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Table 5 TEAEs reporting in each treatment group during the initial 8-week treatment Period 1

From: A randomized placebo controlled clinical trial to evaluate the efficacy and safety of minocycline in patients with Angelman syndrome (A-MANECE study)

 

Placebo N = 12

Minocyclin 8 week N = 22

TEAEs – n° (%) patients

1 (8.3)

4 (18.8)

Number of TEAEs

1

4

Infection

1

 

Constipation

Diarrhea

 

1

Cutaneous alterations

 

1

Coloration dental

  

Nauseas

 

1

Edemas

Increase urine concentration

 

1

Serious adverse events – n° of patients (%)

0

0

TEAEs leading to treatment discontinuation N (%) patients

0

1 (4.5)a

  1. aVertiginous Syndrome.No alterations in laboratory test