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Pulmicort

Ingredients: Budesonide
Average User Review Score
* Based on 207 reviews from across the web.
Wikipedia

Budesonide (BUD), sold under the brand name Pulmicort among others, is a steroid medication. It is available as an inhaler, pill, and nasal spray. The inhaled form is used in the long term management of asthma and chronic obstructive pulmonary disease (COPD). The nasal spray is used for allergic rhinitis and nasal polyps. The pills may be used for inflammatory bowel disease including Crohn's disease and ulcerative colitis.

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* Extracted from FDA Adverse Event Reports for all drugs with the same active ingredients.

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Druginformer Identified Side Effects: Somnolence, Bone loss, Adrenalitis

Posted By Anonymous in askapatient.com on July 11, 2015 @ 12:00 am

Side Effects: Bone loss, 3 inches in height. Fatigue, adrenal gland problems. When I first started taking it I asked dr about side effects. He said not to worry as I wouldn't be taking it t...

Druginformer Identified Side Effects: Scar

Posted By Anonymous in askapatient.com on February 26, 2015 @ 12:00 am

... daughter is diagnosed with asthma.attacks are sporadic the last one was a week ago,previous to that it was last August.the doctor has been asking is to give her pulmicort.extremely scared of the side...

Druginformer Identified Side Effects: Mental impairment, Weight decreased

Posted By Anonymous in askapatient.com on August 27, 2014 @ 12:00 am

Side Effects: Side effects my son experienced;aggressiveness,weight loss, fidgety, and unable to focus.

Druginformer Identified Side Effects: Dry mouth, Contusion

Posted By Anonymous in fdb.rxlist.com on June 15, 2014 @ 12:00 am

... been taking Pulmicort for several years now, and it has allowed me to keep my asthma under control where other medications failed. I am dealing with side effects such as dry mouth, bruising easy, and ...

Druginformer Identified Side Effects: Feeling abnormal, Aggression, Disturbance in attention

Posted By Anonymous in askapatient.com on February 21, 2014 @ 12:00 am

... pulmicort on and off for 2 years. I had always noticed aggressive behavior while taking it. He had just been on it for 2 weeks and his teacher made the comment to me today how "spaced out" he had been...

Druginformer Identified Side Effects: Aggression

Posted By Anonymous in askapatient.com on September 23, 2013 @ 12:00 am

Side Effects: My son too became very agressive on this. I wish I had discontinued it a long time ago because not only are his teeth stained but he is also in the 5th percentile for height. ...

Druginformer Identified Side Effects: None

Posted By Anonymous in askapatient.com on May 2, 2013 @ 12:00 am

Side Effects: great for short term use to help with breathing difficulties

Druginformer Identified Side Effects: None

Posted By Anonymous in askapatient.com on January 15, 2013 @ 12:00 am

Side Effects:

Druginformer Identified Side Effects: Adverse drug reaction, Rash, Weight increased

Posted By Anonymous in askapatient.com on August 19, 2012 @ 12:00 am

... I started the pulmicort, then the next doctors appointment (6 weeks later) I had gained 12 POUNDS 2 lbs per week when before I was gaining 3-4lbs per 6 weeks. Nothing in my diet changed except I now g...

Druginformer Identified Side Effects: Sleep disorder

Posted By Anonymous in askapatient.com on August 18, 2012 @ 12:00 am

... he get cold specially if he is going to start going to a day care si I don't know what to do ?? He was having some steroid twice a day but I didn't like it I notice changes no sleeping at night waking...


* 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.