Sinus bradycardia is found among people who take Hydrocortisone, especially for people who are male, 60+ old also take medication Furosemide, and have Prostate cancer . We study 15,694 people who have side effects while taking Hydrocortisone from FDA and social media. Among them, 43 have Sinus bradycardia. Find out below who they are, when they have Sinus bradycardia and more.
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Hydrocortisone has active ingredients of hydrocortisone. It is often used in addison's disease. (latest outcomes from Hydrocortisone 16,768 users)
Sinus bradycardia (an unusually slow heartbeat due to heart disease) has been reported by people with high blood pressure, atrial fibrillation/flutter, multiple sclerosis, depression, pain (latest reports from 7,548 Sinus bradycardia patients).
On Oct, 21, 2016
15,694 people reported to have side effects when taking Hydrocortisone.
Among them, 43 people (0.27%) have Sinus Bradycardia
* Approximation only. Some reports may have incomplete information.
** Reports from social media are used.
How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.
I had a TBI one year ago. Took out my pituitary. Focalin has been good. Was able to back off on hydrocort but had adverse reactions to. Kenalog nerve block (for migraine) and beta blocker. I had to self-diagnose. For those who have POTS there is a TVAM procedure that provides hope. We persevere in a medical area in which there is so little knowledge.
Last year in my ecg sinus bradycardia was detected. Although i am an active healthy male with no medications, my doctor ignored the situation saying it must be healthy for me. However recently i have noticed i have small level of erectile dysfunction. Is there anything i should do. Or is it just ...
ISN'T IT A MED. FACT THAT THE DOSE OF HYDRO CORTISONE NEEDS TO BE DOUBLED WHEN HAVING AN ACUTE INFECTION? DUE TO ADRENAL INSUFFICIENCY, I'VE TAKEN 30 MGS. DAILY FOR 5 DECADES. MY CURRENT, NEW PCP DENIED THIS.
I had a TBI one year ago. Took out my pituitary. Focalin has been good. Was able to back off on hydrocort but had adverse reactions to. Kenalog nerve block (for migraine) and beta blocker. I had to self-diagnose. For those who have POTS there is a TVAM procedure that provides hope. We persevere ...
Hi, have been on hydrocortisone for 15 years due to pituitary tumour discovered when 8 months pregnant - now been told have hypothyroidism and on Levothyorixne low dosage ....I have put on nearly 14lbs in 3 months ! Fed up being told these drugs are straight replacements
I'm glad to see I'm not alone in this! Thank you to whoever was active enough & cared enough to start this and get this information our so it becomes know. I'm a 40 yr old female that suffers from both CRPS + TOCS. I also suffer fromPolyendocrine Autoimmune Disorder (Addison' + Hashimoto's + ...
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