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Bupropion Hydrochloride Related Crush Syndrome

Official FDA Reports0
Social Media Events3

  This report is for all products sharing this active ingredient. For more details, please use our Workbench for research on individual brands like Wellbutrin.


Explanation

The quarterly trend chart illustrates changing levels of adverse events over time. Results from both the FDA Adverse Event Database (AERS) and adverse events extracted from social media by Druginformer are plotted side-by-side for easy comparison.


List of Possible Side Effects Reported

Report Date Dosage Indication Outcome Country Gender Age Weight (lbs)

* DrugInformer calculates alarm using a proprietary algorithm. Alarm should not be taken as an ofiicial signal from the FDA or other regulatory entity.


Social Media Comments From Around the Web

The following are comments from users that experienced side effects while taking Milnacipran Hydrochloride

Wellbutrin Xl

Side Effects: Crushing , miserable, debilitating panic attacks. Slightly increased sex drive and improvement in SSRI related anorgasmia.

This was a painful experience. The only positive thin...


Source:" WELLBUTRIN XL: Side effects, ratings, ...

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Did the author experience crush syndrome while taking wellbutrin xl?

What is this?

Wellbutrin

... long as I can remember but didn't seek treatment until a couple of years ago. All of my life I never knew if I was going to wake up to severe, uncontrollable irritability, crushing sadness, or extreme...


Source:" WELLBUTRIN: Side effects, ratings, and...

View full report on drug related crush syndrome

Did the author experience crush syndrome while taking wellbutrin?

What is this?

Bupropion Hydrochloride

... a full blown manic episode with psychosis (detachment from reality, auditory hallucinations) requiring nightmarish week's stay in local psych ward. Followed by months of crushing depression so severe ...


Source:" EFFEXOR XR: Side effects, ratings, and...

View full report on drug related crush syndrome

Did the author experience crush syndrome while taking bupropion hydrochloride?

What is this?

Tell us about your Experience with Bupropion Hydrochloride Related Crush Syndrome

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Share Your Experience

Druginformer Identified Side Effects: Crying, Crush syndrome, Anorgasmia, Depression, Disability, Libido increased, Panic attack

Posted By Anonymous in askapatient.com on January 11, 2012 @ 12:00 am

Side Effects: Crushing, miserable, debilitating panic attacks. Slightly increased sex drive and improvement in SSRI related anorgasmia. This was a painful experience. The only positive thin...

Druginformer Identified Side Effects: Tremor, Constipation, Dizziness, Malaise, Tinnitus, Crush syndrome, Amnesia, Apathy, Dry mouth, Hyperhidrosis, Irritability, Loss of libido, Mood altered

Posted By Anonymous in askapatient.com on August 22, 2008 @ 12:00 am

Side Effects: Increased sweating,short term memory loss,decreased ability to concentrate,ringing in ears,tremors,dizziness,some decrease in libido,constipation,dry mouth I have had mood pro...

Druginformer Identified Side Effects: Feeling cold, Hypomania, Crush syndrome, Depression, Hallucination, auditory, Mania, Psychotic disorder

Posted By Anonymous in askapatient.com on November 17, 2006 @ 12:00 am

... are fallible. Beware. Now Dx of bipolar type 1 even though I'm 62 and never had mania before, nor has anyone in my family been bipolar. Due to mania, taken off Effexor cold turkey. Because I dropped i...



* Warning: The facts and figures contained in these reports are accurate to the best of our capability; however, our metrics are only meant to augment your medical knowledge, and should never be used as the sole basis for selecting a new medication. As with any medical decision, be sure to work with your doctor to ensure the best choices are made for your condition.

* About FAERS: The FDA Adverse Event Reporting System (FAERS) is used by FDA for activities such as looking for new safety concerns that might be related to a marketed product, evaluating a manufacturer's compliance to reporting regulations and responding to outside requests for information. Reporting of adverse events is a voluntary process, and not every report is sent to FDA and entered into FAERS. The FAERS database may contain duplicate reports, the report quality is variable, and many factors may influence reporting (e.g., media attention, length of time a drug is marketed, market share). For these reasons, FAERS case reports cannot be used to calculate incidence or estimates of risk for a particular product or compare risks between products.