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News > Methotrexate Shortage Has Many With Arthritis Concerned, Too
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Methotrexate Shortage Has Many With Arthritis Concerned, Too

Rheumatoid arthritis and juvenile arthritis patients who can't tolerate oral methotrexate are most vulnerable.

By Jennifer Davis

2/17/12 A shortage of an injectable version of the drug methotrexate has been all over the news lately, sparking outrage and concern on behalf of children with a certain type of leukemia who can’t get their life-saving medication. But some people who have inflammatory types of arthritis and rely on the drug to keep their disease under control are also concerned about access to methotrexate.

“For the most part, this should be a manageable situation for arthritis patients,” says Donald Miller, PharmD, a professor of pharmacy practice at North Dakota State University, in Fargo. That’s because the majority of people with arthritis who take methotrexate – which is used in the treatment of rheumatoid arthritis, psoriatic arthritis, lupus and certain types of juvenile arthritis – use the pill form. There is no shortage of that right now.  

The root of the problem lies with the preservative-free, injectable form of methotrexate. Very high doses of it are used to treat pediatric cancer patients, and that is the form of the medication that is running dangerously low.

And now that shortage is increasing demand on other, injectable forms of methotrexate. “When you get shortages with even one product, it does have a ripple effect on everything else,” Miller says.

In this case, the form of injectable methotrexate with preservatives is being affected. It is used by arthritis patients (at much lower doses than cancer patients) when methotrexate pills don’t provide enough relief or cause unpleasant side effects. Some people may still be able to fill their prescriptions for injectable methotrexate at certain locations. For those who can’t, there are other options that may work for them until the shortage is resolved – which could be within two weeks, federal health officials said Thursday.

The shortage developed after one of the major suppliers of the preservative-free injectable medication, Ben Venue Laboratories, shut down an Ohio plant in November because of manufacturing problems identified during inspections by the Food and Drug Administration, or FDA, and other global regulatory agencies. Manufacturers of the type with preservatives are now reporting shortages due to increased demand.

In response to growing concerns that the medication shortage will worsen, the FDA said that Ben Venue will now release its emergency supplies of the injectable, which were produced before the shutdown, and two other manufacturers will step up production.

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Tate
04 May 2012, 19:14
I also take the injectable. I am 16 and swiched to the injectable form the eight pills and like the shot better.The shot is so much better than the pills. I am lucky to have some left but I hope this gets resolved quickly especially for this who need it to save their life. God bless all
mw
06 Apr 2012, 22:24
almost a year ago my daughter was diagnosed with ALL. We were told that we caught it early and was given a rundown of steps needed to be taken in order for her cure. and not even a year later in a 2-3 year plan one of the most important drugs, used to help cure her, is running dangerously low. as a parent i'm terrified. when will this be resolved before we are seriouls affected. my daughter is 4 years old.
Amber
29 Mar 2012, 18:48
I, too, take the inj. form of mtx. It's so frustrating in the article, "just take the pills". Like many others, the pills make me soooooo sick. I'm stuck in the bed for days just from the nausea. Let's see, would I rather be stuck in bed from nausea & hurt, or just hurt at and least be up some? Someone else mentioned the mouth ulcers & it going thru your liver. It's not good. Was lucky & have a little left. After that, if this shortage isn't resolved, I'll have to look for something else. Good luck all!
Steve L. Epp
29 Mar 2012, 13:58
I, too, used to take the injectable years ago, when a shortage developed. Ever since, I've been on the tablets, 7 every Friday. Thank goodness for the tabs! Now I'm on a drug trial that's working wonders, along with my methotrexate.
Ruby
27 Feb 2012, 23:52
I've been on gabapentin (generic neuronton) for 10 years for neuropathy caused by sjogren's syndrome. It helps with pain, but doesn't get rid of it completely.
Irish
26 Feb 2012, 15:04
I have been taking the injection of methotrexate for many years now and because my body does not absorb meds as well in pill form. I do well on the shots and but the naseau (msp) is bad right after taking it but the next day is all good. This med has helped me tremendously over the years and hopefully the maufacturers will produce more so those cancer patients can stay well.
Tara
25 Feb 2012, 10:33

Please read my comment about Neurotin because it may help you also. I am so sorry you are still suffering and would like to share what's helping me. I feel lucky after reading your comments. I take 7 Methotrexate pills per week and have no problems. I also did the injections but hated giving them to myself and asked to go back on the pills. I am also on Humira 40mg. injections and feel pretty good but had to have Morton Neuroma surgery(removal of nerve) in my foot. I just wanted to share that my primary care provider just gave me a prescription for Nuerotin 300mg. to take just once a day at bedtime for pain that I still had from having the nerve taken out of my foot and not being able to sleep at night. It has helped me with a lot of my body pain. My doctor thought since I've had pain for over 5 years that it's programed in my head and that this medicine can help redirect my brain to not have this pain. It's a very low dose and has helped with sleeping and the pain. It was developed for seizures but didn't work well but worked for people with fibromialgia, menopause, RA and many other ailments pertaining to problems with sleeping and/or pain. Google the medication and read about the good comments people are blogging about it. I've been on it for a week and feel much better.
Rebecca Mancini
24 Feb 2012, 22:53
It is so nice to read what you all have to say, and not feel so alone. The RA has changed every part of my life. I am now on SS and can no longer work. The first time I was on the injectable it took about 6 months to start working. As soon as I was feeling "good" I ended up in the hospital with a virus that made me sick for months. I have been back on it for 8 months now. Two moths ago they added Cimzia to my list of meds....What is worse..the sleeping all the time, the pain, or the depression from feeling so useless to your family......Thx again for making me feel like I am not alone.
Melissa Bennett
23 Feb 2012, 06:23
I was on the pills for a while for psoriatic arthritis, but they made be very sick for days. I had to come off the med for a while, and when the doc started me back up, I asked for the shot(which is amazing considering I hate needles). I'd rather deal with the shot then being sick and having the ulcers with the pills. I hope they get this shortage issue taken care of soon.
Doreen
23 Feb 2012, 01:53
I am so worried because I am on the injectable MTX and I believe it has kept me out of the hospital. My doctor is trying desperately to find a biological for my desease but so far no luck. I ended up in the hopital 2 X's 2010 for my shoulder and hip when I couldn't walk. I pray for all of you who need this medication. It is actually heartening to hear of others who suffer like me. I feel so alone so much. I get frustrated from well thinking friends and loved ones who keep telling me about all the natural miracle cures because they don't understand this dibilitating desease. The Lord give each of you strength. Thanks for listening to me vent.
Becky
22 Feb 2012, 20:24
I had been taking the injectable form of MTX, and I think the type without the preservatives has less side effects. I stopped using it regularily in August and then went back on it in November and had frequent bouts of vomiting, so I am no longer taking MTX. Not sure how my rheumatologist is going to feel about this when he finds out next week. The side effects from MTX are just too much for me, I end up having to stay in bed the next day after I take it.
Tula
21 Feb 2012, 22:01
Wow, I've been taking the pills (8 per week) for 25 years with no problems. I take them over 24 hours, though, and not all at once, so maybe that mitigates the side effects somewhat. It's bad enough we have to deal with severe diseases without being unable to get our meds when we need them. I try to keep an extra supply around - paid for off insurance, since they don't like you having more than you're currently taking. I asked my doctor for a second set of prescriptions so I could get a backup supply, since mail order can be unreliable and slow.

Kathy
21 Feb 2012, 20:52
I take 8 pills per week & Folic acid daily to help keep the ulcers away. Doesn't always work but it really helps. Try hard to keep acidic foods at a minimum as well. Still have flares but it's better than before did nothing. I grew up with a doctor that told my parents it was "growing pains" sure wish those growing pains would have stopped when I stopped growing!!!
Kathryn Brooks
21 Feb 2012, 19:29
I have been taking SC MTX for over a year. Now taking by mouth when I can't get the injectable. The oral form makes me extremely nauseous, causes oral lesions, is not effective. I have frequent flairs. Had to double my prednisone last week.
Eileen
21 Feb 2012, 13:56
Since when does other global regulatory agencies inspect our drug manufacture companies. To what extent do these agencies effect what is approved andis not approved? How stupid of me to think all along that thefood and drug agency looked out for us and our health. Eileen
Vicki
21 Feb 2012, 12:33
I, personally, rely on my sub q injectable methotrexate for the stabilization of my RA. The oral pills make me sick. I am trying to get off the higher doses of prednisone to save my organs. This is not a simple disease to regulate. Arthritis should be put in the same catagory as a "pediatric cancer drug." This disease is debilitating and will never go away! It cripls many young people! Let's not forget how important treatment is for Rheumatoid arthritis!
Eddie
21 Feb 2012, 11:55
Fortunately, I am able to take the oral methotrexate, which is good thing since I don't care for needles.

Unfortunately there are far too many children who depend on injectable version to survive, along with many adults who can't take the oral and need the injectable version just to be able to function and be relatively pain free. I know I wouldn't be able to function without my prescription.

My heart goes out to all those who need this medication and either are not able to find it, or have the funds to purchase it.
CONNIE
21 Feb 2012, 11:07
I fortunately have not had to use the shots, but I do use the Voteran Gel for quick relief until my pain meds kick in.
I feel sorry for those that are affected by this shortage. On top of their illness & pain,they will have to deal with LOCATING their medication.
I do have a suggestion if they have to take the oral MTX.
I did have various side effects at the beginning of my treatment. I did as many suggested to take it at night, well I did but I took it after my dinner. Now I take my 7 little pills with my dinner. The trick is that I eat a few bites, take the pills and then finish my meal. Seems to work for me.
Kim
21 Feb 2012, 10:59
MOST fellow Juv Arthritis patients I know - use the Inj - NOT the PILLS,..... Pills aused nausea yes,... but Mostly Horrible Mouth Ulcers AND was told it wasnt as good, having to go through the stomach & liver,.... etc,.... So we have been on the Inj Preservative (Spoke of in this article) for 4 of the 5 years of her life so far.....
lee ann serie
21 Feb 2012, 09:19
i have used .6cc of methotrexate for several years. i switched after 7 years when pills started making me throw up. the last month, i have had very bad pain for the entire week after my shot. thought it might be the bottle, so i used a new one. same thing. so the doctor took me off and put me on 1 5mg prednisoine. 2 if i need it. the pain seem to have gone away since it is out of my system. i may try it again later. sad these meds are so dangerous.

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