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Has anyone got experience of Prucalopride or Fluconazole?
Gastro has prescribed me a week of the antifungal Fluconazole for suspected Candida and a months trial of Prucalopride for poor oesophageal and gut peristalis (contractions that move food along).
Apparently Prucalopride can in rare cases give you headaches, I suffer from headaches anyway but they have been exacerbated by things like medications in the past which I had to stop as a result of that. Apparently it is a seretonin agonist. The doctor said that reduced peristalsis is often associated with hyper mobility of which I do have some of, so am getting referred to rheumatology, not sure what could do about it however. My swallowing problems first started after a bout of glandular fever.
Have either of these medications helped anyone here or caused further problems. I’m always cautious of risks because they often get played down by mainstream medicine and it is not often recognised that ME patients can be more likely to be adversely effected by them.
Gastro has prescribed me a week of the antifungal Fluconazole for suspected Candida and a months trial of Prucalopride for poor oesophageal and gut peristalis (contractions that move food along).
Apparently Prucalopride can in rare cases give you headaches, I suffer from headaches anyway but they have been exacerbated by things like medications in the past which I had to stop as a result of that. Apparently it is a seretonin agonist. The doctor said that reduced peristalsis is often associated with hyper mobility of which I do have some of, so am getting referred to rheumatology, not sure what could do about it however. My swallowing problems first started after a bout of glandular fever.
Have either of these medications helped anyone here or caused further problems. I’m always cautious of risks because they often get played down by mainstream medicine and it is not often recognised that ME patients can be more likely to be adversely effected by them.