Ruxolitinib
Common brands: Jakafi, Opzelura, Jakafi Xr, Aspirin 325, Aspirin 81
Top reporter: Incyte Corporation
Janus Kinase Inhibitor [EPC]Kinase Inhibitor [EPC]Corticosteroid [EPC]Nonsteroidal Anti-inflammatory Drug [EPC]Platelet Aggregation Inhibitor [EPC]
69,262
Total Reports
39,069
Serious Reports
9,621
Death Reports
30
Reported Reactions
Death Report Ratio: High (13.89%)
Patient Demographics
Reported Adverse Reactions (30)
Side effects reported in FDA adverse event reports for Ruxolitinib.
| # | Reaction | Reports | % of Total |
|---|---|---|---|
| 1 | OFF LABEL USE | 13,948 | |
| 2 | DEATH | 6,288 | |
| 3 | FATIGUE | 5,973 | |
| 4 | ANAEMIA | 3,032 | |
| 5 | HAEMOGLOBIN DECREASED | 2,933 | |
| 6 | PLATELET COUNT DECREASED | 2,668 | |
| 7 | DIARRHOEA | 2,624 | |
| 8 | PRODUCT DOSE OMISSION ISSUE | 2,491 | |
| 9 | ASTHENIA | 2,485 | |
| 10 | DIZZINESS | 2,458 | |
| 11 | HEADACHE | 2,371 | |
| 12 | PRODUCT AVAILABILITY ISSUE | 2,276 | |
| 13 | PNEUMONIA | 2,113 | |
| 14 | NAUSEA | 2,086 | |
| 15 | DRUG INEFFECTIVE | 2,079 | |
| 16 | WEIGHT INCREASED | 1,951 | |
| 17 | DYSPNOEA | 1,944 | |
| 18 | PAIN | 1,807 | |
| 19 | PRURITUS | 1,728 | |
| 20 | SPLENOMEGALY | 1,722 | |
| 21 | MALAISE | 1,573 | |
| 22 | PYREXIA | 1,526 | |
| 23 | PLATELET COUNT INCREASED | 1,509 | |
| 24 | FALL | 1,488 | |
| 25 | CONTUSION | 1,479 | |
| 26 | PRODUCT DOSE OMISSION | 1,373 | |
| 27 | THROMBOCYTOPENIA | 1,337 | |
| 28 | WHITE BLOOD CELL COUNT INCREASED | 1,321 | |
| 29 | ARTHRALGIA | 1,297 | |
| 30 | DRUG DOSE OMISSION | 1,250 |
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.