Three times symptoms and conditions

My 13 year old sister is a normal active teenager. She received the first Gardasil shot last October with Hep B. In November, she received the second Gardasil shot with the meningitis vaccine. Right before Christmas, she started experiencing tingling in her hands and fingers. Two days before the New Year, her knees swelled three times their normal size and were extremely painful. It took two weeks for her knees to become only slightly swollen. Several doctors and a specialist in pediatric arthritis later, she was diagnosed with chronic arthritis. She had no previous joints issue at all. She has been on medication for a year. We can only hope she has juvenile arthritis and that it will go in remission. Unfortunately, her wrists have started to hurt recently.

After much research by my mom and myself, we have come to the conclusion her spontaneous arthritis was a result of Gardasil. Most likely the combination of Gardasil and the meningitis vaccine was the cause. It should be noted that the FDA allowed Merck to fast-track Gardasil for approval. The Gardasil vaccine was never tested with the meningitis vaccine; however, most physicians give multiple vaccines at one time.

My name is Heather I am now 32 years old I took levaquin when i was 29. After i took levaquin I went on a roller coaster ride I have yet to be able to get off of. First when i took it I had the worst night mares i have ever had only to wake up to a splitting headache and a very sore body. took another one the next day same reaction.I figured it was the bronchitis that was causing the problem. on the third day i was worse still I could hardly move. I stopped taking the drug. after another two days i felt better. two weeks later I was out with my father and he noticed a rash on my legs. I was also starting to get little blood blisters. I started to become concerned and the next day after going to the zoo with my family i came home and my legs were swollen three times there normal size and very sore. I put them up just to find the felt like play dough had been stuffed in to them and I had blood blisters the size of pencil erasers. I made an appointment to see the doctor. he said and i Quote " Heather I have No idea what the Hell you have" he sent me to a specialist. between the time of my first appointment and the appointment with the specialist my legs stopped working from the hips down i was 90% paralyzed (not spelled right ) they just wouldn't work right. My ten year old daughter was helping me get to the bathroom. I was soooo sick i had a headache all the time couldn't eat or sleep and when i did it was only for a few hours I couldn't move very well and to get up out of bed hurt so bad i almost fell every morning. by the time i had gotten to the specialist I had gone to the E.R. three times for the pain.and the last time was because my toes stopped moving altogether. at the appointment the doctor ran all kinds of tests checking me for everything from S.T.D.s (which i have been happily married for years) to Lupus. I felt Like and 80 year old Lady And like i said i was only 29. after the extensive tests and everything coming back normal the doctor put me on a steriod. for 4 months i was told i had to take prednisone After the first dose i could move again I still hurt but i could move.But now i had the side effect from that. i was gaining weight like it was going out of style, but at least i could move. after the 4 months things seemed normal kinda. I could move but if i sit still to long my legs go numb not fall sleep go completely numb even if i am standing to long. I am still afraid that i will wake up again feeling like i did that Fall three years ago. I still have problems but im not sure they are tied in but it wouldn't surprise me in the least. I only took three Pills of Levaquin three years ago!!!! How long does this stuff hang on really??????

I haven't actually started it yet but am seriously considering it. I been using normal pill BC and I have used the ortho evra patch before I got off BC to have a child. here is my story of why I want to try and for those who are still considering it.

First off, I usually get sick every month with the pill when I start a new pack, not all BC pill did it as I am on Loestrin now and on Yaz before that and they didn't make me sick, but they are lower doses. However, I loved ortho evra, it was great except for the sticky ring where lint get stuck on you from around the edges, but that was just a small negative for me. However, I got off it before all the controversy about how it has three times theh rate of blood clots forming than BC pills, so I am a little worried about going back on it and my docs don't really prescribe it either, and suggested the nuvaring.

Well I went on Yaz post birth and couldn't understand why I was so tired all the time, every one kept saying it is because you have a new baby but i don't believe it was that because my child is a really easy child who sleeps through the night and took her naps. i just wanted to sleep all the time and still feel this way even after switching to loestrin which is similar to Yaz. I wasn't tired like this on Ortho evra and my doc told me that the ring is similar in like the patch.

so I am sorry for all those of you who have had bad experiences and the only thing I think I can do is try it for myself cause, when something bad or negative happens everyone hears about it but that is not the case when something is good. Everyone's body is different and reacts differently to medication. So I am going to go ahead and try I think to see how it affects me cause I don't think I can get any worse and I am not ready to have another child yet. I am currently on an antidepressant for about 5 weeks now and still am having my constant tired wanting to sleep feeling, this is why I think it is the BC. Hopefully i won't have too many side effects but I am willing to give it a try as I do know women who have used it and said that they liked it.

I had Kenalog injections a few days ago for MyoFacial Pain Syndrome. They are used for Trigger Points in the body that cause severe muscle spasms.
I have experienced these spasms for about three years. The first three times I had the injections I had no side effects. But the relief from the pain only lasted about three weeks.
So the nurse practitioner upped the dosage the other day. Since that evening I have been suffering from chills, sweating, fatigue, lost appetite, anxiety, aching muscles, and insomnia. I wake in the night several times sweating.
The pain in my upper back has subsided now but am not sure it was worth it.
I called their office but have not heard back from them.
Am so tired from suffering already and I hope the side effects subside very soon!

I have been taking Methimazole for exactly 1 week. I am 26. This is the second time to take these same drugs. Methimazole along with a beta-blocker, Propranolol. My thyroid had been back to normal for 2 years. This time, I started off taking one three times daily, then just one a day, now I was instructed that I should take three once daily. My tests just came back and I am extremely thyrotoxic and have Grave's Disease. I have had headaches on and off this week, today I have had a headache most of the day. My heart is still palpitating but my strength is coming back. Last week before starting the drugs was much worse. I could barely move my body hurt so bad, felt like I had a fever, fatigue...the works

Oh my goodness.....my daughter, age 17, had her first injection in June 2008, started losing her hair w/in a month. We thought it was form straightening, some high lightening etc. She had blood work done which showed she was anemic...strange, as 2yrs prior her blood work was stellar, and she had not changed her diet, or physical activity. She increased her iron and protein intake (along w/ supplements).....three months later, and after her second injection, iron was still anemic....worse actually, and her hair loss significant.I found this website last night....and I am floored......I called MERCK today and spoke to a representative wh o was not aware of the hair loss issue, but said that in their case studies, Autoimmune Hemolytic Anemia was a side effect.....which leads to hair loss itself.....so I am researching now what to do next.....anyone else have this issue??????

My daughter is no longer on advair, but when she was I thought she was a hypochondriac. She had asthma since age 3 and by the time she was in 4th grade she was put on advair. She gained weight in her face and stomach. She would have trouble concentrating on her school work, stayed moody. She would lash out for little or no reason. She always had some ache or pain. Almost every day either her head hurt or her stomach hurt. It was would last under an hour each time

She started having muscle pains. had to be in a walking cast twice for soft tissue damage to her ankle. She would have no idea how it got hurt. If she crawled on her knees playing she would get fluid on her knees. She would have knee pain off and on for a weeks at a time. All the time we were at one doctor or another. Every one of them said her asthma medicine would not cause this. The last straw was when in 6th grade her shoulders would pop out of place if she tried to do push ups in gym. She had to have physical therapy three times a week for three months. Even though the doctors told me not to she has been off of advair for 4 years now. All of the side effects went away with the except for the problems with her shoulders. She has to do exercises a few time a week to keep the muscle's strong to hold them in place.

recently was prescribed simvastatin. Pharmacist advised that 50% of people will experience severe muscle & joint pain and burning in the muscles. I can see by reading the site that this is true. Must try since cholesteral and bp are high and dr thinks at 51 I had two mini strokes (tia's). If I experience the severe pain that is discussed i will stop taking. Thank you for all the info! This site is awesome.

All I can say is that since having it inserted in Oct. 2007 I began rigorous training to lose extra weight for a breast reduction, I found it extremely difficult to lose 1 POUND let alone 20. Went to the gyn who inserted it and she was not sympathetic at all she said women over thirty just have those problems.....What problem? Walking/jogging at least 5 miles three times weekly, drop your caloric intake by more than half AND STILL ABSOLUTELY NO WEIGHT LOSE?? I am at my ideal weight, just the far end of it and seriously after 7 months training not one pound lost. New gyn thought Mirena might be the cause, I had it removed two days ago and I already feel a difference in my energy levels!!

I completed the cycle of taking this drug. The next day I started to itch all over the body, followed by numbness in my jaws, pain in all joints of the body, chest pain, back pain and cramps in my leg. Lack of sleep due to itching. I continue to have this and it has been nearly two weeks. The doctor has advised me to take Advil (200mg) three tablets three times a day and to take a Benadryl at night time. I started this yesterday and it gave me some relief continue to see when I will be fit again. I recommend that this drug should be banned.

I was prescribed a generic for keflex (cephalexin), 500mg three times a day for 10 days for cellulitis(skin infection through an insect bite). My gastrointestinal tract went totally haywire as soon as I started taking the medication, bad stomach upset. The infection subsided in a couple of days but started having stomach cramps and the diarrhea continues for almost a month till I started taking probiotics to replenish all the flora in the gi tract.
It has been almost a month after I stopped taking this medication and now experience phantosmia( phantom smell ), in my case smelling smoke/exhaust fumes at random times throughout the day. I mentioned this symptom to the doc and according to here, it is one of the side effects asked me to hang in there for 5 more months before I can consult an ENT specialist.

I hate this pill. Im nauseated, cramping, bloated, angry, have high axiety, cry at the drop of a hat, leg pain, headaches, bubbles in my stomach. and it even gave me an infection canadisis (like a yeast infection of the skin). which I found out was actually a symptom of this pill! I want to switch so bad. But i have been on and off this freaking pill three times this year. Im worried that if i switch to a different birth control I'll just experience new horrible symptoms. Luckily no weight gain though. but horrible break outs as well.

I'm a 45 yr old female, I've been on Singular for many years (originally for allergies and then asthma too) and have quit three times due to "possible" side effects and tried other asthma medicines. Inhalers make my GERD worse and I'm anxious all the time. I have to say Singular is the only thing that really works for my asthma and I keep going back to it because it does work. Also, I found that when I quit and expected my depression, headaches or fibromyalgia to go away they didn't... so I own these symptoms now regardless of Singular. I've always had mild depression and anxiety and all the prescription drugs for this I find are really too strong and are made worse then by Singular. For mild depression I find taking SAMe and St. John's Wort to really help me. Can't say if it would help others but you might look into it. I think it's important that doctors understand a link with depression and Singular but for some of us there's not another choice.

I am a 37 year old female that went to the ER 3 days ago for chest tightness & extremely high blood sugar. I have had high blood pressure in the past years but as of a year ago when I was diagnosed as being diabetic my blood pressure has been normal about 117/75 so I go to the ER and they give me 2 EKG's and a heart monitor for 24hrs and put me through a stress test,they also give me this little pill and say it will help me, well not feeling well and wanting to feel good again I take the pill no questions asked. I have never felt so tired in my life. I thought well chest pains will do that to you so I dismissed it. I know they were making sure I do not have a heart attack but, my blood pressure seems to be going lower and lower and I am more tired by the minute, they released me from the hospital and gave me a million RX's including toprol and lisinopril both of whch lower blod pressure ??? do they want me to pass out? so yesterday I took the toprol only and felt like I was sinking , my thinking seemed foggy and my legs felt rubbery. I am sooooo glad I found this site because I will not take this drug ever again I already suffer weight issues being diabetic I don't need anything else. I would prefer to be interested in sex and be able too function this drug seems like it is more negative than it is worth. I think I will stick with the lisinopril, and why would they give me two blood pressure meds when my blood pressure is already normal??? If anyone has a comment please let me know I am very scared about this whole thing

I'm 39 years old with two very healthy children. That said, I got my Mirena because I was having prolonged extremely heavy periods and my regular doctor thought it was the cause of the extreme chronic anemia that I suffer from. My serum ferritin count (amount of iron stored int eh body) was 2 the lowest point of normal serum ferritin is 10-12. My ob/gyn disagreed as did I. There is something else wrong we've just not found it yet.

The Mirena helped with the bleeding to a point. I still have a period for weeks at a time but not so badly that I have to change pads and tampons by the hour, ony two or three times a day now. Turns out that my period apparently wasn't the cause of the anemia because it hasn't gotten any better.

My hair is much thinner, I've lost 40 pounds. I'm tired a lot with memory loss. Ready for a shock? I'm 5ft8 and I weigh 225 and 92/63 is my at work on my feet all day blood pressure. I don't attribute any of that to Mirena, maybe I should. I think Mirena might have prolonged if not saved my life.

However, it has been steadily losing its effectiveness I think because of my age and fluctuating hormonal levels and because my body was so starved for hormones before it was inserted that maybe it was just used up faster...I don't really know. What I do know is in the past 3 or 4 months is that I started having cramps, bleeding more heavily and even longer and my sex drive started either completely failing me or going the direct opposite and being way on out there (not that the hubby minds all that much)

I'm going to have it removed next Friday. I might have it replaced. I might not.

I got the Mirena after my 2nd child in April 2007 at the age of 25. It was very painful and I can handle pain I had just done completely natural child birth to a 9 pound baby. I bleed for the first three months. With really bad cramps!!
However until seeing this website I never realized that all these things that have been happening to me are probably from the Mirena. The last 6 months I have been having anxiety attacks, dizziness, headaches, mood swing, acne, and I have been so tired I thought I was pregnant, now after today I believe it is from the Mirena. I am going to call my doctor and have it removed!!!

Two days ago, I needed to drink two doses of gastrographin one hour apart two hours before an abdominal CT. Not more than 20 minutes after drinking the first does with 12 oz. of cranberry juice I felt a burning sensation in my eyes and they started to water. I also felt disoriented for a moment or two, similar to what one might feel when they are driving tired and they have a hard time keeping their eyes open. By the time I had started drinking the second dose, I had diarrhea and visited the bathroom three times before setting off for my CT appointment.

Once reaching the medical facility, I used the restroom twice more within 40 minutes time before my scan. I feel like I am telling you way more than I would tell anyone else however it was remarkable to me to have to visit the toilet five times in less than three hours! I was made to drink a third dose just prior to my scan and given an IV dose of contrast. Throughout the remainder of the day I felt out of sorts: loss of appetite, lethargic, thirsty, and although less frequent visits to the toilet were necessary, I continued to have diarrhea.

The next morning I awoke with the most enormous headache. I have never had a hangover but what I felt was what I imagine a hangover would feel like . . . I felt crummy! I still had the diarrhea and I was drinking water like a mermaid out of water.

Today, two days later, I feel like I am back to normal. I attribute the crummy side effects I experienced to the gastrofrafin but not being knowledgeable about such things, I decided to research possible side effects on the web. So that's how I got here.

I have been on this medication for about 3-4 months now, and I have NEVER passed out or fainted before in my life and I have done it three times already since I've been on this medicine. I have had an increased amount of hair loss . But other than feeling very dizzy, then nauseas, then hot flashes and then passing out.... not too many other side effects. Has anyone else experienced this?

My mom took Levaquin for a sinus infection and within three days of starting the medicine her kidneys began to fail. Her heart rate and blood pressure were elevated. After 6 months of going to doctor after doctor, she was diagnosed with chronic kidney disease and high blood pressure. Now she is on dialysis three times a week. The kicker...she had just had a complete physical with a blood work up three weeks prior to taking Levaquin and she was absolutely fine. Now, she's dying of chronic kidney disease.

I was taking 500mg three times a day. After 1 week I developed severe joint pain and swelling in my fingers. I got an itchy rash on the bridge of my nose and over my eyes and inside my nose. The joint pain continued to my knees and toes. I have been off of the medication 3 weeks and I am just starting to feel a little normal. a different doctor put me on 800 mg of Ibupropen 3 times a day and after reading up on the side effects of Cephalexin I began taking Benadryl which has helped a lot.

I have had so many shots of
Corticosteroids/NSAIDS/Steroids:

Triamcinolone Acetonide, Kenalog, Depo-Mardol, Lidocaine, Marvaine, Toradol, Epinephrine, Bextra, Xylocaine, Isovue.......on and on and now I do not walk hardly anymore.

I am married, no sex whatsoever! I stayed away from my husband for 3 years almost, living at my apartment. I just moved out by Eviction March 2, 2008. I did not pay rent for one year. I applied for disability since 1995. Won ALJ decision September 2006. I appealed the case being opened back to 1995. I wanted it go go back futher. Just appealed it again in 2008.

Okay, I am a simpleton out here needing a HERO to Take A Stand and Advocate for me.

I do not live with my husband. I live at his mother's home so that he comes and takes cares of us at the same time. She is 90 now. Can you imagine this? I have been reduced to a cripple.

I am a prisoner laid to rest by the BIG DRUG COMPANIES MISLEADING ME, IN NOT KNOWING ABOUT THE DISEASES THAT WOULD ATTACK ME IN THE ONLY LIFE THAT I HAVE.

I wonder if my hip bones have collasped. I have terrible bone pain.

I waddle like a duck, side to side with extreme pain until I freeze up and fall, but mostly, I live with a cane at my side when going out and about.

I now need a wheelchair.

From 1980's, 1990's and now all the way to 2008. I have all medicals.

It was not until 2003-2004 that my life took a turn for the worse.

Hips pain, arms pain, shoulders pain, pain in the Thorasic area to the tail bone area, right groin pain/pubic area pain/gentials, stomach sores/cut out, pain on the scalp, calves feel hard in side/stiff at all times, hamstrings are short,open sores have been on my face, arms and neck lasting for 4-6 mths, low back pain....all of me has been injected with the above crap.

I was doing quite well in life until 2004 when this Orthopedic doctor had shot my left shoulder 3 times.

After this June 2004 event above, and by September 2004 I had walking problems, blamed only on Fibromyalgia, DX 1989.

They took one blood test for Polyrheumatica.

I was fed 20 something meds in 2004.

By 2005 I was devestated in life, health and even wanting to be alive. For one full year I lived on the pot, using Lidocaine up the butt 3-4 times a day for the pain.

Now, looking back at this part, no wonder I had extreme skin blisters, hives, rashes, extreme sweating....this Lidocaine for rectum pain was harming me and no one took me off of it. I finally had my pharmacy tell me this was so wrong to be using 134.00 a month for over one year for pain. I stopped!!!! he seemed to say that I was being harmed.

Suddenly, at my clinic, all of my primary doctors began to do trigger point injections weekly, monthly and for 4 years for my Fibromyalgia comlaint. DX in 1989.

Many NSAIDS for one year, 2003-2004.

In 2003 I had a new denture and a few teeth extracted so that I smiled great when got married April 2003.

By August 2003 I was off the State HMO, had housing city of salem voucher for 5 years at my apartment and was planning to move out and be at my husband's home, but...by September 2003 I was already in some medical exams, new meds and was being normal to a point.

By late 2003 to mid-2004 I was feeling strange about my health. I felt as if I was being sucked dry of any fluids, weird to say, but it felt as if...hard to explain.

I was dizzy, vertigo, some balance problems and like itching, sweating and extreme fatigue. I felt like i was melting. My muscles felt like jello. I had no ability to stay upward on my spine.

I did complain to my dentist and doctors that I was feeling numb on my face and gums by may 2003.

After 2 years, leaving room for a possible lawsuit on the dentist/OS, I filed, had one deposition and my lawyer walked.

I had laughing gas for teeth extractions/numbing shots.

I thought that GAS/SHOTS was to be blamed, maybe the tools they used, or the water and I worked this case to the bitter end, sad to say, that a Lawyer Walked On Me.

By 2004 I did not know what hit me with my health issues..dentists/new meds/new marriage/new doctors involved.

I was in a drug stupor, taking almost 30 drugs from this clinic in 2004.

Prescribed and the samples of Vioxx, Mobic, Celebrex and Bextra.

I had so many Toradol shots to my spine and hips at this clinic and thought they had crippled me.

This doctor humiliated me.

Told me that I was a nut.

I now needed long term counseling with all of the body ailments they all told me. My primary doctor told me many times that NONE OF THE SPECIALIST NEEDED OR WANTED TO SEE ME FOR ANYTHING.

Nothing was hardly affecting me when I got married April 2003. I was a knock out!

The Gastro doctor had me on his 3 drugs also, including that daily Lidocaine up my butt. He did the endoscopy and colonscopy, bloodwork and he said I had Atrophic Mucosa.

He was in direct conflict with my Neurologist who did his own work and he claimed that I was Gluten sensitive, a Celiac now. He gave B12 shots and Folic Acid on top of all the other crap that I was taking.

The Hospital did a spinal tap and may tests.

The pain specialist did his epidurals 2 times.

I have had every NSAID they prescribed me.

I had sleeping pills.

I had anti-depressants.

I had Vicodin to Percacets and then they tried to get me on Methadone. One week on that crap was all.

I notice that Depo-Medrol, Marcaine, Lidocaine was mostly used thru out my life.

The pain specialist above that I used in 2006, also shot me with the epidurals 2 times before 2006, and the O.H.S.U. also shot me with all the above when they DX me with Fibromyalgia 1989.

Then many Toradol and Kenalog shots.

I live with daily diarrhea since 2005-2008.

My legs are always red every day with any walking, sleeping, sitting, balance is off, waddling gait.

My feet pain is as if I walk on glass or rocks....sharp pain now for 4 months.

Arachnoiditis fits me well. I have spoken with the doctor/expert that can test me.

I have been searching since early 2004.

I have no way to know who or what to blame.

I even thought that the MRI's Contrast Agents harmed me starting from the past to now.

I left the clinic that stole my life from me and now have a new doctor at Kaiser Permanente.

I am scared of all doctors now.

I have 4-5 meds right now.

Not one doctor or specialist will DX me. I have a thought below...

I fought the medical community WORLD WIDE back in 2002-2003 with the President Dr. Richard Willner, of Retired Association of Physcians and Surgeons. My two other sisters were in this heated debate.

I was told to expect danger at any time after this online 30 page cruel attack by the doctors on my wrongful death of my mother by her doctors/nursing home/hospital.

I proved this case.

The lawyer in Portland, Or. Judy Snyder told me I did extremely well proving this death was murder...but the Medical Consultant who did the summary of this death was hushed up!!! Later on, after another summary by Medical Consultant, she told me that we would be lucky to get $10,000 for a Nusiance Claim. I tried to get one Lawyer before the statues ran, but no luck. I heard that the Elder Abuse Statues ran for 7 years and to try for that. Oh well, I tried.

Joanie K.

I used Neutrogena Summer Glow Daily Moisturizer with helioplex SPF 20 on my arms and broke out in a terrible rash on the inside of my arms at the point of my elbow bend. I used the product about three times. My skin is fiery red, bumpy, and has developed scaliness. It seems to be taking a very long time to go away. This seems to be a dangerous product--one that was not very well researched.

I was just discharged from the hospital on Saturday. I had been taking Yasmin for almost two years now and until recently, had no problems. Last Wednesday I went to the ER for severe pain and inability to breath with my left lung. They admitted me after finding a blood clot in the right, as a result of Yasmin! Turns out, I had pneumonia in the left and since I had no symptoms that the clot was there, the pneumonia saved my life! I too had to take those fun Lovenox shots in the stomach and now I'm on Coumadin for 6 months. I am 29 years old, never smoked a day in my life. I do not drink, I am a healthy weight and I work out regularly. I do not have a history of blood clots in the family. How could this happen especially with a drug my doctors told me was safe?

With the amount of occurrences, I'm interested in a class action lawsuit as well. I will never take a birth control pill again EVER.

Has anyone had extreme heavy bleeding/clots after having the Mirena removed? This is day 3. The last time I had such heavy bleeding I had just had my son. When do you start to worry about the bleeding?

I am 30 years old and have been put on Depo Lupron after a laproscopy to help with endometriosis. I am 2 months into a 6 month course (one shot every 3 months) of Depo Lupron and my life has drastically changed. I started feeling life altering hot flashes and night sweats two days after the first shot and nearly drown myself in sweat 24 hours a day. I experienced a little postpardum depression after giving birth 6 years ago but have found myself sunk into a sinking hole of depression and anger like I've never felt before. I bawl at McDonald's commercials and become enraged if the dishwasher isn't loaded properly! I am ecstatic one minute and severely depressed the next. I have even had thought of suicide since being on this shot. I am normally a very outgoing, athletic, cheerful, happy person - but since taking this shot, I have become a stanger in my own head. I tell my family all the time that I need to "go stick my head in the freezer" to cool off because of the horrific hot flashes. I have to carry a handheld fan with me 24 hours a day and sleep with ice packs to keep cool. Since the shot started 2 months ago, I have lost all sexual drive, am thoroughly exhausted by 9am and find myself crying at my desk at work by late afternoon because I am so tired. My family thinks I am going crazy and I've never fought more with my husband. My daughter has gone to grandma's for awhile because I'm just so tired and irritable that I feel like an awful mother. Migraines have also come full circle since the onset of the shot as well as blurred vision and shaky hands. I'm a little achy throughout the as well. I know that everyone responds to medication differently, but I'm finding a lot of people with the same side effects as myself and have to wonder why the doctors don't warn patients about these types of problems before prescribing medications such as Depo Lupron. I don't think I'll be going back for the second shot. Could it get any worse?