Review: could Prazosin hydrochloride cause Ileal atresia?
Summary: there is no Ileal atresia reported by people who take Prazosin hydrochloride yet.
We study 298 people who have side effects while taking Prazosin hydrochloride from FDA and social media. Find out below who they are, when they have Ileal atresia and more.
You are not alone: join a support group for people who take Prazosin hydrochloride and have Ileal atresia >>>
Prazosin hydrochloride has active ingredients of prazosin hydrochloride. It is often used in post-traumatic stress disorder. (latest outcomes from 392 Prazosin hydrochloride users)
Ileal atresia (intestinal atresia (absence of a normal opening)) has been reported by people with depression, thrombosis, epilepsy. (latest reports from 26 Ileal atresia patients)
On Mar, 31, 2015: No report is found
Get connected: join our support group of prazosin hydrochloride and ileal atresia on
Do you have Ileal Atresia while taking Prazosin Hydrochloride?
You are not alone! Join a support group on :
- support group for people who take Prazosin hydrochloride
- support group for people who have Ileal Atresia
Drugs in real world that are associated with:
Could your condition cause:
- A study of drug interactions between Nuvigil, Prazosin Hydrochloride, Viagra, Vitamin D, Prednisone, Pravastatin Sodium, Lisinopril, Bystolic, Zolpidem, Vitamin C, Lexapro, Lorazepam, Hydrocodone Bitartrate And Acetaminophen for a 68-year old man with Tiredness, Ptsd, Erectile Dysfunction, General Physical Condition, Polymyalgia Rheumatica, High Blood Cholesterol, Blood Pressure Increased, Coronary Artery Disease, Sleep Disorder Due To General Medical Condition, Insomnia Type, Generalized Anxiety Disorder, Depression Suicidal, Anxiety Disorder, Chronic Pain. The patient has Tinnitus, Sleep Apnea, Erectile Dysfunction, Elevated Mood, Polymyalgia Rheumatica, Coronary Artery Disease, Major Depressive Disorder, Ptsd
- A study of drug interactions between Melatonin, Prazosin Hydrochloride, Magnesium Sulfate, Magnesium Citrate, Fish Oil, Vitamin D, Mirtazapine, Remeron, Remeron Soltab, Tryptophan for a 35-year old man with Sleep Lack Of (ptsd), In Conjunction With Remeron/mirtazapine To Block/prevent Nightmares, Lack Of Strength, Balance Disorder, Living Will, Depression. The patient has Spasms Of The Hands Or Feet, Weight Gain, Anxiety Disorder, Agitation, Vulnerable To Suggestion, Piss/crap Self, Abdominal Pain Lower, Hyperactive Sight, Smell And Sound Sensory, Slow Response To Stimuli, Blurred Vision, Black Outs/time Loss, Dizziness, Fainting, Pulmonary Embolism, Pulmonary Hypertension, Nightmares, Depression, Depression Suicidal, Suicidal Ideation, Poisoning
Recent Prazosin hydrochloride related drug comparison:
- Comparions of Zestoretic, Prazosin Hydrochloride for a 40-year old woman who has HBP & PTSD
- Comparions of Propranolol Hydrochloride, Guanfacine Hydrochloride, Prazosin Hydrochloride for a 52-year old man who has High Blood Pressure
- Comparions of Amlodipine Besylate, Minipress, Metoprolol Tartrate, Micardis for a 61-year old man who has Hypertension
- Comparions of Propranolol Hydrochloride, Prazosin Hydrochloride for a 52-year old man who has High Blood Pressure
- Comparions of Clonazepam, Lithium Carbonate, Quetiapine Fumarate, Warfarin Sodium, Prazosin Hydrochloride for a 40-year old woman who has PTSD
NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT considered.
WARNING: Please DO NOT STOP MEDICATIONS without first consulting a physician since doing so could be hazardous to your health.
DISCLAIMER: All material available on eHealthMe.com is for informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified healthcare provider. All information is observation-only, and has not been supported by scientific studies or clinical trials unless otherwise stated. Different individuals may respond to medication in different ways. Every effort has been made to ensure that all information is accurate, up-to-date, and complete, but no guarantee is made to that effect. The use of the eHealthMe site and its content is at your own risk.
You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).
If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.