Budesonide
Common brands: Pulmicort Flexhaler, Tarpeyo, Pulmicort Respules, Uceris, Eohilia
Top reporter: H2-Pharma Llc
Corticosteroid [EPC]Nonsteroidal Anti-inflammatory Drug [EPC]Proton Pump Inhibitor [EPC]Benzodiazepine [EPC]Provitamin D2 Compound [EPC]
57,446
Total Reports
27,593
Serious Reports
3,617
Death Reports
30
Reported Reactions
Death Report Ratio: High (6.30%)
Patient Demographics
Reported Adverse Reactions (30)
Side effects reported in FDA adverse event reports for Budesonide.
| # | Reaction | Reports | % of Total |
|---|---|---|---|
| 1 | DYSPNOEA | 6,478 | |
| 2 | DRUG INEFFECTIVE | 6,199 | |
| 3 | OFF LABEL USE | 5,989 | |
| 4 | ASTHMA | 4,768 | |
| 5 | FATIGUE | 3,534 | |
| 6 | COUGH | 3,252 | |
| 7 | HEADACHE | 3,149 | |
| 8 | DIARRHOEA | 2,787 | |
| 9 | CONDITION AGGRAVATED | 2,769 | |
| 10 | NAUSEA | 2,717 | |
| 11 | PNEUMONIA | 2,635 | |
| 12 | WHEEZING | 2,449 | |
| 13 | MALAISE | 2,245 | |
| 14 | PYREXIA | 2,179 | |
| 15 | PAIN | 2,172 | |
| 16 | WEIGHT DECREASED | 2,032 | |
| 17 | ARTHRALGIA | 1,829 | |
| 18 | DIZZINESS | 1,823 | |
| 19 | ABDOMINAL PAIN | 1,721 | |
| 20 | VOMITING | 1,707 | |
| 21 | PRODUCT USE IN UNAPPROVED INDICATION | 1,700 | |
| 22 | PRODUCT DOSE OMISSION ISSUE | 1,682 | |
| 23 | THERAPEUTIC PRODUCT EFFECT INCOMPLETE | 1,637 | |
| 24 | HYPERTENSION | 1,633 | |
| 25 | ASTHENIA | 1,626 | |
| 26 | RASH | 1,582 | |
| 27 | WEIGHT INCREASED | 1,552 | |
| 28 | LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES | 1,477 | |
| 29 | CHEST DISCOMFORT | 1,403 | |
| 30 | COLITIS ULCERATIVE | 1,388 |
Important Disclaimer
FDA adverse event reports are submitted voluntarily and do not prove causation. A reported reaction does not mean the drug caused it. Drugs with more users naturally have more reports. Always consult your doctor or pharmacist before making medication decisions.