Anyone using adalimumab?
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annie21 成员Posts:4我很担心从Adalimumab开始，但是我已经待了8个月了，结果良好，到目前为止没有副作用。我发现注射易于自我管理。它确实有些刺痛，但很快就会过去。我只是希望我已经开始更快地使用它，因为已经造成了很多关节损失。
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Skybird 成员Posts:3Thanks so much Annie I’m just so nervous I guess . Hoping I have the same results as you0
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氨基 成员Posts:29嗨，天鸟
I have just started adalimumab and like you was really anxious about it, but I've done 2 injections now and they're pretty easy to do yourself, you simply just have to press the injection pen down on your skin and the pen does its thing. Like annie21 said, it does sting a little when the medicine is going in but it really isn't that bad and feels fine within about 10 seconds or so. I always take mine out of the fridge about 40 minutes before hand so it can get up to room temperature as this reduces the stinging apparently. I've felt a bit blurgh after the injections but then I do seem to get side effects from most medications so that's probably more just me lol.
Once you've got the first one done, I bet you'll feel much better about it, but it's totally understandable that you feel nervous about it as its something new to have to deal with with.
让我们知道你是怎么做到的
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GrahamD 成员Posts:3I am afraid that I have some negative feedback on Adalimumab normally called Humira. Before taking this medicine or any of the biologicals please ensure you have read the small print. You should also have a very frank discussion with your prescribing Doctor on the potential side effects of taking these drugs.
我服用了药物，最终患有全球神经病，如果您阅读了副作用，您会看到100中的1个。但是让我清楚地知道，有99个人没有副作用，所以我只是不幸的人。
我现在正在使用另一个生物学（secukunimab），到目前为止，它没有造成副作用，因此请不要将我的评论作为您不应该服用药物的陈述。这仅仅是警告您需要冒险评估服用药物潜在的潜在下降一侧的潜在方向。更重要的是，您的开处方医生应该在服用药物之前与您进行这些讨论。
There are thousands who are benefiting from these drugs but remember there are a few who now have serious side effects from taking them.Thats life Im afraid?
最后是您的决定。
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chris_r ModeratorPosts:524Hi@GrahamD
欢迎to the forum. I see you are posting already which is great,but I just want to welcome you to the inline community.
您说您正在使用一种称为secukunimab的药物，到目前为止，目前正在有所帮助，没有副作用，并且患有银屑病关节炎。
You don't say as far as I can see on all your posts how long you have had psoriatic arthritis it would be good to know a little bit about your arthritic story.
Meanwhile keep on posting and enjoy chatting to others
最好的克里斯汀
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Janp72 成员Posts:4嗨，天鸟,
I’ve been on Adalimumab since just before Christmas. I was scared to death of starting, having read all the side effects, but having suffered from Rheumatoid Arthritis for several years I made the decision to try it because my pain was becoming unbearable and I had no quality of life.
I’m happy to say I have had no side effects (yet), the injections are really easy to do.... it’s just like an epipen, and there will always be someone you can contact if you have any queries or problems.
祝您好运，我希望它对您和对我所做的能力一样。
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Elmbow 成员Posts:80Adalimumab has been great for me. I've been on other biologics before that were okay but this one really made a difference. No bad side effects and you only take it once a fortnight. It's the best there is, the gold standard; it's unlucky that your condition is bad enough to need it, but you're also lucky you get to try it when many around the world do not. I wish you all the best with it.
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kayzea42 成员Posts:2I'm currently on steroids and just received my adalimumab. I'm very concerned that the patient alert card that came with the jabs states that the serious side effects include heart failure and cancer.... I'm worried to say the least.
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安娜 ModeratorPosts:624Hello@kayzea42and welcome to the online community,
It’s understandable to be a little worried about starting a new drug treatment for your RA such as adalimumab, especially when you read the contraindications. The drug itself is considered a game changer for many people with inflammatory arthritis such as RA and as you can see from the posts above, many people have few side effects. Perhaps you’d like to read the Versus Arthritis page on the new anti-TNF treatments which include adalimumab - there are some interesting personal stories at the end of people whose lives were improved by taking the drug:
It might also be worthwhile talking to your Rheumatologist or GP about your concerns - they will be able to discuss with you the risks and benefits.
Best wishes and do let us know how you’re getting on. Keep posting as you’ll find that the forum is full of friendly supportive people who will be happy to share their experiences with you.
安娜（mod）
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