Ofatumumab
Common brands: Kesimpta, Vitamin D, Neurontin, Gralise, Gaba 300-Ezs
Top reporter: Novartis Pharmaceuticals Corporation
CD20-directed Cytolytic Antibody [EPC]Provitamin D2 Compound [EPC]Corticosteroid [EPC]Nonsteroidal Anti-inflammatory Drug [EPC]Alkylating Drug [EPC]
32,441
Total Reports
28,553
Serious Reports
750
Death Reports
30
Reported Reactions
Death Report Ratio: Moderate (2.31%)
Patient Demographics
Reported Adverse Reactions (30)
Side effects reported in FDA adverse event reports for Ofatumumab.
| # | Reaction | Reports | % of Total |
|---|---|---|---|
| 1 | FATIGUE | 5,478 | |
| 2 | HEADACHE | 4,593 | |
| 3 | PYREXIA | 3,534 | |
| 4 | PAIN | 3,524 | |
| 5 | CHILLS | 3,459 | |
| 6 | INFLUENZA LIKE ILLNESS | 2,850 | |
| 7 | NAUSEA | 1,791 | |
| 8 | MULTIPLE SCLEROSIS RELAPSE | 1,661 | |
| 9 | COVID-19 | 1,515 | |
| 10 | ASTHENIA | 1,477 | |
| 11 | MULTIPLE SCLEROSIS | 1,439 | |
| 12 | GAIT DISTURBANCE | 1,414 | |
| 13 | HYPOAESTHESIA | 1,379 | |
| 14 | FEELING ABNORMAL | 1,345 | |
| 15 | MALAISE | 1,340 | |
| 16 | DIZZINESS | 1,298 | |
| 17 | NASOPHARYNGITIS | 1,241 | |
| 18 | DRUG INEFFECTIVE | 1,215 | |
| 19 | PAIN IN EXTREMITY | 1,158 | |
| 20 | INJECTION SITE PAIN | 1,008 | |
| 21 | INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION | 980 | |
| 22 | COUGH | 979 | |
| 23 | FALL | 972 | |
| 24 | ARTHRALGIA | 965 | |
| 25 | URINARY TRACT INFECTION | 948 | |
| 26 | ACCIDENTAL EXPOSURE TO PRODUCT | 915 | |
| 27 | VOMITING | 909 | |
| 28 | BACK PAIN | 899 | |
| 29 | MYALGIA | 889 | |
| 30 | MUSCULAR WEAKNESS | 862 |
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.