Drug
Adalimumab-aqvh
Important: Reactions below are the flagged terms from this drug’s
FAERS report history (min. 3 co-reports per term) — PRR/ROR indicate
disproportionality in spontaneous reporting, not causation.
Data from FDA FAERS via openFDA. Last recalculated: 2026-09-14.
| Reaction | Co-reports (a) | PRR | ROR | Signal | |
|---|---|---|---|---|---|
| 1 | Device Malfunction | 28 | 90.1 | 126.3 | signal |
| 2 | Accidental Exposure To Product | 34 | 73.6 | 112.8 | signal |
| 3 | Product Packaging Quantity Issue | 3 | 59.4 | 61.3 | signal |
| 4 | Product Complaint | 6 | 52.0 | 55.3 | signal |
| 5 | Device Leakage | 10 | 51.1 | 56.8 | signal |
| 6 | Device Failure | 3 | 42.8 | 44.1 | signal |
| 7 | Device Defective | 3 | 40.1 | 41.3 | signal |
| 8 | Injury Associated With Device | 3 | 32.2 | 33.2 | signal |