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Table 4 TEAEs occurring in ≥ 10% of patients and any grade 3/4 TEAEs*

From: Evaluation of an alternative ruxolitinib dosing regimen in patients with myelofibrosis: an open-label phase 2 study

Preferred term, n (%)

Ruxolitinib (N = 45)

TEAEs

Grade 3/4 TEAEs

Any

42 (93.3)

17 (37.8)

Anemia

12 (26.7)

9 (20.0)

Fatigue

10 (22.2)

0

Arthralgia

9 (20.0)

0

Nausea

8 (17.8)

0

Thrombocytopenia

8 (17.8)

1 (2.2)

Dizziness

7 (15.6)

1 (2.2)

Abdominal pain

6 (13.3)

0

Cough

6 (13.3)

0

Diarrhea

6 (13.3)

0

Edema peripheral

6 (13.3)

0

Muscle spasms

6 (13.3)

0

Pain in extremity

6 (13.3)

0

Back pain

5 (11.1)

0

Contusion

5 (11.1)

0

Umbilical hernia

0

1 (2.2)

Cholelithiasis

0

1 (2.2)

Dehydration

0

1 (2.2)

Blood creatine phosphokinase increased

0

1 (2.2)

Blood triglycerides increased

0

1 (2.2)

Lipase increased

0

1 (2.2)

Hyperkalemia

0

1 (2.2)

Hypermagnesemia

0

1 (2.2)

Myelodysplastic syndrome

0

1 (2.2)

  1. TEAE treatment-emergent adverse event
  2. *Safety-evaluable population
  3. Myelodysplastic syndrome was the only grade 4 TEAE