Discussions tagged “PAH”

I was recently prescribed Tracleer 125mg Tablets for my Pulmonary Arterial Hypertension (PAH). I've been on them for about a month now, and I'm curious to hear from others who have experience with this medication. What has your experience been like? Have you noticed any significant improvements in your ability to exercise or any concerning side effects? I've been lucky to avoid any serious issues, but I do experience some nose irritation and flushing. I know that everyone's experience can be different, so any insights or advice would be greatly appreciated.

I recently started using Ventavis 10mcg/ml Inhalation Sol for my pulmonary arterial hypertension (PAH). It's been a bit of a roller coaster so far. On one hand, it's helped me breathe easier and improved my exercise tolerance. On the other hand, I've experienced some side effects like headaches and flushing. I'm curious to hear from others about their experiences with this medication. Have you found it helpful? Do you have any tips for managing the side effects? I'd love to hear your stories and any advice you might have. Also, if anyone has dealt with more serious side effects, please share your experience and how you handled it. Let's support each other and share as much information as possible.

I've been on Remodulin for about a year now to manage my pulmonary arterial hypertension (PAH). It's been a journey, to say the least. The continuous infusion can be challenging, but it's made a significant difference in my symptoms. I was wondering if anyone else has tips for managing side effects or dealing with the pump? Also, has anyone had experiences with both subcutaneous and intravenous infusions? I'd love to hear your thoughts and advice.

I was recently prescribed Adcirca 20mg Tablets for pulmonary arterial hypertension (PAH). I've heard it can be quite effective, but I'm also concerned about the potential side effects. Has anyone here had experience with this medication? Specifically, I'm curious about the more severe side effects like allergic reactions, Stevens-Johnson syndrome, changes in hearing or vision, or long-lasting erections. Any insights or shared experiences would be greatly appreciated.

Has anyone tried Tyvaso for pulmonary arterial hypertension (PAH)? I've been prescribed Tyvaso 0.6mg/ml Inh Sol (2.9ml) and I'm curious about how effective it is for improving exercise ability and reducing symptoms like shortness of breath. I've read about some serious side effects, so I'd love to hear real-life experiences—both good and bad. How do you manage any side effects? Any tips on using this medication effectively would be appreciated.