Review: could Wellbutrin xl cause Posterior capsule rupture?
Summary: there is no Posterior capsule rupture reported by people who take Wellbutrin xl yet.
We study 11,492 people who have side effects while taking Wellbutrin xl from FDA and social media. Find out below who they are, when they have Posterior capsule rupture and more.
You are not alone: join a support group for people who take Wellbutrin xl and have Posterior capsule rupture >>>
Wellbutrin xl has active ingredients of bupropion hydrochloride. It is often used in depression. (latest outcomes from 13,319 Wellbutrin xl users)
Posterior capsule rupture
Posterior capsule rupture (tear in the posterior capsule identified at the time of surgery) has been reported by people with hypothyroidism, sinusitis, enlarged prostate. (latest reports from 26 Posterior capsule rupture patients)
On Apr, 28, 2015: No report is found
Get connected: join our support group of wellbutrin xl and posterior capsule rupture on
Do you have Posterior Capsule Rupture while taking Wellbutrin Xl?
You are not alone! Join a support group on :
- support group for people who take Wellbutrin xl
- support group for people who have Posterior Capsule Rupture
Drugs in real world that are associated with:
Could your condition cause:
- A study of drug interactions between Minocycline Hydrochloride, Zoloft, Wellbutrin Xl for a 42-year old woman with Bacterial Infection, Depression. The patient has Blood Clot In The Legs
- A study of drug interactions between Lexapro, Trazodone Hydrochloride, Wellbutrin Xl for a 47-year old woman with GAD, Sleep Disorder, Major Depressive Disorder. The patient has Vaginal Yeast Infection
- A study of drug interactions between Xanax, Singulair, Ultram Er, Triamterene And Hydrochlorothiazide, Nexium, Levoxyl, Wellbutrin Sr, Atenolol, Gabapentin for a 57-year old woman with Anxiety Disorder, Allergic Sinusitis, Fibromyalgia, Fluid Retention, Acid Reflux, Hyperthyroidism, Depression, High Blood Pressure, Meniers.
- A study of side effects of Wellbutrin for a 29-year old woman with Chronic Depression. The patient has Fluid Retention
- A study of drug interactions between Ibuprofen, Vascepa, Bupropion Hydrochloride, Venlafaxine Hydrochloride, Acetazolamide for a 62-year old woman with Headache, High Blood Cholesterol, Anxiety, Apprehension, Feeling Uptight, Jitters, Stress, Stress And Anxiety, Tension, Anxiety, Pseudotumor Cerebri. The patient has Hdl/cholesterol Ratio Decreased, Blood Triglycerides Increased, Hypercholesterolemia
Recent Wellbutrin xl related drug comparison:
- Comparions of Cymbalta, Wellbutrin Xl for a 37-year old woman who has Depression
- Comparions of Wellbutrin, Effexor Xr for a 54-year old woman who has Menopausal Symptoms
- Comparions of Adderall, Trazodone Hydrochloride, Wellbutrin, Lexapro for a 29-year old woman who has Depression
- Comparions of Brintellix, Remeron, Wellbutrin Xl, Lexapro, Paxil for a 40-year old man who has Depression
- Comparions of Hydrocodone Bitartrate And Acetaminophen, Quetiapine Fumarate, Rozerem, Bupropion Hydrochloride, Vivitrol for a 42-year old woman who has Overweight
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.