Because my husband mentioned chest pain/tightness at his diagnosis of PF early September, he was referred for a treadmill test. However at the appointment, the specialist nurse declined to do one as she said it would make him too breathless. Instead he was referred for a stress echo test where they inject something to make your heart race plus a dye. This has indicated some narrowing of an artery and he has been referred for an angiogram. He has also been prescribed beta blockers and nitrates. I'm a little worried about the beta blockers having read that they slow your heartbeat and can cause lung spasm in people with lung conditions.
I know absolutely every possible side effect has to be listed so I'm looking for experiences of anyone with PF who is also on beta blockers.