Experiences with

Atimos Modulite

My doctor changed my inhaler from Atimos modulite to Serevent. I've been using it for two days. My question is how long do you have to use serevent for it to take full effect? Have any of you had experience with this inhaler? Thank you for all your replies.

There I received a prescription for Atimos modulite 12, Flixotide 250. In case of infection, additional Pulmicort and Salbutamol to the nebuliser. I checked all these new drugs to see if they were on the NHS list. It turned out that they are.

my pharmacy have told me they won’t be ordering any more of my Clenil Modulite 200 as it’s been discontinued.

I have been on Clenil Modulite for two years now and over that time I have experienced problems relating to the inhalers. The past two Clenil inhalers I have had have both clogged up and I haven't been able to get any medication out of them.

I need to stop my duaklir genuair and clenil modulite and try something else as I absolutely can't do anything at the moment because of my breathing. Still really breathless after 2 weeks of finishing my clarithromycin and not improving.

I have just been prescribed Qvar 100 after I had to stop taking Seretide 125 due to side effects. I was prescribed the Seretide a week ago as the Clenil inhaler wasn't doing much to control my asthma (waking up several times a night, needing my ventolin inhaler multiple times a day etc). The Seretide

or so on a morning and after a month or more of feeling no better at all, the nurse said she would try something different, and to stop all the different inhalers and try the Asthma treatment using only the maintenance inhaler which is Clenil Modulite and keep the blue ventolin to use if needed,

My profile is up to date. I am coming up on the 18 months of ADT for my Gleason 9 OMCRPC. Treatments : 18 months ADT + 10 months Xtandi+ successful IMRT to pelvis for tumor and lymph nodes and successful SBRT to rib met. Last PSMA PET showed possible nodes . I now have 9 months of undetectable PSA (due

Had 20 sessions of IMRT late October to early November, 2024. Started getting diarrhea in early 2025 that is still happening. Asked my RO if the radiation caused this delayed reaction and he didn't think so because it didn't happen during or immediately after radiation ended. I am not so sure as I did

I've told my TULSA history previously. Had TULSA ablation of 70% of prostate in 2019, G=7a and clean MRI afterward for 4 years. Last year MRI found new tumor, and biospy G 3+4 with PNI .....but only 5% of 2 cores were G4. Prostate size 10ml and PSA=1.2 Doctor did a PSMA in December and found nothing

Back in October, my PSMA PET scan revealed, besides a sub-centimeter lymph node lesion, a concerning lesion on my R frontal lobe of my skull, with uptake from the radioactive tracer. No other bone mets. My oncologists were all skeptical of this finding, but we agreed to do a brain MRI after I was finished

Underwent HDR BT October 2020 to treat 6(3+3), 7(3+4), and one unknown tumor missed by TRUS. Late 2024 PSA doubles from 1.51 ng/ml to 3.28 in 4 months, then to 5.08 four months later. Last Thur/Fri underwent PSMA PET and MRI at Roswell Park, Buffalo, NY. Major worry of metastasis is off the table

I've been on Orgovyx + Abi + 5mg Prednisone now for 3 months. I've had to hound my doc for an A1C and lipid profile, since these are known to affect them. My A1c has moved from the upper range of normal to well within diabetes. It was 5.5 and is now 6.7, ouch. That 5mg of prenisone is like eating

Hey Guys, I would like to glean some collective wisdom/experience from this amazing group. The end of this month will mark my one year anniversary of Salvage radiation therapy IMRT / IGRT Conventional Fractionation 7000 cGy / 35 fractions to prostate fossa concurrent with 5000 cGy / 25 fractions

Post my dad’s PC diagnosis in Dec 2024(PSA:38) with semi vesicle invasions, we started firmagon injection. After 3 month firmagon, dad’s MRI review shows left semi vesicle involvement,PSA dropped from 38 to 1.4. Doc suggests prostatectomy. Post second opinion with RO we were advised to undergo VMAT

I started 24 months of Orgovyx and Nubeqa back in October. And I completed 28 fractions of IMRT two weeks ago. I have noticed a not-insignificant case of gynecomastia that has progressed over the past month or two. No tenderness associated with this by the way. After meeting with my MedOnc last week

I'm 78 years old. In May/June 2024 I had 44 sessions of IMRT. I've been on Orgovyx for one year. The ADT is really affecting me - I've gone from a very active happy life to one that is quite dreary. The main SEs are lack of energy and weakness. My urologist and RO want me on Orgovyx for at least

I was told SBRT is not appropriate for high risk GS 9? Could Prostox confirm this over IMRT or CMRT?

Hello Everyone. Been a little while since I've posted but, unfortunately, I am back ; ) I am 57. Had RP in October (2020). Pathology was G9 pT3bN1M0 with ECE, SVI and positive margin. Had 39 IMRT salvage radiation sessions with 18 months of ADT (Lupron and Zytiga). PSA was less than .05 and testosterone

I was diagnosed with oligometastatic PCa in Feb 2022 (see my profile). I had one met in my right iliac crest. I had 37 fractions of IMRT (including to the met) and completed 2 years of ADT which ended in April 2024. My PSA has been undetectable (<0.025 ng/mL) in my three monthly tests since June 2022