Hay fever symptoms and conditions

Both my husband and my son have had Kenalog Injections for Hay Fever for quite a few years. I heard recently that long term use of this injection for hay fever can cause osteoporosis in the bones. My husband has spinal trouble and my 40 year old son has trouble with the joints in his elbow. Does anyone else have any similar problems

I had the Mirena for 5yrs & had it replaced this past April. I had loved it (no menses) but little did I know of the adverse side effects that were plaguing me. I always had some depression, but wrote it off to cyclical hormones; cystic acne that seemed to be getting worse as the years went by; heart palpitations; NO libido; anxiousness. All this seemed to happen slowly over time for me. Once I had the new one inserted, I started noticing the part in my hair was becoming thinner, like balding; developed an eczema/rash on the back of my neck at the hairline; I felt like my hay fever was non-stop & got an ear infection/sinusitis for the first time ever; then the headaches which most recently turned into a migraine with visual changes coupled with insomnia. And I ached all over like I had the flu all the time. I had no clue that the Mirena could do this until I started researching & read the PHYSICIAN insert info! I discovered that out of 21 "adverse effects" I had at least 13 of them! I was mortified - being a Ob/Gyn RN, I felt I was really misled by the manufacturer & my doctors. I could not take the headaches & insomnia any longer. A week ago, desperate & could not wait until an appt., I went into the bathroom, pulled the strings myself & removed the sucker (being a RN, I have to tell you not to do that; I was willing to take the heat should something bad happen!). Over this last week, a HUGE difference for the better. NO headaches, insomnia, body aches, skin is clearing & my mood is getting better. I actually am feeling frisky for my hubby even (who by the way will be having a vasectomy in the next couple weeks & was fully supportive of me doing this). I am so disappointed as I LOVED the no period thing, but I am not willing to risk my well-being over that!

I just looked at this site to see what side effects people are experiencing with this medication. Here is my experience: I went to see my ENT doctor-this is a great practice and I still have full confidence in their abilities despite what happened to me. I have been having trouble with lots of sinus headaches, and my tonsils becoming infected. However, I have severe hay fever type allergies so most of the time I put up with my symptoms and they go away. However, I knew that I probably needed an antibiotic because my symptoms were getting worse and I had caught a flu-cold thing on top of it. When I went to the ENT she said she thinks that my tonsils may need to come out and prescribed 10 days of Avelox along with a sinus rinse (saline only) she was concerned because I am allergic to a lot of antibiotics (mostly I get hives) so she gave me Avelox. I did not read the side effects before taking it. The reason being I get nervous taking antibiotics as it is because of my allergies and tend to freak myself out. So I just read the part about drinking lots of water, no vitamins,etc.. Even though I had a cold-flu thing I did not take my Allegra or even Tylenol to ease my other symptoms and no vitamins (which I usually take) I only took the Avelox. I also chose to take it at night because on the bottle it warned of dizziness or drowsiness. I have small children to take care of so I couldn't be dizzy during the day! The first night I took it around 10:00-I had trouble falling asleep, felt kind of woozy and high. However, I didn't worry about it cause I knew it could happen. I fell asleep and woke in the night feeling totally freaked out. I kept thinking someone was going to break in the house, I felt really scared for no reason. I wanted to wake up my husband so bad but I didn't because he had the flu and needed some rest. After that I kept drifting in and out of sleep and my mouth kept watering and watering. The next morning I told him to go in the bathroom and read the side effects to HIMSELF-I only wanted to know if what I mentioned was in there. He said yes. I continued to take the drug the next night-this time I felt lots better like my infection was clearing and the woozy feeling was less than the night before which made me happy. But again during the night I felt freaked out and had trouble sleeping all night. The next day I got diarrhea. Again, I figured minor side effects, I need to stick with this and clear up my infection. I took the pill for 5 nights. There were several times during the day that I weird pains (but not super painful-more annoying) a pain in my thumb, my hand, my shoulder, my calf. It was only here or there-not too big of a deal but I thought it was weird. Then I had something happen with my daughter (a family type emergency) which led to lots of crying and drama the entire day. That night I took the drug again (This was actually last night-the 5th time taking it) Again, trouble sleeping but better than the nights before. I woke at 6 this morning to get my daughter ready for school and as soon as I got out of bed I almost fell down. My legs and arms felt SO heavy I can't even describe it. I could barely make it across the room, then the dizziness hit and I started to feel really bad, I started to black out. I laid down on the floor and started sweating, felt like a cold feeling through my body and then my body started going numb. At first I thought "Oh god, I am having an anxiety attack of some kind from all the stress the day before." but it just got worse and worse, I felt like I was having trouble breathing and swallowing. The worst part was if I even tried to LIFT my head off the floor I started to black out (my vision was closing around me and my ears were ringing like crazy) then my mind went crazy-am I having a heart attack (no it couldn't be I am 39!) then the weirdest thing happend my thumbs felt like the muscles were cramping and being drawn into the palms of my hands uncontrollably. That is when I started freaking out. I was yelling-my husband had to leap out of the shower.I kept telling him, something is really wrong get me to the hospital. At one point told him to call 911. I seriously thought "this might be it, the end and I am gonna die here cause my stupid husband keeps rubbing me and trying to calm me down instead of calling 911!" Then I think he got freaked out because it just wouldn't stop and every time he tried to lift me up slightly I would start to faint. Finally, the blacking out thing eased enough he could sit me up, then I finally worked me into standing. He got me to the car and we decided to go to the urgent care versus the ER. They turned us away and told us to go to my doctor because of the antibiotic They said they would see me if I wanted but they really thought I should see her because the antibiotic is really strong and could be the problem. I thought they were crazy and I got really pissed off thinking "What the hell? I could be dying here and they want me to see my freaking ENT?!" My husband talked me into leaving because my ENT was in the next door building. Their office was just opening. They took my blood pressure, it was good, my pulse was good, they checked my ear pressure to see if it had to do with the dizziness and I argued my ears are fine! This is different from dizziness I had from past ear infections I was almost blacking out! But, alas one of my ears was off, and had inflammation. Then they gave me a steroid shot. They said that my infection looked gone in my tonsils but they are still concerned about my sinuses and what is going on there. I have to have a CT scan next week. They said they felt what happened to me was a combo of my ear swelling and a reaction to the antibiotic. They did not give me another antibiotic because they said 5 days was sufficient time to kill the infection. I came home today and tried to rest but it was hard because I had the kids. All day it was an effort to move or walk but thank god the other symptoms were going away. Now it is about 11:30 at night, I can't sleep and I was lying here freaking out about my legs being so screwed up. I have stairs and it is all I can do to walk up or down them. I started thinking the doctor may be nuts and that something really horrible is wrong with me (can you say paranoid?!) so I got on my lap top while my husband is asleep next to me. I found this site. Thank god. Now I can calm down and try to get some sleep! I am not dying of some freaky ailment-it IS the Avelox making me feel this way. While mentally I feel so much better and I am going to stop writing this book-I am still pretty concerned about how long the side effects with my legs are going to last. I am also a little freaked about going to the gym even after I do feel better. I will try to write later to let everyone know when my legs get back to normal. If anyone is experiencing the same symptoms I did. Stop taking this medicine and call your doctor right away. I felt so stupid complaining about all this weird stuff-my husband acted like I might be a little nuts! Now I know its the meds!! :)

I had a Kenalog injection on March 24, 2008. It was given to me for allergy, hay fever problems. I am now experiencing constant leg muscle pain and leg and feet cramping. I truly feel this is from the Kenalog. Can someone tell me how long these injections last in your system? I am miserable and would never get this again.
******

I had to take Doxycycline for 3 weeks last August when a tick bite I had developed the classic "bulls eye"... a sign of Lyme disease. Everything went well for the first 10 days then I started getting kind of nervous and couldn't sleep well at night. I was constantly starving, really ravenous and had to eat constantly otherwise the nausea got worse. I was glad when I was finally able to stop taking the meds, BUT then after 24 hours I became depressed and really fuzzy in my head and disoriented. This lasted for another 2-4 days. I'm feeling much better now, but I have noticed that I'm just a lot more sensitive to other stimulants...coffee, sugar, alcohol, chocolate. I know I have a few other allergies, hay fever, food allergies etc. I was just wondering, does anyone else out there who has had a negative reaction to doxy have any other allergies or intolerances, or asthma? How much sugar, either in the form of sweets or alcohol do you usually consume? Daily, weekly, monthly...none at all? Feedback would be greatly appreciated. I would like to get to the root of this problem.

HI, i too have to say i am kind of relieved after reading this website that i am not alone with my experiences of the kenalog injection. I was given kenalog injections to treat hayfever, although i wasn't told the name of the injection. They did help and i probably would of continued this year if it wasn't for the side effects.
I was told that to have one a yr was safe, then just before xmas i noticed a dent on my hip, this started getting larger and looked almost like scare tissue, I too was worried i had some sort of flesh eating disorder. The dent is still there and i will never have that injection again. I also have been experience problems with my hips and pain around my coxis,i am not sure if this too is related to the injection. I was told by my doctor who is very good that the kenalog had eaten my fat tissue causing a dent and that it will get better in time.

I am a 57 year old man, who has been suffering from asthma several years. This spring my doctor put me on Singulair as an additional medicine to my cortisone-inhalator. after one month I feel symptoms of depression an mood-changing, severe ups and downs.
AND - as an additional symptom i have partially lost my feeling in some fingertips, and now parts of my left thumb and even a feeling of "cold2, mostly in my left hand.
anyone who share that symptom?
M.

Can Statins Cause Chronic Low-Grade Myopathy?
Statins (hydroxymethyl glutaryl coenzyme A reductase
inhibitors) are highly effective drugs for reducing serum
cholesterol and low-density lipoprotein cholesterol levels.
Clinical trials have shown that they also reduce risk for
coronary heart disease events, coronary procedures, and
stroke by about one third (1). Millions of people in the
United States and worldwide are being treated with statins.
In clinical trials and in clinical practice, statins have proved
to be remarkably safe.
The one notable side effect of statin therapy is myopathy.
A small fraction of patients who are treated with
statins will develop severe myopathy (2). In the worst cases,
severe myoglobinuria, acute renal failure, and even death
can occur. The incidence of severe myopathy is low, perhaps
1 in 1000 patients (2). Predisposing factors for severe
myopathy appear to include advanced age, relatively low
body weight, female sex, certain medications, use of multiple
medications, multisystem disease, and acute illnesses
or major surgery (3). If statins were avoided or used in low
doses in these circumstances, it is likely that the incidence
of severe myopathy could be greatly reduced.
Less severe forms of myopathy undoubtedly occur. In
some patients, fatigue and muscle pain and weakness develop
with moderately high serum creatine kinase levels
but not acute renal failure. In these cases, the myopathy
resolves when statin therapy is discontinued.
Still more patients report various muscle symptoms—
fatigue, pain, and muscle weakness—but have normal creatine
kinase levels. These symptoms probably are unrelated
to statin therapy in many patients. In middle-aged and
older people, muscle, joint, and tendon symptoms are very
common. Naturally, if a patient takes a medication that is
believed to produce muscle problems, symptoms are often
attributed to the medication. On the other hand, the major
controlled clinical trials have not detected a higher prevalence
of muscle symptoms during statin therapy versus placebo
(1). This failure of detection has generally led clinical
trialists to conclude that statin-associated myopathy with
normal creatine kinase levels essentially does not exist or
that, if it does exist, it cannot be detected above the “background
noise” of muscle symptoms in the general clinicaltrial
population.
Many physicians in clinical practice nonetheless believe
that they can identify a subset of statin-treated patients
who have a unique set of statin-related muscle symptoms.
Some patients clearly relate the onset of muscle
symptoms to initiation of statin therapy. These symptoms
may abate after discontinuation of therapy, only to reappear
when statin therapy is restarted. The number of such
patients is not large, and thus it may have been impossible
to identify them in large clinical trials.
In this issue, Phillips and colleagues (4) report on a set
of studies in four patients who had muscle symptoms during
statin therapy that resolved during placebo use. Quantitatively
measured muscle weakness also resolved during
placebo use. Muscle biopsies were performed in three patients
during statin therapy and then during placebo use.
Several pathologic changes were seen on biopsy specimens
obtained during statin therapy: increased lipid content of
mitochondria, fibers that did not stain for cytochrome oxidase
activity, and ragged red fibers. The authors suggest
that these patients had statin-associated myopathy with
normal serum creatine kinase levels.
Despite the study’s small size, we cannot dismiss these
observations as random variation in muscle structure.
However, these highly suggestive results are clearly preliminary.
The number of patients was small, and all appropriate
controls were not used. Nonetheless, this study is novel
because it used quantitative measures of muscle strength
and muscle biopsy to address the question of myopathy
with normal creatine kinase levels during statin therapy.
To be confirmed, the current data would have to be
extended to many more patients in whom muscle symptoms
are closely correlated with statin use. Reproducibility
of symptoms during therapy and symptom resolution after
discontinuation of statin therapy would be necessary. A
definitive study would have to be carefully designed and
executed. It would need to be double-blinded and placebocontrolled
and include sufficient numbers of patients to
provide a valid statistical comparison. In addition, investigators
would have to carefully consider the appropriate
selection of patients. The development of a registry of candidate
patients at multiple sites could facilitate a multicenter
study.
Is a carefully controlled, sizable study of this type
worth the investment of time and effort? To date, no evidence
indicates that prolonged statin therapy leads to permanent
muscle damage or progressive myopathy in patients
with normal creatine kinase levels. Controlled
clinical trials attest to the general safety of statins, and
symptomatic side effects appear to be limited to a relatively
small proportion of treated patients. In addition, no therapy
prevents or treats statin-induced myopathy, short of
withholding the drug. On the other hand, statins are being
prescribed to millions of people, and are usually continued
throughout the patient’s lifetime. It is certain that statins
cause myopathy in some patients. For these reasons, a valid
argument can be made for a more extensive study of lowgrade
myopathy in patients treated with statins.
In the meantime, physicians should recognize the great
benefit of statin therapy in high-risk patients and their
documented safety for most patients. For high-risk persons,
the proven efficacy for preventing cardiovascular disease
outweighs the unlikely possibility of permanent muscle
damage. Phillips and colleagues’ preliminary results
certainly do not provide adequate information on the spec-
Editorial
www.annals.org 1 October 2002 Annals of Internal Medicine Volume 137 • Number 7 617
trum, scope, or prognosis of myopathy with normal creatine
kinase levels during statin therapy. For these reasons,
prescription of statins for eligible patients should continue
despite the current results. Moreover, before discontinuing
therapy, physicians should carefully evaluate any patient
receiving statins who reports muscle symptoms. In most
cases, the symptoms will be found not to be consistent
with chronic myopathy, and often they will not be related
temporally to statin treatment. High-risk patients in particular
should not be deprived of major cardiovascular risk
reduction just because they display symptoms not clearly
documented to be closely related to statin therapy.
Despite these comments, the actions of statin on muscle
metabolism and structure deserve further investigation
to clarify the confusing area of low-grade myopathy apparently
associated with statin use in a few patients.
Scott M. Grundy, MD, PhD
University of Texas Southwestern Medical Center at Dallas
Dallas, TX 75390-9052
Current Author Address: Scott M. Grundy, MD, PhD, Center for
Human Nutrition and the Departments of Clinical Nutrition and Internal
Medicine, University of Texas Southwestern Medical Center at Dallas,
5323 Harry Hines Boulevard, Y3.206, Dallas, TX 75390-9052.
Potential Financial Conflicts of Interest: Honoraria (from Merck &
Co.; Pfizer, Inc.; Bristol-Myers Squibb; and Bayer); Grants (from Merck
& Co. and Pfizer, Inc.)
Ann Intern Med. 2002;137:617-618.
References
1. Executive Summary of The Third Report of The National Cholesterol Education
Program (NCEP) Expert Panel on Detection, Evaluation, And Treatment
of High Blood Cholesterol In Adults (Adult Treatment Panel III). JAMA. 2001;
285:2486-97.
2. Staffa JA, Chang J, Green L. Cerivastatin and reports of fatal rhabdomyolysis
. N Engl J Med. 2002;346:539-40.
3. Pasternak RC, Smith SC, Bairey-Merz CN, Grundy SM, Cleeman JI, Lenfant
C. ACC/AHA/NHLBI clinical advisory on the use and safety of statins (1)
(2). J Am Coll Cardiol. 2002;40:567-72.
4. Phillips PS, Haas RH, Bannykh S, Hathaway S, Gray NL, Kimura BJ, et al.
Statin-associated myopathy with normal creatine kinase levels. The Scripps Mercy
Clinical Research Center. Ann Intern Med. 2002;137:581-5.
© 2002 American College of Physicians–American Society of Internal
Medicine
Editorial Statins and Low-Grade Myopathy
618 1 October 2002 Annals of Internal Medicine Volume 137 • Number 7 www.annals.org

Here is some perspective for you all. I take Singulair and do well on it and in ACTUAL studies it has one of the safest safety records. Understand that post marketing reporting does not mean there is a correlation between the event and the product. Throughout the life of a drug the companies must disclose any report of side effects reported to them REGARDLESS of causality. A popular antihistamine that is OVER THE COUNTER also has suicidal thinking/behavior listed in its post marketing section. However, just because patients who had reported having these thoughts while taking the product doesn't mean it was a result of the product! Maybe they had a depressive personality and were also on multiple other medicines to treat that. You must look at the "Adverse Reactions, Warnings and Precautions" sections of package inserts to see the side effects that were actually seen in studies. You can die from ulcers derived from over use of aspirin or ibuprofen. Decongestants can throw off your blood pressure and these events are documented in actual studies! Listen to your bodies when taking any med. If you feel differently report it to your doctor.

These are all drugs people, there are potential side effects. There are also side effects to those "natural" over the counter remedies that are not nearly as regulated by the FDA or studies by the drug companies.

To anyone out there who has experienced side effects to singulair timed to when you started it, talk to your doctor, stop taking it and see if it goes away. Same advice for any product prescription or over the counter medicine. Side effects can be a combination of many factors (what other meds are you taking?) But understand for many people this product is the safest and most effective treatment for them. The FDA and Merck are reviewing all information to see if there is any correlation to the reporting. But singulair been around for about 10 years and prescibed to billions of people and is known to be one of the safer medicines out there overall.

In between the legitimate posts on this site I get the sense there is a lot of ambulance chasing going on. People looking to cash in on this big drug companies. We want drugs, we want them cheap and with no side effects which is not a reality. Keep stepping up the regulation and make the companies hire more lawers to protect themselves and jump through even more hoops and see what happens to the price and access to new meds. Even better, see how regulation has impacted the development of new medicines around the world (here's a tip, it will dramatically decrease). Drug companies certainly aren't perfect but which industry is?

Please, when taking any medicine over the counter, prescription or herbal supplement listen to your bodies to see if the potential benefits of the product outway the risks or side effects. Report any changes to your doctor.

I have been on mirena now for 10 months. I was on the depo for 10 years prior. I loved my depo adn only went off of it after Kaiser said I could not do it any longer. I was told that mirena was a god send and a lot like my depo. I can say that the combination of depo and mirena I have not had any period at all. but that is where the happiness ends. I have experienced moths of breast pain. it hurt to touch them let alone put anything on them. after about 6 months and numerous trips to the vet it disappeared. then I got a small rash on my neck and by my arms. went to dermatology and since then I have been there, or to my primary or an allergist every week since then. the rough severley itchy skin is constant. remarkably every 29 - 32 days it fades for 2 days or so and just when I am sure it is going away wham back it comes and each time it is getting worse and worse. having never had any skin problems before I believed the doctors tha tit was folliculitus, then they said dermatitus, then they said uticaria and then hives or the last straw i was causing it that it was in my head. i just got a new allergist and while she doesn't knwo if it is my mirena she can tell me I have histamine levels that are off the chart. my husband is allergic to a lot so we already use free & clear everything and my housse is spotless but I am still being told it is soemthing I am doing to myself. I have also been reevaluating my things and I relaize I have been experiencing a lot of numbness and joint pain. so much so that my primary sent me to a rhuematlogist and he ran every test for lupus, and many other diseaeses adn even cancer. I was going crazy. Iwas beginning to think maybe I was mental. I have since been researching mirena and I am finding it so much more than what the pamphlet says. I finally got the nerve to call my ob, adn she ahs since been researching things with me and we know for sure that no matter what next week I get my mirena removed. I am just feeling so alone and depressed. I am 33 years old and instead of enjoying my new marriage I am contemplating a divorce becasue I do not want him to be stuck with soemone who might be crazy. seeking support and anyone else who feels this way.

If you are a woman or have a daughter PLEASE READ.......

Please be very careful before getting a Kenalog injection especially if you are a woman or for your daughter. In March my 13 year old daughter received one Kenalog injection for hay fever. Now almost 4 MONTHS later it is a 2 inch indentation with dark bruising all around it. She has also had her period the entire time with maybe a 1-2 day break between them. It has taken this long for the doctors to say the bleeding is from the Kenalog injection. I never would have allowed them to give this to her if I had known of these side effects. She has been put through test after test and no end in site. Now my 13 year old will have to go on birth control to stop the bleeding and there will prob. be side effects from that as well. I was shocked to find this site and now how many lives this drug is hurting. Now my daughter is suffering, all from 1 SHOT.

All you are Hypochondriacs. If one person says this medicine is causing this, then of course; you all have the same problem "some how." Isn't this weird? It is called the "placebo effect." Normally all the people involved in the testing are given "Lisinopril" (or some other drug), then the placebo group is given a vitamin supplement, the group receving the vitamin supplement is being told they are receving "Lisinopril." Mysteriously?, the "placebo group" is all feeling better and their symptoms are gone. This is due to the fact that all these people in the "placebo group" have interacted with eachother and have told eachother "I feel better" than of course everybody feels better. So WEIRD!! So, my point is this forum is all your peoples "placebo group." If you guys never heard of these side effects from this forum you would have never experinced them. Hypochondriacs all of you are. This is a very good medicine that is helping all of you make up for your peoples lack of self-disipline to control your diet or exercise enough to lower your blood pressure naturally. So be thankful. Lets not complain about false side effects because John has them. I wonder what the side-effects of that cheese burger are that caused high blood pressure. It is funny, I don't see a forum for that. So deal with your so called "side-effects" that are associsted with "Lisinopril" or go on a diet people. Get over it!!

Firstly I am Male, aged 48. Suffer from really bad Hay Fever for years now and the same Doctor has administered Kenalog to me for about 6 years, once a year but twice this year. I am suffering dreadful pains in my ankles and lower back and a different doctor today has suggested it is the onset of Arthritis. After quizzing me more I mentioned having taken Kenalog for several years ( I thought it had no relationship whatsoever my current ailment) she has lectured me NOT to use it again. She suggests that it could be a contributing factor to my "Arthritis"( hope I'm spelling that right) Anyway, now I know! But, trouble is, what to do next summer..I really will suffer without it.

I take singulair and do fine with it, helps my allergies, upper resp. and hay fever, I dont want to quit. but my grandson takes it. He is 5 now. It really helps his asthema in the winter. I take him off as soon as possible because he gets so irratible. Easily angered, what some would call spoiled. My husband says he cant tell the difference, but I really can. We do spoil him, but he is such a good child, it is hard to tell sometimes- but I really know and he is different. The angry factor. It just isnt the same when he is off the granules. What is going on with this medicine???

Had a one time cortisone injection in 2004 for severe hay fever. Was a miracle shot! However, one side effect I personally experienced was a menstrual period that lasted 51 days. Took a one time cortisone shot this year, 2005, and once again, the same thing has happened. My Dr. has been a practicing allergist for some 50+ years and has NEVER heard of this side effect, until me. Just want to help anyone else out there who may have had the same problem, but did not relate it to the shot.

I Have Been Taking Kenalog For the past 20 years For Very Bad hay fever Nothing Else Worked As i Have Tried the lot.
I have 1 injection a year around May Time And the relief that it gives is fantastic this year my new doctor suggested as i am now 44 that i try and not use it

It is now June 23rd and i cant take anymore my appoinment for my Jab Is tomorrow and i cant wait for the relief that it will bring.
i have had (touch Wood) No Side Affects That I know Of and will keep on using the product >

I have been on Levoxyl for several years, and it is the only medication I can't live without. I can give up my oral diabetes meds by going low carb, my allergy meds and suffer the hay fever, but Levoxyl is my friend. My levels are low normal, borderline if you will, but I have had muscle fatigue since I was a teenager. When I started the med, I could climb stairs without aching, style my hair without my arms trembling. My thin hair filled in and though it is fine, it is full of volume. The pharmacy switched me to the new generic and within three months, I was aching, my hair was thinning, I was 35 and felt 88. Switched back to the brand name, and am well again. The only negative is I have to drink a LOT of water to stayhydrated, but have to do that w/ the diabetes anyway. Alot of the sideeffects I'm reading here sound like dehydration problems. The anxieties, the fatigues. If you aren't drinking your 64oz of water a day, try it and see if it helps.

I started suffering from hay fever the summer between my jr. and senior high school year; I am now 48. When I was about 20 my cousin referred me to his doctor for a Kenalog shot for the hayfever. For several years I took at least one, sometimes two shots in the fall. I never had any problems that I couldn't live with...the only thing I noticed was irregular monthly cycle (especially the years I had 2 shots) for several months following and loss of smell. However, for anyone who suffers from hayfever, irregular periods and not being able to smell are gladly sacrificed for the relief Kenalog provided. I never experienced the dents or other problems I've read about.

As I got older I've "outgrown" hayfever. I'm really glad as my original doctor died and it became difficult to find a doctor who would administer the injection. I'd hate to still be suffering from the sneezing, watery eyes, etc. I do notice my skin is much more sensitive to plants and grasses now.

Two of my children developed hay fever about the same time as I. I'm ready to tell me son to ask the PCP about Kenalog but after reading other people's experiences, am reluctant. As my daughter is pregnant, I won't say anything to her.

OK, I'll stop.

Use kenalog for the first time last year and couldnt believe how good it was , after one injection I went back to Telfast 180mg which worked ok. This year , been on the Telfast 180mg and no effect on my hayfever at all , been sent home from work a couple of times due to it being really bad.
am back at docs this afternoon and gonna ask for it again , just to get past the worse of the hay fever

I took it at 60mg a day for 3 days then 10mg a day for 4 days for severe allergies (hay fever). I have had terrible headaches every day, frustration to no end, hot flashes. On day 2 I had severe leg pains in both legs that went away with in a few hours. I've had a lot of problems concentrating. My mind feels like it's racing constantly. My cheeks are puffy (moon face) started within day 2 and day 3..at this point my cheeks just hurt inside..ah. It's really uncomfortable. I've had strange/bizarre moments of anger/rage that are a bit frightening. Today is my last day of taking it, at last! It has helped a lot with my allergies though. I usually have cold feet and hands and since I've been on this all have been roasty toasty. Oh day 2 I did have a brief dizzy moment where I saw black spots before my eyes for a few seconds that scared me. The hunger pains are annoying. The headache starts in the morning and builds through out the day. If I lay down for a while and get a few brief nods off of sleep..it seems to do the trick. It's wierd. I don't recognize my face in the mirror much really. Not a good feeling.

Dec. 02 was issued by RX Amibid DM 30-600Cr Qty 60 Two twice per day,acct heavy lung congestion. Ater condition cleared did not refill Rx in expectation of reoccurance in future. As during course of usage noticed an effect of alleviationc of PN intoes and fingers. Thinking it"s just a fluke or way of PN, until this May during another heavy chest congestion Hay Fever_ Asthma and another ongoing round of Amibid DM, the PN has abated again. AQm wonering if this could be an alternatine means of treating Pn other than Neurontin?? Any Dr. or Pharn care to respond for or agaqinst? Thanks

I've taken the kenalog shot for severe hay-fever and allergy-induced asthma three or four times in the last 7 years, always in the Spring when I reach a point that I can't take a single breath without coughing up phlegm from my lungs. Once I received the shot while pregnant. My doctor told me it was safe, and would have the side-effect of helping to develop the baby's lungs a little early. In my case that was a good thing, because I tend to deliver prematurely, and this baby was born 4 weeks early. She is four years old now, and healthy, strong, happy, intelligent and developing completely normally.

I have had no side-effects at all. Instead, I was *less* moody due to not being sick all the time with allergies and finally sleeping. I was finally able to sleep through the night without waking myself up coughing, or because my mouth closed and I couldn't breathe, which happened constantly. I stopped snoring, and could breathe and smell again, go outdoors without fluids immediately pouring from my eyes and nose and filling my lungs, and enjoy sunshine, blue sky and clean air again instead of being imprisoned in my house due to such severe allergies.

The shots clear up my allergy symptoms for 2-3 months, and by then the plants I'm most allergic to have ceased producing pollens for the year.

The severity of my allergy symptoms seem to cycle, so that I have only needed to resort to the kenalog shot every other year or every three years. Tomorrow (Monday morning) I'm seeing the doctor to get a kenalog shot for this year.