In 2006 I had a biopsy done on both turbinates, it showed no disease (was on prednisone), my nose did not heal properly, so i had another surgery to remove the scar tissue, and a final surgery to correct a deviated septum. I now have a hole in my septum, swollen glands and very large/hard crusting in my nose. The last 2 surgeries were back to back in Nov 2007. I have also had a very bad headache in the front of my head since then as well. I have seen ENT's, Rheumatologists, and even a Neurologist at UCLA. Has anyone else had a similar problem? Any solution or advice? I am going to see one more ENT at UCLA on Jan 5th. I am currently taking prednisone and Celebrex for inflammation/headache.

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Laura L replied: "try this, it is simple, easy and won't hurt you . It might cure the infection for you like it did me. I use it to cure sinus infections. THere are many kinds of bacteria that live in the sinuses, and this gets rid of all the bad ones!.This is the only thing that really helped me --- my Dr. told me about a sinus wash that will kill bacteria. you need distilled water sea salt liquid chlorophyll and colloidal silver from the health food store. in a glass mix 1/4 cup water with a pinch of salt and heat to body temperature. add 5 drops each silver and chlorophyll and mix. using a large dropper (like one used for infant medication) drop 2 full droppersfull into one side of the nose while laying down. Turn the head and let it drain out the other nostril. Be sure to have paper towels handy. or just use a neti pot, I like this better. The silver kills the bacteria and there are several hundred kind that can live in the sinus cavities and anti biotics don't get rid of them all. Do this twice a day for a week, mixing up the mixture fresh each time. Then do it once a week for maintenance. There is nothing in this that will hurt you, and it cured me. I do not have to take claritin, or antibiotics anymore. best wishes"

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